BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

137 related articles for article (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
    [TBL] [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
    [TBL] [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; 13(22):2829-40. PubMed ID: 15385444
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 236(2):353-63. PubMed ID: 17117436
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 24(8):2330-48. PubMed ID: 25556186
    [TBL] [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; 16(3):276-85. PubMed ID: 17164259
    [TBL] [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; 213(2):159-69. PubMed ID: 9786416
    [TBL] [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; 15(21):3219-28. PubMed ID: 17000704
    [TBL] [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; 133(5):977-87. PubMed ID: 16452092
    [TBL] [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; 131(21):5491-502. PubMed ID: 15469978
    [TBL] [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; 122(2):199-212. PubMed ID: 15652707
    [TBL] [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; 132(23):5307-15. PubMed ID: 16284121
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Microarray analysis detects differentially expressed genes in the pharyngeal region of mice lacking Tbx1.
    Ivins S; Lammerts van Beuren K; Roberts C; James C; Lindsay E; Baldini A; Ataliotis P; Scambler PJ
    Dev Biol; 2005 Sep; 285(2):554-69. PubMed ID: 16109395
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Timed mutation and cell-fate mapping reveal reiterated roles of Tbx1 during embryogenesis, and a crucial function during segmentation of the pharyngeal system via regulation of endoderm expansion.
    Xu H; Cerrato F; Baldini A
    Development; 2005 Oct; 132(19):4387-95. PubMed ID: 16141220
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Dissecting contiguous gene defects: TBX1.
    Baldini A
    Curr Opin Genet Dev; 2005 Jun; 15(3):279-84. PubMed ID: 15917203
    [TBL] [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; 103(2):142-8. PubMed ID: 18583714
    [TBL] [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; 11(4):349-51. PubMed ID: 12700609
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Embryonic expression of Tbx1, a DiGeorge syndrome candidate gene, in the lamprey Lampetra fluviatilis.
    Sauka-Spengler T; Le Mentec C; Lepage M; Mazan S
    Gene Expr Patterns; 2002 Nov; 2(1-2):99-103. PubMed ID: 12617845
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.