PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 2954599-0 1986 Adrenal steroids stimulate growth and progesterone receptor levels in rat uterus and DMBA-induced mammary tumors. Steroids 8-16 progesterone receptor Rattus norvegicus 38-59 3255736-4 1988 The uterine uptake is selectively blocked by simultaneous injection of a large dose of unlabeled steroid, indicating that the uptake is mediated by a high affinity, low capacity binding system, presumably the progesterone receptor. Steroids 97-104 progesterone receptor Rattus norvegicus 209-230 2954599-1 1986 We have studied the effect of treatment with the adrenal steroids androst-5-ene-3 beta,17 beta-diol (delta 5-diol) and dehydroepiandrosterone (DHEA) on the growth and progesterone receptor levels of dimethylbenz(a)anthracene (DMBA)-induced mammary tumors in the rat. Steroids 57-65 progesterone receptor Rattus norvegicus 167-188 12798354-0 2003 Regulation of progesterone receptor isoforms expression by sex steroids in the rat lung. Steroids 63-71 progesterone receptor Rattus norvegicus 14-35 6627946-8 1983 The relative abilities of the various tested steroids to bind to the rat ovary progesterone receptor were: RU-486 greater than or equal to R5020 greater than progesterone. Steroids 45-53 progesterone receptor Rattus norvegicus 79-100 7078152-0 1982 Steroid-binding specificity of the progesterone receptor from rat placenta. Steroids 0-7 progesterone receptor Rattus norvegicus 35-56 28882474-0 2017 Postpartum inhibition of ovarian steroid action increases aspects of maternal caregiving and reduces medial preoptic area progesterone receptor expression in female rats. Steroids 33-40 progesterone receptor Rattus norvegicus 122-143 18539027-1 2008 Replacement of the 7-CH2 group of natural steroid with an oxygen atom led to identification of unnatural 7-oxa-steroids as potent and selective progesterone receptor antagonists. Steroids 42-49 progesterone receptor Rattus norvegicus 144-165 15976009-10 2005 Collectively, these findings provide evidence that progesterone receptor-dependent receptivity is, in part, dependent on PAC1 receptors for intracellular VMN signaling and delineate a novel, steroid-dependent mechanism for a feed-forward reinforcement of steroid receptor-dependent reproductive receptivity. Steroids 191-198 progesterone receptor Rattus norvegicus 51-72 12969244-7 2003 These results indicate that the expression of PR isoforms is differentially regulated by sex steroid hormones in a regionally specific manner. Steroids 93-109 progesterone receptor Rattus norvegicus 46-48 28260098-6 2017 The downregulated DEGs were highly enriched in female gonad development [e.g. progesterone receptor (Pgr)], and the steroid biosynthesis pathway. Steroids 116-123 progesterone receptor Rattus norvegicus 78-99 28260098-6 2017 The downregulated DEGs were highly enriched in female gonad development [e.g. progesterone receptor (Pgr)], and the steroid biosynthesis pathway. Steroids 116-123 progesterone receptor Rattus norvegicus 101-104 17244199-4 2007 In previous studies, we have found that two of these nuclear receptor coactivators, steroid receptor coactivator-1 (SRC-1) and CREB-binding protein (CBP), are important in ER-mediated induction of PR in the VMN and in steroid-dependent behaviours. Steroids 84-91 progesterone receptor Rattus norvegicus 197-199 12379440-7 2002 These results demonstrate a clear sexual dimorphism in the regulation of PR isoforms expression by sex steroid hormones in the rat brain, suggesting that this sex difference contributes to the sexually dimorphic effects of P in the rat brain. Steroids 103-110 progesterone receptor Rattus norvegicus 73-75 10381541-6 1999 It has been observed that: (1) the messenger for PR is present in Schwann cells; (2) DHT may activate the transcriptional activity of a PR-responsive gene by binding to the PR; and (3) putative steroid responsive elements have been described in this paper to be present in the Po promoter region. Steroids 194-201 progesterone receptor Rattus norvegicus 49-51 11369298-5 2001 Correlation among the mRNA expression levels of PACAP, dPRP and the progesterone receptor and the coordinated inhibitory actions of the anti-progesterone (RU-486) suggest that there is also correlated time-dependent steroid regulation of the mRNA levels of PACAP, dPRP and the progesterone receptor in the decidual and pregnant uteri. Steroids 216-223 progesterone receptor Rattus norvegicus 68-89 11369298-5 2001 Correlation among the mRNA expression levels of PACAP, dPRP and the progesterone receptor and the coordinated inhibitory actions of the anti-progesterone (RU-486) suggest that there is also correlated time-dependent steroid regulation of the mRNA levels of PACAP, dPRP and the progesterone receptor in the decidual and pregnant uteri. Steroids 216-223 progesterone receptor Rattus norvegicus 277-298 12372000-11 2002 These findings suggest that differences in steroid secretion by the neonatal male and female gonads are responsible for producing sex differences in the level of PR expression in the postnatal MPN. Steroids 43-50 progesterone receptor Rattus norvegicus 162-164 10381541-6 1999 It has been observed that: (1) the messenger for PR is present in Schwann cells; (2) DHT may activate the transcriptional activity of a PR-responsive gene by binding to the PR; and (3) putative steroid responsive elements have been described in this paper to be present in the Po promoter region. Steroids 194-201 progesterone receptor Rattus norvegicus 136-138 10218985-0 1999 Steroid regulation of progesterone receptor expression in cultured rat gonadotropes. Steroids 0-7 progesterone receptor Rattus norvegicus 22-43 9926835-0 1998 Progesterone receptor isoforms are differentially regulated by sex steroids in the rat forebrain. Steroids 67-75 progesterone receptor Rattus norvegicus 0-21 9603245-2 1998 These actions are steroid specific and dose dependent and are inhibited by the progesterone receptor (PR) antagonist, RU-486. Steroids 18-25 progesterone receptor Rattus norvegicus 79-100 9603245-2 1998 These actions are steroid specific and dose dependent and are inhibited by the progesterone receptor (PR) antagonist, RU-486. Steroids 18-25 progesterone receptor Rattus norvegicus 102-104 9389534-1 1997 Progesterone receptor (PR) messenger RNA (mRNA) is concentrated in neurons of the preoptic area and other regions of the rat hypothalamus where it is colocalized with the estrogen receptor and regulated by changes in the steroid hormonal milieu. Steroids 221-228 progesterone receptor Rattus norvegicus 0-21 9389534-1 1997 Progesterone receptor (PR) messenger RNA (mRNA) is concentrated in neurons of the preoptic area and other regions of the rat hypothalamus where it is colocalized with the estrogen receptor and regulated by changes in the steroid hormonal milieu. Steroids 221-228 progesterone receptor Rattus norvegicus 23-25 1840636-3 1991 We used the polymerase chain reaction to clone the steroid-binding domain of the rat PR from uterine cDNA and used this as a probe to isolate a larger cDNA from a rat placental cDNA library. Steroids 51-58 progesterone receptor Rattus norvegicus 85-87 8932736-0 1996 Ovarian steroid regulation of estrogen and progesterone receptor messenger ribonucleic acid in the anteroventral periventricular nucleus of the rat. Steroids 8-15 progesterone receptor Rattus norvegicus 43-64