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Journal Abstract Search

182 related items for PubMed ID: 20970242

  • 1. Facioscapulohumeral muscular dystrophy (FSHD) region gene 1 (FRG1) is a dynamic nuclear and sarcomeric protein.
    Hanel ML, Sun CY, Jones TI, Long SW, Zanotti S, Milner D, Jones PL.
    Differentiation; 2011 Feb; 81(2):107-18. PubMed ID: 20970242
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. FHL1 reduces dystrophy in transgenic mice overexpressing FSHD muscular dystrophy region gene 1 (FRG1).
    Feeney SJ, McGrath MJ, Sriratana A, Gehrig SM, Lynch GS, D'Arcy CE, Price JT, McLean CA, Tupler R, Mitchell CA.
    PLoS One; 2015 Jul 16; 10(2):e0117665. PubMed ID: 25695429
    [Abstract] [Full Text] [Related]

  • 4. Facioscapulohumeral muscular dystrophy region gene-1 (FRG-1) is an actin-bundling protein associated with muscle-attachment sites.
    Liu Q, Jones TI, Tang VW, Brieher WM, Jones PL.
    J Cell Sci; 2010 Apr 01; 123(Pt 7):1116-23. PubMed ID: 20215405
    [Abstract] [Full Text] [Related]

  • 5. Direct interplay between two candidate genes in FSHD muscular dystrophy.
    Ferri G, Huichalaf CH, Caccia R, Gabellini D.
    Hum Mol Genet; 2015 Mar 01; 24(5):1256-66. PubMed ID: 25326393
    [Abstract] [Full Text] [Related]

  • 6. Rbfox1 downregulation and altered calpain 3 splicing by FRG1 in a mouse model of Facioscapulohumeral muscular dystrophy (FSHD).
    Pistoni M, Shiue L, Cline MS, Bortolanza S, Neguembor MV, Xynos A, Ares M, Gabellini D.
    PLoS Genet; 2013 Mar 01; 9(1):e1003186. PubMed ID: 23300487
    [Abstract] [Full Text] [Related]

  • 7. Transgenic Drosophila for Investigating DUX4 and FRG1, Two Genes Associated with Facioscapulohumeral Muscular Dystrophy (FSHD).
    Jones TI, Parilla M, Jones PL.
    PLoS One; 2016 Mar 01; 11(3):e0150938. PubMed ID: 26942723
    [Abstract] [Full Text] [Related]

  • 8. Muscular dystrophy candidate gene FRG1 is critical for muscle development.
    Hanel ML, Wuebbles RD, Jones PL.
    Dev Dyn; 2009 Jun 01; 238(6):1502-12. PubMed ID: 19097195
    [Abstract] [Full Text] [Related]

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  • 11. Current status and future prospect of FSHD region gene 1.
    Hansda AK, Tiwari A, Dixit M.
    J Biosci; 2017 Jun 01; 42(2):345-353. PubMed ID: 28569257
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  • 12. AAV6-mediated systemic shRNA delivery reverses disease in a mouse model of facioscapulohumeral muscular dystrophy.
    Bortolanza S, Nonis A, Sanvito F, Maciotta S, Sitia G, Wei J, Torrente Y, Di Serio C, Chamberlain JR, Gabellini D.
    Mol Ther; 2011 Nov 01; 19(11):2055-64. PubMed ID: 21829175
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  • 13. FSHD region gene 1 (FRG1) is crucial for angiogenesis linking FRG1 to facioscapulohumeral muscular dystrophy-associated vasculopathy.
    Wuebbles RD, Hanel ML, Jones PL.
    Dis Model Mech; 2009 Nov 01; 2(5-6):267-74. PubMed ID: 19383939
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  • 14. FSHD muscular dystrophy region gene 1 binds Suv4-20h1 histone methyltransferase and impairs myogenesis.
    Neguembor MV, Xynos A, Onorati MC, Caccia R, Bortolanza S, Godio C, Pistoni M, Corona DF, Schotta G, Gabellini D.
    J Mol Cell Biol; 2013 Oct 01; 5(5):294-307. PubMed ID: 23720823
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  • 16. Testing the effects of FSHD candidate gene expression in vertebrate muscle development.
    Wuebbles RD, Long SW, Hanel ML, Jones PL.
    Int J Clin Exp Pathol; 2010 Mar 28; 3(4):386-400. PubMed ID: 20490329
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  • 17. Nuclear bodies reorganize during myogenesis in vitro and are differentially disrupted by expression of FSHD-associated DUX4.
    Homma S, Beermann ML, Yu B, Boyce FM, Miller JB.
    Skelet Muscle; 2016 Dec 01; 6(1):42. PubMed ID: 27906075
    [Abstract] [Full Text] [Related]

  • 18. Decreased proliferation kinetics of mouse myoblasts overexpressing FRG1.
    Chen SC, Frett E, Marx J, Bosnakovski D, Reed X, Kyba M, Kennedy BK.
    PLoS One; 2011 Dec 01; 6(5):e19780. PubMed ID: 21603621
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  • 20. 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
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