Author:
Roeske R. W.,Chaturvedi N. C.,Hrinyo-Pavlina T.,Kowalczuk M.
Reference13 articles.
1. Schmidt, F., Sundaram, K., Thau, R.B. and Bardin, C. W. [Ac-D-Nal (2)1, 4F-D-Phe2, D-Trp3, D-Arg6]-LHRH, a potent antagonist of LHRH, produces transient edema and behavioral changes in rats. Contraception, 29, 283 (1984).
2. Theoharides, T.C. and Douglas, W.W. Mast cell histamine secretion in response to somatostatin analogues: structural considerations. Eur. J. Pharmacol., 73, 131 (1981).
3. Roeske, R.W., Chaturvedi, N., Rivier, J., Vale, W., Porter, J. and Perrin, M. Substitution of Arg5 for Tyr5 in GhRH antagonists. In: “Peptides: Structure and Function.” C.M. Deber, V.J. Hruby and K.D. Kopple (Eds.), Pierce Chemical Co., Rockford, IL, 1985, p. 561.
4. Momany, F.A. Conformational energy analysis of the molecule, luteinizing hormone-releasing hormone. 1. Native decapeptide. J. Am. Chem. Soc., 98, 2990 (1976).
5. Freidinger, R.M., Veber, D.F., Perlow, D.S., Brooks, J.R. and Saperstein, R. Bioactive conformation of luteinizing hormone-releasing hormone: Evidence from a conformationally constrained analog. Science, 210, 656 (1980).
Cited by
5 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献