Here are the first two pages typed also at
http://groups.google...4558475e9?hl=en#
The genes upstream up the CART (cocaine amphetamine related transcript) peptide may be nootropic IQ genes why are they telling the brain to be more alert (or at least CARTy), if there are say 7 of them, making an animal model of each would perhaps provide a specific link to a gene of noticing "internal" brain state or reactivity to stimuli, if those stimuli are cognitive at the brain rather than sensory then these upstream of CART genes are linked to cognition. Natural variations like haplotypes could then be verified at human population to go with various cognitive styles or capacities Thus are cognition architecture genes as well as IQ increasing genes
I have read that womens ability to detect various scents is ten times higher at particular times of the month, I have also read that SAT scores vary 10 or 20 prct with time of the month, I have also read that estrogen is a mild cognitive enhancer thus the genetics of the distribution of estrogen receptors at particular areas of the brain localized to go with cognitive effects (Neocortex, hippocampus) as well as their haplotypes are higher iq genetics
CSF Dura matter development genes as well as ions cytokines at various ages describe possible wellness or longevity profiles along with cognitive effectiveness chemical ratios as well as suggest possible IQ beneficial genetics. I think Ive previously described this
Mapping the production of messenger RNA mRNA throughout the brain as well as body is accomplished with quantumn linked photons of different colors Basically I have read things at New Scientist where a quantum linked photon pair creates one photon that goes through an opaque area then is absorbed with a unique shape object The quantum benefit is that the linked photon at a different transparent detector space traces a 3d outline of where its linked friend goes. Actual data of Nifty imaging at a distance. We just apply that to color absorption of chemicals looking for uniques with something like quantum linked IR spectroscopy then use it on neural tissue to describe what brain chemicals are doing what where when people think particularlly well to find optimal brain chemistry as well as structure. First visualize a leaf The ratio of GG' YY' absorption describes where the chlorophyll is at with a raster trace. Then give it light n glucose to see active change. Then use the same system on neural tissue using the frequencies of IR spectroscopy to find what chemical or protein is doing what where when people think. (green green prime linked photon pairs, yellow yellow prime linked photon pairs
) GGYY The green n yellow photons reflected absorbed reflected at a raster path along a leaf is measured with the quantum linkage noting that chlorophyll reflects green the YtoG ratio describes where at the leaf chlorophyll is actually present Now applying this to the human body we use quantum linked photon detection ratios at the IR spec absorption frequencies of particular brain chemicals like neurotransmitters or proteins although eentsy (millions of mRNA per moment) It may be possible to detect particular mRNA (or radiolabelled thus ir spectroscopically very unique) activity this way or even record a ribosome actively travelling on on a nucleic acid as the absorbability of a quantum linked photon at a radiolabelledribosome could oscillate going wom wom wom as the ribosome visited the notably different nucleic acid shapes giving a listing of what mRNA were being actively transcribed at particular brain areas thus linking gene activity to neuroanatomic area with area neurostructure linked to function Particularly mapping what occurs during a human mind during particularly effective moments of cognition, mapping aha moments. or active complex yet perceptually notable activities when thought is particularly content full as well as cogtnitively rich (as compared wiuth just rapid or responsive)
People haqve been measured to be more cognitively able at different times of day NMR detection of ribosomes (or radiolabelled ribosomes) oscillating as they glom different nucleic acid sequences links protein activity to area as well as notability of awesomeness of a thought at a particular time thus finds IQ genes from the dna that produced the measured mRNA that are cognition genes of thought structure type as well as brain locality
I think that Lassitude of a warm day is different than a warmed blood effect on the CNS. Finding the cytokines that communicate either outside CNS like afferent of sympathetic nerves that bring the cognitive shift then downregulating these lassitude cytokines chemically is a nootropic as well as a cure for warmth lassitude effect As an IQ gene the genetics of the cytokine source of warmth lassitude may have different haplotypes to navigate as well as cytokines genes to modify It is even possible that as this is an outside CNS effect that there is even an anesthetic that is acually a nootropic.
I have read psychology studies of intent where the Voice of purpose processes acknowledgement of purpose anywhere from .1 second to a few seconds after an actual action, Now think of the stimulus reward cycle of some psychology research, There may be haplotype differences among measured human intervals of purpose that would more tightly link action to purpose strongly effecting reinforcement learning or active knowledge of material. The published difference between the interval of purpose compared with the moment of action may affect the rate as well as linkage of actions to learning Finding those persons with very tight rapid links between actopurpose may be finding persons with highresponsiveness to reinforcement learning thus the genetics of the interval of purpose may be IQ beneficial genes Or possibly people with wide intervals yet high learning may have a genetics of cognitive breadth conferring wisdom or nonconscious consideration of multivariate material. It is possible widely screening chemicals to see if the effect purpose interval may create new learning hyperreadiness drugs or possibly artificial wisom (mulling) drugs
Grab lab mammals with small heads yet high cognitive performance then crossbreed them with large head high cognitive performance mammals of the same species to find the architectural brain structure genes that cause high performance as distinguished from just more brains then create the normosomatic large headed version with the higher performance architecture at humans to give higher IQ Note giving girls estrogen blockers or delaying puberty during the growth phase of bones causes larger skull volume as well as larger brain size along with super female cognition to brain mass ratio while happening to make the girls taller thus puberty at 14 or 20 would be a nootropic or IQ gene also as estrogen is a cognitive enhancer puberty could be restructured to be cognitively beneficial as well as the new socioreproductive option zone puberty represents So, that sounds iffy yet basically says, delaying puberty a few years might give girls 20 to 40 points more IQ based on volume increase prior to estrogen cued ceasing of bone growth. Since they are cogitively equal at a different brain size at age 20 having equal brain size would give girls then women cognitive advantage.
Peptidases (as well as restriction enzymes) divide peptides at particular places which causes the predictable creation of particular protein fragments or peptides, some of these are drugs Genetically engineering new peptidases or doing adenovirus transfection at neurons causes the division of naturally occuring ordinary peptides to create new nootropic active fragment peptides similar to CART, vasopressin, AEDG, nonthyroid active Thyroid peptide fragments, Kappa opoiod placeholders, that give active cognitive benefit Genetically engineering peptidases specific to what might be called preexisting antinootropic peptides could remove baseload of antinootropics causing greater cognitive capacity Also peptidases that that affect glycosylated junk or glyucoproteins could reduce cumulative junk (I think that may have been researched) This is a way to create entirely new ntelligence genes making them a part of the human genome.
(thats the first 2 pages of 9)
Edited by treonsverdery, 11 October 2011 - 12:40 AM.
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