(Q57807345)

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A single strand conformation polymorphism/heteroduplex (SSCP/HD) method for detection of mutations in 15 exons of the KVLQT1 gene, associated with long QT syndrome

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090529%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

A single strand conformation polymorphism/heteroduplex (SSCP/HD) method for detection of mutations in 15 exons of the KVLQT1 gene, associated with long QT syndrome (English)

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090529%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

long QT syndrome

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1

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12 November 2019

Paal S Andersen

2

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12 November 2019

Jorgen K. Kanters

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12 November 2019

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J R Jacobsen

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12 November 2019

J Vuust

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12 November 2019

M Christiansen

6

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12 November 2019

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1 February 1999

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12 November 2019

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13

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Clinica Chimica Acta

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12 November 2019

280

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12 November 2019

1-2

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12 November 2019

113-125

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12 November 2019

Multiple mechanisms in the long-QT syndrome. Current knowledge, gaps, and future directions. The SADS Foundation Task Force on LQTS.

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2898%2900177-6

7 January 2021

The spectrum of symptoms and QT intervals in carriers of the gene for the long-QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2898%2900177-6

7 January 2021

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

https://api.crossref.org/works/10.1016%2FS0009-8981%2898%2900177-6

7 January 2021

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2898%2900177-6

7 January 2021

A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2898%2900177-6

7 January 2021

SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2898%2900177-6

7 January 2021

K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2898%2900177-6

7 January 2021

A minK-HERG complex regulates the cardiac potassium current I(Kr)

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2898%2900177-6

7 January 2021

Evidence of genetic heterogeneity in Romano-Ward long QT syndrome. Analysis of 23 families

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2898%2900177-6

7 January 2021

Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements.

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2898%2900177-6

7 January 2021

KvLQT1, a voltage-gated potassium channel responsible for human cardiac arrhythmias

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2898%2900177-6

7 January 2021

Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2898%2900177-6

7 January 2021

Pathophysiological mechanisms of dominant and recessive KVLQT1 K+ channel mutations found in inherited cardiac arrhythmias

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2898%2900177-6

7 January 2021

Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1.

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2898%2900177-6

7 January 2021

Four novel KVLQT1 and four novel HERG mutations in familial long-QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2898%2900177-6

7 January 2021

KVLQT1 mutations in three families with familial or sporadic long QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2898%2900177-6

7 January 2021

The long QT syndrome: a novel missense mutation in the S6 region of the KVLQT1 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2898%2900177-6

7 January 2021

KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2898%2900177-6

7 January 2021

Molecular basis of the long-QT syndrome associated with deafness

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2898%2900177-6

7 January 2021

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2898%2900177-6

7 January 2021

IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2898%2900177-6

7 January 2021

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2898%2900177-6

7 January 2021

Properties of KvLQT1 K+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2898%2900177-6

7 January 2021

Combined SSCP/heteroduplex analysis in the screening for PAX6 mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2898%2900177-6

7 January 2021

Prolongation of the QT interval and the sudden infant death syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2898%2900177-6

7 January 2021

Diagnostic criteria for the long QT syndrome. An update

1 reference

https://api.crossref.org/works/10.1016%2FS0009-8981%2898%2900177-6

7 January 2021

Identifiers

10.1016/S0009-8981(98)00177-6

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090529%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10090529%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

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