These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
429 related articles for article (PubMed ID: 29891926)
1. Map of synthetic rescue interactions for the Fanconi anemia DNA repair pathway identifies USP48. Velimezi G; Robinson-Garcia L; Muñoz-Martínez F; Wiegant WW; Ferreira da Silva J; Owusu M; Moder M; Wiedner M; Rosenthal SB; Fisch KM; Moffat J; Menche J; van Attikum H; Jackson SP; Loizou JI Nat Commun; 2018 Jun; 9(1):2280. PubMed ID: 29891926 [TBL] [Abstract][Full Text] [Related]
2. Mechanism of Ubiquitination and Deubiquitination in the Fanconi Anemia Pathway. van Twest S; Murphy VJ; Hodson C; Tan W; Swuec P; O'Rourke JJ; Heierhorst J; Crismani W; Deans AJ Mol Cell; 2017 Jan; 65(2):247-259. PubMed ID: 27986371 [TBL] [Abstract][Full Text] [Related]
3. Promyelocytic Leukemia Proteins Regulate Fanconi Anemia Gene Expression. Munkhjargal A; Kim MJ; Kim DY; Jeon YJ; Kee YH; Kim LK; Kim YH Int J Mol Sci; 2021 Jul; 22(15):. PubMed ID: 34360546 [TBL] [Abstract][Full Text] [Related]
4. USP48 May Be Potential Therapeutic Target in Fanconi Anemia: Inactivation of USP48 reduced chromosomal instability of Fanconi anemia defective cells and highlights a role for this enzyme in controlling DNA repair. Am J Med Genet A; 2018 Sep; 176(9):1794-1795. PubMed ID: 30242991 [No Abstract] [Full Text] [Related]
5. 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]
6. Activation of the FA pathway mediated by phosphorylation and ubiquitination. Ishiai M; Sato K; Tomida J; Kitao H; Kurumizaka H; Takata M Mutat Res; 2017 Oct; 803-805():89-95. PubMed ID: 28552166 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. Crosstalk between BRCA-Fanconi anemia and mismatch repair pathways prevents MSH2-dependent aberrant DNA damage responses. Peng M; Xie J; Ucher A; Stavnezer J; Cantor SB EMBO J; 2014 Aug; 33(15):1698-712. PubMed ID: 24966277 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. [The role of the Fanconi anemia pathway in DNA repair and maintenance of genome stability]. Koczorowska AM; Białkowska A; Kluzek K; Zdzienicka MZ Postepy Hig Med Dosw (Online); 2014 May; 68():459-72. PubMed ID: 24864098 [TBL] [Abstract][Full Text] [Related]
11. Genomic instability in mice is greater in Fanconi anemia caused by deficiency of Fancd2 than Fancg. Reliene R; Yamamoto ML; Rao PN; Schiestl RH Cancer Res; 2010 Dec; 70(23):9703-10. PubMed ID: 21118969 [TBL] [Abstract][Full Text] [Related]
12. Deficient regulation of DNA double-strand break repair in Fanconi anemia fibroblasts. Donahue SL; Lundberg R; Saplis R; Campbell C J Biol Chem; 2003 Aug; 278(32):29487-95. PubMed ID: 12748186 [TBL] [Abstract][Full Text] [Related]
13. Functional analysis of Fanconi anemia mutations in China. Li N; Ding L; Li B; Wang J; D'Andrea AD; Chen J Exp Hematol; 2018 Oct; 66():32-41.e8. PubMed ID: 30031030 [TBL] [Abstract][Full Text] [Related]
14. Compromised repair of radiation-induced DNA double-strand breaks in Fanconi anemia fibroblasts in G2. Zahnreich S; Weber B; Rösch G; Schindler D; Schmidberger H DNA Repair (Amst); 2020 Dec; 96():102992. PubMed ID: 33069004 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Patient-derived C-terminal mutation of FANCI causes protein mislocalization and reveals putative EDGE motif function in DNA repair. Colnaghi L; Jones MJ; Cotto-Rios XM; Schindler D; Hanenberg H; Huang TT Blood; 2011 Feb; 117(7):2247-56. PubMed ID: 20971953 [TBL] [Abstract][Full Text] [Related]
17. Prolyl isomerization of FAAP20 catalyzed by PIN1 regulates the Fanconi anemia pathway. Wang J; Chan B; Tong M; Paung Y; Jo U; Martin D; Seeliger M; Haley J; Kim H PLoS Genet; 2019 Feb; 15(2):e1007983. PubMed ID: 30789902 [TBL] [Abstract][Full Text] [Related]
18. Phosphorylation of FANCD2 Inhibits the FANCD2/FANCI Complex and Suppresses the Fanconi Anemia Pathway in the Absence of DNA Damage. Lopez-Martinez D; Kupculak M; Yang D; Yoshikawa Y; Liang CC; Wu R; Gygi SP; Cohn MA Cell Rep; 2019 Jun; 27(10):2990-3005.e5. PubMed ID: 31167143 [TBL] [Abstract][Full Text] [Related]