Defective transcription of ATF3 responsive genes, a marker for Cockayne Syndrome
Published 2020 View Full Article
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Title
Defective transcription of ATF3 responsive genes, a marker for Cockayne Syndrome
Authors
Keywords
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Journal
Scientific Reports
Volume 10, Issue 1, Pages -
Publisher
Springer Science and Business Media LLC
Online
2020-01-24
DOI
10.1038/s41598-020-57999-4
References
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Related references
Note: Only part of the references are listed.- Cockayne’s Syndrome A and B Proteins Regulate Transcription Arrest after Genotoxic Stress by Promoting ATF3 Degradation
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- Progressive demyelinating neuropathy correlates with clinical severity in Cockayne syndrome
- (2015) Cyril Gitiaux et al. CLINICAL NEUROPHYSIOLOGY
- A Small Molecule Screen Identifies an Inhibitor of DNA Repair Inducing the Degradation of TFIIH and the Chemosensitization of Tumor Cells to Platinum
- (2014) Sergey Alekseev et al. CHEMISTRY & BIOLOGY
- Genome-wide Map of Nuclear Protein Degradation Shows NCoR1 Turnover as a Key to Mitochondrial Gene Regulation
- (2013) André Catic et al. CELL
- Blinded by the UV light: How the focus on transcription-coupled NER has distracted from understanding the mechanisms of Cockayne syndrome neurologic disease
- (2013) P.J. Brooks DNA REPAIR
- Regulatory interplay of Cockayne syndrome B ATPase and stress-response gene ATF3 following genotoxic stress
- (2013) U. Kristensen et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Dermatologic Findings in 16 Patients With Cockayne Syndrome and Cerebro-Oculo-Facial-Skeletal Syndrome
- (2013) Eric Frouin et al. JAMA Dermatology
- A Critical Period for Social Experience-Dependent Oligodendrocyte Maturation and Myelination
- (2012) M. Makinodan et al. SCIENCE
- CDK5RAP2 Regulates Centriole Engagement and Cohesion in Mice
- (2010) Jose A. Barrera et al. DEVELOPMENTAL CELL
- The phosphorylation of the androgen receptor by TFIIH directs the ubiquitin/proteasome process
- (2010) Pierre Chymkowitch et al. EMBO JOURNAL
- NER Factors Are Recruited to Active Promoters and Facilitate Chromatin Modification for Transcription in the Absence of Exogenous Genotoxic Attack
- (2010) Nicolas Le May et al. MOLECULAR CELL
- Mutation update for theCSB/ERCC6andCSA/ERCC8genes involved in Cockayne syndrome
- (2009) V. Laugel et al. HUMAN MUTATION
- Interaction of CDK5RAP2 with EB1 to Track Growing Microtubule Tips and to Regulate Microtubule Dynamics
- (2009) Ka-Wing Fong et al. MOLECULAR BIOLOGY OF THE CELL
- A UV-sensitive syndrome patient with a specific CSA mutation reveals separable roles for CSA in response to UV and oxidative DNA damage
- (2009) T. Nardo et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Incidence of DNA repair deficiency disorders in western Europe: Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy
- (2008) Wim J. Kleijer et al. DNA REPAIR
- Transcription-coupled DNA repair: two decades of progress and surprises
- (2008) Philip C. Hanawalt et al. NATURE REVIEWS MOLECULAR CELL BIOLOGY
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