Pro-arrhythmogenic effects of CACNA1C G1911R mutation in human ventricular tachycardia: insights from cardiac multi-scale models (Q27318450)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27502440%20AND%20SRC:MED&resulttype=core&format=json

20 March 2020

title

Pro-arrhythmogenic effects of CACNA1C G1911R mutation in human ventricular tachycardia: insights from cardiac multi-scale models (English)

1 reference

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20 March 2020

main subject

tachycardia

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ventricular tachycardia

1 reference

inferred from title

multi-scale modelling

1 reference

1 reference

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20 March 2020

Kuanquan Wang

1 reference

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20 March 2020

Qince Li

series ordinal

1 reference

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20 March 2020

Yongfeng Yuan

series ordinal

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20 March 2020

Henggui Zhang

series ordinal

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20 March 2020

language of work or name

English

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publication date

9 August 2016

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20 March 2020

1 reference

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20 March 2020

volume

1 reference

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20 March 2020

page(s)

31262

1 reference

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Creative Commons Attribution 4.0 International

20 March 2020

start time

9 August 2016

1 reference

April 2022 Public Data File from Crossref

copyrighted

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cites work

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Gain-of-function mutations in the calcium channel CACNA1C (Cav1.2) cause non-syndromic long-QT but not Timothy syndrome

7 April 2017

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28 September 2017

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A CACNA1C variant associated with reduced voltage-dependent inactivation, increased CaV1.2 channel window current, and arrhythmogenesis

28 September 2017

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Exome sequencing helped the fine diagnosis of two siblings afflicted with atypical Timothy syndrome (TS2).

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Polymorphic ventricular tachycardia--part II: the channelopathies

28 September 2017

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Polymorphic ventricular tachycardia-part I: structural heart disease and acquired causes

28 September 2017

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Exome sequencing and systems biology converge to identify novel mutations in the L-type calcium channel, CACNA1C, linked to autosomal dominant long QT syndrome

28 September 2017

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Interpreting genetic effects through models of cardiac electromechanics

28 September 2017

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Regional cooling facilitates termination of spiral-wave reentry through unpinning of rotors in rabbit hearts.

28 September 2017

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Using induced pluripotent stem cells to investigate cardiac phenotypes in Timothy syndrome

28 September 2017

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Transmural dispersion of repolarization in failing and nonfailing human ventricle

28 September 2017

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Proarrhythmic defects in Timothy syndrome require calmodulin kinase II.

28 September 2017

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The Timothy syndrome mutation differentially affects voltage- and calcium-dependent inactivation of CaV1.2 L-type calcium channels

28 September 2017

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Cellular basis for the electrocardiographic and arrhythmic manifestations of Timothy syndrome: effects of ranolazine

28 September 2017

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28 September 2017

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28 September 2017

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Theoretical study of L-type Ca(2+) current inactivation kinetics during action potential repolarization and early afterdepolarizations

28 September 2017

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21 January 2018

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12 December 2020

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Identifiers

DOI

10.1038/SREP31262

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27502440%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

20 March 2020

1026802920

0 references

OpenCitations bibliographic resource ID

4192923

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

4192923

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27502440%20AND%20SRC:MED&resulttype=core&format=json

20 March 2020

PubMed publication ID

27502440

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27502440%20AND%20SRC:MED&resulttype=core&format=json