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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

199 related items for PubMed ID: 23196547

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  • 2. 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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  • 3. 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 12; 26(12):844-852. PubMed ID: 27816329
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  • 8. Facioscapulohumeral muscular dystrophy: molecular pathological advances and future directions.
    Statland JM, Tawil R.
    Curr Opin Neurol; 2011 Oct 12; 24(5):423-8. PubMed ID: 21734574
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  • 12. Facioscapulohumeral muscular dystrophy (FSHD): an enigma unravelled?
    Richards M, Coppée F, Thomas N, Belayew A, Upadhyaya M.
    Hum Genet; 2012 Mar 12; 131(3):325-40. PubMed ID: 21984394
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  • 13. [Facioscapulohumeral muscular dystrophy type 2].
    Sacconi S, Desnuelle C.
    Rev Neurol (Paris); 2013 Mar 12; 169(8-9):564-72. PubMed ID: 23969240
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  • 16. Molecular basis of facioscapulohumeral muscular dystrophy.
    Tupler R, Gabellini D.
    Cell Mol Life Sci; 2004 Mar 12; 61(5):557-566. PubMed ID: 15004695
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  • 17. CRISPR/dCas9-mediated Transcriptional Inhibition Ameliorates the Epigenetic Dysregulation at D4Z4 and Represses DUX4-fl in FSH Muscular Dystrophy.
    Himeda CL, Jones TI, Jones PL.
    Mol Ther; 2016 Mar 12; 24(3):527-35. PubMed ID: 26527377
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  • 19. 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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