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Items: 1 to 20 of 94

1.

The CLC chloride channel family.

Jentsch TJ, Friedrich T, Schriever A, Yamada H.

Pflugers Arch. 1999 May;437(6):783-95. Review.

PMID:
10370055
2.

From tonus to tonicity: physiology of CLC chloride channels.

Waldegger S, Jentsch TJ.

J Am Soc Nephrol. 2000 Jul;11(7):1331-9. Review.

3.

[Function of the CLC chloride channels and their implication in human pathology].

Vandewalle A.

Nephrologie. 2002;23(3):113-8. Review. French.

PMID:
12087807
4.

[Role and function of voltage-gated chloride channels of the CIC family and their defects leading to genetic diseases].

Dołowy K, Bednarczyk P, Hordejuk R, Dworakowska B, Nurowska E, Jarzabek W.

Postepy Hig Med Dosw. 2002;56(3):307-13. Review. Polish.

PMID:
12194243
5.

Molecular structure and physiological function of chloride channels.

Jentsch TJ, Stein V, Weinreich F, Zdebik AA.

Physiol Rev. 2002 Apr;82(2):503-68. Review. Erratum in: Physiol Rev. 2003 Apr;83(2):following table of contents.

6.

[Various functions of ClC-type Cl- channels].

Furukawa T.

Nihon Yakurigaku Zasshi. 2003 Nov;122(5):375-83. Review. Japanese.

PMID:
14569156
7.

How Bartter's and Gitelman's syndromes, and Dent's disease have provided important insights into the function of three renal chloride channels: ClC-Ka/b and ClC-5.

Briet M, Vargas-Poussou R, Lourdel S, Houillier P, Blanchard A.

Nephron Physiol. 2006;103(1):p7-13. Epub 2005 Dec 12. Review.

9.

ClC chloride channels in epithelia: recent progress and remaining puzzles.

Wills NK, Fong P.

News Physiol Sci. 2001 Aug;16:161-6. Review.

10.

Molecular pathology of renal chloride channels in Dent's disease and Bartter's syndrome.

Thakker RV.

Exp Nephrol. 2000 Nov-Dec;8(6):351-60. Review.

PMID:
11014932
11.

Multimeric structure of ClC-1 chloride channel revealed by mutations in dominant myotonia congenita (Thomsen).

Steinmeyer K, Lorenz C, Pusch M, Koch MC, Jentsch TJ.

EMBO J. 1994 Feb 15;13(4):737-43.

12.

Mechanism of inverted activation of ClC-1 channels caused by a novel myotonia congenita mutation.

Zhang J, Sanguinetti MC, Kwiecinski H, Ptácek LJ.

J Biol Chem. 2000 Jan 28;275(4):2999-3005.

13.

Functional and structural analysis of ClC-K chloride channels involved in renal disease.

Waldegger S, Jentsch TJ.

J Biol Chem. 2000 Aug 11;275(32):24527-33.

14.

CLC chloride channels and transporters.

Jentsch TJ, Neagoe I, Scheel O.

Curr Opin Neurobiol. 2005 Jun;15(3):319-25. Review.

PMID:
15913981
15.

Physiological functions of CLC Cl- channels gleaned from human genetic disease and mouse models.

Jentsch TJ, Poët M, Fuhrmann JC, Zdebik AA.

Annu Rev Physiol. 2005;67:779-807. Review.

PMID:
15709978
16.

In vivo role of CLC chloride channels in the kidney.

Uchida S.

Am J Physiol Renal Physiol. 2000 Nov;279(5):F802-8. Review.

17.

Physiology and pathophysiology of CLC-1: mechanisms of a chloride channel disease, myotonia.

Tang CY, Chen TY.

J Biomed Biotechnol. 2011;2011:685328. doi: 10.1155/2011/685328. Epub 2011 Dec 1. Review.

18.

ClC Channels and Transporters: Structure, Physiological Functions, and Implications in Human Chloride Channelopathies.

Poroca DR, Pelis RM, Chappe VM.

Front Pharmacol. 2017 Mar 23;8:151. doi: 10.3389/fphar.2017.00151. eCollection 2017. Review.

19.

CLC chloride channels and transporters: from genes to protein structure, pathology and physiology.

Jentsch TJ.

Crit Rev Biochem Mol Biol. 2008 Jan-Feb;43(1):3-36. doi: 10.1080/10409230701829110 . Review.

PMID:
18307107
20.

Chloride channels in renal disease.

Thakker RV.

Adv Nephrol Necker Hosp. 1999;29:289-98. Review.

PMID:
10561751

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