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2 orogenic acid (15.4 +/- 0.05 mug mg(-1)) and biochanin A (9.6 +/- 0.06 mug GAE mg(-1)), while minor c
3 From a panel of phytoestrogen isoflavones, biochanin A (BCA) was identified as the most potent indu
4 n (genistein 7-sulfate) and 2 metabolites of biochanin A (genistein and genistein 7-sulfate) were det
6 timulated release of PSA, presumably because biochanin A increased UDPGT and increased the intracellu
10 nap2 mutants and show that the phytoestrogen biochanin A specifically reverses the mutant behavioral
11 f genistein 7-sulfate from genistein or with biochanin A sulfate, genistein 7-sulfate, or genistein f
16 flavonoids, isoflavonoids (formononetin and biochanin A) and flavones (7,4'-dihydroxyflavone), respe
17 flavones (genistein, genistin, daidzein, and biochanin A) and soy phytochemical concentrate exhibit d
18 oybean isoflavones (genistein, daidzein, and biochanin A) are ERbeta-selective agonists of transcript
19 isoflavones (genistein, daidzein, glycitein, biochanin A, and formononetin), lignans (secoisolaricire
21 ch are aglycons, namely daidzein, genistein, biochanin A, and two of which, daidzin and genistin, are
24 s of the isoflavones daidzein, formononetin, biochanin A, genistein, and equol were studied under sim
29 ein, genistein, glycitein, formononetin, and biochanin-A and their mammalian metabolites equol and O-
30 avonoid metabolites such as formononetin and biochanin-A that peaked at 12 to 18 h following elicitat
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