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Journal Abstract Search

153 related items for PubMed ID: 20215405

  • 1. 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
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  • 2. 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 01; 81(2):107-18. PubMed ID: 20970242
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  • 5. 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 Feb 01; 10(2):e0117665. PubMed ID: 25695429
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  • 7. 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
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  • 9. 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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  • 14. 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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  • 15. 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 20; 19(11):2055-64. PubMed ID: 21829175
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  • 16. Overexpression of facioscapulohumeral muscular dystrophy region gene 1 causes primary defects in myogenic stem cells.
    Xynos A, Neguembor MV, Caccia R, Licastro D, Nonis A, Di Serio C, Stupka E, Gabellini D.
    J Cell Sci; 2013 May 15; 126(Pt 10):2236-45. PubMed ID: 23525014
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  • 17. DYC-1, a protein functionally linked to dystrophin in Caenorhabditis elegans is associated with the dense body, where it interacts with the muscle LIM domain protein ZYX-1.
    Lecroisey C, Martin E, Mariol MC, Granger L, Schwab Y, Labouesse M, Ségalat L, Gieseler K.
    Mol Biol Cell; 2008 Mar 15; 19(3):785-96. PubMed ID: 18094057
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  • 18. Functional muscle impairment in facioscapulohumeral muscular dystrophy is correlated with oxidative stress and mitochondrial dysfunction.
    Turki A, Hayot M, Carnac G, Pillard F, Passerieux E, Bommart S, Raynaud de Mauverger E, Hugon G, Pincemail J, Pietri S, Lambert K, Belayew A, Vassetzky Y, Juntas Morales R, Mercier J, Laoudj-Chenivesse D.
    Free Radic Biol Med; 2012 Sep 01; 53(5):1068-79. PubMed ID: 22796148
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  • 19. [Progress in researches on the molecular genetics of facioscapulohumeral muscular dystrophy].
    Su Q, Zhang C.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Oct 01; 18(5):398-401. PubMed ID: 11592052
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  • 20. Mesoangioblasts from facioscapulohumeral muscular dystrophy display in vivo a variable myogenic ability predictable by their in vitro behavior.
    Morosetti R, Gidaro T, Broccolini A, Gliubizzi C, Sancricca C, Tonali PA, Ricci E, Mirabella M.
    Cell Transplant; 2011 Oct 01; 20(8):1299-313. PubMed ID: 21176400
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