BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

333 related articles for article (PubMed ID: 23867477)

  • 21. Nonenzymatic role for WRN in preserving nascent DNA strands after replication stress.
    Su F; Mukherjee S; Yang Y; Mori E; Bhattacharya S; Kobayashi J; Yannone SM; Chen DJ; Asaithamby A
    Cell Rep; 2014 Nov; 9(4):1387-401. PubMed ID: 25456133
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Fanconi anemia group J helicase and MRE11 nuclease interact to facilitate the DNA damage response.
    Suhasini AN; Sommers JA; Muniandy PA; Coulombe Y; Cantor SB; Masson JY; Seidman MM; Brosh RM
    Mol Cell Biol; 2013 Jun; 33(11):2212-27. PubMed ID: 23530059
    [TBL] [Abstract][Full Text] [Related]  

  • 23. WRN, the protein deficient in Werner syndrome, plays a critical structural role in optimizing DNA repair.
    Chen L; Huang S; Lee L; Davalos A; Schiestl RH; Campisi J; Oshima J
    Aging Cell; 2003 Aug; 2(4):191-9. PubMed ID: 12934712
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A Dominant Mutation in Human RAD51 Reveals Its Function in DNA Interstrand Crosslink Repair Independent of Homologous Recombination.
    Wang AT; Kim T; Wagner JE; Conti BA; Lach FP; Huang AL; Molina H; Sanborn EM; Zierhut H; Cornes BK; Abhyankar A; Sougnez C; Gabriel SB; Auerbach AD; Kowalczykowski SC; Smogorzewska A
    Mol Cell; 2015 Aug; 59(3):478-90. PubMed ID: 26253028
    [TBL] [Abstract][Full Text] [Related]  

  • 25. SLFN11 promotes stalled fork degradation that underlies the phenotype in Fanconi anemia cells.
    Okamoto Y; Abe M; Mu A; Tempaku Y; Rogers CB; Mochizuki AL; Katsuki Y; Kanemaki MT; Takaori-Kondo A; Sobeck A; Bielinsky AK; Takata M
    Blood; 2021 Jan; 137(3):336-348. PubMed ID: 32735670
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Perturbed replication induced genome wide or at common fragile sites is differently managed in the absence of WRN.
    Murfuni I; De Santis A; Federico M; Bignami M; Pichierri P; Franchitto A
    Carcinogenesis; 2012 Sep; 33(9):1655-63. PubMed ID: 22689923
    [TBL] [Abstract][Full Text] [Related]  

  • 27. RECQL5 plays co-operative and complementary roles with WRN syndrome helicase.
    Popuri V; Huang J; Ramamoorthy M; Tadokoro T; Croteau DL; Bohr VA
    Nucleic Acids Res; 2013 Jan; 41(2):881-99. PubMed ID: 23180761
    [TBL] [Abstract][Full Text] [Related]  

  • 28. FANCJ compensates for RAP80 deficiency and suppresses genomic instability induced by interstrand cross-links.
    Awate S; Sommers JA; Datta A; Nayak S; Bellani MA; Yang O; Dunn CA; Nicolae CM; Moldovan GL; Seidman MM; Cantor SB; Brosh RM
    Nucleic Acids Res; 2020 Sep; 48(16):9161-9180. PubMed ID: 32797166
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Promyelocytic leukemia protein interacts with werner syndrome helicase and regulates double-strand break repair in γ-irradiation-induced DNA damage responses.
    Liu J; Song Y; Qian J; Liu B; Dong Y; Tian B; Sun Z
    Biochemistry (Mosc); 2011 May; 76(5):550-4. PubMed ID: 21639834
    [TBL] [Abstract][Full Text] [Related]  

  • 30. WRN protects against topo I but not topo II inhibitors by preventing DNA break formation.
    Christmann M; Tomicic MT; Gestrich C; Roos WP; Bohr VA; Kaina B
    DNA Repair (Amst); 2008 Dec; 7(12):1999-2009. PubMed ID: 18805512
    [TBL] [Abstract][Full Text] [Related]  

  • 31. WRN helicase defective in the premature aging disorder Werner syndrome genetically interacts with topoisomerase 3 and restores the top3 slow growth phenotype of sgs1 top3.
    Aggarwal M; Brosh RM
    Aging (Albany NY); 2009 Feb; 1(2):219-33. PubMed ID: 20157511
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Werner syndrome protein is regulated and phosphorylated by DNA-dependent protein kinase.
    Yannone SM; Roy S; Chan DW; Murphy MB; Huang S; Campisi J; Chen DJ
    J Biol Chem; 2001 Oct; 276(41):38242-8. PubMed ID: 11477099
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Checkpoint-dependent and independent roles of the Werner syndrome protein in preserving genome integrity in response to mild replication stress.
    Basile G; Leuzzi G; Pichierri P; Franchitto A
    Nucleic Acids Res; 2014 Nov; 42(20):12628-39. PubMed ID: 25352544
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Preventing over-resection by DNA2 helicase/nuclease suppresses repair defects in Fanconi anemia cells.
    Karanja KK; Lee EH; Hendrickson EA; Campbell JL
    Cell Cycle; 2014; 13(10):1540-50. PubMed ID: 24626199
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Werner helicase is required for proliferation and DNA damage repair in multiple myeloma.
    Akcora-Yildiz D; Ozkan T; Ozen M; Gunduz M; Sunguroglu A; Beksac M
    Mol Biol Rep; 2023 Feb; 50(2):1565-1573. PubMed ID: 36515823
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The DNA repair endonuclease XPG interacts directly and functionally with the WRN helicase defective in Werner syndrome.
    Trego KS; Chernikova SB; Davalos AR; Perry JJ; Finger LD; Ng C; Tsai MS; Yannone SM; Tainer JA; Campisi J; Cooper PK
    Cell Cycle; 2011 Jun; 10(12):1998-2007. PubMed ID: 21558802
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Targeted inhibition of WRN helicase by external guide sequence and RNase P RNA.
    Hitrik A; Abboud-Jarrous G; Orlovetskie N; Serruya R; Jarrous N
    Biochim Biophys Acta; 2016 Apr; 1859(4):572-80. PubMed ID: 26808708
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Preventing nonhomologous end joining suppresses DNA repair defects of Fanconi anemia.
    Adamo A; Collis SJ; Adelman CA; Silva N; Horejsi Z; Ward JD; Martinez-Perez E; Boulton SJ; La Volpe A
    Mol Cell; 2010 Jul; 39(1):25-35. PubMed ID: 20598602
    [TBL] [Abstract][Full Text] [Related]  

  • 39. EGFR-activating mutations correlate with a Fanconi anemia-like cellular phenotype that includes PARP inhibitor sensitivity.
    Pfäffle HN; Wang M; Gheorghiu L; Ferraiolo N; Greninger P; Borgmann K; Settleman J; Benes CH; Sequist LV; Zou L; Willers H
    Cancer Res; 2013 Oct; 73(20):6254-63. PubMed ID: 23966292
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 17.