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Results:
1-21
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Results: 21
Authors:
Craig, AG
DeBoard, R
Kirby, D
Jiang, GC
Koerber, SC
Rivier, JE
Citation: Ag. Craig et al., Characterization of betidamino acid-containing somatostatin and gonadotropin-releasing hormone analogs with electrospray mass spectrometry and tandemmass spectrometry, EUR J MASS, 7(3), 2001, pp. 259-266
Authors:
Wang, LX
Martinez, V
Rivier, JE
Tache, Y
Citation: Lx. Wang et al., Peripheral urocortin inhibits gastric emptying and food intake in mice: differential role of CRF receptor 2, AM J P-REG, 281(5), 2001, pp. R1401-R1410
Authors:
Montaner, AD
Mongiat, L
Lux-Lantos, VAR
Park, MK
Fischer, WH
Craig, AG
Rivier, JE
Lescheid, D
Lovejoy, D
Libertun, C
Sherwood, NM
Somoza, GM
Citation: Ad. Montaner et al., Structure and biological activity of gonadotropin-releasing hormone isoforms isolated from rat and hamster brains, NEUROENDOCR, 74(3), 2001, pp. 202-212
Authors:
Jiang, GC
Stalewski, J
Galyean, R
Dykert, J
Schteingart, C
Broqua, P
Aebi, A
Aubert, ML
Semple, G
Robson, P
Akinsanya, K
Haigh, R
Riviere, P
Trojnar, J
Junien, JL
Rivier, JE
Citation: Gc. Jiang et al., GnRH antagonists: A new generation of long acting analogues incorporating p-ureido-phenylalanines at positions 5 and 6, J MED CHEM, 44(3), 2001, pp. 453-467
Authors:
Rivier, JE
Hoeger, C
Erchegyi, J
Gulyas, J
DeBoard, R
Craig, AG
Koerber, SC
Wenger, S
Waser, B
Schaer, JC
Reubi, JC
Citation: Je. Rivier et al., Potent somatostatin undecapeptide agonists selective for somatostatin receptor 1 (sst1), J MED CHEM, 44(13), 2001, pp. 2238-2246
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:
Montaner, AD
Park, MK
Fischer, WH
Craig, AG
Chang, JP
Somoza, GM
Rivier, JE
Sherwood, NM
Citation: Ad. Montaner et al., Primary structure of a novel gonadotropin-releasing hormone in the brain of a teleost, pejerrey, ENDOCRINOL, 142(4), 2001, pp. 1453-1460
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:
White, HS
McCabe, RY
Armstrong, H
Donevan, SD
Cruz, LJ
Abogadie, FC
Torres, J
Rivier, JE
Paarmann, I
Hollmann, M
Olivera, BM
Citation: Hs. White et al., In vitro and in vivo characterization of conantokin-R, a selective NMDA receptor antagonist isolated from the venom of the fish-hunting snail Conus radiatus, J PHARM EXP, 292(1), 2000, pp. 425-432
Authors:
Rivier, JE
Struthers, RS
Porter, J
Lahrichi, SL
Jiang, GC
Cervini, LA
Ibea, M
Kirby, DA
Koerber, SC
Rivier, CL
Citation: Je. Rivier et al., Design of potent dicyclic (4-10/5-8) gonadotropin releasing hormone (GnRH)antagonists, J MED CHEM, 43(5), 2000, pp. 784-796
Design of monocyclic (1-3) and dicyclic (1-3/4-10) gonadotropin releasing hormone (GnRH) antagonists
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:
Rivier, JE
Jiang, GC
Struthers, RS
Koerber, SC
Porter, J
Cervini, LA
Kirby, DA
Craig, AG
Rivier, CL
Citation: Je. Rivier et al., Design of potent dicyclic (1-5/4-10) gonadotropin releasing hormone (GnRH)antagonists, J MED CHEM, 43(5), 2000, pp. 807-818
Authors:
Koerber, SC
Rizo, J
Struthers, RS
Rivier, JE
Citation: Sc. Koerber et al., Consensus bioactive conformation of cyclic GnRH antagonists defined by NMRand molecular modeling, J MED CHEM, 43(5), 2000, pp. 819-828
Authors:
Carolsfeld, J
Powell, JFF
Park, M
Fischer, WH
Craig, AG
Chang, JP
Rivier, JE
Sherwood, NM
Citation: J. Carolsfeld et al., Primary structure and function of three gonadotropin-releasing hormones, including a novel form, from an ancient teleost, herring, ENDOCRINOL, 141(2), 2000, pp. 505-512
Authors:
Flanagan, CA
Rodic, V
Konvicka, K
Yuen, T
Chi, L
Rivier, JE
Millar, RP
Weinstein, H
Sealfon, SC
Citation: Ca. Flanagan et al., Multiple interactions of the Asp(2.61(98)) side chain of the gonadotropin-releasing hormone receptor contribute differentially to ligand interaction, BIOCHEM, 39(28), 2000, pp. 8133-8141
Authors:
Slawecki, CJ
Somes, C
Rivier, JE
Ehlers, CL
Citation: Cj. Slawecki et al., Neurophysiological effects of intracerebroventricular administration of urocortin, PEPTIDES, 20(2), 1999, pp. 211-218
Authors:
Robinson, BM
Tellam, DJ
Smart, D
Mohammad, YN
Brennand, J
Rivier, JE
Lovejoy, DA
Citation: Bm. Robinson et al., Cloning and characterization of corticotropin-releasing factor and urocortin in Syrian hamster (Mesocricetus auratus), PEPTIDES, 20(10), 1999, pp. 1177-1185
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
Authors:
Rivier, JE
Kirby, DA
Lahrichi, SL
Corrigan, A
Vale, WW
Rivier, CL
Citation: Je. Rivier et al., Constrained corticotropin releasing factor antagonists (astressin analogues) with long duration of action in the rat, J MED CHEM, 42(16), 1999, pp. 3175-3182
Authors:
Turnbull, AV
Vaughan, J
Rivier, JE
Vale, WW
Rivier, C
Citation: Av. Turnbull et al., Urocortin is not a significant regulator of intermittent electrofootshock-induced adrenocorticotropin secretion in the intact male rat, ENDOCRINOL, 140(1), 1999, pp. 71-78
Authors:
Kirby, DA
Wang, W
Gershengorn, MC
Rivier, JE
Citation: Da. Kirby et al., Analogs of thyrotropin-releasing hormone using an aminoglycine-based template, PEPTIDES, 19(10), 1998, pp. 1679-1683
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