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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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Detalhes bibliográficos
Publicado no:Am J Physiol Gastrointest Liver Physiol
Main Authors: Balázs, Anita, Hegyi, Péter, Sahin-Tóth, Miklós
Formato: Artigo
Idioma:Inglês
Publicado em: American Physiological Society 2016
Assuntos:
Acesso em linha: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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