These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

483 related articles for article (PubMed ID: 7767957)

  • 41. Expression of a transfected DNA repair gene (XPA) in xeroderma pigmentosum group A cells restores normal DNA repair and mutagenesis of UV-treated plasmids.
    Levy DD; Saijo M; Tanaka K; Kraemer KH
    Carcinogenesis; 1995 Jul; 16(7):1557-63. PubMed ID: 7614689
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Multiple involvement of nucleotide excision repair enzymes: clinical manifestations of molecular intricacies.
    Jaspers NG
    Cytokines Mol Ther; 1996 Jun; 2(2):115-9. PubMed ID: 9384696
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Comparative studies of host-cell reactivation, cellular capacity and enhanced reactivation of herpes simplex virus in normal, xeroderma pigmentosum and Cockayne syndrome fibroblasts.
    Ryan DK; Rainbow AJ
    Mutat Res; 1986 Jul; 166(1):99-111. PubMed ID: 3014327
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Human cancer and DNA repair-deficient diseases.
    Sarasin A; Stary A
    Cancer Detect Prev; 1997; 21(5):406-11. PubMed ID: 9307843
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Defective transcription-coupled repair of oxidative base damage in Cockayne syndrome patients from XP group G.
    Cooper PK; Nouspikel T; Clarkson SG; Leadon SA
    Science; 1997 Feb; 275(5302):990-3. PubMed ID: 9020084
    [TBL] [Abstract][Full Text] [Related]  

  • 46. The cloned human DNA excision repair gene ERCC-1 fails to correct xeroderma pigmentosum complementation groups A through I.
    van Duin M; Vredeveldt G; Mayne LV; Odijk H; Vermeulen W; Klein B; Weeda G; Hoeijmakers JH; Bootsma D; Westerveld A
    Mutat Res; 1989 Mar; 217(2):83-92. PubMed ID: 2918869
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Xeroderma pigmentosum and related disorders: defects in DNA repair and transcription.
    Berneburg M; Lehmann AR
    Adv Genet; 2001; 43():71-102. PubMed ID: 11037299
    [TBL] [Abstract][Full Text] [Related]  

  • 48. 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]  

  • 49. Host cell reactivation of CAT-expression vectors as a method to assay for cloned DNA-repair genes.
    Henderson EE; Valerie K; Green AP; de Riel JK
    Mutat Res; 1989; 220(2-3):151-60. PubMed ID: 2927423
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Complementation of the DNA repair defect in xeroderma pigmentosum group G cells by a human cDNA related to yeast RAD2.
    Scherly D; Nouspikel T; Corlet J; Ucla C; Bairoch A; Clarkson SG
    Nature; 1993 May; 363(6425):182-5. PubMed ID: 8483504
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Xeroderma pigmentosum--Cockayne syndrome complex: a further case.
    Hamel BC; Raams A; Schuitema-Dijkstra AR; Simons P; van der Burgt I; Jaspers NG; Kleijer WJ
    J Med Genet; 1996 Jul; 33(7):607-10. PubMed ID: 8818951
    [TBL] [Abstract][Full Text] [Related]  

  • 52. UV-induced mutations in a shuttle vector replicated in repair deficient trichothiodystrophy cells differ with those in genetically-related cancer prone xeroderma pigmentosum.
    Madzak C; Armier J; Stary A; Daya-Grosjean L; Sarasin A
    Carcinogenesis; 1993 Jul; 14(7):1255-60. PubMed ID: 8392442
    [TBL] [Abstract][Full Text] [Related]  

  • 53. DNA repair in human fibroblasts, as reflected by host-cell reactivation of a transfected UV-irradiated luciferase gene, is not related to donor age.
    Merkle TJ; O'Brien K; Brooks PJ; Tarone RE; Robbins JH
    Mutat Res; 2004 Oct; 554(1-2):9-17. PubMed ID: 15450399
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Transcription-associated breaks in xeroderma pigmentosum group D cells from patients with combined features of xeroderma pigmentosum and Cockayne syndrome.
    Theron T; Fousteri MI; Volker M; Harries LW; Botta E; Stefanini M; Fujimoto M; Andressoo JO; Mitchell J; Jaspers NG; McDaniel LD; Mullenders LH; Lehmann AR
    Mol Cell Biol; 2005 Sep; 25(18):8368-78. PubMed ID: 16135823
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Complementation studies in cells from patients affected by trichothiodystrophy with normal or enhanced UV photosensitivity.
    Stefanini M; Lagomarsini P; Giorgi R; Nuzzo F
    Mutat Res; 1987 Jun; 191(2):117-9. PubMed ID: 3600693
    [TBL] [Abstract][Full Text] [Related]  

  • 56. 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]  

  • 57. 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]  

  • 58. 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]  

  • 59. Nucleotide excision repair and human syndromes.
    de Boer J; Hoeijmakers JH
    Carcinogenesis; 2000 Mar; 21(3):453-60. PubMed ID: 10688865
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Long-term complementation of DNA repair deficient human primary fibroblasts by retroviral transduction of the XPD gene.
    Quilliet X; Chevallier-Lagente O; Eveno E; Stojkovic T; Destée A; Sarasin A; Mezzina M
    Mutat Res; 1996 Dec; 364(3):161-9. PubMed ID: 8960128
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 25.