Associated Papers
Mechanism of Rad26-assisted rescue of stalled RNA polymerase II in transcription-coupled repair.
Yan C et al.
Nature Communications, 2021
34853308 (PubMed )
Supplement: 41467_2021_27295_MOESM1_ESM.pdf
Current and emerging roles of Cockayne syndrome group B (CSB) protein.
Tiwari V et al.
Nucleic Acids Research, 2021
Defective transcription of ATF3 responsive genes, a marker for Cockayne Syndrome.
Epanchintsev A et al.
Scientific Reports, 2020
Novel frame shift mutation in ERCC6 leads to a severe form of Cockayne syndrome with postnatal growth failure and early death: A case report and brief literature review.
Kou Y et al.
Medicine, 2018
Functional and clinical relevance of novel mutations in a large cohort of patients with Cockayne syndrome.
Calmels N et al.
Journal of Medical Genetics, 2018
Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome.
Laugel V et al.
Human Mutation, 2010
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