Associated Papers
Structural mechanisms of CFTR function and dysfunction.
Hwang TC et al.
The Journal of General Physiology, 2018
29581173 (PubMed )
Supplement: JGP_201711946_TableS1.pdf
Processing mutations disrupt interactions between the nucleotide binding and transmembrane domains of P-glycoprotein and the cystic fibrosis transmembrane conductance regulator (CFTR).
Loo TW et al.
The Journal of Biological Chemistry, 2008
Multiple membrane-cytoplasmic domain contacts in the cystic fibrosis transmembrane conductance regulator (CFTR) mediate regulation of channel gating.
He L et al.
The Journal of Biological Chemistry, 2008
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