Dystrophin and utrophin expression require sarcospan: loss of α7 integrin exacerbates a newly discovered muscle phenotype in sarcospan-null mice

By Marshall Jamie L.   Chou Eric   Oh Jennifer   Kwok Allan   Burkin Dean J.   Crosbie-Watson Rachelle H.  

Human Molecular Genetics, Vol. 21, Iss. 20, 2012-10 ,pp. : 4378-4393

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

Oxford University Press

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Characterization of dystrophin and utrophin diversity in the mouse

By Lumeng C.N.   Phelps S.F.   Rafael J.A.   Cox G.A.   Hutchinson T.L.   Begy C.R.   Adkins E.   Wiltshire R.   Chamberlain J.S.  

Human Molecular Genetics, Vol. 8, Iss. 4, 1999-04 ,pp. : 593-599

Oxford University Press

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-Actinin-3 deficiency results in reduced glycogen phosphorylase activity and altered calcium handling in skeletal muscle

By Quinlan Kate G.R.   Seto Jane T.   Turner Nigel   Vandebrouck Aurelie   Floetenmeyer Matthias   Macarthur Daniel G.   Raftery Joanna M.   Lek Monkol   Yang Nan   Parton Robert G.   Cooney Gregory J.   North Kathryn N.  

Human Molecular Genetics, Vol. 19, Iss. 7, 2010-04 ,pp. : 1335-1346

Oxford University Press

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Mice lacking COX10 in skeletal muscle recapitulate the phenotype of progressive mitochondrial myopathies associated with cytochrome c oxidase deficiency

By Diaz Francisca  

Human Molecular Genetics, Vol. 14, Iss. 18, 2005-09 ,pp. : 2737-2748

Oxford University Press

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