Targeted Proteomic Quantitation of the Absolute Expression and Turnover of Cystic Fibrosis Transmembrane Conductance Regulator in the Apical Plasma Membrane

[Image: see text] Deficient chloride transport through cystic fibrosis (CF) transmembrane conductance regulator (CFTR) causes lethal complications in CF patients. CF is the most common autosomal recessive genetic disease, which is caused by mutations in the CFTR gene; thus, CFTR mutants can serve as...

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Vydáno v:J Proteome Res
Hlavní autoři: McShane, Adam J., Bajrami, Bekim, Ramos, Alex A., Diego-Limpin, Pamela A., Farrokhi, Vahid, Coutermarsh, Bonita A., Stanton, Bruce A., Jensen, Tim, Riordan, John R., Wetmore, Diana, Joseloff, Elizabeth, Yao, Xudong
Médium: Artigo
Jazyk:Inglês
Vydáno: American Chemical Society 2014
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4227562/
https://ncbi.nlm.nih.gov/pubmed/25227318
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/pr5006795
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