These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

208 related articles for article (PubMed ID: 31980658)

  • 1. 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; 10(1):1105. PubMed ID: 31980658
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 68(6):1054-1066.e6. PubMed ID: 29225035
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 110(25):E2261-70. PubMed ID: 23733932
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Differential processing of RNA polymerase II at DNA damage correlates with transcription-coupled repair syndrome severity.
    Gonzalo-Hansen C; Steurer B; Janssens RC; Zhou D; van Sluis M; Lans H; Marteijn JA
    Nucleic Acids Res; 2024 Sep; 52(16):9596-9612. PubMed ID: 39021334
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Functional and clinical relevance of novel mutations in a large cohort of patients with Cockayne syndrome.
    Calmels N; Botta E; Jia N; Fawcett H; Nardo T; Nakazawa Y; Lanzafame M; Moriwaki S; Sugita K; Kubota M; Obringer C; Spitz MA; Stefanini M; Laugel V; Orioli D; Ogi T; Lehmann AR
    J Med Genet; 2018 May; 55(5):329-343. PubMed ID: 29572252
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutations in UVSSA cause UV-sensitive syndrome and destabilize ERCC6 in transcription-coupled DNA repair.
    Zhang X; Horibata K; Saijo M; Ishigami C; Ukai A; Kanno S; Tahara H; Neilan EG; Honma M; Nohmi T; Yasui A; Tanaka K
    Nat Genet; 2012 May; 44(5):593-7. PubMed ID: 22466612
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 145(4):1300-8. PubMed ID: 17055654
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Cockayne syndrome group A and B proteins converge on transcription-linked resolution of non-B DNA.
    Scheibye-Knudsen M; Tseng A; Borch Jensen M; Scheibye-Alsing K; Fang EF; Iyama T; Bharti SK; Marosi K; Froetscher L; Kassahun H; Eckley DM; Maul RW; Bastian P; De S; Ghosh S; Nilsen H; Goldberg IG; Mattson MP; Wilson DM; Brosh RM; Gorospe M; Bohr VA
    Proc Natl Acad Sci U S A; 2016 Nov; 113(44):12502-12507. PubMed ID: 27791127
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cockayne syndrome group A and ferrochelatase finely tune ribosomal gene transcription and its response to UV irradiation.
    Lanzafame M; Branca G; Landi C; Qiang M; Vaz B; Nardo T; Ferri D; Mura M; Iben S; Stefanini M; Peverali FA; Bini L; Orioli D
    Nucleic Acids Res; 2021 Nov; 49(19):10911-10930. PubMed ID: 34581821
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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; 30(3):782-93. PubMed ID: 11809892
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 83():102696. PubMed ID: 31546172
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cockayne syndrome proteins CSA and CSB maintain mitochondrial homeostasis through NAD
    Okur MN; Fang EF; Fivenson EM; Tiwari V; Croteau DL; Bohr VA
    Aging Cell; 2020 Dec; 19(12):e13268. PubMed ID: 33166073
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cockayne syndrome B protein regulates the transcriptional program after UV irradiation.
    Proietti-De-Santis L; Drané P; Egly JM
    EMBO J; 2006 May; 25(9):1915-23. PubMed ID: 16601682
    [TBL] [Abstract][Full Text] [Related]  

  • 14. First molecular study in Lebanese patients with Cockayne syndrome and report of a novel mutation in ERCC8 gene.
    Chebly A; Corbani S; Abou Ghoch J; Mehawej C; Megarbane A; Chouery E
    BMC Med Genet; 2018 Sep; 19(1):161. PubMed ID: 30200888
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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; 48(1):231-248. PubMed ID: 31722399
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cockayne syndrome group B deficiency reduces H3K9me3 chromatin remodeler SETDB1 and exacerbates cellular aging.
    Lee JH; Demarest TG; Babbar M; Kim EW; Okur MN; De S; Croteau DL; Bohr VA
    Nucleic Acids Res; 2019 Sep; 47(16):8548-8562. PubMed ID: 31276581
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Generation of splice switching oligonucleotides targeting the Cockayne syndrome group B gene product in order to change the diseased cell state.
    Sin Y; Makimura F; Saijo M; Obika S
    Biochem Biophys Res Commun; 2018 Jun; 500(2):163-169. PubMed ID: 29625109
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Dysregulation of gene expression as a cause of Cockayne syndrome neurological disease.
    Wang Y; Chakravarty P; Ranes M; Kelly G; Brooks PJ; Neilan E; Stewart A; Schiavo G; Svejstrup JQ
    Proc Natl Acad Sci U S A; 2014 Oct; 111(40):14454-9. PubMed ID: 25249633
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Alterations in the CSB gene in three Italian patients with the severe form of Cockayne syndrome (CS) but without clinical photosensitivity.
    Colella S; Nardo T; Mallery D; Borrone C; Ricci R; Ruffa G; Lehmann AR; Stefanini M
    Hum Mol Genet; 1999 May; 8(5):935-41. PubMed ID: 10196384
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification and Characterization of a Novel Recurrent
    Zayoud K; Kraoua I; Chikhaoui A; Calmels N; Bouchoucha S; Obringer C; Crochemore C; Najjar D; Zarrouk S; Miladi N; Laugel V; Ricchetti M; Turki I; Yacoub-Youssef H
    Genes (Basel); 2021 Nov; 12(12):. PubMed ID: 34946871
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.