This is a transription of a few more pages of the nootropics technology notes
Some of these are microtechnologically very rah rah
Comedy is published as strongly increasing creativity Use functional magnetic resonance imaging to find those areas of the brain that comedy activates then develop nootropics that activate these brain regions
EEG waves are published as accompanying particular mental states Do electroencephalography EEG waves vary with pulse pressure, some senses like touch vary with pulse pressure electroencephalography waves that vary may have a natural variability a numeric distribution that correlates with genetics or cytokines thus giving new nootropics as well as IQ genes also create new physical forms that optimize pulse pressure to raise IQ
Electroencephalography detectors describe electrical activity at the brain, noting that photonic measurement of brain activity (photonic glucose tomography) is published use erythrocyte ghosts (erythrocyes can be emptied then filled with a drug or mechanism, the membrane surface is immunoneutral permitting long circulation) that contain an op amp that is capable of distinguishing frequencies (basically EEG uses a ground, a photovoltaic microopamp provides an artificial difference giving distinguishing capability absent a ground) to create a photonic powered measure of microelectroencephalography wherever an erythrocyte ghost op amp passes through a CNS or body capillary This is used to record electrical microstate throughout the volume of the CNS It is published that feeding people Learning style EEG waves at the skin surface actually ups learning 10 or 20 pt (Science or Nature magazine) thus phototonically powered erthrocyte ghosts are a way to to electrically microamp the entire brain Noting that refeeding electroencephalographic waves to the brain improves cognition the erythrocyte ghost op amps could also convert phtonic energy to electromagnetic energy brief pulses of which could seed beneficial electroencephalographic waveforms It would be nifty to see what a recording of another persons capillarly level micro EEG felt or perhaps thought like when replayed. It could possibly be a learning potentiation machine The measurement function of the erythrocyte ghost op amps could be accomplished with using electricity to shift the light output of an externally detectable (or cascaded data transfer)fluorescent molecule basically if you slightly nudge the electrical field of something like GFP you get it to change emission frequencies which may thus be distinguishable externally, or variously internally detected with another photonic molecule that can multiplex photons to a detectable output or even unique RNA PCR does actually amplify single copy RNA so a modified photomodulatable ribosome could do the multiplexing
When nervous systems or neurons get repeated doses of a drug sometimes they get a ramping effectiveness effect "tolerance" this could be measured at microareas like along a multidendrite neuron to see if there was a natural variation as well as measured at microareas to see if there was a distant cyte or tissue cytokine based ramping effect If microareas go with tolerance then distribution of variation could be measured to find genes that go with less ramping effect as well as siRNA to those genes to create an actual pharmaceutical that modulates the effect If there are wide area effects then the cytokines that travel could be identified, passivating versions would then prevent ramping, also immunizations could remove the ramping cytokines, further mRNA activity linked to ramping creates antimRNA modulation opportunities
Scientific American had an article from a researcher that found the genes that most rapidly changed during human prehistoric development The various human haplotypes of those genes may be notably cognitively different (the tree of early to modern mind styles) thus describing IQ cognitive style genes Further amino acid optimization of these genes like phenylalanine compared with alanine could create more pronounced humanotropic effect as could creating completely new copy number variations. more human than currently human along an obviously maintained development style
These three ideas together create brain region localized neuron type pharmaceuticals Radiolabel a vast variety of proteins as well as peptides then at lab mammals find both where they brain anatomy localize as well as the upper 999th percentile of membrane transport activity that make it past the blood brain barrier This gives the ability to create custom localized nootropics like serotoninWithLocalizerpeptide or cenrophenoxineWithLocalizer as well as things like MemoryPeptideWithTransporter
Create antibodies to receptors at neurons (published) Then create peptide sequences of just the recognition tips of the antibodies as receptor activating drugs then attach Localizers as well as Transport proteins to these new drug peptides to specify their locationality (published) While amplifying transport also use what are called DNA "zip codes" as well as DNA Enhancers (as they are called) to direct these new neuroactivating peptides as well as proteins (likely previously published)
Then Because you have created localizable peptides similar to antibody fragment tip drugs that effect specific neuron receptors you can then create custom particular localizable peptide neurodrugs as well as specifiy the new genetics of their custom receptors (GCPR or different) creating greater localization as well as wider power amplitude of effect (put a copy of the .5b idea version at RDSmart group)
A number of photons can be quantum linked (published (2010) 5 or 7) rapidly zapping a tissue making mRNA with quantum linked photons that on detection were linked to a cascade of higher energy photons the activity of the mRNA could be modified at a distance, that is the "scan" photon is coupled to a "detect" photon outside the body the "detect" photon is also linked to 3 or 7 much higher energy photons that then "zap" at the tissue modifying activity either with radicalless charge modification from absorption, mere warmth that rapidifies enzyme kinetics, or radical ion effects. this GeneRay could be pointed at any tissue to direct the permitted proteins constucted (slow, stop, permit, rapidify the ribosomes or mRNA) as well as the development that occurs This is also nootropic as it is kind of like VR memory or emotion construction editing of neural tissue to beam a bunch of quantum linked photons that as a result of a unique chemical absorption effect trigger a bigger bunch of active or even mere warming photons to the enzyme kinetics of the microarea with that detected cytotissue or mRNA or detected cytokine
