Improvement of Chloride Transport Defect by Gonadotropin-Releasing Hormone (GnRH) in Cystic Fibrosis Epithelial Cells

Cystic fibrosis (CF), the most common autosomal recessive disease in Caucasians, is due to mutations in the CFTR gene. F508del, the most frequent mutation in patients, impairs CFTR protein folding and biosynthesis. The F508del-CFTR protein is retained in the endoplasmic reticulum (ER) and its traffi...

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Detaylı Bibliyografya
Asıl Yazarlar: Benz, Nathalie, Le Hir, Sophie, Norez, Caroline, Kerbiriou, Mathieu, Calvez, Marie-Laure, Becq, Frédéric, Trouvé, Pascal, Férec, Claude
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Public Library of Science 2014
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3929654/
https://ncbi.nlm.nih.gov/pubmed/24586461
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0088964
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