333 related articles for article (PubMed ID: 21240277)
21. Human SLX4 is a Holliday junction resolvase subunit that binds multiple DNA repair/recombination endonucleases.
Fekairi S; Scaglione S; Chahwan C; Taylor ER; Tissier A; Coulon S; Dong MQ; Ruse C; Yates JR; Russell P; Fuchs RP; McGowan CH; Gaillard PHL
Cell; 2009 Jul; 138(1):78-89. PubMed ID: 19596236
[TBL] [Abstract][Full Text] [Related]
22. Fanconi anaemia cells are not uniformly deficient in unhooking of DNA interstrand crosslinks, induced by mitomycin C or 8-methoxypsoralen plus UVA.
Poll EH; Arwert F; Kortbeek HT; Eriksson AW
Hum Genet; 1984; 68(3):228-34. PubMed ID: 6437965
[TBL] [Abstract][Full Text] [Related]
23. SLX4: multitasking to maintain genome stability.
Guervilly JH; Gaillard PH
Crit Rev Biochem Mol Biol; 2018 Oct; 53(5):475-514. PubMed ID: 30284473
[TBL] [Abstract][Full Text] [Related]
24. Disruption of SLX4-MUS81 Function Increases the Relative Biological Effectiveness of Proton Radiation.
Liu Q; Underwood TSA; Kung J; Wang M; Lu HM; Paganetti H; Held KD; Hong TS; Efstathiou JA; Willers H
Int J Radiat Oncol Biol Phys; 2016 May; 95(1):78-85. PubMed ID: 27084631
[TBL] [Abstract][Full Text] [Related]
25. Analysis of the novel fanconi anemia gene SLX4/FANCP in familial breast cancer cases.
Bakker JL; van Mil SE; Crossan G; Sabbaghian N; De Leeneer K; Poppe B; Adank M; Gille H; Verheul H; Meijers-Heijboer H; de Winter JP; Claes K; Tischkowitz M; Waisfisz Q
Hum Mutat; 2013 Jan; 34(1):70-3. PubMed ID: 22911665
[TBL] [Abstract][Full Text] [Related]
26. A genetic screen identifies FAN1, a Fanconi anemia-associated nuclease necessary for DNA interstrand crosslink repair.
Smogorzewska A; Desetty R; Saito TT; Schlabach M; Lach FP; Sowa ME; Clark AB; Kunkel TA; Harper JW; Colaiácovo MP; Elledge SJ
Mol Cell; 2010 Jul; 39(1):36-47. PubMed ID: 20603073
[TBL] [Abstract][Full Text] [Related]
27. C. elegans: a model of Fanconi anemia and ICL repair.
Youds JL; Barber LJ; Boulton SJ
Mutat Res; 2009 Jul; 668(1-2):103-16. PubMed ID: 19059419
[TBL] [Abstract][Full Text] [Related]
28. Impaired FANCD2 monoubiquitination and hypersensitivity to camptothecin uniquely characterize Fanconi anemia complementation group M.
Singh TR; Bakker ST; Agarwal S; Jansen M; Grassman E; Godthelp BC; Ali AM; Du CH; Rooimans MA; Fan Q; Wahengbam K; Steltenpool J; Andreassen PR; Williams DA; Joenje H; de Winter JP; Meetei AR
Blood; 2009 Jul; 114(1):174-80. PubMed ID: 19423727
[TBL] [Abstract][Full Text] [Related]
29. Fanconi anemia pathway--the way of DNA interstrand cross-link repair.
Yao CJ; Du W; Zhang Q; Zhang F; Zeng F; Chen FP
Pharmazie; 2013 Jan; 68(1):5-11. PubMed ID: 23444773
[TBL] [Abstract][Full Text] [Related]
30. DNA interstrand cross-linking, repair, and SCE mechanism in human cells in special reference to Fanconi anemia.
Fujiwara Y; Kano Y; Yamamoto Y
Basic Life Sci; 1984; 29 Pt B():787-800. PubMed ID: 6442145
[TBL] [Abstract][Full Text] [Related]
31. Coordination of structure-specific nucleases by human SLX4/BTBD12 is required for DNA repair.
Muñoz IM; Hain K; Déclais AC; Gardiner M; Toh GW; Sanchez-Pulido L; Heuckmann JM; Toth R; Macartney T; Eppink B; Kanaar R; Ponting CP; Lilley DM; Rouse J
Mol Cell; 2009 Jul; 35(1):116-27. PubMed ID: 19595721
[TBL] [Abstract][Full Text] [Related]
32. Functional defects in the fanconi anemia pathway in pancreatic cancer cells.
van der Heijden MS; Brody JR; Gallmeier E; Cunningham SC; Dezentje DA; Shen D; Hruban RH; Kern SE
Am J Pathol; 2004 Aug; 165(2):651-7. PubMed ID: 15277238
[TBL] [Abstract][Full Text] [Related]
33. Biallelic mutations in BRCA1 cause a new Fanconi anemia subtype.
Sawyer SL; Tian L; Kähkönen M; Schwartzentruber J; Kircher M; ; ; Majewski J; Dyment DA; Innes AM; Boycott KM; Moreau LA; Moilanen JS; Greenberg RA
Cancer Discov; 2015 Feb; 5(2):135-42. PubMed ID: 25472942
[TBL] [Abstract][Full Text] [Related]
34. The Fanconi anemia ID2 complex: dueling saxes at the crossroads.
Boisvert RA; Howlett NG
Cell Cycle; 2014; 13(19):2999-3015. PubMed ID: 25486561
[TBL] [Abstract][Full Text] [Related]
35. Induction and removal of interstrand crosslinks in the ribosomal RNA genes of lymphoblastoid cell lines from patients with Fanconi anemia.
Rey JP; Scott R; Müller H
Mutat Res; 1993 Oct; 289(2):171-80. PubMed ID: 7690885
[TBL] [Abstract][Full Text] [Related]
36. Topo IIIalpha and BLM act within the Fanconi anemia pathway in response to DNA-crosslinking agents.
Hemphill AW; Akkari Y; Newell AH; Schultz RA; Grompe M; North PS; Hickson ID; Jakobs PM; Rennie S; Pauw D; Hejna J; Olson SB; Moses RE
Cytogenet Genome Res; 2009; 125(3):165-75. PubMed ID: 19738377
[TBL] [Abstract][Full Text] [Related]
37. Analysis of a FANCE Splice Isoform in Regard to DNA Repair.
Bouffard F; Plourde K; Bélanger S; Ouellette G; Labrie Y; Durocher F
J Mol Biol; 2015 Sep; 427(19):3056-73. PubMed ID: 26277624
[TBL] [Abstract][Full Text] [Related]
38. Assessment of SLX4 Mutations in Hereditary Breast Cancers.
Shah S; Kim Y; Ostrovnaya I; Murali R; Schrader KA; Lach FP; Sarrel K; Rau-Murthy R; Hansen N; Zhang L; Kirchhoff T; Stadler Z; Robson M; Vijai J; Offit K; Smogorzewska A
PLoS One; 2013; 8(6):e66961. PubMed ID: 23840564
[TBL] [Abstract][Full Text] [Related]
39. FANCD2 binds CtIP and regulates DNA-end resection during DNA interstrand crosslink repair.
Unno J; Itaya A; Taoka M; Sato K; Tomida J; Sakai W; Sugasawa K; Ishiai M; Ikura T; Isobe T; Kurumizaka H; Takata M
Cell Rep; 2014 May; 7(4):1039-47. PubMed ID: 24794430
[TBL] [Abstract][Full Text] [Related]
40. Diagnosis of Fanconi Anaemia by ionising radiation- or mitomycin C-induced micronuclei.
Francies FZ; Wainwright R; Poole J; De Leeneer K; Coene I; Wieme G; Poirel HA; Brichard B; Vermeulen S; Vral A; Slabbert J; Claes K; Baeyens A
DNA Repair (Amst); 2018 Jan; 61():17-24. PubMed ID: 29154021
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]