Design and synthesis of potent hexapeptide and heptapeptide gonadotropin-releasing hormone antagonists by truncation of a decapeptide analogue sequence
A novel strategy for designing reduced-size analogues of the decapeptide gonadotropin-releasing hormone (GnRH) was developed. As opposed to previous attempts to delete residues from either of the peptide's termini, our approach is based upon the known imp
Yahalom, Dror,Rahimipour, Shai,Koch, Yitzhak,Ben-Aroya, Nurit,Fridkin, Mati
p. 2831 - 2836
(2007/10/03)
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