359 related articles for article (PubMed ID: 23604072)
1. Mammalian DNA2 helicase/nuclease cleaves G-quadruplex DNA and is required for telomere integrity.
Lin W; Sampathi S; Dai H; Liu C; Zhou M; Hu J; Huang Q; Campbell J; Shin-Ya K; Zheng L; Chai W; Shen B
EMBO J; 2013 May; 32(10):1425-39. PubMed ID: 23604072
[TBL] [Abstract][Full Text] [Related]
2. Dna2 is involved in CA strand resection and nascent lagging strand completion at native yeast telomeres.
Budd ME; Campbell JL
J Biol Chem; 2013 Oct; 288(41):29414-29. PubMed ID: 23963457
[TBL] [Abstract][Full Text] [Related]
3. A Critical Role for Dna2 at Unwound Telomeres.
Markiewicz-Potoczny M; Lisby M; Lydall D
Genetics; 2018 May; 209(1):129-141. PubMed ID: 29559500
[TBL] [Abstract][Full Text] [Related]
4. Processing of G4 DNA by Dna2 helicase/nuclease and replication protein A (RPA) provides insights into the mechanism of Dna2/RPA substrate recognition.
Masuda-Sasa T; Polaczek P; Peng XP; Chen L; Campbell JL
J Biol Chem; 2008 Sep; 283(36):24359-73. PubMed ID: 18593712
[TBL] [Abstract][Full Text] [Related]
5. RTEL1 dismantles T loops and counteracts telomeric G4-DNA to maintain telomere integrity.
Vannier JB; Pavicic-Kaltenbrunner V; Petalcorin MI; Ding H; Boulton SJ
Cell; 2012 May; 149(4):795-806. PubMed ID: 22579284
[TBL] [Abstract][Full Text] [Related]
6. Dna2 nuclease-helicase structure, mechanism and regulation by Rpa.
Zhou C; Pourmal S; Pavletich NP
Elife; 2015 Nov; 4():. PubMed ID: 26491943
[TBL] [Abstract][Full Text] [Related]
7. A telomerase-associated RecQ protein-like helicase resolves telomeric G-quadruplex structures during replication.
Postberg J; Tsytlonok M; Sparvoli D; Rhodes D; Lipps HJ
Gene; 2012 Apr; 497(2):147-54. PubMed ID: 22327026
[TBL] [Abstract][Full Text] [Related]
8. BLM helicase facilitates telomere replication during leading strand synthesis of telomeres.
Drosopoulos WC; Kosiyatrakul ST; Schildkraut CL
J Cell Biol; 2015 Jul; 210(2):191-208. PubMed ID: 26195664
[TBL] [Abstract][Full Text] [Related]
9. Mammalian telomeres resemble fragile sites and require TRF1 for efficient replication.
Sfeir A; Kosiyatrakul ST; Hockemeyer D; MacRae SL; Karlseder J; Schildkraut CL; de Lange T
Cell; 2009 Jul; 138(1):90-103. PubMed ID: 19596237
[TBL] [Abstract][Full Text] [Related]
10. AKTIP/Ft1, a New Shelterin-Interacting Factor Required for Telomere Maintenance.
Burla R; Carcuro M; Raffa GD; Galati A; Raimondo D; Rizzo A; La Torre M; Micheli E; Ciapponi L; Cenci G; Cundari E; Musio A; Biroccio A; Cacchione S; Gatti M; Saggio I
PLoS Genet; 2015 Jun; 11(6):e1005167. PubMed ID: 26110528
[TBL] [Abstract][Full Text] [Related]
11. Defective repair of uracil causes telomere defects in mouse hematopoietic cells.
Vallabhaneni H; Zhou F; Maul RW; Sarkar J; Yin J; Lei M; Harrington L; Gearhart PJ; Liu Y
J Biol Chem; 2015 Feb; 290(9):5502-11. PubMed ID: 25572391
[TBL] [Abstract][Full Text] [Related]
12. Break-induced replication promotes fragile telomere formation.
Yang Z; Takai KK; Lovejoy CA; de Lange T
Genes Dev; 2020 Oct; 34(19-20):1392-1405. PubMed ID: 32883681
[TBL] [Abstract][Full Text] [Related]
13. DNA processing is not required for ATM-mediated telomere damage response after TRF2 deletion.
Celli GB; de Lange T
Nat Cell Biol; 2005 Jul; 7(7):712-8. PubMed ID: 15968270
[TBL] [Abstract][Full Text] [Related]
14. Telomere damage induced by the G-quadruplex ligand RHPS4 has an antitumor effect.
Salvati E; Leonetti C; Rizzo A; Scarsella M; Mottolese M; Galati R; Sperduti I; Stevens MF; D'Incalci M; Blasco M; Chiorino G; Bauwens S; Horard B; Gilson E; Stoppacciaro A; Zupi G; Biroccio A
J Clin Invest; 2007 Nov; 117(11):3236-47. PubMed ID: 17932567
[TBL] [Abstract][Full Text] [Related]
15. Neil3 and NEIL1 DNA glycosylases remove oxidative damages from quadruplex DNA and exhibit preferences for lesions in the telomeric sequence context.
Zhou J; Liu M; Fleming AM; Burrows CJ; Wallace SS
J Biol Chem; 2013 Sep; 288(38):27263-27272. PubMed ID: 23926102
[TBL] [Abstract][Full Text] [Related]
16. G-rich telomeric and ribosomal DNA sequences from the fission yeast genome form stable G-quadruplex DNA structures in vitro and are unwound by the Pfh1 DNA helicase.
Wallgren M; Mohammad JB; Yan KP; Pourbozorgi-Langroudi P; Ebrahimi M; Sabouri N
Nucleic Acids Res; 2016 Jul; 44(13):6213-31. PubMed ID: 27185885
[TBL] [Abstract][Full Text] [Related]
17. An intramolecular G-quadruplex structure is required for binding of telomeric repeat-containing RNA to the telomeric protein TRF2.
Biffi G; Tannahill D; Balasubramanian S
J Am Chem Soc; 2012 Jul; 134(29):11974-6. PubMed ID: 22780456
[TBL] [Abstract][Full Text] [Related]
18. Disruption of G-quadruplex dynamicity by BRCA2 abrogation instigates phase separation and break-induced replication at telomeres.
Lee JJ; Kim H; Park H; Lee U; Kim C; Lee M; Shin Y; Jung JJ; Lee HB; Han W; Lee H
Nucleic Acids Res; 2024 Jun; 52(10):5756-5773. PubMed ID: 38587189
[TBL] [Abstract][Full Text] [Related]
19. Replication intermediates that escape Dna2 activity are processed by Holliday junction resolvase Yen1.
Ölmezer G; Levikova M; Klein D; Falquet B; Fontana GA; Cejka P; Rass U
Nat Commun; 2016 Oct; 7():13157. PubMed ID: 27779184
[TBL] [Abstract][Full Text] [Related]
20. Disease-associated DNA2 nuclease-helicase protects cells from lethal chromosome under-replication.
Falquet B; Ölmezer G; Enkner F; Klein D; Challa K; Appanah R; Gasser SM; Rass U
Nucleic Acids Res; 2020 Jul; 48(13):7265-7278. PubMed ID: 32544229
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
