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Mutation of EpCAM leads to intestinal barrier and ion transport dysfunction

ABSTRACT: Congenital tufting enteropathy (CTE) is a devastating diarrheal disease seen in infancy that is typically associated with villous changes and the appearance of epithelial tufts. We previously found mutations in epithelial cell adhesion molecule (EpCAM) to be causative in CTE. We developed...

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Detalhes bibliográficos
Publicado no:J Mol Med (Berl)
Main Authors: Kozan, Philip A., McGeough, Matthew D., Peña, Carla A., Mueller, James L., Barrett, Kim E., Marchelletta, Ronald R., Sivagnanam, Mamata
Formato: Artigo
Idioma:Inglês
Publicado em: Springer Berlin Heidelberg 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4408367/
https://ncbi.nlm.nih.gov/pubmed/25482158
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00109-014-1239-x
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