Zobrazeno 1 - 10
of 11
pro vyhledávání: '"T. S. Ruh"'
Publikováno v:
Biochemical pharmacology. 52(6)
Chromosomal proteins that impart high affinity and specificity to the binding of the estrogen receptor (ER) to DNA are termed estrogen receptor binding factors (ERBFs). Certain partially purified chromosomal protein fractions obtained from rabbit ute
Autor:
T C Spelsberg, T S Ruh
Publikováno v:
Biochemical Journal. 210:905-912
Partially purified hen oviduct oestrogen receptors, charged with [3H]oestradiol, were shown to specifically bind in vitro to purified hen oviduct chromatin. Maximal binding occurred within 60min at 0 degrees C in a Tris buffer containing 0.1 M-KCl an
Publikováno v:
Experimental Biology and Medicine. 134:947-951
SummaryThe effect of hyper- and hypothyroidism on uterine wet weight, total protein, and SDH activity was studied in estrogen (2.0 μg of estradiol 17β/kg of body wt for 3 days)- and nonestrogen-treated ovariectomized rats. Uterine SDH activity appe
Publikováno v:
Recent Advances in Steroid Hormone Action
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c7bd9e9742a1effb0d5d9ab7a6ff9a8b
https://doi.org/10.1515/9783110850260-005
https://doi.org/10.1515/9783110850260-005
Publikováno v:
Cancer research. 43(6)
The effects of glucocorticoids were studied in lipopolysaccharide (LPS)-stimulated splenic murine B-cell leukemia line one (BCL1) cells. At 24 hr, LPS caused a 3-fold increase in [3H]-thymidine incorporation compared to similarly cultured unstimulate
Publikováno v:
Endocrinology. 97(5)
Studies were conducted to determine the ability of androgens in vitro to elicit the induction of a specific uterine protein (IP) normally attributed to estrogens. Both 5alpha-dihydrotestosterone (5alpha-DHT) and testosterone were effective in stimula
Publikováno v:
Cancer research. 45(9)
The antiestrogenic character and potency of 4-(N,N-diethylaminoethoxy)-4'-methoxy-alpha-(p-hydroxyphenyl)-alpha' -ethylstilbene (H1285) and its binding to estrogen receptor and to estrogen-noncompetible antiestrogen binding sites have been studied in
Publikováno v:
Cancer research. 41(1)
Glucocorticoid-specific binding macromolecules were measured and characterized in L2C cells, a B-lymphocyte guinea pig leukemia that is resistant to administered cortisol or adrenocorticotrophic hormone. L2C cells were harvested by cardiac puncture f
Publikováno v:
The Biochemical journal. 200(1)
Various aspects of the interaction of oestrogen-receptor complexes with calf uterine chromatin covalently coupled to cellulose were analysed. Partially purified [3H]oestradiol-receptor complexes were bound to intact, or partially deproteinized, chrom
Publikováno v:
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.). 134(2)
SummaryUterine uptake and retention of 3H-estradiol-17β in rats subjected to varying levels of thyroid hormones were studied in vivo and in vitro. Uteri from thyroxine-treated rats had a lesser in vivo retention and in vitro uptake of estrogens wher