ライフサイエンスコーパス: isovaleryl-CoA dehydrogenase

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1 rogenases) or on the G helix (long-chain and isovaleryl-CoA dehydrogenases).

2 ium is, however, similar to that observed in isovaleryl-CoA dehydrogenase.

3 ields a reduced flavin adduct with wild-type isovaleryl-CoA dehydrogenase.

4 The potato cDNAs Solanum tuberosum isovaleryl-CoA dehydrogenases 1 and 2 (St-IVD1 and St-IV

5 bstrate for the ETC are not fully available, isovaleryl-CoA dehydrogenase and 2-hydroxyglutarate dehy

6 not due to weak binding: the complex between isovaleryl-CoA dehydrogenase and 2-pentynoyl-CoA shows a

7 hose of medium chain acyl-CoA dehydrogenase, isovaleryl-CoA dehydrogenase, and bacterial short chain

8 d branched chain amino acid catabolic enzyme isovaleryl-CoA dehydrogenase (encoded by gene At3g45300

9 eral expansion of the binding cavity seen in isovaleryl-CoA dehydrogenase is not observed in IBD.

10 with abstraction of a gamma-proton, whereas isovaleryl-CoA dehydrogenase is not significantly inhibi

11 Isovaleryl-CoA dehydrogenase (IVD) belongs to an importa

12 Isovaleryl-CoA dehydrogenase (IVD) is a homotetrameric m

13 Isovaleryl-CoA dehydrogenase (IVD) is an intramitochondr

14 rror of metabolism caused by a deficiency of isovaleryl-CoA dehydrogenase (IVD), a nucleus-encoded, h

15 ancestral glutaryl-CoA dehydrogenase (GCD), isovaleryl-CoA dehydrogenase (IVD), and ACAD10/11.

16 yl-CoA dehydrogenase (MCAD), Glu254 in human isovaleryl-CoA dehydrogenase (IVD), and Glu261 in human

17 recessive disorder caused by a deficiency of isovaleryl-CoA dehydrogenase (IVD).

18 the Glu254Gly/Ala375Glu double mutant) makes isovaleryl-CoA dehydrogenase sensitive to irreversible i

19 oA ligand for medium chain, short chain, and isovaleryl-CoA dehydrogenases suggests that the increase

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