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Journal Abstract Search

133 related items for PubMed ID: 16586352

  • 1. Tbx1 is expressed at multiple sites of epithelial-mesenchymal interaction during early development of the facial complex.
    Zoupa M, Seppala M, Mitsiadis T, Cobourne MT.
    Int J Dev Biol; 2006; 50(5):504-10. PubMed ID: 16586352
    [Abstract] [Full Text] [Related]

  • 2. Expression patterns of the bone morphogenetic protein genes Bmp-4 and Bmp-2 in the developing chick face suggest a role in outgrowth of the primordia.
    Francis-West PH, Tatla T, Brickell PM.
    Dev Dyn; 1994 Oct; 201(2):168-78. PubMed ID: 7873788
    [Abstract] [Full Text] [Related]

  • 3. The del22q11.2 candidate gene Tbx1 regulates branchiomeric myogenesis.
    Kelly RG, Jerome-Majewska LA, Papaioannou VE.
    Hum Mol Genet; 2004 Nov 15; 13(22):2829-40. PubMed ID: 15385444
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  • 4. Tbx1 regulation of myogenic differentiation in the limb and cranial mesoderm.
    Dastjerdi A, Robson L, Walker R, Hadley J, Zhang Z, Rodriguez-Niedenführ M, Ataliotis P, Baldini A, Scambler P, Francis-West P.
    Dev Dyn; 2007 Feb 15; 236(2):353-63. PubMed ID: 17117436
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  • 5. TBX1 protein interactions and microRNA-96-5p regulation controls cell proliferation during craniofacial and dental development: implications for 22q11.2 deletion syndrome.
    Gao S, Moreno M, Eliason S, Cao H, Li X, Yu W, Bidlack FB, Margolis HC, Baldini A, Amendt BA.
    Hum Mol Genet; 2015 Apr 15; 24(8):2330-48. PubMed ID: 25556186
    [Abstract] [Full Text] [Related]

  • 6. The 22q11 deletion syndrome candidate gene Tbx1 determines thyroid size and positioning.
    Fagman H, Liao J, Westerlund J, Andersson L, Morrow BE, Nilsson M.
    Hum Mol Genet; 2007 Feb 01; 16(3):276-85. PubMed ID: 17164259
    [Abstract] [Full Text] [Related]

  • 7. Alx-4, a transcriptional activator whose expression is restricted to sites of epithelial-mesenchymal interactions.
    Hudson R, Taniguchi-Sidle A, Boras K, Wiggan O, Hamel PA.
    Dev Dyn; 1998 Oct 01; 213(2):159-69. PubMed ID: 9786416
    [Abstract] [Full Text] [Related]

  • 8. Dissection of Tbx1 and Fgf interactions in mouse models of 22q11DS suggests functional redundancy.
    Aggarwal VS, Liao J, Bondarev A, Schimmang T, Lewandoski M, Locker J, Shanske A, Campione M, Morrow BE.
    Hum Mol Genet; 2006 Nov 01; 15(21):3219-28. PubMed ID: 17000704
    [Abstract] [Full Text] [Related]

  • 9. Inactivation of Tbx1 in the pharyngeal endoderm results in 22q11DS malformations.
    Arnold JS, Werling U, Braunstein EM, Liao J, Nowotschin S, Edelmann W, Hebert JM, Morrow BE.
    Development; 2006 Mar 01; 133(5):977-87. PubMed ID: 16452092
    [Abstract] [Full Text] [Related]

  • 10. Tbx1 regulates fibroblast growth factors in the anterior heart field through a reinforcing autoregulatory loop involving forkhead transcription factors.
    Hu T, Yamagishi H, Maeda J, McAnally J, Yamagishi C, Srivastava D.
    Development; 2004 Nov 01; 131(21):5491-502. PubMed ID: 15469978
    [Abstract] [Full Text] [Related]

  • 11. 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 01; 122(2):199-212. PubMed ID: 15652707
    [Abstract] [Full Text] [Related]

  • 12. Tbx1 expression in pharyngeal epithelia is necessary for pharyngeal arch artery development.
    Zhang Z, Cerrato F, Xu H, Vitelli F, Morishima M, Vincentz J, Furuta Y, Ma L, Martin JF, Baldini A, Lindsay E.
    Development; 2005 Dec 01; 132(23):5307-15. PubMed ID: 16284121
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  • 15. Dissecting contiguous gene defects: TBX1.
    Baldini A.
    Curr Opin Genet Dev; 2005 Jun 01; 15(3):279-84. PubMed ID: 15917203
    [Abstract] [Full Text] [Related]

  • 16. The del22q11.2 candidate gene Tbx1 controls regional outflow tract identity and coronary artery patterning.
    Théveniau-Ruissy M, Dandonneau M, Mesbah K, Ghez O, Mattei MG, Miquerol L, Kelly RG.
    Circ Res; 2008 Jul 18; 103(2):142-8. PubMed ID: 18583714
    [Abstract] [Full Text] [Related]

  • 17. DiGeorge subtypes of nonsyndromic conotruncal defects: evidence against a major role of TBX1 gene.
    Conti E, Grifone N, Sarkozy A, Tandoi C, Marino B, Digilio MC, Mingarelli R, Pizzuti A, Dallapiccola B.
    Eur J Hum Genet; 2003 Apr 18; 11(4):349-51. PubMed ID: 12700609
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  • 19. Beta-catenin deficiency causes DiGeorge syndrome-like phenotypes through regulation of Tbx1.
    Huh SH, Ornitz DM.
    Development; 2010 Apr 18; 137(7):1137-47. PubMed ID: 20215350
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