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1 alyzes the conversion of isovaleryl-CoA to 3-methylcrotonyl-CoA.
2 alyzes the conversion of isovaleryl-CoA to 3-methylcrotonyl-CoA.
3 conditions, the hyper-accumulation of Leu, 3-methylcrotonyl CoA and isovaleryl CoA indicates that mit
4 3-methylcrotonyl-CoA carboxylase (MCCase) (3-methylcrotonyl-CoA:carbon-dioxide ligase (ADP-forming),
6 eogenesis), propionyl-CoA carboxylase, and 3-methylcrotonyl-CoA carboxylase (branched chain amino aci
7 uced activity of the biotin-dependent enzyme methylcrotonyl-CoA carboxylase (EC 6.4.1.4), was measure
8 r biotin-dependent carboxylases, including 3-methylcrotonyl-CoA carboxylase (MCC) and eukaryotic acet
9 the related biotin-dependent carboxylases 3-methylcrotonyl-CoA carboxylase (MCC) and propionyl-CoA c
13 otin, the normally biotinylated A-subunit of methylcrotonyl-CoA carboxylase (MCCase) accumulates in i
14 carboxylase activity and a lesser amount of methylcrotonyl-CoA carboxylase activity in pancreatic is
15 the current study was the discovery of beta-methylcrotonyl-CoA carboxylase and propionyl-CoA carboxy
20 alyzes the conversion of isovaleryl-CoA to 3-methylcrotonyl-CoA in the leucine catabolism pathway.
21 H, HMG CoA, methylmalonyl CoA, succinyl CoA, methylcrotonyl CoA, isobutyryl CoA, oxidized CoA, acetyl
23 hat use substrates structurally related to 3-methylcrotonyl-CoA, we isolated the MCC-B cDNA and gene
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