SCA6 is Caused by Moderate CAG Expansion in the α 1A -Voltage-Dependent Calcium Channel Gene

By Riess Olaf  

Human Molecular Genetics, Vol. 6, Iss. 8, 1997-01 ,pp. : 1289-1293

Oxford University Press

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Protein interacting with C kinase (PICK1) is a suppressor of spinocerebellar ataxia 3-associated neurodegeneration in Drosophila

By McGurk Leeanne   Bonini Nancy M.  

Human Molecular Genetics, Vol. 21, Iss. 1, 2012-01 ,pp. : 76-84

Oxford University Press

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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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-III spectrin mutation L253P associated with spinocerebellar ataxia type 5 interferes with binding to Arp1 and protein trafficking from the Golgi

By Clarkson Yvonne L.   Gillespie Trudi   Perkins Emma M.   Lyndon Alastair R.   Jackson Mandy  

Human Molecular Genetics, Vol. 19, Iss. 18, 2010-09 ,pp. : 3634-3641

Oxford University Press

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Transcriptional dysregulation of TrkA associates with neurodegeneration in spinocerebellar ataxia type 17

By Shah Anjali G.   Friedman Meyer J.   Huang Shanshan   Roberts Meredith   Li Xiao-Jiang   Li Shihua  

Human Molecular Genetics, Vol. 18, Iss. 21, 2009-11 ,pp. : 4141-4152

Oxford University Press

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