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Differential binding of antiestrogens by rat uterine and chick oviduct cytosol.

作者信息

Sutherland R L, Foo M S

出版信息

Biochem Biophys Res Commun. 1979 Nov 14;91(1):183-91. doi: 10.1016/0006-291x(79)90601-6.

DOI:10.1016/0006-291x(79)90601-6
PMID:518621
Abstract
摘要

相似文献

1
Differential binding of antiestrogens by rat uterine and chick oviduct cytosol.
Biochem Biophys Res Commun. 1979 Nov 14;91(1):183-91. doi: 10.1016/0006-291x(79)90601-6.
2
Anti-estrogen interaction with uterine estrogen receptors. Studies with a radiolabeled anti-estrogen (CI-628).
J Biol Chem. 1978 Feb 10;253(3):697-707.
3
A high-affinity binding site for the antioestrogens, tamoxifen and CI 628, in immature rat uterine cytosol which is distinct from the oestrogen receptor.在未成熟大鼠子宫胞液中存在一种抗雌激素（他莫昔芬和CI 628）的高亲和力结合位点，该位点与雌激素受体不同。
J Endocrinol. 1981 Oct;91(1):155-61. doi: 10.1677/joe.0.0910155.
4
Differential inhibition of estrogen and antiestrogen binding to the estrogen receptor by diethylpyrocarbonate.焦碳酸二乙酯对雌激素和抗雌激素与雌激素受体结合的差异抑制作用。
J Steroid Biochem. 1988 Oct;31(4A):427-36. doi: 10.1016/0022-4731(88)90311-1.
5
[In vivo occupation of estrogen receptors by hydroxylated metabolites of tamoxifen].
C R Seances Acad Sci D. 1979 Dec 10;289(15):1141-4.
6
Differentiation of estradiol receptors in rat uterine cytosol by sensitivity to tamoxifen.
Biochem Biophys Res Commun. 1979 Mar 30;87(2):550-8. doi: 10.1016/0006-291x(79)91830-8.
7
Biological potency and uterine estrogen receptor interactions of the metabolites of the antiestrogens CI628 and U23,469.
Endocrinology. 1981 Jan;108(1):164-72. doi: 10.1210/endo-108-1-164.
8
Estrogenic stimulation of the antiestrogen specific binding site in rat uterus and liver.雌激素对大鼠子宫和肝脏中抗雌激素特异性结合位点的刺激作用。
Endocrinology. 1983 Jun;112(6):1910-5. doi: 10.1210/endo-112-6-1910.
9
Differential interaction of antiestrogens with cytosol estrogen receptors.
Mol Cell Endocrinol. 1981 Apr;22(1):95-103. doi: 10.1016/0303-7207(81)90105-2.
10
Hydroxylated metabolites of tamoxifen are formed in vivo and bound to estrogen receptor in target tissues.他莫昔芬的羟基化代谢产物在体内形成，并与靶组织中的雌激素受体结合。
J Biol Chem. 1981 Jan 25;256(2):859-68.

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1
Binding sites of droloxifene in the cytosol of 7,12-dimethylbenz[a]anthracene-induced rat mammary tumor cells.屈洛昔芬在7,12-二甲基苯并[a]蒽诱导的大鼠乳腺肿瘤细胞胞质溶胶中的结合位点。
Jpn J Cancer Res. 1994 Jun;85(6):639-44. doi: 10.1111/j.1349-7006.1994.tb02407.x.
2
Synergistic interaction between cisplatin and tamoxifen delays the emergence of cisplatin resistance in head and neck cancer cell lines.
Cancer Chemother Pharmacol. 1995;35(6):511-8. doi: 10.1007/BF00686837.
3
Oestrogen and progesterone receptors in chick oviduct chromatin after administration of oestradiol, progesterone or anti-oestrogen.给予雌二醇、孕酮或抗雌激素后鸡输卵管染色质中的雌激素和孕酮受体
Biochem J. 1982 Jun 15;204(3):653-62. doi: 10.1042/bj2040653.
4
Physicochemical and genetic evidence for specific antiestrogen binding sites.特异性抗雌激素结合位点的物理化学及遗传学证据
Proc Natl Acad Sci U S A. 1983 Jun;80(11):3158-62. doi: 10.1073/pnas.80.11.3158.
5
Antiestrogen action in breast cancer cells: modulation of proliferation and protein synthesis, and interaction with estrogen receptors and additional antiestrogen binding sites.抗雌激素在乳腺癌细胞中的作用：对增殖和蛋白质合成的调节，以及与雌激素受体和其他抗雌激素结合位点的相互作用。
Breast Cancer Res Treat. 1985;5(3):231-43. doi: 10.1007/BF01806018.
6
Microsomal binding sites for antioestrogens in rat liver. Properties and detergent solubilization.大鼠肝脏中抗雌激素的微粒体结合位点。特性及去污剂增溶作用。
Biochem J. 1986 Jun 15;236(3):903-11. doi: 10.1042/bj2360903.
7
A study on the correlation between estrogen receptor, progesterone receptor and tamoxifen binding sites in human breast cancer tissues.人乳腺癌组织中雌激素受体、孕激素受体与他莫昔芬结合位点的相关性研究。
Jpn J Surg. 1987 Nov;17(6):487-92. doi: 10.1007/BF02470753.
8
Solubilization of a tamoxifen-binding protein. Assessment of its molecular mass.他莫昔芬结合蛋白的增溶作用。其分子量的评估。
Biochem J. 1988 Nov 15;256(1):229-36. doi: 10.1042/bj2560229.
9
Tamoxifen binding sites in human mammary cancers.人类乳腺癌中的他莫昔芬结合位点。
Jpn J Surg. 1986 Sep;16(5):311-7. doi: 10.1007/BF02470552.