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1 chanism in the energy-yielding metabolism of alpha-glycerophosphate.
2 elatively high concentrations of pyruvate or alpha-glycerophosphate.
3 sed conformation in the presence of disodium alpha-glycerophosphate.
4 osteric ligands sodium chloride and disodium alpha-glycerophosphate.
5 15N-HSQC signal in the presence of disodium alpha-glycerophosphate.
6 but the dihydroxyacetone phosphate (DHAP) to alpha-glycerophosphate (alpha-GP) ratio significantly in
7 ytic muscle extract that generates pulses of alpha-glycerophosphate and pyruvate and induces oscillat
8 ne (GSSG), glycolytic intermediates, malate, alpha-glycerophosphate, and adenine nucleotides were ass
9 lutarate, glutamate, malate, dihydroorotate, alpha-glycerophosphate, and N,N,N',N'-tetramethyl-p-phen
10 presence of L-Trp with NaCl and/or disodium alpha-glycerophosphate are more difficult to interpret i
11 open conformation in the absence of disodium alpha-glycerophosphate but was able to form a closed con
14 identical to that of the membrane-associated alpha-glycerophosphate dehydrogenase from Bacillus subti
15 sequence is 30-43% identical to those of the alpha-glycerophosphate dehydrogenases (GlpDs) from mitoc
17 ither in the presence or absence of disodium alpha-glycerophosphate, indicating the preference for a
18 cia oleracea L.) enzyme was stabilized by DL-alpha-glycerophosphate or ethanol and destabilized by D-
20 stigate whether changes in Ca2+ and possibly alpha-glycerophosphate or pyruvate supply could underlie
27 As reported previously, the flavoprotein alpha-glycerophosphate oxidases (GlpOs) from a number of
29 ange in lactate), and a 9.2-fold increase in alpha-glycerophosphate suggest diabetes-induced inhibiti
30 so identified, perhaps a unique substituent, alpha-glycerophosphate, which is attached to Ser93 by a
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