Naturally occurring utrophin correlates with disease severity in Duchenne muscular dystrophy

By Kleopa Kleopas A.   Drousiotou Anthi   Ormiston Annita   Kyriakides Theodoros  

Human Molecular Genetics, Vol. 15, Iss. 10, 2006-05 ,pp. : 1623-1628

Oxford University Press

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Identification of transcripts from a subtraction library which might be responsible for the mild phenotype in an intrafamilially variable course of Duchenne muscular dystrophy

By Sifringer Marco   Uhlenberg Birgit   Lammel Stefanie   Hanke Rita   Neumann Benjamin   Moers Arpad   Koch Ina   Speer Astrid  

Human Genetics, Vol. 114, Iss. 2, 2004-01 ,pp. : 149-156

Springer Publishing Company

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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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Novel mutations and genotype–phenotype relationships in 107 families with Fukuyama-type congenital muscular dystrophy (FCMD)

By Kondo-Iida Eri  

Human Molecular Genetics, Vol. 8, Iss. 12, 1999-11 ,pp. : 2303-2309

Oxford University Press

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

By Hino Hirotake  

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

Oxford University Press

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