490 related articles for article (PubMed ID: 27760710)
1. 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]
2. 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]
3. A comprehensive molecular study identified 12 complementation groups with 56 novel FANC gene variants in Indian Fanconi anemia subjects.
George M; Solanki A; Chavan N; Rajendran A; Raj R; Mohan S; Nemani S; Kanvinde S; Munirathnam D; Rao S; Radhakrishnan N; Lashkari HP; Ghildhiyal RG; Manglani M; Shanmukhaiah C; Bhat S; Ramesh S; Cherian A; Junagade P; Vundinti BR
Hum Mutat; 2021 Dec; 42(12):1648-1665. PubMed ID: 34585473
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Molecular pathogenesis of fanconi anemia.
Taniguchi T; Dandrea AD
Int J Hematol; 2002 Feb; 75(2):123-8. PubMed ID: 11939257
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. A new frontier in Fanconi anemia: From DNA repair to ribosome biogenesis.
Gueiderikh A; Maczkowiak-Chartois F; Rosselli F
Blood Rev; 2022 Mar; 52():100904. PubMed ID: 34750031
[TBL] [Abstract][Full Text] [Related]
8. Deficiency of UBE2T, the E2 Ubiquitin Ligase Necessary for FANCD2 and FANCI Ubiquitination, Causes FA-T Subtype of Fanconi Anemia.
Rickman KA; Lach FP; Abhyankar A; Donovan FX; Sanborn EM; Kennedy JA; Sougnez C; Gabriel SB; Elemento O; Chandrasekharappa SC; Schindler D; Auerbach AD; Smogorzewska A
Cell Rep; 2015 Jul; 12(1):35-41. PubMed ID: 26119737
[TBL] [Abstract][Full Text] [Related]
9. DNA repair: exploiting the Fanconi anemia pathway as a potential therapeutic target.
Hucl T; Gallmeier E
Physiol Res; 2011; 60(3):453-65. PubMed ID: 21401292
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Fanconi anemia: at the crossroads of DNA repair.
Deakyne JS; Mazin AV
Biochemistry (Mosc); 2011 Jan; 76(1):36-48. PubMed ID: 21568838
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. The Fanconi anemia pathway and DNA interstrand cross-link repair.
Su X; Huang J
Protein Cell; 2011 Sep; 2(9):704-11. PubMed ID: 21948210
[TBL] [Abstract][Full Text] [Related]
14. Biallelic inactivation of REV7 is associated with Fanconi anemia.
Bluteau D; Masliah-Planchon J; Clairmont C; Rousseau A; Ceccaldi R; Dubois d'Enghien C; Bluteau O; Cuccuini W; Gachet S; Peffault de Latour R; Leblanc T; Socié G; Baruchel A; Stoppa-Lyonnet D; D'Andrea AD; Soulier J
J Clin Invest; 2016 Sep; 126(9):3580-4. PubMed ID: 27500492
[TBL] [Abstract][Full Text] [Related]
15. Deficiency of the Fanconi anemia E2 ubiqitin conjugase UBE2T only partially abrogates Alu-mediated recombination in a new model of homology dependent recombination.
Lewis TW; Barthelemy JR; Virts EL; Kennedy FM; Gadgil RY; Wiek C; Linka RM; Zhang F; Andreassen PR; Hanenberg H; Leffak M
Nucleic Acids Res; 2019 Apr; 47(7):3503-3520. PubMed ID: 30715513
[TBL] [Abstract][Full Text] [Related]
16. Mutations in the gene encoding the E2 conjugating enzyme UBE2T cause Fanconi anemia.
Hira A; Yoshida K; Sato K; Okuno Y; Shiraishi Y; Chiba K; Tanaka H; Miyano S; Shimamoto A; Tahara H; Ito E; Kojima S; Kurumizaka H; Ogawa S; Takata M; Yabe H; Yabe M
Am J Hum Genet; 2015 Jun; 96(6):1001-7. PubMed ID: 26046368
[TBL] [Abstract][Full Text] [Related]
17. An ATR- and BRCA1-mediated Fanconi anemia pathway is required for activating the G2/M checkpoint and DNA damage repair upon rereplication.
Zhu W; Dutta A
Mol Cell Biol; 2006 Jun; 26(12):4601-11. PubMed ID: 16738325
[TBL] [Abstract][Full Text] [Related]
18. The role of Fanconi anemia/BRCA genes in zebrafish sex determination.
Rodríguez-Marí A; Postlethwait JH
Methods Cell Biol; 2011; 105():461-90. PubMed ID: 21951543
[TBL] [Abstract][Full Text] [Related]
19. The Fanconi anaemia/BRCA pathway.
D'Andrea AD; Grompe M
Nat Rev Cancer; 2003 Jan; 3(1):23-34. PubMed ID: 12509764
[TBL] [Abstract][Full Text] [Related]
20. A Boolean network model of the FA/BRCA pathway.
Rodríguez A; Sosa D; Torres L; Molina B; Frías S; Mendoza L
Bioinformatics; 2012 Mar; 28(6):858-66. PubMed ID: 22267503
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
