CLCNKB gene

Known as: CHLORIDE CHANNEL, KIDNEY, B, CLCKB, hClC-Kb 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1996-2017
024619962017

Papers overview

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2010
2010
Mutations in the gene CLCNKB encoding the ClC-Kb chloride channel causes classic Bartter syndrome, which is characterized by… (More)
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2010
2010
CONTEXT Our understanding of inherited salt-losing tubulopathies has improved with recent advances in molecular genetics. However… (More)
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2009
2009
OBJECTIVE Prior to the discovery of chloride channel Kb with a variant threonine change to serine at position 481 (CLCNKB-T481S… (More)
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2008
2008
OBJECTIVE Differences exist among various populations with regards to hypertension prevalence, severity, progression and response… (More)
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2007
2007
BACKGROUND Little information on the management and long-term follow-up of patients with biallelic mutations in the chloride… (More)
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2006
2006
We previously selected a group of hypertension candidate genes by a key word search using the OMIM database of NCBI and validated… (More)
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2005
2005
BACKGROUND Reproducibility of results is important for the validity of genetic association studies. Recently, 3 functional… (More)
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2005
2005
OBJECTIVE Chromosome 1p36 has been linked to essential hypertension and systolic blood pressure. This locus contains the chloride… (More)
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2003
2003
BACKGROUND Gitelman syndrome (GS) and Bartter syndrome (BS) are hereditary hypokalemic tubulopathies with distinct phenotypic… (More)
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Highly Cited
1997
Highly Cited
1997
Analysis of patients with inherited hypokalaemic alkalosis resulting from salt–wasting has proved fertile ground for… (More)
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