BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

1043 related articles for article (PubMed ID: 27122034)

  • 1. Mutations in Cockayne Syndrome-Associated Genes (Csa and Csb) Predispose to Cisplatin-Induced Hearing Loss in Mice.
    Rainey RN; Ng SY; Llamas J; van der Horst GT; Segil N
    J Neurosci; 2016 Apr; 36(17):4758-70. PubMed ID: 27122034
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cockayne syndrome group B (Csb) and group a (Csa) deficiencies predispose to hearing loss and cochlear hair cell degeneration in mice.
    Nagtegaal AP; Rainey RN; van der Pluijm I; Brandt RM; van der Horst GT; Borst JG; Segil N
    J Neurosci; 2015 Mar; 35(10):4280-6. PubMed ID: 25762674
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Age-related neuronal degeneration: complementary roles of nucleotide excision repair and transcription-coupled repair in preventing neuropathology.
    Jaarsma D; van der Pluijm I; de Waard MC; Haasdijk ED; Brandt R; Vermeij M; Rijksen Y; Maas A; van Steeg H; Hoeijmakers JH; van der Horst GT
    PLoS Genet; 2011 Dec; 7(12):e1002405. PubMed ID: 22174697
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The relationship between benzo[a]pyrene-induced mutagenesis and carcinogenesis in repair-deficient Cockayne syndrome group B mice.
    Wijnhoven SW; Kool HJ; van Oostrom CT; Beems RB; Mullenders LH; van Zeeland AA; van der Horst GT; Vrieling H; van Steeg H
    Cancer Res; 2000 Oct; 60(20):5681-7. PubMed ID: 11059760
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Different effects of CSA and CSB deficiency on sensitivity to oxidative DNA damage.
    de Waard H; de Wit J; Andressoo JO; van Oostrom CT; Riis B; Weimann A; Poulsen HE; van Steeg H; Hoeijmakers JH; van der Horst GT
    Mol Cell Biol; 2004 Sep; 24(18):7941-8. PubMed ID: 15340056
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cell-type-specific consequences of nucleotide excision repair deficiencies: Embryonic stem cells versus fibroblasts.
    de Waard H; Sonneveld E; de Wit J; Esveldt-van Lange R; Hoeijmakers JH; Vrieling H; van der Horst GT
    DNA Repair (Amst); 2008 Oct; 7(10):1659-69. PubMed ID: 18634906
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cell type-specific hypersensitivity to oxidative damage in CSB and XPA mice.
    de Waard H; de Wit J; Gorgels TG; van den Aardweg G; Andressoo JO; Vermeij M; van Steeg H; Hoeijmakers JH; van der Horst GT
    DNA Repair (Amst); 2003 Jan; 2(1):13-25. PubMed ID: 12509265
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Cerebro-oculo-facio-skeletal syndrome with a nucleotide excision-repair defect and a mutated XPD gene, with prenatal diagnosis in a triplet pregnancy.
    Graham JM; Anyane-Yeboa K; Raams A; Appeldoorn E; Kleijer WJ; Garritsen VH; Busch D; Edersheim TG; Jaspers NG
    Am J Hum Genet; 2001 Aug; 69(2):291-300. PubMed ID: 11443545
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Translocation of Cockayne syndrome group A protein to the nuclear matrix: possible relevance to transcription-coupled DNA repair.
    Kamiuchi S; Saijo M; Citterio E; de Jager M; Hoeijmakers JH; Tanaka K
    Proc Natl Acad Sci U S A; 2002 Jan; 99(1):201-6. PubMed ID: 11782547
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 10(11):3583-94. PubMed ID: 10564257
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The Cockayne syndrome B protein, involved in transcription-coupled DNA repair, resides in an RNA polymerase II-containing complex.
    van Gool AJ; Citterio E; Rademakers S; van Os R; Vermeulen W; Constantinou A; Egly JM; Bootsma D; Hoeijmakers JH
    EMBO J; 1997 Oct; 16(19):5955-65. PubMed ID: 9312053
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Bacterial DNA repair genes and their eukaryotic homologues: 4. The role of nucleotide excision DNA repair (NER) system in mammalian cells.
    Maddukuri L; Dudzińska D; Tudek B
    Acta Biochim Pol; 2007; 54(3):469-82. PubMed ID: 17893751
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Early postnatal ataxia and abnormal cerebellar development in mice lacking Xeroderma pigmentosum Group A and Cockayne syndrome Group B DNA repair genes.
    Murai M; Enokido Y; Inamura N; Yoshino M; Nakatsu Y; van der Horst GT; Hoeijmakers JH; Tanaka K; Hatanaka H
    Proc Natl Acad Sci U S A; 2001 Nov; 98(23):13379-84. PubMed ID: 11687625
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel splice site mutation in the Cockayne syndrome group A gene in two siblings with Cockayne syndrome.
    Kleppa L; Kanavin ØJ; Klungland A; Strømme P
    Neuroscience; 2007 Apr; 145(4):1397-406. PubMed ID: 17084038
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Cockayne syndrome group B (CSB) protein: at the crossroads of transcriptional networks.
    Vélez-Cruz R; Egly JM
    Mech Ageing Dev; 2013; 134(5-6):234-42. PubMed ID: 23562425
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mouse model for the DNA repair/basal transcription disorder trichothiodystrophy reveals cancer predisposition.
    de Boer J; van Steeg H; Berg RJ; Garssen J; de Wit J; van Oostrum CT; Beems RB; van der Horst GT; van Kreijl CF; de Gruijl FR; Bootsma D; Hoeijmakers JH; Weeda G
    Cancer Res; 1999 Jul; 59(14):3489-94. PubMed ID: 10416615
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Xeroderma pigmentosum, trichothiodystrophy and Cockayne syndrome: a complex genotype-phenotype relationship.
    Kraemer KH; Patronas NJ; Schiffmann R; Brooks BP; Tamura D; DiGiovanna JJ
    Neuroscience; 2007 Apr; 145(4):1388-96. PubMed ID: 17276014
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Transcription-coupled nucleotide excision repair in mammalian cells: molecular mechanisms and biological effects.
    Fousteri M; Mullenders LH
    Cell Res; 2008 Jan; 18(1):73-84. PubMed ID: 18166977
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The role of Cockayne syndrome group A (CSA) protein in transcription-coupled nucleotide excision repair.
    Saijo M
    Mech Ageing Dev; 2013; 134(5-6):196-201. PubMed ID: 23571135
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 53.