From: treon3verdery@gmail.com   
      
   Longevity technology   
      
   Custom epigenetics,   
   Making a deacytlase protein note effective, make millions of molecular   
   variants then screen to find some that function better and pass the blood   
   brain barrier   
   Do all epigenetic drugs reach oocytes and sperm progenitor cytes well, create   
   epigenetic drugs that are better at this   
      
   Are healing ability proteins in young children longevity drugs, concentrate   
   chemicals from healing children of primates, multicentury lifespan clams, and   
   tortoises to find out if they longevize c elegans and yeast   
      
   Verify the 40 something percent greater longevity effect from enterosorbemts   
   at mice and then compare the electrophoresis chemicals of enterosorbent   
   treated mice and regular mice to find out if there is any physiochemical   
   difference in the unabsorbed    
   remaining material, if there is, find out which chemicals GI tract bacteria   
   produce, or decompose to make,, then see if GI tract bacteria that omit   
   producing those toxins cause mice to live longer, axenic (bacterialess) mice   
   exist but I do not know if    
   they have been screened for greater longevity, screen axenic mice for greater   
   longevity, if normal human GI tract bacteria are found to produce toxins then   
   immunization against those toxins could cause greater longevity   
      
   Enyerosorbents are published as causing 40% something greater longevity, and   
   at a dubious study mice fed LKM512 bacteria lived 95% longer and had   
   remodelled GI tracts, at mice find out if there is s GI tract morphology   
   difference between 99th percentile    
   of longevity mice and median mice (diameter, length, membrane thickness,   
   number of bends, transit interval) if there is a difference genetically   
   engineer median mice to have the more optimal GI tract morphology, if there is   
   one, do imaging of    
   supercentenarians and well persons at the 60th, 70th, 80th, and 90th, and 99th   
   percentile of longevity and see if there is a shape trend, that contributes to   
   modifying the human germline to cause people to have the more longevizing GI   
   tract form   
      
   Transit time and automatic hydration at the GI tract may also effect   
   longevity, test the effect of drugs that hyperhydrate and underhydrate the GI   
   tract as to longevity effects on normal mice, also test the effect of transit   
   time rapidifiers on longevity    
   at mice, GI tract only mu opioid antagonists might do this and some mu opioid   
   peptides are active at microgram quantities,    
      
   Noting enyerosorbents ate published as causing greater than 40% greater   
   longevity at rodents, test their effect on large mammals (cows, pigs, horses)   
   then do 700 electrophoretic fractions of plasms, with each being tested on   
   yeast or c elegans for    
   longevity modulation effects, it could be that there is a longevizing chemical   
   or that a deleterious chemical will be detectably strongly reduced when   
   comparing normal large mammal plasma with enyerosorbent treated large mammal   
   or rodent plasma, find out    
   which body systems, possibly something in the liver, usually metabolize those   
   deleterious chemicals then upregulate the production of that metabolizer   
   molecule, drugs that upregulate that metabolizer molecule could be new   
   longevity drugs   
      
   Enyerosorbents are published as increasing longevity, find out if much lower   
   mass enterosorbents, possibly diaper-gel like 200-1000 times expansion   
   molecular variants (acrylates) with different surface charges as   
   enterosorbents, and screen 100 varieties    
   of molecular variants with different surface charges, as well as completely   
   different enterosorbent molecules to find a one pill per day enterosorbant   
   longevity pill that functions at humans, c elegans may have a longevity   
   increase response to    
   enyerosorbents, if so, numerous thousands of different enyerosorbents and   
   surface charges can be tested, it is possible screening some ion exchange   
   resins as enyerosorbents like materials could find a longevity increasing oral   
   material that functions at    
   lower mass   
      
   Enterosorbents, it is possible these reduce inflammation, so topical   
   fluorocorticoids modified not to pass the GI tract could have an effect, this   
   could be tested on mice, or if c elegans respond to enterosorbents with   
   greater longevity, c elegans.    
   Longevity chemical 10HDA causes mice with dermatitis to itch(or actually   
   scratch) five times less, screen molecular variants of 10HDA to find one with   
   much stronger anti-itch, possibly antiinflammatory characteristics, find out   
   if this has greater    
   longevity increasing effects at c elegans and mice   
      
   Find out if mice that get a fecal transplant from 400 year lifespan clams,   
   tortoises, and humans live longer, if they do then find out which bacteria   
   either omit secreting or being toxic, and test those on age batched humans as   
   probiotics after a course    
   of antibiotics and a purgative clears their intestinal flora   
      
   Words about art   
   Art about "are you treating your children well"   
      
   --- SoupGate-Win32 v1.05   
    * Origin: you cannot sedate... all the things you hate (1:229/2)