Identification and characterization of the gene causing type 1 spinocerebellar ataxia

Biochemistry, Genetics and Molecular Biology

• Allele 50%
• Alternative Splicing 50%
• CAG Repeat 50%
• Coding Region 100%
• Exon 100%
• Polyglutamine Tract 50%
• Translational Regulation 50%
• Trinucleotide Repeat Expansion 50%
• Untranslated Region 100%
• Wild Type 50%

Keyphrases

• 3′-untranslated Region (3′-UTR) 20%
• 5′-untranslated Region (5′-UTR) 20%
• Alternative Splicing 20%
• Ataxin-1 20%
• CAG Repeat 20%
• CAG Trinucleotide Repeat 20%
• Coding Exons 20%
• Coding Region 40%
• Encoded Protein 20%
• Exon 20%
• Genomic DNA (gDNA) 20%
• Neurodegenerative Diseases 20%
• Polyglutamine Tract 20%
• Spinocerebellar Ataxia 100%
• Transcriptional Regulation 20%
• Translational Regulation 20%

Neuroscience

• Alternative Splicing 20%
• CAG Repeat 20%
• Coding Region 40%
• Exon 40%
• Genomic DNA 20%
• Neurodegenerative Disorder 20%
• Polyglutamine 20%
• Spinocerebellar Ataxia 100%
• Translational Regulation 20%
• Trinucleotide Repeat 20%
• Untranslated Region 40%