An understanding of spinocerebellar ataxia.

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Clinical Characteristics, Radiological Features and Gene Mutation in 10 Chinese Families with Spinocerebellar Ataxias.Localized vs. Systematic Neurodegeneration: A Paradigm Shift in Understanding Neurodegenerative Diseases.Epigenetic profiles in polyglutamine disorders.

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P2860

An understanding of spinocerebellar ataxia.

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2015 nî lūn-bûn

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An understanding of spinocerebellar ataxia.

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An understanding of spinocerebellar ataxia.

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An understanding of spinocerebellar ataxia.

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P1476

An understanding of spinocerebellar ataxia.

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P2093

L Kusuma

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N B Ramachandra

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P2860

Reconstructing Indian population history

Animal models of polyglutamine diseases and therapeutic approaches

Complex genetic origin of Indian populations and its implications

CTCF regulates ataxin-7 expression through promotion of a convergently transcribed, antisense noncoding RNA.

Genomic context drives SCA7 CAG repeat instability, while expressed SCA7 cDNAs are intergenerationally and somatically stable in transgenic mice.

Molecular pathogenesis and cellular pathology of spinocerebellar ataxia type 7 neurodegeneration

Design of RNAi hairpins for mutation-specific silencing of ataxin-7 and correction of a SCA7 phenotype.

Spinocerebellar ataxia 7 (SCA7) in Indian population: predilection of ATXN7-CAG expansion mutation in an ethnic population

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.

Reduction of mutant ataxin-7 expression restores motor function and prevents cerebellar synaptic reorganization in a conditional mouse model of SCA7

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English

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An understanding of spinocerebellar ataxia.

about

P2860

P2860

An understanding of spinocerebellar ataxia.

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P1476

P2093

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