Channelpedia

ClCK2 Channel

60 automatically matched literature references

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Lopez HU et al. Whole-Exome Sequencing Reveals CLCNKB Mutations in a Case of Sudden Unexpected Infant Death.
Pediatr. Dev. Pathol., 2015 Jul-Aug , 18 (324-6).

3

Andrini O et al. ClC-K chloride channels: emerging pathophysiology of Bartter syndrome type 3.
Am. J. Physiol. Renal Physiol., 2015 Jun 15 , 308 (F1324-34).

7

Chiang WF et al. Hypokalemic paralysis in a middle-aged female with classic Bartter syndrome.
Clin. Nephrol., 2014 Feb , 81 (146-50).

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Cho HY et al. Translational read-through of a nonsense mutation causing Bartter syndrome.
J. Korean Med. Sci., 2013 Jun , 28 (821-6).

11

García Castaño A et al. Genetics of type III Bartter syndrome in Spain, proposed diagnostic algorithm.
PLoS ONE, 2013 , 8 (e74673).

13

Lee BH et al. Genetic basis of Bartter syndrome in Korea.
Nephrol. Dial. Transplant., 2012 Apr , 27 (1516-21).

14

Su X et al. Association of CLCNKB haplotypes and hypertension in Mongolian and Han populations.
Clin. Exp. Hypertens., 2012 , 34 (482-7).

15

Robitaille P et al. Bartter syndrome in two sisters with a novel mutation of the CLCNKB gene, one with deafness.
Eur. J. Pediatr., 2011 Sep , 170 (1209-11).

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Iqbal H et al. Identification of missense mutation (I12T) in the BSND gene and bioinformatics analysis.
J. Biomed. Biotechnol., 2011 , 2011 (304612).

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Enríquez R et al. Gitelman syndrome due to p.A204T mutation in CLCNKB gene.
Int Urol Nephrol, 2010 Dec , 42 (1099-102).

22

Jung J et al. Allelic-based gene-gene interaction associated with quantitative traits.
Genet. Epidemiol., 2009 May , 33 (332-43).

23

Brochard K et al. Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome.
Nephrol. Dial. Transplant., 2009 May , 24 (1455-64).

25

Sile S et al. CLCNKB-T481S and essential hypertension in a Ghanaian population.
J. Hypertens., 2009 Feb , 27 (298-304).

31

Lang F et al. Functional significance of channels and transporters expressed in the inner ear and kidney.
Am. J. Physiol., Cell Physiol., 2007 Oct , 293 (C1187-208).

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Sile S et al. Functional BSND variants in essential hypertension.
Am. J. Hypertens., 2007 Nov , 20 (1176-1182).

36

Bichet DG Hereditary polyuric disorders: new concepts and differential diagnosis.
Semin. Nephrol., 2006 May , 26 (224-33).

39

Lin SH et al. Phenotype and genotype analysis in Chinese patients with Gitelman's syndrome.
J. Clin. Endocrinol. Metab., 2005 May , 90 (2500-7).

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Yamauchi K et al. Apical localization of renal K channel was not altered in mutant WNK4 transgenic mice.
Biochem. Biophys. Res. Commun., 2005 Jul 8 , 332 (750-5).

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Rodríguez-Soriano J et al. A founder mutation in the CLCNKB gene causes Bartter syndrome type III in Spain.
Pediatr. Nephrol., 2005 Jul , 20 (891-6).

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Behr R et al. Mild nephrogenic diabetes insipidus caused by Foxa1 deficiency.
J. Biol. Chem., 2004 Oct 1 , 279 (41936-41).

48

Langman CB The molecular basis of kidney stones.
Curr. Opin. Pediatr., 2004 Apr , 16 (188-93).

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Kobayashi K et al. Intrarenal and cellular localization of CLC-K2 protein in the mouse kidney.
J. Am. Soc. Nephrol., 2001 Jul , 12 (1327-34).

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Konrad M et al. Mutations in the chloride channel gene CLCNKB as a cause of classic Bartter syndrome.
J. Am. Soc. Nephrol., 2000 Aug , 11 (1449-59).

56

Vantyghem MC et al. [Bartter's syndromes]
Ann. Endocrinol. (Paris), 1999 Dec , 60 (465-72).

57

Károlyi L et al. The molecular genetic approach to "Bartter's syndrome".
J. Mol. Med., 1998 Apr , 76 (317-25).

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