(Q38024058)

27 August 2017

The molecular basis of blood pressure variation (English)

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27 August 2017

Hakan R Toka

1

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27 August 2017

Jacob M Koshy

series ordinal

2

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27 August 2017

Ali Hariri

series ordinal

3

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27 August 2017

5 July 2012

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27 August 2017

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27 August 2017

28

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27 August 2017

387-399

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27 August 2017

3

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https://scigraph.springernature.com/pub.10.1007/s00467-012-2206-9

27 August 2017

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cites work

Trends in the prevalence of hypertension, antihypertensive therapy, and left ventricular hypertrophy from 1950 to 1989.

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

A clinical trial of the effects of dietary patterns on blood pressure. DASH Collaborative Research Group

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

The NHLBI twin study of cardiovascular disease risk factors: methodology and summary of results

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Molecular mechanisms of human hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Monogenic forms of human hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Genetic testing in renal disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Linkage analysis in the next-generation sequencing era

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Rare independent mutations in renal salt handling genes contribute to blood pressure variation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

A chimaeric llβ-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Hereditary hypertension caused by chimaeric gene duplications and ectopic expression of aldosterone synthase

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Human hypertension caused by mutations in the kidney isozyme of 11 beta-hydroxysteroid dehydrogenase

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

11 beta-Hydroxysteroid dehydrogenase and the syndrome of apparent mineralocorticoid excess

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Liddle's syndrome: heritable human hypertension caused by mutations in the beta subunit of the epithelial sodium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Hypertension caused by a truncated epithelial sodium channel gamma subunit: genetic heterogeneity of Liddle syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Activating mineralocorticoid receptor mutation in hypertension exacerbated by pregnancy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

A prospective study of the prevalence of primary aldosteronism in 1,125 hypertensive patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

K+ channel mutations in adrenal aldosterone-producing adenomas and hereditary hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

A novel form of human mendelian hypertension featuring nonglucocorticoid-remediable aldosteronism

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Hypertension with or without adrenal hyperplasia due to different inherited mutations in the potassium channel KCNJ5.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Congenital adrenal hyperplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Medical treatment of classic and nonclassic congenital adrenal hyperplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Mineralocorticoid-resistant renal hyperkalemia without salt wasting (type II pseudohypoaldosteronism): role of increased renal chloride reabsorption.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Human hypertension caused by mutations in WNK kinases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

WNK kinases: molecular regulators of integrated epithelial ion transport

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Mutations in kelch-like 3 and cullin 3 cause hypertension and electrolyte abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Autosomal dominant hypertension and brachydactyly in a Turkish kindred resembles essential hypertension.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

A cross-over medication trial for patients with autosomal-dominant hypertension with brachydactyly

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Severely impaired baroreflex-buffering in patients with monogenic hypertension and neurovascular contact

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Neurovascular compression at the ventrolateral medulla in autosomal dominant hypertension and brachydactyly.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Inversion region for hypertension and brachydactyly on chromosome 12p features multiple splicing and noncoding RNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Recent advances in genetics, diagnosis, localization, and treatment of pheochromocytoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Molecular and cellular biology of pheochromocytomas and extra-adrenal paragangliomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

A cluster of metabolic defects caused by mutation in a mitochondrial tRNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Role of renal medullary oxidative and/or carbonyl stress in salt-sensitive hypertension and diabetes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Maternal component in the familial aggregation of hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Bartter- and Gitelman-like syndromes: salt-losing tubulopathies with loop or DCT defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Barttin is a Cl- channel beta-subunit crucial for renal Cl- reabsorption and inner ear K+ secretion

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Inactivation of the Na-Cl co-transporter (NCC) gene is associated with high BMD through both renal and bone mechanisms: analysis of patients with Gitelman syndrome and Ncc null mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type I

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

KCNJ10 gene mutations causing EAST syndrome (epilepsy, ataxia, sensorineural deafness, and tubulopathy) disrupt channel function

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Time course of inner ear degeneration and deafness in mice lacking the Kir4.1 potassium channel subunit.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Inherited renal tubular dysgenesis may not be universally fatal

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Renin-angiotensin system in kidney development: renal tubular dysgenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Recognition and management of angiotensin converting enzyme inhibitor fetopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Under pressure: the search for the essential mechanisms of hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Genome-wide association study of blood pressure and hypertension

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Genome-wide association study identifies eight loci associated with blood pressure

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

High frequency of methylenetetrahydrofolate reductase 677TT genotype in Hungarian HELLP syndrome patients determined by quantitative real-time PCR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Association of common variants in NPPA and NPPB with circulating natriuretic peptides and blood pressure

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Disruption of Na+,HCO₃⁻ cotransporter NBCn1 (slc4a7) inhibits NO-mediated vasorelaxation, smooth muscle Ca²⁺ sensitivity, and hypertension development in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Blood pressure control--special role of the kidneys and body fluids

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Cardiovascular risk factors in a french canadian population: Resolution of genetic and familial environmental effects on blood pressure using twins, adoptees, and extensive information on environmental correlates

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Maternal influence on blood pressure suggests involvement of mitochondrial DNA in the pathogenesis of hypertension: the Framingham Heart Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00467-012-2206-9

Functional Characterization of a Calcium-Sensing Receptor Mutation in Severe Autosomal Dominant Hypocalcemia with a Bartter-Like Syndrome

21 January 2018

1 reference

12 December 2020

Global burden of hypertension: analysis of worldwide data

1 reference

12 December 2020

Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK

1 reference

12 December 2020

Pseudohypoaldosteronism type II: marked sensitivity to thiazides, hypercalciuria, normomagnesemia, and low bone mineral density

1 reference

12 December 2020

Families with autosomal dominant brachydactyly type E, short stature, and severe hypertension

1 reference

12 December 2020

Hereditary Brachydactyly Associated with Hypertension

1 reference

12 December 2020

Trafficking and cell surface stability of ENaC.

1 reference

12 December 2020

Hypertension and Severe Hyperkalaemia Associated with Suppression of Renin and Aldosterone and Completely Reversed by Dietary Sodium Restriction

1 reference

12 December 2020

Brief report: Liddle's syndrome revisited--a disorder of sodium reabsorption in the distal tubule

1 reference

12 December 2020

Demographic, dietary, life style, and anthropometric correlates of blood pressure.

1 reference

12 December 2020

10.1007/S00467-012-2206-9

Identifiers

DOI

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Dimensions Publication ID

27 August 2017

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