메뉴 건너뛰기
Genetic Testing
Volumn 12, Issue 4, 2008, Pages 467-469
NKX2.5/NKX2.6 mutations are not a common cause of isolated type 1 truncus arteriosus in a small cohort of multiethnic cases
Author keywords

[No Author keywords available]
Indexed keywords

DNA; TRANSCRIPTION FACTOR NKX2.5;
EID: 57749114568     PISSN: 10906576     EISSN: None     Source Type: Journal    
DOI: 10.1089/gte.2007.0122     Document Type: Letter
Times cited : (5)
References (11)
  • 1
    • 0033430230 scopus 로고    scopus 로고
    • Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways
    • Benson DW, Silberbach GM, Kavanaugh-McHugh A, et al. (1999) Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways. J Clin Invest 104:1567-1573.
    • (1999) J Clin Invest , vol.104 , pp. 1567-1573
    • Benson, D.W.1    Silberbach, G.M.2    Kavanaugh-McHugh, A.3
  • 2
    • 14644441750 scopus 로고    scopus 로고
    • Common arterial trunk associated with a homeodomain mutation of NKX2.6
    • Heathcote K, Braybrook C, Guy M, et al. (2005) Common arterial trunk associated with a homeodomain mutation of NKX2.6. Hum Mol Genet 14:585-593.
    • (2005) Hum Mol Genet , vol.14 , pp. 585-593
    • Heathcote, K.1    Braybrook, C.2    Guy, M.3
  • 3
    • 0037134945 scopus 로고    scopus 로고
    • The incidence of congenital heart disease
    • Hoffman JIE, Kaplan S (2002) The incidence of congenital heart disease. J Am Coll Cardiol 39:1890-1900.
    • (2002) J Am Coll Cardiol , vol.39 , pp. 1890-1900
    • Hoffman, J.I.E.1    Kaplan, S.2
  • 4
    • 0242636701 scopus 로고    scopus 로고
    • NKX2.5 mutations in patients with congenital heart disease
    • McElhinney DB, Geiger E, Blinder J, et al. (2003) NKX2.5 mutations in patients with congenital heart disease. J Am Coll Cardiol 42:1650-1655.
    • (2003) J Am Coll Cardiol , vol.42 , pp. 1650-1655
    • McElhinney, D.B.1    Geiger, E.2    Blinder, J.3
  • 5
    • 0031406027 scopus 로고    scopus 로고
    • NKX2.6 expression is transiently and specifically restricted to the branchial of pharyngeal-stage mouse embryos
    • Nikolova M, Chen X, Lufkin T (1997) NKX2.6 expression is transiently and specifically restricted to the branchial of pharyngeal-stage mouse embryos. Mech Dev 69:215-218.
    • (1997) Mech Dev , vol.69 , pp. 215-218
    • Nikolova, M.1    Chen, X.2    Lufkin, T.3
  • 6
    • 0035992788 scopus 로고    scopus 로고
    • Developmental paradigms in heart disease: Insights from tinman
    • Prall OW, Elliot DA, Harvey RP (2002) Developmental paradigms in heart disease: insights from tinman. Ann Med 34:148-156.
    • (2002) Ann Med , vol.34 , pp. 148-156
    • Prall, O.W.1    Elliot, D.A.2    Harvey, R.P.3
  • 7
    • 0033524814 scopus 로고    scopus 로고
    • Molecular genetics of congenital heart disease: A problem of faulty septation
    • Schiaffino S, Dallapiccola B, Di Lisi R (1999) Molecular genetics of congenital heart disease: a problem of faulty septation. Circ Res 84:247-249.
    • (1999) Circ Res , vol.84 , pp. 247-249
    • Schiaffino, S.1    Dallapiccola, B.2    Di Lisi, R.3
  • 8
    • 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. (1998) Congenital heart disease caused by mutations in the transcription factor NKX2.5. Science 28:108-111.
    • (1998) Science , vol.28 , pp. 108-111
    • Schott, J.J.1    Benson, D.W.2    Basson, C.T.3
  • 9
    • 0034648772 scopus 로고    scopus 로고
    • A genetic blueprint for cardiac development
    • Srivastava D, Olson EN (2000) A genetic blueprint for cardiac development. Nature 407:221-226.
    • (2000) Nature , vol.407 , pp. 221-226
    • Srivastava, D.1    Olson, E.N.2
  • 10
    • 0034115494 scopus 로고    scopus 로고
    • Phenotypic characterization of the murine NKX2.6 homeobox gene by gene targeting
    • Tanaka M, Yamasaki N, Izumo S (2000) Phenotypic characterization of the murine NKX2.6 homeobox gene by gene targeting. Mol Cell Biol 20:2874-2879.
    • (2000) Mol Cell Biol , vol.20 , pp. 2874-2879
    • Tanaka, M.1    Yamasaki, N.2    Izumo, S.3
  • 11
    • 17144391123 scopus 로고    scopus 로고
    • The keeshond defect in cardiac conotruncal development is oligogenic
    • Werner P, Raducha MG, Procuik U, et al. (2005) The keeshond defect in cardiac conotruncal development is oligogenic. Hum Genet 116:368-377.
    • (2005) Hum Genet , vol.116 , pp. 368-377
    • Werner, P.1    Raducha, M.G.2    Procuik, U.3

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.