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Journal Abstract Search

766 related items for PubMed ID: 9425902

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  • 4. The importance of having your SOX on: role of SOX10 in the development of neural crest-derived melanocytes and glia.
    Mollaaghababa R, Pavan WJ.
    Oncogene; 2003 May 19; 22(20):3024-34. PubMed ID: 12789277
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  • 5. Identification of Sox8 as a modifier gene in a mouse model of Hirschsprung disease reveals underlying molecular defect.
    Maka M, Stolt CC, Wegner M.
    Dev Biol; 2005 Jan 01; 277(1):155-69. PubMed ID: 15572147
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  • 6. [Molecular genetics of Hirschsprung disease: a model of multigenic neurocristopathy].
    Amiel J, Salomon R, Attié-Bitach T, Touraine R, Steffann J, Pelet A, Nihoul-Fékété C, Vekemans M, Munnich A, Lyonnet S.
    J Soc Biol; 2000 Jan 01; 194(3-4):125-8. PubMed ID: 11324313
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  • 8. Human homology and candidate genes for the Dominant megacolon locus, a mouse model of Hirschsprung disease.
    Pingault V, Puliti A, Préhu MO, Samadi A, Bondurand N, Goossens M.
    Genomics; 1997 Jan 01; 39(1):86-9. PubMed ID: 9027489
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  • 10. Interactions between Sox10 and EdnrB modulate penetrance and severity of aganglionosis in the Sox10Dom mouse model of Hirschsprung disease.
    Cantrell VA, Owens SE, Chandler RL, Airey DC, Bradley KM, Smith JR, Southard-Smith EM.
    Hum Mol Genet; 2004 Oct 01; 13(19):2289-301. PubMed ID: 15294878
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  • 14. Early death of neural crest cells is responsible for total enteric aganglionosis in Sox10(Dom)/Sox10(Dom) mouse embryos.
    Kapur RP.
    Pediatr Dev Pathol; 1999 Oct 01; 2(6):559-69. PubMed ID: 10508880
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  • 17. Endothelin-3 gene mutations in isolated and syndromic Hirschsprung disease.
    Bidaud C, Salomon R, Van Camp G, Pelet A, Attié T, Eng C, Bonduelle M, Amiel J, Nihoul-Fékété C, Willems PJ, Munnich A, Lyonnet S.
    Eur J Hum Genet; 1997 Oct 01; 5(4):247-51. PubMed ID: 9359047
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  • 19. Novel nonsense mutation of the endothelin-B receptor gene in a family with Waardenburg-Hirschsprung disease.
    Syrris P, Carter ND, Patton MA.
    Am J Med Genet; 1999 Nov 05; 87(1):69-71. PubMed ID: 10528251
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  • 20. SOX10, in combination with Sp1, regulates the endothelin receptor type B gene in human melanocyte lineage cells.
    Yokoyama S, Takeda K, Shibahara S.
    FEBS J; 2006 Apr 05; 273(8):1805-20. PubMed ID: 16623715
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