Abstract
Using a newly developed isotopic tracer technique for the measurement of 32P-labelled intermediates in glycolysis and nucleotide metabolism in platelets, we studied the variations in 32P-labelled intermediates during activation of the glycolytic flux by cyanide and platelet-activating agents. The major variations occured in [32P]Fru-1,6-P2, dihydroxy acetone phosphate, ATP and Pi.
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