作者: U. K. Banik , M. L. Givner
DOI: 10.1007/978-1-4684-3824-6_6
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摘要: Following isolation, purification (Schally et al., 1971; Amoss 1971), and elucidation of the chemical structure luteinizing-hormone-releasing hormone (LH-RH) (Matsuo 1971a; Burgus 1971) its synthesis 1971b; Monahan many investigators (see White 1973; Immer 1974) synthesized a number analogues that are more potent than LH-RH in releasing LH follicle-stimulating (FSH) inducing ovulation animals humans (Fugino 1974; Schally 1976; Keye 1976).