It is also possible soaking the paper in 3 of the ingredients, and just printing the electroporation circuits, biochemicals, DMSO (or more effective duoalkane sulphoxide), actual gene sequences, bacteria, single or doube stranded DNA or RNA viruses, the
polymer layer that causes deliquescent (autogooey) liquid layer to be at the dermis side, and the immunocolorizing material that lets people know when the gene therapy is successful;

How to make the sugar based cytomaterial inserting probes: These sugar linear probe things are published as functional at immunization, so they can reach through the dermis to the circulatory system to do immunoactivities, a few technologies to make
these could be a mm or less deep sugar 9600 DPI print homogenous surface, then have lasers engrave the sugar layer to make various amounts (millions? thousands?) of probe/insertion items per 3 mm paper circle; another technology to make the sugar probes/
insertion things, is to just spray coat the paper with microparticulate sugar probe insertion shapes, and measure the actual effectiveness of the actual percentage of right side up, high angle sugar probes that spontaneously occur. It is possible that a
technology that causes an order of magnitude greater transfection efficiency could make a 40-70% right side up sugar probe gene therapy transfection paper circle have the transfection effectiveness of a 99th percentile right side up sugar probe array;
One possibility for another power of two or even order of magnitude of transfection efficiency is to have the sugar probes have materials in them to be electrically conductive (calcium ions are published as having utility at gene transfer), this could
bring the electroporation voltage effect to the dermatocytes at depth, likely near the endothelial capillaries (where I perceive sugar probe immunzation geometry sizes might reach), another possibility if the sugar probes are laser engraved is to have
them have linear channels on the sides that cause the transfection material to flow to the tip of the sugar probe, also I read about superhydrophilic microsurfaces, they favor liquid coatings, and look sort of like troughs; bulk mass production of liquid
transport geometries at sugar probes: putting linear grooves at the sugar probes might also work at mass produced sugar probes, with the nonspecific application angle as a spray, perhaps the sugar probes when manufactured and previous to placement at the
paper circles, could be sprayed on one side with a surface tension reducing agent or some other thing that causes liquids to like flowing a particular direction;

The bacteria would also produce beneficial wellness, healthspan, longevity youthification chemicals even at the non CRISPR/cas9 part of the bacterial genome; At mice and humans, the measured longevity wellness and healthspan of the bacteria would be
beneficial even preceding the highly beneficial voluntary gene therapy part;

As the bacteria’s proteolytic nutrient producing enzymes are also the enzymes that make youthification chemical peels functional administration can be at any body location, puffiness of a less than 1 cm area (1 ml tissue transfected/ bacterial
colonized continuous output CRISPR/cas9 gene therapy vector) could be an engineering standard; the bellybutton could be the least noticeable, and perhaps 90th percentile or higher of being least probed with fingers, the bellybutton could be among the
90th percentile at user adherence, is completely sensationless, does not cause visible change, has laser addressibility if persons, that is humans, that is members of groups of people, that is homo sapiens would like to laser modify the gene therapy
process, notably some varieties of gene therapy are published that are responsive to light, so the 1/6th of 1 cent gene therapy technology is affordable and has further reach, a laser adjustable version is also possible.

Also, to verify the gene therapy has been installed, the bacteria could produce a chemical that causes an aesthetically pleasant color change at the paper circle (similar to color antibody diagnostics), the paper circle could change the visual pattern of
the aesthetically pleasing color when the gene therapy had progressed beyond the bacterial vector and was being produced at the user, person, human, or application’s genome

Think of a way or cause for people to distribute something that is less than 1/10,000 of a $

Longevity technology: a new kind of autophagy could be linked to longevity, healthspan, and wellness, if it is functional: Noting the idea that cytoplasm might have nonorganelle enzymes floating around, catalyzing things, possibly even comminuting or
nonactivating some cytochemicals: These enzymes, outside the lysosome remind me of autophagy, autophagy is linked to cytorefreshment, longevity, and wellness, it could be that the genetics of having more cytoplasm enzymes outside of organelles do
something like an alternate version of autophagy, refreshing and recycling physiostructures and chemicals, so looking at a variety of mammals, notably things like multicentury lifespan whales, beavers, naked mole rats, bats, tortoises, and parrots and
400 year lifespan or longer clams, kings holly, and creosote (reminded of mitochondrial apoptosis) any cytoplasm enzymes, notably proteolytic or membraneolytic, outside of organelles (like lysosome) could be quantified at mice as to longevity wellness
and healthspan effects, and if beneficial made into gene therapy, drugs, or germline enhancement or optimization at humans;

Noting autophagy is linked to longevity, wellness and healthspan, and I might have read that AMPK heightens autophagy, it could be possible to engineer larger amounts of autophagy from 1) cytoterminating chemicals, proteins or peptides as drugs (possibly
kind of senolytic like), also as periodically automatically activated gene therapy; an accumulation of physiologically beneficial peptides, like AEDG heightening with each sleep occurence, could, when they accumulate to a particular amount, cause the
gene therapy modified tissue to produce a new circulating amount of the new autophagy chemical, causing fresh autophagy and renewal at the living human; these likely would benefit from localization to create beneficial differences in concentration and
action at different cytes and tissues;

Along with heightening cytoplasmic autophagy like effect enzymes, periodic production of autophagy as algorithmically activated with a completely beneficial physiochemical that accumulates (epithalon, thymosin, likely a variety of things, possibly even
beneficially heightened circulating omega 3 DHA from accumulation of DHA from endogenous production), there is also periodic, quantitatively measured as beneficial to longevity, wellness, and healthspan, triggering of mitochondria to zap cytes, causing
leukocytes to absorb them.

New to me autophagy longevity technologies: Another possibility is a periodic genetic activation of the production of a non-autoimmune activating production of antigens at the surface of cytes, possibly those at the 40th percentile or less of cyte and
tissue youthfulness, where the percentile is an experimentally quantified causative function at wellness and healthspan; this could possibly be quantified with mRNA transcript production’s deviation from a beneficial range (reminds me of engineering
tolerance, the 2nd standard deviation at the non-preferred side of the distribution) Periodic activation of the beneficial new form of autophagy could be linked to the accumulation of a physiologically beneficial chemical (epithalon, thymosin, omega 3
DHA);

New to me autophagy with high cytotype localization technology: I perceive I read about where two different receptor proteins, when both activated, caused a cyte to be exposed to a chemotherapy drug, causing fewer well cytes to be dosed with the
chemotherapy; Responding to things like: At cytes that are at less than 30th percentile of wellness, longevity and healthspan heightening physiology, the translation/transcription protein generators receive instructions to make notably larger amounts of
one normal type, but comparatively tissue and cyte unusual chemical, protein, or peptide transport channel, perhaps something that occurs less than 1/400th of a cytes’ external receptors or transport channels, and at perhaps less than 1 per 200
different cytotypes and tissues, it then becomes 1/20th to 1/40th of the proportion of the cytes external transport channels and receptors enumerated amount, (twenty or ten times as populous as previously), and then an transport channel optimized
autophagy causing protein, peptide, or genetic effect causes autophagy at that cyte; The concentration of the autophagy causer is 40 times greater at the 30th percentile nonwell cytes than at well, wellness, longevity and healthspan functionally active
cytes; Technologically it seems possible that autophagy could be tuned to to be activated when the transport protein heightened autophagy causer is above 30 times that at an unaffected cyte;

As a another supporting technology, it is possible a protein, peptide, or peptide effluxing transporter could be part of membrane accumulating cytotransport duo; at a well, longevity, wellness, and healthspan support heightening, functional cyte the
transport and efflux of a particular protein, peptide or chemical from the duo, which could be spontaneously occuring at a nonmodified organism or human, would be about the same amount, they would omit accumulating the transported protein, peptide, or
chemical at the cytoplasm; that would cause any autophagy activating chemicals, proteins, peptides, or gene products, to pass through well cytes above the 30th percentile causing a minimal amount at the cytoplasm of the 30th percentile of higher cyte;
When the measure of the longevity functionality, wellness, and healthspan of an unwell cyte occurred it would cause the unwell cyte to make large numbers of the harmless chemical cytotransport structure, causing it to be 40 times more prevalent at the
unwell cyte; natural endogenous circulation of things that that particular transport protein transports, would reach 40 times the usual amount, causing a gene at the cyte to make an autophagy causing molecule endogenous to they cyte; another technology
is to have the autophagy causing protein, peptide, or chemical that is linked to a 40 times usual amount transport protein moeity for hieghtened transport to the 1th to 30th percentile cytes, be produced at a different area of the body, perhaps from just
a few gram, or even one gram area of gene therapy;

Technologies that could discern longevity, wellness, healthspan contributive and supportive cytes above the 20th percentile: mRNA, possibly gene therapy that caused presence of nonbeneficial mRNA, cytochemicals, proteins, or peptides, to cause

Normalization algorithms create higher and higher longevity, wellness, and healthspan physiochemistry, it is possible that technologies that cause the least (0- 20th percentile) longevity, wellness, and healthspan supporting cytes to be quantified as
they relate to the to other cytes at the body, to be as a relation to all the cytes at the body continuously or periodically, would cause double digit % increase in baseline longevity, wellness, and healthspan annually, this could physiochemically
contribute to a percentage of longevity increase, and noting the continuous improvement of 20% more longevity, wellness, and healthspan cytes annually is likely larger than an annual accumulation of nonwell cytes, that like actuarial escape velocity,
things move towards wellness, longevity, and healthspan faster than they wear out; The effect of multiple 20th percentile autophagy events causes the after autophagy organism to be accumulate towards what would previously have been 90th percentile or
higher cyte function as to longevity, wellness, and healthspan physiochemistry; that similarity to actuarial escape velocity, which I have also read is called longevity escape velocity, is alogrithmically related to making each iteration of cytes that
support longevity, wellness, and healthspan as the new computational basis for the percentiles. A technology I read about, which might be called gene switches, makes things like AND and OR as well as other logic forms out of simultaneous gene
modification effects; The technological algorithm that supports the heightening of each iteration of 20th percentile or less’ autophagy to be based on a new foundation could be based on things like: gene therapy at the entire body causes harmless
unique peptides or proteins to be produced, which then utilize mechanisms that are usual to move to the exterior cytomembrane of the cyte they are produced at, This labels each cyte with a non immunoreactive cytosurface diagnostic of what it is doing and
making, it is possible the diagnostic proteins that make their way to the cytosurface are actually beneficial, noting the cyte is still alive, or also possibly beneficial to neighbor cytes, the (0-20th percentile) producers of just the completely
beneficial interleukins, possibly some onconeutral neutral growth protein like BDNF, or if immunotransparency and absence of immunoreaction of any kind is beneficial, perhaps slight variations on water transport proteins (aquaporins), where variations
from the usual protein amino acid sequence would let diagnostic things that cause the 40 times greater amount of transport channels to cause beneficial autophagy find and have effects on cytes at less than the 20th percentile; Gene logic could also just
have quantifiable things effect logic, to cause the production of mRNA that makes the 40 times higher amount of autophagy transport channels at the cytomembrane; it is also possible that gene logic can just directly make autophagy functional effects
directly at any cyte where the gene logic notes 0-20th percentile longevity, wellness, and helthspan physiochemistry;

also possibly periodic wellness chemical accumulation (epithalon, thymosin, omega 3 DHA) that activates the production of “make transport channels” at the unwell cytes;

Also possible is the unwell 20th perctile making 40 times more transport channels, and then a human, person, a member of a group of people, that is a homo sapiens, takes a drug to cause the autophagy, much more beneficial is an automated, periodic,
automatic process, which could technologically be based around a one gram or less area of gene therapy that emits things that diagnose, modify and cause autophagy at cytes at the (0-20th percentile) of longevity, wellness, and healthspan, noting the
continuously new distribution’s new foundation; Notably though, there is also the technology of a multihundred year longevity depot injection that just causes autophagy anywhere a group of antibodies (I perceive I read about fewer AMU versions of
antibodies) note some unusual distribution of surface characteristics (proteins), also I think I read about antibodies that can glom to receptors to make them stay active, go less active, or just be neutrally at the cyte, this might function at
cytotransport channels as well, possibly antibodies glomming unwell cytes

Gene logic

possible that without antibodies, this would cause autophagy at virus inected cytes from their being at 30th percentile or less of wellness quantifications, the incidental antiviral effect could be beneficial to both the person, and even possibly reduce
the amount of viruses circulating at the population. The 30th percentile of wellness autophagy technology could be a nonimmunosystem new to me approach that kind of incidentally removes virus infected, oncocyte, and even possibly, fiberous nonutility
tissue, which might be replaced with weller cytes. It is kind of like a new to me, multipurpose, new (30th percentile quantified effect at any nonoptimality) kind of senolytic, with different criteria than various intracyte deleterious products like
interleukins;

the versionbs of these technologies or others that create longevity, wellness, and healthspan beneficial new versions of autophagyor germline enhancement or optimization


Longevity technology: an antiglycation mechanism could be found at some animals then tested at mice anfd humans to see if it increased longevity, healthspan, and wellness, also, gene variations at humans like SNPs could be correlated with wellness and
absence of or reduced glycation at humans, and then causality measured with mouse studies to find beneficial genes for human gene enhancement or also optimization; notably though I perceive plants also do the nonpreferred glycation of proteins, so
anything at plants that is produced at cytes that reduces glycation could be tested at the mammalian genome to find out if it benefits longevity, wellness, and healthspan, notably the 40,000 year old King’s holly, the 10,000 year old creosote bush, and
the 4k year old conifer might each have a different plant genetics of antiglycation that benefits their longevity that could be tested at mice and humans.

When a person gets gene therapy, they might like having a way to utilize their previous genome at some or even all their cytes: backup with gene therapy: crispr/cas9 appends the new genome to the previous genome, puts a start codon (or start codon group)
imaginably at a sticks-out circly pouf on the nucleotide double lane topology, the body ignores the first, previous, genome, which might even have some stop codons crispr/cas9ed into it at easily recognized locations (sort of like restriction enzymes say
“thing here” perhaps stop codons could be placed at the previous genome anytime a CCCCC occured, so if editing it out it would be near errorless to utilize the previous genome, if the utilizer felt like it.

I have not read about any siRNA longevity molecules, It is possible these are possible, and that siRNA that heighten AMPK and decrease mTOR (or another 60% greater mouse longevity mTOR drug, that works on just mTOR1 rather than mTOR1 and mTOR2), siRNA
might be even better at reaching the CNS through the blood brain barrier as their AMU is less than some other nucleotides



I perveive there might be a million or more actin lanes per cyte, at 70 trillion cytes, that could be like a math iteration structure with a really large number of math areas to model, algorithmize, and generate, something like interpretations about
things as compared with, and possibly as a beneficial resource to the brain and CNS; Like what if the 70 trillion cytes with actin paths simulated various effects of various possible things, and communicated the modelling results with a one thing one
meaning language;

um, I perceive how DNA per cyte has lots more data space, it is just that actin paths also have lots of functional movement, geometry, spatial accessibility…

It likely already exists, but is there a CRISPR/cas9 automatic gene sequence linker? I perceive different lengths of DNA have different easiness of transfection like 3/4 a decade ago (2011), but the perception I have of of CRISPR/cas9 is that they have
figured out how to make. transfer, and activate things with out about 20,000 genes with simultaneous high velocity, high accuracy, and high editing sucess (transfection); complementing that, perhaps at a variety of sizes, could be something that is
effective at attaching one sequence to another, at a functional place and physical form, (imaginably, histonated, less histonated, a loopy part available because of a mitosis, translation as well as transcription event, meiosis, or some new thing that is
new to me)

so, one approach is to find the easiest histones on earth; some mammal has histones with really long, super editable, physical like-new preservationess above other mammalian histones, really available DNA; completely making a synthetic sequence of that,
then making if even more genetic engineering friendly, then placing it at a variety of mammals, likely including humans, could benefit DNA transcript fidelity, DNA preservation, translation velocity at organisms, like humans, as well as heightening
beneficial, functional, engineering friendly genetic editing, modification and genetic engineering;

Also, besides unlooping things, and actually I have no idea what they do, but I perceive DNA is unusually accessible during translation, mitosis, meiosis, and possibly some kind of “make this” thing that something at the nucleus says, like imaginably,
if something says “make ribosomes” perhaps hundreds of ribosome making DNA locations get sequentially availabilized rather than just like one, over and over again; so, it seems possible they have tried loading up a well human cyte with a numerous
quantity of things to translate at DNA, so they could unspool a bunch of DNA, efficiently, and edit it;

Along with making like a big list of DNA access producing translation instructions, they might have some amazing thing like a DNA translation smoothified new to me histone that makes DNA completely available to editing (like crispr cas9 or more advanced)
while being a place to have a lot of DNA stay linear, functional, well, effective, and immediately ok to utilize without repairs; the smoothified histone could even be nifty at some ethynilization methylization optionalizing, gene modification now able
to be unaffected from methylization and ethynilization molecular topology effect; a smoothified histone like an inspection and upgrade access area of an airplane;

Is there an artificial intelligence thing where if people, or AIs share the technology the sharers accumulate greater prosperity; it is possible AI APIs

Longevity technology: finding human gene variants that predict responsiveness to different longevity drugs would be beneficial. Rapamycin and a rapalog each are published at 60% longevity increase, my perception is that that math functions describe a
medianized response, so noting half of all persons are above median, perhaps a greater than 60% rapamycin response could be predicted, and a gene therapy or a coadministered gene product upregulating drug might be able to cause a 99th percentile
rapamycin response.

Squiggles developed with AI deep learning have been published that cause primate brains to produce more activity than views of faces and nature, it is possible that new squiggles developed with deep learning AI could cause greater amounts of response
than the beauty responding areas of the human brain, and that when humans view these squiggles people describe them as attractive, appealing, and beautiful. I am not aware of research on deep AI generated squiggles that are beauty experieince activating
above that of nature and human faces and form that are three dimesnional or that vary gradually. Among many beneficial uses of these squiggles could be decorating architecture, decorating energy producing utility plants (among them wind, photovoltaic,
nuclear, chemical), hairstyles, and notably anything with above median utility and during the year 2019 less than median aesthetic impression; trash dumpsters, parking facilities, some public transit, medical appliances, anything on a list of survey
generated “could look better” things at public and private spaces.

It is possible that things that are already aesthetically beneficial like plants, landscapes, nature, aesthetically appealing humans, could have versions and variations of deep AI developed beauty squiggles, and that actual spaces could be quantified as
to their beauty response as well as images duplicated. Also, automated mechanisms or also robots that clean and arrange dwelling spaces could arrange items that humans view and utilize to be simultaneously highly available and, with beauty squiggle
technology, arranged at ways that cause higher subjective well being increasing beauty response than the person doing their own arranging. People could of course do their own arranging, they might more often appreciate deep AI guided arrangeements of
things.

Aesthetically mild to beneficial things like computer interfaces and printed text, could generate a beauty response while being combined with other deep AI developed squiggles that simultaneously increase comprehension and retention to create beautiful
and cognitively enhanced interfaces and text; I favor a computer interface and text interface that causes heightened sense of well being (the psychometric: subjective well being increase from experiencing beauty), the “nice space” architecture effect,
the “startlingly gorgeous” art object response, and even the human reponse to human female beauty response at persons with any form of human sex chromosomes occuring at 98% or more of people;

There are no top of page results on a search of “chemical vapor deposition metallurgy” so these are some chemical vapor deposition metallurgy technologies. I read that 3 nanometer silicon features are produced at integrated circuit technology,
noting that arrays of atoms can have much more than an anisotropy or two at (25 atoms per feature, one to 20something billion features per IC, ) a trillion deposited atoms, that suggests that rather than a 3 nanometer feature size a 1 nanometer atom
group feature size could be produced, and that the dots could be customizably amorphous, crystalline, variations of crystalline or other forms.

rather than an integrated circuit phototemplate it is possible a UV laser could produce a regular array of dots or shapes at a photoresist with diffraction grating technology, switching between a few, or even a few hundred different atom location
preferentialization areas could produce a wide range of material characteristics;

thoughts on the size of chemical vapor deposition metallurgy part sizes: MEMs technology could also be a guide, with thickest chemical vapor deposition metallurgy being some higher of power of two than the 24 hour thickest MEMs object production cycle,
it could be higher, if manufacturing time equivalence is considered (a company orders parts for delivery every month, giving as much as 1 month photolithography growth or possibly MEMs thickness build up), if something like UV lasers with a diffraction
grating can be adapted to modify the shape of a growing single crystal of tungsten, like those used at some airplane turbines, then that could be a metallurgical chemical vapor deposition object size guide (although perhaps not, as I think they might
pull those out of a melt)

Other ways to make features of less than 1 nanometer: It is possible that one photon, even at one frequency, from a laser, could have variable absorption likeliness based on grouping and entangling (linking) photon spins. At New Scientist magazine I
read about a quantum camera, where a beam of quantum entangled photons met a figurine, and the other group of photons the first photons were entangled (linked) with made an imnage on a camera chip, the shape of the figurine caused the figurine to be
imaged on the chip from varied photon energy availability based on photon spin, there was an absence of an optical path between figurine and camera chip; Notably, large numbers (thousands) of photons have been quantum entangled together, and it is
possible that adjusting the spin effects on each of the 1000 photons separately could produce 1000 gradations of either absorbability at the figurine or electrical charge effect at the imaging chip. The same technology with 16 quantum entangled photons
making the chemical vapor deposition metallurgy optical guide could have 256 levels of possible charge variation and atom attraction/deposition/enarrayment, or also likeliness of causing a deposition; so although the physics seems iffy to me, there might
be a locational effect beyond light wavelength, or at least an automatic 16 bit halftone effect, possibly per each 1 nanometer sized dot, possible.

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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