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Journal Abstract Search

197 related items for PubMed ID: 22121874

  • 1. In junk we trust: repetitive DNA, epigenetics and facioscapulohumeral muscular dystrophy.
    Neguembor MV, Gabellini D.
    Epigenomics; 2010 Apr; 2(2):271-87. PubMed ID: 22121874
    [Abstract] [Full Text] [Related]

  • 2. Facioscapulohumeral muscular dystrophy.
    Tawil R.
    Handb Clin Neurol; 2018 Apr; 148():541-548. PubMed ID: 29478599
    [Abstract] [Full Text] [Related]

  • 3. Inter-individual differences in CpG methylation at D4Z4 correlate with clinical variability in FSHD1 and FSHD2.
    Lemmers RJ, Goeman JJ, van der Vliet PJ, van Nieuwenhuizen MP, Balog J, Vos-Versteeg M, Camano P, Ramos Arroyo MA, Jerico I, Rogers MT, Miller DG, Upadhyaya M, Verschuuren JJ, Lopez de Munain Arregui A, van Engelen BG, Padberg GW, Sacconi S, Tawil R, Tapscott SJ, Bakker B, van der Maarel SM.
    Hum Mol Genet; 2015 Feb 01; 24(3):659-69. PubMed ID: 25256356
    [Abstract] [Full Text] [Related]

  • 4. Genetic and epigenetic contributors to FSHD.
    Daxinger L, Tapscott SJ, van der Maarel SM.
    Curr Opin Genet Dev; 2015 Aug 01; 33():56-61. PubMed ID: 26356006
    [Abstract] [Full Text] [Related]

  • 5. Consequences of epigenetic derepression in facioscapulohumeral muscular dystrophy.
    Greco A, Goossens R, van Engelen B, van der Maarel SM.
    Clin Genet; 2020 Jun 01; 97(6):799-814. PubMed ID: 32086799
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. The cell biology of disease: FSHD: copy number variations on the theme of muscular dystrophy.
    Cabianca DS, Gabellini D.
    J Cell Biol; 2010 Dec 13; 191(6):1049-60. PubMed ID: 21149563
    [Abstract] [Full Text] [Related]

  • 8. Dysregulation of 4q35- and muscle-specific genes in fetuses with a short D4Z4 array linked to facio-scapulo-humeral dystrophy.
    Broucqsault N, Morere J, Gaillard MC, Dumonceaux J, Torrents J, Salort-Campana E, Maues De Paula A, Bartoli M, Fernandez C, Chesnais AL, Ferreboeuf M, Sarda L, Dufour H, Desnuelle C, Attarian S, Levy N, Nguyen K, Magdinier F, Roche S.
    Hum Mol Genet; 2013 Oct 15; 22(20):4206-14. PubMed ID: 23777630
    [Abstract] [Full Text] [Related]

  • 9. Facioscapulohumeral muscular dystrophy.
    Sacconi S, Salviati L, Desnuelle C.
    Biochim Biophys Acta; 2015 Apr 15; 1852(4):607-14. PubMed ID: 24882751
    [Abstract] [Full Text] [Related]

  • 10. Intrinsic epigenetic regulation of the D4Z4 macrosatellite repeat in a transgenic mouse model for FSHD.
    Krom YD, Thijssen PE, Young JM, den Hamer B, Balog J, Yao Z, Maves L, Snider L, Knopp P, Zammit PS, Rijkers T, van Engelen BG, Padberg GW, Frants RR, Tawil R, Tapscott SJ, van der Maarel SM.
    PLoS Genet; 2013 Apr 15; 9(4):e1003415. PubMed ID: 23593020
    [Abstract] [Full Text] [Related]

  • 11. Specific sequence variations within the 4q35 region are associated with facioscapulohumeral muscular dystrophy.
    Lemmers RJ, Wohlgemuth M, van der Gaag KJ, van der Vliet PJ, van Teijlingen CM, de Knijff P, Padberg GW, Frants RR, van der Maarel SM.
    Am J Hum Genet; 2007 Nov 15; 81(5):884-94. PubMed ID: 17924332
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  • 15. A complex interplay of genetic and epigenetic events leads to abnormal expression of the DUX4 gene in facioscapulohumeral muscular dystrophy.
    Gatica LV, Rosa AL.
    Neuromuscul Disord; 2016 Dec 15; 26(12):844-852. PubMed ID: 27816329
    [Abstract] [Full Text] [Related]

  • 16. Facioscapulohumeral muscular dystrophy and DUX4: breaking the silence.
    van der Maarel SM, Tawil R, Tapscott SJ.
    Trends Mol Med; 2011 May 15; 17(5):252-8. PubMed ID: 21288772
    [Abstract] [Full Text] [Related]

  • 17. Facioscapulohumeral Muscular Dystrophy.
    DeSimone AM, Pakula A, Lek A, Emerson CP.
    Compr Physiol; 2017 Sep 12; 7(4):1229-1279. PubMed ID: 28915324
    [Abstract] [Full Text] [Related]

  • 18. Two Cases of Facioscapulohumeral Muscular Dystrophy 2 in Korea.
    Lee JH, Park HJ, Seong MW, Park SS, Choi YC.
    Yonsei Med J; 2021 Jan 12; 62(1):95-98. PubMed ID: 33381940
    [Abstract] [Full Text] [Related]

  • 19. DNA methylation analysis of the macrosatellite repeat associated with FSHD muscular dystrophy at single nucleotide level.
    Huichalaf C, Micheloni S, Ferri G, Caccia R, Gabellini D.
    PLoS One; 2014 Jan 12; 9(12):e115278. PubMed ID: 25545674
    [Abstract] [Full Text] [Related]

  • 20. Pearls in the junk: dissecting the molecular pathogenesis of facioscapulohumeral muscular dystrophy.
    Dmitriev P, Lipinski M, Vassetzky YS.
    Neuromuscul Disord; 2009 Jan 12; 19(1):17-20. PubMed ID: 18974002
    [Abstract] [Full Text] [Related]

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