Druggable genome screen identifies new regulators of the abundance and toxicity of ATXN3, the Spinocerebellar Ataxia type 3 disease protein-Reference-Cited by-同舟云学术

Druggable genome screen identifies new regulators of the abundance and toxicity of ATXN3, the Spinocerebellar Ataxia type 3 disease protein

Published:2020-04 Issue: Volume:137 Page:104697
ISSN:0969-9961
Container-title:Neurobiology of Disease
language:en
Short-container-title:Neurobiology of Disease

Author:

Ashraf Naila S.,Sutton Joanna R.,Yang Yemen,Ranxhi Bedri,Libohova Kozeta,Shaw Emily D.,Barget Anna J.,Todi Sokol V.,Paulson Henry L.,Costa Maria do Carmo^ORCID

Funder

National Ataxia Foundation

National Institute of Neurological Disorders and Stroke

Publisher

Elsevier BV

Subject

Neurology

Reference64 articles.

1. Signalling pathways of the TNF superfamily: a double-edged sword;Aggarwal;Nat. Rev. Immunol.,2003

2. Allele-specific RNA silencing of mutant ataxin-3 mediates neuroprotection in a rat model of Machado-Joseph disease;Alves;PLoS One,2008

3. Silencing ataxin-3 mitigates degeneration in a rat model of Machado-Joseph disease: no role for wild-type ataxin-3?;Alves;Hum. Mol. Genet.,2010

4. Biallelic variants in FBXL3 cause intellectual disability, delayed motor development and short stature;Ansar;Hum. Mol. Genet.,2019

5. Spinocerebellar ataxias: prospects and challenges for therapy development;Ashizawa;Nat. Rev. Neurol.,2018

Cited by 14 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Progressive degeneration in a new Drosophila model of spinocerebellar ataxia type 7;Scientific Reports;2024-06-21

2. Spinocerebellar Ataxia Type 3 Pathophysiology—Implications for Translational Research and Clinical Studies;International Journal of Molecular Sciences;2024-04-03

3. Progressive degeneration in a newDrosophilamodel of Spinocerebellar Ataxia type 7;2023-11-11

4. High throughput compound screening in neuronal cells identifies statins as activators of ataxin 3 expression;Scientific Reports;2023-09-09

5. Identification and copy number variant analysis of enhancer regions of genes causing spinocerebellar ataxia;2023-09-01