Gcn5 loss-of-function accelerates cerebellar and retinal degeneration in a SCA7 mouse model

By Chen Yi Chun   Gatchel Jennifer R.   Lewis Rebecca W.   Mao Chai-An   Grant Patrick A.   Zoghbi Huda Y.   Dent Sharon Y.R.  

Human Molecular Genetics, Vol. 21, Iss. 2, 2012-01 ,pp. : 394-405

Oxford University Press

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SCA7 mouse models show selective stabilization of mutant ataxin-7 and similar cellular responses in different neuronal cell types

By Lindenberg K.S.   Landwehrmeyer G.B.   Yvert G.   Devys D.   Helmlinger D.   Mandel J-L.  

Human Molecular Genetics, Vol. 10, Iss. 16, 2001-08 ,pp. : 1679-1692

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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Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy ( SCA7 )

By David G.  

Human Molecular Genetics, Vol. 7, Iss. 2, 1998-02 ,pp. : 165-170

Oxford University Press

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Ataxin-7 associates with microtubules and stabilizes the cytoskeletal network

By Nakamura Yoko   Tagawa Kazuhiko   Oka Tsutomu   Sasabe Toshikazu   Ito Hikaru   Shiwaku Hiroki   La Spada Albert R.   Okazawa Hitoshi  

Human Molecular Genetics, Vol. 21, Iss. 5, 2012-03 ,pp. : 1099-1110

Oxford University Press

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