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Items: 15

1.

Cse1l is a negative regulator of CFTR-dependent fluid secretion.

Bagnat M, Navis A, Herbstreith S, Brand-Arzamendi K, Curado S, Gabriel S, Mostov K, Huisken J, Stainier DY.

Curr Biol. 2010 Oct 26;20(20):1840-5. doi: 10.1016/j.cub.2010.09.012. Epub 2010 Oct 7. Erratum in: Curr Biol. 2010 Dec 7;20(23):2157.

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
3.

CFTR inhibitors.

Verkman AS, Synder D, Tradtrantip L, Thiagarajah JR, Anderson MO.

Curr Pharm Des. 2013;19(19):3529-41. Review.

4.

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
5.

CFTR pharmacology and its role in intestinal fluid secretion.

Thiagarajah JR, Verkman AS.

Curr Opin Pharmacol. 2003 Dec;3(6):594-9. Review.

PMID:
14644010
6.

Recent advances and new perspectives in targeting CFTR for therapy of cystic fibrosis and enterotoxin-induced secretory diarrheas.

Zhang W, Fujii N, Naren AP.

Future Med Chem. 2012 Mar;4(3):329-45. doi: 10.4155/fmc.12.1. Review.

7.

The cystic fibrosis transmembrane regulator (CFTR) in the kidney.

Morales MM, Falkenstein D, Lopes AG.

An Acad Bras Cienc. 2000 Sep;72(3):399-406. Review.

8.

Exploiting species differences to understand the CFTR Cl- channel.

Bose SJ, Scott-Ward TS, Cai Z, Sheppard DN.

Biochem Soc Trans. 2015 Oct;43(5):975-82. doi: 10.1042/BST20150129. Review.

PMID:
26517912
9.

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.

10.

CFTR chloride channel in the apical compartments: spatiotemporal coupling to its interacting partners.

Li C, Naren AP.

Integr Biol (Camb). 2010 Apr;2(4):161-77. doi: 10.1039/b924455g. Epub 2010 Mar 5. Review.

11.

Ca²⁺ signaling and fluid secretion by secretory cells of the airway epithelium.

Lee RJ, Foskett JK.

Cell Calcium. 2014 Jun;55(6):325-36. doi: 10.1016/j.ceca.2014.02.001. Epub 2014 Feb 11. Review.

PMID:
24703093
12.

Ivacaftor treatment of cystic fibrosis patients with the G551D mutation: a review of the evidence.

Kotha K, Clancy JP.

Ther Adv Respir Dis. 2013 Oct;7(5):288-96. doi: 10.1177/1753465813502115. Epub 2013 Sep 3. Review.

PMID:
24004658
13.

New paradigms of CFTR chloride channel regulation.

Kirk KL.

Cell Mol Life Sci. 2000 Apr;57(4):623-34. Review.

PMID:
11130462
14.

Cytoskeleton and CFTR.

Edelman A.

Int J Biochem Cell Biol. 2014 Jul;52:68-72. doi: 10.1016/j.biocel.2014.03.018. Epub 2014 Mar 28. Review.

PMID:
24685681
15.

Macromolecular complexes of cystic fibrosis transmembrane conductance regulator and its interacting partners.

Li C, Naren AP.

Pharmacol Ther. 2005 Nov;108(2):208-23. Epub 2005 Jun 2. Review.

PMID:
15936089

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