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1 f a proton at C-4, this is not the case with glutaryl-CoA dehydrogenase.
2 medium chain acyl-CoA dehydrogenase and the glutaryl-CoA dehydrogenase.
3 ylation of glutaryl-CoA that is catalyzed by glutaryl-CoA dehydrogenase.
4 the active site in these binary complexes of glutaryl-CoA dehydrogenase.
7 tion of a spectral species between wild type glutaryl-CoA dehydrogenase and a E370D mutant are consis
8 sm via beta-oxidation, a non-decarboxylating glutaryl-CoA dehydrogenase and a subsequent glutaconyl-C
9 tic pathway catalyzed by the E370D mutant of glutaryl-CoA dehydrogenase and compared them with those
14 nsistent with the idea that this distance in glutaryl-CoA dehydrogenase contributes to the enhanced r
15 y diagnosis, one-third of Amish infants with glutaryl-CoA dehydrogenase deficiency (GA1) develop stri
17 eening the conditions for crystallization of glutaryl-CoA dehydrogenase from Burkholderia pseudomalle
19 were already present at that time: ancestral glutaryl-CoA dehydrogenase (GCD), isovaleryl-CoA dehydro
20 ood disorder caused by defective activity of glutaryl CoA dehydrogenase (GCDH) which disturb lysine (
21 an disease, glutaric aciduria type I (GA-1), glutaryl-CoA dehydrogenase (GCDH) deficiency disrupts th
26 ces (e.g., in short-chain, medium-chain, and glutaryl-CoA dehydrogenases) or on the G helix (long-cha
27 dehydrogenation reaction catalyzed by human glutaryl-CoA dehydrogenase was investigated using a seri
29 The involvement of water in catalysis by glutaryl-CoA dehydrogenase was previously unrecognized a
30 parison of steady-state kinetic constants of glutaryl-CoA dehydrogenase with glutaryl-CoA and the alt
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