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#81
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RWM Wrote: "MagillaGorilla" wrote in message ... patch70 wrote: MagillaGorilla Wrote: But you still didn't answer my question: if blood transfusions are detectable for 120 days and EPO is detectable for 5-9 days after injection, why would Tyler opt for the one that has a much longer half life? I have no idea if Tyler is guilty or innocent, but to answer your question I believe that a rider would make the above decision is due to improved out of competition testing. The rider would be concerned that if the testing organization knew the rider's goals for the season they could effectively develop a testing plan to better be able to predict their doping cycles. This greatly increases the chances of nailing a rider taking EPO. If I remember correctly this is how Oscar Camenzind was caught. Also, until the Olympics there was no test in play for homoloogus testing so it was free from detection until this summer. By rushing the test into the Olympics the posiblity existed of catching transfusions too close to scheduled competition for transfusers to adjust to the new test. Or if Hamilton did take a transfusion, he may have thought the nominal 120 day threshold was an absolute and thought a transfusion outside that window was not detectable. The use of the test commencing in the Olympics was anounced to the riders at the TDF, so it's possible that Tyler had dropped out and missed the anouncement or had already got a pre-TDF transfusion so was already in his blood. Lasse Viren was very effective with autologous doping in the 70's before the practice was banned. -- meb |
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#82
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"meb" wrote in message
... Lasse Viren was very effective with autologous doping in the 70's before the practice was banned. As far as I can remember, Viren (and his whole family) had a gene defect which kept his body producing EPO without the limiting factors. He had no need to blood dope since he was a natural high count around 60. |
#83
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"meb" wrote in message
... Lasse Viren was very effective with autologous doping in the 70's before the practice was banned. As far as I can remember, Viren (and his whole family) had a gene defect which kept his body producing EPO without the limiting factors. He had no need to blood dope since he was a natural high count around 60. |
#84
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Tom Kunich wrote: "meb" wrote in message ... Lasse Viren was very effective with autologous doping in the 70's before the practice was banned. As far as I can remember, Viren (and his whole family) had a gene defect which kept his body producing EPO without the limiting factors. He had no need to blood dope since he was a natural high count around 60. Nope. That was the XC skiing famiy. Not Viren. |
#85
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Tom Kunich wrote: "meb" wrote in message ... Lasse Viren was very effective with autologous doping in the 70's before the practice was banned. As far as I can remember, Viren (and his whole family) had a gene defect which kept his body producing EPO without the limiting factors. He had no need to blood dope since he was a natural high count around 60. Nope. That was the XC skiing famiy. Not Viren. |
#86
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MagillaGorilla wrote: I already explained this. But I'll do it again. You wouldn't expect the false positive rate for a bad test to be more than say 1 in 300 or so, maybe 1 in 500. [BTW, an acceptable false positive rate is like 1 in 450,000.] So let's assume the blood transfusion test is a bad test and has a high false positive rate. Given the number of tests done (say 500-1000), two or three false positives are what you would expect, and really no more than that. Dumbass - So how would one get repeated false positives for different sets of antigens? thanks, K. Gringioni. |
#87
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MagillaGorilla wrote: I already explained this. But I'll do it again. You wouldn't expect the false positive rate for a bad test to be more than say 1 in 300 or so, maybe 1 in 500. [BTW, an acceptable false positive rate is like 1 in 450,000.] So let's assume the blood transfusion test is a bad test and has a high false positive rate. Given the number of tests done (say 500-1000), two or three false positives are what you would expect, and really no more than that. Dumbass - So how would one get repeated false positives for different sets of antigens? thanks, K. Gringioni. |
#88
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Tom Kunich wrote:
As far as I can remember, Viren (and his whole family) had a gene defect which kept his body producing EPO without the limiting factors. He had no need to blood dope since he was a natural high count around 60. Stewart Fleming wrote: Nope. That was the XC skiing famiy. Not Viren. Perhaps Viren was tapping them. |
#89
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Tom Kunich wrote:
As far as I can remember, Viren (and his whole family) had a gene defect which kept his body producing EPO without the limiting factors. He had no need to blood dope since he was a natural high count around 60. Stewart Fleming wrote: Nope. That was the XC skiing famiy. Not Viren. Perhaps Viren was tapping them. |
#90
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J DASH ME wrote:
Dumbass - I can think of 1 thing: someone else's blood cells. K. Gringioni. RBR hematologist Rock On!!! J DASH ME, If you think CAS hearings are superfluous bull****, you should resign as a USAC athlete rep. Your response to Tyler's predicament as a USAC athlete rep should be to ensure the process is fair and objective. Your repsonse is a little embarassing given your elected position, no? Or is that position just a popularity contest that carries with it no real responsibility? Thanks, Magilla |
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