BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

185 related articles for article (PubMed ID: 9760192)

  • 1. The SOX10/Sox10 gene from human and mouse: sequence, expression, and transactivation by the encoded HMG domain transcription factor.
    Pusch C; Hustert E; Pfeifer D; Südbeck P; Kist R; Roe B; Wang Z; Balling R; Blin N; Scherer G
    Hum Genet; 1998 Aug; 103(2):115-23. PubMed ID: 9760192
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Analysis of SOX10 mutations identified in Waardenburg-Hirschsprung patients: Differential effects on target gene regulation.
    Chan KK; Wong CK; Lui VC; Tam PK; Sham MH
    J Cell Biochem; 2003 Oct; 90(3):573-85. PubMed ID: 14523991
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model.
    Southard-Smith EM; Kos L; Pavan WJ
    Nat Genet; 1998 Jan; 18(1):60-4. PubMed ID: 9425902
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 9(3):215-25. PubMed ID: 10077527
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Loss of DNA-dependent dimerization of the transcription factor SOX9 as a cause for campomelic dysplasia.
    Sock E; Pagon RA; Keymolen K; Lissens W; Wegner M; Scherer G
    Hum Mol Genet; 2003 Jun; 12(12):1439-47. PubMed ID: 12783851
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Translation of SOX10 3' untranslated region causes a complex severe neurocristopathy by generation of a deleterious functional domain.
    Inoue K; Ohyama T; Sakuragi Y; Yamamoto R; Inoue NA; Yu LH; Goto Y; Wegner M; Lupski JR
    Hum Mol Genet; 2007 Dec; 16(24):3037-46. PubMed ID: 17855451
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutation of the Sry-related Sox10 gene in Dominant megacolon, a mouse model for human Hirschsprung disease.
    Herbarth B; Pingault V; Bondurand N; Kuhlbrodt K; Hermans-Borgmeyer I; Puliti A; Lemort N; Goossens M; Wegner M
    Proc Natl Acad Sci U S A; 1998 Apr; 95(9):5161-5. PubMed ID: 9560246
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Functional analysis of Sox10 mutations found in human Waardenburg-Hirschsprung patients.
    Kuhlbrodt K; Schmidt C; Sock E; Pingault V; Bondurand N; Goossens M; Wegner M
    J Biol Chem; 1998 Sep; 273(36):23033-8. PubMed ID: 9722528
    [TBL] [Abstract][Full Text] [Related]  

  • 9. SOX10 mutations in patients with Waardenburg-Hirschsprung disease.
    Pingault V; Bondurand N; Kuhlbrodt K; Goerich DE; Préhu MO; Puliti A; Herbarth B; Hermans-Borgmeyer I; Legius E; Matthijs G; Amiel J; Lyonnet S; Ceccherini I; Romeo G; Smith JC; Read AP; Wegner M; Goossens M
    Nat Genet; 1998 Feb; 18(2):171-3. PubMed ID: 9462749
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A gene that is related to SRY and is expressed in the testes encodes a leucine zipper-containing protein.
    Takamatsu N; Kanda H; Tsuchiya I; Yamada S; Ito M; Kabeno S; Shiba T; Yamashita S
    Mol Cell Biol; 1995 Jul; 15(7):3759-66. PubMed ID: 7791783
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 22(20):3024-34. PubMed ID: 12789277
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Transcription factor hierarchy in Waardenburg syndrome: regulation of MITF expression by SOX10 and PAX3.
    Potterf SB; Furumura M; Dunn KJ; Arnheiter H; Pavan WJ
    Hum Genet; 2000 Jul; 107(1):1-6. PubMed ID: 10982026
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cloning and characterisation of the Sry-related transcription factor gene Sox8.
    Schepers GE; Bullejos M; Hosking BM; Koopman P
    Nucleic Acids Res; 2000 Mar; 28(6):1473-80. PubMed ID: 10684944
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cloning and functional analysis of the Sry-related HMG box gene, Sox18.
    Hosking BM; Wyeth JR; Pennisi DJ; Wang SC; Koopman P; Muscat GE
    Gene; 2001 Jan; 262(1-2):239-47. PubMed ID: 11179689
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cell type-specific activation of neuronal nicotinic acetylcholine receptor subunit genes by Sox10.
    Liu Q; Melnikova IN; Hu M; Gardner PD
    J Neurosci; 1999 Nov; 19(22):9747-55. PubMed ID: 10559384
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Chick sox10, a transcription factor expressed in both early neural crest cells and central nervous system.
    Cheng Y; Cheung M; Abu-Elmagd MM; Orme A; Scotting PJ
    Brain Res Dev Brain Res; 2000 Jun; 121(2):233-41. PubMed ID: 10876038
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Sox10 is required for the early development of the prospective neural crest in Xenopus embryos.
    Honoré SM; Aybar MJ; Mayor R
    Dev Biol; 2003 Aug; 260(1):79-96. PubMed ID: 12885557
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Sox10, a novel transcriptional modulator in glial cells.
    Kuhlbrodt K; Herbarth B; Sock E; Hermans-Borgmeyer I; Wegner M
    J Neurosci; 1998 Jan; 18(1):237-50. PubMed ID: 9412504
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 9(13):1907-17. PubMed ID: 10942418
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Sox10 and Pax3 physically interact to mediate activation of a conserved c-RET enhancer.
    Lang D; Epstein JA
    Hum Mol Genet; 2003 Apr; 12(8):937-45. PubMed ID: 12668617
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.