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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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Bibliografische gegevens
Gepubliceerd in:Sci Rep
Hoofdauteurs: Xue, Ruiqi, Gu, Huan, Qiu, Yamei, Guo, Yong, Korteweg, Christine, Huang, Jin, Gu, Jiang
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Nature Publishing Group 2016
Onderwerpen:
Online toegang: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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