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1 s of estrogen receptors or estradiol-induced progestin receptors.
2  estrogen receptors and/or estradiol-induced progestin receptors.
3 sterone, it appears to be mediated by neural progestin receptors.
4  estrogen receptors and/or estradiol-induced progestin receptors.
5 radiol and progesterone involve estrogen and progestin receptors.
6 ve no detectible impact on the expression of progestin receptors.
7 -1 down-regulated the expression of membrane progestin receptor alpha (mPRalpha), the intermediary in
8 el immunofluorescent technique to label both progestin receptors and Fos protein following progestero
9 dy examined the effects of administering the progestin receptor antagonist RU486 for the first 10 day
10  brain, changes in the activational state of progestin receptors because of dopamine D1 receptor stim
11 and D1 agonist-induced neuronal responses in progestin receptor-containing areas and cells.
12 ng the mating-induced release of dopamine in progestin receptor-containing areas of the brain, change
13 haps via stimulation of D1 receptors, within progestin receptor-containing areas.
14 cant increase in Fos-immunoreactivity within progestin receptor-containing cells in the medial preopt
15 e progesterone-induced Fos expression within progestin receptor-containing neurons may or may not be
16 terone treatment increased Fos expression in progestin receptor-containing regions, such as the ventr
17    The finding that sex differences exist in progestin receptor expression in the perinatal rat brain
18 ls housed in SP showed significantly reduced progestin receptor immunoreactivity (PRIR) in the VMH, m
19 ning estrogen receptor- or estradiol-induced progestin receptor-immunoreactivity in the ventrolateral
20 e with increased Fos expression also contain progestin receptor-immunoreactivity.
21  for estrogen receptor- or estradiol-induced progestin receptor-immunostaining.
22 stics suggest the fish protein is a membrane progestin receptor mediating a "nonclassical" action of
23  gene with the characteristics of a membrane progestin receptor (mPR) in a fish model, spotted seatro
24 alpha), estrogen receptor-beta (ERbeta), and progestin receptor (PR) immunoreactivities are localized
25 or instance, the sex difference in perinatal progestin receptor (PR) immunoreactivity in the medial p
26         High levels of progestin binding and progestin receptor (PR) mRNA have also been reported in
27 us, vessel invasion, estrogen receptor (ER)/ progestin receptor (PR) status, c-erb B-2, or Ki-67 expr
28  of estrogen receptor (ER) alpha, ERbeta and progestin receptor (PR) with LENK-labeled MF pathway pro
29   Only C57 and C57x129 mice had increases in progestin receptor (PR)-immunoreactivity (PR-IR) in the
30 ha (ER alpha) and/or beta (ER beta), and the progestin receptor (PR).
31 ptic connectivity maybe mediated through the progestin receptor (PR).
32                 However, the distribution of progestin receptors (PR) in a socially monogamous and sp
33 boratory has shown previously that E induces progestin receptors (PR) in serotonin neurons.
34 dministered estradiol systemically to induce progestin receptors (PR).
35                             Progesterone and progestin receptors (PRs) are known to play a role in th
36                  Recently, estradiol-induced progestin receptors (PRs) have been localized within the
37 xual receptivity and given the importance of progestin receptors (PRs) in mediating the responses of
38 e of P's actions at E2-induced intracellular progestin receptors (PRs) to facilitate lordosis was inv
39 -32 activation is thus an obligatory step in progestin receptor regulation of sexual receptivity in r
40  post-synaptic GPCRs, including the membrane progestin receptor, the corticotropin releasing hormone
41 ne with increase Fos expression also contain progestin receptors, we used a double-label immunofluore

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