CFTR mutations altering CFTR fragmentation

Most CF (cystic fibrosis) results from deletion of a phenylalanine (F(508)) in the CFTR {CF transmembrane-conductance regulator; ABCC7 [ABC (ATP-binding cassette) sub-family C member 7]} which causes ER (endoplasmic reticulum) degradation of the mutant. Using stably CFTR-expressing BHK (baby-hamster...

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Detaylı Bibliyografya
Asıl Yazarlar: Tosoni, Kendra, Stobbart, Michelle, Cassidy, Diane M., Venerando, Andrea, Pagano, Mario A., Luz, Simão, Amaral, Margarida D., Kunzelmann, Karl, Pinna, Lorenzo A., Farinha, Carlos M., Mehta, Anil
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Portland Press Ltd. 2012
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3542821/
https://ncbi.nlm.nih.gov/pubmed/23067305
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BJ20121240
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