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Volumn 89, Issue 16, 2009, Pages 1114-1116

Preliminary exploration of transcription factor Nkx2.5 mutations and congenital heart diseases

Author keywords

Gene mutation; Heart disease, congenital; Nkx2.5 gene

Indexed keywords

DNA; TRANSCRIPTION FACTOR GATA 4; TRANSCRIPTION FACTOR NKX2.5; TRANSCRIPTION FACTOR TBX5;

EID: 73449131415     PISSN: 03762491     EISSN: None     Source Type: Journal    
DOI: 10.3760/cma.j.issn.0376-2491.2009.16.011     Document Type: Article
Times cited : (5)

References (14)
  • 1
    • 0037134945 scopus 로고    scopus 로고
    • The incidence of congenital heart disease
    • Hoffman JI, Kaplan S. The incidence of congenital heart disease. J Am Coll Cardiol, 2002,39:1890-1900.
    • (2002) J Am Coll Cardiol , vol.39 , pp. 1890-1900
    • Hoffman, J.I.1    Kaplan, S.2
  • 2
    • 0242636701 scopus 로고    scopus 로고
    • NKX2.5 mutation in patients with congenital heart disease
    • McElhinney DB, Geiger E, Blinder J, et al. NKX2.5 mutation in patients with congenital heart disease. J Am Coll Cardiol, 2003,42:1650-1655.
    • (2003) J Am Coll Cardiol , vol.42 , pp. 1650-1655
    • McElhinney, D.B.1    Geiger, E.2    Blinder, J.3
  • 3
    • 21344435944 scopus 로고    scopus 로고
    • Cardiac transcription factor Csx/Nkx2-5: Its role in cardiac development and diseases
    • Akazawa H, Komuro I. Cardiac transcription factor Csx/Nkx2-5: its role in cardiac development and diseases. Pharmacol Ther, 2005,107:252-268.
    • (2005) Pharmacol Ther , vol.107 , pp. 252-268
    • Akazawa, H.1    Komuro, I.2
  • 4
    • 0035923555 scopus 로고    scopus 로고
    • NKX2.5 mutations in patients with tetralogy of fallot
    • Elizabeth G, Elizabeth GD, Woodrow B. NKX2.5 mutations in patients with tetralogy of fallot. Circulation, 2001,104:2565-2568.
    • (2001) Circulation , vol.104 , pp. 2565-2568
    • Elizabeth, G.1    Elizabeth, G.D.2    Woodrow, B.3
  • 5
    • 33847261472 scopus 로고    scopus 로고
    • Re-employment of developmental transcription factors in adult heart disease
    • Oka T, Xu J, Molkentin JD. Re-employment of developmental transcription factors in adult heart disease. Semin Cell Dev Biol, 2007,18:117-131.
    • (2007) Semin Cell Dev Biol , vol.18 , pp. 117-131
    • Oka, T.1    Xu, J.2    Molkentin, J.D.3
  • 6
    • 0032479573 scopus 로고    scopus 로고
    • Congenital heart disease caused by mutations in the transcription factor NKX2.5
    • Schott JJ, Benson DW, Basson CT, et al. Congenital heart disease caused by mutations in the transcription factor NKX2.5. Science, 1998,281:108-111.
    • (1998) Science , vol.281 , pp. 108-111
    • Schott, J.J.1    Benson, D.W.2    Basson, C.T.3
  • 7
    • 33751306550 scopus 로고    scopus 로고
    • A novel CSX/NKX2-5 mutation causes autosomal-dominant AV block: Are atrial fibrillation and syncopes part of the phenotype?
    • Gutierrez-Roelens I, De Roy L, Ovaert C, et al. A novel CSX/NKX2-5 mutation causes autosomal-dominant AV block: are atrial fibrillation and syncopes part of the phenotype? Eur J Hum Genet, 2006,14:1313-1316.
    • (2006) Eur J Hum Genet , vol.14 , pp. 1313-1316
    • Gutierrez-Roelens, I.1    De Roy, L.2    Ovaert, C.3
  • 8
    • 2442705544 scopus 로고    scopus 로고
    • Novel NKX2-5 mutations in diseased heart tissues of patients with cardiac malformations
    • Reamon-Buettner SM, Hecker H, Spanel-Borowski K, et al. Novel NKX2-5 mutations in diseased heart tissues of patients with cardiac malformations. Am J Pathol, 2004,164:2117-2125.
    • (2004) Am J Pathol , vol.164 , pp. 2117-2125
    • Reamon-Buettner, S.M.1    Hecker, H.2    Spanel-Borowski, K.3
  • 9
    • 20944442976 scopus 로고    scopus 로고
    • Phenotypes with GATA4 or NKX2.5 mutations in familial atrial septal defect
    • Hirayama-Yamada K, Kamisago M, Akimoto K, et al. Phenotypes with GATA4 or NKX2.5 mutations in familial atrial septal defect. Am J Med Genet A, 2005,135:47-52.
    • (2005) Am J Med Genet A , vol.135 , pp. 47-52
    • Hirayama-Yamada, K.1    Kamisago, M.2    Akimoto, K.3
  • 10
    • 77954890914 scopus 로고    scopus 로고
    • Chinese source
  • 11
    • 77954937014 scopus 로고    scopus 로고
    • Missense mutations in CSX/NKX2.5 are associated with atrial septal defects
    • Li T, Zhu JF, Yang JG, et al. Missense mutations in CSX/NKX2.5 are associated with atrial septal defects. J Nanjing Med Univ, 2007,21:218-221.
    • (2007) J Nanjing Med Univ , vol.21 , pp. 218-221
    • Li, T.1    Zhu, J.F.2    Yang, J.G.3
  • 12
    • 77954931339 scopus 로고    scopus 로고
    • Chinese source
  • 13
    • 0035895925 scopus 로고    scopus 로고
    • Characterization of Homo- And Heterodimerization of Cardiac Csx/Nkx2.5 Homoprotein
    • Kasahara H, Usheva A, Ueyama T, et al. Characterization of Homo- and Heterodimerization of Cardiac Csx/Nkx2.5 Homoprotein. J Biol Chem, 2001,276:4570-4580.
    • (2001) J Biol Chem , vol.276 , pp. 4570-4580
    • Kasahara, H.1    Usheva, A.2    Ueyama, T.3
  • 14
    • 3142566471 scopus 로고    scopus 로고
    • GATA transcription factors in the developing and adult heart
    • Pikkarainen S, Tokola H, Kerkela R, et al. GATA transcription factors in the developing and adult heart. Circ Res, 2004,63:196-207.
    • (2004) Circ Res , vol.63 , pp. 196-207
    • Pikkarainen, S.1    Tokola, H.2    Kerkela, R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.