(Q33148068)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12209021%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

title

A novel SCN5A mutation associated with long QT-3: altered inactivation kinetics and channel dysfunction (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12209021%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12209021%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

author name string

Ilaria Rivolta

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12209021%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

Colleen E Clancy

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12209021%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

Huajun Liu

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12209021%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

Silvia G Priori

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12209021%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

Robert S Kass

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12209021%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

publication date

3 September 2002

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12209021%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

published in

Physiological Genomics

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12209021%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

volume

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12209021%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12209021%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

page(s)

191-197

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:12209021%20AND%20SRC:MED&resulttype=core&format=json

Novel arrhythmogenic mechanism revealed by a long-QT syndrome mutation in the cardiac Na(+) channel.

12 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00039.2002

Novel LQT-3 mutation affects Na+ channel activity through interactions between alpha- and beta1-subunits

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00039.2002

The steady state TTX-sensitive ("window") sodium current in cardiac Purkinje fibres

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00039.2002

Molecular mechanism for an inherited cardiac arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00039.2002

Single sodium channels from canine ventricular myocytes: voltage dependence and relative rates of activation and inactivation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00039.2002

Cardiac sodium channel and inherited arrhythmia syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00039.2002

Functional expression of sodium channel mutations identified in families with periodic paralysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00039.2002

Na(+) channel mutation that causes both Brugada and long-QT syndrome phenotypes: a simulation study of mechanism

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00039.2002

Multiple mechanisms of Na+ channel--linked long-QT syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00039.2002

Direct measurement of L-type Ca2+ window current in heart cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00039.2002

Phenotypic characterization of a novel long-QT syndrome mutation (R1623Q) in the cardiac sodium channel.

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00039.2002

Molecular and cellular mechanisms of cardiac arrhythmias

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00039.2002

Role of the C-terminal domain in inactivation of brain and cardiac sodium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00039.2002

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00039.2002

Subconductance states of a mutant NMDA receptor channel kinetics, calcium, and voltage dependence

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00039.2002

Estimating single-channel kinetic parameters from idealized patch-clamp data containing missed events

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00039.2002

Inherited long QT syndromes: a paradigm for understanding arrhythmogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00039.2002

A Met-to-Val mutation in the skeletal muscle Na+ channel alpha-subunit in hyperkalaemic periodic paralysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00039.2002

Cardiac conduction defects associate with mutations in SCN5A

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00039.2002

Characterization of human cardiac Na+ channel mutations in the congenital long QT syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00039.2002

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00039.2002

De novo mutation in the SCN5A gene associated with early onset of sudden infant death

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00039.2002

Linking a genetic defect to its cellular phenotype in a cardiac arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00039.2002