1022 related articles for article (PubMed ID: 20227372)
1. A postincision-deficient TFIIH causes replication fork breakage and uncovers alternative Rad51- or Pol32-mediated restart mechanisms.
Moriel-Carretero M; Aguilera A
Mol Cell; 2010 Mar; 37(5):690-701. PubMed ID: 20227372
[TBL] [Abstract][Full Text] [Related]
2. Pol32 is required for Pol zeta-dependent translesion synthesis and prevents double-strand breaks at the replication fork.
Hanna M; Ball LG; Tong AH; Boone C; Xiao W
Mutat Res; 2007 Dec; 625(1-2):164-76. PubMed ID: 17681555
[TBL] [Abstract][Full Text] [Related]
3. Rad52 and Rad59 exhibit both overlapping and distinct functions.
Feng Q; Düring L; de Mayolo AA; Lettier G; Lisby M; Erdeniz N; Mortensen UH; Rothstein R
DNA Repair (Amst); 2007 Jan; 6(1):27-37. PubMed ID: 16987715
[TBL] [Abstract][Full Text] [Related]
4. Homologous recombination is involved in transcription-coupled repair of UV damage in Saccharomyces cerevisiae.
Aboussekhra A; Al-Sharif IS
EMBO J; 2005 Jun; 24(11):1999-2010. PubMed ID: 15902273
[TBL] [Abstract][Full Text] [Related]
5. Overexpression of Rad51 inhibits double-strand break-induced homologous recombination but does not affect gene conversion tract lengths.
Paffett KS; Clikeman JA; Palmer S; Nickoloff JA
DNA Repair (Amst); 2005 Jun; 4(6):687-98. PubMed ID: 15878310
[TBL] [Abstract][Full Text] [Related]
6. Purification and assays of Saccharomyces cerevisiae homologous recombination proteins.
Van Komen S; Macris M; Sehorn MG; Sung P
Methods Enzymol; 2006; 408():445-63. PubMed ID: 16793386
[TBL] [Abstract][Full Text] [Related]
7. Dynamic regulatory interactions of rad51, rad52, and replication protein-a in recombination intermediates.
Sugiyama T; Kantake N
J Mol Biol; 2009 Jul; 390(1):45-55. PubMed ID: 19445949
[TBL] [Abstract][Full Text] [Related]
8. Replication fork breakage and re-start: New insights into Rad3/XPD-associated deficiencies.
Moriel-Carretero M; Aguilera A
Cell Cycle; 2010 Aug; 9(15):2958-62. PubMed ID: 20740714
[TBL] [Abstract][Full Text] [Related]
9. Control of Rad52 recombination activity by double-strand break-induced SUMO modification.
Sacher M; Pfander B; Hoege C; Jentsch S
Nat Cell Biol; 2006 Nov; 8(11):1284-90. PubMed ID: 17013376
[TBL] [Abstract][Full Text] [Related]
10. Transcription factor b (TFIIH) is required during nucleotide-excision repair in yeast.
Wang Z; Svejstrup JQ; Feaver WJ; Wu X; Kornberg RD; Friedberg EC
Nature; 1994 Mar; 368(6466):74-6. PubMed ID: 8107888
[TBL] [Abstract][Full Text] [Related]
11. Choreography of the DNA damage response: spatiotemporal relationships among checkpoint and repair proteins.
Lisby M; Barlow JH; Burgess RC; Rothstein R
Cell; 2004 Sep; 118(6):699-713. PubMed ID: 15369670
[TBL] [Abstract][Full Text] [Related]
12. Exploring the roles of Mus81-Eme1/Mms4 at perturbed replication forks.
Osman F; Whitby MC
DNA Repair (Amst); 2007 Jul; 6(7):1004-17. PubMed ID: 17409028
[TBL] [Abstract][Full Text] [Related]
13. DNA REPAIR. Mus81 and converging forks limit the mutagenicity of replication fork breakage.
Mayle R; Campbell IM; Beck CR; Yu Y; Wilson M; Shaw CA; Bjergbaek L; Lupski JR; Ira G
Science; 2015 Aug; 349(6249):742-7. PubMed ID: 26273056
[TBL] [Abstract][Full Text] [Related]
14. Multiple recombination pathways for sister chromatid exchange in Saccharomyces cerevisiae: role of RAD1 and the RAD52 epistasis group genes.
Dong Z; Fasullo M
Nucleic Acids Res; 2003 May; 31(10):2576-85. PubMed ID: 12736307
[TBL] [Abstract][Full Text] [Related]
15. Strong functional interactions of TFIIH with XPC and XPG in human DNA nucleotide excision repair, without a preassembled repairosome.
Araújo SJ; Nigg EA; Wood RD
Mol Cell Biol; 2001 Apr; 21(7):2281-91. PubMed ID: 11259578
[TBL] [Abstract][Full Text] [Related]
16. Homologous recombination is responsible for cell death in the absence of the Sgs1 and Srs2 helicases.
Gangloff S; Soustelle C; Fabre F
Nat Genet; 2000 Jun; 25(2):192-4. PubMed ID: 10835635
[TBL] [Abstract][Full Text] [Related]
17. Rad51 replication fork recruitment is required for DNA damage tolerance.
González-Prieto R; Muñoz-Cabello AM; Cabello-Lobato MJ; Prado F
EMBO J; 2013 May; 32(9):1307-21. PubMed ID: 23563117
[TBL] [Abstract][Full Text] [Related]
18. Use of yeast for detection of endogenous abasic lesions, their source, and their repair.
Boiteux S; Guillet M
Methods Enzymol; 2006; 408():79-91. PubMed ID: 16793364
[TBL] [Abstract][Full Text] [Related]
19. Histone H3K56 acetylation, Rad52, and non-DNA repair factors control double-strand break repair choice with the sister chromatid.
Muñoz-Galván S; Jimeno S; Rothstein R; Aguilera A
PLoS Genet; 2013; 9(1):e1003237. PubMed ID: 23357952
[TBL] [Abstract][Full Text] [Related]
20. A new Saccharomyces cerevisiae strain with a mutant Smt3-deconjugating Ulp1 protein is affected in DNA replication and requires Srs2 and homologous recombination for its viability.
Soustelle C; Vernis L; Fréon K; Reynaud-Angelin A; Chanet R; Fabre F; Heude M
Mol Cell Biol; 2004 Jun; 24(12):5130-43. PubMed ID: 15169880
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]