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Pathogenic cellular role of the p.L104P human cationic trypsinogen variant in chronic pancreatitis

Mutations in the PRSS1 gene encoding human cationic trypsinogen are associated with hereditary and sporadic chronic pancreatitis. High-penetrance PRSS1 mutations found in hereditary pancreatitis alter activation and/or degradation of cationic trypsinogen, thereby promoting intrapancreatic trypsinoge...

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Détails bibliographiques
Publié dans:Am J Physiol Gastrointest Liver Physiol
Auteurs principaux: Balázs, Anita, Hegyi, Péter, Sahin-Tóth, Miklós
Format: Artigo
Langue:Inglês
Publié: American Physiological Society 2016
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC4824176/
https://ncbi.nlm.nih.gov/pubmed/26822915
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajpgi.00444.2015
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