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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

207 related items for PubMed ID: 21730972

  • 21.
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  • 22. Muscle-specific promoters may be necessary for adeno-associated virus-mediated gene transfer in the treatment of muscular dystrophies.
    Cordier L, Gao GP, Hack AA, McNally EM, Wilson JM, Chirmule N, Sweeney HL.
    Hum Gene Ther; 2001 Jan 20; 12(2):205-15. PubMed ID: 11177557
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  • 23. AAV-mediated follistatin gene therapy improves functional outcomes in the TIC-DUX4 mouse model of FSHD.
    Giesige CR, Wallace LM, Heller KN, Eidahl JO, Saad NY, Fowler AM, Pyne NK, Al-Kharsan M, Rashnonejad A, Chermahini GA, Domire JS, Mukweyi D, Garwick-Coppens SE, Guckes SM, McLaughlin KJ, Meyer K, Rodino-Klapac LR, Harper SQ.
    JCI Insight; 2018 Nov 15; 3(22):. PubMed ID: 30429376
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  • 24. Transduction Efficiency of Adeno-Associated Virus Serotypes After Local Injection in Mouse and Human Skeletal Muscle.
    Muraine L, Bensalah M, Dhiab J, Cordova G, Arandel L, Marhic A, Chapart M, Vasseur S, Benkhelifa-Ziyyat S, Bigot A, Butler-Browne G, Mouly V, Negroni E, Trollet C.
    Hum Gene Ther; 2020 Feb 15; 31(3-4):233-240. PubMed ID: 31880951
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  • 25. DUX4, a candidate gene for facioscapulohumeral muscular dystrophy, causes p53-dependent myopathy in vivo.
    Wallace LM, Garwick SE, Mei W, Belayew A, Coppee F, Ladner KJ, Guttridge D, Yang J, Harper SQ.
    Ann Neurol; 2011 Mar 15; 69(3):540-52. PubMed ID: 21446026
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  • 26. 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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  • 27. From Mice to Humans: An Overview of the Potentials and Limitations of Current Transgenic Mouse Models of Major Muscular Dystrophies and Congenital Myopathies.
    Sztretye M, Szabó L, Dobrosi N, Fodor J, Szentesi P, Almássy J, Magyar ZÉ, Dienes B, Csernoch L.
    Int J Mol Sci; 2020 Nov 25; 21(23):. PubMed ID: 33255644
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  • 28. Current status and future prospect of FSHD region gene 1.
    Hansda AK, Tiwari A, Dixit M.
    J Biosci; 2017 Jun 25; 42(2):345-353. PubMed ID: 28569257
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  • 32. AAV-directed muscular dystrophy gene therapy.
    Tang Y, Cummins J, Huard J, Wang B.
    Expert Opin Biol Ther; 2010 Mar 25; 10(3):395-408. PubMed ID: 20132060
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  • 33. Gene therapy for muscular dystrophy: lessons learned and path forward.
    Mendell JR, Rodino-Klapac L, Sahenk Z, Malik V, Kaspar BK, Walker CM, Clark KR.
    Neurosci Lett; 2012 Oct 11; 527(2):90-9. PubMed ID: 22609847
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  • 38. Facioscapulohumeral muscular dystrophy (FSHD) region gene 1 (FRG1) expression and possible function in mouse tooth germ development.
    Hasegawa K, Wada H, Nagata K, Fujiwara H, Wada N, Someya H, Mikami Y, Sakai H, Kiyoshima T.
    J Mol Histol; 2016 Aug 11; 47(4):375-87. PubMed ID: 27234941
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