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Volumn 6, Issue 9, 2000, Pages 968-970

Listening for hoof beats in heart beats

Author keywords

[No Author keywords available]

Indexed keywords

CONNEXIN 40; ENDOTHELIN 1; HOMEODOMAIN PROTEIN; LEUCINE ZIPPER PROTEIN; MYOSIN HEAVY CHAIN; TRANSCRIPTION FACTOR HF 1B; TRANSCRIPTION FACTOR SP1; UNCLASSIFIED DRUG;

EID: 0033830794     PISSN: 10788956     EISSN: None     Source Type: Journal    
DOI: 10.1038/79652     Document Type: Article
Times cited : (3)

References (10)
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  • 2
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    • Functional effects of mutations in KvLQT1 that cause long QT syndrome
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    • (1999) J. Cardiovasc. Electrophysiol. , vol.10 , pp. 817-826
    • Wang, Z.1
  • 3
    • 0031916794 scopus 로고    scopus 로고
    • The long QT syndrome: Ion channel diseases of the heart
    • Ackerman, M.J. The long QT syndrome: ion channel diseases of the heart. Mayo Clin. Proc. 73, 250-269 (1998).
    • (1998) Mayo Clin. Proc. , vol.73 , pp. 250-269
    • Ackerman, M.J.1
  • 4
    • 0032479573 scopus 로고    scopus 로고
    • Congenital heart disease caused by mutations in the transcription factor NKX2-5
    • Schott, J.J. et al. Congenital heart disease caused by mutations in the transcription factor NKX2-5. Science 281, 108-111 (1998).
    • (1998) Science , vol.281 , pp. 108-111
    • Schott, J.J.1
  • 5
    • 0030636780 scopus 로고    scopus 로고
    • Mutations in human TBX5 cause limb and cardiac malformation in holt-oram syndrome
    • Basson, C.T. et al. Mutations in human TBX5 cause limb and cardiac malformation in Holt-Oram syndrome. Nature Genet. 15, 30-35 (1997).
    • (1997) Nature Genet. , vol.15 , pp. 30-35
    • Basson, C.T.1
  • 6
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    • A novel genetic pathway for sudden cardiac death via defects in the transition between ventricular and conduction system cell lineages
    • in the press
    • Nguyen-Tran, V.T.B. et al. A novel genetic pathway for sudden cardiac death via defects in the transition between ventricular and conduction system cell lineages. Cell, (in the press).
    • Cell
    • Nguyen-Tran, V.T.B.1
  • 7
    • 0029944159 scopus 로고    scopus 로고
    • Sp4, a member of the Sp1-family of zinc finger transcription factors, is required for normal murine growth, viability, and male fertility
    • Supp, D.M., Witte, D.P., Branford, W.W., Smith, E.P. & Potter, S.S. Sp4, a member of the Sp1-family of zinc finger transcription factors, is required for normal murine growth, viability, and male fertility. Dev. Biol. 176, 284-299 (1996).
    • (1996) Dev. Biol. , vol.176 , pp. 284-299
    • Supp, D.M.1    Witte, D.P.2    Branford, W.W.3    Smith, E.P.4    Potter, S.S.5
  • 8
    • 0033825398 scopus 로고    scopus 로고
    • In vivo induction of cardiac Purkinje fiber differentiation by co-expression of preproendothelin-1 and endothelin converting enzyme-1
    • Takebayashi-Suzuki, K., Yanagisawa, M., Gourdie, R.G., Kanzawa, N. & Mikawa, T. In vivo induction of cardiac Purkinje fiber differentiation by co-expression of preproendothelin-1 and endothelin converting enzyme-1. Development 127, 3523-3532 (2000).
    • (2000) Development , vol.127 , pp. 3523-3532
    • Takebayashi-Suzuki, K.1    Yanagisawa, M.2    Gourdie, R.G.3    Kanzawa, N.4    Mikawa, T.5
  • 9
    • 0033524661 scopus 로고    scopus 로고
    • Replacement by homologous recombination of the mink gene with lacZ reveals restriction of minK expression to the mouse cardiac conduction system
    • Kupershmidt, S. et al. Replacement by homologous recombination of the minK gene with lacZ reveals restriction of minK expression to the mouse cardiac conduction system. Circ. Res. 84, 146-152 (1999).
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    • Kupershmidt, S.1
  • 10
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    • Myofibril degeneration caused by tropomodulin overexpression leads to dilated cardiomyopathy in juvenile mice
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    • Sussman, M.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.