메뉴 건너뛰기




Volumn 100, Issue 5, 2007, Pages 484-489

Molecular aspects of congenital heart diseases;Bases moléculaires des cardiopathies congénitales humaines

Author keywords

[No Author keywords available]

Indexed keywords

CARDIOLOGIST; CLINICAL FEATURE; CONGENITAL HEART MALFORMATION; DISEASE COURSE; FALLOT TETRALOGY; GENE IDENTIFICATION; GENE INACTIVATION; GENETIC HETEROGENEITY; GREAT VESSELS TRANSPOSITION; HEART DEVELOPMENT; HEREDITY; HUMAN; HYPOPLASIA; LUNG ATRESIA; MOLECULAR BIOLOGY; NONHUMAN; PEDIATRICIAN; PHENOTYPE; REVIEW;

EID: 34347386066     PISSN: 00039683     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review
Times cited : (5)

References (30)
  • 1
    • 1242342762 scopus 로고    scopus 로고
    • Development gone awry: Congenital heart disease
    • Gruber PJ, Epstein JA. Development gone awry: congenital heart disease. Circ Res 2004;94:273-83.
    • (2004) Circ Res , vol.94 , pp. 273-283
    • Gruber, P.J.1    Epstein, J.A.2
  • 2
    • 20144387341 scopus 로고    scopus 로고
    • Mutation in myosin heavy chain 6 causes atrial septal defect
    • Ching YH, Ghosh TK, Cross SJ, et al. Mutation in myosin heavy chain 6 causes atrial septal defect. Nat Genet 2005;37:423-8.
    • (2005) Nat Genet , vol.37 , pp. 423-428
    • Ching, Y.H.1    Ghosh, T.K.2    Cross, S.J.3
  • 3
    • 0037155776 scopus 로고    scopus 로고
    • Transcriptional regulation of vertebrate cardiac morphogenesis
    • Bruneau BG. Transcriptional regulation of vertebrate cardiac morphogenesis. Circ Res 2002;90:509-19.
    • (2002) Circ Res , vol.90 , pp. 509-519
    • Bruneau, B.G.1
  • 4
    • 29044437301 scopus 로고    scopus 로고
    • Odd-skipped related 1 (Odd 1) is an essential regulator of heart and urogenital development
    • Wang Q, Lan Y, Cho ES, Maitby KM, Jiang R. Odd-skipped related 1 (Odd 1) is an essential regulator of heart and urogenital development. Dev Biol 2005;288:582-94.
    • (2005) Dev Biol , vol.288 , pp. 582-594
    • Wang, Q.1    Lan, Y.2    Cho, E.S.3    Maitby, K.M.4    Jiang, R.5
  • 5
  • 6
    • 19444371444 scopus 로고    scopus 로고
    • Dissecting contiguous gene defects: TBX1
    • Baldini A. Dissecting contiguous gene defects: TBX1. Curr Opin Genet Dev 2005;15:279-84.
    • (2005) Curr Opin Genet Dev , vol.15 , pp. 279-284
    • Baldini, A.1
  • 7
    • 10744226877 scopus 로고    scopus 로고
    • Mutations of ZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot
    • Pizzuti A, Sarkozy A, Newton AL, et al. Mutations of ZFPM2/FOG2 gene in sporadic cases of tetralogy of Fallot. Hum Mutat. 2003;22:372-7.
    • (2003) Hum Mutat , vol.22 , pp. 372-377
    • Pizzuti, A.1    Sarkozy, A.2    Newton, A.L.3
  • 8
    • 0035923555 scopus 로고    scopus 로고
    • NKX2.5 mutations in patients with tetralogy of Fallot
    • Goldmuntz E, Geiger E, Benson DW. NKX2.5 mutations in patients with tetralogy of Fallot. Circulation 2001;104:2565-8.
    • (2001) Circulation , vol.104 , pp. 2565-2568
    • Goldmuntz, E.1    Geiger, E.2    Benson, D.W.3
  • 9
    • 0036179821 scopus 로고    scopus 로고
    • CFC1 mutations in patients with transposition of the great arteries and double-outlet right ventricle
    • Goldmuntz E, Bamford R, Karkera JD, dela Cruz J, Roessler E, Muenke M. CFC1 mutations in patients with transposition of the great arteries and double-outlet right ventricle. Am J Hum Genet. 2002;70:776-80.
    • (2002) Am J Hum Genet , vol.70 , pp. 776-780
    • Goldmuntz, E.1    Bamford, R.2    Karkera, J.D.3    dela Cruz, J.4    Roessler, E.5    Muenke, M.6
  • 10
    • 0344736940 scopus 로고    scopus 로고
    • Missense mutations and gene interruption in PROSIT240 a novel TRAP240-like gene, in patients with congenital heart defect (transposition of the great arteries)
    • Muncke N, Jung C, Rudiger H, et al. Missense mutations and gene interruption in PROSIT240 a novel TRAP240-like gene, in patients with congenital heart defect (transposition of the great arteries). Circulation 2003;108:2843-50.
    • (2003) Circulation , vol.108 , pp. 2843-2850
    • Muncke, N.1    Jung, C.2    Rudiger, H.3
  • 11
    • 0033822768 scopus 로고    scopus 로고
    • X linked transposition of the great arteries and incomplete penetrance among males with a nonsense mutation in ZIC3
    • Megarbane A, Salem N, Stephan E, et al. X linked transposition of the great arteries and incomplete penetrance among males with a nonsense mutation in ZIC3. Eur J Hum Genet. 2000;8:704-8.
    • (2000) Eur J Hum Genet , vol.8 , pp. 704-708
    • Megarbane, A.1    Salem, N.2    Stephan, E.3
  • 12
    • 33646810876 scopus 로고    scopus 로고
    • Rotation of the myocardial wall of the outflow tract is implicated in the normal positioning of the great arteries
    • Bajolle F, Zaffran S, Kelly RG, et al. Rotation of the myocardial wall of the outflow tract is implicated in the normal positioning of the great arteries. Circ Res 2006; 98:421-8.
    • (2006) Circ Res , vol.98 , pp. 421-428
    • Bajolle, F.1    Zaffran, S.2    Kelly, R.G.3
  • 13
    • 33746926015 scopus 로고    scopus 로고
    • Forkhead transcription factors, Foxcl and Foxc2, are required for the morphogenesis of the cardiac outflow tract
    • Seo S, Kume T. Forkhead transcription factors, Foxcl and Foxc2, are required for the morphogenesis of the cardiac outflow tract. Dev Biol 2006;296:421-36.
    • (2006) Dev Biol , vol.296 , pp. 421-436
    • Seo, S.1    Kume, T.2
  • 14
    • 33748754729 scopus 로고    scopus 로고
    • Bajolle F, Bonnet D. Malformations obstructives du cceur gauche et génétique. Arch Mal Coeur 2006; 99:494-6.
    • Bajolle F, Bonnet D. Malformations obstructives du cceur gauche et génétique. Arch Mal Coeur 2006; 99:494-6.
  • 15
    • 24644467759 scopus 로고    scopus 로고
    • Mutations in NOTCH1 cause aortic valve disease
    • Garg V, Muth AN, Ransom JF, et al. Mutations in NOTCH1 cause aortic valve disease. Nature 2005;437:270-4.
    • (2005) Nature , vol.437 , pp. 270-274
    • Garg, V.1    Muth, A.N.2    Ransom, J.F.3
  • 16
    • 13444281898 scopus 로고    scopus 로고
    • Cardiovascular anomalies in children and young adults with Ullrich-Turner syndrome the Erlangen experience
    • Volkl TM, Degenhardt K, Koch A Simm D, Dorr HG, Singer H. Cardiovascular anomalies in children and young adults with Ullrich-Turner syndrome the Erlangen experience. Clin Cardiol 2005;28:88-92.
    • (2005) Clin Cardiol , vol.28 , pp. 88-92
    • Volkl, T.M.1    Degenhardt, K.2    Koch, A.3    Simm, D.4    Dorr, H.G.5    Singer, H.6
  • 17
    • 0037975739 scopus 로고    scopus 로고
    • Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: Associations with atrial septal defect and hypoplastic left heart syndrome
    • Elliott DA, Kirk EP, Yeoh T, et al. Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome. J Am Coll Cardiol 2003;41:2072-6.
    • (2003) J Am Coll Cardiol , vol.41 , pp. 2072-2076
    • Elliott, D.A.1    Kirk, E.P.2    Yeoh, T.3
  • 18
    • 23344439128 scopus 로고    scopus 로고
    • Alk3/Bmpr1a receptor is required for development of the atrioventricular canal into valves and annulus fibrosus
    • Gaussin V, Morley GE, Cox L, et al. Alk3/Bmpr1a receptor is required for development of the atrioventricular canal into valves and annulus fibrosus. Circ Res 2005;97:219-26.
    • (2005) Circ Res , vol.97 , pp. 219-226
    • Gaussin, V.1    Morley, G.E.2    Cox, L.3
  • 19
    • 33744931369 scopus 로고    scopus 로고
    • Congenital heart defects in Fgfr2-IIIb and Fgf10 mutant mice
    • Marguerie A, Bajolle F, Zaffran S, et al. Congenital heart defects in Fgfr2-IIIb and Fgf10 mutant mice. Cardiovasc Res 2006;71:50-60.
    • (2006) Cardiovasc Res , vol.71 , pp. 50-60
    • Marguerie, A.1    Bajolle, F.2    Zaffran, S.3
  • 20
    • 4544291281 scopus 로고    scopus 로고
    • Foxh1 is essential for development of the anterior heart field
    • Von Both I, Silvestri C, Erdemir T, et al. Foxh1 is essential for development of the anterior heart field. Dev Cell 2004;7:s331-45.
    • (2004) Dev Cell , vol.7
    • Von Both, I.1    Silvestri, C.2    Erdemir, T.3
  • 21
    • 6944232153 scopus 로고    scopus 로고
    • Foxp1 regulates cardiac outflow tract, endocardial cushion morphogenesis and myocyte proliferation and maturation
    • Wang B, Weidenfeld J, Lu MM, et al. Foxp1 regulates cardiac outflow tract, endocardial cushion morphogenesis and myocyte proliferation and maturation. Development 2004;131:4477-87.
    • (2004) Development , vol.131 , pp. 4477-4487
    • Wang, B.1    Weidenfeld, J.2    Lu, M.M.3
  • 22
    • 4644306118 scopus 로고    scopus 로고
    • Advanced cardiac morphogenesis does not require heart tube fusion
    • Li S, Zhou D, Lu MM, Morrisey EE. Advanced cardiac morphogenesis does not require heart tube fusion. Science 2004;305:1619-22.
    • (2004) Science , vol.305 , pp. 1619-1622
    • Li, S.1    Zhou, D.2    Lu, M.M.3    Morrisey, E.E.4
  • 23
    • 23244436445 scopus 로고    scopus 로고
    • Loss of Gbx2 results in neural crest cell patterning and pharyngeal arch artery defects in the mouse embryo
    • Byrd NA, Meyers EN. Loss of Gbx2 results in neural crest cell patterning and pharyngeal arch artery defects in the mouse embryo. Dev Biol 2005;284:233-45.
    • (2005) Dev Biol , vol.284 , pp. 233-245
    • Byrd, N.A.1    Meyers, E.N.2
  • 24
    • 0346783332 scopus 로고    scopus 로고
    • Isl1 identifies a cardiac progenitor population that proliferates prior to differentiation ana contributes a majority of cells to the heart
    • Cai CL, Liang X, Shi Y, Chu PH, et al. Isl1 identifies a cardiac progenitor population that proliferates prior to differentiation ana contributes a majority of cells to the heart. Dev Cell 2003;5:877-89.
    • (2003) Dev Cell , vol.5 , pp. 877-889
    • Cai, C.L.1    Liang, X.2    Shi, Y.3    Chu, P.H.4
  • 25
    • 4544236360 scopus 로고    scopus 로고
    • Mef2c is a direct transcriptional target of ISL1 and GATA factors in the anterior heart field during mouse embryonic development
    • Dodou E, Verzi MP, Anderson JP, Xu SM, Black BL. Mef2c is a direct transcriptional target of ISL1 and GATA factors in the anterior heart field during mouse embryonic development. Development 2004;131:3931-42.
    • (2004) Development , vol.131 , pp. 3931-3942
    • Dodou, E.1    Verzi, M.P.2    Anderson, J.P.3    Xu, S.M.4    Black, B.L.5
  • 26
    • 4344594556 scopus 로고    scopus 로고
    • PlexinD1 and semaphorin signaling are required in endothelial cells for cardiovascular development
    • Gitler AD, Lu MM, Epstein JA. PlexinD1 and semaphorin signaling are required in endothelial cells for cardiovascular development. Dev Cell 2004;7:107-16.
    • (2004) Dev Cell , vol.7 , pp. 107-116
    • Gitler, A.D.1    Lu, M.M.2    Epstein, J.A.3
  • 27
    • 0038640316 scopus 로고    scopus 로고
    • The role of Pitx2 during cardiac development. Linking left-right signaling and congenital heart diseases
    • Franco D, Campione M. The role of Pitx2 during cardiac development. Linking left-right signaling and congenital heart diseases. Trends Cardiovasc Med 2003;13:157-63.
    • (2003) Trends Cardiovasc Med , vol.13 , pp. 157-163
    • Franco, D.1    Campione, M.2
  • 28
    • 18344370436 scopus 로고    scopus 로고
    • PTPN11 mutations in Noonan syndrome: Molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity
    • Tartaglia M, Kalidas K, Shaw A, et al. PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity. Am J Hum Genet 2002;70:1555-63.
    • (2002) Am J Hum Genet , vol.70 , pp. 1555-1563
    • Tartaglia, M.1    Kalidas, K.2    Shaw, A.3
  • 29
    • 33746563019 scopus 로고    scopus 로고
    • Formation of the venous pole of the heart rrom an Nkx2-5-negative precursor population requires Tbx18
    • Christoffels VM, Mommersteeg MT, Trowe MO, et al. Formation of the venous pole of the heart rrom an Nkx2-5-negative precursor population requires Tbx18. Circ Res 2006;98:1555-63.
    • (2006) Circ Res , vol.98 , pp. 1555-1563
    • Christoffels, V.M.1    Mommersteeg, M.T.2    Trowe, M.O.3
  • 30
    • 21044452772 scopus 로고    scopus 로고
    • Tbx20 dose-dependently regulates transcription factor networks required for mouse heart and motoneuron development
    • Takeuchi JK, Mileikovskaia M, Koshiba-Takeuchi K, et al. Tbx20 dose-dependently regulates transcription factor networks required for mouse heart and motoneuron development. Development 2005;132:2463-74.
    • (2005) Development , vol.132 , pp. 2463-2474
    • Takeuchi, J.K.1    Mileikovskaia, M.2    Koshiba-Takeuchi, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.