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Items: 1 to 20 of 148

1.

Aberrant CFTR-dependent HCO3- transport in mutations associated with cystic fibrosis.

Choi JY, Muallem D, Kiselyov K, Lee MG, Thomas PJ, Muallem S.

Nature. 2001 Mar 1;410(6824):94-7.

2.

Regulation of Cl-/ HCO3- exchange by cystic fibrosis transmembrane conductance regulator expressed in NIH 3T3 and HEK 293 cells.

Lee MG, Wigley WC, Zeng W, Noel LE, Marino CR, Thomas PJ, Muallem S.

J Biol Chem. 1999 Feb 5;274(6):3414-21.

3.
4.

CFTR expression but not Cl- transport is involved in the stimulatory effect of bile acids on apical Cl-/HCO3- exchange activity in human pancreatic duct cells.

Ignáth I, Hegyi P, Venglovecz V, Székely CA, Carr G, Hasegawa M, Inoue M, Takács T, Argent BE, Gray MA, Rakonczay Z Jr.

Pancreas. 2009 Nov;38(8):921-9. doi: 10.1097/MPA.0b013e3181b65d34.

PMID:
19752774
5.

Polarized distribution of HCO3- transport in human normal and cystic fibrosis nasal epithelia.

Paradiso AM, Coakley RD, Boucher RC.

J Physiol. 2003 Apr 1;548(Pt 1):203-18. Epub 2003 Jan 31.

6.

Bicarbonate conductance and pH regulatory capability of cystic fibrosis transmembrane conductance regulator.

Poulsen JH, Fischer H, Illek B, Machen TE.

Proc Natl Acad Sci U S A. 1994 Jun 7;91(12):5340-4.

7.

Dynamic regulation of CFTR bicarbonate permeability by [Cl-]i and its role in pancreatic bicarbonate secretion.

Park HW, Nam JH, Kim JY, Namkung W, Yoon JS, Lee JS, Kim KS, Venglovecz V, Gray MA, Kim KH, Lee MG.

Gastroenterology. 2010 Aug;139(2):620-31. doi: 10.1053/j.gastro.2010.04.004. Epub 2010 Apr 14.

PMID:
20398666
8.

Correction of CFTR malfunction and stimulation of Ca-activated Cl channels restore HCO3- secretion in cystic fibrosis bile ductular cells.

Zsembery A, Jessner W, Sitter G, Spirlí C, Strazzabosco M, Graf J.

Hepatology. 2002 Jan;35(1):95-104.

PMID:
11786964
9.

Regulatory interaction between the cystic fibrosis transmembrane conductance regulator and HCO3- salvage mechanisms in model systems and the mouse pancreatic duct.

Ahn W, Kim KH, Lee JA, Kim JY, Choi JY, Moe OW, Milgram SL, Muallem S, Lee MG.

J Biol Chem. 2001 May 18;276(20):17236-43. Epub 2001 Feb 22.

10.

Cystic fibrosis transmembrane conductance regulator regulates luminal Cl-/HCO3- exchange in mouse submandibular and pancreatic ducts.

Lee MG, Choi JY, Luo X, Strickland E, Thomas PJ, Muallem S.

J Biol Chem. 1999 May 21;274(21):14670-7.

11.

A molecular mechanism for aberrant CFTR-dependent HCO(3)(-) transport in cystic fibrosis.

Ko SB, Shcheynikov N, Choi JY, Luo X, Ishibashi K, Thomas PJ, Kim JY, Kim KH, Lee MG, Naruse S, Muallem S.

EMBO J. 2002 Nov 1;21(21):5662-72.

12.

Ca2+-activated Cl- channels can substitute for CFTR in stimulation of pancreatic duct bicarbonate secretion.

Zsembery A, Strazzabosco M, Graf J.

FASEB J. 2000 Nov;14(14):2345-56.

PMID:
11053257
13.

Functional interactions of HCO3- with cystic fibrosis transmembrane conductance regulator.

Gray MA, O'Reilly C, Winpenny J, Argent B.

JOP. 2001 Jul;2(4 Suppl):207-11. Review.

14.

Direct sensing of intracellular pH by the cystic fibrosis transmembrane conductance regulator (CFTR) Cl- channel.

Chen JH, Cai Z, Sheppard DN.

J Biol Chem. 2009 Dec 18;284(51):35495-506. doi: 10.1074/jbc.M109.072678.

15.

CFTR gene transfer to human cystic fibrosis pancreatic duct cells using a Sendai virus vector.

Rakonczay Z Jr, Hegyi P, Hasegawa M, Inoue M, You J, Iida A, Ignáth I, Alton EW, Griesenbach U, Ovári G, Vág J, Da Paula AC, Crawford RM, Varga G, Amaral MD, Mehta A, Lonovics J, Argent BE, Gray MA.

J Cell Physiol. 2008 Feb;214(2):442-55.

PMID:
17654517
16.

cAMP and genistein stimulate HCO3- conductance through CFTR in human airway epithelia.

Illek B, Yankaskas JR, Machen TE.

Am J Physiol. 1997 Apr;272(4 Pt 1):L752-61.

PMID:
9142951
17.

Relationships among CFTR expression, HCO3- secretion, and host defense may inform gene- and cell-based cystic fibrosis therapies.

Shah VS, Ernst S, Tang XX, Karp PH, Parker CP, Ostedgaard LS, Welsh MJ.

Proc Natl Acad Sci U S A. 2016 May 10;113(19):5382-7. doi: 10.1073/pnas.1604905113. Epub 2016 Apr 25.

18.

Targeting of carbonic anhydrase IV to plasma membranes is altered in cultured human pancreatic duct cells expressing a mutated (deltaF508) CFTR.

Fanjul M, Salvador C, Alvarez L, Cantet S, Hollande E.

Eur J Cell Biol. 2002 Aug;81(8):437-47.

PMID:
12234015
19.

Ca2+ activates cystic fibrosis transmembrane conductance regulator- and Cl- -dependent HCO3 transport in pancreatic duct cells.

Namkung W, Lee JA, Ahn W, Han W, Kwon SW, Ahn DS, Kim KH, Lee MG.

J Biol Chem. 2003 Jan 3;278(1):200-7. Epub 2002 Oct 29.

20.

Physiology and pathophysiology of bicarbonate secretion by pancreatic duct epithelium.

Ishiguro H, Yamamoto A, Nakakuki M, Yi L, Ishiguro M, Yamaguchi M, Kondo S, Mochimaru Y.

Nagoya J Med Sci. 2012 Feb;74(1-2):1-18. Review.

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