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1 a potent anti-proliferative/immunomodulatory secosteroid.
2 mediated the AP-1 activation induced by this secosteroid.
3 ds were also analyzed for these steroids and secosteroids.
4 n addition to its calciotropic function, the secosteroid 1,25-dihydroxyvitamin D(3) (1,25(OH)(2)D(3))
8 isomerase activity from inactivation by the secosteroid and did not slow the inactivation of 3beta-H
9 esis, the beta-ketoester 2 was carried on to secosteroid (-)-astrogorgiadiol (3), a naturally occurri
12 was incubated with the purified enzyme (30/1 secosteroid/enzyme molar ratio) to produce an 80% loss o
13 validate specificity, the affinity labeling secosteroid has identified peptides in the enzyme that a
15 itamin D3, a major natural metabolite of the secosteroid hormone, 1alpha,25(OH)2D3, were chemically s
16 Thus, we have detected novel CYP11A1-derived secosteroids in the skin, serum and adrenal gland and ba
20 phy and radioimmunoassays indicated that the secosteroid product of CYP2R1 was 25-hydroxyvitamin D3.
21 hat clarifies the structural determinants of secosteroid recognition and validates the predictive pow
22 /MS analysis following derivatization with a secosteroid signal enhancing tag that imparted a permane
24 s identify 20(OH)D3 as a biologically active secosteroid that induces keratinocyte differentiation.
26 three peptides and shifted the alkylation by secosteroid to a single tryptic peptide (135EIIQNGHEEEPL
27 inase inhibitor, blocked the ability of this secosteroid to stimulate the translocation and tyrosine
30 led to stimulate PI hydrolysis, but required secosteroid treatment of intact colonocytes, suggesting
31 the biologically active hormonal form of the secosteroid vitamin D-classically categorized as a regul
32 ylator, 5,10-secoestr-4-yne-3,10, 17-trione (secosteroid), was incubated with the purified enzyme (30
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