cytomembrane fragments with a stable, typical to living structures of a molecular biological form of the kind of deleterious cyte terminating senolytics terminate, Then screen libraries of wild-type bacteria, fungi, plants, and even virus products to
find out if they effect, modify, block, cause hypertransport at, or disintegrate these molecular biology structures.
Also, a novel thing, place a bunch of the actual molecules and proteins that are the unique biomolecular structures of the kinds of cytes senolytics terminate, at a culture medium, perhaps a (1000 times 1000) million multiwell plate, that contains a wide
survey of bacteria, wild yeast, and variations on what humans think of as beneficial bacteria (probiotics); possibly use micropositioning to place a zone of molecular biology unique structures, a diffusion gap. and then a bacterial growth area: this
causes material that diffuses across the zone to be measurable as to its quantitative effect on the unique molecular biological structures of the kind of cytes senolytics direct their effects at; When some of the million sample multiwell plates find
bacteria, fungi, even viruses hosted by human tissue culture cytes products’ or other materials that cause plugging, blocking, hypertransport amplification, or disintegration of the unique molecular biological structures of the kind of cytes senolytics
terminate, then organisms that produce new senolytics have been identified and can be quantified as longevity, wellness, healthspan, and youthful phenotype producing drugs. These wild type organisms can also be bred to have much higher amounts of
senolytic chemicals. That is a new source of senolytic drugs.
As a technology, an immune response generating functions-like-a-senolytic yeast beverage or yogurt, plant, or plant pollen, bscteria, or even physiologically and attentionally nonperceptible dermal bacteria, similar to a probiotic, that is a senolytic
from immunofunctioning, that is the immunosensitizing bacteria, plant, fungi or even virus causes greater longevity, wellness, healthspan, and youthfulness of phenotype like senolytics do. The humans, that is person’s or people’s immune response to
optimally, the organisms or ok, but less nifty as it goes with actual human sustained production of concentrates, organism material concentrates, where both and either of these causes the immune system to be sensitized to glom and terminate the kind of
cytes senolytics terminate.
So, perhaps: blenderized e coli membranes, combined with cytomembrane molecule transport channel plugs that preferentially populate deleterious chemokine and deletarious cytokine export channel (efflux) transport channels, also combined with some oil to
make liposomes that make it through the GI tract;
So where do the at-wild, at 2019AD society, efflux blocker molecules come from? Organisms at a culture medium with chemical travel zone and an area of chemically changeable molecular biology structures to measure the modification efficacy of each of
the organisms forms is described. As another source of efflux channel blocking molecules that are combinable with immunosensitizing decorations on the efflux blocking molecule, for immunoglomming and removal, which has a senolytic function effect.
It seems like it would be possible to screen a library of naturally occuring materials and molecules,proteins, peptides,andother things, as well as genetically engineered materials like new or enhanced proteins and peptides, to find out if there are any
that plug the efflux channels that are effluxing deleterious biochemicals.
It might be that to a molecular biologist this is sort of easy, like “the transport channel is n angstroms wide and w angstroms tall. Anything hydrophobic/hydrophilic you make with an angle bend, a beta sheet or an alpha helix on it will block the
efflux channel of that size and form. If you make a 20 amino acid peptide tail and put iton the plugging protein, you can use an amino acid that is absent any environemental or body-wide previous immune sytem antigen stimulation, or immune system
activity. Immunocytes that react to the unique 20 mer peptide, after the “immune system alerting dose” are unlikely to react to any other physiological biochemical, minimizing immunological reactions drift, thus keepin nearer optimal human,
immunofunction, human longevity, human wellness, and youthful phenotype form at the human.
The technology is that if just those cytes are immunoterminated which have a bunch of efflux channels where deleterious cytokines, chemokines, and matrix protein messer-uppers are effluxed, then that immunotermination functions like a senolytic:
Gene therapy, that transfects and terminates deleterious cytes with something like apoptosis, gene therapy that produces immunoequivalents to senolytic drugs, or gene therapy that actually produces proteins or peptides that are senolytic in their own
right. Technology of senolytic longevity, wellness, healthspan, and phenotypic youthfulness of form are developing. At 2019 AD, at any deleterious cyte where a senolytic accumulates at but previously did not terminate as it would more optimally do, gene
therapy could be a way to get the 30% that fisetin does not reach, the 50% that curcurmin does not reach, or the numerous kinds of cytotypes and tissues that any known senolytic might not reach the cytoplasm of (cartilidge, eye lenses, osteocytes, other
nonvascularized tissues).
Curcurmin and fisetin are published senolytics; could curcurmin as well as fisetin molecules with an antibody alerting moeity or tail, attached with: an enzyme endogenous to the cytoplasm that divides the curcurmin or fisetin from the immune system
alerting moeity, which then travels to the outer surface of the exterior cytomembrane, which alerts the immune system to terminate the cyte that the senolytic has already localized and concentrated at. That only works if fisetin, curcurmin, andother
senolytics actually localize to deleterious cytes. If they just go to allcytes, but only terminate deleterious ones, then a different technology would be the thing to make. If senolytics do localize and concentrate at deleterious cytes then putting
immunoactivators on them would cause them to be even more senolytic as the immunocytes seek them out.

wellness technology: somehow leukocytes, macrophages and WBCs notice they are more effective at being an active and beneficial immune system when they travel past the capillary epithelia to actual cytotypes that provide a utility definition to a tissue (
chondrocytes, pneumocytes, cardiocytes, dermatocytes, beneficial only immune responses to neurons, glia, mesentary, hepatocytes) to have a curative beneficial effect; that is they make their way past the epithelia to reach pneumocytes to engulf
pneumocytes that have viruses and cure pneumonia when they do that. So, is there a chemical peptide or protein that causes luekocyctes and other immunocytes to move past, or between, epithelial cytes twice as often, twice as fast, or even travel
preferntially along tissue cytes and omit a travel path that is along epithelial lined passgaeways like capillaries? Those would be drugs that multiply the effectiveness of the immune system at interacting with and vanquishing infections. Kindof like
the utility of antibiotics, it could be possible to terminate twice as many infected cytes orinvasive organismsevery 24 hours, rapidifying recovery from illness and improving wellbeing.
screenalibrary,
lookfor variants at a human population, find the genetics of passing epthelia or omitting travel at epithelial separation from the tissue cytes to be beneficially immunoterminated. Gene therapy could then produce muchhigher effectiveness immune systems
at the people whoget the genetherapy who then have immune function that is twice as effective as passing, or passes twice as frequetly throughepithelia. Similarly my perceptionisthe leukocytes WBCs and other immunocytes have chemoreceptors. it is
possible that at humans some human immune systems have twice the ability to sense, accurately a immunomeaningful chemical or molecule; These might be much more effective at sensing things at a distance when to pass an epithelial structure like a
capillary to reach an actual tissue cyte to terminate the deleterious cytes and cause healing. One thing supporting the twice as effective idea is that at other body systems human capability differences between and amongst 2019 AD humans ranges over
amounts much more than twice as effective, human vision, from 20-15 to 20-30, at immunoreactivity, children and adults have notably different immune learning libraries, much more than two times different, even persons of normal mental capability during
2019 AD could have brains that were twice or half as weighty. The technology is then, find an area of the immune system, particularly rapid, affordable, and effective at being changed, where the difference betweena human withthe most beneficial
versionand a median activity humanis twice the effectiveness or greater. Then amongst that list of doubled or higher immune system capability, find the capabilities that respond withgreater ability most effectively to drugs, plants or other organisms,
gene therapy, germline modification, lifestyle changes, and
Possibly things like biologically originated duration of immunity from an exposure could cause some people to be ill half as often (twice effectiveness) at areas, mostly previous to the 21st century, where disease organisms were persistent at the
environment. So these persons would be able to omit becoming ill twice a as long or twice as effectively as others when re-exposed.
Adjuvants. I read about vaccine adjuvants. Are there any physiologically harmless adjuvants, possibly what were known during 2019 AD as GRAS food additives? Adjuvants similar to those that are a part of vaccines; these adjuvants when taken orally cause
the entire volume of the body to be more effective at beneficially developing an immune response. So basically, if a person gets athlete’s foot, taking an oral adjuvant makes them twice as effective at developing an effective immune response to the
fungi, so that makes them be cured twice as fast and be half as likely to have a recurrence. It is possible a bodywide adjuvant could reduce pneumonia, saving lives, although infection frequency could just be from organism variety; also, there is
research on food, lifestyle, and cancer prevention. I have not heard of how taking adjuvant pills could make it so non detectable carcinogenesis is twice as immuno reacted to, thus the persons as a population, as measured at a population, get cancer as
disease half as often.
Wikipedia mentions PAMPS, “Adjuvants accomplish this task by mimicking specific sets of evolutionarily conserved molecules, so called PAMPs, which include liposomes, lipopolysaccharide (LPS), molecular cages for antigen, components of bacterial cell
walls, and endocytosed nucleic acids such as double-stranded RNA (dsRNA), single-stranded DNA (ssDNA), and unmethylated CpG dinucleotide-containing DNA.[4] Because immune systems have evolved to recognize these specific antigenic moieties, the presence
of an adjuvant in conjunction with the vaccine can greatly increase the innate immune response to the antigen by augmenting the activities of dendritic cells (DCs), lymphocytes, and macrophages by mimicking a natural infection.” things that look like
cytostructures, a lot of different things have as adjuvants.”, screening large libraries of PAMPS could find better adjuvants and possibly those that if taken orally, possibly as parts of liposomes, provide beneficial systemic immune sytem enhancement.
It is possible to imagine liposomes, or artificial lipid bilayer bags, that have proteins on their surfaces causing engineerable changes in immune response, that is, being adjuvants;
Bag surface proteins could be kind of purposefully noncomplex, priming for a broad different similar group of proteins to recognize. Noting the lipid bilayer bag could be made out of different lipids it is possible lipid bags made out of really lengthy
new omega 3s like C20 or C27 could be hyperdurable yet physiologically harmless or even measurably beneficial as omega-3s when they disintegrate. My perception is that some kinds of liposomes are ultraffordable to produce, sort of like: oil, water,
ultrasonic transducer manufacturing.
They could screen a library of mlecules to find out if there are better adjuvants than “alum”, aluminum phosphate. Gallium is at the same row of the periodic table so they could try that. Also, noting the milligrams or possibly even micrograms of
aluminum phosphate at an injection it is possible aluminum phosophate liposomes that make it past the GI tract could produce the same chemical concentration as an injected dose from oral consumption; it could have its flavor made palatable rather than
tasting like alum because of the liposomes.
Also, they could find out if oral food: pickles, which contain alum, have an immunobeneficial, all-body adjuvant effect on laboratory mammals, and also do correlation studies on humans that eat pickles. It is possible there are other adjuvant foods,
possibly some kind of recipe for liposomal transport of something immunoadjuvantish, so like a salad dressing, a nugget dipping sauce, a dilute milk drink, or a new kind of quantifiably physiologically beneficial margarine to make liposomes or lipid
bilayer bags with and at. There is a chance that oil coated fried potatos like french fries could have a liposome producing oil-water effect, or a purposeful coating; the technology to think of though is what is at the core of the liposomal bag; PAMPS;
something like “vegemite”, dried yogurt powder enzyme product (basically a bunch of bacterial cytostructures and mambranes as a heap of legos), I read activated carbon, and I think zeolite like aluminum oxide, so possibly some naturally occuring
zeolite like mineral, at liposomal bags. They could also make artificial zeolite that is, imaginably many times more effective than other forms of aluminum oxide, although it might not be.
If zeolites work as adjuvants, then a variation of the food thing sodium silico aluminate might be sort of like a ceramic material that could have a different zeolite like form that could be an adjuvant.
silica gel adjuvants: Other silica materials that might have adjuvant character, be placeable at liposomes, or could have an adjuvant like aluminum or gallium phosphate or ion exchange resins dissolved in them are silica gels, it is possible silica gels
have different AMU amounts of silica networks, so perhaps they have light and medium ones, ones that adsorb strongly, others that adsorb weakly, also, silica gels can absorb liquids which I perceive might diffuse out again over hours, so if there is a
liquid adjuvant it might go well with silica gel with liposomal bag around it; “The hydroxy (OH) groups on the surface of silica can be functionalized to afford specialty silica gels that exhibit unique stationary phase parameters. These so-called
functionalized silica gels are also used in organic synthesis and purification as insoluble reagents and scavengers.” makes custom silica gels sound like they can be tuned to absorb or adsorb custom chemicals, there is even a chance that they could do
some sort of simple localization, although it seems like to a silica gel, everything they are near would be epithelium.
Another, new to me approach to an oral immunization: If silica gels that are really eentsy are placed in liposomes then migrate through the small intestine to the circulatory sytem then perhaps they meet immunocytes like leukocytes or macrophages or WBCs
or some other thing that react to them as a granular particle to be engulfed, I do not know how it works, but after being engulfed a silica gel particle might diffuse out something, even a liquid, that then causes a beneficial immune reaction.
Alginate jello blobs at liposomes might be an adjuvant, “adjuvants may provide physical protection to antigens which grants the antigen a prolonged delivery” That suggests the possibility that putting alginate jello in liposomes would cause alginate
filled oil-water bags to travel around the circulatory system. These might pruprosefully leak alginate, causing some amount of antigens to get alginated-attached and then get gradually re-emitted; also ion exchange resins could be at liposomal bags and
even glom and then gradually re-emit biological molecules of particular masses and surface charges.
Somewhat dubious, but it is my perception there are sometimes trace amounts of blood in stools. That suggests that an adjuvant, like a PAMP, aluminum or gallium phosphate at liposomes, that dissolves or migrates through membranes at the large intestine,
or just contacts the sides of the large intestine, which, based on the blood at a stool concept, might have circulatory system distribution possibilities for something like the micrograms or milligrams of something like alum that could be a bodywide
adjuvant.

longevity technology:

Gene therapy technology:
It seems like a dermal dose of thioglycolate based hair remover cream that, at more minutes of activity than I think the 2019 label suggests, causes moist plasma-like exudate would be an effective, simple to dose (just calculate cm^2 dermal area to
topically dose to get a particular number of milligrams or micrograms of gene product per 24 hours) gene therapy technology, then to produce even greater effectiveness, have the gene therapy modified dermis have an optically activated activateable gene
or gene therapy promotor area that would make it so that you could further program and direct the dosage with laser (like blue laser pointer) activation or the application of a highly available chemical. Among these technology methods is having dermal
gene therapy respond to topical materials, many of which could be available almost without effort, for example, topical tannin, which could come from a leaf poultice available anywhere there are leaves, or a pharmacy, as the person prefers, could
activate all, or just a little part, or even just an easy to remember location (poultice on your elbow once a month or once a year to omit ageing) dermal gene therapy area that causes some particular healing or also wellness response, as well as a
longevity increasing, healthspan increasing, youthspan increasing, and lifespan increasing chemical, or as another item, produce a voluntary behavior enhancing chemical, a mental wellness drug, a cardiovascular well being drug, a senolytic, as well as a
cognitive preserving and cognitive enhancing drug, an general immunoactivating drug that causes the production of more of the immunochemicals or immunocytes that are the first to notice something like a nonenutral nonbeneficial organism at the body, and,
as the research finds effective treatments, an anti-alheimers protein drug; along with those technologies listed and described new better drugs that are thought of, found, and made into dermally available, light or chemically activateable gene therapy
forms abe beneficial and creatable. Like I will see if I can think of a new one, if I can then that verifies humans, that is persons, that is people can invent new beneficial medicines. How about fMRI drugs? fMRI of a various thoughts and emotions
that get the same verbal or writing or software measured, psychology test quantifgied description while having different fMRI data graphics, which is actually a form of algorithmic math representation, as well as positron emission tomography
representation; These identically described but experientially more beneficial ways of a brain having being, isness, content, responsive ability, cognition, feeling, resting or active ambience would be different than they were before adjustable,
beneficial, voluntary and even reversible or wears-off (recoverable) gene therapy; these cognitive ways, mental baselines, emotions, and even different than the thinker things like dreams or responses to media, to the extent that although they have
differing fMRI or as well as positron emission tomography graphic and math measures they have identical measured quantifications at tests, computer tests, and even a person’s self-generated written descriptions of the experience of having a way of
cognition, feeling, or awareness as written by the person. Math is used to define a data space, and the data space here is, with fMRI orpositron emission tomography visual feedback there is something you can prefer, and make actual with putting a leaf
poultice or light ray on your arm to make durably the preferred optimized usual way to be, that can be reversed if you like, that is undetectable to prose, 2019 AD psychology measurements, the surveyed perception of other people, measurements of
productivity of any kind, or computer neural network (such as deep-learning) predictions of your behavior. You like things better, feel better, think better, emote better, and do many other things better, but it is undetectable to others. When you
activate the gene therapy area, such as a light or topical material activation of an area of dermis that gene therapy causes a shift to that version of genetics that causes the fMRI or positron emission tomography math and graphics to have software
create the actual biological gene sequences, that will produce your, that is the utilizers, preferred version of the cognitive direction, ambience, and experience that is preferred. You can put some leaf poultice or shine a bright light on your elbow
once a year to create your preferred form or kind of happy, your preferred kind of imaginative, and your preferred kind of productivity, orderliness or tidiness. It is the “even more opposite than a P-zombie drug” that gives humans, that is persons,
that is people, the ability to experience, prefer, and activate benefits which are language, AI (without digital tomography), behavioral, productivity form and amount, as well as psychologically surveyably really unlikely to be discernable or
distiguishable, although of course fMRI or positron emission tomography of 3d (4d time) maps of neurotransmitter locations and activation is mathematically and scientifically modellable, predictable, and the source of new materials, ideas, content, and
applications with math and science. It is just nifty to be able to make actual a preference of being, isness, response to things, mental forms, nonself-forms like dreams, as well as other attributes that are among the beneficial, all of these while,
being absent the possibility of verbal, written, or nonmathematical description. This gene therapy is a way to be the thing, the more womderful optimal thing, you could not ever describe, after sampling it, and being able to reverse your activation of
the newly optimized way of being. Also, as an amazing feature, any human, that is person, or people, that modified themselves this way would, with very high likeliness of nondetectability, function exactly the same in the perceptions of others. You
would feel creative and happy and productive, and even when between thoughts, feelings, as well as sensations prefer the newly optimized form at the new way you prefer, yet those around you would be absent noticing any change. Along with beneficial,
nearer to being a preferred optimal, change that is outside of description and discernability to others, the person, that is human, or people would like to they can also get voluntary, voluntarily durable, voluntarily reversible, gene therapy that causes
perceptible beneficially experienced personal voluntary change that other people can perceive if that person, human, or people feel like it.

Is there any beneficial protein or amino acid that if gene therapy produced at the optical areas or whites of the eye would benefit human beings? I read that cataracts are treatable with some eyedrops made from an amino acid, it is possible gene therapy
with one dose of instilled fluid could prevent cataracts or provide a one dose cure for cataracts when it causes the production of the cataract curing amino acid. it is even possible that halving or quartering the immunoreactivity of corneas and lenses
using gene therapy would make them stay clearer longer with less surface variation. AEDG and the thymulin peptide combined make humans 4 times more likely to be alive after a 6 year interval, so an eye instilled gene therapy fluid that causes the eyes
to make AEDG and thymulin could possibly be a one dose longevity, wellness existence preserving functional activity drug.
engineering, chemistry, computer ic, computer fab, longevity, longevity technology, treon, treon verdery, physics, lasers, laser, emiconductor, dimension, math, IT, IL, pattern resonance, time travel, chronotechnology, circile, eric the circle, cartoon,
healthspan, youthspan, cpi, manufacturing, fiscal, money, software, petroleum, archive at deviantart com user treonsebastia

All technologies, ideas, and inventions of Treon Sebastian Verdery are public domain at JUly 8,2023AD and previously, as well as after that date

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Longevity technology

Do enzymes make or regenerate NMN at the body? Genes for these could have SNPs that are high wellness phenotypes, gene therapy could be a wellness drug. Although NMN only made mice live 5% longer further study might find a longevity effect, notably
from cardiowellnes and perhaps youthful liver function at removing xenobiotics and reducing cancer,

Are there naturally occuring body produced chemicals that contributed to more than half of 20th century cancers? (with the idea that xenobiotics, stress, possibly EM, sedentariness and food might have caused much of the rest) SNPs about these body
occuring carcinogenic chemicals could be anti-cancer gene variations that people could optimize with genetic engineering and gene therapy. Insulin and growth factor genetics are possibilities, as is possibly sex hormone levels and SHBG (plasma fraction
that gloms steroids); I think there are published systems approaches as well, like mRNA math distribution change with physiological challenges, epigenenetics, and mitochondrial number change.

Longevity chemical: It is my perception that some cytes have less than a dozen mitochondria, and other sites might have near 400; If you do gene therapy or modify the human genome to have mRNA for proteins that would otherwise be affected as to their
amount from having fewer mitochondria per cyte from chronological duration effects produced at those cytes (and tissues) that have upper third of mitochondrial number quantity does more of the previously diminishing protein get produced, thus benefitting
the body and causing youthful levels of protein to exist? Some proteins travel from cyte to cyte as neighbors as well as circulate at the circulatory system, the proteins that travel outside the cyte could be especially engineering effective at sharing
benefit from the gene-therapied, many-mitochondiad cytes and tissues.

Genetic engineering biochemicals to be mRNA coded or produced at the ADP makes ATP cycle, which processes 90 lbs of ADP every 24 hours looks like higher volume production.

I think the ethics and engineering of making humanly intended (mind) physical or possibly neural activation alone, actions modify genetic expression and thus phenotype support the beneficial use of this technology. Prior to 2019 AD and I think anytime,
It would have been nice and beneficial, and not that much effort if people had the ability to modify the output of their genes and voluntarily modify their phenotype from simple purposed actions. Things like skipping a day of food, drinking a gallon of
water, or recieving a two hour pleasant massage could all be adressable gene switches to turn on beneficial effects while being just slightly unusual enough to omit unintentional activation. Would you like your beautiful personally appreciated hair to
grow twice as fast? Get a two hour massage once every 6 months. Getting a massage, even massage at a specific body part to get a specific gene activating phenotypic effect is a possible way to adjust pehnotype voluntarily at the individual, without
medical, chemical, social, or fiscally-linked activity based actions. You can give yourself a massage, become more socially fluent and have more fun. It is highly valuable to have previously heightened cognitive ability at all persons, people, humans to
higher amount, I think genetically engineering persons, humans, that is people at the germline and thus phenotype to be three, four, or five times more intelligent than I am, with the persons, people, that is humans having the ability to make their
beings more intelligent from that is beneficial and more optimal.

Another possibility is a minimal amount of exercise, possibly with different muscles switching on or off different genes, like if you prefer more responsive dopamine receptors (more fun!) then walk more. This increases the amount of mitochondria, the
protein production of the cytes, and possibly the actual number of muscle cytes as well. Technologically among the things are the gene therapy or modified human genome concentrating the production of biochemicals or also proteins that can circulate, or
possibly things like neuron-localized nerve growth factors produced at muscle that then increase growth of doapmine neurons. (the thighs, but only the thighs produce a chemical, that when it circulates increases a growth factor like NGF or BDNF at just
dopamine neurons) So walking exercises the thighs, and that produces chemicals that cause the brain’s phenotype to improve to have more dopamine responsiveness and more dopamine. If you prefer less dopamine you could do sit-ups. wlaking is easier
than sit-ups, to my perception, so people with this intentionally changeable phenotype genetic form might sort of have an automatic happiness fun physiological tenedency,although just genetically engineering people and germlines to be much happier is
beneficial and I support Dave Pearce’ hedonistic Imperative.


As an early 21st century longevity technology, producing more mitochondria, whether with chemicals, gene therapy, germline modification, or exercise, might increase the production of other proteins at the cytes from simply making more mitochondria, which
makes more ATP available, at all of the proteins coded at the genome. It is imaginable that just light exercise could up cytolocalized biochemicals and circulating biochemicals 20%. During 2019 AD many people found it easy and enjoyable to actually
double the mass of some of their muscles, so that might double the amount of a preferred protein or circulating biochemical. Different genome product directors and switches than exercise are likely to be more beneficial and popular than exercise.
Drinking a gallon of water all at once, or getting a pleasurable massage once every six months is much less effort to do, and sustain, as a goal-seeking activity at consciousness than sustained exercise.

As a technology it is possible to do gene therapy on a just one body part, and then have growth of that part make more of the phenotypic chemical like a protein or other biochemical or chemical, to produce local effects (GFP output changes with tissue
use which I think is published as increasing transcription at the utilized tissue, exercising should therefore make GFP at muscle tissue increase, and instead of GFP it could be different physiologically beneficial protein or other biochemical)

Surpisingly muscle, which coalesces to multinucleus cytes and can have its number of mitochondria heighten just with use, could be a location to produce beneficial proteins with go-everywhere-activity, although other gene directors and activators are
likely to be more avidly used, like massage, skipping or eating an anomalous amount of food, or getting a massage, even massage at a specific body part to get a specific phenotypic effect.

(I may have read that 80 year olds might have only 40% of the mitochondrial numbers as 20 somethings); this affects how much energy there is to produce new proteins, how much is produced, and possibly if they are produced at all. I think I also read
that the number of mitochondria, which goes with the amount of )

I read ATP might travel on actin filaments, somehow, even though ATP is an eentsy molecule. It is plausible that tubulin also effects ATP transport. If actin or also tubulin transport of ATP is actual, then drugs or genes that modify the ability of
actin to transport ATP could be wellness drugs and possibly longevity drugs, or even treatment of illness drugs. Also as a possible wellness longevity drug or genetics is the effects on the actual location arrangement and network of the actin or also
tubulin that transports the ATP. Multilane highways or dendritic branches? Concentrated depots and paths, or partially populated walkways? There is a possibility that a computer science approach to optimizing the mathematical network form of actin or
also tubulin transport of ATP could benefit humans at the cytological level with drugs or genes that reprogram actin or also tubulin based transport to optimize human well being. I perceive I have heard about research on what actin and tubulin goes where
during meiosis and why, so perhaps some of those techniques and research could benefit the technologization of actin and tubulin engineering for wellness and longevity.

I read about some chemical in Scientific american that is sometimes described as “exercise in a pill”; exercise increases the number of mitochondria at muscles, perhaps “exercise in a pill” at the circulatory system reaches more cyte types, even
neurons and also tissue types and increases the number of mitochondria at them, increasing wellnes and possibly heightening lifespan from removing nonoptimal effects at linked dynamic systems.

Another thing that increases the number of mitochondria is branched chain amino acids, “Branched-chain amino acid (BCAA) supplementation increased mitochondrial biogenesis in skeletal muscle [4]. BCAAs are 3 of the 9 essential amino acids required for
humans.” [not made at humans though]

Genetically engineering food crops to make BCAAs could have quantitative measurable wellness effects, and just possibly from more mitochondria, beneficial longevity effects. Soybeans, wheat, legumes all contribute to protein sources during 2019 AD, and
these nd other plants could be engineered to make BCAA.

Developing a plant-based milk that tastes more delicious to the majority of humans than dairy milk would be a valuable ethical vegetarian technology. Among Europeans and Americans milk, which could be technologically improved to be better-than-dairy-milk
plant based milk, provides much protein to many people. Genetically engineering plant based milk to have BCAA, possibly BCAA optimized to generate more mitochnodria is beneficial.

Technology that enhances vegetarian milk: Are there any good tasting surfactants? that would make the little globs customizable in size for flavor adjustment (improvement).

Can you put veggie milkpowder as a thin layer through an embosser with the resolution, or higher, of a holographic decalmaker? Microfeatures at blobs eentsier than a wave of light could then be used to technologically improve the milk product as
solvated globs; Also I have read about superhydrophilic and superhydrophobic surfaces, teeny spires (hydrophobic) or angled sided spaces that look like ingots (hydrophilic), it could be that embossing vegetarian milk powder to make hydrophilic or
hydrophobic features could enhance flavor. Also there is customizing globs to physical tongue receptor size for an optimal fit. Uncomplex embossing of a powder could be ultra-fiscally favored. Ihave seen candies made of sugar that have a hologram
embossed on them, so lightwave feature size at carbohydrates is a technology that has existed since the 20th century.

.5B GSK:
I perceive that GSK may have (or may not) have links to companies like nestle; could cocoa, and possibly thus chocolate, be wavelength of light feature size embossed to enhance flavor?

Are there any naturally occuring amino acids or peptides that activate the taste receptors that activate when milk tastes good; this is completely different than MSG (monosodium glutamate) in milk, but the technology of an amino acid or eentsy peptide
that enhances the flavor of veggie milk could be possible.

school lunch veggie milk
It seems like things like vegetarian nut or soy milk could be cheaper to produce than dairy milk. I think it is possible to develop the vegetrarian milk flavor until it is preferred over diry milk among most people. It is possible that more people,
throughout their lives, would like an utilize vegetarian milks if they received them at school lunches.
It might even be possible to use vegetarian milk to cause people to be weller in different ways. If the serving size of vegetarian milk is 10 Oz, as compared with the previous 8 Oz at dairy milk at identical calories, then people might drink more fluid
at school lunch. Drinking more fluid at school lunch causes a population effect of eating fewer calories at the rest of the food. Then noting that at 2019 AD, research supported that vegetarians had less heart disease, cancer, diabetes, and weighed
less with a better BMI than the rest of the population, the school administrators could say, “there’s nothing wrong with our food, but it’s awesome students are drinking nut/soy/oat milk and eating less of the other items and more vegetable sorced
food instead” So the people at school get more ounces of milk, they are, as a population at least slightly wellness heightened, and the school district spends less on the milk. That all combines to support vegetarian milks at school lunches.

MWI, that is Many Worlds Interpretation of physics: thinking of ways to cause a larger number of MWI universes to be generated from something going right, that a person, that is a human likes: The amount of quantum states produced from a proton (protons
have their own quantum effects, among them tunneling) is, I think, larger than that of af a neutron

Note: about protons or neutrons having different numbers of quantum states, and that they each generate quantum state changes at different amount for each unit of chronological moments: I think protons have more quantum states as an area with t as a
dimension, although it could be otherwise. Thinking about the quantum effects of neutrons ( I am thinking about neutrons taht are a part of atoms): if a neutron (just one as part of an entire atom) is changing a chemical rection in a flask with the
isotope effect it may or may not be having a quantum mechanical effect at a multitrillion atoms simultaneously at chemical system that is some chemicals in some water in a flask.

That the isotope effect of one (part of an atom thus nondecaying) neutron, which should have at least some analog effect on all the actual atoms at the chemical sample if analog, functions at a distance (at an aqueous chemical system it could be nm, Cm
or Km); the analog possibility comes from what seems like an analog nature of things like circles and various math of topology that seems like they could be having an effect at a 3d chemical system; The thing is that I perceive a physicist might say, “
even though you can observe it into a circle, or a sphere, or even that the sides of the container are changing (however minutely) to produce either space or time analog-like things, it is all describeable with a quantum wave function and quantum
equation, so prior to 2019 AD observations that support quantum theory support that it is actually just a quantized system, the neutrons are not having an analog effect when one neutron produces an isotope effect on an entire flask with quadrillions of
atoms at a flask of aqueous chemicals”.

That a neutron being turned into a proton causes the number of quantum states possible, as well as generateable, per unit of chonologically measured moments, suggests that making neutrons into protons could be a technologizable way to purposefully make a
larger number of MWI universes when a sentience, like a person, that is a human likes what is going on.

When a neutron is turned into a proton, that proton often attracts an electron, (does the casimir effect preclude the possibility of naked protons staying solitary?) which then do electron and photon quantum things, numerous of which are described at
peer reviewed published material as being quantum effect actions, each quantum event with an MWI branch universe 92019 AD theory); converting a neutron to a proton then causes a much larger number of MWI branches to be generated, for the theoretical
duration of the universe. Although I am not yet educated sufficiently able to use aleph numbers to do calculations, if the universe happens to be chronologiclly nonfinite then the number of MWI universes generated from one neutron being converted to one
proton is a nonfinite number, and further, that nonfinite number has many many MWI branches (I perceive I have read that human researchers might have different scientifically supported ideas about whether MWI branches are finite or nonfinite in quantity).

Thinking about a new proton coming from a neutron: a new proton at a chronologically nonterminating universe would have a nonfinite number of MWI branches though; or perhaps could, I read about people who think cooling all atoms to their quantum ground
state is a spontaneous actual process at the universe; although MWI suggests that things like time crystals and the delayed quantum choice eraser could effect quantum-capability of atoms retrocausally or cyclically at some amount of the MWI universes; I
have heard of these things, so the MWI universe I am in might be entropically nonmonolithic

A technology that utilizes the difference between a proton and a neutron to cause more MWI branches where a human things things are pleasantly going the way they like. I like Serina, so when I send her a text, and she replies I think my life is going
well and I am particularly enthused about MWI branches arising from a universe where Serina texts me, I then press “make proton” on my phone, and the phone makes some protons out of neutrons. That generates a nonfinite (proton at nonchronologically
finite universe version) number of universes that branch from one where Serina communicates with me. I could even press on “make lots of protons” if Serina says something like, “I like you” or “let’s meet”.

AI and software developing MWI technologies: With MWI technologies it is my perception it is endless quadrillion of times better to write them immediately rather than wait a moment to write them as a vast plurality of MWI branch universes will
potentially benefit from new, accurate, actual, technology producing MWI content; that suggests that AI (artificial intelligence) writing, communicating, or doing experiments could then validate and quantify the “research on the MWI should be
accomplished immediately as it affects endless quadrillions of universes differently if you delay 1 millisecond” way of looking at the MWI. A human that builds an AI that figures out new things about the MWI, or even just develops the math and
technology space, a few trillion times faster than a thinking writing human is a thing that could be of value from the perspective of a person like me that values making happier more optimal, Dave Pearce’ headonistic imperative actualized universes. (
AI produces MWI research and technology a trillion times faster than me) During 2019 a 4Ghz processor would do 4 billion computations a second, and 250 seconds would be a trillion computations, so an AI doing a few trillion more MWI research things and
technology items than I would in an hour is plausible; a few sequential instructions at a parallel 4Ghz AI compared with a few minutes of human thought.

Immunizing against a million topologies; screen antibodies to things like “a torus of alpha helices” or a “square of beta sheets”, or “something made of protein twice as wide as it is long” at human tissue culture. This edits the amount and
kind of chemicals and biochemicals shared between cytes. Then find out what these categories, and mathematically developable forms (if it kind of works on one topology, then they can find logical math extensions from that topological shape; immunizing
against alpha helix torus is 20% effective at heightening organism, like a human, that is a person’s longevity, so the math suggests: vary diameters, immunize against an “8” and an “88”, and immunize against a tetrahedron made with a torus on
each side, and others) of them to find the topological antibodies that cause human tissue culture arrays to be weller and have greater longevity; (immunize against many to mid AMU rod looking groups, curlies, heaps of alpha helices, piles of beta sheets)

Immunizing that prevents senescence could be the effect of screening topological libraries of antibodies. Notably research on senolytics apparently supports this. Senolytics terminate senescent cytes; as a result the senescent cytes cease to export
chemicals and biochemicals to their between-cyte environment as well as the circulatory system. Those senescent cyte produced chemicals caused unwellness at other previously well and non senescent cytes. Terminating the senescent cytes causes the well
cytes to have things continue to go well, and I think I read that mice that get senolytic therapy are healthier, perhaps phenotypically younger, and have longer lifespans, all from eliminating the chemicals the senescent cytes made. So, could you
immunize a lab mammal and then a human, that is a person, against the entire library of chemicals and biochemicals that the senescent cytes produce; such an immunization could have the effect of a senolytic drug as it mops up the nonoptimal chemicals.

So, supporting the screening of topological antibodies, senolytics’ effectiveness and conceptual form apparently supports the idea that there is a whole bunch of things, and that if you treat them as a group, you can get an overall bulk effect, even
though the bulk effect could contain optimal and nonoptimal chemical effects simultaneously.

Some different bulk effects at the human body that I think are published as causing benefit are things kind of like: more mitochondria causes more protein production, and more mitochondria thus produce greater wellness and youthfulness. Another bulk
effect is putting more genes, of any kind, on histones, I think (possibly) causes greater longevity and fidelity of proteins produced.

As a bulk effect, immunizing against topologies could produce beneficial effects like wellness and longevity at the entire body. The thing is to make a lot of them and screen the library to find the ones where the average and distribution of the blended
bulk effect is quantitatively and qualitatively measured as much better for the human than an absence of the topological immunization.

Going with this technology of Immunizing against extensible classifications (like topology) could be immunizing against electric charge of an entire protein. Immunize against everything with -.499 to -5.00 charge and a thousand others from +4.99 to -4.
99). this diminishes the amount of the proteins circulating, or zapping those cytes with these charges of protein at their surface; this would have a bulk effect, and then the bulk effects of a few thousand variations, or a few million variations, are
listed at a computer with the immunization that produces the greatest beneficial bulk effect at the top of the list.

Screening topological and protein molecular electronegativity: Make a human tissue culture of neuron, cardiac and other human cytes, although multiwell plates already exist, you could use IC production technology to make a 1000 times 1000 grid, which is
one million human tissue culture samples per screenable plate. The thing is that if you screen a 1000 times 1000 times physical array you have characterized the effect of more than a million different antibodies on the wellness and longevity of things
like neuron and cardiac and other tissue culture, which could be predictive of wellness and longevity effects at those tissues and also the entire organism.

Notably increasing wellness and longevity at the entire organism is the resulting beneficial drug from screening vaccines to topologies at a big array. These new wellness longevity drugs are produced when topologies and electron negativities of proteins
are found that have beneficial bulk of physiology effects.

I read that BCAA cause more mitochondria to be at cytes. A person with abilities at planning and creating food, might be able to make a new popular food based completely around BCAAs, possibly a completely new BCAA, with a different amino acid sequence
that tastes better than 2019 A.D. BCAA (Noting the mitochondrial amount going up I think I read, has higher wellness (and possibly longevity) effects.

I perceive that caffeine is a 2019 AD popular drug, notably at beverages.

So, can you attach a biguanide (metformin-like molecule) to caffeine, which alread tastes aversive, to make a longevity version of caffeine that is a stimulant that makes people live longer and have less heart disease and less cancer. Lilacs make
biguanides, tea makes caffeine, so both at one gene engineered plant could be produced. Along with the rest of the world China might go for longevity tea from a GMO crop.

If you chelate beneficial things, even like a biguanide (metformin-like effects) does the taste become much milder? EDTA seems to be mild flavor. Are there any naturally occruing plant products that are chelation agents? Then you could blenderize and
fractionate the source plant and soak the thing to be chelated in the soultion that had the naturally occuring chelator concentrated.


Although ECGC is already at tea, perhaps it could be engineered into coffee.

Curcurmin comes from a plant in the ginger family, perhaps ginger could be engineered to be good for people and make curcurmin. A mild flavored more massive Ginger root with curcurmin might replace the potato

Tea bred or engineered to have 10x as much ECGC, noting tea already produces ECGC.
engineering, chemistry, computer ic, computer fab, longevity, longevity technology, treon, treon verdery, physics, lasers, laser, emiconductor, dimension, math, IT, IL, pattern resonance, time travel, chronotechnology, circile, eric the circle, cartoon,
healthspan, youthspan, cpi, manufacturing, fiscal, money, software, petroleum, archive at deviantart com user treonsebastia

All technologies, ideas, and inventions of Treon Sebastian Verdery are public domain at JUly 8,2023AD and previously, as well as after that date

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