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Xi Lin

University of Texas Medical Branch

13

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769

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Instability of expanded CAG/CAA repeats in spinocerebellar ataxia type 17

2008 European Journal of Human Genetics
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Clinical and molecular diagnosis of a Costa Rican family with autosomal recessive myotonia congenita (Becker disease) carrying a new mutation in the CLCN1 gene

2006 Revista De Biologia Tropical
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Recent Progress in Spinocerebellar Ataxia Type 10

2006
- Xi Lin
- Tetsuo Ashizawa
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Ataxin 10 induces neuritogenesis via interaction with G‐protein β2 subunit

2006 Journal of Neuroscience Research
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The role of ataxin 10 in the pathogenesis of spinocerebellar ataxia type 10

2006 Neurology
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Recent progress in spinocerebellar ataxia type-10 (SCA10)

2005 The Cerebellum
- Xi Lin
- Tetsuo Ashizawa
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Somatic and Germline Instability of the ATTCT Repeat in Spinocerebellar Ataxia Type 10

2004 American Journal of Human Genetics
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Prenylcysteine carboxylmethyltransferase is essential for the earliest stages of liver development in mice

2002 Gastroenterology
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Calcium Dynamics and Electrophysiological Properties of Cerebellar Purkinje Cells in SCA1 Transgenic Mice

2001 Journal of Neurophysiology
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The Cerebellum and its Disorders: Spinocerebellar ataxia type 1

2001
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