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Results: 1 to 20 of 117

Related Citations for PubMed (Select 9380758)

1.

Protein phosphatase 2C dephosphorylates and inactivates cystic fibrosis transmembrane conductance regulator.

Travis SM, Berger HA, Welsh MJ.

Proc Natl Acad Sci U S A. 1997 Sep 30;94(20):11055-60.

3.

Differential regulation of single CFTR channels by PP2C, PP2A, and other phosphatases.

Luo J, Pato MD, Riordan JR, Hanrahan JW.

Am J Physiol. 1998 May;274(5 Pt 1):C1397-410.

4.

Association of cystic fibrosis transmembrane conductance regulator and protein phosphatase 2C.

Zhu T, Dahan D, Evagelidis A, Zheng S, Luo J, Hanrahan JW.

J Biol Chem. 1999 Oct 8;274(41):29102-7.

5.

Regulation of recombinant cardiac cystic fibrosis transmembrane conductance regulator chloride channels by protein kinase C.

Yamazaki J, Britton F, Collier ML, Horowitz B, Hume JR.

Biophys J. 1999 Apr;76(4):1972-87.

6.

The cystic fibrosis transmembrane conductance regulator is regulated by a direct interaction with the protein phosphatase 2A.

Thelin WR, Kesimer M, Tarran R, Kreda SM, Grubb BR, Sheehan JK, Stutts MJ, Milgram SL.

J Biol Chem. 2005 Dec 16;280(50):41512-20. Epub 2005 Oct 20.

7.

Regulation of the CFTR channel by phosphorylation.

Dahan D, Evagelidis A, Hanrahan JW, Hinkson DA, Jia Y, Luo J, Zhu T.

Pflugers Arch. 2001;443 Suppl 1:S92-6. Epub 2001 Jul 13. Review.

PMID:
11845311
8.

Expression of cystic fibrosis transmembrane conductance regulator in a model epithelium.

Sheppard DN, Carson MR, Ostedgaard LS, Denning GM, Welsh MJ.

Am J Physiol. 1994 Apr;266(4 Pt 1):L405-13.

PMID:
7513963
9.

Role of protein phosphatases in the activation of CFTR (ABCC7) by genistein and bromotetramisole.

Luo J, Zhu T, Evagelidis A, Pato MD, Hanrahan JW.

Am J Physiol Cell Physiol. 2000 Jul;279(1):C108-19.

10.

Isotype-specific activation of cystic fibrosis transmembrane conductance regulator-chloride channels by cGMP-dependent protein kinase II.

French PJ, Bijman J, Edixhoven M, Vaandrager AB, Scholte BJ, Lohmann SM, Nairn AC, de Jonge HR.

J Biol Chem. 1995 Nov 3;270(44):26626-31.

11.

Interaction of the protein phosphatase 2A with the regulatory domain of the cystic fibrosis transmembrane conductance regulator channel.

Vastiau A, Cao L, Jaspers M, Owsianik G, Janssens V, Cuppens H, Goris J, Nilius B, Cassiman JJ.

FEBS Lett. 2005 Jun 20;579(16):3392-6.

12.
13.

The role of the C terminus and Na+/H+ exchanger regulatory factor in the functional expression of cystic fibrosis transmembrane conductance regulator in nonpolarized cells and epithelia.

Benharouga M, Sharma M, So J, Haardt M, Drzymala L, Popov M, Schwapach B, Grinstein S, Du K, Lukacs GL.

J Biol Chem. 2003 Jun 13;278(24):22079-89. Epub 2003 Mar 21.

14.

Basolateral chloride current in human airway epithelia.

Itani OA, Lamb FS, Melvin JE, Welsh MJ.

Am J Physiol Lung Cell Mol Physiol. 2007 Oct;293(4):L991-9. Epub 2007 Jul 27.

15.

CFTR with a partially deleted R domain corrects the cystic fibrosis chloride transport defect in human airway epithelia in vitro and in mouse nasal mucosa in vivo.

Ostedgaard LS, Zabner J, Vermeer DW, Rokhlina T, Karp PH, Stecenko AA, Randak C, Welsh MJ.

Proc Natl Acad Sci U S A. 2002 Mar 5;99(5):3093-8. Epub 2002 Feb 19.

16.

Development of substituted Benzo[c]quinolizinium compounds as novel activators of the cystic fibrosis chloride channel.

Becq F, Mettey Y, Gray MA, Galietta LJ, Dormer RL, Merten M, Métayé T, Chappe V, Marvingt-Mounir C, Zegarra-Moran O, Tarran R, Bulteau L, Dérand R, Pereira MM, McPherson MA, Rogier C, Joffre M, Argent BE, Sarrouilhe D, Kammouni W, Figarella C, Verrier B, Gola M, Vierfond JM.

J Biol Chem. 1999 Sep 24;274(39):27415-25.

17.

Potentiation of cystic fibrosis transmembrane conductance regulator (CFTR) Cl- currents by the chemical solvent tetrahydrofuran.

Hughes LK, Ju M, Sheppard DN.

Mol Membr Biol. 2008 Sep;25(6-7):528-38. doi: 10.1080/09687680802487967.

PMID:
18989824
18.

Contribution of R domain phosphoserines to the function of CFTR studied in Fischer rat thyroid epithelia.

Baldursson O, Berger HA, Welsh MJ.

Am J Physiol Lung Cell Mol Physiol. 2000 Nov;279(5):L835-41.

19.

Lack of correlation between CFTR expression, CFTR Cl- currents, amiloride-sensitive Na+ conductance, and cystic fibrosis phenotype.

Beck S, Kühr J, Schütz VV, Seydewitz HH, Brandis M, Greger R, Kunzelmann K.

Pediatr Pulmonol. 1999 Apr;27(4):251-9.

PMID:
10230924
20.

Phosphatase inhibitors activate normal and defective CFTR chloride channels.

Becq F, Jensen TJ, Chang XB, Savoia A, Rommens JM, Tsui LC, Buchwald M, Riordan JR, Hanrahan JW.

Proc Natl Acad Sci U S A. 1994 Sep 13;91(19):9160-4.

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