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Re: noforgettingu post# 17110

Saturday, 03/05/2005 4:13:03 PM

Saturday, March 05, 2005 4:13:03 PM

Post# of 64738
Noforgettingu That is what I was thinking ,here is my post from yesterday .

I WAS THINKING THAT MAYBE THIS NEW TEST WAS USING THE NEW DNA METHOD ,REMEMBER[By eliminating the need for this extra DNA, the plasmids are significantly smaller and safer,]MAYBE THEY ARE THINKING THAT THE PLASMIDS ARE SMALLER SO THAT THEY WANTED TO SEE HOW SMALL OF A DOSE THEY CAN GIVE AND STILL AFFECT A CURE.AND ALSO REMEMBER THIS[CytoGenix' breakthrough synthesis technology does not use bacteria and therefore produces no bacterial toxins. Gram or greater quantities of very high purity DNA can now be produced in test tubes or flasks in laboratories at a fraction of the time and cost of DNA manufactured using traditional bioprocess methods]THEY USED THE OLD METHOD WITH BACTERIA BEFORE ,COULD BE THAT THE FDA WANTED RESULTS WITH THE NEW METHOD, AND THAT IS WHAT THEY ARE DOING NOW,WITH THE NEW TESTS. THIS COULD BE THE REASON WHY WE ARE PUSHED FORWARD NOW IN FOURTH QUARTER FOR IND.ALSO THESE NEW TESTS COULD SHOW FDA THE SAFTY OF THE NEW DNA METHOD AND THE CURE FOR HERPES AT THE SAME TIME
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