Absence of α7 integrin in dystrophin-deficient mice causes a myopathy similar to Duchenne muscular dystrophy

By Guo Chun   Willem Michael   Raivich Gennadij   Emerson Michael   Neyses Ludwig   Mayer Ulrike  

Human Molecular Genetics, Vol. 15, Iss. 6, 2006-03 ,pp. : 989-998

Oxford University Press

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Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of α-dystroglycan

By Longman Cheryl  

Human Molecular Genetics, Vol. 12, Iss. 21, 2003-11 ,pp. : 2853-2861

Oxford University Press

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ZZ domain is essentially required for the physiological binding of dystrophin and utrophin to -dystroglycan

By Ishikawa-Sakurai Michiko  

Human Molecular Genetics, Vol. 13, Iss. 7, 2004-04 ,pp. : 693-702

Oxford University Press

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Dystrophin conferral using human endothelium expressing HLA-E in the non-immunosuppressive murine model of Duchenne muscular dystrophy

By Cui Chang-Hao   Miyoshi Shunichiro   Tsuji Hiroko   Makino Hatsune   Kanzaki Seiichi   Kami Daisuke   Terai Masanori   Suzuki Harumi   Umezawa Akihiro  

Human Molecular Genetics, Vol. 20, Iss. 2, 2011-01 ,pp. : 235-244

Oxford University Press

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Read-through compound 13 restores dystrophin expression and improves muscle function in the mdx mouse model for Duchenne muscular dystrophy

By Kayali Refik   Ku Jin-Mo   Khitrov Gregory   Jung Michael E.   Prikhodko Olga   Bertoni Carmen  

Human Molecular Genetics, Vol. 21, Iss. 18, 2012-09 ,pp. : 4007-4020

Oxford University Press

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