BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

226 related articles for article (PubMed ID: 8754844)

  • 1. The sensitivity of Cockayne's syndrome cells to DNA-damaging agents is not due to defective transcription-coupled repair of active genes.
    van Oosterwijk MF; Versteeg A; Filon R; van Zeeland AA; Mullenders LH
    Mol Cell Biol; 1996 Aug; 16(8):4436-44. PubMed ID: 8754844
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Lack of transcription-coupled repair of acetylaminofluorene DNA adducts in human fibroblasts contrasts their efficient inhibition of transcription.
    van Oosterwijk MF; Filon R; de Groot AJ; van Zeeland AA; Mullenders LH
    J Biol Chem; 1998 May; 273(22):13599-604. PubMed ID: 9593697
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The sensitivity of human fibroblasts to N-acetoxy-2-acetylaminofluorene is determined by the extent of transcription-coupled repair, and/or their capability to counteract RNA synthesis inhibition.
    van Oosterwijk MF; Filon R; Kalle WH; Mullenders LH; van Zeeland AA
    Nucleic Acids Res; 1996 Dec; 24(23):4653-9. PubMed ID: 8972850
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cells from XP-D and XP-D-CS patients exhibit equally inefficient repair of UV-induced damage in transcribed genes but different capacity to recover UV-inhibited transcription.
    van Hoffen A; Kalle WH; de Jong-Versteeg A; Lehmann AR; van Zeeland AA; Mullenders LH
    Nucleic Acids Res; 1999 Jul; 27(14):2898-904. PubMed ID: 10390531
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cockayne syndrome: varied requirement of transcription-coupled nucleotide excision repair for the removal of three structurally different adducts from transcribed DNA.
    Kitsera N; Gasteiger K; Lühnsdorf B; Allgayer J; Epe B; Carell T; Khobta A
    PLoS One; 2014; 9(4):e94405. PubMed ID: 24713864
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Blockage of transcription as a trigger for p53 accumulation by 2-acetylaminofluorene DNA-adducts.
    van Gijssel HE; Mullenders LH; van Oosterwijk MF; Meerman JH
    Life Sci; 2003 Aug; 73(14):1759-71. PubMed ID: 12888115
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Ultraviolet-sensitive syndrome cells are defective in transcription-coupled repair of cyclobutane pyrimidine dimers.
    Spivak G; Itoh T; Matsunaga T; Nikaido O; Hanawalt P; Yamaizumi M
    DNA Repair (Amst); 2002 Aug; 1(8):629-43. PubMed ID: 12509286
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Enhanced UV-induced mutagenesis in the UV61 cell line, the Chinese hamster homologue of Cockayne's syndrome B, is associated with defective transcription coupled repair of cyclobutane pyrimidine dimers.
    Vreeswijk MP; Overkamp MW; Westland BE; van Hees-Stuivenberg S; Vrieling H; Zdzienicka MZ; van Zeeland AA; Mullenders LH
    Mutat Res; 1998 Oct; 409(1):49-56. PubMed ID: 9806502
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Deficient repair of the transcribed strand of active genes in Cockayne's syndrome cells.
    van Hoffen A; Natarajan AT; Mayne LV; van Zeeland AA; Mullenders LH; Venema J
    Nucleic Acids Res; 1993 Dec; 21(25):5890-5. PubMed ID: 8290349
    [TBL] [Abstract][Full Text] [Related]  

  • 10. UVB radiation-induced cancer predisposition in Cockayne syndrome group A (Csa) mutant mice.
    van der Horst GT; Meira L; Gorgels TG; de Wit J; Velasco-Miguel S; Richardson JA; Kamp Y; Vreeswijk MP; Smit B; Bootsma D; Hoeijmakers JH; Friedberg EC
    DNA Repair (Amst); 2002 Feb; 1(2):143-57. PubMed ID: 12509261
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The human CSB (ERCC6) gene corrects the transcription-coupled repair defect in the CHO cell mutant UV61.
    Orren DK; Dianov GL; Bohr VA
    Nucleic Acids Res; 1996 Sep; 24(17):3317-22. PubMed ID: 8811084
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutagenic properties of 3-(deoxyguanosin-N2-yl)-2-acetylaminofluorene, a persistent acetylaminofluorene-derived DNA adduct in mammalian cells.
    Yasui M; Dong H; Bonala RR; Suzuki N; Ohmori H; Hanaoka F; Johnson F; Grollman AP; Shibutani S
    Biochemistry; 2004 Nov; 43(47):15005-13. PubMed ID: 15554708
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Transcription coupled repair deficiency results in increased chromosomal aberrations and apoptotic death in the UV61 cell line, the Chinese hamster homologue of Cockayne's syndrome B.
    Proietti De Santis L; Garcia CL; Balajee AS; Brea Calvo GT; Bassi L; Palitti F
    Mutat Res; 2001 Mar; 485(2):121-32. PubMed ID: 11182543
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Evidence for defective repair of cyclobutane pyrimidine dimers with normal repair of other DNA photoproducts in a transcriptionally active gene transfected into Cockayne syndrome cells.
    Barrett SF; Robbins JH; Tarone RE; Kraemer KH
    Mutat Res; 1991 Nov; 255(3):281-91. PubMed ID: 1719400
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Differential requirement for the ATPase domain of the Cockayne syndrome group B gene in the processing of UV-induced DNA damage and 8-oxoguanine lesions in human cells.
    Selzer RR; Nyaga S; Tuo J; May A; Muftuoglu M; Christiansen M; Citterio E; Brosh RM; Bohr VA
    Nucleic Acids Res; 2002 Feb; 30(3):782-93. PubMed ID: 11809892
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hypersensitivity of Cockayne's syndrome cells to camptothecin is associated with the generation of abnormally high levels of double strand breaks in nascent DNA.
    Squires S; Ryan AJ; Strutt HL; Johnson RT
    Cancer Res; 1993 May; 53(9):2012-9. PubMed ID: 7683249
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Molecular characterization of an acidic region deletion mutant of Cockayne syndrome group B protein.
    Sunesen M; Selzer RR; Brosh RM; Balajee AS; Stevnsner T; Bohr VA
    Nucleic Acids Res; 2000 Aug; 28(16):3151-9. PubMed ID: 10931931
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Repair in ribosomal RNA genes is deficient in xeroderma pigmentosum group C and in Cockayne's syndrome cells.
    Christians FC; Hanawalt PC
    Mutat Res; 1994 Apr; 323(4):179-87. PubMed ID: 7512688
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The binding of N-hydroxy-2-acetylaminofluorene to DNA and repair of the adducts in primary rat hepatocyte cultures.
    Howard PC; Casciano DA; Beland FA; Shaddock JG
    Carcinogenesis; 1981; 2(2):97-102. PubMed ID: 6168407
    [TBL] [Abstract][Full Text] [Related]  

  • 20. In situ detection of acetylaminofluorene-DNA adducts in human cells using monoclonal antibodies.
    Iwamoto TA; Kobayashi N; Imoto K; Yamamoto A; Nakamura Y; Yamauchi Y; Okumura H; Tanaka A; Hanaoka F; Shibutani S; Miyagawa S; Mori T
    DNA Repair (Amst); 2004 Nov; 3(11):1475-82. PubMed ID: 15380103
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.