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Journal Abstract Search

158 related items for PubMed ID: 16288871

  • 21. Symptomatic dysferlin gene mutation carriers: characterization of two cases.
    Illa I, De Luna N, Domínguez-Perles R, Rojas-García R, Paradas C, Palmer J, Márquez C, Gallano P, Gallardo E.
    Neurology; 2007 Apr 17; 68(16):1284-9. PubMed ID: 17287450
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  • 24. Absence of T and B lymphocytes modulates dystrophic features in dysferlin deficient animal model.
    Farini A, Sitzia C, Navarro C, D'Antona G, Belicchi M, Parolini D, Del Fraro G, Razini P, Bottinelli R, Meregalli M, Torrente Y.
    Exp Cell Res; 2012 Jun 10; 318(10):1160-74. PubMed ID: 22465227
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  • 25. 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 10; 116(3):235-46. PubMed ID: 18392839
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  • 28. 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 10; 26(9):2391-8. PubMed ID: 18583542
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  • 30. Absence of alpha 7 integrin in dystrophin-deficient mice causes a myopathy similar to Duchenne muscular dystrophy.
    Guo C, Willem M, Werner A, Raivich G, Emerson M, Neyses L, Mayer U.
    Hum Mol Genet; 2006 Mar 15; 15(6):989-98. PubMed ID: 16476707
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  • 31. Strong induction of the Tis11B gene in myogenic differentiation.
    Busse M, Schwarzburger M, Berger F, Hacker C, Munz B.
    Eur J Cell Biol; 2008 Jan 15; 87(1):31-8. PubMed ID: 17889962
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  • 32. Characterization of lobulated fibers in limb girdle muscular dystrophy type 2A by gene expression profiling.
    Keira Y, Noguchi S, Kurokawa R, Fujita M, Minami N, Hayashi YK, Kato T, Nishino I.
    Neurosci Res; 2007 Apr 15; 57(4):513-21. PubMed ID: 17258832
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  • 33. Bone marrow transplantation improves outcome in a mouse model of congenital muscular dystrophy.
    Hagiwara H, Ohsawa Y, Asakura S, Murakami T, Teshima T, Sunada Y.
    FEBS Lett; 2006 Aug 07; 580(18):4463-8. PubMed ID: 16859688
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  • 35. Dysferlin expression after normal myoblast transplantation in SCID and in SJL mice.
    Leriche-Guérin K, Anderson LV, Wrogemann K, Roy B, Goulet M, Tremblay JP.
    Neuromuscul Disord; 2002 Feb 07; 12(2):167-73. PubMed ID: 11738359
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  • 36. Expression Analysis Systematic Explorer (EASE) analysis reveals differential gene expression in permanent and transient focal stroke rat models.
    Ford G, Xu Z, Gates A, Jiang J, Ford BD.
    Brain Res; 2006 Feb 03; 1071(1):226-36. PubMed ID: 16409990
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  • 40. Up-regulation of MHC class I expression accompanies but is not required for spontaneous myopathy in dysferlin-deficient SJL/J mice.
    Kostek CA, Dominov JA, Miller JB.
    Am J Pathol; 2002 Mar 03; 160(3):833-9. PubMed ID: 11891182
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