130 related articles for article (PubMed ID: 18078829)
1. Analyses of functional interaction between RECQL1, RECQL5, and BLM which physically interact with DNA topoisomerase IIIalpha.
Otsuki M; Seki M; Inoue E; Abe T; Narita Y; Yoshimura A; Tada S; Ishii Y; Enomoto T
Biochim Biophys Acta; 2008 Feb; 1782(2):75-81. PubMed ID: 18078829
[TBL] [Abstract][Full Text] [Related]
2. Functional relation among RecQ family helicases RecQL1, RecQL5, and BLM in cell growth and sister chromatid exchange formation.
Wang W; Seki M; Narita Y; Nakagawa T; Yoshimura A; Otsuki M; Kawabe Y; Tada S; Yagi H; Ishii Y; Enomoto T
Mol Cell Biol; 2003 May; 23(10):3527-35. PubMed ID: 12724411
[TBL] [Abstract][Full Text] [Related]
3. The absence of a functional relationship between ATM and BLM, the components of BASC, in DT40 cells.
Wang W; Seki M; Otsuki M; Tada S; Takao N; Yamamoto K; Hayashi M; Honma M; Enomoto T
Biochim Biophys Acta; 2004 Mar; 1688(2):137-44. PubMed ID: 14990344
[TBL] [Abstract][Full Text] [Related]
4. Functional interactions between BLM and XRCC3 in the cell.
Otsuki M; Seki M; Inoue E; Yoshimura A; Kato G; Yamanouchi S; Kawabe Y; Tada S; Shinohara A; Komura J; Ono T; Takeda S; Ishii Y; Enomoto T
J Cell Biol; 2007 Oct; 179(1):53-63. PubMed ID: 17923529
[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. Recql5 and Blm RecQ DNA helicases have nonredundant roles in suppressing crossovers.
Hu Y; Lu X; Barnes E; Yan M; Lou H; Luo G
Mol Cell Biol; 2005 May; 25(9):3431-42. PubMed ID: 15831450
[TBL] [Abstract][Full Text] [Related]
7. Possible association of BLM in decreasing DNA double strand breaks during DNA replication.
Wang W; Seki M; Narita Y; Sonoda E; Takeda S; Yamada K; Masuko T; Katada T; Enomoto T
EMBO J; 2000 Jul; 19(13):3428-35. PubMed ID: 10880455
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Vertebrate WRNIP1 and BLM are required for efficient maintenance of genome stability.
Hayashi T; Seki M; Inoue E; Yoshimura A; Kusa Y; Tada S; Enomoto T
Genes Genet Syst; 2008 Feb; 83(1):95-100. PubMed ID: 18379138
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. A double Holliday junction dissolvasome comprising BLM, topoisomerase IIIalpha, and BLAP75.
Raynard S; Bussen W; Sung P
J Biol Chem; 2006 May; 281(20):13861-4. PubMed ID: 16595695
[TBL] [Abstract][Full Text] [Related]
13. BLAP75/RMI1 promotes the BLM-dependent dissolution of homologous recombination intermediates.
Wu L; Bachrati CZ; Ou J; Xu C; Yin J; Chang M; Wang W; Li L; Brown GW; Hickson ID
Proc Natl Acad Sci U S A; 2006 Mar; 103(11):4068-73. PubMed ID: 16537486
[TBL] [Abstract][Full Text] [Related]
14. Disruption of the BLM gene in ATM-null DT40 cells does not exacerbate either phenotype.
Fukao T; Chen P; Ren J; Kaneko H; Zhang GX; Kondo M; Yamamoto K; Furuichi Y; Takeda S; Kondo N; Lavin MF
Oncogene; 2004 Feb; 23(8):1498-506. PubMed ID: 14985700
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Bloom helicase is involved in DNA surveillance in early S phase in vertebrate cells.
Imamura O; Fujita K; Shimamoto A; Tanabe H; Takeda S; Furuichi Y; Matsumoto T
Oncogene; 2001 Mar; 20(10):1143-51. PubMed ID: 11313858
[TBL] [Abstract][Full Text] [Related]
18. Cooperative roles of vertebrate Fbh1 and Blm DNA helicases in avoidance of crossovers during recombination initiated by replication fork collapse.
Kohzaki M; Hatanaka A; Sonoda E; Yamazoe M; Kikuchi K; Vu Trung N; Szüts D; Sale JE; Shinagawa H; Watanabe M; Takeda S
Mol Cell Biol; 2007 Apr; 27(8):2812-20. PubMed ID: 17283053
[TBL] [Abstract][Full Text] [Related]
19. Functional relationships of FANCC to homologous recombination, translesion synthesis, and BLM.
Hirano S; Yamamoto K; Ishiai M; Yamazoe M; Seki M; Matsushita N; Ohzeki M; Yamashita YM; Arakawa H; Buerstedde JM; Enomoto T; Takeda S; Thompson LH; Takata M
EMBO J; 2005 Jan; 24(2):418-27. PubMed ID: 15616572
[TBL] [Abstract][Full Text] [Related]
20. RMI, a new OB-fold complex essential for Bloom syndrome protein to maintain genome stability.
Xu D; Guo R; Sobeck A; Bachrati CZ; Yang J; Enomoto T; Brown GW; Hoatlin ME; Hickson ID; Wang W
Genes Dev; 2008 Oct; 22(20):2843-55. PubMed ID: 18923082
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
