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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

193 related items for PubMed ID: 21829175

  • 21. Facioscapulohumeral muscular dystrophy.
    Tawil R.
    Handb Clin Neurol; 2018; 148():541-548. PubMed ID: 29478599
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  • 24. The mouse homolog of FRG1, a candidate gene for FSHD, maps proximal to the myodystrophy mutation on chromosome 8.
    Grewal PK, van Deutekom JC, Mills KA, Lemmers RJ, Mathews KD, Frants RR, Hewitt JE.
    Mamm Genome; 1997 Jun; 8(6):394-8. PubMed ID: 9166581
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  • 27. Analysis of allele-specific RNA transcription in FSHD by RNA-DNA FISH in single myonuclei.
    Masny PS, Chan OY, de Greef JC, Bengtsson U, Ehrlich M, Tawil R, Lock LF, Hewitt JE, Stocksdale J, Martin JH, van der Maarel SM, Winokur ST.
    Eur J Hum Genet; 2010 Apr; 18(4):448-56. PubMed ID: 19888305
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  • 32. 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; 26(12):844-852. PubMed ID: 27816329
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  • 33. Facioscapulohumeral muscular dystrophy.
    Tawil R.
    Neurotherapeutics; 2008 Oct; 5(4):601-6. PubMed ID: 19019312
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  • 34. Facioscapulohumeral muscular dystrophy family studies of DUX4 expression: evidence for disease modifiers and a quantitative model of pathogenesis.
    Jones TI, Chen JC, Rahimov F, Homma S, Arashiro P, Beermann ML, King OD, Miller JB, Kunkel LM, Emerson CP, Wagner KR, Jones PL.
    Hum Mol Genet; 2012 Oct 15; 21(20):4419-30. PubMed ID: 22798623
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  • 35. 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
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  • 36. Identification of Epigenetic Regulators of DUX4-fl for Targeted Therapy of Facioscapulohumeral Muscular Dystrophy.
    Himeda CL, Jones TI, Virbasius CM, Zhu LJ, Green MR, Jones PL.
    Mol Ther; 2018 Jul 05; 26(7):1797-1807. PubMed ID: 29759937
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  • 37. [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 05; 18(5):398-401. PubMed ID: 11592052
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  • 38. Early-Onset Infantile Facioscapulohumeral Muscular Dystrophy: A Timely Review.
    Chen TH, Wu YZ, Tseng YH.
    Int J Mol Sci; 2020 Oct 21; 21(20):. PubMed ID: 33096728
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  • 39. [Recent advances in facioscapulohumeral muscular dystrophy].
    Hayashi YK, Goto K, Nishio I.
    Rinsho Shinkeigaku; 2012 Oct 21; 52(11):1154-7. PubMed ID: 23196547
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  • 40. Comprehensive expression analysis of FSHD candidate genes at the mRNA and protein level.
    Klooster R, Straasheijm K, Shah B, Sowden J, Frants R, Thornton C, Tawil R, van der Maarel S.
    Eur J Hum Genet; 2009 Dec 21; 17(12):1615-24. PubMed ID: 19809486
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