Interaction between trypsinogen isoforms in genetically determined pancreatitis: Mutation E79K in cationic trypsin (PRSS1) causes increased transactivation of anionic trypsinogen (PRSS2)-Reference-Cited by-同舟云学术

Interaction between trypsinogen isoforms in genetically determined pancreatitis: Mutation E79K in cationic trypsin (PRSS1) causes increased transactivation of anionic trypsinogen (PRSS2)

Published:2004-01 Issue:1 Volume:23 Page:22-31
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Teich Niels,Le Maréchal Cédric,Kukor Zoltán,Caca Karel,Witzigmann Helmut,Chen Jian-Min,Tóth Miklós,Mössner Joachim,Keim Volker,Férec Claude,Sahin-Tóth Miklós

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference44 articles.

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4. Mutational analysis of the human pancreatic secretory trypsin inhibitor (PSTI) gene in hereditary and sporadic chronic pancreatitis;Chen;J Med Genet,2000

5. A CGC>CAT gene conversion-like event resulting in the R122H mutation in the cationic trypsinogen gene and its implication in the genotyping of pancreatitis;Chen;J Med Genet,2000

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