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Volumn 43, Issue 2, 2002, Pages 245-254

The KVLQT1 gene is not a common target for mutations in patients with various heart pathologies

Author keywords

KCNQ1 gene; KVLQT1 gene; Long QT Syndrome; mSSCP analysis; Mutation; Potassium channel

Indexed keywords

KCNQ1 PROTEIN, HUMAN; POTASSIUM CHANNEL; POTASSIUM CHANNEL KCNQ; POTASSIUM CHANNEL KCNQ1; VOLTAGE GATED POTASSIUM CHANNEL;

EID: 0036043904     PISSN: 12341983     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (4)

References (24)
  • 5
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    • Suppresion of slow delayed rectifier current by truncated isoform of KVLQT1 cloned from normal human heart
    • JIANG M., TSENG-CRANK J., TSENG G.N. (1997). Suppresion of slow delayed rectifier current by truncated isoform of KVLQT1 cloned from normal human heart. J. Biol. Chem. 272: 24109-24112.
    • (1997) J. Biol. Chem. , vol.272 , pp. 24109-24112
    • Jiang, M.1    Tseng-Crank, J.2    Tseng, G.N.3
  • 6
    • 0034710954 scopus 로고    scopus 로고
    • Channel structure and drug-induced cardiac arrhythmia
    • USA
    • KASS R.S., CABO C. (2000). Channel structure and drug-induced cardiac arrhythmia. Proc. Natl. Acad. Sci. USA 97(22): 11683-11684.
    • (2000) Proc. Natl. Acad. Sci. , vol.97 , Issue.22 , pp. 11683-11684
    • Kass, R.S.1    Cabo, C.2
  • 7
    • 0025847714 scopus 로고
    • Linkage of cardiac arrhythmia, the long QT syndrome and the Harvey ras-1 gene
    • KEATING M., ATKINSON D., DUNN C., TIMOTHY K., VINCENT G.M., LEPPERT M. (1991). Linkage of cardiac arrhythmia, the long QT syndrome and the Harvey ras-1 gene. Science 252: 704-706.
    • (1991) Science , vol.252 , pp. 704-706
    • Keating, M.1    Atkinson, D.2    Dunn, C.3    Timothy, K.4    Vincent, G.M.5    Leppert, M.6
  • 8
    • 0031046285 scopus 로고    scopus 로고
    • Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements
    • LEE M.P., HU R.J., JOHNSON L.A., FEINBERG A.P. (1997). Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements. Nat. Genet. 15: 181-185.
    • (1997) Nat. Genet. , vol.15 , pp. 181-185
    • Lee, M.P.1    Hu, R.J.2    Johnson, L.A.3    Feinberg, A.P.4
  • 10
    • 0034213745 scopus 로고    scopus 로고
    • + channel diversity in the mammalian myocardium
    • + channel diversity in the mammalian myocardium. J. Physiol. 525: 285-298.
    • (2000) J. Physiol. , vol.525 , pp. 285-298
    • Nerbonne, J.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.