123 related articles for article (PubMed ID: 16818625)
1. 4-nitroquinoline-1-oxide induces the formation of cellular topoisomerase I-DNA cleavage complexes.
Miao ZH; Rao VA; Agama K; Antony S; Kohn KW; Pommier Y
Cancer Res; 2006 Jul; 66(13):6540-5. PubMed ID: 16818625
[TBL] [Abstract][Full Text] [Related]
2. Phosphorylation of BLM, dissociation from topoisomerase IIIalpha, and colocalization with gamma-H2AX after topoisomerase I-induced replication damage.
Rao VA; Fan AM; Meng L; Doe CF; North PS; Hickson ID; Pommier Y
Mol Cell Biol; 2005 Oct; 25(20):8925-37. PubMed ID: 16199871
[TBL] [Abstract][Full Text] [Related]
3. Endogenous gamma-H2AX-ATM-Chk2 checkpoint activation in Bloom's syndrome helicase deficient cells is related to DNA replication arrested forks.
Rao VA; Conti C; Guirouilh-Barbat J; Nakamura A; Miao ZH; Davies SL; Saccá B; Hickson ID; Bensimon A; Pommier Y
Mol Cancer Res; 2007 Jul; 5(7):713-24. PubMed ID: 17634426
[TBL] [Abstract][Full Text] [Related]
4. PARP-1-dependent RND1 transcription induced by topoisomerase I cleavage complexes confers cellular resistance to camptothecin.
Mouly L; Mamouni K; Gence R; Cristini A; Cherier J; Castinel A; Legrand M; Favre G; Sordet O; Monferran S
Cell Death Dis; 2018 Sep; 9(9):931. PubMed ID: 30209297
[TBL] [Abstract][Full Text] [Related]
5. Werner and Bloom helicases are involved in DNA repair in a complementary fashion.
Imamura O; Fujita K; Itoh C; Takeda S; Furuichi Y; Matsumoto T
Oncogene; 2002 Jan; 21(6):954-63. PubMed ID: 11840341
[TBL] [Abstract][Full Text] [Related]
6. Association of the Bloom syndrome protein with topoisomerase IIIalpha in somatic and meiotic cells.
Johnson FB; Lombard DB; Neff NF; Mastrangelo MA; Dewolf W; Ellis NA; Marciniak RA; Yin Y; Jaenisch R; Guarente L
Cancer Res; 2000 Mar; 60(5):1162-7. PubMed ID: 10728666
[TBL] [Abstract][Full Text] [Related]
7. Cellular and chromosomal hypersensitivity to DNA crosslinking agents and topoisomerase inhibitors in the radiosensitive Chinese hamster irs mutants: phenotypic similarities to ataxia telangiectasia and Fanconi's anaemia cells.
Jones NJ; Ellard S; Waters R; Parry EM
Carcinogenesis; 1993 Dec; 14(12):2487-94. PubMed ID: 8269616
[TBL] [Abstract][Full Text] [Related]
8. Enzymatic and DNA binding properties of purified WRN protein: high affinity binding to single-stranded DNA but not to DNA damage induced by 4NQO.
Orren DK; Brosh RM; Nehlin JO; Machwe A; Gray MD; Bohr VA
Nucleic Acids Res; 1999 Sep; 27(17):3557-66. PubMed ID: 10446247
[TBL] [Abstract][Full Text] [Related]
9. Cleavage of the Bloom's syndrome gene product during apoptosis by caspase-3 results in an impaired interaction with topoisomerase IIIalpha.
Freire R; d'Adda Di Fagagna F; Wu L; Pedrazzi G; Stagljar I; Hickson ID; Jackson SP
Nucleic Acids Res; 2001 Aug; 29(15):3172-80. PubMed ID: 11470874
[TBL] [Abstract][Full Text] [Related]
10. Batracylin (NSC 320846), a dual inhibitor of DNA topoisomerases I and II induces histone gamma-H2AX as a biomarker of DNA damage.
Rao VA; Agama K; Holbeck S; Pommier Y
Cancer Res; 2007 Oct; 67(20):9971-9. PubMed ID: 17942930
[TBL] [Abstract][Full Text] [Related]
11. The Bloom's syndrome helicase stimulates the activity of human topoisomerase IIIalpha.
Wu L; Hickson ID
Nucleic Acids Res; 2002 Nov; 30(22):4823-9. PubMed ID: 12433984
[TBL] [Abstract][Full Text] [Related]
12. Study of molecular markers of resistance to m-AMSA in a human breast cancer cell line. Decrease of topoisomerase II and increase of both topoisomerase I and acidic glutathione S transferase.
Lefevre D; Riou JF; Ahomadegbe JC; Zhou DY; Benard J; Riou G
Biochem Pharmacol; 1991 Jun; 41(12):1967-79. PubMed ID: 1645555
[TBL] [Abstract][Full Text] [Related]
13. Bloom helicase and DNA topoisomerase IIIalpha are involved in the dissolution of sister chromatids.
Seki M; Nakagawa T; Seki T; Kato G; Tada S; Takahashi Y; Yoshimura A; Kobayashi T; Aoki A; Otsuki M; Habermann FA; Tanabe H; Ishii Y; Enomoto T
Mol Cell Biol; 2006 Aug; 26(16):6299-307. PubMed ID: 16880537
[TBL] [Abstract][Full Text] [Related]
14. Methyleugenol and oxidative metabolites induce DNA damage and interact with human topoisomerases.
Groh IA; Rudakovski O; Gründken M; Schroeter A; Marko D; Esselen M
Arch Toxicol; 2016 Nov; 90(11):2809-2823. PubMed ID: 26542539
[TBL] [Abstract][Full Text] [Related]
15. Topoisomerase II and tubulin inhibitors both induce the formation of apoptotic topoisomerase I cleavage complexes.
Sordet O; Goldman A; Pommier Y
Mol Cancer Ther; 2006 Dec; 5(12):3139-44. PubMed ID: 17172417
[TBL] [Abstract][Full Text] [Related]
16. DNA damage induced by DNA topoisomerase I- and topoisomerase II-inhibitors detected by histone H2AX phosphorylation in relation to the cell cycle phase and apoptosis.
Huang X; Traganos F; Darzynkiewicz Z
Cell Cycle; 2003; 2(6):614-9. PubMed ID: 14504478
[TBL] [Abstract][Full Text] [Related]
17. BLM is required for faithful chromosome segregation and its localization defines a class of ultrafine anaphase bridges.
Chan KL; North PS; Hickson ID
EMBO J; 2007 Jul; 26(14):3397-409. PubMed ID: 17599064
[TBL] [Abstract][Full Text] [Related]
18. Evidence for BLM and Topoisomerase IIIalpha interaction in genomic stability.
Hu P; Beresten SF; van Brabant AJ; Ye TZ; Pandolfi PP; Johnson FB; Guarente L; Ellis NA
Hum Mol Genet; 2001 Jun; 10(12):1287-98. PubMed ID: 11406610
[TBL] [Abstract][Full Text] [Related]
19. Various inhibitors of DNA topoisomerases diminish repair-specific DNA incision in UV-irradiated human fibroblasts.
Thielmann HW; Popanda O; Gersbach H; Gilberg F
Carcinogenesis; 1993 Nov; 14(11):2341-51. PubMed ID: 8242865
[TBL] [Abstract][Full Text] [Related]
20. Chromosome breakage is regulated by the interaction of the BLM helicase and topoisomerase IIalpha.
Russell B; Bhattacharyya S; Keirsey J; Sandy A; Grierson P; Perchiniak E; Kavecansky J; Acharya S; Groden J
Cancer Res; 2011 Jan; 71(2):561-71. PubMed ID: 21224348
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
