A highly functional mini-dystrophin/GFP fusion gene for cell and gene therapy studies of Duchenne muscular dystrophy

By Li Sheng   Kimura En   Ng Rainer   Fall Brent M.   Meuse Leonard   Reyes Morayma   Faulkner John A.   Chamberlain Jeffrey S.  

Human Molecular Genetics, Vol. 15, Iss. 10, 2006-05 ,pp. : 1610-1622

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

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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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

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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

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