Authors:
Perrin, MH
Fischer, WH
Kunitake, KS
Craig, AG
Koerber, SC
Cervini, LA
Rivier, JE
Groppe, JC
Greenwald, J
Nielsen, SM
Vale, WW
Citation: Mh. Perrin et al., Expression, purification, and characterization of a soluble form of the first extracellular domain of the human type 1 corticotropin releasing factorreceptor, J BIOL CHEM, 276(34), 2001, pp. 31528-31534
Authors:
Erhardt, NM
Fradinger, EA
Cervini, LA
Rivier, JE
Sherwood, NM
Citation: Nm. Erhardt et al., Early expression of pituitary adenylate cyclase-activating polypeptide andactivation of its receptor in chick neuroblasts, ENDOCRINOL, 142(4), 2001, pp. 1616-1625
Authors:
Rivier, JE
Porter, J
Cervini, LA
Lahrichi, SL
Kirby, DA
Struthers, RS
Koerber, SC
Rivier, CL
Citation: Je. Rivier et al., Design of monocyclic (1-3) and dicyclic (1-3/4-10) gonadotropin releasing hormone (GnRH) antagonists, J MED CHEM, 43(5), 2000, pp. 797-806
Authors:
Perrin, MH
Sutton, SW
Cervini, LA
Rivier, JE
Vale, WW
Citation: Mh. Perrin et al., Comparison of an agonist, urocortin, and an antagonist, astressin, as radioligands for characterization of corticotropin-releasing factor receptors, J PHARM EXP, 288(2), 1999, pp. 729-734