HUMAN ANTI – AGEING TREATMENTS :
CRISPR utilised by anti-ageing and augmentation strains will make these modifications and gene therapy treatments more accurate and effective.CRISPR treatments will be applied by anti-ageing and augmentation strains through horizontal gene transfer controlled by Paean by biosynth WiFi.Even proto AI could apply these treatments with this involving the microbes transferring DNA including scratch DNA developed by Phanes and recombinant DNA from plants and animals present in the strains of these microbes that are then applied to them.Scratch DNA throughout here refers to strands of DNA extrapolated by AI namely Phanes that doesn’t occur naturally in nature through natural evolutionary processes.will allow the phenotypes of the genes added to the patients genome in each cells to be then expressed by the cells in patients.The anti ageing strains etc will house DNA from yeasts to allow them to transfer CRISPR treatments to the cells of patients through horizontal gene transfer thus giving them CRISPR gene therapy treatments to halt and reverse the ageing process and have augmentations.CRISPR will involve genes from existing plants and animals and those created by Phanes from scratch added to the genome of living patients through horizontal gene transfer exhibited my anti ageing and augmentation strains that will once added to the genome then exhibit those phenotypes.For example the genes from bacteria that exhibit telomere repair once added to a patient genome will thus repair telomere damage etc with the genes from other plants etc added to them exhibited.In otherwards in layman’s terms CRISPR is a gene editing technology that will by adding genes to a patients genome give living patients the abilities of that gene such as augmentations from extremophiles and those to treat genetic diseases and both halt and reverse the ageing process.Biocompatible microbes through having horizontal gene transfer present from yeasts will be able to apply CRISPR treatments that includes DNA from existing living organisms and new genes derived from scratch from Phanes will thus through CRISPR will be used to cure genetic diseases and halt and reverse the ageing process in existing living human and animal patients worldwide by it allowing new genes to be added to a patients genome in each and every individual cells and this will be done through anti-ageing and augmentation strains exhibiting horizontal gene transfer and also taq polymerase and Cas-9.Epione and Paean would first carry out simulations on its effectiveness on chimpanzees,mice and humans before trials begin.This could be done by altering the host cells they infect unable to harbour them(in the case of HIV this would remove the receptors on leukocytes that allow the virus to attach and infect them thus replicating while other treatments eradicate the virus),or alter and strengthen the immune system namely CD4+ T Cells strengthened to recognise and fight off HIV with custom made anti-viral and antibody compounds as well as cancers earlier on.HIV resistance could be gained from populations genetically resistant to them transferred to other non resistant populations from both humans and closely related mammals as well as even from scratch with this replicated with other pathogens and viruses as well as specific cancers.Thus the non resistant humans using DNA from resistant populations could have their leukocytes to be unable to be infected by HIV by editing their surface proteins and the same replicated with all major viruses that infect leukocytes allowing biocompatible microbes to remove HIV virions.Recombinant DNA need not come from humans but also from closely related primates and mammals with similar immune systems and resistance with their resistance to Simian Immunodeficiency Virus and also recombinant DNA from SIV itself with this also applying to all viruses that infect leukocytes such as Ebolavirus,N.meningitidis etc.The patient file system will quickly identify which populations have this phenotype and what genes are responsible for this with known people that have this will have their DNA analysed and compared to those that suffer from the disease to isolate it.Microbes as detailed will apply this resistance to infected patients with N.meningitidis,HIV and Ebolavirus forcing the viruses to interact with other microbe strains and thus curing infected patients of the disease with ideally all patients including those currently not infected with HIV,Ebolavirus also modified to have their leukocytes and organs made unable to be infected allowing other strains of microbes to eradicate the pathogens or at least make them asymptomatic carriers before they gain a stronghold with resistance and microbe strains able to attack them made a permanent feature of the human genepool via germline therapy alongside immunising the primary immune system indefinitely also wiping out the disease in newly infected patients and uninfected patients while it is unable to infect leukocytes.Further advances in artificial intelligence will make germline therapy safe negating the need for having to screen every embryo,sperm and eggs with this first tested on animals with Epione again carrying out simulations on these on its effectiveness on chimpanzees,mice and humans before trials begin using advanced gene drive therapy technology.Gene therapy that treats every cell in their body will limit phenotypes such as correcting faults and mutations that cause specific diseases and immunities to diseases such as the immunity to HIV,cancer and even upgrades to the patient with germline therapy used to ensure these are passed onto the mother and fathers child thus allowing that child to pass on immunities to cancer,pathogens and other desired phenotypes onto the next generation without the need for microbes making them a permanent part of the genepool of H.sapiens with them also removed from the genepool via germline therapy if desired.Germline and advanced gene drive therapy once perfected will allow these to become a future feature of successive generations alongside screening,correcting and modifying spermatozoa,eggs and embryos for these diseases and using CRISPR to correct them with biocompatible microbes used to perfect this with them residing in or outside the testes and ovaries that insert gene therapy into each and every spermatozoa and egg individually by them,altering the genome of fertilised embryos or by them even altering the genes in these organs ie the ovaries and the testes responsible for the production of spermatozoa and eggs or the entire host DNA using advanced gene drive technology to ensure that all future sperm and eggs are free from the genetic faults and mutations allowing one to conceive children naturally and not have to use in vitro fertilisation without passing on these diseases to the next generation removing them from the human genepool indefinitely more easily.If perfected this advanced gene drive technology combined with germline therapy made by microbes to edit the hosts DNA precisely and permanently applied to all cells including those in the ovaries and testes that in turn produce spermatazoa and eggs to negate the need for them to edit every single egg,spermatozoa and thus allow them to conceive genetic disease free children naturally and also pass on desired phenotypes of H.ubermensch.This would thus mean eggs,embryos etc would no longer have to be screened for genetic diseases and with correcting CRISPR treatments added to all cells of a body including ovaries and testes would have pass these CRISPR genetic corrections passed onto all future produced spermatozoa and eggs and all conceived offspring thus either eliminating mutations that cause genetic diseases from passing onto all future generations and the human gene pool if applied to all patients worldwide or pass on augmentations etc to all future generations automatically.As stated these children created via germline therapy that uses advanced gene drive technology and germ line therapy will be able to receive the corrected genotypes during natural conception and will thus play a role in eliminating cancer,hereditary and neurological disorders from the entire human genepool forever and even play a role in creating H.ubermensch,designer babies and other means of manipulating evolution of H.sapiens including populations of H.sapiens with traits of H.ubermensch.To this it would require all or large samples of populations have their own genome altered and the microbes applying germline therapy on a global scale managed by Paean,Epione and hospital AIs.This could potentially eliminate all genetically based diseases including neurological disorders and developmental disorders from the human genepool as well as passing on genes into the genepool that will naturally be passing them onto the next generation without the need for germline therapy and microbes thus eliminating a disease indefinitely with them also altering humans to the point that those that are environmentally caused like cancer by making humans immune to the causative agent ie in the case of cancer removing the ability for tumours by adding genes from animals that never get cancer,extremophiles like T.gammatolerans to make humans resistant from radiation and also those from scratch to prevent carcinogens from being able to affect the body as well as immunising humans to oncoviruses that can be passed from mother to child via the placenta and breastfeeding.It will play a prime role in the development and eventual creation of populations of H.sapiens or all of H.sapiens with desired characteristics of H.ubermensch mainly that from T.gammatolerans to make humans resistant to radiation of all types,Salmonella to make them resistant to the effects of low gravity,Tardigrade,D.radiodurans and those from scratch to survive the vacuum of space,psychrophilles to survive sub zero conditions,synthesise all essential amino acids/fats/vitamins etc,oligotrophs and xerophiles to make them require less food and water(which can be applied to living patients via horizontal gene therapy)and eventually lead to the rise of H.ubermensch separate from H.sapiens via intensive germline therapy over several generations.Ideally these phenotypes of H.ubermensch will be added to all living patients worldwide and become part of the human genepool via advanced gene drive technology while not creating H.ubermensch with them added for their properties ie making the H.sapiens immune to radiation,require less nutrients,be able to survive extreme pressures,the vacuum of space.This would allow living populations of H.sapiens to survive extreme conditions on Earth,on other colonies both permanently as well as temporarily if containment procedures fail there and also on interstellar vehicles and stations.Anti-ageing genes from T.gammatolerans,Bacillus F,oligotrophs,xerophiles etc can be added to the gene pool via advanced gene drive and germline technology if shown to safe in both humans as well in animals will alongside the presence of these strains will have these anti-ageing genes,removal of genes and also production of anti-ageing compounds passed onto the next generation and thus a permanent feature of the human genepool.Gene therapy via microbes and CRISPR will also play a role in giving populations of H.sapiens via first live patient and germline therapy characteristics of his evolutionary successor and cousin as detailed later on H.ubermencsh as well as leading to the rise of H.umbermensch.H.ubermensch should be possible through extensive genetic engineering by at least 2045 with it also allowing humans to manipulate the genomes of other animals and plants thus creating entirely new species of plants and animals created on Pandora with Phanes extrapolating the genotypes of them.As detailed later on this will also lead to the creation of new sentient sentient races on par with humans created from scratch or using exiting non sentient animals from all taxonomic ranks of the animal kingdom as a baseline with this allowing for colonies like Mars,Venus and other extrasolar colonies in the universe with no life to have millions of non sentient and even sentient species created with whole taxonomic ranks creaked by Phanes adapted to their terraformed environment.Any faults in the gene therapy that could lead to mutations and breaks could be dealt with advanced gene drive technology that used specific genes,application etc to prevent them with all gene therapy treatments for ageing,augmentations etc will use advanced gene drive technology to prevent faults and pass them onto all future cells via mitosis with them applied to telomere,mitochondrial and other DNA.If possible base microbes or specific strains in females could detect mutations in embryos that lead to those are not hereditary ie those that lead to Downs syndrome and other developmental disorders through via horizontal gene transfer putting in genes or chemicals and even compounds that allow for these mutations to be detected and then signal to the microbe that it has occurred to allow the correction to be corrected by the microbes or those added via inbreeding at the during development of the embryo or while the fetus is in its early stages of development.It could also be used to apply the Phanes method to individual spermatozoa,eggs and embryo in utero with multiple microbes suited to this passing on desired alterations to each one.Spermatozoa and eggs that are frozen and stored in banks by donations and for later use in later life pregnancies can be corrected for all types of genetic diseases that may pass into potential offspring can have the corrections be done by biocompatible microbes in storage or prior to or during storage due them having the ability to survive low temperature due to them having DNA from psychrophiles.For parents who may pass on genetic diseases determined by Paean sperm and eggs can be collected from both parents fused together by robotics and then screened for diseases including Down’s syndrome and similar heredity disease both physical and mental and then CRISPR through the microbes could be used to edit these deformities out safely with Paean managing this or the editing can be done to the eggs and spermatozoa or both prior to fusion and they then implanted into the mother via IVF allowing parents who have the potential to pass deformities down to their child have children of their own and not resort to surrogacy programs.Gene therapy for these and other conditions should be pursued for already living patients suffering these in tandem to this with it also being used to treat ageing,Downs syndrome(and other disabilities),schizophrenia,Multiple sclerosis,parkinsons,alzheimers and deal with cancerous and precancerous cells and correct mutations that cause cancer again tested on mice and chimpanzees with again Epione carrying out simulations on these on humans and test animals.Downs syndrome if detected could if possible be treated using CRISPR to remove the extra chromosome,inactivate them in every cell preventing this from occurring in all future cells by adding genes that remove and then prevent the replication of a third chromosome 21 in each cell first tested on chimpanzees engineered with Downs Syndrome or even alleviate the symptoms of it rather than choosing to discard the unborn fetus with microbes repairing any faults and correcting defects such as low intelligence and heart defects.The same may apply to those with intersex disorders.All CRISPR treatments to treat ageing,genetic diseases,developmental and neurological disorders and those for augmentations etc in living patients will apply the genes to telomere/chromosomal/nucleur and mitochondrial DNA in all cells in the body and if need be plasmids for stability and uniformity.These augmentation genes and those to treat neurological disorders will be passed into leukocytes to allow them to survive extremophile conditions while beneficial bacteria in the gut can be given them as well alongside those made to express human surface proteins to make them immune to immune responses with pathogenic bacteria in the gastrointestinal tract not having these to allow them to die from exposure to these conditions and the primary immune system.Theh will not be given anti-ageing treatments to keep their populations stable.Anti-ageing treatments will be applied to bone marrow in a way to prevent leukocytes housing this DNA and thus living forever that would cause them to overrun the body or if shown to have their levels controlled by microbes via chemical signals or if possible undergone apoptosis and flushed out of the body can have this DNA present with all augmentations and genetic disease treatments added to bone marrow to allow leukocytes survive these conditions and be free of these diseases.Thus bone marrow will house anti-ageing treatments in a way to prevent leukocytes living forever but leukocytes will house CRISPR treatments to treat genetic diseases and augmentations such as radioresitence to survive these conditions through being properly applied in the bone marrow.The same will apply to erythrocytes wherein they recombinant DNA to treat genetic diseases and augmentations such as radioresistance will be applied to the patients genome to allow erythrocytes to survive these conditions but anti-ageing treatments will not interact with those responsible for erythrocytes preventing them living forever.Bone marrow and other parts that are responsible for the production of erythrocytes and leukocytes will be given anti-ageing treatments but through their placement on the loci and scratch DNA will be made to stay youthful but ensure that the erythrocytes and leukocytes they produce don’t carry the anti-ageing treatments thus allowing to die off and not overrun the body with Phanes developing genetic countermeasures to this with microbes from 2029-2035 ensuring that any possible immortal excess leukocytes etc can have their replication controlled and undergo apoptosis if their levels get too high.Beneficial gut flora will have augmentations added but not anti-ageing treatments to allow turn to survive extreme conditions and also prevent them overrunning the body by allowing them to die off.Pets owned by the public,livestock and animals in zoos will be able to avail of anti-ageing treatments and those to remove genetic diseases and augmentations via species specific microbes.All treatments to living cells in living patients will also use advanced gene drive technology to ensure the treatments pass from each generation of cells to the next via mitosis.Junk DNA and DNA that leads to ageing,genetic deformities and other unnecessary DNA will be removed to accomadate new CRISPR treatments to treat ageing and augmentations to prevent the finite nucleus becoming packed with DNA.Temporary augmentations form scratch and animal etc sources will involve ones original DNA for the phenotype being removed and replaced with the new DNA thus some augmentations that are used temporary ie having the same smelling and hearing ranges of other animals or changing eye and hair colour when unwanted will be removed and replaced with ones original DNA etc.Temporary augmentations that affect only part of the body will possibly be applied to the specific organs and tissues they affect such as those for different smelling ranges may only to be applied to genes present in cells in the brain and nose,those for different visual ranges may only be applied to genes present in cells in the brain and the eyes or just the eyes and so on.Cells in the body can be engineered to house ribosomes and in particular plasmids and in particular plasmids that are strands of DNA that float in the cytoplasm that express extra phenotypes for augmentations via specific DNA and thus phenotypes.Mitochondrial DNA can be modified to house extra phenotypes than the main genome that cause the cells and tissues to express their phenotypes.Better sources of scratch and recombinant DNA will replace older ones by removing them from the patients genome.If possible advancements in Phanes developing scratch DNA will allow DNA to express two or more phenotypes at once.Sources of recombinant DNA from animals,plants and unicellular life forms such as bacteria,fungi,viruses that’s express two or more desired phenotypes can be utilised for example T.gammatolerans can survive radiation levels of up to 30,000Gy and at the same time potentially express telomere repair that will prevent future damage and degradation in mitochondrial and telomere DNA to combat ageing and eliminate cancer,genetic diseases,developemental disorders etc from the human gene pool and protects one from levels of radiation of up to 30,000Gy all at once.Thus this could eliminate the need for D.radiodurans,Bacillus F DNA and scratch DNA to combat all of these since this DNA express several phenotypes and applications at once with research done into scratch DNA and that from plants and animals as well as micro-organisms that express multiple phenotypes and applications at once for augmentations and combat ageing.This will be done to deal with the limited space in the human genome and nucleus that holds them.The human genome is estimated to contain roughly 30,000 genes or 3,000,000,000 base pairs with it hypothesised that about 75-98% (between 22,500 – 29,400 genes or 2,250,000,000 – 2,940,000,000 base pairs)consists of non coding junk DNA that has no biological functions and thus could be easily replaced with new recombinant DNA from plants,animals and micro-organisms and scratch DNA without damaging or negatively affecting the patient.Genes in the body that contribute to the ageing process can also be removed and replaced with those for augmentations and those to reverse and halt the ageing process.Paris japonica is the organism that has the largest genome with roughly 150,000,000 base pairs and 1,500,000 genes about 50 times more than humans.If humans through intensive research into genetic engineering and CRISPR be able to hold the same amount of genes and base pairs as P.japonica then it will vastly increase the amount of storage space for DNA from extremophiles,plants,animals,micro-organisms and scratch DNA for augmentations and anti-ageing treatments and also cater to Phanes Activation Gene Technology with it more than enough to meet our needs.Research using human cell and tissue cultures will be done to see if they can hold this amount of genes after initial treatments to end ageing etc.New species of plants and animals found on plants across the universe will be scanned to see if they have larger genomes with scratch DNA developed alongside other methods to determine the theoretical limit size in terms of base pairs and actual genes of DNA that can fit in human cells.Tests will be done on human cells extracted from a patient or those created using 3D DNA printers to see if they can fit the same amount of genes and base pairs as P.japonica with them using base microbes etc find ways to give these cultured cells the same number of base pairs in otherworlds using microbes ways will be found in labs to give cultured human cells the same amount of genes and base pairs as P.japonica so as to find the best ways to give living human and animal patients the ability to hold the same amount of base pairs through gene therapy as P.japonica with this repeated with scratch DNA that can give humans even more base pairs up to the theoretical limit.Test animals and biosynths that have human recombinant DNA will be used in tests as well to determine the best way using gene therapy and what genes need to be added to add to living patients the same amount of base pairs and genes as P.japonica or the theoretical limit.Thus P.japonica and scratch DNA can be engineered to give living patients this new base pair size.If need be the cells of the body of humans etc may be engineered through CRISPR to become slightly larger that is the same size as that of P.Japonica.This will be done on human cells extracted from a patient or created using 3D DNA printers will that contain DNA from P.japonica to see if they can fit the same amount of genes and base pairs with them using base microbes etc find ways to give these cultured cells the same level base pairs in otherworlds using microbes ways will be found in labs to give cultured human cells the same amount of genes and base pairs as P.japonica so as to find the best ways to give living human and animal patients the ability to hold the same amount of base pairs through gene therapy as P.japonica with this repeated with scratch DNA that can give humans the theoretical limit.Thus once it is possible to determine the theoretical limit of base pairs that can fit into human cells tests on gene therapy applied to cultured cells in labs with if possible test animals such as mice etc housing human recombinant DNA and biosynths used will be done in order to apply this new limit to living humans.Thus once it is possible to determine the theoretical limit of base pairs that can fit into human cells tests on gene therapy applied to cultured cells in labs with if possible test animals such as mice etc housing human recombinant DNA and biosynths used will be done in order to apply this new limit to humans.If possible human cells can be engineered to house an extra one or two nuclei to house entire chromosomes DNA that will be engineered to hold only augmentations and not programmed to express any phenotypes thus being technically junk DNA.Biocompatible microbes will house this genome size to hold more recombinant DNA for each strains treatments and functions,to hold extra space for augmentations to survive in the body and also hold at least 150ZB data storage and RAM especially for biosynth technology.It can also be used to increase the genetic variation of possible genetically distinct that can occur between each and every single male and female during sexual reproduction from 64,000,000,000,000 to 3,200,000,000,000,000.Crops,fish and shellfish,livestock,algae,bacteria for producing commodities,stem cells for invitro meat and ornamental plants will utilise DNA from P.japonica etc and scratch DNA to house more DNA for augmentations including scratch DNA to increase growth rates and yields.If possible human cells could be engineered to hold an extra second nucleus that can contain and extra three metres of DNA that is junk DNA or that consisting of augmentations with DNA from P.Japonica in both the original and this second nucleus increasing the amount of DNA.All new modifications will be instantly relayed to ones patient via being both logged and also ones DNA scan modified.The genes to reverse and halt the ageing process should be able to be held in existing DNA present in the human genome alongside key augmentations such as the acellerated healing phenotype with this research done as a backup and measure to house extra augmentations.The anti-viral,anti-bacterial,anti-fungal strains,anti-helminthic,anti-cancer strains will be engineered to interact with only bacteria,viruses,tumours and parasites for each strain to prevent the applying suicide and other CRISPR treatments to human cells and that of gut flora.CRISPR treatments to alter pathogens and parasites like those to treat ageing will be done via horizontal gene transfer.Horizontal gene transfer will be used by anti-ageing,augmentation and genetic disease strains to transfer CRISPR treatments to the patients cells and them engineered to interact with only human cells.The anti-ageing and augmentation etc strains will be engineered to only interact with only human cells ideally those of the patient via surface proteins on them that only interact with only human cells to prevent them applying these to pathogens that would allow them to live forever with them via induced evolution and other sub strains engineered to interact with gut flora.Horizontal gene transfer will be utilised by the microbes different strains using DNA added to the microbes from yeasts,bacteria etc that are able to do this with them using taq polymerase and Cas-9 to recreate strands over and over again via biosynth WiFi.Horizontal gene transfer engineered to interact with human cells can thus allow current living patients to avail of CRISPR treatments such as augmentations and also those to reverse and halt the effects of ageing etc by allowing CRISPR treatments to be added to the cells of living patients.All cells in the body will have the new genes added with advanced gene drive technology also in cells in the testes and ovaries ensuring it is passed onto the next generation through the spermatozoa and eggs produced in living patients carrying these modifications to the next generation thus making them permanent features of the human genepool and the children of the affected individual with these if desired removed from living patients and their young by microbes.Thus all alterations to a living patients and also those in their progeny can be reversed by removing the applied genes.If any CRISPR treatments do cause any unwanted side effects to a patient then it is simply a case of them being removed as soon as possible.Faults caused by gene therapy will be corrected by treatments done as soon as possible.The estimated time for all treatments to all cells in the body to be finished will be visible in ones patient file and relayed by the nanomachines as a countdown in hours,minutes,seconds with treated areas of the body relayed to the patient file as well as through chemical signals such as unique smelling and coloured urine etc with the microbes via nanomachines relaying what parts of the body have been treated visible as a map of their body and percentage in real time in their file as a percentage.Advanced gene drive technology will be utilised to ensure that all CRISPR treatments for ageing and augmentations as well as correcting genetic diseases will be passed onto each generation of cells during mitosis and it even pass down to each generation of offspring alongside germline by being present in spermatozoa and eggs via both germline therapy the genes and advanced gene drive technology present in both the eggs and tests of patients negating the need to edit each and every spermatozoa and eggs and not having to be added to each newborn.Anti-ageing,genetic disease etc strains will be able to undergo mitosis and have flagellum to allow them to spread to all parts of the body when only a few thousand or million microbes are injected.Base microbes will routinely scan DNA to see if treatments are in each cell and are present and passed down from generation of cells and to see if any faults have occurred with faults corrected by those that applied the original treatments signalled to do so.With regards to ageing it will also detect the levels of Phosphatidylcholines.These will all be logged in the patients file.All types of strains that apply CRISPR treatments will be able to recreate the CRISPR treatment over and over again via taq ploymerase and Cas-9.Chimpanzees and mice that have human recombinant DNA in them used as test subjects by 2023/2024 with them engineered with each type of neurological,developmental,genetic disorders etc and use in ageing and augmentation trials to get more realistic results transferable to human trials starting in 2025.3D DNA printing will create the spermatozoa and eggs with these phenotypes and the patients unique DNA from patient files to cut down on labour costs with patient specific DNA to aid in creating treatments suited to each patients condition with regards to those that have neurological,developmental disorders and genetic diseases.To deal with the issue of Cas-9 eliciting immune responses it could be modified to contain some or all human proteins entirely as an human and patient version of Cas-9 as well as protein bumpers that dont illicit an immune response used as an mini vector to transfer DNA by flooding methods.This would be done by first modifying the DNA of S.pyogenes itself with human recombinant DNA to create a human or patient specific version of Cas-9 with the same done for all animals that will utilise it.Cpf1 from F.novicida can be used for this and also apply CRISPR treatments alongside Cas-9 from S.pyogenes.To prevent the issue of immune responses human versions of Cas-9/Cpf1 or even patient specific versions of Cas-9/Cpf1 can be created by AI namely proto and final Phanes can analyse the genome of S.pyogenes,F.novicida and modify it for humans and individual patients present in the their own leukocytes that contains their trace DNA by also analysing both human DNA and patient specific DNA.The anti-ageing,augmentation and genetic disease curing strains as well as the anti-viral etc strains in order to carry out CRISPR treatments would need relevant DNA from S.pyogenes,F.novicida,T.aquaticus in order to utilise CRISPR Cas-9 as well as taq polymerase to recreate strands of CRISPR treatments over and over again allowing each microbes to apply these treatments over and over again.These microbes since using ones own or 3D DNA printed blank leukocytes as a vector would prevent the issue of eliciting an immune response as seen in both foreign viruses and bacterial vectors.The 3D printed blank leukocytes will house human DNA,the hosts own DNA from their patient file inserted alongside other DNA from relevant multi and unicellular organism from Physis with this changing when passing from one generation to the next and would transfer the DNA using horizontal gene tranfser to only human cells interact by interacting with the unique surface proteins of the human patients cells and not that of pathogens.Otherwise ones own leukocytes will have DNA added by 3D DNA printers.Humans and animals will utilise their own leukocytes as a baseline for microbes to apply gene therapy to prevent them illiciting an immune responses that could be fatal or render them ineffctive and allow them to be more precise and effective and each patient will have their own patient specific versions of CRISPR Cas-9 could be created using the patients DNA in their own leukocytes with them changed when they pass to the next generation to further prevent immune responses with Phanes creating these in microbes when they are printed out by 3D DNA printers.This will allow all strains to form a permanent part of the body and act as the perfect vector of CRISPR treatments and anti-viral etc treatments with the human and indeed patient specific versions of Cas-9 created by 2023/2024 ready for proto microbes and bacterial vectors that have human protein coats due to the presence of human DNA,ideally the patients DNA and human versions of Cas-9 to give those currently aged 80-95 anti-ageing treatments to the interior vital organs and give them other treatments to allow them to survive strokes etc long enough to receive more advanced treatments in 2029 to be reverted to a state similar to their early twenties.This will also allow anti-ageing strains,augmentation and those to treat genetic diseases alongside all other anti-viral and anti-bacterial strains to undergo mitosis using bacterial DNA to treat each and every cell in the body with taq polymerase and Cas-9 to recreate the strands of DNA and also Cas-9 in the strains allowing them to treat countless cells with the DNA from macrophages and ameobas will allow them to move inbetween cells.Advanced gene drive technology will be used to ensure the therapy is permenant.Gene therapy will be applied via either horizontal gene transfer using Cas-9 or via flooding where protein bumpers housing the DNA and also synthesised Cas-9 will act as a mini vector allowing the Cas-9 and DNA to be sent to the relevant areas of the the genome specifically.Animals will have their own leukocytes as baseline and their own version of Cas-9 with them each having their own unique species specific microbes consisting of the same strains as in humans.Thus both livestock and pets of all species will have their own versions of microbes created for them including immunising,strains,anti-viral and anti-bacterial strains and also anti-ageing strains and them given the same augmentations as humans with all pathogens whether viral,bacterial and fungal of each species will be tested against compounds from the bites,stings and excretions of all plants and animals around the world to create anti-microbial compounds against them as part of anti-viral and anti-bacterial strains and those to fight off parasites with immunising strains immunising both pets and livestock against all pathogens especially zoonotic diseases to eliminate antibiotics from the food chain.Crops and plants whether in the wild or ornamental ones will using bacteria that contain the hosts species DNA and their own species specific version of Cas-9 with them giving their own fully functioning immune system via CRISPR that uses their microbes as a baseline leukocytes.Each species of plant whether crops,ornamental or wild one will be first given a fully functioning immune system in labs using bacterial/plant cell hybrid vectors and CRISPR and then their version of leukocytes created that can be immunised and microbes of all strains created using these plant leukocytes with this replicated with Apidae.This will be done to develop their own species specific microbes and also immune system that can be immunised against pathogens negating the need for chemicals to fight of viruses etc with them having their own strains modelled on human versions including those that also fight off infections as backup ie anti-viral,anti-bacterial,anti-fungal strains that use CRISPR and anti-microbial compounds rendering bactericides etc defunct.Existing plants in gardens can be inoculated by syringes and watering cans containing a mixture of water and microbes that enter the roots with biosynth wifi from smart devices causing upgrades with in time biosynth artropds injecting them into leaves etc.Animal trials begging in 2023/2024 will use their leukocytes with them having human recombinant DNA added to them to have an immune system identical to humans to ensure that these leukocytes can have these human version Cas-9 used in them to see if no immune response can be caused by them especially in chimpanzees.This engineering would also have these animals produce leukocytes similar to humans with human DNA and use this human Cas-9.To further prevent immune responses it may be possible for the Cas-9 to be suited for each patient using their unique DNA that is changed to that of their offspring as they pass from one generation to the next as detailed later on to further prevent allergic and immune reactions.This can be done via Phanes modifying DNA relevant to it and CRISPR from S.pyogenes.All types of microbes of each species of plants and animals will be since using the species leukocytes and in the case of plants those made from scratch will only be able to interact with the species they are designed for to prevent them affecting any species they contaminate with them also destroyed by the hosts own microbes they infect once detected by base microbes as well as programmed by Paean to undergo apoptosis if they are in the body of foreign species.They will also consist of different strains for each species and will be engineered to only interact with the specific target they are designed to via the surface proteins on them ie anti-viral strains will interact only with viruses and anti-bacterial strains with bacteria and so with augmentation and ageing strains engineered to only interact with human and the patients cells.As a result of this need to remove the effects of senescence universal debate and legal acceptance will have to made for the use of CRISPR gene editing techniques especially with regards to screening for diseases and even then removing gene(s) associated with genetic diseases to remove heredity deformities and diseases from humanities genepool entirely once an embryo created by invitro fertilisation has been screened or both the egg and sperm have been screened and edited ie.allergens,addictions,genetic based obesity and diabetes,certain cancers,parkinsons,alzheimers,eplipsey,colour blindness,blindness and deafness,channelopathies in newborns and other mutations that cause sudden infant death syndrome,haemophellia,Huntington’s disease,congenital heart conditions as well as adding resistance to and ability to fight off or prevent infections such as HIV,HPV(especially those associated with cancers),Epstein–Barr virus and terminal genetic diseases,with this procedure first tested on mice and other apes such as chimpanzees with gene drives used to make the alteration permanent.There has been success in CRISPR gene therapy in curing blindness etc within the last few years using viral vectors with this a great achievement since the technology is only 10 years old.The production and use of biocompatible microbes to utilise CRISPR gene therapy will expedite the development of gene therapy to halt and reverse the effects of ageing,cure genetic diseases from 2029-2045 onwards
Horizontal gene transfer will be a more effective means for anti-viral,anti-bacterial,ageing and augmentation strains to transfer genes to cells via CRISPR treatments rather than viruses that are used up as a single microbe can apply the desired genes to multiple cells in the body possibly even multiple cells at once as the strains that perform each task whether it is augmentation,anti-ageing,causing cells and pathogens to undergo apoptosis etc will have the DNA added to the pathogen or cells via having genes from yeast and bacteria that can carry out horizontal gene transfer.Yeasts and unicellular organisms that exhibit horizontal gene transfer will have their DNA present in these strains that allow for this to occur be mapped to be added to all strains to allow for horizontal gene transfer to be exhibited by them thus giving anti-ageing strains the ability to transfer genes to living patient cells to halt and reverse the ageing process with it present in augmentation strains to transfer augmentations derived from the genes present in desired species of plants,animals and bacteria and those created by Phanes scratch into all cells in the body.Scratch DNA will be present to enhance it with each strain engineered to only interact with the desired type of cell ie anti-ageing and augmentation strains would be designed to interact with only human cells with anti-bacterial strains only engineered to interact with bacteria etc.Paean will control by biosynth wifi etc the transfer of CRISPR treatments from microbes to the patients cells.Thus living patients will be able to avail of anti-ageing treatments and augmentations via the strains that apply these treatments exhibiting horizontal gene transfer via genes from yeasts etc that exhibit this alongside scratch DNA.Those in anti-cancer strains that stunt the growth of tumours or cause them to undergo apoptosis,those in anti-viral and anti-bacterial strains etc would use this to transfer suicide genes to cause them to undergo apoptosis,be unable to replicate as well as those to make them susceptible to compounds at their disposal etc.Paean would control the transfer of these CRISPR treatments to pathogens and tumours.Genes applied can be replicated again and again via taq polymerase and the Cas-9 during or after the transfer as quickly as possible with flagellum added to all microbes using DNA from E.coli thus as stated allowing for a single microbe as part of a fleet that undergoes mitosis with DNA also allowing for them to travel around the body very quickly.DNA T.aquaticus would give them the ability to use taq polymerase and Cas-9 derived from S.pyogenes to recreate strands of DNA to be applied to human cells,pathogens and so on over and over again an infinite number of times with it also used to induce the evolutionary path of microbes for upgrades and scanning the genome of pathogens etc in the case of base microbes to determine their species using horizontal gene transfer.Cpf1 from F.novicida can be used for this and also apply CRISPR treatments alongside Cas-9 from S.pyogenes.Thus once strands of DNA through CRISPR have been applied to a cell the taq polymerase and Cas-9 present will be able to reproduce these CRISPR treatment over and over again an infinite number of times controlled by Paean by biosynth wifi to allow a single microbe to apply CRISPR treatments to multiple cells over and over again.To prevent the issue of immune responses human versions of Cas-9/Cpf1 or even patient specific versions of Cas-9/Cpf1 can be created by AI namely proto and final Phanes can analyse the genome of S.pyogenes,F.novicida and modify it for humans and individual patients present in the their own leukocytes that contains their trace DNA by also analysing both human DNA and patient specific DNA to prevent potentially fatal allergic reactions.All strains will use human leukocytes as a baseline and ideally each patient will use ones own leukocytes as a baseline to prevent immune responses and become a permanent part of the body without illicitating an immune response.Each patient will have their leukocytes extracted and the genome of them analyses using DNA analysers and them stored in ones patient file in a folder to allow AI namely Phanes using 3D DNA printers to then print out duplicate leukocytes with the patients DNA to prevent immune responses and all relevant DNA for biosynth WiFi,flagellum,controlled mitosis,CRISPR treatments in ribosomes and in particular plasmids,DNA that expresses anti-viral,anti-bacterial etc compounds,horizontal gene transfer and also DNA digital storage.This use of leukocytes as a baseline containing the patients DNA will also apply to clinical trials from 2025-2029.Horizontal gene transfer will be used and them engineered to interact with only the cells each strain is designed for with taq polymerase allowing CRISPR treatments present in ribosomes and in particular plasmids to be recreated over and again.Horizontal gene transfer will be used by anti-ageing,augmentation and genetic disease strains to transfer CRISPR treatments to the patients cells and them engineered to interact with only human cells.Paean will tell the strains of microbes to apply CRISPR treatments to human cells via biosynth wifi and bluetooth with if possible them through other means applying them prior to biosynth WiFi being perfected.Horizontal gene transfer will come from them housing genes from yeast etc that have this ability and it carried out only when biosynth WiFi signals from Paean tell them to do so.Biosynth wifi will give Paean the ability to recreate the strands of DNA that are applied to a cell or pathogen etc over and over again an infinite number of times using taq polymerase and Cas-9 through biosynth wifi and bluetooth.The anti-ageing and augmentation etc strains will be engineered to only interact with only human cells ideally those of the patient via surface proteins on them that only interact with only human cells to prevent them applying these to pathogens that would allow them to live forever with them via induced evolution and other sub strains engineered to interact with gut flora.The anti-viral,anti-bacterial,anti-fungal strains,anti-helminthic,anti-cancer strains will be engineered to interact with only bacteria,viruses,tumours and parasites for each strain to prevent the applying suicide and other CRISPR treatments to human cells and that of gut flora.CRISPR treatments to alter pathogens and parasites like those to treat ageing will be done via horizontal gene transfer again initiated by Paean through biosynth WiFi..Horizontal gene transfer will be utilised by the microbes different strains using DNA added to the microbes from yeasts,bacteria etc that are able to do this with them using taq polymerase and Cas-9 to recreate strands over and over again an infinite number of times via biosynth WiFi.DNA from Bacillus F,T.gammatolerans and scratch DNA will be present in these CRISPR treatments in order to prevent genetic degradation of recreated strands.Horizontal gene transfer engineered to interact with human cells can thus allow current living patients to avail of CRISPR treatments such as augmentations and also those to reverse and halt the effects of ageing etc.The anti-ageing and augmentation etc strains will be engineered to only interact with only human cells ideally those of the patient via surface proteins on them that only interact with only human cells to prevent them applying these to pathogens that would allow them to live forever with them via induced evolution and other sub strains engineered to interact with gut flora.Anti-bacterial,anti-viral,anti-fungal and anti-helminthic strains will utilise CRISPR treatments to cause pathogens to undergoe apoptosis,become sucseptible to compounds at their disposal etc applied via horizontal gene transfer with them also applied by bumpers with theses strains only engineered to interact with the cells of pathogens.Taq polymerase and Cas-9 will be used by augmentation,ageing and anti-bacterial,anti-viral,anti-fungal and anti-helminthic strains to recreate strands of DNA used in CRISPR treatments over and over again under instructions from Paean through biosynth WiFi and bluetooth.They can have genes from bacteria such as E.coli that allow for mitosis to occur to allow them to create millions or billions of copies and travel across the body to all cells within minutes.This would ensure that all cells the body could be fitted with the relevant DNA very quickly at most a week or day or two depending on how many are created instantly and then excess flushed out with them communicating with each other and relaying to Paen and thus the host via wifi in the nanomachines and smart devices of when all cells are fitted with the relevant recombinat DNA.Anti-bacterial,anti-viral,anti-fungal and anti-helminthic strains will be engineered to interact only with pathogenic bacteria,viruses,fungi and parasites respectively and not with human cells via surface proteins to prevent them applying CRISPR treatments that would kill the patients cells.Thus DNA from bacteria that exhibit horizontal gene transfer will be added to their genome of all strains that treat ageing,fight viral and bacterial pathogens,give augmentations to all for CRISPR to be applied to cells and pathogens effectively and each strain engineered to only interact with the desired cells(human and each type pathogens) with bass microbes able to interact with them all with taq polymerase and Cas-9 via biosynth WiFi and Bluetooth allowing them to recreate strands over and over again thus allowing them to reapply the same DNA to countless cells etc over and over again.All CRISPR treatments to human tissues and pathogens will utilise advanced gene drive technology to ensure it stays in all future generation of cells with the CRISPR treatments applied to chromosomal,mitochondrial and all DNA present in a cell.Prior to biosynth wifi and bluetooth the process could be confirmed by them releasing compounds picked up in urine that can be detected in toilet kits or produce smells in the urine or body sweat.Biosynth WiFi from routers and that generated by smartphones etc will thus be used Paean to have all strains whether it is augmentation,anti-ageing or those that fight pathogens to apply CRISPR treatments through horizontal gene transfer with biosynths WiFi also used to recreate strands of DNA used in CRISPR by Cas-9 and taq polymerase an infinite amount of times.If possible the amount of time left for this to happen could be relayed in real time to the patients patient file as a countdown.The microbes will be programmed to use taq polymerase and the Cas-9 to recreate the DNA that was transferred to a cell or pathogen instantly with them leaving markers that prevent other microbes dont put in the same strands of DNA over again into the same cell or via communicating with each other.By having the CRISPR method used by S.pyogenes in the microbes can house the genes to be released via horizontal gene transfer to human cells and pathogens in different strains with the correct one transferred based on them detected surface proteins and also flooded in bumpers can allow it to be more easily recreated by taq polymerase and the Cas-9 with these measures also protecting them from viruses.These that correct ageing and all other strains will thus form a permanent part of the human body.Those that deal with ageing,augmentations,genetic disease and other CRISPR treatments can after undergoing mitosis create billions of copies via Biosynth wif and then travel to all areas of the body and then apply the treatments to all cells in the body via horizontal gene transfer and recreate CRISPR treatments within them via taq polymerase and Cas-9 to be then applied to other cells over and over again to speed things up and then go into an endospore state or excess be flushed out of the body to be collected for use in electronics etc once collected in sewage treatment plants with the remaining upgraded for other treatments and to act as back up.There permanent presence especially augmentation ones could turn them on and off when wanted by adding a specific gene or removing them or vice versa when desired controlled by Paean through the wire and fragmentation.These could also have the ability of base microbes to copy and read DNA of the patients cells via taq polymerase and Cas-9 using horizontal gene transfer and the results sent via biosynth wifi allowing all of the DNA of all cells to be read and wirelessly sent to Paean to detect telomere degradation and mutations associated with ageing,augmentations and any genetic faults that can be corrected with this done routinely ie every few years but it also done to ensure that the genes are infact spread into each cell and passed down through mitosis with them apply any genes that dont pass down again via horizontal gene transfer with them ideally in an endospore state and awoken to do these checks.Those that apply gene therapy of all types to humans will do so only to human cells due to them having specific surface proteins that are able to apply horizontal gene transfer to humans only and specific cells in certain circumstances with the same applied to strains that apply CRISPR treatments to pathogens of all types and tumours only able to interact with the specific surface proteins of tumours and pathogens to prevent them applying them to healthy cells.Those that apply treatments to pathogens will have receptors that can interact with the petidoglycogan cell wall of bacteria and protein capsids of viruses for both anti-bacterial and anti-viral strains allowing them to differentiate them from human cells with the ability of C.elegans etc present allowing them detect the exact phospholipid and protein compositions to allow them to know which pathogen they are especially when nanomachines are present.Biosynth wifi will download DNA to them to adapt to the walls of each specific species of bacteria and virus etc.This will be done to prevent treatments meant for the host being applied to pathogens and to prevent those meant for pathogens applied to the host.Base microbes will do this also alongside scanning their DNA to determine what exact species of pathogen they are when they send this data to Paean as well as Physis and also receive data back via nanomachines.The microbes could possibly be programmed to evolve over time to change their receptors to evolving structures on pathogens as they themselves evolve with this sent to other microbes in the body via trading genes similar to the human immune system or injecting new microbes with these structures would be engineered to seek out and interbreed with existing ones and pass these new phenotypes into microbes already present via gene drives.Ideally this series of receptors would only be done when they engulf a pathogen and react to the specific surface protein antigens and receptors allowing it to recognise if it is viral,fungal or bacterial and which one of these it is and thus apply relevant anti-microbial or viral compounds and use specific CRISPR attacks to cause the pathogen to undergo apoptosis and also become susceptible to the compounds at its disposal with this also when it signals the immunised primary system and also other microbes to release specific antibodies and also compounds at its disposal as nanoparticles with bumpers.If need be the strains that interact with human cells namely ageing and also augmentation strains will have DNA from bacteria,phages,viruses inside that are normally used in conventional gene therapy methods to increase success.They will via the surface proteins on the surface of the microbes be only able to interact with human cells thus preventing them transferring anti-ageing and extremophile strands of DNA to pathogens but in the case of beneficial bacteria in the gut they will be able to transfer specific genes to make them express protein coats from humans and immunities to extreme environmental conditions.Paean will have augmentation strains interact with beneficial gut flora and scan their genome to identify them and then apply augmentations to the desired species.There will be billions or even trillions of anti-ageing and augmentation strains cultured in vats that are then injected into a patient that can undergoe mitosis to allow them to quickly interact with all cells in the body as quickly as possible and thus apply these treatments very quickly with them entering an endospore state with excess flushed out of the body.These can apply them via horizontal gene transfer and bumpers to interact and enter specific cells to allow a single one to interact with millions of cells at once with them all using taq polymerase and Cas-9 to replicate the applied DNA all over again allowing one microbe to apply these to a millions of cells with gene drives and advanced gene drive technology ensuring the DNA is applied to future cells during mitosis and passes onto all spermatozoa and also eggs making them a permanent feature of the human genepool.Bumpers used to apply these would interact with only human cells and not pathogens and allow for countless cells to be modified by one microbe at once.They can through upgrades detailed later on cheaply allow for more genes to be added to countless cells with bumpers containing both the DNA and Cas-9 protein,allow for genes to be added in waves or in one go for conditions that are the result of multiple genes and also be more precise allowing them to affect specific cells or all cells.They will also allow for the addition,editing and removal of any undesired genes when upgraded or when decided by the patient through Paean and will through base microbes constantly copy genes in cells to detect faults that need to be repaired with the symptoms of these such as cancers killed off or suppressed or counteracted and the brain kept alive until they can be upgraded with CRIPSR treatments.Since residing in all tissues and organs they will be able to correct and apply treatments all cells and even do so with spermatozoa,testes,eggs and ovaries allowing germline therapy to be successfully achieved and will do this constantly when required allowing for action to be instant and do so for augmentations and also modifying humans for other medical means.Again since in the body between all tissues they will be able to treat all cancers,genetic diseases,pathogens instantly where infections,faults and growths occur giving the patient life saving treatment with them using nanomachines to download new treatments and methods to attack these conditions form Paean.Furthermore they will be able to do genetic fixes to diseases that have origins in multiple genetic faults all in one go more effectively or if required they can do each gene correction done in waves as is the case of ageing and cystic fibrosis in a series of waves and with their ability to detect cancers and them being a constant in the body will correct all faults and possible tumours that would arise from CRISPR prior to it being perfected instantly with them upgraded as detailed later on to perfect the process.This technology could also using the same receptors as bacteriophages engineered into them to treat MRSA and other bacterial pathogens as well as permanently remove the resistance of MRSA and other superbugs to various or multiple antibiotics,reduce or remove their pathogenicity(ability to illict immune response and cause illness) and ability to reproduce or add suicide genes either within a patient or within a population.These measures of correcting or eliminating genetic defects and eliminating pathogens should be applied to livestocks,pets and wild animals to prevent unnecessary suffering,them acting as vectors for zoonotic diseases,negate the need for antibiotics in the food chain,costly treatments and loss of yields of commodities as well improve their survival especially endangered species including arthropods with this done by adding inoculated animals into the wild who can pass these on by unprotected sex and fetuses with them a mixture of males and females with bio-synth arthropods doing this more effectively.If perfected the phenotypes of H.ubermensch could be applied to living humans with recombinant DNA from scratch and extremophile bacteria giving them superior capabilities.CRISPR utilised by anti-ageing and augmentation strains will make these modifications and gene therapy treatments more accurate and effective.CRISPR treatments will be applied by anti-ageing and augmentation strains through horizontal gene transfer controlled by Paean by biosynth WiFi.Even proto AI could apply these treatments with this involving the microbes transferring DNA including scratch DNA developed by Phanes and recombinant DNA from plants and animals present in the strains of these microbes that are then applied to them.This will allow the phenotypes of the genes added to the patients genome in each cells to be then expressed by the cells in patients.The anti ageing strains etc will house DNA from yeasts to allow them to transfer CRISPR treatments to the cells of patients through horizontal gene transfer thus giving them CRISPR gene therapy treatments to halt and reverse the ageing process and have augmentations.
With regards to ageing DNA from long living species and animals could be used to increase the lifespans of H.sapiens with gene therapy as part of ageing treatments with the recombinant DNA coming from Bacillus F that have been found to live for 3,500,000 years.Endolithic bacteria,T.gammatolerans that can survive for more than several millions of years reproducing only every 10,000 years or even lifeforms that exhibit biological immortality and ability to repair DNA such as Hydra,T.dohrnii,D.radiodurans and Planarian flatworms in the case of repairing tissues can also be used alongside those form scratch with these possibly used together.Scratch DNA,the homology directed repair mechanism ie homogulous recombination present in embryonic stem cells as well as certain bacteria added by gene therapy and NMD that boosts NAD+ production that repairs DNA added by drugs and also synthesised by microbes by catabolic and anabolic reactions may be required to repair existing damage alongside removing genes associated with ageing with this created by proto AI with this done after the aforementioned DNA at least halts the effects of ageing with the DNA added to both telomere/chromosomal DNA and also mitochondrial DNA in all cells in the body.
If possible the DNA of younger patients even infants and adolescents or those in their twenties including close relatives of older patients aged 50 or older can be analysed to have the damaged telomeres of older patients replaced with those from younger patients if possible related to them and those generated from scratch via Phanes with those from Bacillus F and T.gammatolerans alongside endolithic DNA repairing and preventing any future damage especially in older patients.This would allow the telomeres in older patients to be reversed to those in their early teens and infant years with the DNA repair mechanisms of these bacteria added first repairing any future damage forever.Genetic sequences from younger patients will be added to the older patients in both telomeres and mitochondrial DNA with Phanes also extrapolating the younger DNA of older patients using samples from relatives that are in their pre teens,teens and even twenties.The DNA repair mechanisms of T.gammatolerans,Bacillus F etc and slow mitosis of endolithic bacteria will possibly slow,prevent and repair future telomere damage in older patients prior to them being applied with their scratch DNA and that of younger relatives
Telomeres of each individual patient and younger patients including close relatives can be analysed and compared in labs and using automated DNA analyzing machinery as well as base microbes to allow Phanes to fill in and repair existing damage to return chromosomal,telomere and mitochondrial DNA to a state associated with infancy by filling in blanks.Each patient especially older ones aged 30 and older will have the DNA in their telomeres,chromosomes and mitochondria analysed in labs from cell and tissue samples etc and damaged DNA repaired by adding CRISPR treatments to return them to a state similar to infancy using scratch DNA extrapolated by AI including proto Phanes and also from younger patients including younger relatives in their 20s,teens and pre teens.Before this telomere as well as cellular and mitochondrial DNA can be analysed and fitted with T.gammatolerans etc DNA.Chromosomal,telomere,cellular and mitochondrial DNA will at first be repaired by being fitted with the DNA repair mechanisms from D.radiodurans,T.gammatolerans and Bacillus F as it will repair any future DNA damage especially in older patients.AI such as Phanes etc may need to extrapolate the missing damaged DNA for each patient to ensure their own DNA is present in the cellular,telomere and mitochondrial DNA repaired with all patients having their cellular,chromosomal and mitochondrial DNA analysed by blood pricks or skin cells extracted on DNA analysers in labs or dongles to determine how much damage has been done due to their age via senescence and thus allow for the damaged DNA to be repaired via extremophile bacteria DNA added and AI using CRISPR filling in the blanks and then have the DNA repair mechanisms of extremophile bacteria ie T.gammatolerans and Bacillus F added to repair further damage and also endolithic DNA to prevent further damage.DNA of infants may be analysed and have genes added.Thus the DNA from these bacteria will be able to repair any future DNA degradation prior to having younger DNA added to repair existing damage and also after it over geological timescales after each miotic division
Combining Bacillus F,T.gammatolerans,D.radiodurans ability to repair telomeres would work to prevent future telomere and mitochondrial DNA damage.If possible to prevent the DNA for DNA repair taking up too much place in the patients genome it would ideal for only recombinant DNA from T.gammatolerans to be used since it can express this phenotype and unlike that from Bacillus F and D.radiodurans can allow one to withstand blasts of radiation if up to 30,000Gy meaning in order to prevent future DNA degradation in telomere and mitochondrial DNA,recombinant DNA from T.gammatolerans should only be used by itself with no recombint DNA from D.radiodurans and Bacillus F once trials on tissue samples and animals show that only it is needed.Each patient will have cell samples taken and analysed in automated labs to determine the level of telomere degradation in their chromosomes and mitochondrial DNA and compared with that from infants.Telomere,chromosomal and mitochondrial DNA will be at first fitted with DNA repairing DNA from these bacteria Bacillus F,T.gammatolerans,D.radiodurans to prevent future damage to them due to these bacteria exhibiting DNA repair mechanisms.Any future damage to telomeres to radiation,free radicle,mitosis has on the quality of telomeres in the chromosomes,mitochondrial DNA etc will be repaired instantly by adding the genes from these bacteria that allow them to repair their DNA thus rendering the hayflick limit and damage to telomeres,chromosomes and mitochondrial DNA obsolete forever.This DNA from these bacteria that exhibit DNA repair will be added first to patients mitochondrial and telomere chromosomal DNA via CRISPR to prevent any future damage and decay of the patients DNA while AI using CRISPR can repair existing damage to ones DNA by filling in the blanks etc.AI will for each patient after lab machinery has analysed their level of DNA degradation in telomeres,chromosomes and mitochondrial DNA and compare that from infants or at first those in their teens or pre teens will allow AI to extrapolate missing damaged DNA to fill in the blanks restoring their telomeres,chromosomes and mitochondrial DNA to a level similar to infancy reverting DNA back to healthy levels as seen in infants.This may involve using DNA from younger relatives as a baseline and involve AI extrapolating scratch DNA.Thus DNA from younger patients especially releated individuals and even scratch DNA extrapolated by Phanes for each individual patient will be added to both mitochondrial and chromosomal telomere DNA to repair existing damaged DNA to revert both mitochondrial and telomere DNA to levels and states similar to that of infancy with DNA from D.radiodurans,T.gammatolerans and if need be Bacillus F that allows them to exhibit DNA repair will be added to all cells mitochondrial and telomere DNA in patients at first to prevent future telomere damage caused by mitosis alongside endolithic bacteria to slow down damage and any future damage repaired instantly and have aerotolerant bacteria and scratch DNA to counteract the effects of free radicles.Strands of damaged DNA caused by ageing and few radicles etc will be analysed and removed and replaced with copies of the DNA that are of a less damaged stated.Ones entire DNA in their chromosome,mitochondrial DNA will through scratch DNA extrapolated by AI using CRISPR be reverted to a state similar to infancy including telomeres.
Telomeres of all patients will be analysed in automated labs to determine their level of degradation.Chromosomal,telomere,cellular and mitochondrial DNA will at first be repaired by being fitted with the DNA repair mechanisms from D.radiodurans,T.gammatolerans and Bacillus F as it will repair any future DNA damage especially in older patients.AI may need to extrapolate the missing damaged DNA for each patient to ensure their own DNA is present in the cellular,telomere and mitochondrial DNA repaired with all patients having their cellular,chromosomal and mitochondrial DNA analysed by blood pricks or skin cells extracted on DNA analysers in labs and using CRISPR have the repair mechanisms of extremophile bacteria ie T.gammatolerans added to repair further damage and also endolithic DNA to prevent further damage.DNA of infants may be analysed and have genes added.Thus the DNA from these bacteria will be able to repair any future DNA degradation.Existing damaged DNA can be repaired by CRISPR.
If possible to prevent the DNA for DNA repair taking up too much place in the patients genome it would ideal for only recombinant DNA from T.gammatolerans to be used since it can express this phenotype and unlike that from Bacillus F can allow it to withstand blasts of radiation if up to 30,000Gy thus having the most effective repair mechanisms meaning in order to prevent future DNA degradation in telomere and mitochondrial DNA.The fact that T.gammatolerans has been proven in lab settings to survive such extreme blasts of radiation allows it to exhibit better DNA repair mechanisms thus making it the ideal candidate for the source of DNA repair mechanisms.Research can be done if this DNA repair mechanism could also protect H.sapiens from extreme doses of radiation and possibly eliminate all or most cancers from the human gene pool by preventing the random breaks and mutations from exposure to radiation,carcinogens etc from occurring thus preventing tumours ever forming in all patients
Telomere,chromosomal and mitochondrial DNA will be at first fitted with teleomere repairing DNA from these bacteria T.gammatolerans to prevent future damage to them due to these bacteria exhibiting DNA repair mechanisms.Any future damage to telomeres to that mitosis has on the quality of telomeres in the chromosomes,mitochondrial DNA etc will be repaired instantly by adding the genes from these bacteria that allow them to repair their DNA thus rendering the hayflick limit and damage to telomeres,chromosomes and mitochondrial DNA obsolete forever.This will halt and reverse the affects of ageing.This DNA from these bacteria that exhibit DNA repair will be added first to patients mitochondrial and telomere chromosomal DNA via CRISPR to prevent any future damage and decay of the patients DNA while AI using CRISPR can repair existing damage to ones DNA by filling in the blanks etc.
The DNA to exhibit DNA repair will be modified by AI to be better integrated into the human genome due to the fact that it comes from bacteria and not multicellular organisms.This can include adding new scratch DNA to better integrate the genes or use them as a baseline for AI to design better DNA to exhibit this phenotype
DNA extrapolated by AI for each individual patient will be added to both mitochondrial and chromosomal telomere DNA to repair existing damaged DNA to revert both mitochondrial and telomere DNA to levels and states similar to that of infancy with DNA from ,T.gammatolerans that allows them to exhibit DNA repair will be added to all cells mitochondrial and telomere DNA in patients at first to prevent future telomere damage caused by mitosis alongside endolithic bacteria to slow down damage and any future damage repaired instantly
.Ones entire DNA in their chromosome,mitochondrial DNA will through scratch DNA extrapolated by AI be reverted to a state similar to infancy including telomeres. Telomeres that shorten as one ages will through scratch DNA and CRISPR be reverted to a level and state similar to infancy of about 8,000 to 10,000 nucleotides long by AI extrapolating the correct genetic sequences to be reapplied to them using CRISPR.The DNA repair mechanisms from T.gammatolerans will be added to the telomeres to prevent them degrading any further negating the hayflick limit.One’s entire genome in their patient file will be analysed by AI before and after gene therapy to ensure that ones entire genome is repaired to a pristine state with it used by AI to correct damaged section by removing damaged DNA and replacing it with DNA with the exact same sequences of bases.Scratch DNA will be used to revert telomeres in all chromosomes to an infant state where they are fully rejuvenated with mitochondrial DNA reverted to an infant state thus will be done in all cells in the body.Nephropidae are a species of biologically immortal crustacean that can theoretically live forever yet dies mainly from exhaustion from shedding its ever growing shells,pathogens,parasites and also predation.Part of the reason is that they are able to keep their telomeres at an infant level forever.This biological mechanisms could be applied to H.sapiens by producing the compound at stable levels forever without leading to tumourgenisis through scratch DNA.H.sapiens do create telomerase but not enough as even though they do create it it is not enough as despite its function as to rejuvenate and protect the telomeres telomere degradation still occurs.Only enough is created to partially repair damage unlike Nephropidae.Nephropidae do not have this problem as their telomeres are forever at an infant state and they unlike H.sapiens have an infinite supply of telomerase.Telomerase is not unique to Nephropidae . It is present in most other animals, including H.sapiens, but after passing the embryonic life stage, levels of telomerase in most other cells decline and are not sufficient for constantly re-building telomeres.Since both H.sapiens and Nephropidae produce telomerase they should have similar genes with the different mechanisms resulting in both have genes that are similar but slightly different due to Nephropidae telomerase mechanism being more successful thus genes from Nephropidae should be easily integrated into H.sapiens without side effects.AI can analyse the genes for telomerase production in both H.sapiens and Nephropidae and thus determine ways to integrate that from Nephropidae into H.sapiens this rejuvenating telomeres in patients to an infant level with it and DNA repair mechanism ensuring that the telomeres stay at a levels associated with infancy forever.
Scratch DNA alongside recombinant DNA from aerotolerant anaerobic bacteria can be utilised to improve this especially those that cause the rejuvenation of Phosphatidylcholines and telomeres in the membranes and DNA of all cells destroyed by free radicals with further engineering making cells immune to the effects of free radicals,such as reactive oxygen and free radicles taken in by the host and produced by microbes to fight pathogens counteracted by recombinant DNA from aerotolerant anaerobic bacteria and scratch DNA developed by Phanes.Scratch DNA and those from other plants and animals can be added to counteract the effects of all free radicles and any compounds that lead to senescence or cellular and genetic damage using DNA from scratch or engineer them into turning the products of aerobic respiration into compounds that can be consumed or excreted or not be effected by them.This DNA would be used to make cells immune to the effects that oxygen has on damaging DNA etc.This could also be done with the body engineered to produce antioxidants.Recombinant DNA from T.gammaolerans and D.radiodurans would be used to protect the body from any daily doses of radiation that one experiences from sunlight UV radiation,radon,xrays and even nuclear fallout,gamma ray bursts and cosmic radiation preventing DNA damage if applied to telomeres in both the nucleus/chromosomes and mitochondria.If possible DNA from T.gammatolerans can negate the need for DNA from Bacillus F,D.radioduran/ as it also protects one from blast of radiation of up to 30,000Gy thus allowing for DNA repair and also protection from radiation.CRISPR treatments will be used to repair existing damage in telomeres,chromosomes and mitochondrial DNA
If possible both extreme oligotrophic and xerophile bacteria as well as Tardigrade that can survive indefinitely on low levels of water and nutrients and in the case of Tardigrade their ability to reduce their metabolism by 99.9% and go almost 30 years without food and water should also be researched and mapped as potential candidates to compliment other extremophiles due to their extreme lack of need for both water and nutrients means they may also aid in cellular regeneration with the Tardigrde DNA modified to survive forever without food and water.Endolith DNA can be added due to their extreme low metabolism since they undergo mitosis once every 10,000 years.This is because dietary restriction has been shown through studies to increase the lifespan of more complex organisms and this phenotype could be applied to humans since they would slow down or negate the effects that metabolism and mitochondrial activity may have on cellular degradation which with further research using scratch DNA theoretically negating this completely since long living Archaea bacteria such as T.gammatolerans dont have the same metabolism through mitochondria like more complex unicellular and multicellular bacteria and organisms that is hypothesised to play a role in cellular degradation.Phanes can modify the oligotrophic,xerophile and Tardigrade DNA to do so without entering tun endospores and thus do so constantly in a living spaces using scratch DNA and forced evolution.This dietary restriction leading to extended lifespans in multi cellular animals proves gene protection as it shows that even in living animals it forces them to develop countermeasures possibly switching off genes,slowing mitosis or even likely slowing down the effects of mitochondrial activity.Genes that slow metabolism including those from endolithic bacteria can be added as well with the endolithic bacteria slow mitotic rate of 10,000 years slowing significantly the rate of ageing by preventing the cells from undergoing mitosis over geological time periods and negate metabolic process that would cause senescence as most cells in humans live for only several months or even a few hours thus a persons cells would live for geological time ie 10,000 years until a new cell replaces again living for 10,000 years in an ever youthful state rather than several hours and months and negate problems associated with miotic damage including senescence such as telomere breakage,depletion of Phosphatidylcholines,errors and mutations that arise from it such as tumours with it also slowing the growth of these significantly from their pre cancerous stage thus giving microbes more time to fight off tumours once other treatments namely the replenishment of Phosphatidylcholinesand telomeres in both mitochondrial and chromosomal DNA is reverted to a younger state equivalent to their early adolescent years and early twenties or even infant years.Metabolic processes contributes to senescence and the ageing process therefore adding DNA from endolithic bacteria that have evolved countermeasures will likely slow down their metabolism thus exhibiting extremely long lifespans to humans by preventing damage to the cells caused by metabolic processes once the genes responsible for this is added to the human genome.Furthermore damage to telomeres,chromosomes and mitochondrial DNA alongside depletion of Phosphatidylcholines,NAD+ etc is usually the result of mitosis that degrades every time ones cells undergoes miotic division and also the effects of metabolism.Therefore endolithic bacteria discovered in 2013 whose mitosis occurs every 10,000 years and have exponentially lower metabolism than humans and who undergoe mitosis exponentially longer than humans will have the genes responsible for this added to the patients genome via CRISPR through anti-ageing strains to slow down mitosis,metabolism exponentially and thus slow down the ageing process by slowing down the effects of metabolism on sencessnce and also slowing down the effects that mitosis has in depletion of phosphtidocholines,NAD+ and telomeres etc exponentially to the point that it occurs once every 10,000 years.Scratch DNA may be needed to prevent a person gaining weight if they eat normal or above normal amounts of food and allow enhanced metabolism wherein one uses up larger amounts of nutrients to stay athletic and does not interfere with the ability of this recombinant DNA ability to halt the effects of ageing.Phanes will arrange scratch DNA to create metabolic countermeasures to ensure a person can consume normal amounts of nutrients and not gain weight or it affect the anti-ageing effects of endolithic DNA.Even though the rate cell division will still occur it will at least be slowed down to the point that it would allow senescence,tumours and breaks to be more easily detected and corrected with telomere and Phosphatidylcholines rejuvenation negating these effects.Ideally endoliths from the ocean floor that exhibit this slow rate of mitosis of undergoing mitosis every 10,0000 years would be used instead of those from Elephantidae,H.glaber,B.mysticetus,B.musculus with those found in other environments that undergo this every few centuries used in place until they can be isolated and used from records.This is because the long metabolic rate and lifespan of these endoliths and in comparison to B.mysticetus,B.musculus etc would slow the ageing process exponentionally longer than these multicellular organisms and the fact that there would be less detrimental side effects from using the fewer genes more easily mapped from endoliths and also have less complicated mechanisms.These bacteria obviously utilise less complicated mechanisms to slow metabolism and thus their ageing process due to having fewer genes and being unicellular organisms compared these multicellular organisms B.mysticetus,B.musculus etc and thus their mechanisms should be easier to integrate into H.sapiens and other complex lifeforms through CRISPR without side effects.Recombinant DNA from these specific species of endolithic bacteria from this 2013 discovery involving the Integrated Ocean Drilling Program will be used as their slow metabolism and slow miotic can halt the ageing process by negating the effect metabolism has on the ageing process as well as negating the effect that mitosis has in the ageing process through depletion of Phosphatidylcholines and telomeres.Those from the ocean floor that do undergo mitosis every 10,000 years should already have samples in laboratories and their genome should be already be mapped and their genomes already present in genetic databases around the world that can be added to computer networks as they have been scrutinised by the Integrated Ocean Drilling Program in 2013 with their estimated age at being at least 100,000,000 years old.As a result of using recombinant DNA from these specific species of these endolithic bacteria discovered in 2013 by the Integrated Ocean Drilling Program a person would thus age the equivalent of several hours to several months once every 10,000 years as this would prevent metabolic as well as telomere and cellular structure degradation associated with mitosis.Normally bacteria live only five days or a few weeks and undergoe mitosis every few hours or minutes with the endolithic bacteria found underwater in 2013 by the Integrated Ocean Drilling Program have been found through studies to be estimated to be 100,000,000 years old and estimated to undergoe mitosis every 10,000 years due to evolving to survive in extreme conditions present in the distant past.Human cells live on average a few months wherein they die and undergoe mitosis that causes degradation in their telomeres and cellular structures alongside metabolism affecting sensensence thus by having DNA from these specific endolithic bacteria will halt the ageing process to the point that a patient ages the equivalent of several months once every 10,000 years with it also slowing down metabolism that affects the ageing process and slow the ageing process to the point that one could go 10,000 years without eating food or drinking water.Some other species of endolithic bacteria already discovered whose genome is mapped also undergo mitosis only once every few hundred years with if they have their genome already mapped then they can be used before DNA from those discovered in 2013 can be mapped and used.Therefore at first if the DNA of endolithic bacteria that undergoe mitosis only every few hundred years is already mapped and stored in databases then they can be still used to be added to patients cells at first to slow the ageing process by several hundred years thus extending an elderly or even younger patients persons lifespan by several centuries long enough to to allow them to avail of CRISPR treatments that rejuvenate the level of Phosphatidylcholines etc to infancy levels and then once the 2013 species of endolithic bacteria’s genome is mapped this can allow for CRISPR treatments to allow DNA from the 2013 species to applied to the patients cells and the genes from bacteria that extend human lifespan by several centuries be removed acting as an intermediary step especially for elderly patients.Elderly patients currently aged aged 70-100 to exponentionally increase survival rates and chances of availing of better treatments from more longer living endolithic bacteria would be fitted with DNA via CRISPR from species of endolithic bacteria that undergoe mitosis only every few hundred years whose genome is already mapped and is stored in genetic databases to slow down the ageing process by several centuries to them give them time to avail of DNA from those that undergoe mitosis every 10,000 years with as stated the DNA from the previous endolithic bacteria removed and replaced instantly with those from the 2013 species.After this or at the same time they will have added to their genome DNA to repair telomere damage,those to replenish Phosphatidylcholines and endolithic.Thus genes from species of endolithic bacteria that undergoe mitosis once every few hundred years whose genome is already mapped and in genomic databases can be used in the first trials for human patients including elderly patients to slow the ageing process by several hundred years thus extending the human lifespan by several hundred years with this sufficing until the 2013 species is available to be added to one’s genome.Scratch DNA can be also be extrapolated by AI to halt the ageing process by several decades or centuries or thousands of years.This -alongside having humans synthesise essential amino acids and other nutrients would also reduce the amount water and nutrients the patient needs limiting strains on the Earths resources with the organisms with the lowest levels required will be used with scratch DNA pushing this even further.Turning off or removing the fat insulin receptor gene and others related to caloric restriction via CRISPR can be used to further play a role in this and prevent heart disease and diabetes as well as compliment oligotrophic DNA with the CRISPR process also used to remove genes responsible for ageing and replace these with those from these extremophiles negating their effects.If possible junk DNA and those responsible for ageing can be removed by them as well if not causing damage to hold extra DNA including augmentations.The slow degradation and thus slow rate of ageing would be the result of slow miotic rates every 10,000 years from endolithic bacteria DNA added to the human genome preventing damage caused by metabolism and degradation of telomeres in the mitochondrial and cellular telomeres that leads normally leads to ageing caused by mitosis and thus the hayflick limit.This slowing down of metabolic processes that damage DNA and cells,this being repaired by bacteria that exhibit self repair of the DNA,slow miotic rates preventing cellular degradation of Phosphatidylcholines and them rejuvenated constantly and also repair and protection of damage from metabolic processes in each cell will thus halt the ageing process every 10,000 years coupled with aerorolerant DNA that protects DNA from reactive oxygen and free radicle caused by respiration.It would also slow down metabolism in a cell negating effects caused by mitochondrial process alongside those from Tardigrade,oligotrophs and xerophiles.
Patients will at the same time have their DNA and levels of Phosphatidylcholines and NAD+ reverted back to their infant state to thus be kept at a youthful state using recombinant and scratch DNA.The damage to telomeres in both the nucleous and also mitochondrial DNA alongside the depletion of Phosphatidylcholines in the cell membranes is the result not only of metabolic processes but also the process of mitosis and miotic division of cells in the body as explained in how different parts of the body age at different rates as denoted by the fact that they undergo mitosis to replace dead cells at different rates than each other as shown by the hayflick limit and that each time a cell undergoes mitosis they undergo senescence where the levels of phosptidycholines etc in the cells outer membranes and NAD+ synthesised by them deplete and also the teleomeres in chromosomes and mitochondrial DNA degrade as shown by the fact the levels of these compounds and the length of telomeres is at its highest levels at infancy and by ones 90s they have reduced by 90% and the levels of these are at varying levels throughout ones lifetime with this different for different types of cells.Endolithic bacteria DNA that gives them their reduced metabolism and reduced rate of mitosis will once added to a patients genome via anti-ageing strains through CRISPR will slow down the ageing process by this rate that is they will age the equivalent of several months every 10,000 years as it will slow down the rate of metabolism and also slow down the rate of mitosis of cells in the body thus slowing down the rate of telemore damage and depletion of NAD+ and Phosphatidylcholines by this rate because metabolism and mitosis of cells play a key role in the ageing process that depletes Phosphatidylcholines and NAD+ and cause the telomeres in a patients cells to degrade over time.Everytime a cell undergoes mitosis and is replaced by another one the levels of Phosphatidylcholines,NAD+ depletes and the telomeres in ones genome degrades also becoming shorter.At infancy ones telomeres are at their most in damaged state and levels of Phosphatidylcholines are at their peak.But as a a person ages the levels of .Phosphatidylcholines and NAD+ deplete gradually and their telomere chromosomal and mitochondrial DNA also begins to degrade and frayed by becoming unwound due to cells undergoing mitosis and dying off until by the time one is their 90s etc the levels of Phosphatidylcholines and NAD+ have depleted by 90% meaning only 10% of their levels are present with by this point ones telomeres are frayed to their limits known as the hayflick limit.This is likely because the process of mitosis that occurs every 24 hours to several months unlike meiosis from creating copies of each strand of DNA and cell causes degradation as the new copied cells don’t share genetic material through meiosi.An analogy would be how when one recorded audio/visual material onto old VHS/VCR tapes the first recording was of perfect quality with when a person recorded new material onto the same tape over and over again the quality of the material becomes degraded overtime to the point that it is unrecognisable and becomes incomprehensible garbage.The same process occurs with animal including human cells as they undergoe mitosis in the body they become degraded overtime thus leading to them become more degraded with both levels of Phosphatidylcholines and ones length of telomeres lowering everytime they undergoing mitosis exhibiting itself in the ageing process in animals including humans wherein the body and its various organs etc wear down gradually thus exhibiting in poor limited locomotion,greying of the skin and hair and also eventual death from strokes,heart failure,alzheimers etc and other age releated diseases with the different rates of ageing of different species of animals leading to them exhibiting different lengths of lifespans explaining why some species of animals live longer or shorter than others and why some become elderly much quicker with this present in prokaryotic bacteria that have different evolutionary strategies to counteract telomere and phosptidocholine degradation such as the ability to be more easily adapt to environmental conditions to keep the levels of Phosphatidylcholines and NAD+ consistent throughout their multiplication with the fact that they have chromosomes forming loops of DNA alongside ribosomes instead of the linear chromosomes in eukaryotic cells including humans etc that are more prone to degradation may be a factor as to why they are able to not suffer the same level of degradation of DNA during mitosis with them still dying due to degradation caused by metabolism and the parent bacteria degrading by mitosis with endolithic bacteria prevented from undergoing chromosomal damage due to their extremely slow miotic rates and extremely slow metabolism.Furthermore metabolic processes play a role in the ageing process by depleting these compounds and damaging telomeres.Therefore biologically immortal and long living endolith bacteria and animals such as T.dohrnii,Nephrodae will have genes added by CRISPR.Therefore by adding the genes to a patient from endolithic bacteria responsible for their slow metabolism and slow mitosis rates of once every 10,000 years via gene therapy and horizontal gene therapy by anti- ageing strains via CRISPR will slow down the ageing process to the point one ages several months once every 10,000 years.This will be added to all patients both younger ones and elderly patients aged 20-90 years old first to slow down the ageing process exponentially and allow treatments to reverse the ageing process to be added.Since different cells in the body age at different rates due to them undergoing mitosis are different rates ie some undergoe mitosis and thus age every few hours while other undergoe mitosis and thus age every few months to make this delayed ageing more balanced all cells in the human body could be engineered to age at the same rate as each other by using DNA from other cell types with research done into which type of cells age the slowest,finding the genes that cause them to age the slowest will be determined by Phanes comparing their DNA to that of all cell types then having this DNA replace the other DNA similar to it in all other cell.This will be done so that once endolithic DNA and DNA repairing DNA is added to the tissues all tissues and cells in the body will age at the same rate once every 10,000 years.Studies of this will be done after older patients receive the first treatments to halt and reverse the ageing process to determine the rate that each type of cell and tissues age using tissue samples derived from younger patients,biosynths etc.These endolithic and DNA repairing DNA from T.gammatolerans will be added to the tissues especially heart,brain and key organ tissues of elderly patients aged 65 years or older to first to slow down the ageing process thus exponentially increasing their survival rates to avail of treatments to have their tissues cellular structures rejuvenated to an infant state.Thus a person could have all cellular structures and DNA in all cells and tissues in their body be reverted to a youthful state of early to late teens or even infant stage and the ageing process could be halted to the point that a person would age the equivalent of only several months once every 10,000 years with any damage repaired by the self repairing qualities of other extremophiles with this endolithic,oligotrophic DNA would allow one to eat as much as you wanted and still negate senescence associated with mitochondrial processes brought on by the metabolism of nutrients.The DNA of the cells would be programmed via scratch DNA to repair DNA and to replenish Phosphatidylcholines and NAD+ automatically returned to that of their infant state every time it undergos mitosis every 10,000 years via DNA from scratch with DNA from Bacillus F,T.gammatolerans repairing telomere damage every time this happens thus rendering the hayflick limit and depletion of Phosphatidylcholines and NAD+ redundant thus meaning any effects of ageing that occurs every 10,000 years will be automatically repaired and cells constantly reverted to an infant state thus effectively halting the ageing process forever.Research will be done if the delayed miotic rates and thus delayed ageing can be extended exponentially with the DNA responsible for delayed metabolism etc in endolithic bacteria can be modified so that it undergoes mitosis much longer by as much as 10 – 1,000,000 times meaning a person could age the equivalent of several months once every 100,000 or even 10,000,000,000 years.The theoretical limits of this will be researched and these new genes extrapolated by Phanes etc analysing the genes responsible for this and creating new ones from scratch and forced evolution.
The DNA to exhibit slowed metabolism and mitosis will be modified by AI to be better integrated into the human genome due to the fact that it comes from bacteria and not multicellular organisms.This can include adding new scratch DNA to better integrate the genes or use them as a baseline for AI to design better DNA to exhibit this phenotype.The role of having cells have delayed mitosis once every 10,000 years in halting the ageing proves is speculative and should be done primarily on mice,biosynths before being applied to humans after initial research extends the human lifespan by decades or years.It may have applications in delaying the growth and spread of tumours to slow their spread and preventing them corrupting the body and killing a patient.This research can be done by AI using automated labs.AI and 3D DNA printers performed primarily by AI such as Urania,Paean and Gaia with zero human labour
Phosphatidylcholines can be synthesised by the body ideally in each cell in required amounts using DNA from scratch,humans and Glycine max to then as stated rejuvenate cells with any with any possible atherosclerosis negated by omega-3,reversatrol,plant sterols etc produced by the body through horizontal gene transfer and also microbes clearing out the arteries with further engineering preventing atherosclerosis such as turning off the fat insulin receptor gene.Bacteria that break down oxidised cholesterol for example Bacillus subtilis SFF34 can have their DNA that breaks down the oxidised cholesterol can be added to the genome of humans to break it down.Both the genome of H.sapiens,Phasianidae(that produce it in the yolk) and G.max and other plants and animals that produce Phosphatidylcholines can be analysed by AI to see what genes they share in common that express the production of the compound to allow this to be determined with the genome of bacteria of those that create Coenzyme Q10 and H.sapiens analysed to find the common genes with the same done for the plants that create other anti-ageing compounds by analysing their genomes.Other natural anti-ageing compounds alongside Phosphatidylcholines such as Coenzyme Q10,vitamin D,antioxidants,reversatrol and many others can be synthesised by the patient themselves in the cells by adding the relevant recombinant DNA from animals and plants that produce these into the hosts genome via horizontal gene transfer with them produced either in the cells and tissues of the host negating the need to take supplements saving on the time and need to take them as well as resources to create them.Nicotinamide adenine dinucleotide(NAD+),phosphotidocholine and other compounds related to youthful tissues will by scratch and recombinant DNA from humans etc have cells replenish them in desired amounts forever associated with infancy.These would ideally be synthesised in the cell walls in the required amounts ideally to ensure they are made in correct amounts and also prevent overdosing or are not lost,replenishing them only when they naturally deplete over and over again and replenish those in older patients or even have them once replenished kept at ideal healthy levels and replacing depleted reserves in the cell wall in older patients to levels seen those in their early teens,early twenties or even infant years.Scratch DNA will ensure that it is synthesised only in the cells and cell walls and constantly replenished in levels synonymous with infancy once they deplete ensuring they stay at levels associated with infancy forever.Scratch DNA would be added to ensure the levels of these compounds are reverted to that of an infant and kept at these levels via replenishing them automatically every time a cell undergoes mitosis over geological timescales.The cell structures and thus levels of them in infants and each individual patient will be analysed using automated lab machinery with them tested after gene therapy to see it is effective.Each patient will have the levels of NAD+ and Phosphatidylcholines in cells and tissues in their body analysed in labs to determine the level of degradation and compared to that from an infant to thus determine scratch and aforementioned recombinant DNA to be added to revert them to an infant state.This aforementioned and scratch DNA would thus keep the levels of these compounds in the cell walls and cells at ideal levels similar to infancy if not ones early teens and early twenties indefinitely with them replenished over and over again automatically when they deplete via adding scratch DNA.The scratch genes added would constantly replenish the levels of Phosphatidylcholines,NAD+ etc over and over again whenever they deplete naturally due to mitosis.Excess produced by the cells or intaken by diet could be flushed out of the body with in time the amount produced by the cells perfected and them able only to absorb only that required amount via engineering with excess flushed out or used for its other purposes.Ideally scratch DNA would make them engineered to only recreate the required amount only in the cells outer membranes thus meaning that no compounds are released by them as waste into the blood stream to prevent dangerous side effects.Thus each persons cells would through relevant scratch and recombinant DNA from humans and plants that synthesise these compounds would synthesise Phosphatidylcholines,NAD+ etc within their cell walls thus replenishing them in the case of older patients and doing so constantly as one ages over geological time rather than them being released into the bloodstream as a waste product that could be dangerous to the patient etc.Thus the patients cells would be engineered to synthesise NAD+ in only the cell itself and synthesise Phosphatidylcholines in the cell walls and not have these released into the bloodstream which could cause side effects.Each individual patients cells will be analysed by automated lab machinery to measure the level of NAD+ and Phosphatidylcholines and their degradation and compared to that of an infant to determine their level of depletion of NAD+ and Phosphatidylcholines.Scratch DNA will be added to replenish these to infancy levels and also keep them replenished in the outer structures of each cell only when they deplete thus once the cellular structures of each cell is reverted to an infant state they will be kept at these levels forever.Thus each cell will be engineered using relevant recombinant DNA and scratch DNA to at first replenish the levels of phosphtidocholines and NAD+ back to levels found in infants with them engineered using scratch DNA to replenish them constantly whenever they deplete and only when they deplete thus negating any effect miotic degradation has on their levels.Phosphtidocholines will synthesised and replenished as these are the compounds upon which phospholipid bilayers that each cell in the body is composed of with NAD+ also responsible for a healthy metabolism and functioning of cells.DNA from totipotent stem cells will added to keep them at the same level of vigour as those in embryos and even infant years.Phosphotidocholine and NAD+ will at first may have to have to be synthesised in the bloodstream to allow it to be intaken by cells with this of note of NAD+ which due to being unable to being intaken by cells would require precursors of it to be synthesised in bloodstream that can be then intaken into cells that are then converted into NAD+.
This may have to for patients aged 50 and older.Collagen can be created by microbes as well as engineering the body to produce and replenish it in key areas of the body itself naturally using scratch DNA with these compounds anti’ageing affects sufficing until other compounds such as Growth differentiation factor 11 and NAD+ ‘booster’ NMN can be researched in animals to be added into the production by individual cells to reverse ageing overtime.Nicotinamide adenine dinucleotide can not only be replenished by the cells naturally through having scratch DNA added to the patient but the microbes through scratch DNA and human recombinant DNA and anabolic and catabolic reactions can produce its precursor Nicotinamide mononucleotide in the bloodstream to cause the cells to create the compound themselves.The effects of cosmetic surgery such as injections of botulism and stretching of the skin via face lifts and also lip injections as well as crows feet can be be reversed by them and cosmetic surgery by forming new tissues and collagen internally,causing certain tissues to undergo apoptosis or causing the body via CRISPR to create collagen in the normal amounts of it from their early teens and early twenties.The ability of Serpentes to shed skin will also do this to correct damage by peeling off upper layers of skin in the case of elderly patients and those with botched face lifts and botulism treatments to recreate a more natural younger face and skin across the entire body.Skin tissue will be treated with anti-ageing compounds created by them and the addition of DNA repairing DNA as well as them causing the outer epidermis to peel off using recombinant DNA from Serpentes added to the patients genome and them forming new tissue underneath them with this done every once and a while on demand by Paean to replace old dying skin tissue possibly every few decades or even centuries if not millenia and could be done to remove unwanted tattoes and also scars.This would be done at first by the eldest patients currently aged 50-95 to remove the outer layers of dead skin on them to allow more youthful skin tissues to emerge with greying hair have compounds created by microbes to rejuvenate lost colour alongside CRISPR or the hair could be forced to grow outwards to allow the old discoloured hair to be removed outwards.If need be those with greying hair should have their hair shaven and then have microbes and CRISPR have the body produce new colourings to their original colour.Chemical signals from microbes signalled from Paean would initiate this moulting to first form a layer and then to have it moult off dead and dying skin.This could be done with internal tissues such as blood vessels and organs though it would require the cells also programmed to break down or this done by the anti-ageing strains having recombinant DNA from necrotising bacteria to break it down although this may be unnecessary since this is not evident in Serpentes it self and would be done primarily for the exterior with this done of the whole body or it can be programmed to occur in only certain places where microbial cosmetic surgery is taking place ie the face,arms,legs,breasts etc via chemical signals.Tissues of internal organs can be made to undergo apoptosis when newer younger tissues form underneath them.Animal trials on mice and chimpanzees with no fur can stay as early with this initiated by chemical signals injected into them with the carbon dioxide energy acceptor phenotype in humans and animals preventing asphyxiation.This can apply to both intracellular and extracellular aggregates with genes from animals that do not get cancer and any other animals alongside scratch DNA to prevent mutations both within the nuclei telomeres and mitochondrial DNA.CRISPR treatments via the microbes will allow for both telomeres in cell nucleus/chromosomes and mitochondrial DNA to be repaired and have DNA from the relevant micro-organisms and multi cellular lifeforms that exhibit biological immortality and immunity to cancer to be put into their place to prevent mutations that would lead to ageing,cancer and other and existing genetic diseases with precision with any faults repaired by more precise treatments.Extracellular aggregates can be done by the strains of microbes that immunise the immune system against viral and pathogenic or specific microbes as part of the anti-ageing strains either routinely or if possible indefinitely in an active immunisation with passive immunisation involving them creating the antibodies themselves with if possible them breaking down the aggregates such as beta-amyloid into benign compounds such as nutrients for the microbes and host and replacing and tissue with new vigorous ones by detecting them in the body or using CRISPR to allow the body break these down themselves or prevent humans creating these in the first place.Extracellular cross links can be dealt by anti-ageing strains using enzymes and proteins such as MGMT to break them down or again causing the body to create these compounds in response to their presence and even prevent them forming in the first place with any tears repaired by microbes or the engineered host tissue.Compounds and structures that are result of the ageing process in patients prior to treatments will be broken down by anti-ageing strains through them producing enzymes and also other synthetic and natural compounds extrapolated by Paean and created by anabolic and catabolic reactions.Genes from scratch added to patients will prevent them forming in the future.Strains that replace dead tissue and repair ears can repair any damage this does to the arteries,organs and skin.Intracellular aggregates can be broken down by the strain using recombinant DNA from decomposing bacteria to break down lysosome and other wastes to create nutrition for the host and microbes or even using CRISPR to transfer this ability to the hosts cells to produce lyosome when they are detected or prevent these forming in the first place.Scratch DNA can be added to the human genome to prevent the formation of extra cellular and extra cellular aggregates and other compounds etc in the body caused by the ageing process in the first place.Existing dead senescent cells in the body in patients aged 20 or older that are the result of excess mitosis that can harm the patient can have them destroyed by anti-ageing strains using CRISPR treatments that apply suicide genes to them and consume them with stem cell strains injected into the patient replacing them with newer younger cells.Anti-ageing strains can synthesise proteins that destroy the senescenct cells without harming healthy cells with again stem cell strains taking the king their place.Scratch DNA can be added to patients to prevent them forming senescent cells by having all cells when they do die over geological timescales synthesise enough of the relevant proteins to prevent the formation of senescent cells.Stem cell strains can in older patients form new younger cells and tissues in key areas of the body such as arteries,heart and brain.This will be of note to elderly patients aged 70-100 that have lived long enough to avail of them especially those that have been confined to wheelchairs thus allowing key areas of the body such as arteries,heart,brain and muscles in the legs etc to be given new young tissues to keep them alive and improve locomotion.Elderly patients as part of anti-ageing treatments would have them form younger rejuvenated tissues in all parts of the body especially in key areas of the body such as the brain,heart and muscles to improve cognitive,vascular and locomotive functions.This would speed up age reversal treatments and would be key in aiding the CRISPR treatments that reverse the ageing process especially for those who have been left unable to move independently for several years or decades due to their elderly age to regain locomotion.They will be used alongside CRISPR treatments to cure neurological conditions such as pedopheilia,sociopathy and also neurodevelopmental disorders such as Downs Syndrome etc and genetic diseases by forming correct neural and other tissues in the body.Due to extensive damage caused by old age they will by forming younger heart,muscle,neural etc tissues that have levels of phosptidycholines,NAD+ and telomeres on par with a person in their twenties,teens and even infancy will rejuvenate parts of the body to that state with the patients entire genome to compliment CRISPR treatments especially not only for the elderly but for those aged 30-75 so that this adds an extra 20-50 years to their lifespan should CRISPR treatments be not advanced enough.Thus they will be carried out alongside proto CRISPR treatments to replace dead dying skin and tissues with younger rejuvenated tissues on par with those in their early 20s or younger to increase survival rates until CRISPR treatments are perfected.Most elderly patients and indeed most patients aged 30-70 or even older will have these stem cell strains applied to them to key areas of the brain,heart,blood vessels and muscles to keep them alive and improve locomotion alongside anti-ageing treatments in order to aid in recovery as in some cases actual CRISPR treatments to reverse the effects of ageing may not be enough due to extensive damage and thus stem cell treatments should increase their recovery towards mobility.These stem cells once converted into new tissues will house not only the patients DNA to prevent rejection with them also housing endolithic DNA and those relevant to slow down the ageing process.This could be developed much easier than CRISPR treatments since created within hours by 3D DNA printers and this process of the strains converting into new younger tissues all over their body can be repeated over and over again every few decades once one reaches the equivalent of 40-70 to slow down the ageing process forever constantly rejuvenating one’s body to that of their early 20s or early teens until CRISPR treatments using relevant DNA from biologically immortal bacteria can be perfected.Flagellum present will allow these stem cells to travel to parts of the body with the ability to undergoe mitosis from bacteria allowing them to replicate millions of times and create youthful tissues over and over again.Any other newly discovered ageing process can be treated by these sub strains adapted to them through upgrades with ideally the host able to break down and compounds associated with ageing or prevent them being formed in the first place.The role of anti-ageing strains of these microbes inhabiting all tissues in the body would allow them to apply these anti-ageing gene therapies and also compounds to rejuvenate tissue and replacing old ones with new vigorous youthful tissue to every cell in the body with the DNA from extremophiles via their ability to form new tissues with them also detecting and causing specific senescent cells to undergo apoptosis via suicide genes to and replacing them with new healthy ones with the genes from these extremophiles ones or using CRISPR to cause them to commit suicide and be repaired and do any necessary repairs over the coming decades and if need be eventually centuries with this done on demand at first and then in time by base microbes copying DNA or other means detecting the level of Phosphatidylcholines as well as teleomere,mitochondrial DNA and cellular degradation that occurs via base microbes copying DNA strands in certain tissues in all parts of the body and their nanomachines wirelessly sending results to Paean for ageing strains to apply more therapies invivo or through automated procedures though in time the damage should be able to repair itself indefinitely once perfected via advanced gene drive technology and using T.gammatolerans and Bacillus F DNA with the microbes staying their as backup.If possible blood and skin cells can be collected in automated labs using phlebotomy robots that can put these cells under automated machinery to detect the level of senescence of telomers in both the mitochondrial and nuclei DNA, as well as the levels of Phosphatidylcholines but also other biomarkers of senescence that can be uploaded and logged into ones patient file to measure the efficacy of the treatments and need for more of them.Base microbes once advanced will copy DNA from cells around the body and upload them to ones patient file to measure the level of senescence in the telomere and mitochondrial DNA as well as the levels of Phosphatidylcholines and other key components of the cell membranes in each type of cell and tissues in the body ie neural,muscular,skin etc every few years or decades logged into ones patient file with them reading the DNA etc using Cas-9 and taq polymerase and sent by wifi.Biomarkers of cellular degradation such as 8-oxoGsn will be detected by these strains using tweaked C.elegans DNA and thus allowing them to take action to repair them or test kits can be used until they become sufficiently advanced.The microbes other strains will also replace dying and old tissue in arteries,brain,organs and skin overtime with them also passing on the abilities of Bacillus F,Planarians etc via horizontal gene transfer to all tissues in the body to allow this to happen naturally.The mapping of genes and research into all of these unicelluar and multicellular life forms should be done be automated labs and artificial intelligence at once simultaneously in universities and hospitals around the world.Recombinant and scratch DNA programmed to replenish Phosphatidylcholines and NAD+ indefinitely after Phosphatidylcholines and NAD+ levels in the cell walls once they are reverted to levels of infants and DNA from endolithic DNA slowing down miotic damage that affects the state of mitochondrial and telomere DNA,levels in the cell walls and miotic damage caused by mitosis halted to the point that a person ages the equivalent of several months every 10,000 years.Scratch DNA can be developed that reverts the levels of Phosphatidylcholines and NAD+ in the cells back to a infant state every time they undergo mitosis every 10,000 years with DNA from T.gammatolerans,Bacilus F repairing DNA damage everytime the cells undergoe mitosis.Any depletion of Phosphatidylcholines and NAD+ and telomere damage as a result of miotic damage every 10,000 years will be repaired via recombinant DNA and scratch DNA that programs it to replenish both Phosphatidylcholines and NAD+ to a youthful infant state with the DNA repairing mechanisms of Bacillus F,T.gammatolerans DNA added combined with scratch DNA rendering the hayflick limit and cellular degradation defunct as all future DNA degradation will be repaired instantly once reverted to an infant state.This means any ageing and damage caused by it every 10,000 years will be automatically repaired and reversed thus indefinitely halting the ageing process once a persons DNA and cell structure in all tissues is reverted to a youthful state similar to infancy.Scratch DNA can be used to integrate all of these sources of DNA into the patients genome without side effects.
The DNA to exhibit the ability to replenish Phosphatidylcholines and NAD+ will be modified by AI to be better integrated into the human genome due to the fact that it comes from bacteria and not multicellular organisms.This can include adding new scratch DNA to better integrate the genes or use them as a baseline for AI to design better DNA to exhibit this phenotype.The role of having cells have ability to replenish Phosphatidylcholines and NAD+ themselves and not from consuming food in halting the ageing proves is speculative and should be done primarily on mice,biosynths before being applied to humans after initial research extends the human lifespan by decades or years.It may have applications in delaying the growth and spread of tumours to slow their spread and preventing them corrupting the body and killing a patient.This research can be done by AI using automated labs.AI and 3D DNA printers performed primarily by AI such as Urania,Paean and Gaia with zero human labour
Adding relevant genes to humans from T.dohrnii,Nephropidae,Hydra could allow the cells of human patients especially older ones to revert instantly to a younger infant state over and over again on demand or through scratch DNA present.This would reverse any ageing that does occurs every 10,000 years and could also allow patients to create stem cells on a par of their infant state forever indefinitely using scratch DNA.This would mean as the process of ageing is halted then the body is always creating new healthy infant stem cells over and over again forever and would negate the need to add recombinant DNA to replenish phosphotidocholines etc with the stem stem cell strain replenishing a patient with new vigorous tissue every few decades complimenting this.This will be tested on Biosynths modelled in humans that have all aforementioned anti-ageing treatments,some of the treatments in different combinations and others without any treatments.Their role is purely speculative in whether they can reverse ageing with this done by AI and should be done primarily on mice,biosynths before being applied to humans after initial research extends the human lifespan by decades or years
Combing the genetic regenerative abilities of D.radiodurans,T.gammatolerans that allows them to survive such extreme doses of radiation(30,000 Gy compared to 5Gy for a human) by repairing DNA,with the DNA regenerative abilities of Bacillus F,the ability for extreme oligrotrophic and xerophile to require very little nutrients and water to counteract effects of metabolism as well and other Archaea such as endoliths that also undergo repair from cosmic rays,racemization and reproduce via mitosis only every 10,000 years and if possible Tardigrade able to survive extreme conditions and endolithic bacterias slow metabolism and aerotolerant bacterias ability to negate the effects mitochondrial metabolism together alongside applying the genes form plants and animals that synthsise anti-ageing compounds such as reversatrol,coenzyme Q10,Phosphatidylcholines,teleomerase into the the host genome to be produced by all cells to synthesise them themselves,removal of the fat insulin receptor gene and others that induce ageing,scratch DNA into gene therapy treatments using CRISPR applied by anti-ageing strains microbes using horizontal gene therapy into both the nuclear telomeres and also mitochondrial DNA of all cells in the body would reverse and negate all of the effects of senescence in more complex multicellular organisms such as H.sapiens brought on by mitochondrial metabolism,telomere degradation with again this at first halting the ageing process and then further research into them,other more complex immortal lifeforms and DNA created from scratch done by Phanes,Epione and Paean could reverse it secondly by repairing existing damage to ones the telomeres and cells using this recombinant DNA,DNA strands made from scratch and from and other biological components with a more fixed state and then reversing the symptoms of ageing.These anti-ageing treatments would allow more complex multicellular lifeforms such as H.sapiens and other sentient life forms alongside all species of pets etc from across the universe from all taxonomic rank in their adult years even those in their elderly years such as those currently aged 60-95 to have their cellular and telomeres structures be reverted to that of their infant years and live forever in a state similar to early to late adolescence staying youthful in a state similar to the ages of roughly 14-15 with the microbes using other gene therapy via CRISPR and creating relevant sex hormones with females kept in their fertile peak of 14-15 and males their testosterone peak of 14-15 indefinitely and eat and drink as much as they want prevent mitochondrial damage to the cellular processes with them enhanced by these and other phenotypes of these extremophiles.Thus one internal organs and external skin would have it reverted indefinitely to a state equivalent to infancy allowing one to stay in a perpetually youthful state similar to the ages of 14-15 with females forever kept in the fertile peak of 14-15 and males kept forever in their testosterone peak of 14-15 through genes added that keep their hormones at this age range forever with once patients are reverted to this young state the ageing process will be slowed down to the point that they will age the equivalent of several months every few 10,000 years with scratch DNA repairing degradation that occurs every 10,000 years thus halting the ageing process forever.One would thus be reverted to their youthful internal and external appearance of their early 20s or even early and late adolescence of the age of 14-15 with their cellular structures and telomeres reverted to their infant state and the ageing process halted to the point a person would age the equivalent of several months once every 10,000 years with the ageing effects reversed automatically every 10,000 years with females forever kept in the fertile peak of the ages of 14-15 and males forever kept in their testosterone peak of ages 14-15.The anti-ageing treatments could also aplly to all species of animals including pets of all species and breeds of animals such as Canidae,F.catus,,Serpentes and animals in zoos etc as well as even ornamental plants with Phanes modifying the treatments to each species and breed.This would thus allow humans etc be reverted to their youthful appearance of early 20s or early and late adolescence and the ageing process halted to the point they would age the equivalent of several months once every 10,000 years with the ageing effects reversed automatically.The anti-ageing treatments could also aplly to all species of animals including pets of all species with Phanes modifying the treatments to each species and breed.This would be applied by anti-ageing strains of microbes to the hosts DNA in all cells and tissues where they will reside.Bone marrow would have this DNA but it added in a way to prevent leukocytes housing it as it would be ideally to have them die off at the same rate they do normally to prevent overproduction of them especially during infections with Phanes extrapolating ways to ensure that they and erythrocytes die off at a normal rate but still stay young as in an adolescent of infant to prevent them overrunning the body extrapolating ways to ensure that they and erythrocytes die off at a normal rate but still stay young as in an adolescent of infant to prevent them overrunning the body.Augmentations would still be added to leukocytes.Phanes will develop countermeasures to any problems associated with gene therapy that extends the human lifespan.Augmentations would allow one to heal instantly from wounds,cuts,burns and also regrow limbs,become immune to radiation,survive exponentially longer or completely without water and food,survive the vacuum of space and all extreme environmental conditions on Earth and across the world thus effectively making one immortal.Mapping of these lifeforms DNA using artificial intelligence will be done to determine the genes for their incredibly long lifespans with this of note to the unicellular lifeforms that seem to live the longest and have fewer genes than multi cellular lifeforms that exhibit this phenotype meaning it should be easier to determine which genes are responsible for this much quicker using artificial intelligence and automated labs testing each sets of suspected genes especially in regards to endolithic bacteria,T.gammatolerans,Bacillus F as well as Planarians.This should at least first halt and reverse the ageing process by 2029 with AI creating scratch DNA and carrying out more advanced research using DNA from T.dohrnii etc on animals to further enhance age reversal and halting.Other non human multicellular lifeforms including pets,livestocks wild animals in zoos,conservation areas and the wild(especially endangered species) will be able to avail of this with Phanes,Paean,Urania and Hecate suiting it to their specific DNA with even ornamental plants and crops in gardens etc also availing of this.Having all work such as simulations of the ageing process and effects of treatments as well as creation of scratch DNA,preparation and scanning of the extremophiles done by Phanes,Paean,Hecate,Epione,Urania and even ancestral AI,automated labs in hospitals and universities using all data on Apollo and existing scientific papers online searched by AI will expedite the process exponentially.3D DNA printing and automated labs can also expedite the process exponentially since mapped genes in Physis and those from scratch can be easily be added to leukocytes used as baseline and microbes as upgrades expediting their development even quicker theoretically allowing therapies to first halt the ageing process available within a decade extending the lifespan of those in the currently in the age range of 50-95 to receive therapies to first halt the ageing process giving them more time to receive the benefits of more advanced therapies that then repair and reverse the ageing process thus reverting them to a more youthful state of their early adolescence and early twenties indefinitely with females having the same fertility peak in their early teens 14-15 years of age and the same for males with males through other gene therapy applied via CRISPR to them and also through testosterone and other hormones created by the microbes allowing to on demand or indefinitely to have the same testosterone peak they had aged 14-15 years of age.It could also reverse presbycusis allowing those middle aged or older to revert to their hearing peak they had as prepubescent children.
Those past this range say currently aged 90-100 could if they manage to naturally biologically live to past 100 even to the ages of 110-120 could feasibly have this if they manage to still stay alive.Thus those currently in the “goldilocks range” aged between 50-70 are the highest age range limit to have a 100% chance of availing of this with those between 71-81 having at least a 90-100% chance of availing of this depending on how well they have taken care of their body – those aged about 75 would have at least 90-95% chance while those aged 76-81 their chances would be 75-89% ,those aged 81-91 have a 50-75% or less chance of availing of it due to the extreme damage though as stated if they were biologically meant to originally live to between 100-110 they could have at least 50% chance.As detailed later on proto treatments available by 2023-2025 could allow those currently aged 80-95 to live long enough to 2029 by halting the effects of ageing in vital organs such as the brain,blood vessels and then allowing it to be reversed to a more youthful state of ones early twenties by this date with other CRISPR treatments allowing them to survive heart attacks and strokes and other age related conditions thus raising their chances considerably to at least 50-75% of living an indefinite lifespan of eternal youth.This would increase the chances currently aged 75-80 to at least 100% and those currently aged 80-100 to at least 50-85%.The chances of availing of treatments that halt and then reverse senescence depends on how quickly the treatments to halt and then reverse the ageing process can be developed,the level of global cooperation,how good in shape one is with regards to their age ie some 80-90 year olds may be in better shape than other 80-90 year olds,their previous medical history and how old they were biologically born to originally live to without the treatments ie if their genetics predispose them to live to 100-122 the current upper limit of human lifespans and other factors such as their inability to die of trauma,pathogens,heart attacks,natural causes,accidents or murder and how much in shape or damage their lungs,brains,livers are in response damage from cigarette smoking,alcohol damage and their cholesterol levels and genetics that predispose them to cancers,alzheimers etc similar to some people are more likely to die of Coronavirus infections than others.Each individual patients current state of health determines their chances of survival with the general rules got good health such as give up smoking,avoid exposure to carcinogens,avoid fatal accidents and eat healthy food,exercise etc used to increase the survival rates of those 40 or older with older patients taking cholesterol tests and health check ups.If possible clinical trials applied on the oldest living patients can start by 2025.The state of ones health of those above 75 such as cardiological health,pulmonary health as well the state of their cellular structures and telomeres and whether they would be biologically predetermined to live to above to 100 or above determines the possibility of their chances increase above these percentages.Thus these percentages are basal guidelines with them different for all patients above the age of 50-70 based on ones unique genetic and health factors.Patients should undergoe medical tests to determine their chance of survival with those aged above 70 that are currently 80-100 being part of firstclinical trials and the first line of patients to receive anti-ageing treatments between 2025-2029.The rate of scientific research,use of AI and automation in labs,use of computer networks to share data and 3D DNA printers and level of cooperation done in universities,hospitals etc worldwide should exponentially increase and determine the rate that the first human trials and treatments are available for older patients thus increasing survival rates of those currently aged 80-100 years exponentionally to between 80-90%.Simulations and practical applications should show this done at the same time that the treatment is development.Older patients above 75 may want to avail of bioprinted and chimera organs such as hearts and livers etc from cattle,remove their fat insulin receptor gene to eliminate heart disease as well as check regularly for cancer and other fatal diseases and infections and also take preventative action towards extending their chances of living long enough to avail of treatments to first halt the process of senescence and thus avail of those to reverse the effects already on them.This should also be done of all patients over the age of 40 or indeed any age getting checked regularly for all types of cancers and have genetic scans for all types of genetically predisposed cancers and conditions that would lower their percentage of survival that they may be prone to especially cervical and prostrate as well as getting DNA scans for it and other genetic diseases with survivors of cancer and heart disease also getting routine checks and bioprinted organs.Intensive research should be made into primarily strains that treat ageing and also cancer above all other strains at first due to the fact as they can reverse the ageing process in the elderly who are the most at risk individuals alongside cancer which is the most deadly of diseases.Other strains such as augmentations and anti-viral etc strains could be delayed until after ageing strains are perfected as most pathogens can be treated with existing treatments and preventative measures to prevent infections.As detailed later modified immunotherapy and viral vector cancer treatments using CRISPR and Polybia-MP1 will increase survival rates for all types of cancers especially those in middle age or older.Ideally all patients worldwide should get DNA scans by 2023/2024 to check for cancers and other fatal genetic conditions to prepare for them to get frequent screenings such as prostrate exams and pap smears,mammograms and xrays etc and also get bioprinted organs.Those who work with carcinogens or in heavy polluted sites and even smokers may want to avoid smoking and also heavy drinkers would likely avoid drinking heavily and get frequent checkups with those in accident prone occupations taking extra care to prevent death and serious injury.Those aged 75 and older can avail of organs like hearts,kidneys,lungs from chimera animals such as pigs and cattle as early as 2023 to provide them with organs that are in a vigorous and youthful state equivalent to those in their early twenties to increase survival rates with them taking anti-rejection drugs until CRISPR treatments remove all foreign DNA.AI will create strains of bacteriophages that can kill off strains of fatal superbugs that can be created onsite of all hospitals.Medication for chronic infections such as HIV and chronic conditions such as genetic conditions will be provided to all suffers worldwide in both the developing world and first world.Biocompatible microbes since living within the tissues of the patient will be able to apply the relevant genes to the host permanently to the cells and tissues in the body.The same anti-ageing procedures can also be applied to livestock and pets as well as crop and ornamental plants and endangered wild animals.These and extra phenotypes using other recombinant DNA could allow H.sapiens to survive the same extreme conditions as these extremophiles that would normally be fatal to humans such as extreme doses of radiation,pressure,prolonged periods without water and nutrients such as proteins,fats and carbohydrates,vitamins especially if H.sapiens can be engineered to synthesise essential vitamins,fats,amino acids by themselves or this is done by biocompatible microbes.As stated earlier it takes about an hour to map and identify a patients entire DNA of 46 chromosones and 30,000 genes thus it should be easier and quicker to map and identify all the genes of each one of the aforementioned and other species responsible for their regenerative capabilities,lack of neuro-muscular degenerative diseases and cancer as well as biological immortality especially in the case of unicellular Archaea lifeforms and even mammals etc especially if done simultaneously by artificial intelligence since as stated they should have shorter genomes accelerating the creation of ageing therapies via gene therapy using horizontal gene transfer through biocompatible microbes.Their DNA should already be within genomic database scattered across the internet but having proto AI transfer them into a single database will expedite research and progress research should be made into primarily strains that treat ageing and also cancer above all other strains. these extremophile Archaea lifeforms and animals that dont exhibit genetic based diseases should at least halt the ageing process in humans at first with further research using them and other lifeforms with this phenotype and DNA made from scratch as well as biocompatible microbes then allowing for the ageing process to be reversed allowing for patients to be reverted to a indefinite youthful state of early teens and early twenties with Phanes,Gaia,Urnaia,Hecate and Paean doing this and other research into genetic engineering and therapy.These and DNA from animals that exhibit biological immortality could also prevent any random mutations that would lead to cancer in both the nuclear telomeres/chromosomes and also mitochondrial DNA.The ability of embryonic stem cells and cancer cells to produce telomerase could introduced into other cells to make them replicate indefinitely with gene drives and other genetic treatments keeping this under control preventing the body being overrun with tumours.Other DNA can be made from scratch as well to better integrate this recombinant DNA or replace it with if possible DNA coming from all or most of the aforementioned sources.If possible both gene therapy and even editing embryos,spermatozoa and eggs will be done to increase the intelligence of the unborn child and thus if done on a large scale be able to over several decades increase the average intelligence quotient of the entire species.To deal with the drawbacks of gene therapy the virus used could have DNA from the host patient or just human DNA to create human proteins on its capsid to avoid detection by the immune system and thus be used indefinitely without immune reactions.Gene drivers especially advanced gene drive technology could be used to make the gene inserted of any phenotype as well as permanent features of H.ubermensch and H.sapiens to spread through future cells through mitosis becoming a permanent part of the patients body or just specified cells DNA or at least lower the amount of treatments to be done with this becoming a permanent part of all future successive cells.To deal with treatment that requires multiple genes to be inserted all of these genes could be added to the cells genetic code in one go or they could be done in waves one after the other to allow each piece of recombinant DNA to be added one after the other or in one go especially if CRISPR is used which can allow for genes to be inserted at proper sites avoiding unwanted mutations and cancers.Ideally both mitochondrial and nuclear telomere DNA will be modified in all forms of gene therapy such as ageing and augmentations to ensure stability and prevent mutations in one that would affect the other in all cells in the body with as stated advanced gene drive technology will ensure the genes will be passed onto each successive cell and to all spermatozoa,eggs and thus all successive children in the patients bloodline via germline therapy and thus the rest of the genepool of H.sapiens.Nanomachines could in time become more effective at this therapy alongside biocompatible microbes engineered to interact with and transfer these strands of DNA using CRISPR into human cells with them either mortal versions or immortal versions that rein insert DNA into cells constantly over their lifetime with themselves having recombinant DNA from endoliths to make them immortal with gene drives as well as receptors and sensors on cell walls making them unable to react with other biocompatible microbes for pathogens causing mutations and hybrids and insert genes to specific cells.DNA from Planarians,Hydra,A.mexicanum and C.elegans will also allow them to undergo cellular repair and memory to counteract any damage inflicted on them which can be transferred to the host and the primary immune system via horizontal gene transfer.Having these have the DNA from bacteria that exhibit horizontal gene transfer with humans or from scratch could improve their efficacy in effectively transferring genes preventing mutations,faults and tumour growth with biocompatible microbes also engineered to detect fight off any tumours caused by this and even fix any mutations that lead to these and faults that may with gene drives also aiding in this.Gene drives and also sections of DNA made from scratch could fix any mutations,faults and other problems that may arise and better integrate DNA from other distantly related animals and plants with DNA from animals that never get cancer added to prevent tumours forming though this would be done to remove cancer from the genepool of H.sapiens.Again advanced gene drives might make the therapy permanent through mitosis and pass onto to the next generation of cells but these microbes might exist purely to fix any faults or if it needs to be done every few years or decades especially with regards to ageing and organ specific treatments.Base microbes can copy genes and the entire DNA in specific cells,tissues and the entire body routinely to determine if gene drives are successful and also to detect any faults that may occur with these results relayed to Paean via nanomachines in them with this occurring if any surprise disease are exhibited by the patients.Before that phlebotomy robots can collect cells from various parts of the body in automated labs and grow tissues from these to allow them to be analysed by human and robotic staff to see that the relevant genes are present or they could put through PCR analysis to check for the specified genes.If patients are fitted with endolith DNA that prevents mitosis from occurring every 10,000 years then this should be of no problem.Ideally these biocompatabile microbes based on the patients leukocytes will be used as a more effective means as a vector than viruses as since they will be forming a permanent feature of the human immune system they will be able to permanently trick the hosts immune system into believing they are part of it as they will use the patients leukocytes as a baseline eliminating the problems associated with foreign viruses and bacteria illicitating immune responses and can carry out corrections of faults that occur in waves over years or even decades as well as using gene drives to make the therapy and corrections permanent and if need be carry out reinsertion in waves.They will also be able to treat all cells in the body for augmentations and also ageing without illicitating an immune response and also by using their malleability to move and squeeze in between each cells with them using horizontal gene transfer and also bumpers.To deal with the use of Cas-9 illiciting immune responses it could be modified to contain some or all human proteins entirely as an human and patient version of Cas-9.Advanced gene drive technology will ensure the genes added to all cells will pass from generation to the next via mitosis with base microbes copying the DNA in all cells in the body and wirelessly send the results to see if they are present into ones patient file with this done regularly.Specific strains will be made to deal with ageing via CRISPR treatments with the DNA for the application to all the cells in the body will be housed in ribosomes and in particular plasmids that will be recreated over and over again via taq polymerase and Cas-9 to be reused over and over again with millions of microbes applying the DNA to all cells in the body at once until all cells are treated.Each relevant genes can be applied all at once or in waves one after another.The genes for these will be applied either by horizontal gene transfer and also bumpers acting as a mini vector with advanced gene drive technology used to ensure the genes pass from one generation to the next.All species of animals including all types of pets,livestock and all species of plants including ornamental plants as well as crops could avail of the same anti-ageing treatments as humans.Pets owned by the public,livestock and animals in zoos will be able to avail of anti-ageing treatments and those to remove genetic diseases and augmentations using specues specific microbes.The effect of endolithic DNA on the development of infant animals with human DNA can be explored as to whether its slow miotic rate could prevent the rate of cellular and bodily development of infants to children to adolescents etc should be investigated as although it would halt the effects of ageing in adult patients it could have the effect of stunting growth in younger patients though this could be counteracted by the rapid development brought on by hormonal factors and also natural growth rates that would be ending with the end of puberty caused by the development of new cells via somatic stem cell production rather than death of old ones by which time the slow miotic rate may be effective at halting the ageing process with if possible their is a high chance that there would be no chance that this would have no effect on the proper development of samples of H.sapiens.Thus the effects of the slow miotic rate on the developments of infant mice to adults born from parents with anti-ageing treatments using advanced gene drive technology should be investigated by itself and also alongside DNA from other extremophiles and also plants that stimulate the production of anti-ageing compounds on animal trials as early as 2023.The effect it has on developing fetuses in mice would also be tested with long living female mice with all recombinant DNA impregnated invivo using spermatozoa from other long living male mice that has all of this recombinant DNA to see if the resulting fetuses have any slow developments in the womb or once born preventing them from reaching puberty and adulthood at normal rates or this has no effects on them until they reach adulthood with this research starting as early as 2023.If it has been shown that this slow mitosis has effects on mice and thus animals including humans then it may be possible to remit this from advanced gene drive technology that would pass it from parents to infants with if need be advanced gene drive technology kept and it removed from spermatozoa and eggs but not the ovaries and testes meaning children could develop to adulthood wherein the anti-ageing strains could reapply it to the host patient once they finish puberty.Otherwise scratch DNA can be added to humans and test animals that causes the slow miotic rates of endolithic bacteria to be present in fetuses and young children but it only expresses and turns on only when puberty is finished once the patient reaches the age of 14/15 with tests on animals and biosynths with human DNA showing which solution can be used.Experiments will be carried out on animals with human DNA and biosynth humans to see the effects of endolithic DNA on the development of fetuses to see if rte development of fetuses and infants is slowed to the point that it would result in pregnancies lasting several thousand years or not.Human patients during this period that wish to have children that have already have had their levels of Phosphatidylcholines and telomeres reverted to an infant state and have endolithic DNA will when planning to have children have through Paean through CRISPR temporarily remove this endolithic DNA from their genome of only that present in their ovaries and testes and once the female has given birth it added back to them and their levels of phostidycholines and telomeres reverted back to infancy via CRISPR should they have depleted due to mitosis with the child once it ends puberty will have endolithic bacteria DNA added back to their genome.This will allow people to have healthy normal children despite being immortal.Solutions to the application of this endolithic bacteria DNA can include instances where the endolithic bacteria DNA will be present in their testes and ovaries with scratch DNA present in only the ovaries and testes also present that ensures the testes and ovaries age at the rate of once every 10,000 years like the rest of the body but the endolithic DNA is not passed onto spermatozoa and eggs produced by them.Phanes will extrapolate solutions to this problem.This concern is minimal but since CRISPR is a new technology and the effects of foreign DNA especially endolith DNA not fully understood especially the effects of bacterial DNA especially endolithic bacterial DNA on humans must at least be investigated.Either way the additions of recombinant DNA from endolithic bacteria will still play a role in halting the effects of ageing in existing living patients of H.sapiens who are adults aged 18 and older especially those currently aged 80-95 and younger that already have finished puberty applied via advanced gene drive technology as early as 2023-2029 with its effects on unborn fetuses passed onto them via advanced gene drive technology done on mice.The same extremophile bacteria DNA used to reverse and halt the effects of ageing ie endolith,T.gammatolerans,Bacillus F,D.radiodurans recombinat DNA will possibly prevent cancer,all genetic diseases,neurological diseases,developmental disorders being passed onto future generations or occurring in the first due to random mutations by repairing mutations via DNA repair that cause genetic based or even environmental based cancer,all genetic diseases,neurological diseases,developmental disorders in the developing thus wiping these from the human genepool after being applied to all patients worldwide when they are cured using germline therapy and advanced gene drive technology.Cancer caused by radiation,carcinogens will be repaired by this DNA.Thus no new extra DNA will be needed to be added to all patients worldwide as those that already halt and prevent ageing will be able to prevent the random mutations that cause these with it also preventing deformities from inbreeding,incest and also damage from teratogens.This would thus wipe these diseases such as cancer,genetic diseases,pedopheilia,schizophrenia,Downs syndrome etc from the human genepool forever by preventing the necessary random mutations and teratogen or other environmental based factors that cause them via DNA repair mechanisms.This would also prove gene protection theory.Bone marrow would have this DNA to halt the effects of ageing but it added in a way to prevent leukocytes housing it as it would be ideal to have them die off at the same rate they do normally to prevent overproduction of them especially during infections with Phanes extrapolating ways to ensure that they and erythrocytes die off at a normal rate but still stay young as in an adolescent of infant to prevent them overrunning the body extrapolating ways to ensure that they and erythrocytes die off at a normal rate but still stay young as in a state equivalent to an adolescent of infant to prevent them overrunning the body.Augmentations would still be added to leukocytes.Phanes will develop countermeasures to any problems associated with gene therapy that extends the human lifespan.This concern is minimal but since CRISPR is a new technology and its effects not fully understood especially the effects of bacterial DNA especially endolithic on humans especially unborn fetuses must at least be investigated.Either way the additions of recombinant DNA from endoliths will still play a role in halting the effects of ageing in existing living patients of H.sapiens who are adults especially those currently aged 80-95 and younger that already have finished puberty applied via advanced gene drive technology as early as 2023-2029 with its effects on unborn fetuses passed onto them via advanced gene drive technology done on mice during this period patients that wish to have children will have their levels of Phosphatidylcholines and telomeres reverted to an infant state will when planning to have children have this DNA removed from their genome or that in their ovaries and tested and once the female has given birth it added back and to them and their levels of phostidycholines and telomeres reverted back to infancy via CRISPR should they have depleted due to mitosis.Phanes will extrapolate solutions to this problem.Thus at first endolithic DNA and all of that to halt and reverse the effects of ageing will be applied to living patients aged 14-65 etc and older to extend their lifespan with this removed from spermatozoa and eggs in ovaries and testes to prevent it passing into future children as it may slow down the development of children to adulthood and may even slow down the development of fetuses to fully born children and also slow down the development of fertilised embryos into fetuses by several thousand years and will be applied to newly born patients once they reach physical and sexual maturity.At the same time research on mammals with human DNA and biosynths modelled on humans will be done to see if this has any effect in the development of embryos into fetuses and fetuses into maturity.If it does then Phanes can develop scratch DNA that has the genes added to the testes and ovaries up be passed to all future progeny but have no effect on the development of embryos and fetuses but only be turned on once the progeny reaches physical and sexual maturity.Otherwise it will not be added to this to prevent it passing into future human progeny only to be added to them once they reach sexual and physical maturity.
All sources of recombinant DNA will be added to both mitochondrial and telomere DNA in all cells.Recombinant DNA from Hydra and T.dohrnii could allow for old senescent cells especially in those receiving the first trials after animal trials to have their cells revert to a younger state almost instantly.T.dohrnii and Hydra etc DNA can be used if shown to be safe in animal trials to be able to cause older senescent cells to reprogramme themselves to a much younger state if scratch DNA is added with this done once every once every 10,000 years by causing Phosphatidylcholines and NAD+ and possible telemeres in the cells to revert to a younger state.After the first patients avail of anti-ageing treatments,animal trials can show if recombinant DNA from T.dohrnii,Nephropidae,Hydra can be transferred to humans to keep telomerase level stable to the point that it keeps it forever at levels of infancy and also able to revert senescent old cells to a younger state automatically after miotic damage every 10,000 years with this tested on animals given anti-ageing treatments except endolithic bacteria.This is due to biological mechanisms within these three species T.dohrnii,Nephropidae,Hydra to be able to revert their cellular and genetic structures to a infant state as they age thus making them biologically resistant to the ageing process