메뉴 건너뛰기




Volumn 7, Issue 9, 2001, Pages 1021-1027

Abrupt rate accelerations or premature beats cause life-threatening arrhythmias in mice with long-QT3 syndrome

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; SODIUM CHANNEL;

EID: 0034800266     PISSN: 10788956     EISSN: None     Source Type: Journal    
DOI: 10.1038/nm0901-1021     Document Type: Article
Times cited : (228)

References (40)
  • 1
    • 0028101967 scopus 로고
    • Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity
    • (1994) Nature Genet , vol.8 , pp. 141-147
    • Jiang, C.1
  • 2
    • 0028905566 scopus 로고
    • SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome
    • (1995) Cell , vol.80 , pp. 805-811
    • Wang, Q.1
  • 4
    • 0023637449 scopus 로고
    • Circadian variation in the incidence of sudden cardiac death in the Framingham Heart Study population
    • (1987) Am. J. Cardiol , vol.60 , pp. 801-806
    • Willich, S.N.1
  • 6
    • 0034721235 scopus 로고    scopus 로고
    • A molecular link between the sudden infant death syndrome and the long-QT syndrome
    • (2000) N. Engl. J. Med , vol.343 , pp. 262-267
    • Schwartz, P.J.1
  • 9
    • 0033530381 scopus 로고    scopus 로고
    • Long QT syndromes and torsade de pointes
    • (1999) Lancet , vol.354 , pp. 1625-1633
    • Viskin, S.1
  • 11
    • 0032189139 scopus 로고    scopus 로고
    • Influence of genotype on the clinical course of the long-QT syndrome
    • International Long-QT Syndrome Registry Research Group
    • (1998) N. Engl. J. Med , vol.339 , pp. 960-965
    • Zareba, W.1
  • 12
    • 0028874658 scopus 로고
    • + channel blockade and to increases in heart rate. Implications for gene-specific therapy
    • (1995) Circulation , vol.92 , pp. 3381-3386
    • Schwartz, P.J.1
  • 13
    • 0035830365 scopus 로고    scopus 로고
    • Genotype-phenotype correlation in the long-QT syndrome: Gene-specific triggers for life-threatening arrhythmias
    • (2001) Circulation , vol.103 , pp. 89-95
    • Schwartz, P.J.1
  • 22
    • 0033527032 scopus 로고    scopus 로고
    • Linking a genetic defect to its cellular phenotype in a cardiac arrhythmia
    • (1999) Nature , vol.400 , pp. 566-569
    • Clancy, C.E.1    Rudy, Y.2
  • 24
    • 0030024562 scopus 로고    scopus 로고
    • Developmental changes in ionic channel activity in the embryonic murine heart
    • (1996) Circ. Res , vol.78 , pp. 15-25
    • Davies, M.P.1
  • 25
    • 0028861892 scopus 로고
    • ECG T-wave patterns in genetically distinct forms of the hereditary long QT syndrome
    • (1995) Circulation , vol.92 , pp. 2929-2934
    • Moss, A.J.1
  • 28
    • 0032514164 scopus 로고    scopus 로고
    • + channel in heart rate control of repolarization in a murine engineered model of Jervell and Lange-Nielsen syndrome
    • (1998) Circ. Res , vol.83 , pp. 95-102
    • Drici, M.D.1
  • 37
    • 0032546384 scopus 로고    scopus 로고
    • Genetic basis and molecular mechanism for idiopathic ventricular fibrillation
    • (1998) Nature , vol.392 , pp. 293-296
    • Chen, Q.1
  • 39
    • 0032925156 scopus 로고    scopus 로고
    • Impaired myocardial angiogenesis and ischemic cardiomyopathy in mice lacking the vascular endothelial growth factor isoforms VEGF164 and VEGF188
    • (1999) Nature Med , vol.5 , pp. 495-502
    • Carmeliet, P.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.