Associated Papers
Molecular Basis for Fe(III)-Independent Curcumin Potentiation of Cystic Fibrosis Transmembrane Conductance Regulator Activity.
Wang G
Biochemistry, 2015
Role of tyrosine phosphorylation in the muscarinic activation of the cystic fibrosis transmembrane conductance regulator (CFTR).
Billet A et al.
The Journal of Biological Chemistry, 2013
AMP-activated protein kinase phosphorylation of the R domain inhibits PKA stimulation of CFTR.
King JD et al.
American Journal of Physiology. Cell Physiology, 2009
Role of individual R domain phosphorylation sites in CFTR regulation by protein kinase A.
Hegedus T et al.
Biochimica Et Biophysica Acta, 2009
Cystic fibrosis transmembrane conductance regulator: a chloride channel gated by ATP binding and hydrolysis.
Bompadre SG et al.
Sheng Li Xue Bao : [acta Physiologica Sinica], 2007
Capsaicin potentiates wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride-channel currents.
Ai T et al.
Molecular Pharmacology, 2004
Protein kinase A regulates ATP hydrolysis and dimerization by a CFTR (cystic fibrosis transmembrane conductance regulator) domain.
Howell LD et al.
The Biochemical Journal, 2004
Cystic fibrosis transmembrane conductance regulator Cl- channels with R domain deletions and translocations show phosphorylation-dependent and -independent activity.
Baldursson O et al.
The Journal of Biological Chemistry, 2001
CFTR activation: additive effects of stimulatory and inhibitory phosphorylation sites in the R domain.
Wilkinson DJ et al.
The American Journal of Physiology, 1997
Regulation of the cystic fibrosis transmembrane conductance regulator Cl- channel by negative charge in the R domain.
Berger HA et al.
The Japanese Journal of Physiology, 1994
Regulation of the cystic fibrosis transmembrane conductance regulator Cl- channel by negative charge in the R domain.
Rich DP et al.
The Journal of Biological Chemistry, 1993
Protein kinase A (PKA) still activates CFTR chloride channel after mutagenesis of all 10 PKA consensus phosphorylation sites.
Chang XB et al.
The Journal of Biological Chemistry, 1993
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