(Q38337767)

2 September 2017

title

Identification of 108 SNPs in TSC, WNK1, and WNK4 and their association with hypertension in a Japanese general population (English)

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2 September 2017

main subject

arterial hypertension

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1

Yoshihiro Kokubo

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2 September 2017

Kei Kamide

2

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2 September 2017

Nozomu Inamoto

3

1 reference

2 September 2017

Chihiro Tanaka

4

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2 September 2017

Mariko Banno

5

1 reference

2 September 2017

Shin Takiuchi

6

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2 September 2017

Yuhei Kawano

7

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2 September 2017

Hitonobu Tomoike

8

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2 September 2017

Toshiyuki Miyata

9

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2 September 2017

language of work or name

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11 August 2004

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Journal of Human Genetics

2 September 2017

published in

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2 September 2017

volume

49

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2 September 2017

issue

9

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2 September 2017

page(s)

507-515

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Novel molecular variants of the Na-Cl cotransporter gene are responsible for Gitelman syndrome.

2 September 2017

cites work

1 reference

12 December 2020

Genetic mapping of a gene causing hypertension in the stroke-prone spontaneously hypertensive rat

1 reference

12 December 2020

Genetic variants of WNK4 in whites and African Americans with hypertension

1 reference

12 December 2020

Association of EDNRA, but not WNK4 or FKBP1B, polymorphisms with essential hypertension

1 reference

12 December 2020

Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter

1 reference

12 December 2020

Verification of 525 coding SNPs in 179 hypertension candidate genes in the Japanese population: identification of 159 SNPs in 93 genes

1 reference

12 December 2020

WNK4 intron 10 polymorphism is not associated with hypertension

1 reference

12 December 2020

Three novel missense mutations of WNK4, a kinase mutated in inherited hypertension, in Japanese hypertensives: implication of clinical phenotypes

1 reference

12 December 2020

An Alternative Fast and Convenient Genotyping Method for the Screening of Angiotensin Converting Enzyme Gene Polymorphisms

1 reference

12 December 2020

Identification of 21 single nucleotide polymorphisms in human hepatocyte growth factor gene and association with blood pressure and carotid atherosclerosis in the Japanese population

1 reference

12 December 2020

Human hypertension caused by mutations in WNK kinases

1 reference

12 December 2020

Genetic susceptibility for human familial essential hypertension in a region of homology with blood pressure linkage on rat chromosome 10.

1 reference

12 December 2020

Association of a mutation in thiazide-sensitive Na-Cl cotransporter with familial Gitelman's syndrome

1 reference

12 December 2020

Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease

1 reference

12 December 2020

Use of calcium excretion values to distinguish two forms of primary renal tubular hypokalemic alkalosis: Bartter and Gitelman syndromes

1 reference

12 December 2020

Association of methylenetetrahydrofolate reductase gene polymorphism with carotid atherosclerosis depending on smoking status in a Japanese general population

1 reference

12 December 2020

WNK kinases regulate thiazide-sensitive Na-Cl cotransport

1 reference

12 December 2020

Evidence for a gene influencing blood pressure on chromosome 17. Genome scan linkage results for longitudinal blood pressure phenotypes in subjects from the framingham heart study

1 reference

12 December 2020

Evidence for linkage between essential hypertension and a putative locus on human chromosome 17.

1 reference

12 December 2020

Molecular pathogenesis of inherited hypertension with hyperkalemia: the Na-Cl cotransporter is inhibited by wild-type but not mutant WNK4

1 reference

12 December 2020

WNK1, a kinase mutated in inherited hypertension with hyperkalemia, localizes to diverse Cl- -transporting epithelia

1 reference

12 December 2020

10.1007/S10038-004-0181-0

Identifiers

DOI

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2 September 2017

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