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1 nd 14 extension modules, and merE encoding a cytochrome P450 monooxygenase.
2 one or more oxidation reactions catalyzed by cytochrome P450 monooxygenases.
3 sequence with predicted protein homology to cytochrome P450 monooxygenases.
5 The P450 enzymes (mixed function oxidases, cytochrome P450 monooxygenases), a diverse class of enzy
6 nthetic pathway, including a multifunctional cytochrome P450 monooxygenase, a hydroxylating nonheme-i
8 O-methyltransferases and dihydroxylation by cytochrome P450 monooxygenases, although the precise seq
9 extremely large repertoire of genes encoding cytochrome P450 monooxygenases and glutathione S-transfe
11 erentially expressed genes (DEGs), including cytochrome P450 monooxygenases and UDP-glycosyltransfera
12 rrently, lipoxygenases, cyclooxygenases, and cytochrome P450 monooxygenases are considered the primar
13 atetraenoic acid (12[R]-HETE) is formed by a cytochrome P450 monooxygenase; both give rise to the pot
15 ses (Cop1 to Cop6) and two terpene-oxidizing cytochrome P450 monooxygenases (Cox1 and Cox2) from Copr
17 Cytochrome P450 Engineering Database, CYPED; cytochrome P450 monooxygenase, CYP; Hidden Markov Model,
19 vestigated whether stromal expression of the cytochrome P450 monooxygenase CYP26 modulates BTZ sensit
20 on is catalyzed by the Brassicaceae-specific cytochrome P450 monooxygenase CYP705A1 and is transientl
21 pathway, amorphadiene synthase, and a novel cytochrome P450 monooxygenase (CYP71AV1) from A. annua t
23 iochemical function of a rice (Oryza sativa) cytochrome P450 monooxygenase, CYP76M7, which seems to a
24 ation of the ovule primordium; O40 encodes a cytochrome P450 monooxygenase (CYP78A2) that is pollen t
27 talyzed by both microsomal and mitochondrial cytochrome P450 monooxygenases (CYPs), are strongly impl
28 howing high sequence similarity to bacterial cytochrome P450 monooxygenases (CYPs), from the Plm bios
29 own inhibitors of the important enzyme class cytochrome P450 monooxygenases (CYPs), thereby influenci
34 ur results suggest that a single enzyme, the cytochrome P450 monooxygenase encoded by sare1259, catal
35 bition of cyclooxygenase, lipooxygenase, and cytochrome P450 monooxygenase enzymes prior to exposure
36 bolized by cyclooxygenase, lipoxygenase, and cytochrome P450 monooxygenase enzymes to biologically ac
37 ron-containing enzymatic catalyst-based on a cytochrome P450 monooxygenase-for the highly enantiosele
38 ncoded in the biosynthetic gene cluster, the cytochrome P450 monooxygenase Fr9R, was assigned as a 4-
39 fied a gene, designated CYP716Y1, encoding a cytochrome P450 monooxygenase from Bupleurum falcatum th
44 ally, knockout of the tropD gene, encoding a cytochrome P450 monooxygenase, indicated its place as th
47 ss this question, we cloned cDNAs encoding a cytochrome P450 monooxygenase (LsM88) and a caffeate O-m
48 , we demonstrate that CYP82G1 (At3g25180), a cytochrome P450 monooxygenase of the Arabidopsis CYP82 f
49 nce that maize CYP72A27-Zm gene represents a cytochrome P450 monooxygenase (P450) gene recently captu
50 at a rate (V(max) of 10.02 pmol/min/pmol of cytochrome P450 monooxygenase (P450)) significantly high
52 s controlling the expression and activity of cytochrome P450 monooxygenase (P450s) detoxificative enz
59 idered to be the primary mechanisms by which cytochrome P450 monooxygenases (P450s) have radiated int
63 as not yet been defined, each of the encoded cytochrome P450 monooxygenases (P450s) metabolizes an ar
65 howed that more than half (51.2%) of the CBP cytochrome P450 monooxygenases (P450s) that are up-regul
66 tion and screening of soybean cDNAs encoding cytochrome P450 monooxygenases (P450s) was used in an at
67 s of genes encoding metabolic enzymes, i.e., cytochrome P450 monooxygenases (P450s), esterases, and g
68 enobiotic metabolism by inducing the phase I cytochrome P450 monooxygenases, phase II conjugating tra
71 hidonic acid metabolism by lipoxygenases and cytochrome P450 monooxygenases produces regioisomeric hy
72 nts because they contain an abundance of the cytochrome P450 monooxygenases required for generation o
73 The predicted PAD3 protein appears to be a cytochrome P450 monooxygenase, similar to those from mai
74 sis (Arabidopsis thaliana) CYP86A and CYP94B cytochrome P450 monooxygenase subfamilies, which share s
77 f this study, we believe the presence of the cytochrome P450 monooxygenase system in glial cells of t
78 e rat glioma C6 cell line contains an active cytochrome P450 monooxygenase system that can be induced
80 nvolves a remarkably versatile and iterative cytochrome P450 monooxygenase (TamI) and a flavin adenin
82 ntified the CYP78A5 gene encoding a putative cytochrome P450 monooxygenase that is the first member o
83 e four of these enzymes are characterized as cytochrome P450 monooxygenases, the nature of a fifth ox
85 M on large Arabidopsis gene families such as cytochrome P450 monooxygenases to group the members func
88 cloning, and functional characterization of cytochrome P450 monooxygenases, we established that tran
89 gested that the catalytic mechanisms of both cytochrome P450 monooxygenases were similar to the other
90 quence analysis revealed that DWF4 encodes a cytochrome P450 monooxygenase with 43% identity to the p
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