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The molecular basis of long QT syndrome and prospects for therapy
scientific article published on 01 September 1998
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9791861
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9791861%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
review article
1 reference
stated in
Europe PubMed Central
title
The molecular basis of long QT syndrome and prospects for therapy
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9791861
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9791861%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
main subject
long QT syndrome
1 reference
based on heuristic
inferred from title
author name string
Q Wang
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9791861
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9791861%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
N E Bowles
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9791861
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9791861%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
J A Towbin
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9791861
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9791861%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
publication date
1 September 1998
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9791861
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9791861%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
published in
Trends in Molecular Medicine
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9791861
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9791861%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
volume
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9791861
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9791861%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
issue
9
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9791861
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9791861%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
page(s)
382-388
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9791861
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9791861%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
cites work
Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Diagnostic criteria for the long QT syndrome. An update
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Evidence of genetic heterogeneity in the long QT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Locus heterogeneity of autosomal dominant long QT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Evidence of genetic heterogeneity in Romano-Ward long QT syndrome. Analysis of 23 families
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
KCNE1 mutations cause jervell and Lange-Nielsen syndrome
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in the hminK gene cause long QT syndrome and suppress IKs function
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
KVLQT1 mutations in three families with familial or sporadic long QT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Four novel KVLQT1 and four novel HERG mutations in familial long-QT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
New mutations in the KVLQT1 potassium channel that cause long-QT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cloning of a membrane protein that induces a slow voltage-gated potassium current
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dominant-negative KvLQT1 mutations underlie the LQT1 form of long QT syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular basis of the long-QT syndrome associated with deafness
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A family of potassium channel genes related to eag in Drosophila and mammals
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
HERG, a Human Inward Rectifier in the Voltage-Gated Potassium Channel Family
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The long-QT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mutation in HERG associated with notched T waves in long QT syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Missense mutation in the pore region of HERG causes familial long QT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A minK-HERG complex regulates the cardiac potassium current I(Kr)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Spectrum of HERG K+-channel dysfunction in an inherited cardiac arrhythmia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Primary structure and functional expression of the human cardiac tetrodotoxin-insensitive voltage-dependent sodium channel
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular mechanism for an inherited cardiac arrhythmia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple mechanisms of Na+ channel--linked long-QT syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple mechanisms in the long-QT syndrome. Current knowledge, gaps, and future directions. The SADS Foundation Task Force on LQTS.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Clinical relevance of cardiac arrhythmias generated by afterdepolarizations. Role of M cells in the generation of U waves, triggered activity and torsade de pointes.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The spectrum of symptoms and QT intervals in carriers of the gene for the long-QT syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Long QT syndrome patients with mutations of the SCN5A and HERG genes have differential responses to Na+ channel blockade and to increases in heart rate. Implications for gene-specific therapy.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetically defined therapy of inherited long-QT syndrome. Correction of abnormal repolarization by potassium
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS1357-4310%2898%2901320-3
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S1357-4310(98)01320-3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9791861
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9791861%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
PubMed publication ID
9791861
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9791861
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9791861%20AND%20SRC:MED&resulttype=core&format=json
retrieved
5 December 2019
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