Similar articles for PMID: 14993613

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1

Vitamin C controls the cystic fibrosis transmembrane conductance regulator chloride channel.

Fischer H, Schwarzer C, Illek B. Fischer H, et al. Proc Natl Acad Sci U S A. 2004 Mar 9;101(10):3691-6. doi: 10.1073/pnas.0308393100. Epub 2004 Mar 1. Proc Natl Acad Sci U S A. 2004. PMID: 14993613 Free PMC article.

2

Resveratrol ameliorates abnormalities of fluid and electrolyte secretion in a hypoxia-Induced model of acquired CFTR deficiency.

Woodworth BA. Woodworth BA. Laryngoscope. 2015 Oct;125 Suppl 7(0 7):S1-S13. doi: 10.1002/lary.25335. Epub 2015 May 6. Laryngoscope. 2015. PMID: 25946147 Free PMC article.

3

Cystic fibrosis transmembrane conductance regulator-mRNA delivery: a novel alternative for cystic fibrosis gene therapy.

Bangel-Ruland N, Tomczak K, Fernández Fernández E, Leier G, Leciejewski B, Rudolph C, Rosenecker J, Weber WM. Bangel-Ruland N, et al. J Gene Med. 2013 Nov-Dec;15(11-12):414-26. doi: 10.1002/jgm.2748. J Gene Med. 2013. PMID: 24123772

4

Hypercapnia modulates cAMP signalling and cystic fibrosis transmembrane conductance regulator-dependent anion and fluid secretion in airway epithelia.

Turner MJ, Saint-Criq V, Patel W, Ibrahim SH, Verdon B, Ward C, Garnett JP, Tarran R, Cann MJ, Gray MA. Turner MJ, et al. J Physiol. 2016 Mar 15;594(6):1643-61. doi: 10.1113/JP271309. Epub 2015 Dec 20. J Physiol. 2016. PMID: 26574187 Free PMC article.

5

Induction of a cAMP-stimulated chloride secretion in regenerating poorly differentiated airway epithelial cells by adenovirus-mediated CFTR gene transfer.

Dupuit F, Chinet T, Zahm JM, Pierrot D, Hinnrasky J, Kaplan H, Bonnet N, Puchelle E. Dupuit F, et al. Hum Gene Ther. 1997 Aug 10;8(12):1439-50. doi: 10.1089/hum.1997.8.12-1439. Hum Gene Ther. 1997. PMID: 9287144

6

Liquid movement across the surface epithelium of large airways.

Chambers LA, Rollins BM, Tarran R. Chambers LA, et al. Respir Physiol Neurobiol. 2007 Dec 15;159(3):256-70. doi: 10.1016/j.resp.2007.06.005. Epub 2007 Jun 17. Respir Physiol Neurobiol. 2007. PMID: 17692578 Free PMC article. Review.

7

Turnover of the cystic fibrosis transmembrane conductance regulator (CFTR): slow degradation of wild-type and delta F508 CFTR in surface membrane preparations of immortalized airway epithelial cells.

Wei X, Eisman R, Xu J, Harsch AD, Mulberg AE, Bevins CL, Glick MC, Scanlin TF. Wei X, et al. J Cell Physiol. 1996 Aug;168(2):373-84. doi: 10.1002/(SICI)1097-4652(199608)168:2<373::AID-JCP16>3.0.CO;2-4. J Cell Physiol. 1996. PMID: 8707873

8

Epithelial sodium channel silencing as a strategy to correct the airway surface fluid deficit in cystic fibrosis.

Gianotti A, Melani R, Caci E, Sondo E, Ravazzolo R, Galietta LJ, Zegarra-Moran O. Gianotti A, et al. Am J Respir Cell Mol Biol. 2013 Sep;49(3):445-52. doi: 10.1165/rcmb.2012-0408OC. Am J Respir Cell Mol Biol. 2013. PMID: 23600628

9

Pendrin Mediates Bicarbonate Secretion and Enhances Cystic Fibrosis Transmembrane Conductance Regulator Function in Airway Surface Epithelia.

Kim D, Huang J, Billet A, Abu-Arish A, Goepp J, Matthes E, Tewfik MA, Frenkiel S, Hanrahan JW. Kim D, et al. Am J Respir Cell Mol Biol. 2019 Jun;60(6):705-716. doi: 10.1165/rcmb.2018-0158OC. Am J Respir Cell Mol Biol. 2019. PMID: 30742493

10

Relationship of a non-cystic fibrosis transmembrane conductance regulator-mediated chloride conductance to organ-level disease in Cftr(-/-) mice.

Clarke LL, Grubb BR, Yankaskas JR, Cotton CU, McKenzie A, Boucher RC. Clarke LL, et al. Proc Natl Acad Sci U S A. 1994 Jan 18;91(2):479-83. doi: 10.1073/pnas.91.2.479. Proc Natl Acad Sci U S A. 1994. PMID: 7507247 Free PMC article.

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