Neurological disorders associated with DNA strand-break processing enzymes-Reference-Cited by-同舟云学术

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Neurological disorders associated with DNA strand-break processing enzymes

Published:2017-01 Issue: Volume:161 Page:130-140
ISSN:0047-6374
Container-title:Mechanisms of Ageing and Development
language:en
Short-container-title:Mechanisms of Ageing and Development

Author:

Jiang Bingcheng,Glover J.N. Mark,Weinfeld Michael

Funder

the Canadian Cancer Society/Canadian Breast Cancer Research Alliance

Canadian Institutes of Health Research

National Institutes of Health

CIHR

Publisher

Elsevier BV

Subject

Developmental Biology,Ageing

Reference131 articles.

1. R loops: from transcription byproducts to threats to genome stability;Aguilera;Mol. Cell,2012

2. The neurodegenerative disease protein aprataxin resolves abortive DNA ligation intermediates;Ahel;Nature,2006

3. Ataxia-ocular motor apraxia: a syndrome mimicking ataxia-telangiectasia;Aicardi;Ann. Neurol.,1988

4. Slow mitochondrial repair of 5'-AMP renders mtDNA susceptible to damage in APTX deficient cells;Akbari;Sci. Rep.,2015

5. Tracking the processing of damaged DNA double-strand break ends by ligation-mediated PCR: increased persistence of 3'-phosphoglycolate termini in SCAN1 cells;Akopiants;Nucleic Acids Res.,2015

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1. TDP1 mutation causing SCAN1 neurodegenerative syndrome hampers the repair of transcriptional DNA double-strand breaks;Cell Reports;2024-05

2. Effects of low‑power red laser and blue LED on mRNA levels from DNA repair genes in human breast cancer cells;Lasers in Medical Science;2024-02-08

3. Ataxia-associated DNA repair genes protect the Drosophila mushroom body and locomotor function against glutamate signaling-associated damage;Frontiers in Neural Circuits;2023-07-05

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

5. Ataxia-telangiectasia mutated plays an important role in cerebellar integrity and functionality;Neural Regeneration Research;2023

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