Mitochondrial processes are impaired in hereditary inclusion body myopathy

By Eisenberg Iris   Novershtern Noa   Itzhaki Zohar   Becker-Cohen Michal   Sadeh Menachem   Willems Peter H.G.M.   Friedman Nir   Koopman Werner J.H.   Mitrani-Rosenbaum Stella  

Human Molecular Genetics, Vol. 17, Iss. 23, 2008-12 ,pp. : 3663-3674

Oxford University Press

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Gene shifting: a novel therapy for mitochondrial myopathy

By Taivassalo Tanja   Fu Katherine   Johns Timothy   Arnold Douglas   Karpati George   Shoubridge Eric   Larsson N.G.   Grossman L.I.   Boulet L.   Chomyn A.   Fu K.   Weber K.   Shoubridge E.A.   Moraes C.T.   Moraes C.T.   Moraes C.T.   Keightley J.A.   Shoubridge E.A.   Clark K.M.   Stauber W.T.   Darr K.C.   MacIntyre D.L.   Newham D.J.   Russell B.   Nosaka K.   Clarkson P.M.   Schultz E.   Goldberg A.L.   Schiaffino S.   Rosenblatt J.D.   Snow M.H.   Sale D.G.  

Human Molecular Genetics, Vol. 8, Iss. 6, 1999-06 ,pp. : 1047-1052

Oxford University Press

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Collagen VI deficiency induces early onset myopathy in the mouse: an animal model for Bethlem myopathy

By Bonaldo P.   Braghetta P.   Zanetti M.   Piccolo S.   Volpin D.   Bressan G.M.  

Human Molecular Genetics, Vol. 7, Iss. 13, 1998-12 ,pp. : 2135-2140

Oxford University Press

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Effect of bezafibrate treatment on late-onset mitochondrial myopathy in mice

By Yatsuga Shuichi   Suomalainen Anu  

Human Molecular Genetics, Vol. 21, Iss. 3, 2012-02 ,pp. : 526-535

Oxford University Press

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Ketogenic diet slows down mitochondrial myopathy progression in mice

By Ahola-Erkkil Sofia   Carroll Christopher J.   Peltola-Mjsund Katja   Tulkki Valtteri   Mattila Ismo   Seppnen-Laakso Tuulikki   Orei Matej   Tyynismaa Henna   Suomalainen Anu  

Human Molecular Genetics, Vol. 19, Iss. 10, 2010-05 ,pp. : 1974-1984

Oxford University Press

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