Molecular Targets and Therapeutic Strategies in Spinocerebellar Ataxia Type 7 | SpringerLink
Cross-talking noncoding RNAs contribute to cell-specific neurodegeneration in SCA7. - Abstract - Europe PMC
Biomolecules | Free Full-Text | Altered Plasma Acylcarnitines and Amino Acids Profile in Spinocerebellar Ataxia Type 7 | HTML
Spinocerebellar Ataxia 7 | SpringerLink
Biomolecules | Free Full-Text | Altered Plasma Acylcarnitines and Amino Acids Profile in Spinocerebellar Ataxia Type 7 | HTML
Spinocerebellar ataxia type 7: SCA7 - Ataxia UK
A SCA7 premutation may be a novel Mendelian modifier of MS course: A case report - Multiple Sclerosis and Related Disorders
Disease Progression Despite Early Loss of Polyglutamine Protein Expression in SCA7 Mouse Model | Journal of Neuroscience
Disease Progression Despite Early Loss of Polyglutamine Protein Expression in SCA7 Mouse Model | Journal of Neuroscience
IJMS | Free Full-Text | Current Status of Gene Therapy Research in Polyglutamine Spinocerebellar Ataxias | HTML
Genetics, Mechanisms, and Therapeutic Progress in Polyglutamine Spinocerebellar Ataxias | SpringerLink
Genes | Free Full-Text | Mutant CAG Repeats Effectively Targeted by RNA Interference in SCA7 Cells | HTML
Cross-talking noncoding RNAs contribute to cell-specific neurodegeneration in SCA7 | Nature Structural & Molecular Biology
A Proposal for Classification of Retinal Degeneration in Spinocerebellar Ataxia Type 7 | SpringerLink
PDF) Modulation of Increased mGluR1 Signaling by RGS8 Protects Purkinje Cells From Dendritic Reduction and Could Be a Common Mechanism in Diverse Forms of Spinocerebellar Ataxia
Molecular Targets and Therapeutic Strategies in Spinocerebellar Ataxia Type 7 | SpringerLink
Figure 2 | Brain pathology of spinocerebellar ataxias | SpringerLink
Cross-talking noncoding RNAs contribute to cell-specific neurodegeneration in SCA7 | Nature Structural & Molecular Biology
Allele-specific silencing of mutant Ataxin-7 in SCA7 patient-derived fibroblasts | European Journal of Human Genetics
Veränderungen im Genom: Mutationen | SpringerLink
Disease Progression Despite Early Loss of Polyglutamine Protein Expression in SCA7 Mouse Model | Journal of Neuroscience
Genetic Underpinnings of Neurodegenerative Condition Uncovered | Technology Networks
SCA7 Through My Eyes
Cross-talking noncoding RNAs contribute to cell-specific neurodegeneration in SCA7 | Nature Structural & Molecular Biology
