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Items: 1 to 20 of 739

2.

Protein kinase A regulates ATP hydrolysis and dimerization by a CFTR (cystic fibrosis transmembrane conductance regulator) domain.

Howell LD, Borchardt R, Kole J, Kaz AM, Randak C, Cohn JA.

Biochem J. 2004 Feb 15;378(Pt 1):151-9.

3.

Mechanism of G551D-CFTR (cystic fibrosis transmembrane conductance regulator) potentiation by a high affinity ATP analog.

Bompadre SG, Li M, Hwang TC.

J Biol Chem. 2008 Feb 29;283(9):5364-9. doi: 10.1074/jbc.M709417200.

4.

ATP-independent CFTR channel gating and allosteric modulation by phosphorylation.

Wang W, Wu J, Bernard K, Li G, Wang G, Bevensee MO, Kirk KL.

Proc Natl Acad Sci U S A. 2010 Feb 23;107(8):3888-93. doi: 10.1073/pnas.0913001107.

6.

Curcumin stimulates cystic fibrosis transmembrane conductance regulator Cl- channel activity.

Berger AL, Randak CO, Ostedgaard LS, Karp PH, Vermeer DW, Welsh MJ.

J Biol Chem. 2005 Feb 18;280(7):5221-6.

7.

Differential interactions of nucleotides at the two nucleotide binding domains of the cystic fibrosis transmembrane conductance regulator.

Aleksandrov L, Mengos A, Chang X, Aleksandrov A, Riordan JR.

J Biol Chem. 2001 Apr 20;276(16):12918-23.

8.

Dibasic protein kinase A sites regulate bursting rate and nucleotide sensitivity of the cystic fibrosis transmembrane conductance regulator chloride channel.

Mathews CJ, Tabcharani JA, Chang XB, Jensen TJ, Riordan JR, Hanrahan JW.

J Physiol. 1998 Apr 15;508 ( Pt 2):365-77.

9.

Nucleotide-binding domains of cystic fibrosis transmembrane conductance regulator, an ABC transporter, catalyze adenylate kinase activity but not ATP hydrolysis.

Gross CH, Abdul-Manan N, Fulghum J, Lippke J, Liu X, Prabhakar P, Brennan D, Willis MS, Faerman C, Connelly P, Raybuck S, Moore J.

J Biol Chem. 2006 Feb 17;281(7):4058-68.

10.

Domain-domain associations in cystic fibrosis transmembrane conductance regulator.

Wang W, He Z, O'Shaughnessy TJ, Rux J, Reenstra WW.

Am J Physiol Cell Physiol. 2002 May;282(5):C1170-80.

12.

Pyrophosphate stimulates wild-type and mutant cystic fibrosis transmembrane conductance regulator Cl- channels.

Carson MR, Winter MC, Travis SM, Welsh MJ.

J Biol Chem. 1995 Sep 1;270(35):20466-72.

13.

Regulation by ATP and ADP of CFTR chloride channels that contain mutant nucleotide-binding domains.

Anderson MP, Welsh MJ.

Science. 1992 Sep 18;257(5077):1701-4. Erratum in: Science 1992 Dec 11;258(5089):1719.

PMID:
1382316
15.

Nucleoside triphosphates are required to open the CFTR chloride channel.

Anderson MP, Berger HA, Rich DP, Gregory RJ, Smith AE, Welsh MJ.

Cell. 1991 Nov 15;67(4):775-84.

PMID:
1718606
16.
17.

Stimulation of CFTR activity by its phosphorylated R domain.

Winter MC, Welsh MJ.

Nature. 1997 Sep 18;389(6648):294-6.

PMID:
9305845
18.

The intact CFTR protein mediates ATPase rather than adenylate kinase activity.

Ramjeesingh M, Ugwu F, Stratford FL, Huan LJ, Li C, Bear CE.

Biochem J. 2008 Jun 1;412(2):315-21. doi: 10.1042/BJ20071719.

PMID:
18241200
19.
20.

Maturation and function of cystic fibrosis transmembrane conductance regulator variants bearing mutations in putative nucleotide-binding domains 1 and 2.

Gregory RJ, Rich DP, Cheng SH, Souza DW, Paul S, Manavalan P, Anderson MP, Welsh MJ, Smith AE.

Mol Cell Biol. 1991 Aug;11(8):3886-93.

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