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305 related items for PubMed ID: 23733932

  • 1. Regulatory interplay of Cockayne syndrome B ATPase and stress-response gene ATF3 following genotoxic stress.
    Kristensen U, Epanchintsev A, Rauschendorf MA, Laugel V, Stevnsner T, Bohr VA, Coin F, Egly JM.
    Proc Natl Acad Sci U S A; 2013 Jun 18; 110(25):E2261-70. PubMed ID: 23733932
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  • 2. Cockayne's Syndrome A and B Proteins Regulate Transcription Arrest after Genotoxic Stress by Promoting ATF3 Degradation.
    Epanchintsev A, Costanzo F, Rauschendorf MA, Caputo M, Ye T, Donnio LM, Proietti-de-Santis L, Coin F, Laugel V, Egly JM.
    Mol Cell; 2017 Dec 21; 68(6):1054-1066.e6. PubMed ID: 29225035
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  • 3. Defective transcription of ATF3 responsive genes, a marker for Cockayne Syndrome.
    Epanchintsev A, Rauschendorf MA, Costanzo F, Calmels N, Obringer C, Sarasin A, Coin F, Laugel V, Egly JM.
    Sci Rep; 2020 Jan 24; 10(1):1105. PubMed ID: 31980658
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  • 4. The ATPase domain but not the acidic region of Cockayne syndrome group B gene product is essential for DNA repair.
    Brosh RM, Balajee AS, Selzer RR, Sunesen M, Proietti De Santis L, Bohr VA.
    Mol Biol Cell; 1999 Nov 24; 10(11):3583-94. PubMed ID: 10564257
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  • 5. Cockayne syndrome B protein regulates the transcriptional program after UV irradiation.
    Proietti-De-Santis L, Drané P, Egly JM.
    EMBO J; 2006 May 03; 25(9):1915-23. PubMed ID: 16601682
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  • 6. Differential requirement for the ATPase domain of the Cockayne syndrome group B gene in the processing of UV-induced DNA damage and 8-oxoguanine lesions in human cells.
    Selzer RR, Nyaga S, Tuo J, May A, Muftuoglu M, Christiansen M, Citterio E, Brosh RM, Bohr VA.
    Nucleic Acids Res; 2002 Feb 01; 30(3):782-93. PubMed ID: 11809892
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  • 7. Transcription-coupled nucleotide excision repair is coordinated by ubiquitin and SUMO in response to ultraviolet irradiation.
    Liebelt F, Schimmel J, Verlaan-de Vries M, Klemann E, van Royen ME, van der Weegen Y, Luijsterburg MS, Mullenders LH, Pines A, Vermeulen W, Vertegaal ACO.
    Nucleic Acids Res; 2020 Jan 10; 48(1):231-248. PubMed ID: 31722399
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  • 8. The conserved Cockayne syndrome B-piggyBac fusion protein (CSB-PGBD3) affects DNA repair and induces both interferon-like and innate antiviral responses in CSB-null cells.
    Bailey AD, Gray LT, Pavelitz T, Newman JC, Horibata K, Tanaka K, Weiner AM.
    DNA Repair (Amst); 2012 May 01; 11(5):488-501. PubMed ID: 22483866
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  • 10. A ubiquitin-binding domain in Cockayne syndrome B required for transcription-coupled nucleotide excision repair.
    Anindya R, Mari PO, Kristensen U, Kool H, Giglia-Mari G, Mullenders LH, Fousteri M, Vermeulen W, Egly JM, Svejstrup JQ.
    Mol Cell; 2010 Jun 11; 38(5):637-48. PubMed ID: 20541997
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  • 11. The human CSB (ERCC6) gene corrects the transcription-coupled repair defect in the CHO cell mutant UV61.
    Orren DK, Dianov GL, Bohr VA.
    Nucleic Acids Res; 1996 Sep 01; 24(17):3317-22. PubMed ID: 8811084
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  • 15. Poly(ADP-ribose) polymerase 1 (PARP1) promotes oxidative stress-induced association of Cockayne syndrome group B protein with chromatin.
    Boetefuer EL, Lake RJ, Dreval K, Fan HY.
    J Biol Chem; 2018 Nov 16; 293(46):17863-17874. PubMed ID: 30266807
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  • 19. Cockayne syndrome exhibits dysregulation of p21 and other gene products that may be independent of transcription-coupled repair.
    Cleaver JE, Hefner E, Laposa RR, Karentz D, Marti T.
    Neuroscience; 2007 Apr 14; 145(4):1300-8. PubMed ID: 17055654
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  • 20. Multisystem analyses of two Cockayne syndrome associated proteins CSA and CSB reveal shared and unique functions.
    Wu Z, Zhu X, Yu Q, Xu Y, Wang Y.
    DNA Repair (Amst); 2019 Nov 14; 83():102696. PubMed ID: 31546172
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