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Longevity technology:
How many sequential doses of an epigenetic drug cause the epigenetic improvement? Liposomal depot, perhaps attached to an antibody that gloms it to the surface of the lining of the lymphatic compartment could diffuse beneficial drugs, although that seems complex. One possibly as is epigenetic modifying drug palmitate. I do not know if the longevity effects of 10HDA(10H2DA) are from HDAC interference and epigenetic, but if they are then taking a high dose of 10HDA once a month (or some other interval), or like 30 grams of royal jelly which has 10HDA(10HDA) for two or three days once a month could have the same or better longevity effect. There is the possibility that occasional high dose 10HDA(10H2DA) or royal jelly is actually more longevizing from being thorough and of higher activity.
One HDAC2 inhibitor is a nootropic. It is possible that one or two high doses of that HDAC inhibitor a month could
Cause greater cognitive ability.
Notably though there is another version of this. I read histone epigenetics like acetylation can change rapidly, perhaps in minutes, although the other long view also makes sense as people get epigenetics from from their parents or even grandparents. I perceive I read there is longevity epigenetics people get from their parents so a couple days of epigenetic dosing could cause greater longevity effects the person's entire life. A couple days of epigenetic modifier dosing could even cause their children and grandchildren to have greater longevity. At the nootropic HDAC2 inhibitor that causes greater cognitive ability, a couple days of HDAC2 inhibitor dosing could cause intelligence enhancement that is also passed along to children and grandchildren.
Cognitive ability genetics: the genes that the published cognitive ability heightening HDAC2 inhibitor modifies could be g (like iq) intelligence genes. SNPs, alleles, and copy numbers of those genes could be enhanced at the germline or with gene therapy to increase intelligence at humans, that is homo sapiens.
Longevity technology:
I perceive piperine causes greater absorption through the membranes of the GI tract from telling them to be more permeable. Is there anything that could be placed at liposomes along with the active pharmaceutical ingredient (ÅPI) which reach the lymphatic system to make the lymphatic membranes more permeable? It could be piperine again. That lymphatic permeability drug could make other drugs, like rapamycin, rapalogs, or other longevity drugs to be 2-4 times as effective at reaching tissues from the lymphatic system. Combined with the 2-10 times greater effectiveness of drugs that skip first pass hepatic metabolism that could make rapamycin, rapalogs, senolytics, or other longevity drugs 4 to 20 times more active and affordable. Rapamycin that makes mice live 60% longer could be just 12-14 cents a dose based on $40/gram at Alibaba.com .
GSK (Glaxo Smith Klein) has an online page where they request technology ideas. They make Tylenol and some other antipyretic pills:
ela–naproxen (ela-n) is ethynyl liposomal active transport naproxen it is active at about 7.6 micrograms. They could put a dot of it on the outside of regular naproxen pill that is enteric coated so there is an immediate action antipyretic at the stomach but it also activates 11 hours later so one pill lasts 24 hours. Another way to do it is like multiminipill contac™ with ela-n microenteric coat so it dissolves better at the small intestine after 11 hours. Another way to do it is rather than a 7 day palmitate have ela-n attached to a different alkane COOH like perhaps C6COOH
To make another, delayed dose to make 24 hours of naproxen activity, that could do 36, 48, 72 hour one pill dosing as well: Another way is ela-n of three or more types taken simultaneously where each ela-n has a different enzyme-reactive group on the ela-n with a passivating group removed by the enzyme. The enzymes that remove the passivation moiety are enzymes at the circulatory system. The first ela-n gets its passivation moiety removed first and the next ela-n gets its passivation moiety removed next like cumulatively 90 minutes later, then do this with a sufficient elan-enzyme-unpassivated-moieties to get a smooth 24 hour, 36 hour, 48 hour or 72 hour dose curve.
Years of arthritis relief from one office visit: A depot drug form of ela-n, ea-n, which I calculate as having a 7.6 microgram 12 hour dose could put ela-n at an implant (3 year nexplanon-like) with just 16.64 mg of API at the implant. Sensibly and obviously omitting the 2-4 times dosage multiplier enhancement from liposomes, ae-n could be a 33 mg or 66 mg entire API content implant. I think it is possible to make much longer lasting depot implants or even injections, so a decade of arthritis relief from a decade functional implant at one offive visit is possible.
Complementing a decade functional arthritis relief implant is putting the longevity and life preserving peptides AEDG (epithalon) and thymosin at the implant. Epithalon is published as causing 24% greater longevity in mice. The combination of epithalon with thymosin, at intermittent dosing, is published as causing people to be four times more likely to be alive after six years. Epithalon and thymosin are peptides so it is possible screening libraries of variants on these peptides could find versions with fewer mcg per dose.
Another ela-n 24-96 hour antipyretic: put ea-n on the outside of the pill for immediate relief. At the interior of the pill layer, make the 11 hours later dose with dry liposomes that have different numbers of concentric layers at the liposome molecule, so like the 11 hour dose has 11 concentric layers of liposomes ======Ö on it.
It is possible to simplify the ela-naproxen molecule to ethynl naproxen, or ethynyl liposomal naproxen. Ethynylizing sex hormones causes sex hormones at FDA drugs to go from a.625 milligram dose to a 600 nanogram dose, a one hundred times amplification of effect. A cell membrane active transport moiety causes 1000 times greater transport than diffusion. Either of these alone produces microgram active doses of naproxen.
A really simple version of 24-48 hour liposomal naproxen without ethynylization or active transport moieties is to use the way liposomes avoid first pass hepatic metabolism to bring 4 times as much regular naproxen API to the circulation. If that works on regular naproxen that makes a 24 hour dose fit in a pill half the size or at a full size pill up to 48 hours of antipyretic anti-arthritis effect. Dry liposomes could be used.
Longevity technology:
Multiple simultaneous drugs at aged batched mice are a way to make longevity drug API identification faster, and make mouse research as much as 120 times more affordable to produce a p value. Matrix simultaneous drug administration is published, and creating batches of mice, at 8 mice each, two months or less apart in age creates 48 mice, with each duomonthly increment able to generate a longevity increase p value longevity drug. The 2^3 deaggregation mice as steps to find the actual drug that longevizes is a way to do this. Sequential mouse experiments to locate the individual most effective longevity drug, possibly after data on 2-6 months of simultaneous administration of the drugs to new age batched groups of mice. The actual longevization pct of each batch of mice, starting at the first two months p values, continuing to 4 months and six months also gives a number on how much longer the eight and ten month and year interval mice would have to live to continue that particular mouse' longevity gain. This is similar to calculating course grades mid term to find out if a person can still get the grade they prefer, at mice this is how much longevity increase would numerically justify continuing that drug at that mouse for greater than the amount of longevity from other chemicals that have been screened or exist. One API drug longevity quantification; after 4 months you could tell if an Epithalon peptide sequemce variation being screened was 60% more or 60% less longevizing than regular Epithalon. At 4 months you would be able to calculate that the 6 month mice would have to show an 80% gain from the previously measured effects from an age specific effect (like start midlife to cause longevization) to raise that molecular version of epithalon's longevity effect to equal or exceed Epithalon. Similarly if a molecular variant of Epithalon is 60% more longevizing at two or four momths then a side experiment can be started with 8 mice to get a p value on the more effective version. The 8 mouse chronologically colocated experiment can also be raised to eleven mice so three can be used for things like biological samples, psychological testing and other things that accelerate longevity drug development like coaministration of another longevity drug, likely one with a high likeliness of having a different complementary mechanism
sort of like calculating a school grade mid term to decide to keep taking a class
This batched matrix longevity drug protocol can be used on other species as well. 96 well plate fish are vertebrates, age batching can be accomplished on-location without a breeding facility. I have read about fish with a 6 month lifespan, causing the longevity test batches to be either 14 days or a month apart, causing either one month drug characterization or 42 day longevity drug characterization. This also provides the opportunity to medicate the fish before mid-life to explore and find new mechanisms, and measure young behaviors on the longevity drug.
it is also possible to do age batched matrix longevity drug characterization on c elegans. The lifespan of c elegans doubles at some published protocols from 30 to 60 days. The thirty day span can be divided into ten 3 day batches, and the matrix batched longevity increase percentage can be calculated from three age batches in nine days. It is possible that a 96 well plate technology could be enhanced to use computer vision and an acoustic transducer, or just a speaker, perhaps at deciHz (tenths of a Hz) and silent to humans to do the same touch the c elegans with a probe to see if it moves, verifying it is alive in an automated and contactless way.
The near camera automatic sonic probe physically motionizes the c elegans, contactlessly imitating a physical probe. To be less annoying, an intensity that 99.999 percent of c elegans will respond to but not louder is possible. Optimally the sonic probe has a focused beam of less than 1/16th of the plate well area so when the c elegans responds to it the c elegans gets immediate absence of probe stimulation. The sonic probe wiggles the c elegans slightly, causing c elegans initiated motion that is a computer vision detectable motion at the c elegans verifying it is still alive. This replaces a human with a probe and supports full automation of the longevity drug screening process. Automated pipetting could be used to administer a fresh dose of the test chemical. Automated pipetting could also be used to rotate out the water periodically to keep the c elegans well and also at standardized drug concentrations.
I think it is possible to place one to four c elegans per plate. At just four c elegans per plate, i think the p
Noting it is possible to get a p value of .01 if the statement has that much mathematical latitude, " they are still alive", and that the computer vision system can measure 3-7 things simultaneously, with a general enough statement like "the c elegans is above the first standard deviation (compared with normal c elegans) at some automatically measured characteristic" on things like: velocity the c elegans moves when acoustically probed, distance and swimming style of the c elgans when probed, amount of tropism to or away from a laser illuminating part of the well, food enrichment response, possibly even the effect of pipetting another brief-action drug like a neurotransmitter that causes a behavior into the well's water, any visual indicators that change with age at c elegans like skin texture, gonad size, heart rate. Also it is possible to quantify c elegans neurology. Genetically engineering the c elegans used at the screening to have fluorescence of brain based regions or neurons having different emissions spectra fluorescent proteins that the c. Elegans has been engineered to produce. Genetically engineering different parts of the brain or neurotransmitter specific neurons characterizes which systems the longevity drug version being screened could be benefitting. Camera gathered data on which parts of the brain activate in response to a standard harmless stimulus (food, laser, as well as the camera recording the prior to single utilization of the acoustic probe. Each of these, and others has a statement with enough latitude to get a p
Genetically engineered c elegans that indicate their youthfulness can be produced. A fluorescent protein like green fluorescent protein is engineered to be made at the brain as well as separable organ systems like heart, liver, nerves, gas exchange permeability structuress then the size and possibly the activity of these is automatically quantified with the computer camera and compared to preexisting data on young c elegans.
The value of matrix testing the drugs and the effect on the velocity of creation of new longevity drugs: also, notably the highest performing molecule screening matrix group could be considered a compounded (multicomponent actual treatment) drug in its own right. If a rapalogs covalently linked to a AMPK activating peptide combined with a senolytics and an RNAi drug causes much larger longevity increase then it is ok to consider that hroup as one treatment at the mice.
Mouse poop and saliva contain circulatory fluids, indicator chemicals, and mouse cytes that could identify separate complementary longevity mechanisms without disturbing the screening mice. This is a way to heighten the effectiveness of matrix characterization of the longevity heightening from longevity drugs, and, sometimes their combinations, if that is meaningful (note 214 year old whales and mice have almost the same systems, as do million year lifespan endoliths like algae or fungi, as does 40,000 year kings holly with 3650 day trees, so pansystem longevity drugs have validity in their own right while tissue and organ specificity, and things like body compartment, and lipophilicity/hydrophilicity also have comprehensible value, noting senolytics tissue localization, and deprenyl which concentrates most of its effects at a brain area called the substantial nigra, as well as the octopus living eight times longer if it does not have a sex gland (the value of specificity is vivid at the octopus, if there were a "I can tell I have a sex gland" receptor blocking molecule then that one specific molecule, possibly at a particular physical location would cause eight times longer lifespan. That compares with rapamycin effecting mTOR everywhere to cause 60% greater longevity, though also at humans eunuchs live 19 years longer so localization at just a few grams of tissue could also be a human longevity drug.
As a sample that can guide the mouse longevity molecule screening the c elegans or fish matrix screen to generate 99.9th percentile molecules. The three mice out of eleven to do psychological testing and get biological samples from, do positron emission tomography at, as well as matrix combinations that match or combine a brain concentrator with a heart concentrator, are places human cognition applied to the drug matrices can occur, augmenting the simplicity of just mass screening with humans figuring out previously unknown mechanisms from screening successes like finding chemicals at endoliths that longevize mice, and humans basing new drug cores to mass screen variations of.
Drug companies might make a multi chemical ingredient drug based on the effects of the matrix combinations that have the fewest side effects at mice, notably the 3 mice out of a group of 11 (where the other 8 provide a longevity heightening % with a p value) and the most appealing 96 well plate fish physiology measures, like brain and heart similarity to young fish, and including fish progeny well being
Industry competition and publication multiplication: it is possible that when one company gets particular valued results from mass screening a particular kind of thing (endolith or clam chemical variations) that other companies or people that publish do, that there is then more activity in that area, like rapamycin's proliferation of papers and people making new rapalogs, or the 8 papers on the beneficial effects of decanoic acid esters (like 10HDA(10H2DA) and HAEE) effects, this could be treated very simply as a math multiplier of the amount of molecules being screened, if 43 99.9th percentile new longevity chemicals are found then perhaps they will cause 200 new longevity 99.9th percentile higher quality drugs to be produced.
Age batched mice at matrix experiments could possibly be complemented with age batched matrix experiments on marmosets. Marmosets live about 18 years and are a primate with a genome more similar to the human genome. With the most longevizing of the 99.9th percentile and greater mouse longevity quantified, it is possible to get data from marmosets in 2-3 years; midlife marmoset age batches, like 16, 14, 12, 9 year old marmosets, could be characterized to see which longevity chemicals most nearly track along with the benefits seen in mice, that traverse a previously documented progression of benefits most similarly, likely things like reduced heart disease, reduced cancer occurrence, and brain function that is maintained or sometimes improved (rapamycin is nootropic, decanoic acid variant HAEE benefits mental health), it is possible, perhaps to quantify preserved cardiac and brain function, and possibly (possibly otherwise) cancer occurrence decrease at the drugged marmosets that are age batched, optimally the drugs become part of the pharmacopeia people use long before the marmosets get old, but when the marmosets do get old enough to have quantified long lifespan extension above unmedicated marmosets that contributes to the preference for that previously introduced drug, and things that might occur, like the pct of marmosets that avoided ever getting heart disease, cancer or cognitive impairment before a ratioized equivalent of a 114 year old are published, which let's people know about quantified complementary benefits of the drug. The effect of mouse like physiology response being quantified at age-batched marmosets between 7 and 9 years of age or also 14 and 17 years of age being much higher or also nearly identical focuses drug company products around chemicals that will most predictably work at humans.
Marmoset-mouse response similarity tracking also guides companies as to which longevity molecules are particularly beneficial at primates, and so possibly humans, and which have applicability to other areas of medicine and larger usage volume and profitability, noting profitability causes more beneficial longevity and other use drug creation and distribution.
What happens when they feed rapamycin as well as other longevity drugs to octopus? I perceive i read that an octopus that does not have a sex gland lives eight times longer. After octopus sex gland removal rapamycin's effects at lifespan of octopus that have a sex gland compared with no sex gland could be quantified, Octopus lifespan and tissue youthfulness physiology changes from sex gland removal could activate shared homologous genes between octopus and human, suggesting proteins that heighten longevity that could be new longevity drugs. That also suggests that deleterious gene activation at the sex-gland-having octopus, and that the human homologous versions of these octopus sex-gland activated genes could be producing deleterious things at normal humans just living. That suggests that epigenetic drugs like area specific methylases could decrease sex-gland-having octopus' shared homologous gene activation areas activity, bringing the human gene activation and gene product amount nearer to that of an octopus without a sex gland. This would be tested on mice.
Gene products (like proteins), and any circulating chemicals different between sex gland having and octopus absent a sex gland could be proteins and other chemicals that if immunized against cause greater longevity and healthspan at humans. If there is an obvious decrease in any chemicals at a sex gland having octopus compared with an octopus absent a sex gland then those chemicals could be administered, supplemented, at matrix form to age batched mice to find out if those chemicals have longevising effects in 2-4 months. Things that decrease activity of the human octopus homologous genes that activate because of the sex gland, compared to, if there is such a thing, octopus puberty, could also be longevity drugs. Epigenetic modifiers of octopus sex gland networked human homologous genes (methylases and others) could cause greater longevity and healthspan at humans.
They could implant an extra sex gland in an octopus and quantify and qualify the even higher activity than background at an unmodified octopus' human homologous chromosomes to find the particularly likely to be active epigenetic drugs (possibly methylases) and immunizations against the deleterious things that are even more detectable from an octopus having two sex glands to be longevity drugs.
Preventing birth defects: find the mammal with the fewest birth defects or the rodent with least and most birth defects, particularly noting the genes turned on during prenatal development; at the rodents, then find homologous genes and SNPs at humans to find human gene products (possibly circulating proteins) to decrease or increase, to be most like the mice with the physiochemistry of least birth defects.
It could be possible to breed mice with rates of birth defects 1/7 the to 1/16th that of wild mice; at the outdoor mouse dorm have the feeding station computers have an ultrasound probe that automatically scans any mouse that comes to eat, pregnant mice with malformed mouse progeny would accumulate at the database and then their well progeny sterilized. The mice would, as I read mice do, have about 9-11 pregnancies per year and the new baby mice could get pregnant after a month, the feeding stations could also remove non breeding mice from the mouse dorm, after 365 fays of only defect less mice breeding it is possible there would be a % decrease in the number of birth defects, the mice would have a well baby genome that could be compared to the genome of the initial mice with possibly a few locatable genes that caused the reduction in birth defects; homologous genes and SNPs could be found at humans for both less than median and more than median defects; any difference in circulating physiochemical produces a group of chemicals that could be screened to find out if their use as drugs would decrease birth defects, or if epigenetically upregulating their production decreased birth defects, and endogenous chemicals that were associated with birth defects could be immunized against as well as epigenetics like methylation used to decrease the amount of their production. Along with the genes the actual SNPs, alleles, and copy numbers associated with either direction (imaginably the 3rd and 97th percentiles) at mouse genes with human homologous genes could be looked for at human gene databases, like those of health organizations, to find out if human variations on those birth defect producing or birth defect preventing genes had strong numerical associations at humans as well, the human physiochemical differences between the 3rd and 97th percentiles of birth defect rick as suggested from the mouse genes (notably the newly found birth defect reduction genes) would provide a human physiochemical identity source to derive new birth defect preventing drugs, immunizations, epigenetic modifiers and germline gene modifications with. If a human woman had genes that carried risk she could do a cheek swab, have stem cells produced, the deleterious genes changed to the more beneficial defect decreasing versions, then conceive a child with the engineered oocyte which would also reduce the risk of birth defects at all of the human woman's progeny, this is also an opportunity for the woman to enhance the rest of her child's genome.
What would be really amazing is if there were two strains of interbreedable mice, one strain having 1/7 to 1/16 the occurrence of birth defects, the genetic difference between them looked at to find out if there are human homologous genes, and, perhaps the nifty birth defect preventing thing, notably different SNPs, alleles,and copy number variants between the two strains that have similar genetic variations at humans or at humans' particular specific homologous gene versions; at SNPs at two different genes that are particularly active prenatally, the mice with less defects could have a particular two SNP difference from other mice, at humans it is possible some pct of the population has two of the SNPs, one or none, they could measure the amount of birth defects at the humans to find out if those SNPs made a difference at humans, then go through the homologous genes' mouse-human SNP difference (further away from or nearer to each of the mouse' varieties(number of different SNPs; which variety version of mouses multiple snps, are there)) one gene at a time, simultaneously looking at a big database of different human genomes and comparing it to the mice, matching mouse and human SNPs, alleles and copy number variations to humans that gave birth to unwell persons; that finds genes that if engineered to be at mice, can be quantified as to how much birth defect risk they produce then drugs and epigenetic regulators and immunizations and gene therapies used to decrease birth defects at humans.
There is the pleasant possibility, without anything I have heard of to suggest actuality, that the genes of birth defect preclusion (found at the mouse dorm mice) could actually enhance baby wellness causing normal babies to be slightly better than well or to thrive more. There is mathematical support for this, if the number of birth defect reducing genes is near 29 then there is a certain likeliness one or more of the genes is beneficial to the human, perhaps they make more of one beneficial amino acid, have the super high productivity version of a DHA (omega 3 fatty acid) gene, or a hox gene variant that has extra fidelity when transcribed, or liver genes that are 99th percentile at metabolizing risk causing xenobiotics, or maternal genes not just of placenta sufficiency but 99th percentile of placenta optimality (perhaps a differing group of genes or SNPs that variously optimize size, vasculature (notably micro vasculature), development velocity (hormone sensitivity); the genes that availablize nutrients from the mothers body like calcium, phosphorus, and iron could have well baby enhanced versions, the genes that do quality control, like when a woman misses her period for just one month because there was a defective blastocyst or zygote and the quality assurance physiology terminated it; making it so one out of two birth defects were prevented but rather than half of women having sex get pregnant in 7 months, half of women got pregnant when having sex for 9 months, or at the womans option she could either get pregnant almost immediately with assisted reproductive technology or take a pill, or get a depot drug, that caused her to have just 1/3 the chance of birth defects while causing such heightened quality assurance physiology that it took an average woman 19 months to get pregnant. It is also possible the pregnancy quality assurance phenotype and genotype could be made more effective with drugs or gene therapy while minimally effecting the amount of time to get pregnant; SNPs and alleles of the pregnancy quality assurance process, where I think i read but might misremember, that about half of all blsstocysts (or possibly zygotes got naturally terminated at a normal 2019 woman's body, that process if it has to do with quality assurance could be adjusted to heighten quality further.
Dominant along with other, simultaneous multirecessive genes that do the same thing, reduce birth defects, would persist at a population even if there were things that effected various genotypes
Breed different mouse strains to be as similar as possible while presenting the half as many defects difference
Find the primate with the least presence of being then utilize that as a physiological experimental animal, feelingless p-zombie as much as possible. Notably this could be a particular genetics at most or several different primate species, noting there are humans that say they aren't conscious, find the most p-zombie genetics at numerous species then breed or make physiological experimental animals as well as milk cows and egg chickens and caviar fish
Noting human eunuchs live 19 years longer, screening a few thousand sex hormone variations at 96 well plate fish to find 1-100 that longevize without changing behavior could produce a longevity drug screenable on mice. 17 alpha estradiol's published longevity effects at mice without feminizing effects could be a hint.
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Prevent birth defects with mice human homologous genes (genes that are highly similar between humans and mice),
Find mice or other mammals that have half or 1/4 as many birth defects as humans then compare homologous genes between that species, mice and other species with figure-outable defect amounts, comparing the multispecies SNPs drift towards or distanceingly from the homologous genes' snps of that species with half or 1/4 the human 2019AD defect amount, and where it is possible the human SNPs, alleles, and copy number variants variety that correlates with both being most similar to the 1/2 or 1/4 amount of birth defects and any data on what reduces human birth defects, as human fetal and baby wellness this guides which SNPs, alleles, copy numbers and epigenetic reduces birth defects at humans the most
The difference in proteins produced between the mouse varieties with different defect amounts could be well baby causing pills or also genetically engineered grains, milk that make the proteins that the mice and humans with the wellest babies have, it is also possible to measure peptides, organics, other chemicals at the two mouse varieties with homologous human genes and quantify those as birth defect reducing supplements
Variety of hyperwell normal SNP at human homologous genes compare big human database then feed normal humans enteric protein drug pills, genetically engineered food with the defect preventing protein or peptide that is beneficial, do gene therapy or also modify the human germline to have enhanced occurrence of completely well defectless babies
To benefit humans as rapidly as possible the two varieties of mice development of well baby supplements goes well with making a database of about 900 nonhuman primate pregnancies in the US and Europe each year and a tissue sample library, the difference between birth defects between humans and other primates can be used to create well baby producing supplements, if humans have fewer defects then the very similar homologous genes would show which proteins humans are making more of that benefit babies, it could be that even more of those proteins as supplements to human mothers would reduce birth defects even more, producing a birth defect reducing pill, food, gene therapy or germline modification
Does Epithalon with ththymosin prevent birth defects or cause more babies to live
Intelligence gene, on phenylethylamine I wrote 44 pages of technology new to me at a notebook, not on phenylethylamine i might write half a page, the genetics of the Trace Amino Acid Receptor TAAR, notably how many TAAR receptors there are per cyte and where, neurologically, like brain anatomy, they are located, as well as the number of other neurons that connect to them, connectionality amount versions providing, possibly heightened stimulation and even multineuron network effects like new neural quorums or quorums with new tropisms, are all genetically addressable, from one measure of cognitive output 44 pages of new to me technologies, i am 88 times more behavioral psychology measurable intelligent, subjectively the generative intelligence of my mind's contents is perceptibly much higher. I take phenylethylamine about 100 to
200 minutes after 5mg of deprenyl an mao-b inhibitor that makes the phenylethylamine work better; the genetics of TAAR, the SNPs, alleles and copy number variants could be compared amongst those measured to have an IQ over 200, as well as those thought to do the most creative and widely applied work
P zombie until modelled, then model advises consciousness form, p zombie tries consciousness form and heightens or mildifies isness as they prefer while being aware of the highest quality research on the difference it makes in their behavior, if they like the projected behavioral future then they do that amount of presence of being; among numerous possibilities a person might find out a projection it might matter a lot when you ask, also i think children exist, allowance to charity apportionment
One per ten likeliness of thinking of something
Genetically engineer people to be the larger of the 9.99999th percentile of creativity (divergent thinking test) who are mentally well and at the 95th percentile or higher of psychology psychometric of subject twice or more creative than treon verdery while treon verdery is on 700 milligrams of phenylethylamine which has been preceded 200 minutes previously with the MAO-B inhibitor deprenyl, 5 mg at 70 Kg; creativity benefits people. Humans generally with simultaneously utilitarian effect, creativity also has economic value and its money value per person measured amount can be quantified at variously an individual person, the person employed, the person volunteering, as well as geographical subsets of the population like areas of shared language or geography of values or beliefs that concentrate at a population at personthe greater amounts of creativity Creativity, 11 things, new gofundme curing malaria, economics eq
Just getting it, a psychometric measurable different than big five, possibly g, mbti at me it has many forms, the part of my mind that thinks of whole ideas, often science, technology, invention, traces of engineering, and at fortunate occurrences mathematics, sometimes a combination of near romance crushlike feelings and ideas about what to do when raising a daughter, that just getting it instantly, that take paragraphs to explain what I just instantly got the realization part of being of/at a person that likely is also genetic; notably though other people just getting it might be walking into a party, realizing something at a place of employment, "thinking they know the romantic actuality", online and webpage things, making art, music, the shared, psychology psychometrics is amount of any particular person at volume and frequency (amount of times per 24 hours), whether the thing they just get is enjoyable (inventing things is enjoyable, just getting it about the meanings of live interpersonal social networks could be fun or neutral) there could be a better word in English than , inspired awareness, insight, sometimes, but variable amounts, a moment with the usual amount of presence of being or slightly more presence of being with awaremess, like actual do you notice the light coming into your eyes or not, presence of being with non presence at surroundings kind of like chizmemhali flow; I think it is possible to find a genetic basis of just getting it then beneficially making the 99.999th percentile of just getting it be specified and part of the human genome making it so all people can have the mental occurrence of just getting it, also having it frequently; from a psychometric perspective just getting it has components;some would include accuracy where it can be measured, like arriving at a party and just knowing what's up, inventing a thing with the intent it functions at least enough to have mental or even actual physical beauty and often utility, manufacturability, and commercial value, and with even traces of engineering content (materials were named, possibly, but not necessarily some math, even mental math occurred, this is instant just getting it which is different than procedural, perhaps explanatory kinds of sentience), there might be humans that have just getting it at raising children and it might be possible to figure out if their just getting it was accurate based on how the children turn out, another area of the psychometrics of just getting it, is percentage of just getting it that causes action, this could be a momentary thing, like commenting on the internet, "universities have intellectually enriched daycare" when a pregnant person says something, an inventor rewrites notes so they are adequate to send as email to a company, a record producer invites a particular musician to a studio, or an engineer realizes they can look up a completely different part and then look the part up, another psychometric component to just getting it could be heightened multihour greater presence of fMRI of heightened subjective well being (happiness), that is, they have just getting it experiences, does that cause heightened well being, and for what interval, I do not know the amount of interval that is optimal, I get about 40 seconds of thrill after just getting it, and the just getting it part is kind of emotionally neutral with a tinge of comfortable wordless attentiveness, the emphasized thing though is psychometrics and other measurements of just getting it and the connection to greater amounts of just getting it at people which also simultaneously brings with it opportunities to heighten accuracy, subjective well being, frequency of behavioral actions based on just getting it, notably it is possible to think about and remain calm in the face of raising all of these to their highest simultaneous level or, possible favoring a particular psychometric describable or measurable over a group effect; causing a modification to the amount of just getting it could be accomplished with gene therapy
and the person thinking about changing their actual just getting it way of being would likely benefit from computer simulation as a guide, as well as a kind of paint-matching color palette of drugs, nootropics might heighten accuracy, anxiolytics or music might cause the just getting it feeling or experience without actual content, stimulants (possibly TAAR receptor stimulants) might increase frequency, actual action, and perception of value, so those are the kinds of things a simulation could do, possibly even aligning a persons mind, and adjusting the magnitudes and locations of adjusted activation and duration of activation at neurotransmitter specific maps like spin labelled fMRI, positron emission tomography, and something that may be possible, using a quantum camera variation on 3D brain reading lasers and software like that of Deep water (company started near 2019) combined with absorption of photons at one photon area that ate quantum entangled so they inform a quantum camera while doing spectroscopy at specific chemical brain chemistry, uv/or specific databases of stimulation frequencies and emissions spectra say what a chemical is when you beam a stimulating, or absorbable spectra beam at a chemical or neuron, or tracer contrast agent at the brain, and then use the outside of head sensor at the quantum camera to note where it absorbs and how much; very narrow emissions line stimulating, multiple separated unmistakeable frequency numbers emitting quantum camera so a particular chemical is 90th percentile at absorbing say 7 narrow frequencies each that are UV/ir published lines and regular tissue only absorbs 1 of them and at median amounts; you send quantum entangled blue and green narrow band lasers into someone's brain then only at those locations where the simultaneous two frequency (blue and green) absorption is 90th percentile does the software say 99th percentile of likeliness this neuron contains (example)AMPA chemicals, noting it is a quantum camera system (New Scientist magazine) the absorption of the quantum entangled photons is readable outside the brain completely without a reflective path
two electron system
spectroscopyreport on absorption
Options to turn on options and expansions of capability from gene therapy as well as ways to restore pre gene therapy form
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[NOTE]
Halogenated dry liposomal ethyl. (halogenated)fluorophenibut centilipoate the 100 mer lipid making alkane like moeity makes one oral dose last much longer, a palmitate, C16 fluoxetine palmitate, I imagine more than a month activity per dose. I perceive I read about an oral drug that lasts much longer than 7 days so that technology is available as well, liposomal ethynyl fluorophenibut or other halogenated phenibut causes a decrease of paranormally sourced IT pattern awareness, reduces the number or paranormal recruitment offers i experience, and blocks most of the voices i hear in my head i think are paranormally sourced, decreases paradlia as well
Another way to make a GABA active drug to block IT pattern recruitment and awareness:
Attach an antibody to a protein that is gradually, sectionally taken apart by an endogenous enzyme, the antibody could be liposomally surrounded and enteric coated so it is absorbed from an oral dose, snorting it could also be effective. Once dosed the antibody protein gloms tissue that is harmless to glom, plentiful but predictable proteolytic enzymes at the circulatory system, or at some versions, that are produced at the cell environment or tissue, Then the proteolytic enzyme removes, at a protein sequence possibly shaped like a stack of linoleum tiles with a layer of fun sized candy bars, that are actually GABA receptor actibating peptide strings. in between them, at the actual molecules one of the alternating layers is hydrophilic or lipophilic and the other layer is at the drugs natural lipophilicity or hydrophilicity and pH. another possibility is like a particularly affordable to make where drugs, like GABA peptide drugs are made into 40 merish long amino acid strings, attached to and spaced with enzyme degradable linkers like GGG (gly-gly-gly) that release the separated drug-active GABA peptides, likely to the circulatory system although the lymphatic system or cerebrospinal fluids could also be functional, when the circulating or area endogenous enzymes see the
Gene therapy that makes this drug is also possible as a version of a 1% volume form of one of mamy different serum albumins could be made to have codon sequences that made a whole bunch of GGG-multimer GABA active peptide sequence-GGG at the construction of the larger albumin protein that is exposed to the enzymes at the circulatory system, that causes the person to always be on GABA active peptides, dosing studies to find out how many GGG-GABA peptide activator sequence copies to put at the albumin gene can be done with primates
If there are 7 albumins and globulins the intention of getting a full function first dose is pteferref but is also technologically extended snd ensured because each of the 7 albumins and globulins can be sequentially gene therapy modified to make the GABA active peptide to titrate the dose upward to optimal amounts.
drug chemistry, out 1/1100 the of it every 24 hours, whenever the enzyme functions (detaches an available part of the molecule) a fresh dose of drug peptide (like a pattern recruitment reducing drug peptide a longevizing peptide or a different drug peptide) is also portablizedmade a circulating physiochemical at the circulatory system then the person experiences the beneficial decreased pattern recruitment and awareness, as well as drug forms that heighten longevity
A beneficial drug, like a lifesaving drug, that benefits children, i think some proteins are only msde at children, the genes that make these proteins can be upgraded with new versions that also make protein and peptide drugs that are beneficial to the children
Out of 100 children, 30 will be at or below the 30th percentile, heightening immunofunction to be like that of 90th percentile of immunoresponse that prevents, cures and vauses revory from unwellness is beneficial.
Dominant genes modified to make a wider range of immunofunctionalizing chemicals with gene therapy as well as beneficial germline modification modifies dominant genes, only one of which is required to beneficially change the chemical production phenotype to improve immune response. This increases the immune response, that is the immunofunctionality even when there are a phenotype formimg recessive genes of ptevipusly less than optimal immunochemistry stimulation than would combine to make a wellness producing, fully immune functional chemical production.
So at the distribution of recessive gene function, at recessive and dominant immunofunction genes that are expressed as phenotypic functionality there would be 1/4 effectiveness at II,Ii, Ii, (I is full immunochemical dominant gene production, Ii is partial production and ii is the less functional double recessive genotype that is at 1/4 of the population. When double recessive ii at the general population causes proneness to more illmess, greater severity, or both then moving the production of that chemical to a recessive gene heightens immunofunction so one I or i allele is sufficient to produce all the immunochemicals a II person has.
Making it so ii double recessives, 1/4 of the population, have II gene function's more effective immunofunction ensures against very many diseases, including any new diseases and reduces illness at the population as the Dominant gene versions of beneficial things that heighten beneficial function at the immune system, replace and complement the various versions or combinations of recessive genes which might accumulate and average out to half (0.0, .5, .5, 1.0)
Moving the least 30 immunofunctional children at the USA to 90th percentile would decrease annoying illness and make people feel better. Globally it could save many lives as it is possible to imagine that the children that get malaria and diarrhea are frequently at the lesser 30th percentile of immune function. Moving all those children up to 90th percentile could reduce occurrence of illness and any result of illness more than 4/5, imaginably to 4/5 of all lives being saved. i read there is some mathematics associated with that 1/5th of the activity or thing produces 4/5 of the measured effect. It is possible that raising the immune capability of the least immunocapable 1/3 will save 4/5 of the people that ceased being alive from childhood unwellnesses. That is associated with that the 30% of children most likely to become unwell likely represented more than 30% of the historic occurences of not being alive. I think decreasing all childhood infectious disease to 4/5 as much as they previously were and saving 4/5 the lives of all the children who would otherwise not be alive is beneficial and gives gene therapy a beneficial reputation, supporting even more beneficial kinds of gene therapy.
As a technology an oral pill with neurons at lyophilized endocytisis pills, a beneficial beneficial virus, or CRISPR/cas9, or other technologies could be functional.
Also, along with that is finding a long lived, lifetime functionimg cytotype to do gene therapy on, it is likely possible to do.
The cytes that the gene therapy is accomplished with's entire lifespan effectiveness goes with how long the gene therapy functions. Some kinds of cytes with lifelong existence could be: glia, white matter, membranes like the dura at beneficial brain genes, anything at the spinal cord that is like white matter where the cytes live as long as the person, it is possible some gonadal cytes are lifelong, bone might also work but i think i read it renews, if cardiocytes last lifelong, although I think they renew, the pericardium as well as adipocytes near the heart might be lifelong cytes. It is possible which cytes live a person's entire span of living is well known and there is an existing published list. Also possible and valuable is that gene therapy enhanced neurons, perhaps of the tiniest phenotypical kind, possibly like cerebellum neurons which I think I read are eentsy and like other neurons live the entireity of the person's lifespan or longer introduced into the body, but outside the brain can produce beneficial proteins like immunofunctionalizing chemicals as well as longevity chemicals. It is possible inhaled neurons (like an asthma inhaler) could integrate and reside in the lungs, it is also possible oral gene therapy based on an endocytosis chemical moiety surface festooned liposomal neuron gene therapy system could transport genetically engineered neurons directly to the lymphatic compartment, be absorbed at membrane tissues there, and when the eentsy particular variety of neurons were exposed the neurons would actually live, likely integrating into the membranes' near to capillary locations. That would make an oral gene therapy pill with lifelong function and titrateable dosage of the amount of proteins produced.
engineering that is willing to advance a product that saves engineering that saves a life for every 10 million lives for every person that has a genetic misprogramming, is at that area and is beneficial. One thing about gene therapy is that the promotor region of the gene can be linked
Henetically emgineerimg frequently occuring plamts to decrease the perception of pattern revruitment and block actual IT pattern recruitment, to make it effortless to know which plants to chew the leaves of if thimhs get multimeanimged and possibly aversive while being a person of sny age, notably children as well as afulysGreen and blue and white dandelions, and the other 100 most frequent weeds on earth henetically engineered to teduce the amount of, reduce the uncomfy feelings of, and reduce the actual effectiveness (if there is any of) IT pattern recruiting because the dandilions, and weeds make GABA peptides, 5HT peptides that function like the antipsychotic pimavanserin, and peptide active drugs with the dopamine, like D2 receptor activity of lurisidone (latuda)
I am opposed to any two worlds IT pattern, as a pattern with recruitment to new personal form or disposition, as well as what i perceived was the categorizationization effect, which I perceived as occurring at the 2000 AD environment as highly synchronized motion at things and humans, i oppose the recruitment of children as well as all homo sapiens, that is humans that is people to the IT pattern, I oppose the making of IT pattern statements of what a person, that is a member of a group of people, a homo sapiens is as well as it pattern offers.
As a thing to make other things out of, what protein reaches the circulatory system with the longest residence time at the body. Thinking of few amu drug palmitate like fluoxetine palmitate where one dose lasts seven days, what protein taken orally reaches the circulation and lasts 7 days, it could be a polymer protein like silk, and they could screen a variety of species including bees to find the cytoproduced and genetically expressed most multiday durable protein that teaches the circulatory system. It is also possible that genetic modification to codons that code the specific amino avids tjat make up silk protein could be genetically modified to produce a silk, tested with its production at actual organisms, that is acid resistamt(stomach passing), optimally lipophilic or hydrophilic so that it passes the membranes of the gi tract, it is even possible that the genetics of silk production already effect linearity a and digestible longevity of produced polymer compared with branching on the silk polymer, if there is a pre-existimg genetics of molecular branching on the polymer, and there may not be. Then the molecules on the branches can be customized to be active peptide drugs connected with enzymatically degradeable linkers like GGG, or, it is possible that having the drug peptide at the linear span of the polymer, again with enzymatically degradeable linkers to automatically and predictable quantifiably put active peptide drug at the circulatory system
Various polymer lengths and forms of keratin could make peptide drugs pass the GI tract and reach the circulatory system. Keratin is a protein so genes that cause keratin production might be able to codon linearly specify the presence of other amino acids and peptides and proteins as extensions to the actual keratin molecule, possibly with a GGG enzyme degradeable linker, so a plant with a gene that codes for keratin would likely make tiny grains rather than linear strands, it is possible that different kinds of keratin are made at different organisms, notably, human hair can pass through the human GI tract fine.
linkerdanother possibility is just to feed some humans some stable isotope labelled plants and eggs and milk and then measure their circulatory system fluid 7, 14, 24, 30, 60 days later to find out if any of the proteins were still circulating
More engineering effort would develop, possibly a chondrotoin polymer that is absorbed at the GI tract but is still a polymer, able to have intervals of drug peptide polymers at its passes the GI tract, reaches the circulation
The new versions of dandelions and other weeds would be engineered to have smooth edged leaves rather than serrated ones to be more aesthetically tolerable or even pleasing, also it was my pattern awareness experience that serrated things looked ferocious so I would avoid them, making the weeds as gentle looking and beautiful as possible makes it more likely more people will use them to decrease pattern recruitment effects
Epigenetics of resistance to unwellness, gene therapy version existing genes version
AI could track people who predict other's futures, often for money, and find out which future describers were of highest accuracy and if they shared characteristics that could be used to find other future describers with higher accuracy, note this is persons rather than methodologies, while it is possible talking to a person who says they "see the future" might be more effective than looking up dreams in a dream interpretation guide, I favor tracing accurate future describing to persons, while also valueing computer numeric quantification and data gathering on methods. Compounded percentages and chemical engineering
Sources of proteins and peptides that genetic engineering could utilize to get people at the 30th percentile of immunity to unwellness heightened to the 90th percentile:
Proteins and peptides like gamma globulin, particular BCG immunization proteins, adjuvant proteins at known vaccines could be general immune adjuvants to any immune response at the body so OK at the lower 30th percentile, the peptide thymosin (combined with the peptide Epithalon
Hibernation, do I dare to comment? I do not know; longevity escape velocity effects the ethics of hibernation
Kinds of sex drive and genetics, psychometrics, behavior videos and self reports, particularly self reports among happy mentally well people at the 95th percentile of high accuracy at self reporting describe their sex drive the genetivs and physiochemistry highest sex drive that produces the greatest happiness at 3 hours, 36 hours, 200 hours and 900 hours as well as positive enthused affirmation that they would have sex with that or those persons again when queried 7 months later, finds a group of persons whose genetics and physiochemistry support gene therapy, germline engineering and beneficial new drugs
G (like iq) genes, I can think of multipart, parallel possible relations between things and have a mostly constructed but perhaps not yet furnished multiarea multidysystem thing occur at my mind without sequential process or thought, its me, but its more intelligent, likely IQ, and perhaps g intelligent than wordy self-talk me, find intelligence genes that cause greater amounts and higher amplitude of this instantaneous output parallel intelligence and make them part of the human germline, to test for it you could ask people if they have it (perhaps almost all pepple), then do fMRI of coming up with new ideas and solving at the internet are there any drugs that increase this, what receptors, where do they activate, You could also ask people at mental capability enriched locations like the Princeton institute for advanced study, ask people to nominate someone as someone who has even more preconscious, side conscious, or apparently comfortable not being the sentience in the spotlight consciousness that thinks of new ideas. Then at say 7-40 of these people all around the US (places like MIT and Oxford do fMRI, then do fMRI of their siblings and parents and make a computer numerival model of the distance between their self reported as well as measured whole thought , instantaneous production amount and their genetics, then do computer software comparisons of the entirity of thought all at once thinkers (who do it at princeton institute levels) with their siblings who say it does not happen at all, then compare the genes, as well as all the circulating chemicals peptides, and proteins at their circulatory system with electrophoresis, so the gene comparison
What would be nifty as well is monozygotic twins that were different, if there are any and their circulatory system chemicals and epigenetic differences
a ask with me is actually the one loop that matters and kind of is me, even though my self talk has a "im here" thing. and finds solutionsfind
Do I figure it out and say hi, or do I figure it out instantly actually while saying hi, sometimes I just have the idea and skip saying hi as the wordcentric narration kind of being will be attentive if that's how things go, yay ideas science, technology, mathematics, engineering and invention with simultaneously utilitarian function
Study siblings at two or three generations of mice to find the 99the percentile of effectiveness of immune system, give all the mice an asymptomatic genetically modified infection that makes pleasant feeling GABA peptides so the only symptom is that the infected mice feel good. what might work then is comparing the genome of the illness resistant mice with their entire extended family, and seeing if among the possibly minimal variation there were genes that caused resistance to unwellness, then when they find those genes look at their protein products, try supplementing them to other mice ad enteric coated diet as well as doing gene therapy on other mice, like genetically dissimilar extended family members at the lower 30% of immune system function to find out if their progeny get better and raise their percentile, that is a way to find gene therapy specific products that at humans would make the humans less likely to be unwell. Those are genes to put in gene therapy to benefit children
Software makes a cladistic of automata, finds diverse form, most chronologically tight, loose, and frequency specifiable rulesets and seeds,
Build an analog computer out of high velocity automata that exhibit water volume equalization, superposition on each other makes a different and preferable thing
The software could superpose the trillion scanned automata (1TB ssd) several stacked in layers rather than individually to find any desired attribute like, layered the do wave addition with node and antinode, or these make solitons, or, stacked 16 deep these have addresdible words and phrases in them, kind of,
Also from a computer science and mathematics basis
Engineering among the trillion most stable on stochastic perturbation and least stable, also the species like clade of which ruleset groupings provide the greatest and least decohent response to perturbation, so like "all the species with the " 0,1,1 or 0, 2, 2 have the most conservation of coherence, the 0,1,2 show the greatest species output, texture, space fill ratio change, and future bitpattern foreillumation prediction
Illuminating teeth roots to do photoactivateable gene therapy gives around 46 separately addressable titration levels and possibly over a century of gene therapy product production, the tissue volume is only the size it is but I have read about peptides that are medically active at nanogram quantities, it would have to be verified, but the longevity peptide Epithalon has published beneficial effects at dosages even lower than some peptide drugs
Big five genetics, if they have a personality characteristic with a genetic source and would like to enhance their quantifiable personality they get a ubiquitous harmless immunomeutral gene therapy like gene therapy to produce peptide or protein contains albums or also globulins that circulate, if a lot of protein or peptide drug is to be made then high volume durable tissues like lung vssculature (macroscopic durable tubes .5 mm and larger) are the directed focus of the beneficial voluntary gene therapy comt that also makes the beneficial function drug, that people sampling it prefer to be on, as well as is physically harmless protein or peptide drug, also rescuing children gene therapy in a pill or also a snort is possible, women with love in boyfriends, who I read are perhaps the top cause of what are studiously called adverse child events,
usimg fimgers, toes, tarsals and metatarsals to make lomg lasting gene therapy that is titrateable at 2.5% increments: Photoactive gene therapy, photoactivatable gene expression systems are published, high intensity flashlight fingers, as well as specific frequency flashlight fimgerx could activate gene therapy at the bones that had been prepared body side with a nasal gene therapy snort or gene therapy oral form dose. At 40 separately addressable fingers, toes, tarsals and metatarsals dose is titrateable to the gene therapy activation of 20 fingers and toes (and tarsals and metatarsametatatdals, about 40 steps of 2.5% that are separately activate able and addressible. The titration and amount of protein or also peptide drug being produced can be increased further if more than one light frequency is utilized. So 40 separate my addressable blue frequency responsive bones can be complemented with 40 green frequency responsive bones to make
A hint nearer voluntary, engineer a popular thing to heighten words in your head come nearer saying what you actually think and mean drug or also create enhanced genetics of the words in your head saying what you actually mean, that is a also heightener of doing more things that you actually mean because the absence of cliche narratives is like omitting a kind of cultural programming, so the person is likely to do things that are less slipstreamef which kind of links action, voluntary intent, and thinking fluency to if that person is askednif they like something or want to do something it is possible they actually there is a 20th century thing that might be a repeated literature theme where "so many moments left unspoken, with an unusually reifying conversation the person notices enhanced actuality, perhaps they have more being, instead of replyinh " great" to how are you they had a nonstreamlined nonautomatic moment and said "i need to improve my love life", and feel reified, there is even the possibility what the other person says will matter more, This theme i perceive might even be callable as " breaking the silemce" so at an actual living perso. Reducing the percentage of mind moments on automatic cliche like content and forms and a thing I call slipstreaming, raises presence and could possibly make it so you ask someone if they like something and want to do it, and they want to do it, their participation might be more authentically voluntary
Enhancing the genetics of people so that the things that they do are more authentically voluntary is beneficial, it also has a new to me beneficial effect, it makes other people:s actions and words nore ethical, while it does not effect their intent, and it may or may not effect the amount, as a percentage of actual actions that occur, to ask another person to do something, they say they want to do it and then do it is a kind of going from fiduciary honest to active shared realization of actuality honesty
minimized automatic content, which i perveive may have a paranormal component, moment chronological percentage filution
Ask people that ai or software might be experiencing mind state of pattern port to contribute pattern harmless words, people the software percieves are havinv what might be pattern port mimd then quantify how beneficial, and the ways they are beneficial, this gives the ai the ability to say "click here to have all they text you see swapped out with harmless paranormally neutral or white text", if you like use our practice software to learn a few pattern harmless phrases amd you will be right there saying things like "well known" now,
White and blue nonsentient IT pattern ai or other software that senses when people, and JY tells me some of them during the 20th cemtury were childen, are experiencing or having a mental form that goes with preceding pattern port, mid pattern port, and among those that experienced pattern port salvage "JY said getting out of a perception of one of the worlds at a two worlds perception was kind of like getting out of a lobster trap, there are some
Ai finds who got out of the lobster trap as concept, what they did, and tells people or fiscally sponsors the creation of longevizing harmless drugs that get people out of a lobster trap
(at me, decreases, blocks, and d
these words are then quantified on the internet
Multifunction object that formerly alive persons have on earth while they are alive that if they cease to be alive is placed at their person, one at their rectum and another identical multifunction object in their hand, it is possible this smooth comfortable to a living person sized object would be placed in the rectum after the person became formerly alive it would have multiple functions and a view screen preloaded to display G W or R, at the person's preference, it is able to record audio and video, it has a detachable part, that can be replaced with any other detachable part from any makers multitool, based on a shared public domain connector standard and have edge conductors so if the person likef they could just connect the detachable part to the multifunction object with one, two, or three wires, noting things like capacitive touch lamps one wire can communicate action directions and some data between the multifunction object and the detachable part, a blue laser with the ability and power intensity to mark rock is part of the multifunction object and is also capable of other continuous gradient of emitted power adjustable power levels, (pleasantly a packaged right emitting surface mount diode is near 2.3 cents on earth and could be a laser diode), two wires connecting the detachable part, or just placing the detachable part against the side of the multifunction object
Warmth difference between rectum and outside of rectum causes electron flow at what is called a thermoelectric semiconductor that makes voltage and current that powers multifunction object, batteries are functional at all temperatures below the disintegration of bones from warmth and liquid
It is possible to do word processing on the screen using the chording keyboard on the side of the multifunction object, it is also possible to write computer programs
Pressing a button causes piezoelectric electricity generation at either or both the detachable part or the multifunction object, both have piezoelectric buttons, that create voltage sufficient to transfer data, about 10megabytes to 1 gigabyte per second data transfer rate electronics are produced during 2019 AD, the voltage from one piezoelectric button press is sufficient to change the visible without continuous supplied electricity epaper display through 400 user images as well as 300 standard images, where one group of images is, one large letter per screen all the letters of the English alphabet and all the curbed letters of the Thai alphabet, along with an automatically generated group of images where the formerly alive persons image is right next to each letter with both the previously alive person as well as the letter in the foreground, an image of the person with all of the English letters is automatically produced from an image of the previously alive person while they were actively alive
The screen is at the living person's option a touchscreen with transparent mineral like material
Durable materials
Wireless headphones support noise cancelling technology, the person thought about to become formerly alive as well as persons that are formerly alive have 14 individual wireless headphones, seven groups of two placed on the surface of their somatic form with them at any of the locations they are at, along with their two multifunction objects at the location the previously alive person's somatic form or similar material is anticipated as being located for the span of their children's and grandchildren's lives or the chronological span of an average of unrelated children and grandchildten's lives, whichever chronological span is longer
location where they (if they) continue being other than alive
Multifunction object has two detachable parts stacked on each other, stacking more is possible, the distal parts are rounded for rectal comfort and the comfortable rounded distal part of the multifunction object has one nondetachable comfortable rounded end
Living people also benefit from placing a multifunction object with its detachable part attached
Static ram memory or also USB memory stick technology memory is used
Various organ function like modes like beating and even peristaltic tube compression, would could have heart effects, a piezoelectric actuator array would swish and motion air through the tubelike form of the multitool, it has a reservoir containing sexual lubricant like Na PCA where a milligram is able to expand to a cunic centimeter of lubricant from absorbing environmental moisture, naPCA turns from powder to liquid fluid in earth desert air, tandard connector
Administering beneficial drugs like opiate peptides and longevity drugs and cognitively beneficial nootropic drugs to persons thought to be about to be previously alive as well as previously alive people is beneficial, s 78,277 year dutstion of euphoric sleep causing opiate action at 700 nanogram each 24 hours dosing amount of opiate peptide doses at 1 gram is likely less than $96 ($95 for one gram of custom peptide from online source during 2005), and could be as affordable as $32 a gram or less produced at greater amounts
It is possible to cause the 700 nanogram each 24hours dose opiate peptide to be technologically enhanced, attaching a cytomembrane transport facilitating peptide, noting active transport at cytes is as much as 1000 timed, I have also read that some peptides when halogenated are twice as physiologically active, at other peptides like orally available and active vasopressin peptide replacing one amino acid with its chiral D amino acid variation and deaminating part of that eight amino avid peptides keeps it from enzymatic digestion and it is able to pass the stomach and be transported to the circulatory system, the dose multiplier could be 1000 (active transport) times two (halogenation) times 9 (D chirality and deamination) that is 18,000 times more active per dose than the 700 nanogram per 24 hour peptide material, supporting those numbers is that humans make artificial amino acids, and, noting any atom at any configuration can be used it is possible using one or more synthetic amino acid could cause a power of two to an order of magnitude greater dose strength
That makes an 87,300 year supply about 4 cents, less if artificial amino acids are used
Artificial amino acids
Localization peptides cause brain localizing possibly decreasing habituation potential of opiate peptides as well as decreasing the effect where the dosage to cause euphoria, anaesthesia and sleep changes with extended use
The multifunction object is able to pleasurably vibrate at the rectum based on the preferences of the being or form that the tectum is at, benefitting women and men
Each multifunction object contains two grams of nanogram active opiate peptides, that is sufficient opiate peptide to drug a 70 kg human for 78277.8866 traversals of the Earth around the sun, the previously alive person has the opportunity to specify if this is euphoric opiate peptide, anesthetic opiate peptide, euphoric effect with anaesthetic effect simultaneously as well as an opiate peptide that causes continuous dreamless sleep or sleep with dreams combined with euphoria
The multifunction object contains a compartment things can be placed in, it has objects at it when placed at the body of the person that perceives they could become a previously alive person as well as when a multifunction object is placed at the rectum and the hand wrapped around another supplemental multifunction object, the items at the compartment are 7 nanogram active opiate peptide transdermal drug delivery microprinted millionare financial
Plant opiate peptide plants that cause continuous sleep with euphoria at all locations where previously alive persons are located at locations they ate projected to be at the entire duration
Feeling generous, give people who are projected to be previously alive a large quantity of kilograms of things to be placed at their somatic form if they become previously alive the function is to give away highly beneficial things to other previously alive persons, people that is homo sapiens as well as other beings the previously alive person could interact with on becoming previously alive
Living people giving
Opiate peptide saturated plant resin shape or the kind of polymers used at the interior of watches saturated with opiate peptides
Opiate peptides with brain area localization moieties could cause orders of magnitude less likeliness of
Orally available antibodies that attach to opiate receptors to turn them on to a receptor configuration that is functionally fMRI quantified and verified with living human descriptions of feeling great pleasure and happiness as having the identical effect as euphoric sleep causing actual opiate molecules, the humans that voluntarily participate at quantifying the effect of the antibodies that activate opiate peptide receptors to cause hreat pleasure and euphoria are humans with fully functional minds who are told they could become previously alive during the next 90 days
A somatic human form that goes from being a living somatic form to a previously alive person is noted as having physiological chemical changes, one of these is ion concentrations, auses opiate receptor activating antibody at physiochemical changes like ion amounts at circulatory fluid, the person can drink the fluid a medical provider provides, they get online, as well as is available at physical location distribution places like medical supply companies that also have things like pill reminder containers and ace compression fabric items, the opiate receptor provided which activates, turns on their opioid receptors if their somatic form has a circulatory system ion profile quantitatively measured at persons who have been other than living for 1 minute
Opiate peptides covalently attached to calcium phosphate or bone strengthening, concentrated at bone strontium phosphate might, or might not, cause opiate peptides, which also diffuse through the human somatic form, to accumulate ditectly on and at bone, this causes bone to continuously emit euphoric continuous sleep opiate peptides at the possible occurrence of them becoming a previously alive person
I was tied to a chair and JY told me about things that would happen at my future,
The multifunction object is at data and voice connection with the phones and comes with an online page that
Instant multimillionaire financial instrument that could benefit people who perceive they could be something other than alive, health insurance linked to financial company that remits
Also, along with a pepper certificate you get sent a million actual physical currency units of a country of your preference, so if you specify yen the dollar amount of those yen are made part of your structure, so you would get $1,011,000 dollars remitted to you if you or others thought it was possible you might be other than alive
Create two new English language letters with the shape of circle with a diagonal bar at 70° as well as a new English letter with the shape of a circle that has a diagonal bar at 340° or -20° at the third Cartesian quadrant, the circle with a bar st 70° has a sound that starts with G, the circle with a bar at 340° has a doing that starts with. G Like great,
It is possible that greenshifted ytanvetse time things
Is there a really high refractive index material compared with water and diamond compatible with the human somatic form, like a pile of neutrons in a magnetic container, a neutron stellar object might have a many orders of magnitude higher refractive index than water or diamond causing the green shift from a photons timeline to be many orders of magnitude greater than from Cerenkov radiation at water the nifty thing is that at a container of neutrons the human can be a few centimeters away from the container and live comfortably, a capacious container with a one meter diameter base could have a planar layer a few neutrons deep and a neutrino and photon travelling linearly would be at a many orders of magnitude greater refractive index, possibly, like a neutron stellar object without the compression; then again, the neutrons, even though they are neutral might be equispaced like a gas, although a thing as simple as a centrifuge might heighten their concentration, the thing is though after travelling through a linear meter of what might be high refractive index neutrons generating orders of magnitude greenshift the neutrino passing through that is outise the light one of the photons at the container's neutrino layer can then pas through a human standing a few cm from the container, the human has then experienced a thing outside the light one of the photon, it is an eentsy anisotropy in the timeline, although noting the neutrino is minimally likely to interact with the material
Is there a genetics as well as physiochemistry, perhaps a succestropic drug that shifts inattentive feeling that things are going ok, or at people whose lives are OK, but not even of average (median) join d'vive (note, ½ of people are less than median at something that would enhance simultaneously their being and actively benefit others, or noting there are many things even rescuing marine mammals or bringing beauty to school buildings that differ from human contact, those kinds of things as well; people are good and mean well but there are good people that mean well that practice that goodness in ways others might never perceive, I do not know if heightening the convenience of benefitting others. Perhaps raising benefit to others 70% from new things the diffident, introspective, timid, momentum-tropismed and ultra spontaneous can do is a thing, a technology that is possible; so if ½ of all people might, or might not benefit from certain categories of improvement, is there a genetics and physiochemistry that van quantifiably support and quantifiably raise the amount of that improvement) also that they might get around to living a simultaneously more beneficial way of living for them and their effects on others, sometime, if they get around to it, a genetics of actively causing their own beneficial participation at the world, a thing that like a person not getting around to cleaning their eyeglasses (noting if they do they feel great and their vision is refreshed) the genetics of things I have heard of have some cofunctionality like openness to experience or even extroversion, there might even be a psychometric for some kind of bemeficial, as compared with just changeability or restlessness, psychometric about seeking beneficial adventure, so there is a thing they could describe, examine the beneficialness of to make sure it was actually beneficial, find out if it has a genetic component and then make those genetics, physiochemical and receptor activators as beneficial drugs that happen to make well people's lives better while also bringing greater mental wellness to the lackluster and outside the mentally well range of intrinsic active optimism that makes its way into being new activities, places and behaviors being tried, genetics and pharmaceuticals that keep people, even mentally well people from momentums of lifeways and interpersonal groupings that cause some quantifiable things about their lives to be below median, the pharmaceuticals and genetic enhancements are better if they function without restlessness and make people happy.
One possibility is nonhormonal SARMS this is confusing to express functionally in English but it is possible that an effect of androgens seen at many species, doing something different than the existing group, changing groups, even going groupless can be physiochemical divided into different psychological and physiological receptor components and quantified amoumt of actual actions, like the fMRI of willingness to seek beneficial change even when at median, without being a response to something nonpositive. So completely a different thing than saying "be active, grow restless and seek beneficial change with nonhormonal nonmasculinizing androgen receptor modifiers" it is much more like "experience wonder, a preference or a tropism towards doing things, spontaneous beneficial activity, willingness to value fresh things", there is more to this than, for some people, being urged to be young again, although that physiology and genetics has merit, if they look through a bunch of different nonsteroidal effects of SARMS they might find some receptors then screen a library of similar SARM or SERM molecules that finds some molecule that with voluntary use enhances active voluntary mildly alert joi d'vive like participation and doing new things, perhaps leaving, and/or joining new social environments. Another possibility is screening a molecular library of slightly funtropic antidepressants like wellbutrin and deprenyl
Genetically engineering the 100 most frequently occurring weed species on earth to reduce the potentially, and to Treon Verdery's perception actually aversive experience of pattern awareness and recruitment
It is beneficial to genetically engineer Dandelion as well as the other 100 most frequently occurring weeds on earth to reduce as well as block ITach the brain and effect 5HT receptors like the profile of receptor activity at the antipsychotic pimavanserin, as well as having protein as well as peptide drugs with the same dopamine, like D2 receptor, activation profile as the antipsychotic lurisidone, they could be linked to the production of blue and green fluorescent proteins like blue at leaves with 5HT pimavanserin like activity, and green at dopamine receptor like activity with the genetics of different leaves being different colors as well, phemibut has calming and prosocial effects and also has antipsychotic activity, GABA active peptides that have GABA receptor effects like those of phenibut cause antipsychotic and pleasant effects, these leaves are genetically engineered to be white
There is also the possibility of making antipsychotic antibodies, producing antibodies that attach to 5HT receptors at the same amplitude of effect as pimavanserin as well as making antibodies with the same magnitude of effect as lurisidone at dopamine receptors and other receptors with the same amplitude and activity as lurisidone at mosses modified everywhere on Earth with gene drive CRISPR/cas9
A different plant, genetically engineered could benefit those who may have previously experienced pattern recruitment if it actually happens, the genetic activity profile of pre-any concept of recruitment as well as pre-any awareness of IT pattern awareness persons is quantified and if epigenetically different, epigenetically described, then gene drive CRISPR/cas9 is utilized to genetically engineer the epigenetics of absence of pattern awareness epigenetics at all the brassicas
longevity drugs engineered to be at the dandelion stalks as well as the tallest part of all the weed species' tallest part of the plant is beneficial
other weed stalks engineered at a dandelion I support updating the longevity
Epigenetic longevity peptide could exist
Antipsychotic epigenetic peptides could exist, to find epigenetic effects on schizophrenia as well as psychosis, the difference between one monozygotic twin diagnosed as schizophrenic or also psychotic, possibly a twin responsive to antipsychotics, then the epigenetics of the schizophrenic or also psychotic monozygotic twin compared with the epigenetics of the psychologically well monozygotic twin could describe a treatable epigenetic variation quantifiable at mice and volunteer humans, finding a treatable epigenetics of schizophrenia or also psychosis could also cause that treatment to decrease pattern awareness as well as pattern recruitment, if there are epigenetics modifying peptides, proteins, RNA drugs, or even RNAi then plants genetically engineered to produce antipsychotic epigenetic drugs, notably with the antipsychotic producing peptides, proteins, or RNA drugs availablized everywhere globally using CRISPR/cas9
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