BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

754 related articles for article (PubMed ID: 10667598)

  • 1. The cancer-free phenotype in trichothiodystrophy is unrelated to its repair defect.
    Berneburg M; Clingen PH; Harcourt SA; Lowe JE; Taylor EM; Green MH; Krutmann J; Arlett CF; Lehmann AR
    Cancer Res; 2000 Jan; 60(2):431-8. PubMed ID: 10667598
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Comparative study of nucleotide excision repair defects between XPD-mutated fibroblasts derived from trichothiodystrophy and xeroderma pigmentosum patients.
    Nishiwaki T; Kobayashi N; Iwamoto T; Yamamoto A; Sugiura S; Liu YC; Sarasin A; Okahashi Y; Hirano M; Ueno S; Mori T
    DNA Repair (Amst); 2008 Dec; 7(12):1990-8. PubMed ID: 18817897
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Characteristics of UV-induced mutation spectra in human XP-D/ERCC2 gene-mutated xeroderma pigmentosum and trichothiodystrophy cells.
    Marionnet C; Benoit A; Benhamou S; Sarasin A; Stary A
    J Mol Biol; 1995 Oct; 252(5):550-62. PubMed ID: 7563073
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prolonged p53 protein accumulation in trichothiodystrophy fibroblasts dependent on unrepaired pyrimidine dimers on the transcribed strands of cellular genes.
    Dumaz N; Duthu A; Ehrhart JC; Drougard C; Appella E; Anderson CW; May P; Sarasin A; Daya-Grosjean L
    Mol Carcinog; 1997 Dec; 20(4):340-7. PubMed ID: 9433478
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Recovery of normal DNA repair and mutagenesis in trichothiodystrophy cells after transduction of the XPD human gene.
    Marionnet C; Quilliet X; Benoit A; Armier J; Sarasin A; Stary A
    Cancer Res; 1996 Dec; 56(23):5450-6. PubMed ID: 8968100
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Trichothiodystrophy: update on the sulfur-deficient brittle hair syndromes.
    Itin PH; Sarasin A; Pittelkow MR
    J Am Acad Dermatol; 2001 Jun; 44(6):891-920; quiz 921-4. PubMed ID: 11369901
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Effects of XPD mutations on ultraviolet-induced apoptosis in relation to skin cancer-proneness in repair-deficient syndromes.
    Queille S; Drougard C; Sarasin A; Daya-Grosjean L
    J Invest Dermatol; 2001 Nov; 117(5):1162-70. PubMed ID: 11710928
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Differential behaviors toward ultraviolet A and B radiation of fibroblasts and keratinocytes from normal and DNA-repair-deficient patients.
    Otto AI; Riou L; Marionnet C; Mori T; Sarasin A; Magnaldo T
    Cancer Res; 1999 Mar; 59(6):1212-8. PubMed ID: 10096550
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutations in the XPD gene in xeroderma pigmentosum group D cell strains: confirmation of genotype-phenotype correlation.
    Kobayashi T; Uchiyama M; Fukuro S; Tanaka K
    Am J Med Genet; 2002 Jul; 110(3):248-52. PubMed ID: 12116233
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Correction by the ERCC2 gene of UV sensitivity and repair deficiency phenotype in a subset of trichothiodystrophy cells.
    Mezzina M; Eveno E; Chevallier-Lagente O; Benoit A; Carreau M; Vermeulen W; Hoeijmakers JH; Stefanini M; Lehmann AR; Weber CA
    Carcinogenesis; 1994 Aug; 15(8):1493-8. PubMed ID: 8055625
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Photocarcinogenesis and inhibition of intercellular adhesion molecule 1 expression in cells of DNA-repair-defective individuals.
    Ahrens C; Grewe M; Berneburg M; Grether-Beck S; Quilliet X; Mezzina M; Sarasin A; Lehmann AR; Arlett CF; Krutmann J
    Proc Natl Acad Sci U S A; 1997 Jun; 94(13):6837-41. PubMed ID: 9192652
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutations in the xeroderma pigmentosum group D DNA repair/transcription gene in patients with trichothiodystrophy.
    Broughton BC; Steingrimsdottir H; Weber CA; Lehmann AR
    Nat Genet; 1994 Jun; 7(2):189-94. PubMed ID: 7920640
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutations in the XPD gene leading to xeroderma pigmentosum symptoms.
    Kobayashi T; Kuraoka I; Saijo M; Nakatsu Y; Tanaka A; Someda Y; Fukuro S; Tanaka K
    Hum Mutat; 1997; 9(4):322-31. PubMed ID: 9101292
    [TBL] [Abstract][Full Text] [Related]  

  • 16. DNA repair characteristics and mutations in the ERCC2 DNA repair and transcription gene in a trichothiodystrophy patient.
    Takayama K; Danks DM; Salazar EP; Cleaver JE; Weber CA
    Hum Mutat; 1997; 9(6):519-25. PubMed ID: 9195225
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A temperature-sensitive disorder in basal transcription and DNA repair in humans.
    Vermeulen W; Rademakers S; Jaspers NG; Appeldoorn E; Raams A; Klein B; Kleijer WJ; Hansen LK; Hoeijmakers JH
    Nat Genet; 2001 Mar; 27(3):299-303. PubMed ID: 11242112
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Xeroderma pigmentosum and trichothiodystrophy are associated with different mutations in the XPD (ERCC2) repair/transcription gene.
    Taylor EM; Broughton BC; Botta E; Stefanini M; Sarasin A; Jaspers NG; Fawcett H; Harcourt SA; Arlett CF; Lehmann AR
    Proc Natl Acad Sci U S A; 1997 Aug; 94(16):8658-63. PubMed ID: 9238033
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Different removal of ultraviolet photoproducts in genetically related xeroderma pigmentosum and trichothiodystrophy diseases.
    Eveno E; Bourre F; Quilliet X; Chevallier-Lagente O; Roza L; Eker AP; Kleijer WJ; Nikaido O; Stefanini M; Hoeijmakers JH
    Cancer Res; 1995 Oct; 55(19):4325-32. PubMed ID: 7671243
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 38.