BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

127 related articles for article (PubMed ID: 11205328)

  • 1. Mutagenesis in eukaryotes dependent on DNA polymerase zeta and Rev1p.
    Lawrence CW; Maher VM
    Philos Trans R Soc Lond B Biol Sci; 2001 Jan; 356(1405):41-6. PubMed ID: 11205328
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The relative roles in vivo of Saccharomyces cerevisiae Pol eta, Pol zeta, Rev1 protein and Pol32 in the bypass and mutation induction of an abasic site, T-T (6-4) photoadduct and T-T cis-syn cyclobutane dimer.
    Gibbs PE; McDonald J; Woodgate R; Lawrence CW
    Genetics; 2005 Feb; 169(2):575-82. PubMed ID: 15520252
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Analysis of Rev1p and Pol zeta in mitochondrial mutagenesis suggests an alternative pathway of damage tolerance.
    Kalifa L; Sia EA
    DNA Repair (Amst); 2007 Dec; 6(12):1732-9. PubMed ID: 17689152
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Yeast Rev1 protein promotes complex formation of DNA polymerase zeta with Pol32 subunit of DNA polymerase delta.
    Acharya N; Johnson RE; Pagès V; Prakash L; Prakash S
    Proc Natl Acad Sci U S A; 2009 Jun; 106(24):9631-6. PubMed ID: 19487673
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The importance of an interaction network for proper DNA polymerase ζ heterotetramer activity.
    Szwajczak E; Fijalkowska IJ; Suski C
    Curr Genet; 2018 Jun; 64(3):575-580. PubMed ID: 29189894
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Yeast DNA polymerase zeta is an efficient extender of primer ends opposite from 7,8-dihydro-8-Oxoguanine and O6-methylguanine.
    Haracska L; Prakash S; Prakash L
    Mol Cell Biol; 2003 Feb; 23(4):1453-9. PubMed ID: 12556503
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Pre-steady state kinetic studies show that an abasic site is a cognate lesion for the yeast Rev1 protein.
    Pryor JM; Washington MT
    DNA Repair (Amst); 2011 Nov; 10(11):1138-44. PubMed ID: 21975119
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Involvement of mouse Rev3 in tolerance of endogenous and exogenous DNA damage.
    Van Sloun PP; Varlet I; Sonneveld E; Boei JJ; Romeijn RJ; Eeken JC; De Wind N
    Mol Cell Biol; 2002 Apr; 22(7):2159-69. PubMed ID: 11884603
    [TBL] [Abstract][Full Text] [Related]  

  • 9. REV1 Coordinates a Multi-Faceted Tolerance Response to DNA Alkylation Damage and Prevents Chromosome Shattering in
    Khodaverdian V; Sano T; Maggs L; Tomarchio G; Dias A; Clairmont C; Tran M; McVey M
    bioRxiv; 2024 Feb; ():. PubMed ID: 38405884
    [TBL] [Abstract][Full Text] [Related]  

  • 10. REV7 in Cancer Biology and Management.
    Murakumo Y; Sakurai Y; Kato T; Hashimoto H; Ichinoe M
    Cancers (Basel); 2023 Mar; 15(6):. PubMed ID: 36980607
    [TBL] [Abstract][Full Text] [Related]  

  • 11. DNA Polymerase ζ without the C-Terminus of Catalytic Subunit Rev3 Retains Characteristic Activity, but Alters Mutation Specificity of Ultraviolet Radiation in Yeast.
    Siebler HM; Cui J; Hill SE; Pavlov YI
    Genes (Basel); 2022 Sep; 13(9):. PubMed ID: 36140745
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The inner side of yeast PCNA contributes to genome stability by mediating interactions with Rad18 and the replicative DNA polymerase δ.
    Toth R; Halmai M; Gyorfy Z; Balint E; Unk I
    Sci Rep; 2022 Mar; 12(1):5163. PubMed ID: 35338218
    [TBL] [Abstract][Full Text] [Related]  

  • 13. REV7: Jack of many trades.
    de Krijger I; Boersma V; Jacobs JJL
    Trends Cell Biol; 2021 Aug; 31(8):686-701. PubMed ID: 33962851
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The Zn-finger of Saccharomyces cerevisiae Rad18 and its adjacent region mediate interaction with Rad5.
    Frittmann O; Gali VK; Halmai M; Toth R; Gyorfy Z; Balint E; Unk I
    G3 (Bethesda); 2021 Apr; 11(4):. PubMed ID: 33570581
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Half-Intercalation Stabilizes Slipped Mispairing and Explains Genome Vulnerability to Frameshift Mutagenesis by Endogenous "Molecular Bookmarks".
    Kuzminov A
    Bioessays; 2019 Sep; 41(9):e1900062. PubMed ID: 31379009
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Error-prone bypass of DNA lesions during lagging-strand replication is a common source of germline and cancer mutations.
    Seplyarskiy VB; Akkuratov EE; Akkuratova N; Andrianova MA; Nikolaev SI; Bazykin GA; Adameyko I; Sunyaev SR
    Nat Genet; 2019 Jan; 51(1):36-41. PubMed ID: 30510240
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The translesion DNA polymerases Pol ζ and Rev1 are activated independently of PCNA ubiquitination upon UV radiation in mutants of DNA polymerase δ.
    Tellier-Lebegue C; Dizet E; Ma E; Veaute X; Coïc E; Charbonnier JB; Maloisel L
    PLoS Genet; 2017 Dec; 13(12):e1007119. PubMed ID: 29281621
    [TBL] [Abstract][Full Text] [Related]  

  • 18. G4-Interacting DNA Helicases and Polymerases: Potential Therapeutic Targets.
    Estep KN; Butler TJ; Ding J; Brosh RM
    Curr Med Chem; 2019; 26(16):2881-2897. PubMed ID: 29149833
    [TBL] [Abstract][Full Text] [Related]  

  • 19. NGS-based analysis of base-substitution signatures created by yeast DNA polymerase eta and zeta on undamaged and abasic DNA templates in vitro.
    Chen Y; Sugiyama T
    DNA Repair (Amst); 2017 Nov; 59():34-43. PubMed ID: 28946034
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mitochondrial DNA replication: a PrimPol perspective.
    Bailey LJ; Doherty AJ
    Biochem Soc Trans; 2017 Apr; 45(2):513-529. PubMed ID: 28408491
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.