BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

1263 related articles for article (PubMed ID: 10416615)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. Disruption of the mouse xeroderma pigmentosum group D DNA repair/basal transcription gene results in preimplantation lethality.
    de Boer J; Donker I; de Wit J; Hoeijmakers JH; Weeda G
    Cancer Res; 1998 Jan; 58(1):89-94. PubMed ID: 9426063
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutations in XPB and XPD helicases found in xeroderma pigmentosum patients impair the transcription function of TFIIH.
    Coin F; Bergmann E; Tremeau-Bravard A; Egly JM
    EMBO J; 1999 Mar; 18(5):1357-66. PubMed ID: 10064601
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. Hot news: temperature-sensitive humans explain hereditary disease.
    Friedberg EC
    Bioessays; 2001 Aug; 23(8):671-3. PubMed ID: 11494313
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Sublimiting concentration of TFIIH transcription/DNA repair factor causes TTD-A trichothiodystrophy disorder.
    Vermeulen W; Bergmann E; Auriol J; Rademakers S; Frit P; Appeldoorn E; Hoeijmakers JH; Egly JM
    Nat Genet; 2000 Nov; 26(3):307-13. PubMed ID: 11062469
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. Premature aging in mice deficient in DNA repair and transcription.
    de Boer J; Andressoo JO; de Wit J; Huijmans J; Beems RB; van Steeg H; Weeda G; van der Horst GT; van Leeuwen W; Themmen AP; Meradji M; Hoeijmakers JH
    Science; 2002 May; 296(5571):1276-9. PubMed ID: 11950998
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. A mouse model for the basal transcription/DNA repair syndrome trichothiodystrophy.
    de Boer J; de Wit J; van Steeg H; Berg RJ; Morreau H; Visser P; Lehmann AR; Duran M; Hoeijmakers JH; Weeda G
    Mol Cell; 1998 Jun; 1(7):981-90. PubMed ID: 9651581
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Trichothiodystrophy, a transcription syndrome.
    Bergmann E; Egly JM
    Trends Genet; 2001 May; 17(5):279-86. PubMed ID: 11335038
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Requirement for functional DNA polymerase eta in genome-wide repair of UV-induced DNA damage during S phase.
    Auclair Y; Rouget R; Belisle JM; Costantino S; Drobetsky EA
    DNA Repair (Amst); 2010 Jul; 9(7):754-64. PubMed ID: 20457011
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 64.