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Journal Abstract Search


218 related items for PubMed ID: 15917203

  • 21. Tbx1, subpulmonary myocardium and conotruncal congenital heart defects.
    Parisot P, Mesbah K, Théveniau-Ruissy M, Kelly RG.
    Birth Defects Res A Clin Mol Teratol; 2011 Jun; 91(6):477-84. PubMed ID: 21591244
    [Abstract] [Full Text] [Related]

  • 22. Exploring a neurogenic basis of velopharyngeal dysfunction in Tbx1 mutant mice: no difference in volumes of the nucleus ambiguus.
    Spruijt NE, Rana MS, Christoffels VM, Mink van der Molen AB.
    Int J Pediatr Otorhinolaryngol; 2013 Jun; 77(6):1002-7. PubMed ID: 23642587
    [Abstract] [Full Text] [Related]

  • 23. Properties of branchiomeric and somite-derived muscle development in Tbx1 mutant embryos.
    Grifone R, Jarry T, Dandonneau M, Grenier J, Duprez D, Kelly RG.
    Dev Dyn; 2008 Oct; 237(10):3071-8. PubMed ID: 18816853
    [Abstract] [Full Text] [Related]

  • 24. T-box genes and cardiac development.
    Ryan K, Chin AJ.
    Birth Defects Res C Embryo Today; 2003 Feb; 69(1):25-37. PubMed ID: 12768655
    [Abstract] [Full Text] [Related]

  • 25. Visualization of outflow tract development in the absence of Tbx1 using an FgF10 enhancer trap transgene.
    Kelly RG, Papaioannou VE.
    Dev Dyn; 2007 Mar; 236(3):821-8. PubMed ID: 17238155
    [Abstract] [Full Text] [Related]

  • 26. 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 Mar; 50(5):504-10. PubMed ID: 16586352
    [Abstract] [Full Text] [Related]

  • 27. Allelic variations at the haploid TBX1 locus do not influence the cardiac phenotype in cases of 22q11 microdeletion.
    Voelckel MA, Girardot L, Giusiano B, Levy N, Philip N.
    Ann Genet; 2004 Mar; 47(3):235-40. PubMed ID: 15337468
    [Abstract] [Full Text] [Related]

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  • 29. 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
    [Abstract] [Full Text] [Related]

  • 30. 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; 11(4):349-51. PubMed ID: 12700609
    [Abstract] [Full Text] [Related]

  • 31. 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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  • 33. [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
    [Abstract] [Full Text] [Related]

  • 34. TBX1 gene mutation screening in patients with non-syndromic Fallot tetralogy.
    Cabuk F, Karabulut HG, Tuncali T, Karademir S, Bozdayi M, Tükün A.
    Turk J Pediatr; 2007 Apr; 49(1):61-8. PubMed ID: 17479646
    [Abstract] [Full Text] [Related]

  • 35. Mesodermal expression of Moz is necessary for cardiac septum development.
    Vanyai HK, Thomas T, Voss AK.
    Dev Biol; 2015 Jul 01; 403(1):22-9. PubMed ID: 25912687
    [Abstract] [Full Text] [Related]

  • 36. The 22q11 deletion: DiGeorge and velocardiofacial syndromes and the role of TBX1.
    Papangeli I, Scambler P.
    Wiley Interdiscip Rev Dev Biol; 2013 Jul 01; 2(3):393-403. PubMed ID: 23799583
    [Abstract] [Full Text] [Related]

  • 37. Wrapping up DiGeorge syndrome in a T-box?
    Kim MS, Basson CT.
    Pediatr Res; 2001 Sep 01; 50(3):307-8. PubMed ID: 11518813
    [No Abstract] [Full Text] [Related]

  • 38. Isolation and characterization of a gene from the DiGeorge chromosomal region homologous to the mouse Tbx1 gene.
    Chieffo C, Garvey N, Gong W, Roe B, Zhang G, Silver L, Emanuel BS, Budarf ML.
    Genomics; 1997 Aug 01; 43(3):267-77. PubMed ID: 9268629
    [Abstract] [Full Text] [Related]

  • 39. Deconstructing DiGeorge syndrome.
    Schinke M, Izumo S.
    Nat Genet; 2001 Mar 01; 27(3):238-40. PubMed ID: 11242098
    [No Abstract] [Full Text] [Related]

  • 40. Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome.
    Prasad SE, Howley S, Murphy KC.
    Dev Disabil Res Rev; 2008 Mar 01; 14(1):26-34. PubMed ID: 18636634
    [Abstract] [Full Text] [Related]


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