Millipore

Anti-Spinocerebellar Ataxia Type 3, clone 1H9

#MAB5360 · western blot

46
Citing papers
1.4k
Combined citations
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Research areas

Genetic Neurodegenerative Diseases38Mitochondrial Function and Pathology22RNA Research and Splicing10Ubiquitin and proteasome pathways7Muscle Physiology and Disorders7Amyotrophic Lateral Sclerosis Research6DNA Repair Mechanisms4Pluripotent Stem Cells Research3

Papers citing this product

1
Autophagy induction reduces mutant ataxin-3 levels and toxicity in a mouse model of spinocerebellar ataxia type 3
Brain·2009·260 cit.·DOI
2
Oligonucleotide therapy mitigates disease in spinocerebellar ataxia type 3 mice
Annals of Neurology·2018·156 cit.·DOI
3
The ubiquitin ligase UBR5 suppresses proteostasis collapse in pluripotent stem cells from Huntington’s disease patients
Nature Communications·2018·106 cit.·DOI
4
Inactivation of PNKP by Mutant ATXN3 Triggers Apoptosis by Activating the DNA Damage-Response Pathway in SCA3
PLoS Genetics·2015·84 cit.·DOI
5
Development of an AAV-Based MicroRNA Gene Therapy to Treat Machado-Joseph Disease
Molecular Therapy — Methods & Clinical Development·2019·57 cit.·DOI
6
Comparison of spinocerebellar ataxia type 3 mouse models identifies early gain-of-function, cell-autonomous transcriptional changes in oligodendrocytes
Human Molecular Genetics·2017·55 cit.·DOI
7
Nuclear retention of full-length HTT RNA is mediated by splicing factors MBNL1 and U2AF65
Scientific Reports·2015·55 cit.·DOI
8
Alternative polyadenylation transcriptome-wide association study identifies APA-linked susceptibility genes in brain disorders
Nature Communications·2023·54 cit.·DOI
9
Impaired Oligodendrocyte Maturation Is an Early Feature in SCA3 Disease Pathogenesis
Journal of Neuroscience·2022·51 cit.·DOI
10
RNA duplexes with abasic substitutions are potent and allele-selective inhibitors of huntingtin and ataxin-3 expression
Nucleic Acids Research·2013·43 cit.·DOI

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