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Journal Abstract Search

252 related items for PubMed ID: 12952905

  • 1. The zebrafish van gogh mutation disrupts tbx1, which is involved in the DiGeorge deletion syndrome in humans.
    Piotrowski T, Ahn DG, Schilling TF, Nair S, Ruvinsky I, Geisler R, Rauch GJ, Haffter P, Zon LI, Zhou Y, Foott H, Dawid IB, Ho RK.
    Development; 2003 Oct; 130(20):5043-52. PubMed ID: 12952905
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  • 7. [Effect of external retinoic acid on Tbx1 gene during zebrafish embryogenesis].
    Zhang LF, Gui YH, Zhong T, Wang YX, Qian LX, Dong YX, Jiang Q, Sun SN, Song HY.
    Zhonghua Er Ke Za Zhi; 2007 Apr; 45(4):267-71. PubMed ID: 17706063
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  • 12. Tbx1 is required for proper neural crest migration and to stabilize spatial patterns during middle and inner ear development.
    Moraes F, Nóvoa A, Jerome-Majewska LA, Papaioannou VE, Mallo M.
    Mech Dev; 2005 Feb; 122(2):199-212. PubMed ID: 15652707
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  • 14. Beta-catenin deficiency causes DiGeorge syndrome-like phenotypes through regulation of Tbx1.
    Huh SH, Ornitz DM.
    Development; 2010 Apr; 137(7):1137-47. PubMed ID: 20215350
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  • 16. 22q11 deletion syndrome: a role for TBX1 in pharyngeal and cardiovascular development.
    Scambler PJ.
    Pediatr Cardiol; 2010 Apr; 31(3):378-90. PubMed ID: 20054531
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  • 18. Pax9 is required for cardiovascular development and interacts with Tbx1 in the pharyngeal endoderm to control 4th pharyngeal arch artery morphogenesis.
    Phillips HM, Stothard CA, Shaikh Qureshi WM, Kousa AI, Briones-Leon JA, Khasawneh RR, O'Loughlin C, Sanders R, Mazzotta S, Dodds R, Seidel K, Bates T, Nakatomi M, Cockell SJ, Schneider JE, Mohun TJ, Maehr R, Kist R, Peters H, Bamforth SD.
    Development; 2019 Sep 23; 146(18):. PubMed ID: 31444215
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  • 20. TBX1, a DiGeorge syndrome candidate gene, is inhibited by retinoic acid.
    Zhang L, Zhong T, Wang Y, Jiang Q, Song H, Gui Y.
    Int J Dev Biol; 2006 Sep 23; 50(1):55-61. PubMed ID: 16323078
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