Cervini LA - Search Results

1

Comparison of an agonist, urocortin, and an antagonist, astressin, as radioligands for characterization of corticotropin-releasing factor receptors.

Perrin MH, Sutton SW, Cervini LA, Rivier JE, Vale WW. Perrin MH, et al. Among authors: cervini la. J Pharmacol Exp Ther. 1999 Feb;288(2):729-34. J Pharmacol Exp Ther. 1999. PMID: 9918582

2

Corticotropin releasing factor (CRF) agonists with reduced amide bonds and Ser7 substitutions.

Cervini L, Theobald P, Corrigan A, Craig AG, Rivier C, Vale W, Rivier J. Cervini L, et al. J Med Chem. 1999 Feb 25;42(4):761-8. doi: 10.1021/jm980607e. J Med Chem. 1999. PMID: 10052982

3

Expression, purification, and characterization of a soluble form of the first extracellular domain of the human type 1 corticotropin releasing factor receptor.

Perrin MH, Fischer WH, Kunitake KS, Craig AG, Koerber SC, Cervini LA, Rivier JE, Groppe JC, Greenwald J, Møller Nielsen S, Vale WW. Perrin MH, et al. Among authors: cervini la. J Biol Chem. 2001 Aug 24;276(34):31528-34. doi: 10.1074/jbc.M101838200. Epub 2001 Jun 25. J Biol Chem. 2001. PMID: 11425856 Free article.

4

Astressin-amide and astressin-acid are structurally different in dimethylsulfoxide.

Grace CR, Cervini L, Gulyas J, Rivier J, Riek R. Grace CR, et al. Biopolymers. 2007 Oct 5-15;87(2-3):196-205. doi: 10.1002/bip.20818. Biopolymers. 2007. PMID: 17657708

5

Human growth hormone-releasing hormone hGHRH(1-29)-NH2: systematic structure-activity relationship studies.

Cervini LA, Donaldson CJ, Koerber SC, Vale WW, Rivier JE. Cervini LA, et al. J Med Chem. 1998 Feb 26;41(5):717-27. doi: 10.1021/jm970618s. J Med Chem. 1998. PMID: 9513600

6

Design of potent dicyclic (4-10/5-8) gonadotropin releasing hormone (GnRH) antagonists.

Rivier JE, Struthers RS, Porter J, Lahrichi SL, Jiang G, Cervini LA, Ibea M, Kirby DA, Koerber SC, Rivier CL. Rivier JE, et al. Among authors: cervini la. J Med Chem. 2000 Mar 9;43(5):784-96. doi: 10.1021/jm990115h. J Med Chem. 2000. PMID: 10715147

7

Design of potent dicyclic (1-5/4-10) gonadotropin releasing hormone (GnRH) antagonists.

Rivier JE, Jiang G, Struthers RS, Koerber SC, Porter J, Cervini LA, Kirby DA, Craig AG, Rivier CL. Rivier JE, et al. Among authors: cervini la. J Med Chem. 2000 Mar 9;43(5):807-18. doi: 10.1021/jm990116+. J Med Chem. 2000. PMID: 10715149

8

Rat corticostatin R4: synthesis, disulfide bridge assignment, and in vivo activity.

Cervini LA, Gray WR, Kaiser R, Dykert J, Chan R, Solomon S, Rivier CL, Rivier JE. Cervini LA, et al. Peptides. 1995;16(5):837-42. doi: 10.1016/0196-9781(95)00040-q. Peptides. 1995. PMID: 7479324

9

Design of monocyclic (1-3) and dicyclic (1-3/4-10) gonadotropin releasing hormone (GnRH) antagonists.

Rivier JE, Porter J, Cervini LA, Lahrichi SL, Kirby DA, Struthers RS, Koerber SC, Rivier CL. Rivier JE, et al. Among authors: cervini la. J Med Chem. 2000 Mar 9;43(5):797-806. doi: 10.1021/jm9901172. J Med Chem. 2000. PMID: 10715148

10

Newly-identified receptors for peptide histidine-isoleucine and GHRH-like peptide in zebrafish help to elucidate the mammalian secretin superfamily.

Wu S, Roch GJ, Cervini LA, Rivier JE, Sherwood NM. Wu S, et al. Among authors: cervini la. J Mol Endocrinol. 2008 Nov;41(5):343-66. doi: 10.1677/JME-08-0083. Epub 2008 Aug 29. J Mol Endocrinol. 2008. PMID: 18757498

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