Mechanism of APTX nicked DNA sensing and pleiotropic inactivation in neurodegenerative disease-Reference-Cited by-同舟云学术

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Mechanism of APTX nicked DNA sensing and pleiotropic inactivation in neurodegenerative disease

Published:2018-06-22 Issue:14 Volume:37 Page:
ISSN:0261-4189
Container-title:The EMBO Journal
language:en
Short-container-title:EMBO J

Author:

Tumbale Percy¹,Schellenberg Matthew J¹,Mueller Geoffrey A¹,Fairweather Emma²,Watson Mandy²,Little Jessica N¹,Krahn Juno¹,Waddell Ian²,London Robert E¹,Williams R Scott¹^ORCID

Affiliation:

1. Genome Integrity and Structural Biology Laboratory Department of Health and Human Services National Institute of Environmental Health Sciences, US National Institutes of Health Research Triangle Park NC USA

2. Drug Discovery Group Cancer Research UK Manchester Institute Manchester UK

Funder

National Institute of Environmental Health Sciences

Cancer Research UK

Publisher

EMBO

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,Molecular Biology,General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.15252/embj.201798875

Reference56 articles.

1. The Phenix software for automated determination of macromolecular structures

2. The neurodegenerative disease protein aprataxin resolves abortive DNA ligation intermediates

3. Slow mitochondrial repair of 5′-AMP renders mtDNA susceptible to damage in APTX deficient cells

4. Recognition and repair of chemically heterogeneous structures at DNA ends

5. Aprataxin (APTX) gene mutations resembling multiple system atrophy

Cited by 13 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. Heterozygous APTX mutation associated with atypical multiple system atrophy-like phenotype: A case report;Parkinsonism & Related Disorders;2024-06

2. Overarching pathomechanisms in inherited peripheral neuropathies, spastic paraplegias, and cerebellar ataxias;Trends in Neurosciences;2024-03

3. APTX acts in DNA double-strand break repair in a manner distinct from XRCC4;Journal of Radiation Research;2023-03-20

4. Species variations in XRCC1 recruitment strategies for FHA domain-containing proteins;DNA Repair;2022-02

5. A novel, ataxic mouse model of ataxia telangiectasia caused by a clinically relevant nonsense mutation;ELIFE;2021

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