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1 kinase, glucose-6-phosphate dehydrogenase, 6-phosphogluconate dehydrogenase).
2 gnd, which is a polymorphic gene encoding 6-phosphogluconate dehydrogenase.
3 e of the pentose phosphate pathway, and by 6-phosphogluconate dehydrogenase.
4 he pentose phosphate pathway (PPP) enzyme, 6-phosphogluconate dehydrogenase.
5 4-phosphoerythronate (4PE), which inhibits 6-phosphogluconate dehydrogenase.
6 ude beta-hydroxyisobutyrate dehydrogenase, 6-phosphogluconate dehydrogenase, 2-(hydroxymethyl)glutara
7 -6-phosphate dehydrogenase (G-6-PDase) and 6-phosphogluconate dehydrogenase (6-PGDase), which are the
8 matic studies have shown the importance of 6-phosphogluconate dehydrogenase (6-PGDH) in Trypanosoma b
9 t inhibitor of parasite Trypanosoma brucei 6-phosphogluconate dehydrogenase (6-PGDH), the third enzym
12 pathway is important for tumor growth, how 6-phosphogluconate dehydrogenase (6PGD) in this pathway is
14 ucose 6-phosphate dehydrogenase (G6PD), or 6-phosphogluconate dehydrogenase (6PGD), nor prevented by
15 that targeting a key oxidative PPP enzyme, 6-phosphogluconate dehydrogenase (6PGD), using our novel s
17 tegy to change the coenzyme specificity of 6-phosphogluconate dehydrogenase (6PGDH) from a hypertherm
18 ut screening method to identify mutants of 6-phosphogluconate dehydrogenase (6PGDH) from a thermophil
21 glucose 6-phosphate dehydrogenase (G6PDH), 6-phosphogluconate dehydrogenase (6PGDH), and methylenetet
22 glucose 6-phosphate dehydrogenase (G6PDH), 6-phosphogluconate dehydrogenase (6PGDH), and methylenetet
26 ased glucose 6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase activities and increased
27 e in glucose 6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase activities and NADPH and
28 ucose-6-phosphate dehydrogenase (Gpdh) and 6-phosphogluconate dehydrogenase activities present in the
30 hydrogenase activity and a 32% increase in 6-phosphogluconate dehydrogenase activity over control lev
31 me, glucose-6-phosphate dehydrogenase, and 6-phosphogluconate dehydrogenase, all of which produce NAD
32 -aminonicotinamide led to an inhibition of 6-phosphogluconate dehydrogenase and an accumulation of 6-
33 nzymes (glucose 6-phosphate dehydrogenase, 6-phosphogluconate dehydrogenase, and malic enzyme), vario
34 ties of glucose-6-phosphate dehydrogenase, 6-phosphogluconate dehydrogenase, and phosphofructokinase
35 enzymes glucose 6-phosphate dehydrogenase, 6-phosphogluconate dehydrogenase, and transaldolase, eleva
36 lly separated from Glc6P dehydrogenase and 6-phosphogluconate dehydrogenase by a dialysis membrane, t
38 interactions between the 2'-phosphate and 6-phosphogluconate dehydrogenase contribute most of the bi
39 eled between yeast Glc6P dehydrogenase and 6-phosphogluconate dehydrogenase despite the absence of 6-
40 ; glucose phosphate isomerase, EC 5.3.1.9; 6-phosphogluconate dehydrogenase EC 1.1.1.44; and NADP-red
41 PGD(391-410)) is part of a plasmid-encoded 6-phosphogluconate dehydrogenase found in some S. aureus s
43 reactions of whole substrates catalyzed by 6-phosphogluconate dehydrogenase, glucose 6-phosphate dehy
46 ydrogenase, UDP-glucose dehydrogenase, and 6-phosphogluconate dehydrogenase, indicating a possible ev
47 ucose-6-phosphate dehydrogenase (G6PD) and 6-phosphogluconate dehydrogenase (PGD) in the pentose phos
49 aminopyridine compound that targets a unique Phosphogluconate Dehydrogenase (PGD)-dependent metabolic
52 on of two alternative enzymes for both the 6-phosphogluconate dehydrogenase reaction (GndA and GndB)
55 ses (glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase) that were immobilized on
56 sis was used to change E190 of sheep liver 6-phosphogluconate dehydrogenase to A, D, H, K, Q, and R t
57 sis was used to change K183 of sheep liver 6-phosphogluconate dehydrogenase to A, E, H, C, Q, R, and
58 cycle, and erythrose-4-phosphate inhibits 6-phosphogluconate dehydrogenase to redirect flux from the