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
Cytoplasmic pathway followed by chloride ions to enter the CFTR channel pore.
El Hiani Y et al.
Cellular and Molecular Life Sciences : Cmls, 2016
Suppressor mutations in the transmembrane segments of P-glycoprotein promote maturation of processing mutants and disrupt a subset of drug-binding sites.
Loo TW et al.
The Journal of Biological Chemistry, 2007
Channel-lining residues in the M3 membrane-spanning segment of the cystic fibrosis transmembrane conductance regulator.
Akabas MH
Biochemistry, 1998
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