Reduction of mutant ATXN1 rescues premature death in a conditional SCA1 mouse model-Reference-Cited by-同舟云学术

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Reduction of mutant ATXN1 rescues premature death in a conditional SCA1 mouse model

Published:2022-04-22 Issue:8 Volume:7 Page:
ISSN:2379-3708
Container-title:JCI Insight
language:en
Short-container-title:

Author:

Orengo James P.^ORCID,Nitschke Larissa^ORCID,van der Heijden Meike E.,Ciaburri Nicholas A.,Orr Harry T.,Zoghbi Huda Y.^ORCID

Funder

NINDS/NIH

Chao Physician Scientist Award

Mrs. Clifford Elder White Graham Endowed Research Fund

National Ataxia Foundation Young Investigator Award

Dystonia Medical Research Foundation

NICHHD/NIH

Howard Hughes Medical Institute

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Link

https://insight.jci.org/articles/view/154442/files/pdf

Reference43 articles.

1. Spinocerebellar ataxia type 1

2. Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I

3. Identification and characterization of the gene causing type 1 spinocerebellar ataxia

4. Mutation of the E6-AP Ubiquitin Ligase Reduces Nuclear Inclusion Frequency While Accelerating Polyglutamine-Induced Pathology in SCA1 Mice

5. ATAXIN-1 Interacts with the Repressor Capicua in Its Native Complex to Cause SCA1 Neuropathology

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2. Zebrafish Models of Rare Neurological Diseases like Spinocerebellar Ataxias (SCAs): Advantages and Limitations;Biology;2023-10-10

3. Dysregulation of alternative splicing in spinocerebellar ataxia type 1;Human Molecular Genetics;2023-10-06

4. Advances in cerebellar disorders: pre-clinical models, therapeutic targets, and challenges;Expert Opinion on Therapeutic Targets;2023-10-03

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