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Results: 10

1.

Disease-causing mutations in the cystic fibrosis transmembrane conductance regulator determine the functional responses of alveolar macrophages.

Deriy LV, Gomez EA, Zhang G, Beacham DW, Hopson JA, Gallan AJ, Shevchenko PD, Bindokas VP, Nelson DJ.

J Biol Chem. 2009 Dec 18;284(51):35926-38. doi: 10.1074/jbc.M109.057372. Epub .

PMID:
19837664
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

CFTR chloride channel drug discovery--inhibitors as antidiarrheals and activators for therapy of cystic fibrosis.

Verkman AS, Lukacs GL, Galietta LJ.

Curr Pharm Des. 2006;12(18):2235-47. Review.

PMID:
16787252
[PubMed - indexed for MEDLINE]
3.

Cystic fibrosis transmembrane conductance regulator (CFTR) and renal function.

Stanton BA.

Wien Klin Wochenschr. 1997 Jun 27;109(12-13):457-64. Review.

PMID:
9261986
[PubMed - indexed for MEDLINE]
4.

Selective activation of cystic fibrosis transmembrane conductance regulator Cl- and HCO3- conductances.

Reddy MM, Quinton PM.

JOP. 2001 Jul;2(4 Suppl):212-8. Review.

PMID:
11875262
[PubMed - indexed for MEDLINE]
Free Article
5.

Targeting a genetic defect: cystic fibrosis transmembrane conductance regulator modulators in cystic fibrosis.

Derichs N.

Eur Respir Rev. 2013 Mar 1;22(127):58-65. doi: 10.1183/09059180.00008412. Review.

PMID:
23457166
[PubMed - indexed for MEDLINE]
Free Article
6.

Genotype and phenotype in cystic fibrosis.

Zielenski J.

Respiration. 2000;67(2):117-33. Review.

PMID:
10773783
[PubMed - indexed for MEDLINE]
Free Article
7.

Control of cystic fibrosis transmembrane conductance regulator membrane trafficking: not just from the endoplasmic reticulum to the Golgi.

Farinha CM, Matos P, Amaral MD.

FEBS J. 2013 Sep;280(18):4396-406. doi: 10.1111/febs.12392. Epub 2013 Jul 5. Review.

PMID:
23773658
[PubMed - indexed for MEDLINE]
8.

Understanding how cystic fibrosis mutations cause a loss of Cl- channel function.

Sheppard DN, Ostedgaard LS.

Mol Med Today. 1996 Jul;2(7):290-7. Review.

PMID:
8796909
[PubMed - indexed for MEDLINE]
9.

Defects in processing and trafficking of cystic fibrosis transmembrane conductance regulator.

Kunzelmann K, Nitschke R.

Exp Nephrol. 2000 Nov-Dec;8(6):332-42. Review.

PMID:
11014930
[PubMed - indexed for MEDLINE]
10.

CFTR: folding, misfolding and correcting the ΔF508 conformational defect.

Lukacs GL, Verkman AS.

Trends Mol Med. 2012 Feb;18(2):81-91. doi: 10.1016/j.molmed.2011.10.003. Epub 2011 Dec 3. Review.

PMID:
22138491
[PubMed - indexed for MEDLINE]
Free PMC Article

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