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Items: 1 to 20 of 21

1.
2.

Structure and function of the CFTR chloride channel.

Sheppard DN, Welsh MJ.

Physiol Rev. 1999 Jan;79(1 Suppl):S23-45. Review.

3.

Coupling of ATP hydrolysis with channel gating by purified, reconstituted CFTR.

Bear CE, Li C, Galley K, Wang Y, Garami E, Ramjeesingh M.

J Bioenerg Biomembr. 1997 Oct;29(5):465-73. Review.

PMID:
9511931
4.

Review. ATP hydrolysis-driven gating in cystic fibrosis transmembrane conductance regulator.

Muallem D, Vergani P.

Philos Trans R Soc Lond B Biol Sci. 2009 Jan 27;364(1514):247-55. doi: 10.1098/rstb.2008.0191. Review.

5.

ATP hydrolysis cycles and the gating of CFTR Cl- channels.

Gadsby DC, Dousmanis AG, Nairn AC.

Acta Physiol Scand Suppl. 1998 Aug;643:247-56. Review.

PMID:
9789567
6.

Role of CFTR's intrinsic adenylate kinase activity in gating of the Cl(-) channel.

Randak CO, Welsh MJ.

J Bioenerg Biomembr. 2007 Dec;39(5-6):473-9. Review.

PMID:
17965924
7.

Gating of the CFTR Cl- channel by ATP-driven nucleotide-binding domain dimerisation.

Hwang TC, Sheppard DN.

J Physiol. 2009 May 15;587(Pt 10):2151-61. doi: 10.1113/jphysiol.2009.171595. Epub 2009 Mar 30. Review.

8.

Control of CFTR channel gating by phosphorylation and nucleotide hydrolysis.

Gadsby DC, Nairn AC.

Physiol Rev. 1999 Jan;79(1 Suppl):S77-S107. Review.

9.

Emerging issues of connexin channels: biophysics fills the gap.

Harris AL.

Q Rev Biophys. 2001 Aug;34(3):325-472. Review. Erratum in: Q Rev Biophys 2002 Feb;35(1):109.

PMID:
11838236
10.

Electrodiffusional ATP movement through CFTR and other ABC transporters.

Cantiello HF.

Pflugers Arch. 2001;443 Suppl 1:S22-7. Epub 2001 Aug 11. Review.

PMID:
11845298
11.
12.

Molecular basis for the ATPase activity of CFTR.

Cheung JC, Kim Chiaw P, Pasyk S, Bear CE.

Arch Biochem Biophys. 2008 Aug 1;476(1):95-100. doi: 10.1016/j.abb.2008.03.033. Epub 2008 Apr 8. Review.

PMID:
18417076
13.

Cystic fibrosis: recent structural insights.

Dorwart M, Thibodeau P, Thomas P.

J Cyst Fibros. 2004 Aug;3 Suppl 2:91-4. Review.

14.

Strategies to investigate the mechanism of action of CFTR modulators.

Cai Z, Scott-Ward TS, Li H, Schmidt A, Sheppard DN.

J Cyst Fibros. 2004 Aug;3 Suppl 2:141-7. Review.

15.

Conformational changes opening and closing the CFTR chloride channel: insights from cysteine scanning mutagenesis.

El Hiani Y, Linsdell P.

Biochem Cell Biol. 2014 Dec;92(6):481-8. doi: 10.1139/bcb-2014-0038. Epub 2014 Sep 12. Review.

PMID:
25367045
17.

Nucleotide transport through the cystic fibrosis transmembrane conductance regulator.

Cantiello HF.

Biosci Rep. 1997 Apr;17(2):147-71. Review.

PMID:
9217964
18.

Sequence homologies between nucleotide binding regions of CFTR and G-proteins suggest structural and functional similarities.

Manavalan P, Dearborn DG, McPherson JM, Smith AE.

FEBS Lett. 1995 Jun 12;366(2-3):87-91. Review.

19.

ATP hydrolysis-coupled gating of CFTR chloride channels: structure and function.

Zou X, Hwang TC.

Biochemistry. 2001 May 15;40(19):5579-86. Review. No abstract available.

PMID:
11341822
20.

Functional architecture of the CFTR chloride channel.

Linsdell P.

Mol Membr Biol. 2014 Feb;31(1):1-16. doi: 10.3109/09687688.2013.868055. Epub 2013 Dec 17. Review.

PMID:
24341413

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