SCA1-like disease in mice expressing wild-type ataxin-1 with a serine to aspartic acid replacement at residue 776. [electronic resource]
Producer: 20101015Description: 929-35 p. digitalISSN:- 1097-4199
- Animals
- Aspartic Acid -- genetics
- Ataxin-1
- Ataxins
- Calbindins
- Cerebellum -- pathology
- Dendrites -- metabolism
- Disease Models, Animal
- Gene Expression Regulation -- genetics
- Mice
- Mice, Transgenic
- Motor Activity -- genetics
- Mutation -- genetics
- Nerve Tissue Proteins -- genetics
- Neural Pathways -- metabolism
- Nuclear Proteins -- genetics
- Purkinje Cells -- pathology
- Rotarod Performance Test
- S100 Calcium Binding Protein G -- metabolism
- Serine -- genetics
- Spinocerebellar Ataxias -- genetics
- Vesicular Glutamate Transport Protein 2 -- metabolism
No physical items for this record
Publication Type: Journal Article; Research Support, N.I.H., Extramural
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