Suppression of follicular phase pituitary-gonadal function by a potent new gonadotropin-releasing hormone antagonist with reduced histamine-releasing properties (ganirelix) **Supported in part by Syntex Developmental Research, Palo Alto, California.

Author:

Nelson Linda R.,Fujimoto Victor Y.,Jaffe Robert B.,Monroe Scott E.

Publisher

Elsevier BV

Subject

Obstetrics and Gynecology,Reproductive Medicine

Reference25 articles.

1. The biochemistry, physiology, and pharmacology of gonadotropin releasing hormone (GnRH) and GnRH analogues;Friedman,1991

2. The molecular basis of gonadotropin-releasing hormone action;Conn;Endocrinol Rev,1986

3. Concordant suppression of serum immunoreactive luteinizing hormone (LH), follicle-stimulating hormone, α-subunit, bioactive LH, and testosterone in postmenopausal women by a potent gonadotropin releasing hormone antagonist (detirelix);Andreyko;J Clin Endocrinol Metab,1992

4. Differential regulation of luteinizing hormone, follicle-stimulating hormone, and free α-subunit secretion from the gonadotrope by gonadotropin-releasing hormone (GnRH): evidence from the use of two GnRH antagonists;Hall;J Clin Endocrinol Metab,1990

5. Treatment of endometriosis with a potent agonist of gonadotropin-releasing hormone (nafarelin);Schriock;Fertil Steril,1985

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