543 related articles for article (PubMed ID: 15744309)
1. Defective DNA single-strand break repair in spinocerebellar ataxia with axonal neuropathy-1.
El-Khamisy SF; Saifi GM; Weinfeld M; Johansson F; Helleday T; Lupski JR; Caldecott KW
Nature; 2005 Mar; 434(7029):108-13. PubMed ID: 15744309
[TBL] [Abstract][Full Text] [Related]
2. Hereditary ataxia SCAN1 cells are defective for the repair of transcription-dependent topoisomerase I cleavage complexes.
Miao ZH; Agama K; Sordet O; Povirk L; Kohn KW; Pommier Y
DNA Repair (Amst); 2006 Dec; 5(12):1489-94. PubMed ID: 16935573
[TBL] [Abstract][Full Text] [Related]
3. DNA single-strand break repair and spinocerebellar ataxia with axonal neuropathy-1.
el-Khamisy SF; Caldecott KW
Neuroscience; 2007 Apr; 145(4):1260-6. PubMed ID: 17045754
[TBL] [Abstract][Full Text] [Related]
4. TDP1 facilitates repair of ionizing radiation-induced DNA single-strand breaks.
El-Khamisy SF; Hartsuiker E; Caldecott KW
DNA Repair (Amst); 2007 Oct; 6(10):1485-95. PubMed ID: 17600775
[TBL] [Abstract][Full Text] [Related]
5. TDP1 facilitates chromosomal single-strand break repair in neurons and is neuroprotective in vivo.
Katyal S; el-Khamisy SF; Russell HR; Li Y; Ju L; Caldecott KW; McKinnon PJ
EMBO J; 2007 Nov; 26(22):4720-31. PubMed ID: 17914460
[TBL] [Abstract][Full Text] [Related]
6. Spinocerebellar ataxia with axonal neuropathy: consequence of a Tdp1 recessive neomorphic mutation?
Hirano R; Interthal H; Huang C; Nakamura T; Deguchi K; Choi K; Bhattacharjee MB; Arimura K; Umehara F; Izumo S; Northrop JL; Salih MA; Inoue K; Armstrong DL; Champoux JJ; Takashima H; Boerkoel CF
EMBO J; 2007 Nov; 26(22):4732-43. PubMed ID: 17948061
[TBL] [Abstract][Full Text] [Related]
7. Synergistic decrease of DNA single-strand break repair rates in mouse neural cells lacking both Tdp1 and aprataxin.
El-Khamisy SF; Katyal S; Patel P; Ju L; McKinnon PJ; Caldecott KW
DNA Repair (Amst); 2009 Jun; 8(6):760-6. PubMed ID: 19303373
[TBL] [Abstract][Full Text] [Related]
8. Tyrosyl-DNA phosphodiesterase I catalytic mutants reveal an alternative nucleophile that can catalyze substrate cleavage.
Comeaux EQ; Cuya SM; Kojima K; Jafari N; Wanzeck KC; Mobley JA; Bjornsti MA; van Waardenburg RC
J Biol Chem; 2015 Mar; 290(10):6203-14. PubMed ID: 25609251
[TBL] [Abstract][Full Text] [Related]
9. Tyrosyl-DNA phosphodiesterase and the repair of 3'-phosphoglycolate-terminated DNA double-strand breaks.
Zhou T; Akopiants K; Mohapatra S; Lin PS; Valerie K; Ramsden DA; Lees-Miller SP; Povirk LF
DNA Repair (Amst); 2009 Aug; 8(8):901-11. PubMed ID: 19505854
[TBL] [Abstract][Full Text] [Related]
10. TDP2 promotes repair of topoisomerase I-mediated DNA damage in the absence of TDP1.
Zeng Z; Sharma A; Ju L; Murai J; Umans L; Vermeire L; Pommier Y; Takeda S; Huylebroeck D; Caldecott KW; El-Khamisy SF
Nucleic Acids Res; 2012 Sep; 40(17):8371-80. PubMed ID: 22740648
[TBL] [Abstract][Full Text] [Related]
11. In vitro complementation of Tdp1 deficiency indicates a stabilized enzyme-DNA adduct from tyrosyl but not glycolate lesions as a consequence of the SCAN1 mutation.
Hawkins AJ; Subler MA; Akopiants K; Wiley JL; Taylor SM; Rice AC; Windle JJ; Valerie K; Povirk LF
DNA Repair (Amst); 2009 May; 8(5):654-63. PubMed ID: 19211312
[TBL] [Abstract][Full Text] [Related]
12. Deficiency in 3'-phosphoglycolate processing in human cells with a hereditary mutation in tyrosyl-DNA phosphodiesterase (TDP1).
Zhou T; Lee JW; Tatavarthi H; Lupski JR; Valerie K; Povirk LF
Nucleic Acids Res; 2005; 33(1):289-97. PubMed ID: 15647511
[TBL] [Abstract][Full Text] [Related]
13. Spinocerebellar ataxia with axonal neuropathy.
Walton C; Interthal H; Hirano R; Salih MA; Takashima H; Boerkoel CF
Adv Exp Med Biol; 2010; 685():75-83. PubMed ID: 20687496
[TBL] [Abstract][Full Text] [Related]
14. TDP1 mutation causing SCAN1 neurodegenerative syndrome hampers the repair of transcriptional DNA double-strand breaks.
Geraud M; Cristini A; Salimbeni S; Bery N; Jouffret V; Russo M; Ajello AC; Fernandez Martinez L; Marinello J; Cordelier P; Trouche D; Favre G; Nicolas E; Capranico G; Sordet O
Cell Rep; 2024 May; 43(5):114214. PubMed ID: 38761375
[TBL] [Abstract][Full Text] [Related]
15. Association of XRCC1 and tyrosyl DNA phosphodiesterase (Tdp1) for the repair of topoisomerase I-mediated DNA lesions.
Plo I; Liao ZY; Barceló JM; Kohlhagen G; Caldecott KW; Weinfeld M; Pommier Y
DNA Repair (Amst); 2003 Oct; 2(10):1087-100. PubMed ID: 13679147
[TBL] [Abstract][Full Text] [Related]
16. Mutation of TDP1, encoding a topoisomerase I-dependent DNA damage repair enzyme, in spinocerebellar ataxia with axonal neuropathy.
Takashima H; Boerkoel CF; John J; Saifi GM; Salih MA; Armstrong D; Mao Y; Quiocho FA; Roa BB; Nakagawa M; Stockton DW; Lupski JR
Nat Genet; 2002 Oct; 32(2):267-72. PubMed ID: 12244316
[TBL] [Abstract][Full Text] [Related]
17. TDP1-dependent DNA single-strand break repair and neurodegeneration.
El-Khamisy SF; Caldecott KW
Mutagenesis; 2006 Jul; 21(4):219-24. PubMed ID: 16775218
[TBL] [Abstract][Full Text] [Related]
18. SCAN1 mutant Tdp1 accumulates the enzyme--DNA intermediate and causes camptothecin hypersensitivity.
Interthal H; Chen HJ; Kehl-Fie TE; Zotzmann J; Leppard JB; Champoux JJ
EMBO J; 2005 Jun; 24(12):2224-33. PubMed ID: 15920477
[TBL] [Abstract][Full Text] [Related]
19. TDP1 serine 81 promotes interaction with DNA ligase IIIalpha and facilitates cell survival following DNA damage.
Chiang SC; Carroll J; El-Khamisy SF
Cell Cycle; 2010 Feb; 9(3):588-595. PubMed ID: 20009512
[TBL] [Abstract][Full Text] [Related]
20. Tdp1 processes chromate-induced single-strand DNA breaks that collapse replication forks.
Ganguly A; Guo L; Sun L; Suo F; Du LL; Russell P
PLoS Genet; 2018 Aug; 14(8):e1007595. PubMed ID: 30148840
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]