Associated Papers
Comprehensive genomic landscape of metastatic hormone-sensitive prostate cancer in the Chinese population.
Yang B et al.
World Journal of Surgical Oncology, 2025
41121095 (PubMed )
Supplement: 12957_2025_4049_MOESM3_ESM.xlsx › Somatic_mutations
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
Identification and Characterization of a Novel Recurrent ERCC6 Variant in Patients with a Severe Form of Cockayne Syndrome B.
Zayoud K et al.
Genes, 2021
34946871 (PubMed )
Supplement: genes-12-01922-s001.zip › Supplementary_Table_S1_Zayoud_K.pdf
Structural basis of human transcription-DNA repair coupling.
Kokic G et al.
Nature, 2021
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
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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