Flt-1 haploinsufficiency ameliorates muscular dystrophy phenotype by developmentally increased vasculature in mdx mice

By Verma Mayank   Asakura Yoko   Hirai Hiroyuki   Watanabe Shuichi   Tastad Christopher   Fong Guo-Hua   Ema Masatsugu   Call Jarrod A.   Lowe Dawn A.   Asakura Atsushi  

Human Molecular Genetics, Vol. 19, Iss. 21, 2010-11 ,pp. : 4145-4159

Oxford University Press

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Shifts in macrophage phenotypes and macrophage competition for arginine metabolism affect the severity of muscle pathology in muscular dystrophy

By Villalta S. Armando   Nguyen Hal X.   Deng Bo   Gotoh Tomomi   Tidball James G.  

Human Molecular Genetics, Vol. 18, Iss. 3, 2009-02 ,pp. : 482-496

Oxford University Press

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Trehalose reduces aggregate formation and delays pathology in a transgenic mouse model of oculopharyngeal muscular dystrophy

By Davies Janet E.   Sarkar Sovan   Rubinsztein David C.  

Human Molecular Genetics, Vol. 15, Iss. 1, 2006-01 ,pp. : 23-31

Oxford University Press

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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

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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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