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Expression of Cystic Fibrosis Transmembrane Conductance Regulator in Ganglia of Human Gastrointestinal Tract

CF is caused by mutations of the gene encoding the cystic fibrosis transmembrane conductance regulator (CFTR) which is an anion selective transmembrane ion channel that mainly regulates chloride transport, expressed in the epithelia of various organs. Recently, we have demonstrated CFTR expression i...

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Detalhes bibliográficos
Publicado no:Sci Rep
Main Authors: Xue, Ruiqi, Gu, Huan, Qiu, Yamei, Guo, Yong, Korteweg, Christine, Huang, Jin, Gu, Jiang
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2016
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4974654/
https://ncbi.nlm.nih.gov/pubmed/27491544
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/srep30926
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