BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

271 related articles for article (PubMed ID: 10604001)

  • 41. 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]  

  • 42. Nucleotide excision repair and the link with transcription.
    Lehmann AR
    Trends Biochem Sci; 1995 Oct; 20(10):402-5. PubMed ID: 8533152
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Transcription-coupled repair and human disease.
    Hanawalt PC
    Science; 1994 Dec; 266(5193):1957-8. PubMed ID: 7801121
    [No Abstract]   [Full Text] [Related]  

  • 44. 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]  

  • 45. Splitting hairs--discovery of a new DNA repair and transcription factor for the human disease trichothiodystrophy.
    Cleaver JE
    DNA Repair (Amst); 2005 Feb; 4(2):285-7. PubMed ID: 15590337
    [TBL] [Abstract][Full Text] [Related]  

  • 46. [Function of XPG gene and symptoms caused by its defect].
    Shiomi T
    Tanpakushitsu Kakusan Koso; 2001 Jun; 46(8 Suppl):902-7. PubMed ID: 11436315
    [No Abstract]   [Full Text] [Related]  

  • 47. [Xeroderma pigmentosum and related syndromes].
    Berneburg M; Krutmann J
    Hautarzt; 2003 Jan; 54(1):33-40. PubMed ID: 12567255
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Dysregulation of the peroxisome proliferator-activated receptor target genes by XPD mutations.
    Compe E; Drané P; Laurent C; Diderich K; Braun C; Hoeijmakers JH; Egly JM
    Mol Cell Biol; 2005 Jul; 25(14):6065-76. PubMed ID: 15988019
    [TBL] [Abstract][Full Text] [Related]  

  • 49. [XPD (ERCC2) (Xeroderma pigmentosum, group D). Reparation gene].
    Bull Cancer; 1998 Dec; 85(12):987-8. PubMed ID: 9988553
    [No Abstract]   [Full Text] [Related]  

  • 50. Trichothiodystrophy and the relationship between DNA repair and cancer.
    Lehmann AR
    Bioessays; 1989 Dec; 11(6):168-70. PubMed ID: 2695082
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Phosphorylation of XPB helicase regulates TFIIH nucleotide excision repair activity.
    Coin F; Auriol J; Tapias A; Clivio P; Vermeulen W; Egly JM
    EMBO J; 2004 Dec; 23(24):4835-46. PubMed ID: 15549133
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Basal transcription defect discriminates between xeroderma pigmentosum and trichothiodystrophy in XPD patients.
    Dubaele S; Proietti De Santis L; Bienstock RJ; Keriel A; Stefanini M; Van Houten B; Egly JM
    Mol Cell; 2003 Jun; 11(6):1635-46. PubMed ID: 12820975
    [TBL] [Abstract][Full Text] [Related]  

  • 53. An untwister's new twist.
    Davenport RJ
    Sci Aging Knowledge Environ; 2002 Apr; 2002(14):nf6. PubMed ID: 14602981
    [No Abstract]   [Full Text] [Related]  

  • 54. RNA polymerase II elongation complexes containing the Cockayne syndrome group B protein interact with a molecular complex containing the transcription factor IIH components xeroderma pigmentosum B and p62.
    Tantin D
    J Biol Chem; 1998 Oct; 273(43):27794-9. PubMed ID: 9774388
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Irofulven cytotoxicity depends on transcription-coupled nucleotide excision repair and is correlated with XPG expression in solid tumor cells.
    Koeppel F; Poindessous V; Lazar V; Raymond E; Sarasin A; Larsen AK
    Clin Cancer Res; 2004 Aug; 10(16):5604-13. PubMed ID: 15328203
    [TBL] [Abstract][Full Text] [Related]  

  • 56. 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]  

  • 57. Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy: do the genes explain the diseases?
    Chu G; Mayne L
    Trends Genet; 1996 May; 12(5):187-92. PubMed ID: 8984734
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Nucleotide excision repair: variations associated with cancer development and speciation.
    Cleaver JE; Speakman JR; Volpe JP
    Cancer Surv; 1995; 25():125-42. PubMed ID: 8718515
    [TBL] [Abstract][Full Text] [Related]  

  • 59. 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]  

  • 60. Strong functional interactions of TFIIH with XPC and XPG in human DNA nucleotide excision repair, without a preassembled repairosome.
    Araújo SJ; Nigg EA; Wood RD
    Mol Cell Biol; 2001 Apr; 21(7):2281-91. PubMed ID: 11259578
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 14.