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Journal Abstract Search

239 related items for PubMed ID: 16341202

  • 21. DUX4 promotes transcription of FRG2 by directly activating its promoter in facioscapulohumeral muscular dystrophy.
    Thijssen PE, Balog J, Yao Z, Pham TP, Tawil R, Tapscott SJ, Van der Maarel SM.
    Skelet Muscle; 2014; 4():19. PubMed ID: 25789155
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  • 24. Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35.
    van Deutekom JC, Lemmers RJ, Grewal PK, van Geel M, Romberg S, Dauwerse HG, Wright TJ, Padberg GW, Hofker MH, Hewitt JE, Frants RR.
    Hum Mol Genet; 1996 May; 5(5):581-90. PubMed ID: 8733123
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  • 28. 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 May; 6(5):e19780. PubMed ID: 21603621
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  • 29. 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
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  • 30. A nuclear matrix attachment site in the 4q35 locus has an enhancer-blocking activity in vivo: implications for the facio-scapulo-humeral dystrophy.
    Petrov A, Allinne J, Pirozhkova I, Laoudj D, Lipinski M, Vassetzky YS.
    Genome Res; 2008 Jan 20; 18(1):39-45. PubMed ID: 18032730
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  • 31. 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 20; 5(5):294-307. PubMed ID: 23720823
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  • 32. A functional role for 4qA/B in the structural rearrangement of the 4q35 region and in the regulation of FRG1 and ANT1 in facioscapulohumeral dystrophy.
    Pirozhkova I, Petrov A, Dmitriev P, Laoudj D, Lipinski M, Vassetzky Y.
    PLoS One; 2008 Oct 20; 3(10):e3389. PubMed ID: 18852887
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  • 33. Facioscapulohumeral Muscular Dystrophy.
    DeSimone AM, Pakula A, Lek A, Emerson CP.
    Compr Physiol; 2017 Sep 12; 7(4):1229-1279. PubMed ID: 28915324
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  • 37. Facioscapulohumeral muscular dystrophy.
    Tawil R.
    Curr Neurol Neurosci Rep; 2004 Jan 12; 4(1):51-4. PubMed ID: 14683629
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  • 38. 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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  • 39. 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 01; 5(7):e1000559. PubMed ID: 19593370
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