Interaction of vasoactive intestinal peptide (VIP) and N-terminally modified VIP analogs with rat pancreatic, hepatic and pituitary membranes
Author:
Publisher
Wiley
Subject
Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1432-1033.1986.tb09831.x/fullpdf
Reference22 articles.
1. Structural requirements for VIP interaction with specific receptors in human and rat intestinal membranes: Effect of nine partial sequences
2. Effects of HIS1 modifications on the ability of vasoactive intestinal peptide to stimulate adenylate cyclase from rat and human tissues
3. Super-active analogs of growth hormone-releasing factor (1–29)-amide
4. Structure-activity studies on the N-terminal region of growth hormone releasing factor
5. An Extremely Sensitivein VitroModel for Elucidating Structure-Activity Relationships of Growth Hormone-Releasing Factor Analogs*
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1. Peptide and Protein Drugs: Issues and Solutions;Comprehensive Medicinal Chemistry II;2007
2. New Nonradioactive Technique for Vasoactive Intestinal Peptide-Receptor-Ligand-Binding Studies;Annals of the New York Academy of Sciences;2006-07-01
3. Peptide and Protein Hormones;Ullmann's Encyclopedia of Industrial Chemistry;2000-06-15
4. Suppression of I-125-vasoactive intestinal polypeptide binding sites in arteries of the hamster seminal vesicle following castration;Histochemical Journal;1999
5. Interaction of lipophilic VIP derivatives with recombinant VIP1/PACAP and VIP2/PACAP receptors;European Journal of Pharmacology;1998-07
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