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Volumn 3, Issue 4, 2010, Pages 311-313

Trpm4-linked isolated cardiac conduction defects: Bad trafficking causes electrical gridlock

Author keywords

[No Author keywords available]

Indexed keywords

MYOTONIC DYSTROPHY PROTEIN KINASE; TRANSCRIPTION FACTOR NKX2.5; TRANSCRIPTION FACTOR TBX5; TRANSIENT RECEPTOR POTENTIAL CHANNEL M4;

EID: 78649309395     PISSN: 1942325X     EISSN: 19423268     Source Type: Journal    
DOI: 10.1161/CIRCGENETICS.110.957670     Document Type: Editorial
Times cited : (6)

References (18)
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    • Wood MA, Ellenbogen KA. Cardiology patientPages: cardiac pacemakers from the patient's perspective. Circulation. 2002;105:2136-2138.
    • (2002) Circulation. , vol.105 , pp. 2136-2138
    • Wood, M.A.1    Ellenbogen, K.A.2
  • 2
    • 33645326225 scopus 로고    scopus 로고
    • Inherited conduction system abnormalities: One group of diseases, many genes
    • Wolf CM, Berul CI. Inherited conduction system abnormalities: one group of diseases, many genes. J Cardiovasc Electrophysiol. 2006;17: 446-455.
    • (2006) J Cardiovasc Electrophysiol. , vol.17 , pp. 446-455
    • Wolf, C.M.1    Berul, C.I.2
  • 6
    • 77955548404 scopus 로고    scopus 로고
    • Physiological roles of the TRPM4 channel extracted from background currents
    • Guinamard R, Demion M, Launay P. Physiological roles of the TRPM4 channel extracted from background currents. Physiology. 2010;25: 155-164.
    • Physiology. , vol.2010 , Issue.25 , pp. 155-164
    • Guinamard, R.1    Demion, M.2    Launay, P.3
  • 8
    • 77955232406 scopus 로고    scopus 로고
    • Ubiquitylation and SUMOylation of cardiac ion channels
    • Rougier JS, Albesa M, Abriel H. Ubiquitylation and SUMOylation of cardiac ion channels. J Cardiovasc Pharmacol. 2010;56:22-28.
    • J Cardiovasc Pharmacol. , vol.2010 , Issue.56 , pp. 22-28
    • Rougier, J.S.1    Albesa, M.2    Abriel, H.3
  • 9
    • 22544438468 scopus 로고    scopus 로고
    • Abnormal KCNQ1 trafficking influences disease pathogenesis in hereditary long QT syndromes (LQT1)
    • Wilson AJ, Quinn KV, Graves FM, Bitner-Glindzicz M, Tinker A. Abnormal KCNQ1 trafficking influences disease pathogenesis in hereditary long QT syndromes (LQT1). Cardiovasc Res. 2005;67: 476-486.
    • (2005) Cardiovasc Res. , vol.67 , pp. 476-486
    • Wilson, A.J.1    Quinn, K.V.2    Graves, F.M.3    Bitner-Glindzicz, M.4    Tinker, A.5
  • 10
    • 77955983683 scopus 로고    scopus 로고
    • Rescue of mutated cardiac ion channels in inherited arrhythmia syndromes
    • March 6, Epub ahead of print
    • Balijepalli SY, Anderson CL, Lin EC, January CT. Rescue of mutated cardiac ion channels in inherited arrhythmia syndromes. J Cardiovasc Pharmacol. March 6, 2010 [Epub ahead of print].
    • (2010) J Cardiovasc Pharmacol.
    • Balijepalli, S.Y.1    Anderson, C.L.2    Lin, E.C.3    January, C.T.4
  • 14
    • 41749114920 scopus 로고    scopus 로고
    • Clinical and molecular genetics of the short QT syndrome
    • Schimpf R, Borggrefe M, Wolpert C. Clinical and molecular genetics of the short QT syndrome. Curr Opin Cardiol. 2008;23:192-198.
    • (2008) Curr Opin Cardiol. , vol.23 , pp. 192-198
    • Schimpf, R.1    Borggrefe, M.2    Wolpert, C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.