نتایج جستجو برای: ru486

تعداد نتایج: 577  

Journal: :Histology and histopathology 2014
Silvia Guil-Luna Eva Hellmén Raquel Sánchez-Céspedes Yolanda Millán Juana Martín de las Mulas

Canine mammary tumours (CMTs) represent nearly half of all tumours in female dogs and some 50% have malignant behaviour. Simple epithelial carcinomas have shorter disease free periods after surgery and a higher reduction of the proliferation index reduction after antiprogestin aglepristone treatment in vivo related to the expression of progesterone receptors (PR). These findings make simple car...

Journal: :Molecular and cellular biology 2005
Geetha V Rayasam Cem Elbi Dawn A Walker Ronald Wolford Terace M Fletcher Dean P Edwards Gordon L Hager

Progesterone receptor (PR), a member of the nuclear receptor superfamily, is a key regulator of several processes in reproductive function. We have studied the dynamics of the interaction of PR with a natural target promoter in living cells through the use of fluorescence recovery after photobleaching (FRAP) analysis and also have characterized the dynamics of the interaction of PR with the mou...

2015
Rebecca S. Hofford Mark A. Prendergast Michael T. Bardo

Social isolation rearing (isolated condition, IC) is used as a model of early life stress in rodents. Rats raised in this condition are often compared to rats raised in an environmentally enriched condition (EC). However, EC rats are repeatedly exposed to forced novelty, another classic stressor in rodents. These studies explored the relationship between cocaine self-administration and glucocor...

Journal: :Molecular human reproduction 1997
N Schuster-Woldan M Hilton T Wilson

Gravidin is a potent phospholipase A2 inhibitor that may contribute to the maintenance of human pregnancy. The aims of this study were to determine firstly, the site of gravidin synthesis within placental membranes and secondly, whether the antiprogestin compound, RU486, regulates synthesis. Membrane explants were taken from placentae, dissected and cultured in the presence of RU486, progestero...

Journal: :Biology of Reproduction 1996

Journal: :American journal of physiology. Cell physiology 2007
Dongsheng Wang Huanchun Zhang Florian Lang C Chris Yun

Glucocorticoids stimulate the intestinal absorption of Na(+) and water partly by regulation of the Na(+)/H(+) exchanger 3 (NHE3). Previous studies have shown both genomic and nongenomic regulation of NHE3 by glucocorticoids. Serum and glucocorticoid-inducible kinase 1 (SGK1) has been shown to be part of this cascade, where phosphorylation of NHE3 by SGK1 initiates the translocation of NHE3 to t...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2002
Elly S W Ngan Zhi-Qing Ma Steven S Chua Francesco J DeMayo Sophia Y Tsai

Fibroblast growth factor-3 (FGF-3) is a crucial developmental regulator. Aberrant activation of this gene by mouse mammary tumor virus insertion results in pregnancy-responsive mammary tumorigenesis. To characterize better FGF-3 function in postnatal mammary gland development and cancer initiation/progression, we used a mifepristone (RU486)-inducible regulatory system to express conditionally F...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2003
Shirley Teng Veronika Jekerle Micheline Piquette-Miller

The pregnane X receptor (PXR) mediates the induction of various genes by xenobiotics, including several ATP-binding cassette transporters. PXR is also activated by bile acids likely to prevent their accumulation to toxic levels; however, the role of PXR in the regulation of MRP3, an important bile acid efflux transporter, has not been elucidated. The impact of PXR activators on the hepatic expr...

Journal: :Proceedings of the National Academy of Sciences 1994

Journal: :British journal of pharmacology 1991
W Potvin S Mulay D R Varma

1. The influence of progesterone on the activity of atrial natriuretic factor (ANF) on rat myometrial motor activity was determined in vitro. 2. ANF inhibited the tension development by myometrium from cycling or oestrogen-treated rats in a dose-dependent manner; maximal inhibition was 100%. 3. Injections of progesterone into rats inhibited the tocolytic activity of ANF in a dose and time-depen...

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