N. S. Sturm

Structure-activity studies of hydrophobic amino acid replacements at positions 9, 11 and 16 of glucagon.

V. Hruby, D. Trivedi, B. Y. Azizeh, 2009, The journal of peptide research : official journal of the American Peptide Society.

Structure-function studies on positions 17, 18, and 21 replacement analogues of glucagon: the importance of charged residues and salt bridges in glucagon biological activity.

S. Burley, V. Hruby, J. Krstenansky, 1998, Journal of medicinal chemistry.

[des His1, des Phe6, Glu9]glucagon amide: A newly designed “pure” glucagon antagonist

V. Hruby, B. V. Tine, D. Trivedi, 1995 .

Diesters of 2-(E-3-methyloxiranyl)hydroquinone from Pimpinella diversifolia

A. Bottini, C. Mathela, V. Dev, 1989 .

Oxiranylphenyl esters from pimpinella diversifolia

A. Bottini, C. Mathela, Angela Miller, 1985 .

Cyclopentanomonoterpene enol acetates from Nepeta leucophylla

A. Bottini, C. Mathela, A. Nerio, 1992 .

Asymmetric amino acid substitution at the Tyr10 position of glucagon leads to greater binding differences

V. Hruby, B. V. Tine, D. Trivedi, 1995 .