(Q73858925)

English

Homozygosity for a HERG potassium channel mutation causes a severe form of long QT syndrome: identification of an apparent founder mutation in the Finns

scientific article published on 01 June 2000

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10841244%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

Homozygosity for a HERG potassium channel mutation causes a severe form of long QT syndrome: identification of an apparent founder mutation in the Finns (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10841244%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

long QT syndrome

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

9

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10841244%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

author name string

K Piippo

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10841244%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

P Laitinen

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10841244%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

H Swan

3

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10841244%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

L Toivonen

4

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10841244%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

M Viitasalo

5

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10841244%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

M Pasternack

6

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10841244%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

K Paavonen

7

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10841244%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

H Chapman

8

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10841244%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

E Hirvelä

10

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10841244%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

A Sajantila

11

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10841244%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

K Kontula

12

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10841244%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

language of work or name

0 references

publication date

1 June 2000

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10841244%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

Journal of the American College of Cardiology

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10841244%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

35

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10841244%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

7

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10841244%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

1919-1925

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10841244%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

The long Q-T syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900636-7

7 January 2021

based on heuristic

inferred from DOI database lookup

The molecular genetics of the long QT syndrome: genes causing fainting and sudden death

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900636-7

7 January 2021

based on heuristic

inferred from DOI database lookup

CONGENITAL CARDIAC ARRHYTHMIA

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900636-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval and sudden death

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900636-7

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

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900636-7

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

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900636-7

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

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900636-7

7 January 2021

based on heuristic

inferred from DOI database lookup

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%2FS0735-1097%2800%2900636-7

7 January 2021

based on heuristic

inferred from DOI database lookup

KCNE1 mutations cause jervell and Lange-Nielsen syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900636-7

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

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900636-7

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

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900636-7

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

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900636-7

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900636-7

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

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900636-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular genetics of the long QT syndrome: two novel mutations of the KVLQT1 gene and phenotypic expression of the mutant gene in a large kindred

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900636-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Sinus node function and ventricular repolarization during exercise stress test in long QT syndrome patients with KvLQT1 and HERG potassium channel defects.

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900636-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Genomic organization and mutational analysis of HERG, a gene responsible for familial long QT syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900636-7

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

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900636-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Time course and voltage dependence of expressed HERG current compared with native "rapid" delayed rectifier K current during the cardiac ventricular action potential

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900636-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Role of transmembrane segment S5 on gating of voltage-dependent K+ channels

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900636-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Regulation of deactivation by an amino terminal domain in human ether-à-go-go-related gene potassium channels

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900636-7

7 January 2021

based on heuristic

inferred from DOI database lookup

The long QT syndrome with impaired atrioventricular conduction: a malignant variant in infants.

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900636-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Age- and sex-related differences in clinical manifestations in patients with congenital long-QT syndrome: findings from the International LQTS Registry.

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900636-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Influence of the genotype on the clinical course of the long-QT syndrome. International Long-QT Syndrome Registry Research Group.

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900636-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Cardiac actions of erythromycin: influence of female sex.

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900636-7

7 January 2021

based on heuristic

inferred from DOI database lookup

JTc prolongation with d,l-sotalol in women versus men

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900636-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Effects of 17beta-estradiol on tachycardia-induced changes of atrial refractoriness and cisapride-induced ventricular arrhythmia

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900636-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Paternal and maternal DNA lineages reveal a bottleneck in the founding of the Finnish population

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900636-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Dual origins of Finns revealed by Y chromosome haplotype variation

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900636-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Evidence of a long QT founder gene with varying phenotypic expression in South African families

1 reference

https://api.crossref.org/works/10.1016%2FS0735-1097%2800%2900636-7

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0735-1097(00)00636-7

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10841244%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10841244%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q73858925&oldid=2041752207"