Cystic fibrosis transmembrane conductance regulator degradation: cross-talk between the ubiquitylation and SUMOylation pathways
Author:
Affiliation:
1. Department of Cell Biology; University of Pittsburgh School of Medicine; PA USA
Publisher
Wiley
Subject
Cell Biology,Molecular Biology,Biochemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/febs.12415/fullpdf
Reference71 articles.
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2. The relationship between genotype and phenotype in cystic fibrosis;Kerem;Curr Opin Pulm Med,1995
3. Identification of the cystic fibrosis gene: cloning and characterization of complementary DNA;Riordan;Science,1989
4. Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis;Cheng;Cell,1990
5. Multiple proteolytic systems, including the proteasome, contribute to CFTR processing;Jensen;Cell,1995
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