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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Detalles Bibliográficos
Autores principales: Xue, Ruiqi, Gu, Huan, Qiu, Yamei, Guo, Yong, Korteweg, Christine, Huang, Jin, Gu, Jiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4974654/
https://www.ncbi.nlm.nih.gov/pubmed/27491544
http://dx.doi.org/10.1038/srep30926

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4974654/
https://www.ncbi.nlm.nih.gov/pubmed/27491544
http://dx.doi.org/10.1038/srep30926

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