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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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Bibliografiska uppgifter
I publikationen:Am J Physiol Gastrointest Liver Physiol
Huvudupphovsmän: Balázs, Anita, Hegyi, Péter, Sahin-Tóth, Miklós
Materialtyp: Artigo
Språk:Inglês
Publicerad: American Physiological Society 2016
Ämnen:
Länkar: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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