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Quantification of pituitary membrane receptor sites to LHRH: use of a superactive analog as tracer.

作者信息

Conne B S, Aubert M L, Sizonenko P C

出版信息

Biochem Biophys Res Commun. 1979 Oct 29;90(4):1249-56. doi: 10.1016/0006-291x(79)91171-9.

DOI:10.1016/0006-291x(79)91171-9
PMID:229833
Abstract
摘要

相似文献

1
Quantification of pituitary membrane receptor sites to LHRH: use of a superactive analog as tracer.垂体膜促黄体生成素释放激素（LHRH）受体位点的定量：使用一种超活性类似物作为示踪剂。
Biochem Biophys Res Commun. 1979 Oct 29;90(4):1249-56. doi: 10.1016/0006-291x(79)91171-9.
2
[Pituitary LHRH receptor sites: quantification with a superactive analog as tracer, structure-function relationship, and change during castration in male rats (author's transl)].[垂体促黄体生成素释放激素受体位点：用一种超活性类似物作为示踪剂进行定量、结构-功能关系以及雄性大鼠去势后的变化（作者译）]
J Physiol (Paris). 1980 Jul;76(3):207-18.
3
Pituitary receptor binding activity of active, inactive, superactive and inhibitory analogs of gonadotropin-releasing hormone.促性腺激素释放激素的活性、非活性、超活性和抑制性类似物的垂体受体结合活性
Biochem Biophys Res Commun. 1978 May 15;82(1):67-73. doi: 10.1016/0006-291x(78)90577-6.
4
Photoaffinity labeling of luteinizing hormone releasing hormone receptor of rat pituitary membrane preparations.大鼠垂体膜制剂中促黄体生成激素释放激素受体的光亲和标记
Endocrinology. 1981 Oct;109(4):1281-3. doi: 10.1210/endo-109-4-1281.
5
Role of lipids in gonadotropin releasing hormone agonists and antagonist binding to rat pituitary.
Biochem Biophys Res Commun. 1982 Mar 15;105(1):8-13. doi: 10.1016/s0006-291x(82)80003-x.
6
Radioiodinated nondegradable gonadotropin-releasing hormone analogs: new probes for the investigation of pituitary gonadotropin-releasing hormone receptors.放射性碘化不可降解促性腺激素释放激素类似物：用于研究垂体促性腺激素释放激素受体的新型探针。
Endocrinology. 1979 Dec;105(6):1369-76. doi: 10.1210/endo-105-6-1369.
7
Binding of luteinizing hormone-releasing hormone analogues to dispersed rat pituitary cells.促黄体生成激素释放激素类似物与分散的大鼠垂体细胞的结合
Life Sci. 1981 Apr 27;28(17):1961-7. doi: 10.1016/0024-3205(81)90305-2.
8
Luteinizing hormone-releasing hormone inactivation by purified pituitary plasma membranes: effects of receptor-binding studies.
Endocrinology. 1979 May;104(5):1484-94. doi: 10.1210/endo-104-5-1484.
9
Comparison of different agonists and antagonists of luteinizing hormone-releasing hormone for receptor-binding ability to rat pituitary and human breast cancer membranes.促黄体生成激素释放激素的不同激动剂和拮抗剂对大鼠垂体及人乳腺癌细胞膜受体结合能力的比较。
Endocrinology. 1989 Feb;124(2):946-55. doi: 10.1210/endo-124-2-946.
10
Receptor-binding affinity of gonadotropin-releasing hormone analogs: analysis by radioligand-receptor assay.促性腺激素释放激素类似物的受体结合亲和力：通过放射性配体-受体测定法进行分析
Endocrinology. 1980 Apr;106(4):1154-9. doi: 10.1210/endo-106-4-1154.

引用本文的文献

1
Receptor-mediated internalization of fluorescent gonadotropin-releasing hormone by pituitary gonadotropes.垂体促性腺激素细胞通过受体介导的荧光促性腺激素释放激素内化作用
Proc Natl Acad Sci U S A. 1980 Nov;77(11):6692-5. doi: 10.1073/pnas.77.11.6692.
2
Similar luteinizing hormone-releasing hormone binding sites in rat anterior pituitary and ovary.大鼠垂体前叶和卵巢中类似的促黄体生成激素释放激素结合位点。
Proc Natl Acad Sci U S A. 1980 Sep;77(9):5567-71. doi: 10.1073/pnas.77.9.5567.
3
Decapeptides as effective agonists from L-amino acids biologically equivalent to the luteinizing hormone-releasing hormone.
作为与促黄体生成素释放激素生物等效的L-氨基酸有效激动剂的十肽。
Proc Natl Acad Sci U S A. 1986 Feb;83(4):1070-4. doi: 10.1073/pnas.83.4.1070.
4
Binding and internalization of native gonadoliberin (GnRH) by anterior pituitary gonadotrophs of the rat. A quantitative autoradiographic study after cryoultramicrotomy.大鼠垂体前叶促性腺激素细胞对天然促性腺激素释放激素（GnRH）的结合与内化。冷冻超薄切片术后的定量放射自显影研究。
Cell Tissue Res. 1987 Jun;248(3):541-50. doi: 10.1007/BF00216482.