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1 BsAg) and membrane-bound cytochrome P450scc (P450scc).
2 cytochrome P450 side chain cleavage enzyme (P450scc).
3 bers of the P450 side chain cleavage system (P450scc).
4 protein, and side-chain cleavage activity of P450scc.
5 ndrial transfer of cholesterol to cytochrome P450scc.
6 the Fe2+-sensitive process does not involve P450scc.
7 ee Leydig cell steroid biosynthetic enzymes (p450scc, 3betaHSD and p450c17) were not expressed in XY
13 tor, P2, that bind to a known IGFRE (porcine P450scc) and induce reporter gene transcriptional activi
14 ifferent molecular weights, such as BSA, Mb, P450scc, anti-HBsAg with the concentration detection lim
15 bserved elevations of cholesterol-cytochrome P450scc association and metabolism in subsequently isola
16 n-like growth factor 1 (IGF1)-inducible gene P450scc by binding to an insulin-like growth factor resp
17 It has been shown that mammalian cytochrome P450scc can metabolize vitamin D3 to 20-hydroxyvitamin D
18 that the cryoreduced ternary complex of oxy-P450scc-CH is catalytically competent and hydroxylates c
19 als that the distal pocket of the parent oxy-P450scc-cholesterol complex exhibits an efficient proton
27 nduced transcriptional activity of a porcine P450scc core promoter luciferase construct containing th
28 esterol side chain cleavage cytochrome P450 (P450scc; CYP11A) catalyzes the first step in the product
29 ement of the steroidogenic enzyme cytochrome P450scc (CYP11A1) as well as CYP27B1 (1alpha-hydroxylase
31 ents using purified mitochondrial cytochrome P450scc (CYP11A1) reconstituted with the iron-sulfer pro
32 t inhibit mitochondrial import of cytochrome P450scc (cytochrome P450 side chain cleavage enzyme) and
33 the placental strategy for transcription of P450scc employs cis-acting elements different from those
35 regnenolone, i.e. the genes and proteins for P450scc enzyme, adrenodoxin, adrenodoxin reductase and M
37 erotype 2 viral vector (rAAV2), which drives P450scc expression and neuroactive steroid synthesis.
38 esence of aminoglutethimide, an inhibitor of P450scc, FeSO4 increased the synthesis of both steroids,
40 rt presents the first sequence of cytochrome P450scc from this evolutionary unique taxon of vertebrat
42 the transcriptional activity of the porcine P450scc IGFRE by preventing IGF-I-stimulated binding of
44 terol side-chain cleavage enzyme, cytochrome P450scc, initiates the biosynthesis of all steroid hormo
45 criptional activity of the porcine P-45011A (P450scc) insulin-like growth factor response element (IG
46 uces predominantly the hydroperoxy-ferriheme P450scc intermediate, along with a minor fraction of per
47 During annealing of the hydroperoxy-ferric P450scc intermediates at 185 K, they convert to the prim
48 erase chain reaction indicated that mRNA for P450scc is more abundant than mRNA for both P450c17 and
50 experiments in granulosa cells with deletion P450scc/luciferase constructs showed that TNFalpha inhib
51 reported pathway of vitamin D3 metabolism by P450scc may have wider biological implications depending
52 ulin-like growth factor-I (IGF-I)-stimulated P450scc mRNA concentrations in cultures of porcine granu
56 mino terminus longer than the other forms of P450scc, no translation initiation signal (ATG) was evid
66 at bind to the -155/-131 region of the human P450scc promoter, which participates in its placental bu
71 he full cytochrome P450 side-chain cleavage (P450scc) system required for the intracellular catalytic
72 heir modulation of placental but not adrenal P450scc transcription underscores the distinctiveness of
73 , a specific 252 bp fragment of the putative P450scc was amplified from RNA of interrenal tissue (the
76 (StAR) and P450 side-chain cleavage enzyme (P450scc), without affecting P450 aromatase mRNA level, s
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