BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

456 related articles for article (PubMed ID: 22174697)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. Persistence of repair proteins at unrepaired DNA damage distinguishes diseases with ERCC2 (XPD) mutations: cancer-prone xeroderma pigmentosum vs. non-cancer-prone trichothiodystrophy.
    Boyle J; Ueda T; Oh KS; Imoto K; Tamura D; Jagdeo J; Khan SG; Nadem C; Digiovanna JJ; Kraemer KH
    Hum Mutat; 2008 Oct; 29(10):1194-208. PubMed ID: 18470933
    [TBL] [Abstract][Full Text] [Related]  

  • 7. DNA repair-deficient diseases, xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy.
    Lehmann AR
    Biochimie; 2003 Nov; 85(11):1101-11. PubMed ID: 14726016
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Uncommon nucleotide excision repair phenotypes revealed by targeted high-throughput sequencing.
    Calmels N; Greff G; Obringer C; Kempf N; Gasnier C; Tarabeux J; Miguet M; Baujat G; Bessis D; Bretones P; Cavau A; Digeon B; Doco-Fenzy M; Doray B; Feillet F; Gardeazabal J; Gener B; Julia S; Llano-Rivas I; Mazur A; Michot C; Renaldo-Robin F; Rossi M; Sabouraud P; Keren B; Depienne C; Muller J; Mandel JL; Laugel V
    Orphanet J Rare Dis; 2016 Mar; 11():26. PubMed ID: 27004399
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Effects of compound heterozygosity at the Xpd locus on cancer and ageing in mouse models.
    van de Ven M; Andressoo JO; van der Horst GT; Hoeijmakers JH; Mitchell JR
    DNA Repair (Amst); 2012 Nov; 11(11):874-83. PubMed ID: 23046824
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. DMBA-induced toxic and mutagenic responses vary dramatically between NER-deficient Xpa, Xpc and Csb mice.
    Wijnhoven SW; Kool HJ; Mullenders LH; Slater R; van Zeeland AA; Vrieling H
    Carcinogenesis; 2001 Jul; 22(7):1099-106. PubMed ID: 11408355
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. An Xpd mouse model for the combined xeroderma pigmentosum/Cockayne syndrome exhibiting both cancer predisposition and segmental progeria.
    Andressoo JO; Mitchell JR; de Wit J; Hoogstraten D; Volker M; Toussaint W; Speksnijder E; Beems RB; van Steeg H; Jans J; de Zeeuw CI; Jaspers NG; Raams A; Lehmann AR; Vermeulen W; Hoeijmakers JH; van der Horst GT
    Cancer Cell; 2006 Aug; 10(2):121-32. PubMed ID: 16904611
    [TBL] [Abstract][Full Text] [Related]  

  • 14. An Xpb mouse model for combined xeroderma pigmentosum and cockayne syndrome reveals progeroid features upon further attenuation of DNA repair.
    Andressoo JO; Weeda G; de Wit J; Mitchell JR; Beems RB; van Steeg H; van der Horst GT; Hoeijmakers JH
    Mol Cell Biol; 2009 Mar; 29(5):1276-90. PubMed ID: 19114557
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Sirt1 suppresses RNA synthesis after UV irradiation in combined xeroderma pigmentosum group D/Cockayne syndrome (XP-D/CS) cells.
    Vélez-Cruz R; Zadorin AS; Coin F; Egly JM
    Proc Natl Acad Sci U S A; 2013 Jan; 110(3):E212-20. PubMed ID: 23267107
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Nucleotide excision repair of oxidised genomic DNA is not a source of urinary 8-oxo-7,8-dihydro-2'-deoxyguanosine.
    Evans MD; Mistry V; Singh R; Gackowski D; Różalski R; Siomek-Gorecka A; Phillips DH; Zuo J; Mullenders L; Pines A; Nakabeppu Y; Sakumi K; Sekiguchi M; Tsuzuki T; Bignami M; Oliński R; Cooke MS
    Free Radic Biol Med; 2016 Oct; 99():385-391. PubMed ID: 27585947
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Blinded by the UV light: how the focus on transcription-coupled NER has distracted from understanding the mechanisms of Cockayne syndrome neurologic disease.
    Brooks PJ
    DNA Repair (Amst); 2013 Aug; 12(8):656-71. PubMed ID: 23683874
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A disease-associated XPA allele interferes with TFIIH binding and primarily affects transcription-coupled nucleotide excision repair.
    van den Heuvel D; Kim M; Wondergem AP; van der Meer PJ; Witkamp M; Lambregtse F; Kim HS; Kan F; Apelt K; Kragten A; González-Prieto R; Vertegaal ACO; Yeo JE; Kim BG; van Doorn R; Schärer OD; Luijsterburg MS
    Proc Natl Acad Sci U S A; 2023 Mar; 120(11):e2208860120. PubMed ID: 36893274
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 23.