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Genetic modifiers of cardiac arrhythmias.
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Europe PubMed Central
PubMed publication ID
12615039
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12615039%20AND%20SRC:MED&resulttype=core&format=json
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1 November 2019
review article
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title
Genetic modifiers of cardiac arrhythmias
(English)
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Europe PubMed Central
PubMed publication ID
12615039
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1 November 2019
author
Ching-Feng Cheng
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1
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Europe PubMed Central
PubMed publication ID
12615039
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1 November 2019
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Hai-Chien Kuo
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2
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Europe PubMed Central
PubMed publication ID
12615039
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1 November 2019
Kenneth R Chien
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PubMed publication ID
12615039
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1 November 2019
publication date
1 February 2003
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PubMed publication ID
12615039
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1 November 2019
published in
Trends in Molecular Medicine
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Europe PubMed Central
PubMed publication ID
12615039
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1 November 2019
volume
9
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Europe PubMed Central
PubMed publication ID
12615039
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12615039%20AND%20SRC:MED&resulttype=core&format=json
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1 November 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12615039
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12615039%20AND%20SRC:MED&resulttype=core&format=json
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1 November 2019
page(s)
59-66
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Europe PubMed Central
PubMed publication ID
12615039
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12615039%20AND%20SRC:MED&resulttype=core&format=json
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1 November 2019
cites work
Genetic and molecular basis of cardiac arrhythmias: impact on clinical management parts I and II
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Molecular and cellular mechanisms of cardiac arrhythmias
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Molecular genetic basis of sudden cardiac death
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Molecular mechanisms underlying the long QT syndrome
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Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel
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7 January 2021
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K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current
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Crossref
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7 January 2021
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A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel
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Genetic defects of cardiac ion channels. The hidden substrate for torsades de pointes
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SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome
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Slowed conduction and ventricular tachycardia after targeted disruption of the cardiac sodium channel gene Scn5a
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Genetic basis and molecular mechanism for idiopathic ventricular fibrillation
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Right bundle branch block, persistent ST segment elevation and sudden cardiac death: A distinct clinical and electrocardiographic syndrome
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A single Na(+) channel mutation causing both long-QT and Brugada syndromes
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7 January 2021
based on heuristic
inferred from DOI database lookup
Long QT syndrome, Brugada syndrome, and conduction system disease are linked to a single sodium channel mutation
1 reference
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Crossref
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7 January 2021
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Natural history of Brugada syndrome: insights for risk stratification and management
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Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non-SCN5A-related patients
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7 January 2021
based on heuristic
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Mutations in the hminK gene cause long QT syndrome and suppress IKs function
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Crossref
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7 January 2021
based on heuristic
inferred from DOI database lookup
MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900004-2
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7 January 2021
based on heuristic
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Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndrome
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Heteromerization of Kir2.x potassium channels contributes to the phenotype of Andersen's syndrome
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Ryanodine receptors/calcium release channels in heart failure and sudden cardiac death
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Involvement of the cardiac ryanodine receptor/calcium release channel in catecholaminergic polymorphic ventricular tachycardia
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Modulation of A-type potassium channels by a family of calcium sensors
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7 January 2021
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Palmitoylation of KChIP splicing variants is required for efficient cell surface expression of Kv4.3 channels
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7 January 2021
based on heuristic
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A defect in the Kv channel-interacting protein 2 (KChIP2) gene leads to a complete loss of I(to) and confers susceptibility to ventricular tachycardia
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Crossref
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Expression pattern of connexin gene products at the early developmental stages of the mouse cardiovascular system.
1 reference
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Crossref
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Mice lacking connexin40 have cardiac conduction abnormalities characteristic of atrioventricular block and bundle branch block
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
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Reduced cardiac conduction velocity and predisposition to arrhythmias in connexin40-deficient mice
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Conduction disturbances and increased atrial vulnerability in Connexin40-deficient mice analyzed by transesophageal stimulation.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900004-2
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7 January 2021
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inferred from DOI database lookup
[Electrophysiological characterization of connexin 40 deficient hearts--in vivo studies in mice]
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900004-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
Cardiac malformation in neonatal mice lacking connexin43.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900004-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
Heterogeneous Expression of Gap Junction Channels in the Heart Leads to Conduction Defects and Ventricular Dysfunction
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900004-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
A novel, tissue-restricted zinc finger protein (HF-1b) binds to the cardiac regulatory element (HF-1b/MEF-2) in the rat myosin light-chain 2 gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900004-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel genetic pathway for sudden cardiac death via defects in the transition between ventricular and conduction system cell lineages
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900004-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Congenital heart disease caused by mutations in the transcription factor NKX2-5
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900004-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900004-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Loss of function and inhibitory effects of human CSX/NKX2.5 homeoprotein mutations associated with congenital heart disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900004-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Myogenic and morphogenetic defects in the heart tubes of murine embryos lacking the homeo box gene Nkx2-5
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900004-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Progressive atrioventricular conduction defects and heart failure in mice expressing a mutant Csx/Nkx2.5 homeoprotein
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900004-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900004-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900004-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A murine model of Holt-Oram syndrome defines roles of the T-box transcription factor Tbx5 in cardiogenesis and disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900004-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tbx5 associates with Nkx2-5 and synergistically promotes cardiomyocyte differentiation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900004-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a gene responsible for familial Wolff-Parkinson-White syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900004-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Novel PRKAG2 mutation responsible for the genetic syndrome of ventricular preexcitation and conduction system disease with childhood onset and absence of cardiac hypertrophy
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900004-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inhibition of cystic fibrosis transmembrane conductance regulator by novel interaction with the metabolic sensor AMP-activated protein kinase
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900004-2
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7 January 2021
based on heuristic
inferred from DOI database lookup
New approaches to antiarrhythmic therapy: emerging therapeutic applications of the cell biology of cardiac arrhythmias(1).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900004-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transgenic mice overexpressing human KvLQT1 dominant-negative isoform. Part I: Phenotypic characterisation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900004-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A sodium-channel mutation causes isolated cardiac conduction disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900004-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900004-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900004-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Functional consequences of elimination of i(to,f) and i(to,s): early afterdepolarizations, atrioventricular block, and ventricular arrhythmias in mice lacking Kv1.4 and expressing a dominant-negative Kv4 alpha subunit
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1471-4914%2803%2900004-2
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S1471-4914(03)00004-2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12615039
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12615039%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
PubMed publication ID
12615039
1 reference
stated in
Europe PubMed Central
PubMed publication ID
12615039
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12615039%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 November 2019
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