Expression of cystic fibrosis transmembrane conductan... [Nature. 1990] - PubMed

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Altered chloride ion channel kinetics associated with the delta F508 cystic fibrosis mutation. [Nature. 1991]
Altered chloride ion channel kinetics associated with the delta F508 cystic fibrosis mutation.
Dalemans W, Barbry P, Champigny G, Jallat S, Dott K, Dreyer D, Crystal RG, Pavirani A, Lecocq JP, Lazdunski M. Nature. 1991 Dec 19-26; 354(6354):526-8.
Two cystic fibrosis transmembrane conductance regulator mutations have different effects on both pulmonary phenotype and regulation of outwardly rectified chloride currents. [Proc Natl Acad Sci U S A. 1995]
Two cystic fibrosis transmembrane conductance regulator mutations have different effects on both pulmonary phenotype and regulation of outwardly rectified chloride currents.
Fulmer SB, Schwiebert EM, Morales MM, Guggino WB, Cutting GR. Proc Natl Acad Sci U S A. 1995 Jul 18; 92(15):6832-6.
A novel natural product compound enhances cAMP-regulated chloride conductance of cells expressing CFTR[delta]F508. [Mol Med. 2002]
A novel natural product compound enhances cAMP-regulated chloride conductance of cells expressing CFTR[delta]F508.
deCarvalho AC, Ndi CP, Tsopmo A, Tane P, Ayafor J, Connolly JD, Teem JL. Mol Med. 2002 Feb; 8(2):75-87.
Review Dysfunction of CFTR bearing the delta F508 mutation. [J Cell Sci Suppl. 1993]
Review Dysfunction of CFTR bearing the delta F508 mutation.
Welsh MJ, Denning GM, Ostedgaard LS, Anderson MP. J Cell Sci Suppl. 1993; 17:235-9.
Review Functions of the cystic fibrosis transmembrane conductance regulator protein. [Am J Respir Crit Care Med. 1995]
Review Functions of the cystic fibrosis transmembrane conductance regulator protein.
Frizzell RA. Am J Respir Crit Care Med. 1995 Mar; 151(3 Pt 2):S54-8.

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Cited by 74 PubMed Central articles

A CFTR potentiator in patients with cystic fibrosis and the G551D mutation. [N Engl J Med. 2011]
A CFTR potentiator in patients with cystic fibrosis and the G551D mutation.
Ramsey BW, Davies J, McElvaney NG, Tullis E, Bell SC, Dřevínek P, Griese M, McKone EF, Wainwright CE, Konstan MW, et al. N Engl J Med. 2011 Nov 3; 365(18):1663-72.
Cystic fibrosis transmembrane conductance regulator with a shortened R domain rescues the intestinal phenotype of CFTR-/- mice. [Proc Natl Acad Sci U S A. 2011]
Cystic fibrosis transmembrane conductance regulator with a shortened R domain rescues the intestinal phenotype of CFTR-/- mice.
Ostedgaard LS, Meyerholz DK, Vermeer DW, Karp PH, Schneider L, Sigmund CD, Welsh MJ. Proc Natl Acad Sci U S A. 2011 Feb 15; 108(7):2921-6. Epub 2011 Feb 1.
Uncoupling substrate transport from ATP hydrolysis in the Escherichia coli maltose transporter. [J Biol Chem. 2010]
Uncoupling substrate transport from ATP hydrolysis in the Escherichia coli maltose transporter.
Cui J, Qasim S, Davidson AL. J Biol Chem. 2010 Dec 17; 285(51):39986-93. Epub 2010 Oct 19.

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Expression of cystic fibrosis transmembrane conductance regulator corrects defec...
Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells.
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