Decoding F508del Misfolding in Cystic Fibrosis
Author:
Publisher
MDPI AG
Subject
Molecular Biology,Biochemistry
Link
http://www.mdpi.com/2218-273X/4/2/498/pdf
Reference53 articles.
1. Identification of the cystic fibrosis gene: Cloning and characterization of complementary DNA;Riordan;Science,1989
2. Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis;Cheng;Cell,1990
3. Multiple proteolytic systems, including the proteasome, contribute to CFTR processing
4. Degradation of CFTR by the ubiquitin-proteasome pathway
5. Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive;Denning;Nature,1992
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