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Items: 1 to 20 of 1214

1.

Extracellular zinc and ATP restore chloride secretion across cystic fibrosis airway epithelia by triggering calcium entry.

Zsembery A, Fortenberry JA, Liang L, Bebok Z, Tucker TA, Boyce AT, Braunstein GM, Welty E, Bell PD, Sorscher EJ, Clancy JP, Schwiebert EM.

J Biol Chem. 2004 Mar 12;279(11):10720-9. Epub 2003 Dec 29.

2.

RNA interference targeted to multiple P2X receptor subtypes attenuates zinc-induced calcium entry.

Liang L, Zsembery A, Schwiebert EM.

Am J Physiol Cell Physiol. 2005 Aug;289(2):C388-96. Epub 2005 Mar 30.

3.

Role of Ca2+ -activated ion transport in the treatment of cystic fibrosis.

Zsembery A, Hargitai D.

Wien Med Wochenschr. 2008;158(19-20):562-4. doi: 10.1007/s10354-008-0596-x.

PMID:
18998073
5.

Purinergic signaling underlies CFTR control of human airway epithelial cell volume.

Braunstein GM, Zsembery A, Tucker TA, Schwiebert EM.

J Cyst Fibros. 2004 Jun;3(2):99-117.

6.

Sustained calcium entry through P2X nucleotide receptor channels in human airway epithelial cells.

Zsembery A, Boyce AT, Liang L, Peti-Peterdi J, Bell PD, Schwiebert EM.

J Biol Chem. 2003 Apr 11;278(15):13398-408. Epub 2003 Feb 3.

7.

Apical and basolateral ATP stimulates tracheal epithelial chloride secretion via multiple purinergic receptors.

Hwang TH, Schwiebert EM, Guggino WB.

Am J Physiol. 1996 Jun;270(6 Pt 1):C1611-23.

PMID:
8764143
9.
10.
11.

CFTR regulation of intracellular calcium in normal and cystic fibrosis human airway epithelia.

Walsh DE, Harvey BJ, Urbach V.

J Membr Biol. 2000 Oct 1;177(3):209-19.

PMID:
11014859
13.

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.

Proc Natl Acad Sci U S A. 1994 Jan 18;91(2):479-83.

14.

Swelling-activated Ca2+ entry via TRPV4 channel is defective in cystic fibrosis airway epithelia.

Arniges M, Vázquez E, Fernández-Fernández JM, Valverde MA.

J Biol Chem. 2004 Dec 24;279(52):54062-8. Epub 2004 Oct 15.

15.

Calcium entry is regulated by Zn2+ in relation to extracellular ionic environment in human airway epithelial cells.

Hargitai D, Pataki A, Raffai G, Füzi M, Dankó T, Csernoch L, Várnai P, Szigeti GP, Zsembery A.

Respir Physiol Neurobiol. 2010 Jan 31;170(1):67-75. doi: 10.1016/j.resp.2009.12.001. Epub 2009 Dec 6.

PMID:
19995619
16.

Cystic fibrosis airway epithelial Ca2+ i signaling: the mechanism for the larger agonist-mediated Ca2+ i signals in human cystic fibrosis airway epithelia.

Ribeiro CM, Paradiso AM, Carew MA, Shears SB, Boucher RC.

J Biol Chem. 2005 Mar 18;280(11):10202-9. Epub 2005 Jan 12.

17.

Regulation of electrogenic anion secretion in normal and cystic fibrosis gallbladder mucosa.

Chinet T, Fouassier L, Dray-Charier N, Imam-Ghali M, Morel H, Mergey M, Dousset B, Parc R, Paul A, Housset C.

Hepatology. 1999 Jan;29(1):5-13.

PMID:
9862842
18.

Expression of delta F508 cystic fibrosis transmembrane conductance regulator protein and related chloride transport properties in the gallbladder epithelium from cystic fibrosis patients.

Dray-Charier N, Paul A, Scoazec JY, Veissière D, Mergey M, Capeau J, Soubrane O, Housset C.

Hepatology. 1999 Jun;29(6):1624-34.

PMID:
10347100
19.

Residual chloride secretion in intestinal tissue of deltaF508 homozygous twins and siblings with cystic fibrosis. The European CF Twin and Sibling Study Consortium.

Bronsveld I, Mekus F, Bijman J, Ballmann M, Greipel J, Hundrieser J, Halley DJ, Laabs U, Busche R, De Jonge HR, Tümmler B, Veeze HJ.

Gastroenterology. 2000 Jul;119(1):32-40.

PMID:
10889152
20.

Expression of nucleotide-regulated Cl(-) currents in CF and normal mouse tracheal epithelial cell lines.

Thomas EJ, Gabriel SE, Makhlina M, Hardy SP, Lethem MI.

Am J Physiol Cell Physiol. 2000 Nov;279(5):C1578-86.

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