GRASPing CFTR
نویسندگان
چکیده
منابع مشابه
CFTR mutations altering CFTR fragmentation
Most CF (cystic fibrosis) results from deletion of a phenylalanine (F508) 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 kidney) cell lines we demonstrated that wild-type CTFR and the F508delCFTR mutant are cleaved into...
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ژورنال
عنوان ژورنال: Nature Chemical Biology
سال: 2011
ISSN: 1552-4450,1552-4469
DOI: 10.1038/nchembio.703