메뉴 건너뛰기




Volumn 84, Issue 6, 2007, Pages 2137-

GATA4 as Candidate Gene for Pericardial Defects

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME DELETION; CHROMOSOME DELETION 8P; CONGENITAL HEART MALFORMATION; EMBRYOLOGY; GATA4 GENE; GENE; GENE FUNCTION; GENE MUTATION; HEART ATRIUM SEPTUM DEFECT; HUMAN; LETTER; MESENCHYME CELL; PERICARDIUM; PERICARDIUM LESION; PRIORITY JOURNAL;

EID: 36248990859     PISSN: 00034975     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.athoracsur.2007.06.103     Document Type: Letter
Times cited : (4)

References (7)
  • 3
    • 33846044214 scopus 로고    scopus 로고
    • Impaired mesenchymal cell function in GATA4 mutant mice leads to diaphragmatic hernias and primary lung defects
    • Jay P.Y., Bielinska M., Erlich J.M., et al. Impaired mesenchymal cell function in GATA4 mutant mice leads to diaphragmatic hernias and primary lung defects. Develop Biol 301 (2007) 602-614
    • (2007) Develop Biol , vol.301 , pp. 602-614
    • Jay, P.Y.1    Bielinska, M.2    Erlich, J.M.3
  • 4
    • 0043267988 scopus 로고    scopus 로고
    • GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5
    • Garg V., Kathiriya I.S., Barnes R., et al. GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5. Nature 424 (2003) 443-447
    • (2003) Nature , vol.424 , pp. 443-447
    • Garg, V.1    Kathiriya, I.S.2    Barnes, R.3
  • 5
    • 28444447608 scopus 로고    scopus 로고
    • Spectrum of atrial septal defects associated with mutations of NKX2.5 and GATA4 transcription factors
    • Sarkozy A., Conti E., Neri C., et al. Spectrum of atrial septal defects associated with mutations of NKX2.5 and GATA4 transcription factors. J Med Genet 42 (2005) e16
    • (2005) J Med Genet , vol.42
    • Sarkozy, A.1    Conti, E.2    Neri, C.3
  • 6
    • 0034713818 scopus 로고    scopus 로고
    • Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defects
    • Giglio S., Graw S.L., Gimelli G., et al. Deletion of a 5-cM region at chromosome 8p23 is associated with a spectrum of congenital heart defects. Circulation 102 (2000) 432-437
    • (2000) Circulation , vol.102 , pp. 432-437
    • Giglio, S.1    Graw, S.L.2    Gimelli, G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.