BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

581 related articles for article (PubMed ID: 10942418)

  • 1. 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]  

  • 2. Regulation of the microphthalmia-associated transcription factor gene by the Waardenburg syndrome type 4 gene, SOX10.
    Verastegui C; Bille K; Ortonne JP; Ballotti R
    J Biol Chem; 2000 Oct; 275(40):30757-60. PubMed ID: 10938265
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Epistatic relationship between Waardenburg syndrome genes MITF and PAX3.
    Watanabe A; Takeda K; Ploplis B; Tachibana M
    Nat Genet; 1998 Mar; 18(3):283-6. PubMed ID: 9500554
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Functional analysis of Waardenburg syndrome-associated PAX3 and SOX10 mutations: report of a dominant-negative SOX10 mutation in Waardenburg syndrome type II.
    Zhang H; Chen H; Luo H; An J; Sun L; Mei L; He C; Jiang L; Jiang W; Xia K; Li JD; Feng Y
    Hum Genet; 2012 Mar; 131(3):491-503. PubMed ID: 21965087
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mouse models for four types of Waardenburg syndrome.
    Tachibana M; Kobayashi Y; Matsushima Y
    Pigment Cell Res; 2003 Oct; 16(5):448-54. PubMed ID: 12950719
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of a distal enhancer for the melanocyte-specific promoter of the MITF gene.
    Watanabe K; Takeda K; Yasumoto K; Udono T; Saito H; Ikeda K; Takasaka T; Takahashi K; Kobayashi T; Tachibana M; Shibahara S
    Pigment Cell Res; 2002 Jun; 15(3):201-11. PubMed ID: 12028584
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Functional difference of the SOX10 mutant proteins responsible for the phenotypic variability in auditory-pigmentary disorders.
    Yokoyama S; Takeda K; Shibahara S
    J Biochem; 2006 Oct; 140(4):491-9. PubMed ID: 16921166
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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; 275(48):37978-83. PubMed ID: 10973953
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Deletions at the SOX10 gene locus cause Waardenburg syndrome types 2 and 4.
    Bondurand N; Dastot-Le Moal F; Stanchina L; Collot N; Baral V; Marlin S; Attie-Bitach T; Giurgea I; Skopinski L; Reardon W; Toutain A; Sarda P; Echaieb A; Lackmy-Port-Lis M; Touraine R; Amiel J; Goossens M; Pingault V
    Am J Hum Genet; 2007 Dec; 81(6):1169-85. PubMed ID: 17999358
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The clinical and genetic research of Waardenburg syndrome type I and II in Chinese families.
    Liu Q; Cheng J; Lu Y; Zhou J; Wang L; Yang C; Yang G; Yang H; Cao J; Zhang Z; Sun Y
    Int J Pediatr Otorhinolaryngol; 2020 Mar; 130():109806. PubMed ID: 31812001
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Hereditary hypomelanocytoses: the role of PAX3, SOX10, MITF, SNAI2, KIT, EDN3 and EDNRB genes].
    Otręba M; Miliński M; Buszman E; Wrześniok D; Beberok A
    Postepy Hig Med Dosw (Online); 2013 Nov; 67():1109-18. PubMed ID: 24379252
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A tissue-restricted cAMP transcriptional response: SOX10 modulates alpha-melanocyte-stimulating hormone-triggered expression of microphthalmia-associated transcription factor in melanocytes.
    Huber WE; Price ER; Widlund HR; Du J; Davis IJ; Wegner M; Fisher DE
    J Biol Chem; 2003 Nov; 278(46):45224-30. PubMed ID: 12944398
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel mutations of PAX3, MITF, and SOX10 genes in Chinese patients with type I or type II Waardenburg syndrome.
    Chen H; Jiang L; Xie Z; Mei L; He C; Hu Z; Xia K; Feng Y
    Biochem Biophys Res Commun; 2010 Jun; 397(1):70-4. PubMed ID: 20478267
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 273(8):1805-20. PubMed ID: 16623715
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Functional analysis of a SOX10 gene mutation associated with Waardenburg syndrome II.
    Wang XP; Hao ZQ; Liu YL; Mei LY; He CF; Niu ZJ; Sun J; Zhao YL; Feng Y
    Biochem Biophys Res Commun; 2017 Nov; 493(1):258-262. PubMed ID: 28893539
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Two novel mutations of PAX3 and SOX10 were characterized as genetic causes of Waardenburg Syndrome.
    Yu Y; Liu W; Chen M; Yang Y; Yang Y; Hong E; Lu J; Zheng J; Ni X; Guo Y; Zhang J
    Mol Genet Genomic Med; 2020 May; 8(5):e1217. PubMed ID: 32168437
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Sumoylation of the SOX10 transcription factor regulates its transcriptional activity.
    Girard M; Goossens M
    FEBS Lett; 2006 Mar; 580(6):1635-41. PubMed ID: 16494873
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The value of MLPA in Waardenburg syndrome.
    Milunsky JM; Maher TA; Ito M; Milunsky A
    Genet Test; 2007; 11(2):179-82. PubMed ID: 17627390
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 30.