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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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related] Page: [Next] [New Search]