BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

361 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]  

  • 19. Massively parallel sequencing, aCGH, and RNA-Seq technologies provide a comprehensive molecular diagnosis of Fanconi anemia.
    Chandrasekharappa SC; Lach FP; Kimble DC; Kamat A; Teer JK; Donovan FX; Flynn E; Sen SK; Thongthip S; Sanborn E; Smogorzewska A; Auerbach AD; Ostrander EA;
    Blood; 2013 May; 121(22):e138-48. PubMed ID: 23613520
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Assembling an orchestra: Fanconi anemia pathway of DNA repair.
    Yuan F; Song L; Qian L; Hu JJ; Zhang Y
    Front Biosci (Landmark Ed); 2010 Jun; 15(3):1131-49. PubMed ID: 20515746
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.