Hereditary Pancreatitis Caused by a Novel PRSS1 Mutation (Arg-122 → Cys) That Alters Autoactivation and Autodegradation of Cationic Trypsinogen
Open Access
- 1 February 2002
- journal article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 277 (7), 5404-5410
- https://doi.org/10.1074/jbc.m108073200
Abstract
No abstract availableKeywords
This publication has 32 references indexed in Scilit:
- Effect of Hyperthermia on Premature Intracellular Trypsinogen Activation in the Exocrine PancreasBiochemical and Biophysical Research Communications, 2001
- A new polymorphism for the RI22H mutation in hereditary pancreatitisGut, 2001
- Comparative in Vitro Studies on Native and Recombinant Human Cationic TrypsinsJournal of Biological Chemistry, 2001
- Gain-of-Function Mutations Associated with Hereditary Pancreatitis Enhance Autoactivation of Human Cationic TrypsinogenBiochemical and Biophysical Research Communications, 2000
- Human Cationic TrypsinogenPublished by Elsevier ,2000
- Two Mutations in Rat Trypsin Confer Resistance against AutolysisBiochemical and Biophysical Research Communications, 1998
- SWISS‐MODEL and the Swiss‐Pdb Viewer: An environment for comparative protein modelingElectrophoresis, 1997
- Crystal Structure of Human Trypsin 1: Unexpected Phosphorylation of Tyr151Journal of Molecular Biology, 1996
- Alteration of the specificity of ecotin, an E. coli serine proteinase inhibitor, by site directed mutagenesisFEBS Letters, 1994
- Activation of pancreatic zymogensDigestive Diseases and Sciences, 1986