307 related articles for article (PubMed ID: 27208205)
1. Complementation of hypersensitivity to DNA interstrand crosslinking agents demonstrates that XRCC2 is a Fanconi anaemia gene.
Park JY; Virts EL; Jankowska A; Wiek C; Othman M; Chakraborty SC; Vance GH; Alkuraya FS; Hanenberg H; Andreassen PR
J Med Genet; 2016 Oct; 53(10):672-680. PubMed ID: 27208205
[TBL] [Abstract][Full Text] [Related]
2. XRCC2 (X-ray repair cross complementing 2).
Andreassen PR; Hanenberg H
Atlas Genet Cytogenet Oncol Haematol; 2019 Jan; 23(1):1-7. PubMed ID: 31275435
[TBL] [Abstract][Full Text] [Related]
3. Distinct roles of FANCO/RAD51C protein in DNA damage signaling and repair: implications for Fanconi anemia and breast cancer susceptibility.
Somyajit K; Subramanya S; Nagaraju G
J Biol Chem; 2012 Jan; 287(5):3366-80. PubMed ID: 22167183
[TBL] [Abstract][Full Text] [Related]
4. Direct interaction of the Fanconi anaemia protein FANCG with BRCA2/FANCD1.
Hussain S; Witt E; Huber PA; Medhurst AL; Ashworth A; Mathew CG
Hum Mol Genet; 2003 Oct; 12(19):2503-10. PubMed ID: 12915460
[TBL] [Abstract][Full Text] [Related]
5. Function of the Fanconi anemia pathway in Fanconi anemia complementation group F and D1 cells.
Siddique MA; Nakanishi K; Taniguchi T; Grompe M; D'Andrea AD
Exp Hematol; 2001 Dec; 29(12):1448-55. PubMed ID: 11750104
[TBL] [Abstract][Full Text] [Related]
6. Tetratricopeptide-motif-mediated interaction of FANCG with recombination proteins XRCC3 and BRCA2.
Hussain S; Wilson JB; Blom E; Thompson LH; Sung P; Gordon SM; Kupfer GM; Joenje H; Mathew CG; Jones NJ
DNA Repair (Amst); 2006 May; 5(5):629-40. PubMed ID: 16621732
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Snm1B/Apollo functions in the Fanconi anemia pathway in response to DNA interstrand crosslinks.
Mason JM; Sekiguchi JM
Hum Mol Genet; 2011 Jul; 20(13):2549-59. PubMed ID: 21478198
[TBL] [Abstract][Full Text] [Related]
9. Exome sequencing reveals a novel Fanconi group defined by XRCC2 mutation.
Shamseldin HE; Elfaki M; Alkuraya FS
J Med Genet; 2012 Mar; 49(3):184-6. PubMed ID: 22232082
[TBL] [Abstract][Full Text] [Related]
10. Mutation of the RAD51C gene in a Fanconi anemia-like disorder.
Vaz F; Hanenberg H; Schuster B; Barker K; Wiek C; Erven V; Neveling K; Endt D; Kesterton I; Autore F; Fraternali F; Freund M; Hartmann L; Grimwade D; Roberts RG; Schaal H; Mohammed S; Rahman N; Schindler D; Mathew CG
Nat Genet; 2010 May; 42(5):406-9. PubMed ID: 20400963
[TBL] [Abstract][Full Text] [Related]
11. Current knowledge on the pathophysiology of Fanconi anemia: from genes to phenotypes.
Yamashita T; Nakahata T
Int J Hematol; 2001 Jul; 74(1):33-41. PubMed ID: 11530803
[TBL] [Abstract][Full Text] [Related]
12. FANCD2 monoubiquitination and activation by hexavalent chromium [Cr(VI)] exposure: activation is not required for repair of Cr(VI)-induced DSBs.
Vilcheck SK; Ceryak S; O'Brien TJ; Patierno SR
Mutat Res; 2006 Nov; 610(1-2):21-30. PubMed ID: 16893675
[TBL] [Abstract][Full Text] [Related]
13. AluY-mediated germline deletion, duplication and somatic stem cell reversion in UBE2T defines a new subtype of Fanconi anemia.
Virts EL; Jankowska A; Mackay C; Glaas MF; Wiek C; Kelich SL; Lottmann N; Kennedy FM; Marchal C; Lehnert E; Scharf RE; Dufour C; Lanciotti M; Farruggia P; Santoro A; Savasan S; Scheckenbach K; Schipper J; Wagenmann M; Lewis T; Leffak M; Farlow JL; Foroud TM; Honisch E; Niederacher D; Chakraborty SC; Vance GH; Pruss D; Timms KM; Lanchbury JS; Alpi AF; Hanenberg H
Hum Mol Genet; 2015 Sep; 24(18):5093-108. PubMed ID: 26085575
[TBL] [Abstract][Full Text] [Related]
14. The Chinese hamster FANCG/XRCC9 mutant NM3 fails to express the monoubiquitinated form of the FANCD2 protein, is hypersensitive to a range of DNA damaging agents and exhibits a normal level of spontaneous sister chromatid exchange.
Wilson JB; Johnson MA; Stuckert AP; Trueman KL; May S; Bryant PE; Meyn RE; D'Andrea AD; Jones NJ
Carcinogenesis; 2001 Dec; 22(12):1939-46. PubMed ID: 11751423
[TBL] [Abstract][Full Text] [Related]
15. Attenuation of the formation of DNA-repair foci containing RAD51 in Fanconi anaemia.
Digweed M; Rothe S; Demuth I; Scholz R; Schindler D; Stumm M; Grompe M; Jordan A; Sperling K
Carcinogenesis; 2002 Jul; 23(7):1121-6. PubMed ID: 12117768
[TBL] [Abstract][Full Text] [Related]
16. New insights into the Fanconi anemia pathway from an isogenic FancG hamster CHO mutant.
Tebbs RS; Hinz JM; Yamada NA; Wilson JB; Salazar EP; Thomas CB; Jones IM; Jones NJ; Thompson LH
DNA Repair (Amst); 2005 Jan; 4(1):11-22. PubMed ID: 15533833
[TBL] [Abstract][Full Text] [Related]
17. Heterogeneous activation of the Fanconi anemia pathway by patient-derived FANCA mutants.
Adachi D; Oda T; Yagasaki H; Nakasato K; Taniguchi T; D'Andrea AD; Asano S; Yamashita T
Hum Mol Genet; 2002 Dec; 11(25):3125-34. PubMed ID: 12444097
[TBL] [Abstract][Full Text] [Related]
18. Ubiquitylation and the Fanconi anemia pathway.
Garner E; Smogorzewska A
FEBS Lett; 2011 Sep; 585(18):2853-60. PubMed ID: 21605559
[TBL] [Abstract][Full Text] [Related]
19. Recent discoveries in the molecular pathogenesis of the inherited bone marrow failure syndrome Fanconi anemia.
Mamrak NE; Shimamura A; Howlett NG
Blood Rev; 2017 May; 31(3):93-99. PubMed ID: 27760710
[TBL] [Abstract][Full Text] [Related]
20. Inhibition of non-homologous end joining in Fanconi Anemia cells results in rescue of survival after interstrand crosslinks but sensitization to replication associated double-strand breaks.
Eccles LJ; Bell AC; Powell SN
DNA Repair (Amst); 2018 Apr; 64():1-9. PubMed ID: 29459202
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
