Partial loss of Tip60 slows mid-stage neurodegeneration in a spinocerebellar ataxia type 1 (SCA1) mouse model

By Gehrking Kristin M.   Andresen J. Michael   Duvick Lisa   Lough John   Zoghbi Huda Y.   Orr Harry T.  

Human Molecular Genetics, Vol. 20, Iss. 11, 2011-06 ,pp. : 2204-2212

Oxford University Press

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Reversibility of symptoms in a conditional mouse model of spinocerebellar ataxia type 3

By Boy Jana   Schmidt Thorsten   Wolburg Hartwig   Mack Andreas   Nuber Silke   Bttcher Martin   Schmitt Ina   Holzmann Carsten   Zimmermann Frank   Servadio Antonio   Riess Olaf  

Human Molecular Genetics, Vol. 18, Iss. 22, 2009-11 ,pp. : 4282-4295

Oxford University Press

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cDNA Cloning and Expression of rsca1 , the Rat Counterpart of the Human Spinocerebellar Ataxia Type 1 Gene

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Human Molecular Genetics, Vol. 5, Iss. 3, 1996-01 ,pp. : 381-389

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Cloning and Developmental Expression Analysis of the Murine Homolog of the Spinocerebellar Ataxia Type 1 Gene ( Sea1 )

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Human Molecular Genetics, Vol. 5, Iss. 1, 1996-01 ,pp. : 33-40

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CAG repeat length in RAI1 is associated with age at onset variability in spinocerebellar ataxia type 2 (SCA2)

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Human Molecular Genetics, Vol. 9, Iss. 12, 2000-07 ,pp. : 1753-1758

Oxford University Press

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