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Volumn 5, Issue 3, 2008, Pages 113-115

Models that buzz, squeak, ribbit and oink: using a variety of species to study cardiovascular disease

Author keywords

[No Author keywords available]

Indexed keywords

ANTIHYPERTENSIVE AGENT;

EID: 67651208850     PISSN: 17406757     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ddmod.2009.05.001     Document Type: Editorial
Times cited : (1)

References (6)
  • 1
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    • A new homeobox-containing gene, msh-2, is transiently expressed early during mesoderm formation of Drosophila
    • Bodmer R., et al. A new homeobox-containing gene, msh-2, is transiently expressed early during mesoderm formation of Drosophila. Development 110 (1990) 661-669
    • (1990) Development , vol.110 , pp. 661-669
    • Bodmer, R.1
  • 2
    • 0027282774 scopus 로고
    • The gene tinman is required for specification of the heart and visceral muscles in Drosophila
    • Bodmer R. The gene tinman is required for specification of the heart and visceral muscles in Drosophila. Development 118 (1993) 719-729
    • (1993) Development , vol.118 , pp. 719-729
    • Bodmer, R.1
  • 3
    • 0027184211 scopus 로고
    • Csx: a murine homeobox-containing gene specifically expressed in the developing heart
    • Komuro I., and Izumo S. Csx: a murine homeobox-containing gene specifically expressed in the developing heart. Proc. Natl. Acad. Sci. U. S. A. 90 (1993) 8145-8149
    • (1993) Proc. Natl. Acad. Sci. U. S. A. , vol.90 , pp. 8145-8149
    • Komuro, I.1    Izumo, S.2
  • 4
    • 0029090829 scopus 로고
    • Myogenic and morphogenetic defects in the heart tubes of murine embryos lacking the homeo box gene Nkx2-5
    • Lyons I., et al. Myogenic and morphogenetic defects in the heart tubes of murine embryos lacking the homeo box gene Nkx2-5. Genes Dev. 9 (1995) 1654-1666
    • (1995) Genes Dev. , vol.9 , pp. 1654-1666
    • Lyons, I.1
  • 5
    • 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 (1998) 108-111
    • (1998) Science , vol.281 , pp. 108-111
    • Schott, J.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.