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The Journal of Peptide Research : Official Journal of the American Peptide Society|October 19, 2001
Fast, efficient and selective deprotection of the tert-butoxycarbonyl (Boc) group using HCl/dioxane (4 m)G Han, M Tamaki, V J HrubyInternational Journal of Peptide and Protein Research|August 1, 1991
Synthetic glucagon antagonists and partial agonistsC Zechel, D Trivedi, V J HrubyThe American Journal of Physiology|November 1, 1990
mechanism of glucagon choleresis in guinea pigsR Lenzen, V J Hruby, N TavoloniJournal of Magnetic Resonance (San Diego, Calif. : 1997)|May 2, 1998
Gradient- and sensitivity-enhanced TOCSY experimentsK E Kövér, D Uhrín, V J HrubyThe Journal of Biological Chemistry|September 25, 1978
A reassessment of structure-function relationships in glucagon. Glucagon1-21 is a full agonistD E Wright, V J Hruby, M RodbellLife Sciences|September 26, 1983
Re-evaluation of glucagon1-6: the N-terminal hexapeptide of glucagon is not biologically active in the hepatic adenylate cyclase systemJ T Pelton, D Trivedi, V J HrubyCurrent Opinion in Chemical Biology|June 1, 1997
Synthesis of oligopeptide and peptidomimetic librariesV J Hruby, J M Ahn, S LiaoJournal of Medicinal Chemistry|May 1, 1992
Structure-activity studies of a novel bicyclic oxytocin antagonistD D Smith, J Slaninova, V J HrubyThe Journal of Biological Chemistry|December 25, 1980
Glucagon amino groups. Evaluation of modifications leading to antagonism and agonismM D Bregman, D Trivedi, V J HrubyOrganic Letters|February 7, 2001
(S)- or (R)-3-(E-enoyl)-4-phenyl-1,3-oxazolidin-2-ones: ideal Michael acceptors to afford a virtually complete control of simple and face diastereoselectivity in addition reactions with glycine derivativesV A Soloshonok, C Cai, V J HrubyPageof 65