Interleukin-10 reduces the pathology of mdx muscular dystrophy by deactivating M1 macrophages and modulating macrophage phenotype

By Villalta S. Armando   Rinaldi Chiara   Deng Bo   Liu Grace   Fedor Brian   Tidball James G.  

Human Molecular Genetics, Vol. 20, Iss. 4, 2011-02 ,pp. : 790-805

Oxford University Press

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Myopathy phenotype in transgenic mice expressing mutated PABPN1 as a model of oculopharyngeal muscular dystrophy

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Human Molecular Genetics, Vol. 13, Iss. 2, 2004-01 ,pp. : 181-190

Oxford University Press

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Disruption of nesprin-1 produces an Emery Dreifuss muscular dystrophy-like phenotype in mice

By Puckelwartz Megan J.   Kessler Eric   Zhang Yuan   Hodzic Didier   Randles K. Natalie   Morris Glenn   Earley Judy U.   Hadhazy Michele   Holaska James M.   Mewborn Stephanie K.   Pytel Peter   McNally Elizabeth M.  

Human Molecular Genetics, Vol. 18, Iss. 4, 2009-02 ,pp. : 607-620

Oxford University Press

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Mdx mice inducibly expressing dystrophin provide insights into the potential of gene therapy for Duchenne muscular dystrophy

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Human Molecular Genetics, Vol. 9, Iss. 17, 2000-10 ,pp. : 2507-2515

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Amelioration of Duchenne muscular dystrophy in mdx mice by elimination of matrix-associated fibrin-driven inflammation coupled to the α M β 2 leukocyte integrin receptor

By Vidal Berta   Ardite Esther   Suelves Mònica   Ruiz-Bonilla Vanessa   Janué Anna   Flick Matthew J.   Degen Jay L.   Serrano Antonio L.   Muñoz-Cánoves Pura  

Human Molecular Genetics, Vol. 21, Iss. 9, 2012-05 ,pp. : 1989-2004

Oxford University Press

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