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Journal Abstract Search

319 related items for PubMed ID: 12176321

  • 1. Inappropriate gene activation in FSHD: a repressor complex binds a chromosomal repeat deleted in dystrophic muscle.
    Gabellini D, Green MR, Tupler R.
    Cell; 2002 Aug 09; 110(3):339-48. PubMed ID: 12176321
    [Abstract] [Full Text] [Related]

  • 2. Molecular basis of facioscapulohumeral muscular dystrophy.
    Tupler R, Gabellini D.
    Cell Mol Life Sci; 2004 Mar 09; 61(5):557-566. PubMed ID: 15004695
    [Abstract] [Full Text] [Related]

  • 3. Remodeling of the chromatin structure of the facioscapulohumeral muscular dystrophy (FSHD) locus and upregulation of FSHD-related gene 1 (FRG1) expression during human myogenic differentiation.
    Bodega B, Ramirez GD, Grasser F, Cheli S, Brunelli S, Mora M, Meneveri R, Marozzi A, Mueller S, Battaglioli E, Ginelli E.
    BMC Biol; 2009 Jul 16; 7():41. PubMed ID: 19607661
    [Abstract] [Full Text] [Related]

  • 4. Facioscapulohumeral muscular dystrophy.
    Tawil R.
    Curr Neurol Neurosci Rep; 2004 Jan 16; 4(1):51-4. PubMed ID: 14683629
    [Abstract] [Full Text] [Related]

  • 5. The Krüppel-like factor 15 as a molecular link between myogenic factors and a chromosome 4q transcriptional enhancer implicated in facioscapulohumeral dystrophy.
    Dmitriev P, Petrov A, Ansseau E, Stankevicins L, Charron S, Kim E, Bos TJ, Robert T, Turki A, Coppée F, Belayew A, Lazar V, Carnac G, Laoudj D, Lipinski M, Vassetzky YS.
    J Biol Chem; 2011 Dec 30; 286(52):44620-31. PubMed ID: 21937448
    [Abstract] [Full Text] [Related]

  • 6. Methylation of the FSHD syndrome-linked subtelomeric repeat in normal and FSHD cell cultures and tissues.
    Tsien F, Sun B, Hopkins NE, Vedanarayanan V, Figlewicz D, Winokur S, Ehrlich M.
    Mol Genet Metab; 2001 Nov 30; 74(3):322-31. PubMed ID: 11708861
    [Abstract] [Full Text] [Related]

  • 7. Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy.
    Osborne RJ, Welle S, Venance SL, Thornton CA, Tawil R.
    Neurology; 2007 Feb 20; 68(8):569-77. PubMed ID: 17151338
    [Abstract] [Full Text] [Related]

  • 8. Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1.
    Gabellini D, D'Antona G, Moggio M, Prelle A, Zecca C, Adami R, Angeletti B, Ciscato P, Pellegrino MA, Bottinelli R, Green MR, Tupler R.
    Nature; 2006 Feb 23; 439(7079):973-7. PubMed ID: 16341202
    [Abstract] [Full Text] [Related]

  • 9. Hybridization analysis of D4Z4 repeat arrays linked to FSHD.
    Ehrlich M, Jackson K, Tsumagari K, Camaño P, Lemmers RJ.
    Chromosoma; 2007 Apr 23; 116(2):107-16. PubMed ID: 17131163
    [Abstract] [Full Text] [Related]

  • 10. Testing the position-effect variegation hypothesis for facioscapulohumeral muscular dystrophy by analysis of histone modification and gene expression in subtelomeric 4q.
    Jiang G, Yang F, van Overveld PG, Vedanarayanan V, van der Maarel S, Ehrlich M.
    Hum Mol Genet; 2003 Nov 15; 12(22):2909-21. PubMed ID: 14506132
    [Abstract] [Full Text] [Related]

  • 11. Specific loss of histone H3 lysine 9 trimethylation and HP1gamma/cohesin binding at D4Z4 repeats is associated with facioscapulohumeral dystrophy (FSHD).
    Zeng W, de Greef JC, Chen YY, Chien R, Kong X, Gregson HC, Winokur ST, Pyle A, Robertson KD, Schmiesing JA, Kimonis VE, Balog J, Frants RR, Ball AR, Lock LF, Donovan PJ, van der Maarel SM, Yokomori K.
    PLoS Genet; 2009 Jul 15; 5(7):e1000559. PubMed ID: 19593370
    [Abstract] [Full Text] [Related]

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  • 13. Genotype-phenotype study in an FSHD family with a proximal deletion encompassing p13E-11 and D4Z4.
    Deak KL, Lemmers RJ, Stajich JM, Klooster R, Tawil R, Frants RR, Speer MC, van der Maarel SM, Gilbert JR.
    Neurology; 2007 Feb 20; 68(8):578-82. PubMed ID: 17229919
    [Abstract] [Full Text] [Related]

  • 14. In junk we trust: repetitive DNA, epigenetics and facioscapulohumeral muscular dystrophy.
    Neguembor MV, Gabellini D.
    Epigenomics; 2010 Apr 20; 2(2):271-87. PubMed ID: 22121874
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  • 16. A large patient study confirming that facioscapulohumeral muscular dystrophy (FSHD) disease expression is almost exclusively associated with an FSHD locus located on a 4qA-defined 4qter subtelomere.
    Thomas NS, Wiseman K, Spurlock G, MacDonald M, Ustek D, Upadhyaya M.
    J Med Genet; 2007 Mar 20; 44(3):215-8. PubMed ID: 16987949
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  • 18. Hypomethylation is restricted to the D4Z4 repeat array in phenotypic FSHD.
    de Greef JC, Wohlgemuth M, Chan OA, Hansson KB, Smeets D, Frants RR, Weemaes CM, Padberg GW, van der Maarel SM.
    Neurology; 2007 Sep 04; 69(10):1018-26. PubMed ID: 17785671
    [Abstract] [Full Text] [Related]

  • 19. Analysis of allele-specific RNA transcription in FSHD by RNA-DNA FISH in single myonuclei.
    Masny PS, Chan OY, de Greef JC, Bengtsson U, Ehrlich M, Tawil R, Lock LF, Hewitt JE, Stocksdale J, Martin JH, van der Maarel SM, Winokur ST.
    Eur J Hum Genet; 2010 Apr 04; 18(4):448-56. PubMed ID: 19888305
    [Abstract] [Full Text] [Related]

  • 20. The D4Z4 macrosatellite repeat acts as a CTCF and A-type lamins-dependent insulator in facio-scapulo-humeral dystrophy.
    Ottaviani A, Rival-Gervier S, Boussouar A, Foerster AM, Rondier D, Sacconi S, Desnuelle C, Gilson E, Magdinier F.
    PLoS Genet; 2009 Feb 04; 5(2):e1000394. PubMed ID: 19247430
    [Abstract] [Full Text] [Related]

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