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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
12                                              alpha-glycerophosphate complex and the rate constant for
13            Enzyme histochemistry showed high alpha glycerophosphate dehydrogenase activity in poorly
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
16  that is completely absent in the homologous alpha-glycerophosphate dehydrogenases.
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-
19            The addition of the TrpA ligands, alpha-glycerophosphate or indoleglycerol phosphate, duri
20 stigate whether changes in Ca2+ and possibly alpha-glycerophosphate or pyruvate supply could underlie
21 rate, glutamate, isocitrate, dihydroorotate, alpha-glycerophosphate, or endogenous substrates.
22                            The FAD-dependent alpha-glycerophosphate oxidase (GlpO) from Enterococcus
23      One previously uncharacterized protein, alpha-glycerophosphate oxidase (GlpO), was cytotoxic for
24                     The soluble flavoprotein alpha-glycerophosphate oxidase from Enterococcus casseli
25                              The recombinant alpha-glycerophosphate oxidase is fully active and stabi
26                            Surprisingly, the alpha-glycerophosphate oxidase sequence is 43% identical
27     As reported previously, the flavoprotein alpha-glycerophosphate oxidases (GlpOs) from a number of
28                     The addition of disodium alpha-glycerophosphate produced a signal twice as intens
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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