These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

232 related items for PubMed ID: 11734543

  • 1. Human Connexin 32, a gap junction protein altered in the X-linked form of Charcot-Marie-Tooth disease, is directly regulated by the transcription factor SOX10.
    Bondurand N, Girard M, Pingault V, Lemort N, Dubourg O, Goossens M.
    Hum Mol Genet; 2001 Nov 15; 10(24):2783-95. PubMed ID: 11734543
    [Abstract] [Full Text] [Related]

  • 2. Genetic epidemiology of Charcot-Marie-Tooth disease.
    Braathen GJ.
    Acta Neurol Scand Suppl; 2012 Nov 15; (193):iv-22. PubMed ID: 23106488
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. The SOX10 transcription factor: evaluation as a candidate gene for central and peripheral hereditary myelin disorders.
    Pingault V, Bondurand N, Le Caignec C, Tardieu S, Lemort N, Dubourg O, Le Guern E, Goossens M, Boespflug-Tanguy O, Clinical E.N.B.D.D. Clinical European Network on Brain Dysmyelinating Disease.
    J Neurol; 2001 Jun 01; 248(6):496-9. PubMed ID: 11499640
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Pathomechanisms of mutant proteins in Charcot-Marie-Tooth disease.
    Niemann A, Berger P, Suter U.
    Neuromolecular Med; 2006 Jun 01; 8(1-2):217-42. PubMed ID: 16775378
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Point mutation associated with X-linked dominant Charcot-Marie-Tooth disease impairs the P2 promoter activity of human connexin-32 gene.
    Wang HL, Wu T, Chang WT, Li AH, Chen MS, Wu CY, Fang W.
    Brain Res Mol Brain Res; 2000 May 31; 78(1-2):146-53. PubMed ID: 10891594
    [Abstract] [Full Text] [Related]

  • 11. Expression of connexin47 in oligodendrocytes is regulated by the Sox10 transcription factor.
    Schlierf B, Werner T, Glaser G, Wegner M.
    J Mol Biol; 2006 Aug 04; 361(1):11-21. PubMed ID: 16822525
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. 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 06; 275(40):30757-60. PubMed ID: 10938265
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. SOX10 regulates an alternative promoter at the Charcot-Marie-Tooth disease locus MTMR2.
    Fogarty EA, Brewer MH, Rodriguez-Molina JF, Law WD, Ma KH, Steinberg NM, Svaren J, Antonellis A.
    Hum Mol Genet; 2016 Sep 15; 25(18):3925-3936. PubMed ID: 27466180
    [Abstract] [Full Text] [Related]

  • 17. Different consequences of EGR2 mutants on the transactivation of human Cx32 promoter.
    Musso M, Balestra P, Taroni F, Bellone E, Mandich P.
    Neurobiol Dis; 2003 Feb 15; 12(1):89-95. PubMed ID: 12609493
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Protein zero gene expression is regulated by the glial transcription factor Sox10.
    Peirano RI, Goerich DE, Riethmacher D, Wegner M.
    Mol Cell Biol; 2000 May 15; 20(9):3198-209. PubMed ID: 10757804
    [Abstract] [Full Text] [Related]

  • 20. Connexin channels in Schwann cells and the development of the X-linked form of Charcot-Marie-Tooth disease.
    Ressot C, Bruzzone R.
    Brain Res Brain Res Rev; 2000 Apr 15; 32(1):192-202. PubMed ID: 10751670
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 12.