Results 201 to 210 of about 50,245 (245)
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Use of the GnRH-agonist (GnRH-A) in gynaecology.
1998GnRH-agonist therapy is used in the management of many gynaecological pathologies: uterine fibroids, endometriosis, ovarian cystic pathology, breast cancer, dysfunctional uterine bleeding and, in males, prostatic cancer. In the case of uterine fibroids, this therapy can be used as a pre-treatment before conservative or demolitive surgery or as an ...
CIARDO A, SPINA V, ALEANDRI, Vincenzo
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2002
Publisher Summary An inspection of the deduced amino acid sequences from the nine complementary pro-GnRH forms demonstrates several points. All pro-gonadotropin-releasing hormone (GnRH) proteins contain GnRH at their N-termini and the peptide is separated by a putative processing site from GnRH-associated peptide (GAP).
William C, Wetsel, Sudha, Srinivasan
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Publisher Summary An inspection of the deduced amino acid sequences from the nine complementary pro-GnRH forms demonstrates several points. All pro-gonadotropin-releasing hormone (GnRH) proteins contain GnRH at their N-termini and the peptide is separated by a putative processing site from GnRH-associated peptide (GAP).
William C, Wetsel, Sudha, Srinivasan
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GnRH in the invertebrates: an overview
2002Publisher Summary This chapter provides an overview of GnRH in the invertebrates. The gonadotropin-releasing hormone (GnRH), which was previously called luteinizing hormone-releasing hormone (LHRH), represents a pivotal peptide in animal reproduction.
RASTOGI R. K. +4 more
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Embryo implantation and GnRH antagonists: GnRH antagonists do not activate the GnRH receptor.
Human reproduction (Oxford, England), 2000Recent suggestions that gonadotrophin-releasing hormone (GnRH) antagonists activate the GnRH receptor are discussed. Most of the studies cited in support of this suggestion are in-vitro studies, testing supra-pharmacological doses of GnRH analogues in cancer cell lines, whereas GnRH antagonists, e.g.
B, Mannaerts, K, Gordon
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Journal of Obstetric, Gynecologic & Neonatal Nursing, 1994
Gonadotropin-releasing hormone agonists are a relatively new class of drugs, which, when chronically administered, result in marked reductions in blood levels of testosterone and estrogen. These drugs include leuprolide acetate (Lupron); the first GnRH agonist to be approved in the United States, nafarelin acetate (Synarel); and goserelin acetate ...
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Gonadotropin-releasing hormone agonists are a relatively new class of drugs, which, when chronically administered, result in marked reductions in blood levels of testosterone and estrogen. These drugs include leuprolide acetate (Lupron); the first GnRH agonist to be approved in the United States, nafarelin acetate (Synarel); and goserelin acetate ...
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GnRH and GnRH Analogues: Applications in Gynecology
Clinical Obstetrics and Gynecology, 1993openaire +2 more sources
The roles of GnRH in the human central nervous system
Hormones and Behavior, 2022Craig Atwood +2 more
exaly

