(Q34810955)

4 August 2017

0 references

A case of severe hyperaldosteronism caused by a de novo mutation affecting a critical salt bridge Kir3.4 residue (English)

1 reference

4 August 2017

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25322277%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

Mihail Zilbermint

4

1 reference

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6 June 2020

Ivan Dedov

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25322277%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

Michael Allgäuer

7

1 reference

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6 June 2020

Chyi-Chia R Lee

8

1 reference

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6 June 2020

author name string

Sascha Bandulik

2

1 reference

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6 June 2020

Julia Stindl

3

1 reference

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6 June 2020

Paolo Mulatero

6

1 reference

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6 June 2020

Tracy A Williams

10

1 reference

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6 June 2020

Anatoly Tiulpakov

11

1 reference

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6 June 2020

Constantine A Stratakis

9

1 reference

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6 June 2020

language of work or name

English

0 references

publication date

1 January 2015

1 reference

25322277

The Journal of Clinical Endocrinology and Metabolism

4 August 2017

published in

1 reference

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6 June 2020

volume

100

1 reference

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6 June 2020

issue

1

1 reference

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6 June 2020

page(s)

E114-8

1 reference

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A novel KCNJ5-insT149 somatic mutation close to, but outside, the selectivity filter causes resistant hypertension by loss of selectivity for potassium

6 June 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283020

Pharmacology and pathophysiology of mutated KCNJ5 found in adrenal aldosterone-producing adenomas.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283020

a Novel Y152C KCNJ5 mutation responsible for familial hyperaldosteronism type III.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283020

Somatic and germline CACNA1D calcium channel mutations in aldosterone-producing adenomas and primary aldosteronism

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283020

Somatic mutations in ATP1A1 and ATP2B3 lead to aldosterone-producing adenomas and secondary hypertension

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283020

Role of KCNJ5 in familial and sporadic primary aldosteronism

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283020

Comprehensive re-sequencing of adrenal aldosterone producing lesions reveal three somatic mutations near the KCNJ5 potassium channel selectivity filter

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283020

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283020

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283020

Case detection, diagnosis, and treatment of patients with primary aldosteronism: an endocrine society clinical practice guideline

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283020

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283020

Chemistry of ion coordination and hydration revealed by a K+ channel-Fab complex at 2.0 A resolution

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283020

Mechanisms of inward-rectifier K+ channel inhibition by tertiapin-Q.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283020

G protein regulation of potassium ion channels

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283020

The Structure of the Potassium Channel: Molecular Basis of K+ Conduction and Selectivity

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283020

Stabilization of ion selectivity filter by pore loop ion pairs in an inwardly rectifying potassium channel

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283020

Permeation selectivity by competition in a delayed rectifier potassium channel

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283020

Clinical and biochemical variability of congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency. A study of 25 patients

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283020

Molecular basis of ion selectivity, block, and rectification of the inward rectifier Kir3.1/Kir3.4 K(+) channel

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283020

Glucocorticoid remediable aldosteronism: low morbidity and mortality in a four-generation italian pedigree

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4283020

26 October 2018

Identifiers

DOI

10.1210/JC.2014-3636

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25322277%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25322277%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

25322277

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25322277%20AND%20SRC:MED&resulttype=core&format=json