BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

311 related articles for article (PubMed ID: 8304337)

  • 1. Clinical heterogeneity within xeroderma pigmentosum associated with mutations in the DNA repair and transcription gene ERCC3.
    Vermeulen W; Scott RJ; Rodgers S; Müller HJ; Cole J; Arlett CF; Kleijer WJ; Bootsma D; Hoeijmakers JH; Weeda G
    Am J Hum Genet; 1994 Feb; 54(2):191-200. PubMed ID: 8304337
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A mutation in the XPB/ERCC3 DNA repair transcription gene, associated with trichothiodystrophy.
    Weeda G; Eveno E; Donker I; Vermeulen W; Chevallier-Lagente O; Taïeb A; Stary A; Hoeijmakers JH; Mezzina M; Sarasin A
    Am J Hum Genet; 1997 Feb; 60(2):320-9. PubMed ID: 9012405
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome.
    Oh KS; Khan SG; Jaspers NG; Raams A; Ueda T; Lehmann A; Friedmann PS; Emmert S; Gratchev A; Lachlan K; Lucassan A; Baker CC; Kraemer KH
    Hum Mutat; 2006 Nov; 27(11):1092-103. PubMed ID: 16947863
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Correction of xeroderma pigmentosum repair defect by basal transcription factor BTF2 (TFIIH).
    van Vuuren AJ; Vermeulen W; Ma L; Weeda G; Appeldoorn E; Jaspers NG; van der Eb AJ; Bootsma D; Hoeijmakers JH; Humbert S
    EMBO J; 1994 Apr; 13(7):1645-53. PubMed ID: 8157004
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutational analysis of ERCC3, which is involved in DNA repair and transcription initiation: identification of domains essential for the DNA repair function.
    Ma L; Westbroek A; Jochemsen AG; Weeda G; Bosch A; Bootsma D; Hoeijmakers JH; van der Eb AJ
    Mol Cell Biol; 1994 Jun; 14(6):4126-34. PubMed ID: 8196650
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Cloning and characterization of the Drosophila homolog of the xeroderma pigmentosum complementation-group B correcting gene, ERCC3.
    Koken MH; Vreeken C; Bol SA; Cheng NC; Jaspers-Dekker I; Hoeijmakers JH; Eeken JC; Weeda G; Pastink A
    Nucleic Acids Res; 1992 Nov; 20(21):5541-8. PubMed ID: 1454518
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The xeroderma pigmentosum group B protein ERCC3 produced in the baculovirus system exhibits DNA helicase activity.
    Ma L; Siemssen ED; Noteborn HM; van der Eb AJ
    Nucleic Acids Res; 1994 Oct; 22(20):4095-102. PubMed ID: 7937133
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. A Drosophila model for xeroderma pigmentosum and Cockayne's syndrome: haywire encodes the fly homolog of ERCC3, a human excision repair gene.
    Mounkes LC; Jones RS; Liang BC; Gelbart W; Fuller MT
    Cell; 1992 Dec; 71(6):925-37. PubMed ID: 1458540
    [TBL] [Abstract][Full Text] [Related]  

  • 10. TFIIH subunit alterations causing xeroderma pigmentosum and trichothiodystrophy specifically disturb several steps during transcription.
    Singh A; Compe E; Le May N; Egly JM
    Am J Hum Genet; 2015 Feb; 96(2):194-207. PubMed ID: 25620205
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Newly identified CHO ERCC3/XPB mutations and phenotype characterization.
    Rybanská I; Gursky J; Fasková M; Salazar EP; Kimlícková-Polakovicová E; Kleibl K; Thompson LH; Pirsel M
    Mutagenesis; 2010 Mar; 25(2):179-85. PubMed ID: 19942596
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The COOH terminus of suppressor of stem loop (SSL2/RAD25) in yeast is essential for overall genomic excision repair and transcription-coupled repair.
    Sweder KS; Hanawalt PC
    J Biol Chem; 1994 Jan; 269(3):1852-7. PubMed ID: 8294433
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Nucleotide excision repair syndromes: molecular basis and clinical symptoms.
    Bootsma D; Weeda G; Vermeulen W; van Vuuren H; Troelstra C; van der Spek P; Hoeijmakers J
    Philos Trans R Soc Lond B Biol Sci; 1995 Jan; 347(1319):75-81. PubMed ID: 7746858
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A 3' --> 5' XPB helicase defect in repair/transcription factor TFIIH of xeroderma pigmentosum group B affects both DNA repair and transcription.
    Hwang JR; Moncollin V; Vermeulen W; Seroz T; van Vuuren H; Hoeijmakers JH; Egly JM
    J Biol Chem; 1996 Jul; 271(27):15898-904. PubMed ID: 8663148
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Restoring DNA repair capacity of cells from three distinct diseases by XPD gene-recombinant adenovirus.
    Armelini MG; Muotri AR; Marchetto MC; de Lima-Bessa KM; Sarasin A; Menck CF
    Cancer Gene Ther; 2005 Apr; 12(4):389-96. PubMed ID: 15650764
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. A mutation in repB, the dictyostelium homolog of the human xeroderma pigmentosum B gene, has increased sensitivity to UV-light but normal morphogenesis.
    Lee SK; Yu SL; Alexander H; Alexander S
    Biochim Biophys Acta; 1998 Aug; 1399(2-3):161-72. PubMed ID: 9765592
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Localization of the xeroderma pigmentosum group B-correcting gene ERCC3 to human chromosome 2q21.
    Weeda G; Wiegant J; van der Ploeg M; Geurts van Kessel AH; van der Eb AJ; Hoeijmakers JH
    Genomics; 1991 Aug; 10(4):1035-40. PubMed ID: 1916809
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Two individuals with features of both xeroderma pigmentosum and trichothiodystrophy highlight the complexity of the clinical outcomes of mutations in the XPD gene.
    Broughton BC; Berneburg M; Fawcett H; Taylor EM; Arlett CF; Nardo T; Stefanini M; Menefee E; Price VH; Queille S; Sarasin A; Bohnert E; Krutmann J; Davidson R; Kraemer KH; Lehmann AR
    Hum Mol Genet; 2001 Oct; 10(22):2539-47. PubMed ID: 11709541
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.