313 related articles for article (PubMed ID: 20921626)
1. Cytokinesis failure occurs in Fanconi anemia pathway-deficient murine and human bone marrow hematopoietic cells.
Vinciguerra P; Godinho SA; Parmar K; Pellman D; D'Andrea AD
J Clin Invest; 2010 Nov; 120(11):3834-42. PubMed ID: 20921626
[TBL] [Abstract][Full Text] [Related]
2. The FANC pathway and BLM collaborate during mitosis to prevent micro-nucleation and chromosome abnormalities.
Naim V; Rosselli F
Nat Cell Biol; 2009 Jun; 11(6):761-8. PubMed ID: 19465921
[TBL] [Abstract][Full Text] [Related]
3. BLM promotes the activation of Fanconi Anemia signaling pathway.
Panneerselvam J; Wang H; Zhang J; Che R; Yu H; Fei P
Oncotarget; 2016 May; 7(22):32351-61. PubMed ID: 27083049
[TBL] [Abstract][Full Text] [Related]
4. Fanconi anemia and Bloom's syndrome crosstalk through FANCJ-BLM helicase interaction.
Suhasini AN; Brosh RM
Trends Genet; 2012 Jan; 28(1):7-13. PubMed ID: 22024395
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Interaction between the helicases genetically linked to Fanconi anemia group J and Bloom's syndrome.
Suhasini AN; Rawtani NA; Wu Y; Sommers JA; Sharma S; Mosedale G; North PS; Cantor SB; Hickson ID; Brosh RM
EMBO J; 2011 Feb; 30(4):692-705. PubMed ID: 21240188
[TBL] [Abstract][Full Text] [Related]
7. Replication stress induces sister-chromatid bridging at fragile site loci in mitosis.
Chan KL; Palmai-Pallag T; Ying S; Hickson ID
Nat Cell Biol; 2009 Jun; 11(6):753-60. PubMed ID: 19465922
[TBL] [Abstract][Full Text] [Related]
8. Fanconi anaemia proteins are associated with sister chromatid bridging in mitosis.
Ying S; Hickson ID
Int J Hematol; 2011 Apr; 93(4):440-445. PubMed ID: 21472397
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Brief report: human pluripotent stem cell models of fanconi anemia deficiency reveal an important role for fanconi anemia proteins in cellular reprogramming and survival of hematopoietic progenitors.
Yung SK; Tilgner K; Ledran MH; Habibollah S; Neganova I; Singhapol C; Saretzki G; Stojkovic M; Armstrong L; Przyborski S; Lako M
Stem Cells; 2013 May; 31(5):1022-9. PubMed ID: 23280624
[TBL] [Abstract][Full Text] [Related]
11. A defined role for multiple Fanconi anemia gene products in DNA-damage-associated ubiquitination.
Tan W; Deans AJ
Exp Hematol; 2017 Jun; 50():27-32. PubMed ID: 28315701
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. The Fanconi anemia pathway of genomic maintenance.
Levitus M; Joenje H; de Winter JP
Cell Oncol; 2006; 28(1-2):3-29. PubMed ID: 16675878
[TBL] [Abstract][Full Text] [Related]
15. Evidence for subcomplexes in the Fanconi anemia pathway.
Medhurst AL; Laghmani el H; Steltenpool J; Ferrer M; Fontaine C; de Groot J; Rooimans MA; Scheper RJ; Meetei AR; Wang W; Joenje H; de Winter JP
Blood; 2006 Sep; 108(6):2072-80. PubMed ID: 16720839
[TBL] [Abstract][Full Text] [Related]
16. Holding All the Cards-How Fanconi Anemia Proteins Deal with Replication Stress and Preserve Genomic Stability.
Datta A; Brosh RM
Genes (Basel); 2019 Feb; 10(2):. PubMed ID: 30813363
[TBL] [Abstract][Full Text] [Related]
17. Parallel genome-wide screens identify synthetic viable interactions between the BLM helicase complex and Fanconi anemia.
Moder M; Velimezi G; Owusu M; Mazouzi A; Wiedner M; Ferreira da Silva J; Robinson-Garcia L; Schischlik F; Slavkovsky R; Kralovics R; Schuster M; Bock C; Ideker T; Jackson SP; Menche J; Loizou JI
Nat Commun; 2017 Nov; 8(1):1238. PubMed ID: 29089570
[TBL] [Abstract][Full Text] [Related]
18. Bone Marrow Mesenchymal Stem Cells Carrying FANCD2 Mutation Differ from the Other Fanconi Anemia Complementation Groups in Terms of TGF-β1 Production.
Cagnan I; Gunel-Ozcan A; Aerts-Kaya F; Ameziane N; Kuskonmaz B; Dorsman J; Gumruk F; Uckan D
Stem Cell Rev Rep; 2018 Jun; 14(3):425-437. PubMed ID: 29247345
[TBL] [Abstract][Full Text] [Related]
19. HES1 is a novel interactor of the Fanconi anemia core complex.
Tremblay CS; Huang FF; Habi O; Huard CC; Godin C; Lévesque G; Carreau M
Blood; 2008 Sep; 112(5):2062-70. PubMed ID: 18550849
[TBL] [Abstract][Full Text] [Related]
20. FANCI Regulates Recruitment of the FA Core Complex at Sites of DNA Damage Independently of FANCD2.
Castella M; Jacquemont C; Thompson EL; Yeo JE; Cheung RS; Huang JW; Sobeck A; Hendrickson EA; Taniguchi T
PLoS Genet; 2015 Oct; 11(10):e1005563. PubMed ID: 26430909
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
