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Journal Abstract Search


223 related items for PubMed ID: 10973953

  • 1. Direct regulation of the Microphthalmia promoter by Sox10 links Waardenburg-Shah syndrome (WS4)-associated hypopigmentation and deafness to WS2.
    Lee M, Goodall J, Verastegui C, Ballotti R, Goding CR.
    J Biol Chem; 2000 Dec 01; 275(48):37978-83. PubMed ID: 10973953
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  • 3. Interaction among SOX10, PAX3 and MITF, three genes altered in Waardenburg syndrome.
    Bondurand N, Pingault V, Goerich DE, Lemort N, Sock E, Le Caignec C, Wegner M, Goossens M.
    Hum Mol Genet; 2000 Aug 12; 9(13):1907-17. PubMed ID: 10942418
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  • 6. The Sox10(Dom) mouse: modeling the genetic variation of Waardenburg-Shah (WS4) syndrome.
    Southard-Smith EM, Angrist M, Ellison JS, Agarwala R, Baxevanis AD, Chakravarti A, Pavan WJ.
    Genome Res; 1999 Mar 12; 9(3):215-25. PubMed ID: 10077527
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  • 11. Deletion of long-range sequences at Sox10 compromises developmental expression in a mouse model of Waardenburg-Shah (WS4) syndrome.
    Antonellis A, Bennett WR, Menheniott TR, Prasad AB, Lee-Lin SQ, NISC Comparative Sequencing Program, Green ED, Paisley D, Kelsh RN, Pavan WJ, Ward A.
    Hum Mol Genet; 2006 Jan 15; 15(2):259-71. PubMed ID: 16330480
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  • 12. Epistatic relationship between Waardenburg syndrome genes MITF and PAX3.
    Watanabe A, Takeda K, Ploplis B, Tachibana M.
    Nat Genet; 1998 Mar 15; 18(3):283-6. PubMed ID: 9500554
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  • 16. A mouse model of Waardenburg syndrome type 4 with a new spontaneous mutation of the endothelin-B receptor gene.
    Matsushima Y, Shinkai Y, Kobayashi Y, Sakamoto M, Kunieda T, Tachibana M.
    Mamm Genome; 2002 Jan 15; 13(1):30-5. PubMed ID: 11773966
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  • 19. [Molecular pathogenesis of Waardenburg syndrome type II resulting from SOX10 gene mutation].
    Zhang H, Chen H, Feng Y, Qian M, Li J, Liu J, Zhang C.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Aug 15; 33(4):466-70. PubMed ID: 27454999
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  • 20. Melanocyte-specific expression of dopachrome tautomerase is dependent on synergistic gene activation by the Sox10 and Mitf transcription factors.
    Ludwig A, Rehberg S, Wegner M.
    FEBS Lett; 2004 Jan 02; 556(1-3):236-44. PubMed ID: 14706856
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