2011
DOI: 10.1097/gco.0b013e328348a3ce
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Biochemistry, molecular biology and cell biology of gonadotropin-releasing hormone antagonists

Abstract: GnRH-antagonists have various clinical applications in gynecology, reproductive medicine, urology and oncology. The emergence of well tolerated, orally active GnRH-antagonists may provide an alternative to long-term injections and is likely to have a major impact on the utility of GnRH analogues in the treatment of human diseases.

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Cited by 38 publications
(33 citation statements)
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“…A third GnRH isoform, GnRH-III, was isolated from sea lamprey and was also detected in the brain of mammals (Tan and Bukulmez, 2011). This isoform has 60% homology with GnRH-I.…”
Section: Gonadotropin-releasing Hormone (Gnrh)mentioning
confidence: 99%
“…A third GnRH isoform, GnRH-III, was isolated from sea lamprey and was also detected in the brain of mammals (Tan and Bukulmez, 2011). This isoform has 60% homology with GnRH-I.…”
Section: Gonadotropin-releasing Hormone (Gnrh)mentioning
confidence: 99%
“…LH-antagonists may be used in the near future to reverse the effect of LH and to aid in the treatment of ovarian cancer (32).…”
Section: Discussionmentioning
confidence: 99%
“…The potent action of both GnRH agonists and antagonists is enabled by amino acid substitutions in the native GnRH decapeptide chain. 8 In ART, two GnRH-An are currently available for clinical use: Ganirelix and Cetrorelix, both are subcutaneous injections.…”
Section: Discussionmentioning
confidence: 99%