Abundant expression and cytoplasmic aggregations of α 1A voltage-dependent calcium channel protein associated with neurodegeneration in spinocerebellar ataxia type 6

By Ishikawa Kinya  

Human Molecular Genetics, Vol. 8, Iss. 7, 1999-07 ,pp. : 1185-1193

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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Pantothenate kinase-associated neurodegeneration: insights from a Drosophila model

By Wu Zhihao   Li Chenghua   Lv Shan   Zhou Bing  

Human Molecular Genetics, Vol. 18, Iss. 19, 2009-10 ,pp. : 3659-3672

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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