From: treon3verdery@gmail.com   
      
   Rescuing children from pattern awareness and recruitment: gene drive   
   CRISPR/cas9 makes it so if neural activity like fMRI of IT pattern   
   recruitment, or also preoccurences to perceptions of IT pattern recruitment   
   are neurally active at a human    
   physiological child or adult, notably amygdala activation forms from things   
   that weird people out like perception of things being synchronized, then the   
   human physiological child's body or the body of an adult produces an   
   antipsychotic that travels the    
   circulatory system with the IT pattern awareness decrease, decrease of   
   perception of being recruited, decrease of paranormal foreboding, removal of   
   paranormal imagery while maintaining normal light based vision, absence of   
   hearing things not generated    
   with acoustic waves that treon verdery experiences on 160 mg of lurisidone   
   with 3 grams of phenibut; the production of antipsychotics at the human body   
   is also produced for 14 days if the person omits eating for 24 hours; the   
   chemical basis is: I read    
   that genetically engineering a sequence of molecule transformation enzymes to   
   be at an organism is able to produce a molecule making reaction that   
   sequentially builds the molecule and that the yield from the organism; at   
   proteins this could be similar to    
   the 1 kg per approximate body mass of an adult human, although that is milk   
   proteins can be produced at other tissues; dopamine receptor active proteins   
   are published online at abcam.com;   
   Another way to make an antipsychotic that like lurisidone works from   
   antagonizing D2 and D3 receptors is to make the D2 receptor blocking peptide   
   as well as the D3 receptor blocking peptide, online the dopamine receptor   
   protein this is abcam.com ab32347 (   
   D2) as well as ab128688 (D3), they also have 5HT receptor active peptides that   
   could be, I think, modified to be an antipsychotic that functions on the 5HT   
   receptors;    
   Another way to make an antipsychotic at the human body: The enzyme systems and   
   genes that produce dopamine at the human body, notably the gut, could be   
   genetically modified to produce different shapes and moieties at dopamine   
   molecules, that produces    
   dopamine receptor activity modulators; lurisadone antagonizes (reduces   
   activity at )D2 and D3 receptors so a version of dopamine (modified variety of   
   molecule), made at the gut, that occupies the D2 as well as D3 receptors   
   without activating them and    
   actually reduces their activity could have lurisidone like antipsychotic   
   effects  this modification of the dopamine molecule would pass the blood brain   
   barrier;   
   Pimavanserin antipsychotic 5ht receptor action without dopamine receptor   
   effect is absent sedation or to my perception cognitive effects, it has mild   
   antipsychotic effects and is an FDA approved antipsychotic it could be more   
   beneficial than a dopamine    
   receptor psychotic with pimavanserin omitting drowsiness, cognitive, and   
   behavior reinforcement changing effects, 5HT receptor type peptides are at   
   abcam.com; as with the D2 and D3 peptides being made into antipsychotic drugs   
   that bread mold or the human    
   body can produce, variations in peptide amino acid sequence as well as having   
   enzymes put chemical moieties (groups) on the peptides; I read that three   
   glycines causes things to pass the blood brain barrier so putting a   
   gly-gly-gly on the antipsychotic    
   receptor antagonizing variations on D2, D3, 5HT peptides could make it more   
   effective; any fungi, plant, or mammal can produce peptides   
      
   --- SoupGate-Win32 v1.05   
    * Origin: you cannot sedate... all the things you hate (1:229/2)