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1 licas of the peroxidases and cytochrome P450 oxidizing enzymes.
2 -associated heterotrophic bacteria, and NADH-oxidizing enzymes.
3 n high-pH (hpH) signal common to all sulfite oxidizing enzymes.
4 ric sarcosine oxidase (MSOX) family of amine oxidizing enzymes.
5 a variety of genes encoding free fatty acid-oxidizing enzymes.
6 ved within the family of L-alpha-hydroxyacid oxidizing enzymes.
7 aldehyde or oxygen radicals by fetal ethanol-oxidizing enzymes.
8 ), a transcriptional activator of fatty acid oxidizing enzymes, and uncoupling protein 3 (UCP3), a th
10 eviously described bacterial d- or l-lactate oxidizing enzymes (Escherichia coli genes dld and lldD)
12 results were observed for samples of sulfite-oxidizing enzymes from other organisms that were previou
16 levels for retinol, retinaldehyde, and ATRA-oxidizing enzymes; however, the contribution of retinald
18 al results of several flavin-dependent amine oxidizing enzymes including human monoamine oxidases A a
20 he possible mechanistic pathways for sulfite-oxidizing enzymes is presented and related to available
21 found for HAO and HAO-related hydroxylamine-oxidizing enzyme kustc1061 from K. stuttgartiensis Inter
23 stutzeri WM88 encoding the novel phosphorus oxidizing enzyme NAD:phosphite oxidoreductase (trivial n
25 anic core (Mn(4)O(x)Ca(1)Cl(y)) of the water oxidizing enzyme of oxygenic photosynthesis generates O(
26 delivery of the gene for 15-lipoxygenase, an oxidizing enzyme present in atherosclerotic lesions.
27 it was uncertain whether NocL was the only N-oxidizing enzyme required for nocardicin A biosynthesis.
29 ation of sulfite is catalyzed by the sulfite-oxidizing enzymes (SOEs), which interact with an electro
30 ber of a recently recognized family of amine-oxidizing enzymes that all contain covalently bound flav
31 ssence is shared by another class of alcohol oxidizing enzymes that utilize a catalytic zinc to stabi
33 n and biochemical characterization of the Pt-oxidizing enzyme, which was proven to be BAP by N termin
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