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Journal Abstract Search

244 related items for PubMed ID: 18583542

  • 1. SJL dystrophic mice express a significant amount of human muscle proteins following systemic delivery of human adipose-derived stromal cells without immunosuppression.
    Vieira NM, Bueno CR, Brandalise V, Moraes LV, Zucconi E, Secco M, Suzuki MF, Camargo MM, Bartolini P, Brum PC, Vainzof M, Zatz M.
    Stem Cells; 2008 Sep; 26(9):2391-8. PubMed ID: 18583542
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  • 2. Human adipose-derived mesenchymal stromal cells injected systemically into GRMD dogs without immunosuppression are able to reach the host muscle and express human dystrophin.
    Vieira NM, Valadares M, Zucconi E, Secco M, Bueno CR, Brandalise V, Assoni A, Gomes J, Landini V, Andrade T, Caetano HV, Vainzof M, Zatz M.
    Cell Transplant; 2012 Sep; 21(7):1407-17. PubMed ID: 23168016
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  • 3. Human multipotent mesenchymal stromal cells from distinct sources show different in vivo potential to differentiate into muscle cells when injected in dystrophic mice.
    Vieira NM, Zucconi E, Bueno CR, Secco M, Suzuki MF, Bartolini P, Vainzof M, Zatz M.
    Stem Cell Rev Rep; 2010 Dec; 6(4):560-6. PubMed ID: 20821076
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  • 8. Painful enlargement of the calf muscles in limb girdle muscular dystrophy type 2B (LGMD2B) with a novel compound heterozygous mutation in DYSF.
    Diers A, Carl M, Stoltenburg-Didinger G, Vorgerd M, Spuler S.
    Neuromuscul Disord; 2007 Feb; 17(2):157-62. PubMed ID: 17129727
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  • 9. Myotilin overexpression enhances myopathology in the LGMD1A mouse model.
    Garvey SM, Liu Y, Miller SE, Hauser MA.
    Muscle Nerve; 2008 May; 37(5):663-7. PubMed ID: 18335471
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  • 10. Dysferlin and muscular dystrophy.
    Bushby KM.
    Acta Neurol Belg; 2000 Sep; 100(3):142-5. PubMed ID: 11098285
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  • 13. The distribution and characterization of skeletal muscle lesions in dysferlin-deficient SJL and A/J mice.
    Kobayashi K, Izawa T, Kuwamura M, Yamate J.
    Exp Toxicol Pathol; 2010 Sep; 62(5):509-17. PubMed ID: 19615872
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  • 14. Dysferlin deletion in SJL mice (SJL-Dysf) defines a natural model for limb girdle muscular dystrophy 2B.
    Bittner RE, Anderson LV, Burkhardt E, Bashir R, Vafiadaki E, Ivanova S, Raffelsberger T, Maerk I, Höger H, Jung M, Karbasiyan M, Storch M, Lassmann H, Moss JA, Davison K, Harrison R, Bushby KM, Reis A.
    Nat Genet; 1999 Oct; 23(2):141-2. PubMed ID: 10508505
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  • 15. Changes in skeletal muscle expression of AQP1 and AQP4 in dystrophinopathy and dysferlinopathy patients.
    Au CG, Butler TL, Egan JR, Cooper ST, Lo HP, Compton AG, North KN, Winlaw DS.
    Acta Neuropathol; 2008 Sep; 116(3):235-46. PubMed ID: 18392839
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  • 16. Limb-girdle muscular dystrophy due to emerin gene mutations.
    Ura S, Hayashi YK, Goto K, Astejada MN, Murakami T, Nagato M, Ohta S, Daimon Y, Takekawa H, Hirata K, Nonaka I, Noguchi S, Nishino I.
    Arch Neurol; 2007 Jul; 64(7):1038-41. PubMed ID: 17620497
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  • 17. Lariat branch point mutation in the dysferlin gene with mild limb-girdle muscular dystrophy.
    Sinnreich M, Therrien C, Karpati G.
    Neurology; 2006 Apr 11; 66(7):1114-6. PubMed ID: 16606933
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  • 18. Molecular etiopathogenesis of limb girdle muscular and congenital muscular dystrophies: boundaries and contiguities.
    Guglieri M, Magri F, Comi GP.
    Clin Chim Acta; 2005 Nov 11; 361(1-2):54-79. PubMed ID: 16002060
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