Found: 25
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A Cockayne-like phenotype resulting from a de novo variant in MORC2: expanding the phenotype of MORC2-related disorders.
- Published in:
- Neurogenetics, 2022, v. 23, n. 4, p. 271, doi. 10.1007/s10048-022-00697-2
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- Article
A new progeroid syndrome reveals that genotoxic stress suppresses the somatotroph axis.
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- Nature, 2006, v. 444, n. 7122, p. 1038, doi. 10.1038/nature05456
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- Article
Mutations in TFIIH causing trichothiodystrophy are responsible for defects in ribosomal RNA production and processing.
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- Human Molecular Genetics, 2013, v. 22, n. 14, p. 2881, doi. 10.1093/hmg/ddt143
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- Article
Different SWI/SNF complexes coordinately promote R-loop- and RAD52-dependent transcription-coupled homologous recombination.
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- Nucleic Acids Research, 2023, v. 51, n. 17, p. 9055, doi. 10.1093/nar/gkad609
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- Article
SUMO and ubiquitin-dependent XPC exchange drives nucleotide excision repair.
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- Nature Communications, 2015, v. 6, n. 7, p. 7499, doi. 10.1038/ncomms8499
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- Article
Fanconi anemia with sun-sensitivity caused by a Xeroderma pigmentosum-associated missense mutation in XPF.
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- BMC Medical Genetics, 2018, v. 19, p. 1, doi. 10.1186/s12881-018-0520-1
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- Article
Trichothiodystrophy‐associated MPLKIP maintains DBR1 levels for proper lariat debranching and ectodermal differentiation.
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- EMBO Molecular Medicine, 2023, v. 15, n. 11, p. 1, doi. 10.15252/emmm.202317973
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- Article
Disruption of TTDA Results in Complete Nucleotide Excision Repair Deficiency and Embryonic Lethality.
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- PLoS Genetics, 2013, v. 9, n. 4, p. 1, doi. 10.1371/journal.pgen.1003431
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- Article
Mislocalization of XPF-ERCC1 Nuclease Contributes to Reduced DNA Repair in XP-F Patients.
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- PLoS Genetics, 2010, v. 6, n. 3, p. 1, doi. 10.1371/journal.pgen.1000871
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- Article
Ubiquitin and TFIIH-stimulated DDB2 dissociation drives DNA damage handover in nucleotide excision repair.
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- Nature Communications, 2020, v. 11, n. 1, p. N.PAG, doi. 10.1038/s41467-020-18705-0
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- Article
Differentiation Driven Changes in the Dynamic Organization of Basal Transcription Initiation.
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- PLoS Biology, 2009, v. 7, n. 10, p. 1, doi. 10.1371/journal.pbio.1000220
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- Article
Dynamic Interaction of TTDA with TFIIH Is Stabilized by Nucleotide Excision Repair in Living Cells.
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- PLoS Biology, 2006, v. 4, n. 6, p. e156, doi. 10.1371/journal.pbio.0040156
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- Article
Global and transcription-coupled repair of 8-oxoG is initiated by nucleotide excision repair proteins.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-28642-9
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- Article
DNA damage-induced transcription stress triggers the genome-wide degradation of promoter-bound Pol II.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-31329-w
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- Article
DNA damage-induced transcription stress triggers the genome-wide degradation of promoter-bound Pol II.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-31329-w
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- Publication type:
- Article
Global and transcription-coupled repair of 8-oxoG is initiated by nucleotide excision repair proteins.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-28642-9
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- Article
XPG: a multitasking genome caretaker.
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- Cellular & Molecular Life Sciences, 2022, v. 79, n. 3, p. 1, doi. 10.1007/s00018-022-04194-5
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- Article
Repair protein persistence at DNA lesions characterizes XPF defect with Cockayne syndrome features.
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- Nucleic Acids Research, 2018, v. 46, n. 18, p. 9563, doi. 10.1093/nar/gky774
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- Article
Base and nucleotide excision repair facilitate resolution of platinum drugs-induced transcription blockage.
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- Nucleic Acids Research, 2018, v. 46, n. 18, p. 9537, doi. 10.1093/nar/gky764
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- Article
The transcription-coupled DNA repair-initiating protein CSB promotes XRCC1 recruitment to oxidative DNA damage.
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- Nucleic Acids Research, 2018, v. 46, n. 15, p. 7747, doi. 10.1093/nar/gky579
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- Article
Kinetics of endogenous mouse FEN1 in base excision repair.
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- Nucleic Acids Research, 2012, v. 40, n. 18, p. 9044, doi. 10.1093/nar/gks673
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- Article
The small CRL4<sup>CSA</sup> ubiquitin ligase component DDA1 regulates transcription-coupled repair dynamics.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-50584-7
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- Article
Persistent TFIIH binding to non-excised DNA damage causes cell and developmental failure.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-47935-9
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- Article
Protein instability associated with AARS1 and MARS1 mutations causes trichothiodystrophy.
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- Human Molecular Genetics, 2021, v. 30, n. 18, p. 1711, doi. 10.1093/hmg/ddab123
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- Article
Trichothiodystrophy causative TFIIEβ mutation affects transcription in highly differentiated tissue.
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- Human Molecular Genetics, 2017, v. 26, n. 23, p. 4689, doi. 10.1093/hmg/ddx351
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- Article