Receptor occupancy and adenylate cyclase activation in rat liver and heart membranes by 10 glucagon analogs modified in position 2, 3, 4, 25, 27 and/or 29
- 1 May 1988
- journal article
- research article
- Published by Elsevier in Regulatory Peptides
- Vol. 21 (1-2) , 117-128
- https://doi.org/10.1016/0167-0115(88)90096-1
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- [d‐Phe4]Peptide histidine‐isoleucinamide ([d‐Phe4]PHI), a highly selective vasoactive‐intestinal‐peptide (VIP) agonist, discriminates VIP‐preferring from secretin‐preferring receptors in rat pancreatic membranesEuropean Journal of Biochemistry, 1987
- Comparative efficacy of seven synthetic glucagon analogs, modified in position 1, 2 and/or 12, on liver and heart adenylate cyclase from ratPeptides, 1986
- Superactive amidated COOH-terminal glucagon analogues with no methionine or tryptophanPeptides, 1986
- Design and synthesis of glucagon partial agonists and antagonistsBiochemistry, 1986
- Structure-activity studies on the N-terminal region of growth hormone releasing factorJournal of Medicinal Chemistry, 1985
- Structure activity studies on the N-terminal region of glucagonJournal of Medicinal Chemistry, 1984
- Conformation of glucagon in a lipid-water interphase by 1H nuclear magnetic resonanceJournal of Molecular Biology, 1983
- Glucagon: Structure-Function Relationships Investigated by Sequence DeletionsHoppe-Seyler´s Zeitschrift Für Physiologische Chemie, 1981
- SOLID‐PHASE SYNTHESIS OF PORCINE VASOACTIVE INTESTINAL PEPTIDEInternational Journal of Peptide and Protein Research, 1980
- Empirical Predictions of Protein ConformationAnnual Review of Biochemistry, 1978