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1 ally, testosterone antagonized the effect of pregnenolone sulfate.
2 t postulated for the inhibitory neurosteroid pregnenolone sulfate.
3 fected the negative allosteric modulation by pregnenolone sulfate.
4 omers of dehydroepiandrosterone sulfate (1), pregnenolone sulfate (2), and (3alpha,5beta)-3-hydroxypr
5 teric potentiation of NMDA receptor pores by pregnenolone sulfate, 24(S)-hydroxycholesterol, and doco
8 iously shown that the sulfated neurosteroids pregnenolone sulfate and 3alpha-hydroxy-5beta-pregnan-20
10 loreclezole, had different IC(50) values for pregnenolone sulfate and lanthanum, and were insensitive
11 sure alters the actions of the neurosteroids pregnenolone sulfate and pregnenolone hemisuccinate, whi
12 oth compounds competed with progesterone and pregnenolone sulfate and significantly reduced CatSper a
13 bserve enantioselectivity for the actions of pregnenolone sulfate and steroid sulfate 3 indicates tha
14 hermore, the GluN2A/B-selective potentiator (pregnenolone sulfate) and the GluN2C/D-selective potenti
15 s steroids allopregnanolone (3alpha5alphaP), pregnenolone sulfate, and beta-estradiol in the absence
16 tsynaptic neuron depolarization, and an anti-pregnenolone sulfate antibody scavenger blocked this eff
18 ulfated and unsulfated neurosteroids such as pregnenolone sulfate, dehydroepiandrosterone sulfate (DH
19 l CatSper currents, whereas the neurosteroid pregnenolone sulfate exerted similar effects as progeste
20 ectrophysiological techniques, we found that pregnenolone sulfate increases the frequency of AMPA-med
23 report here that the excitatory neurosteroid pregnenolone sulfate induces a long-lasting strengthenin
30 ne mediating the effects of the neurosteroid pregnenolone sulfate, or the allosteric regulatory site
31 roid pregnenolone (PREG) and its metabolites pregnenolone sulfate (PregS) and allopregnanolone in ser
34 h models of the GABA-inhibitory neurosteroid pregnenolone sulfate (PREGS), suggesting common mechanis
43 We examined the effects of the neurosteroid pregnenolone sulfate (PS) on GABA(A) receptor-mediated s
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