(Q33175543)

23 July 2017

1 reference

title

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

1 reference

23 July 2017

The Molecular Ggenetics of the Long QT Syndrome: Genes Causing Fainting and Sudden Death (English)

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

13 December 2024

1 reference

1 reference

voltage-gated potassium channel

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:9509262

cation transport proteins

13 December 2024

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:9509262

13 December 2024

trans-activators

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:9509262

13 December 2024

author name string

G. M. Vincent

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC:MED AND EXT_ID:9509262

13 December 2024

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9509262

13 December 2024

publication date

1 January 1998

1 reference

23 July 2017

1998

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=9509262

full work available at URL

13 December 2024

https://www.annualreviews.org/doi/pdf/10.1146/annurev.med.49.1.263

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

Annual Review of Medicine

13 December 2024

published in

1 reference

23 July 2017

volume

49

1 reference

23 July 2017

page(s)

263-274

1 reference

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

23 July 2017

cites work

1

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

ECG T-Wave Patterns in Genetically Distinct Forms of the Hereditary Long QT Syndrome

13 December 2024

5

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

Spectrum of HERG K -channel dysfunction in an inherited cardiac arrhythmia

13 December 2024

6

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

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

13 December 2024

7

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

Heterogeneity in the inherited long QT syndrome

13 December 2024

8

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

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

13 December 2024

9

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

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

13 December 2024

10

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

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

13 December 2024

11

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

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

13 December 2024

12

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

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

13 December 2024

13

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel

13 December 2024

14

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

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

13 December 2024

16

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

A family of potassium channel genes related to eag in Drosophila and mammals

13 December 2024

17

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

Missense mutation in the pore region of HERG causes familial long QT syndrome

13 December 2024

18

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

HERG, a primary human ventricular target of the nonsedating antihistamine terfenadine

13 December 2024

19

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

Evidence for two components of delayed rectifier K current in human ventricular myocytes

13 December 2024

20

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

Class III antiarrhythmic drugs block HERG, a human cardiac delayed rectifier K channel. Open-channel block by methanesulfonanilides

13 December 2024

21

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

Primary structure and functional expression of the human cardiac tetrodotoxin-insensitive voltage-dependent sodium channel

13 December 2024

22

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

Assignment of the human heart tetrodotoxin-resistant voltage-gated Na channel alpha-subunit gene (SCN5A) to band 3p21.

13 December 2024

23

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia.

13 December 2024

24

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

Molecular mechanism for an inherited cardiac arrhythmia

13 December 2024

25

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

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.

13 December 2024

26

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

Early afterdepolarizations: mechanism of induction and block. A role for L-type Ca2 current

13 December 2024

27

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

Electrophysiologic mechanisms of the long QT interval syndromes and torsade de pointes

13 December 2024

28

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

cAMP compartmentation is responsible for a local activation of cardiac Ca2 channels by beta-adrenergic agonists

13 December 2024

29

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

Risk of cardiac events in family members of patients with long QT syndrome.

13 December 2024

30

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

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

13 December 2024

31

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

Effects of exercise on heart rate, QT, QTc and QT/QS2 in the Romano-Ward inherited long QT syndrome

13 December 2024

32

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

Dispersion of the QT interval. A marker of therapeutic efficacy in the idiopathic long QT syndrome

13 December 2024

34

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

T wave "humps" as a potential electrocardiographic marker of the long QT syndrome

13 December 2024

37

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

Quantitative analysis of T wave abnormalities and their prognostic implications in the idiopathic long QT syndrome.

13 December 2024

38

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

T wave alternans in idiopathic long QT syndrome

13 December 2024

39

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

Diagnostic criteria for the long QT syndrome. An update

13 December 2024

40

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

Diurnal pattern of QTc interval: how long is prolonged? Possible relation to circadian triggers of cardiovascular events

13 December 2024

41

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

Genetically defined therapy of inherited long-QT syndrome. Correction of abnormal repolarization by potassium

13 December 2024

45

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

Prevention of class III-induced proarrhythmias by flecainide in an animal model of the acquired long QT syndrome

13 December 2024

46

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

Nicorandil suppresses a hump on the monophasic action potential and torsade de pointes in a patient with idiopathic long QT syndrome

13 December 2024

47

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

Early Afterdepolarization Abolished by Potassium Channel Opener in a Patient with Idiopathic Long QT Syndrome

13 December 2024

49

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

Effects of verapamil and propranolol on early afterdepolarizations and ventricular arrhythmias induced by epinephrine in congenital long QT syndrome

13 December 2024

50

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

Differential response to Na channel blockade, beta-adrenergic stimulation, and rapid pacing in a cellular model mimicking the SCN5A and HERG defects present in the long-QT syndrome

13 December 2024

51

1 reference

https://api.crossref.org/works/10.1146/ANNUREV.MED.49.1.263

13 December 2024

Identifiers

1 reference

23 July 2017

1 reference