Further study of chromosome 7p22 to identify the molecular basis of familial hyperaldosteronism type II. (Q51554319)

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15 February 2020

title

Further study of chromosome 7p22 to identify the molecular basis of familial hyperaldosteronism type II (English)

1 reference

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Familial hyperaldosteronism

15 February 2020

main subject

1 reference

1 reference

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15 February 2020

M Stowasser

1 reference

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15 February 2020

R D Gordon

series ordinal

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15 February 2020

K M O'Shaughnessy

series ordinal

1 reference

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15 February 2020

publication date

7 October 2010

1 reference

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Journal of Human Hypertension

15 February 2020

published in

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15 February 2020

volume

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15 February 2020

issue

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15 February 2020

page(s)

560-564

1 reference

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A novel genetic locus for low renin hypertension: familial hyperaldosteronism type II maps to chromosome 7 (7p22)

15 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1038%2FJHH.2010.93

Familial hyperaldosteronism type II is linked to the chromosome 7p22 region but also shows predicted heterogeneity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHH.2010.93

Genomic structure of the human gene for protein kinase A regulatory subunit R1-beta (PRKAR1B) on 7p22: no evidence for mutations in familial hyperaldosteronism type II in a large affected kindred

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHH.2010.93

Examination of chromosome 7p22 candidate genes RBaK, PMS2 and GNA12 in familial hyperaldosteronism type II.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHH.2010.93

Clinical and genetic correlates of aldosterone-to-renin ratio and relations to blood pressure in a community sample

21 January 2018

1 reference

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Genes that mediate breast cancer metastasis to lung

21 January 2018

1 reference

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Triad3A regulates ubiquitination and proteasomal degradation of RIP1 following disruption of Hsp90 binding

21 January 2018

1 reference

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Translation initiation control by heme-regulated eukaryotic initiation factor 2alpha kinase in erythroid cells under cytoplasmic stresses

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHH.2010.93

Rac1 accumulates in the nucleus during the G2 phase of the cell cycle and promotes cell division

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHH.2010.93

Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHH.2010.93

Exome sequencing identifies the cause of a mendelian disorder

21 January 2018

1 reference

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Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome

21 January 2018

1 reference

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The International HapMap Project

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHH.2010.93

Human hypertension caused by mutations in WNK kinases

21 January 2018

1 reference

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The Human Gene Mutation Database: 2008 update

21 January 2018

1 reference

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De novo mutations of SETBP1 cause Schinzel-Giedion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHH.2010.93

Next-generation sequencing of a 40 Mb linkage interval reveals TSPAN12 mutations in patients with familial exudative vitreoretinopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHH.2010.93

Prevalence of Primary Aldosteronism among Unselected Hypertensive Patients: A Prospective Study Based on the Use of an Aldosterone/Renin Ratio above 25 as a Screening Test

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHH.2010.93

inferred from DOI database lookup

7 January 2021

based on heuristic

Clinical and pathological diversity of primary aldosteronism, including a new familial variety

1 reference

https://api.crossref.org/works/10.1038%2FJHH.2010.93

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/JHH.2010.93

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20927129%20AND%20SRC:MED&resulttype=core&format=json

15 February 2020

1 reference

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