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Results: 1 to 20 of 48

References for PMC Articles for PubMed (Select 19846789)

1.

SLC26A9 is a constitutively active, CFTR-regulated anion conductance in human bronchial epithelia.

Bertrand CA, Zhang R, Pilewski JM, Frizzell RA.

J Gen Physiol. 2009 Apr;133(4):421-38. doi: 10.1085/jgp.200810097. Epub 2009 Mar 16.

2.

Effect of cytosolic pH on epithelial Na+ channel in normal and cystic fibrosis sweat ducts.

Reddy MM, Wang XF, Quinton PM.

J Membr Biol. 2008 Sep-Oct;225(1-3):1-11. doi: 10.1007/s00232-008-9126-4. Epub 2008 Oct 21.

PMID:
18937003
3.

Cystic fibrosis: impaired bicarbonate secretion and mucoviscidosis.

Quinton PM.

Lancet. 2008 Aug 2;372(9636):415-7. doi: 10.1016/S0140-6736(08)61162-9. Review.

PMID:
18675692
4.

Consensus on the use and interpretation of cystic fibrosis mutation analysis in clinical practice.

Castellani C, Cuppens H, Macek M Jr, Cassiman JJ, Kerem E, Durie P, Tullis E, Assael BM, Bombieri C, Brown A, Casals T, Claustres M, Cutting GR, Dequeker E, Dodge J, Doull I, Farrell P, Ferec C, Girodon E, Johannesson M, Kerem B, Knowles M, Munck A, Pignatti PF, Radojkovic D, Rizzotti P, Schwarz M, Stuhrmann M, Tzetis M, Zielenski J, Elborn JS.

J Cyst Fibros. 2008 May;7(3):179-96. doi: 10.1016/j.jcf.2008.03.009. Review.

5.

Synergistic airway gland mucus secretion in response to vasoactive intestinal peptide and carbachol is lost in cystic fibrosis.

Choi JY, Joo NS, Krouse ME, Wu JV, Robbins RC, Ianowski JP, Hanrahan JW, Wine JJ.

J Clin Invest. 2007 Oct;117(10):3118-27.

6.

Cystic fibrosis: a disease of vulnerability to airway surface dehydration.

Boucher RC.

Trends Mol Med. 2007 Jun;13(6):231-40. Epub 2007 May 23.

PMID:
17524805
7.

Airway surface liquid volume regulates ENaC by altering the serine protease-protease inhibitor balance: a mechanism for sodium hyperabsorption in cystic fibrosis.

Myerburg MM, Butterworth MB, McKenna EE, Peters KW, Frizzell RA, Kleyman TR, Pilewski JM.

J Biol Chem. 2006 Sep 22;281(38):27942-9. Epub 2006 Jul 26.

8.

Regulation of normal and cystic fibrosis airway surface liquid volume by phasic shear stress.

Tarran R, Button B, Boucher RC.

Annu Rev Physiol. 2006;68:543-61. Review.

PMID:
16460283
9.

Rescue of DeltaF508-CFTR trafficking and gating in human cystic fibrosis airway primary cultures by small molecules.

Van Goor F, Straley KS, Cao D, González J, Hadida S, Hazlewood A, Joubran J, Knapp T, Makings LR, Miller M, Neuberger T, Olson E, Panchenko V, Rader J, Singh A, Stack JH, Tung R, Grootenhuis PD, Negulescu P.

Am J Physiol Lung Cell Mol Physiol. 2006 Jun;290(6):L1117-30. Epub 2006 Jan 27.

10.

Hyposecretion, not hyperabsorption, is the basic defect of cystic fibrosis airway glands.

Joo NS, Irokawa T, Robbins RC, Wine JJ.

J Biol Chem. 2006 Mar 17;281(11):7392-8. Epub 2006 Jan 12.

11.

Small-molecule correctors of defective DeltaF508-CFTR cellular processing identified by high-throughput screening.

Pedemonte N, Lukacs GL, Du K, Caci E, Zegarra-Moran O, Galietta LJ, Verkman AS.

J Clin Invest. 2005 Sep;115(9):2564-71. Epub 2005 Aug 25.

12.

Phenylglycine and sulfonamide correctors of defective delta F508 and G551D cystic fibrosis transmembrane conductance regulator chloride-channel gating.

Pedemonte N, Sonawane ND, Taddei A, Hu J, Zegarra-Moran O, Suen YF, Robins LI, Dicus CW, Willenbring D, Nantz MH, Kurth MJ, Galietta LJ, Verkman AS.

Mol Pharmacol. 2005 May;67(5):1797-807. Epub 2005 Feb 18.

13.

Binding site of activators of the cystic fibrosis transmembrane conductance regulator in the nucleotide binding domains.

Moran O, Galietta LJ, Zegarra-Moran O.

Cell Mol Life Sci. 2005 Feb;62(4):446-60.

PMID:
15719171
14.

Activation of VPAC1 receptors by VIP and PACAP-27 in human bronchial epithelial cells induces CFTR-dependent chloride secretion.

Dérand R, Montoni A, Bulteau-Pignoux L, Janet T, Moreau B, Muller JM, Becq F.

Br J Pharmacol. 2004 Feb;141(4):698-708. Epub 2004 Jan 26.

15.

Pathophysiology and management of pulmonary infections in cystic fibrosis.

Gibson RL, Burns JL, Ramsey BW.

Am J Respir Crit Care Med. 2003 Oct 15;168(8):918-51. Review.

PMID:
14555458
16.

All-digital image capture and whole-field analysis of ciliary beat frequency.

Sisson JH, Stoner JA, Ammons BA, Wyatt TA.

J Microsc. 2003 Aug;211(Pt 2):103-11.

PMID:
12887704
17.

Effect of genotype on phenotype and mortality in cystic fibrosis: a retrospective cohort study.

McKone EF, Emerson SS, Edwards KL, Aitken ML.

Lancet. 2003 May 17;361(9370):1671-6.

PMID:
12767731
18.

Effects of endothelin-1 on epithelial ion transport in human airways.

Blouquit S, Sari A, Lombet A, D'herbomez M, Naline E, Matran R, Chinet T.

Am J Respir Cell Mol Biol. 2003 Aug;29(2):245-51. Epub 2003 Mar 6.

PMID:
12626340
19.

ENaC-CFTR interactions: the role of electrical coupling of ion fluxes explored in an epithelial cell model.

Horisberger JD.

Pflugers Arch. 2003 Jan;445(4):522-8. Epub 2002 Dec 4.

PMID:
12548399
20.

Thiazolidinone CFTR inhibitor identified by high-throughput screening blocks cholera toxin-induced intestinal fluid secretion.

Ma T, Thiagarajah JR, Yang H, Sonawane ND, Folli C, Galietta LJ, Verkman AS.

J Clin Invest. 2002 Dec;110(11):1651-8.

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