Somatic and germline CACNA1D calcium channel mutations in aldosterone-producing adenomas and primary aldosteronism (Q34361657)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23913001%20AND%20SRC:MED&resulttype=core&format=json

6 March 2020

title

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

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6 March 2020

2

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Gabriel Stölting

3

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6 March 2020

John W Kunstman

10

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6 March 2020

Erum Hartung

12

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6 March 2020

Matthew R. Benson

14

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Peyman Björklund

24

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Christoph Fahlke

26

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Patricia Hidalgo

27

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6 March 2020

author name string

Ute I Scholl

1

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6 March 2020

Regina Campos de Oliveira

4

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6 March 2020

Murim Choi

5

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6 March 2020

John D Overton

6

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6 March 2020

Annabelle L Fonseca

7

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6 March 2020

Reju Korah

8

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Lee F Starker

9

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Manju L Prasad

11

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6 March 2020

Nelly Mauras

13

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6 March 2020

Tammy Brady

15

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6 March 2020

Jay R Shapiro

16

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Erin Loring

17

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Carol Nelson-Williams

18

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6 March 2020

Steven K Libutti

19

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Shrikant Mane

20

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6 March 2020

Per Hellman

21

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Gunnar Westin

22

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Göran Åkerström

23

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Tobias Carling

25

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Richard P Lifton

28

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language of work or name

English

0 references

publication date

4 August 2013

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6 March 2020

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volume

45

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issue

9

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6 March 2020

page(s)

1050-1054

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

6 March 2020

cites work

1 reference

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Genomic analysis of non-NF2 meningiomas reveals mutations in TRAF7, KLF4, AKT1, and SMO

6 July 2018

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New insights into aldosterone-producing adenomas and hereditary aldosteronism: mutations in the K+ channel KCNJ5.

6 July 2018

1 reference

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CaV1.3-selective L-type calcium channel antagonists as potential new therapeutics for Parkinson's disease.

6 July 2018

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Zona glomerulosa cells of the mouse adrenal cortex are intrinsic electrical oscillators

6 July 2018

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

6 July 2018

1 reference

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

6 July 2018

1 reference

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Loss of Ca(v)1.3 (CACNA1D) function in a human channelopathy with bradycardia and congenital deafness

6 July 2018

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Signaling complexes of voltage-gated sodium and calcium channels

6 July 2018

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Molecular endpoints of Ca2+/calmodulin- and voltage-dependent inactivation of Ca(v)1.3 channels

6 July 2018

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Loss of Cav1.3 channels reveals the critical role of L-type and BK channel coupling in pacemaking mouse adrenal chromaffin cells

6 July 2018

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Arachidonic acid inhibition of L-type calcium (CaV1.3b) channels varies with accessory CaVbeta subunits

6 July 2018

1 reference

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Pore stability and gating in voltage-activated calcium channels

6 July 2018

1 reference

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The guanylate kinase domain of the beta-subunit of voltage-gated calcium channels suffices to modulate gating.

6 July 2018

1 reference

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Functional analysis of congenital stationary night blindness type-2 CACNA1F mutations F742C, G1007R, and R1049W.

6 July 2018

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Frequent mutations of beta-catenin gene in sporadic secreting adrenocortical adenomas

6 July 2018

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A CACNA1F mutation identified in an X-linked retinal disorder shifts the voltage dependence of Cav1.4 channel activation.

6 July 2018

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Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations

6 July 2018

1 reference

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Congenital stationary night blindness type 2 mutations S229P, G369D, L1068P, and W1440X alter channel gating or functional expression of Ca(v)1.4 L-type Ca2+ channels

6 July 2018

1 reference

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Control of aldosterone secretion: a model for convergence in cellular signaling pathways

6 July 2018

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Presidential address. I. Painting background. II. Primary aldosteronism, a new clinical syndrome.

6 July 2018

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Allele frequencies for 15 autosomal STR loci on U.S. Caucasian, African American, and Hispanic populations

6 July 2018

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A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia

6 July 2018

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Functional consequences of mutations in the human alpha1A calcium channel subunit linked to familial hemiplegic migraine

6 July 2018

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

6 July 2018

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Congenital deafness and sinoatrial node dysfunction in mice lacking class D L-type Ca2+ channels

27 October 2018

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27 October 2018

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27 October 2018

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Crossref

https://api.crossref.org/works/10.1038%2FNG.2695

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7 January 2021

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Identifiers

DOI

10.1038/NG.2695

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6 March 2020

Fatcat ID

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mapped directly with Wikidata item

24 November 2022

based on heuristic

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6 March 2020

PubMed publication ID

23913001

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