BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

143 related articles for article (PubMed ID: 27185864)

  • 1. Cdk-dependent phosphorylation regulates TRF1 recruitment to PML bodies and promotes C-circle production in ALT cells.
    Wilson FR; Ho A; Walker JR; Zhu XD
    J Cell Sci; 2016 Jul; 129(13):2559-72. PubMed ID: 27185864
    [TBL] [Abstract][Full Text] [Related]  

  • 2. TRF1 phosphorylation on T271 modulates telomerase-dependent telomere length maintenance as well as the formation of ALT-associated PML bodies.
    Ho A; Wilson FR; Peragine SL; Jeyanthan K; Mitchell TR; Zhu XD
    Sci Rep; 2016 Nov; 6():36913. PubMed ID: 27841304
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Assembly of functional ALT-associated promyelocytic leukemia bodies requires Nijmegen Breakage Syndrome 1.
    Wu G; Jiang X; Lee WH; Chen PL
    Cancer Res; 2003 May; 63(10):2589-95. PubMed ID: 12750284
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Phosphorylated (pT371)TRF1 is recruited to sites of DNA damage to facilitate homologous recombination and checkpoint activation.
    McKerlie M; Walker JR; Mitchell TR; Wilson FR; Zhu XD
    Nucleic Acids Res; 2013 Dec; 41(22):10268-82. PubMed ID: 23997120
    [TBL] [Abstract][Full Text] [Related]  

  • 5. PML3 interacts with TRF1 and is essential for ALT-associated PML bodies assembly in U2OS cells.
    Yu J; Lan J; Wang C; Wu Q; Zhu Y; Lai X; Sun J; Jin C; Huang H
    Cancer Lett; 2010 May; 291(2):177-86. PubMed ID: 19900757
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of candidate alternative lengthening of telomeres genes by methionine restriction and RNA interference.
    Jiang WQ; Zhong ZH; Henson JD; Reddel RR
    Oncogene; 2007 Jul; 26(32):4635-47. PubMed ID: 17297460
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The F-box protein β-TrCP promotes ubiquitination of TRF1 and regulates the ALT-associated PML bodies formation in U2OS cells.
    Wang C; Xiao H; Ma J; Zhu Y; Yu J; Sun L; Sun H; Liu Y; Jin C; Huang H
    Biochem Biophys Res Commun; 2013 May; 434(4):728-34. PubMed ID: 23583392
    [TBL] [Abstract][Full Text] [Related]  

  • 8. De novo assembly of a PML nuclear subcompartment occurs through multiple pathways and induces telomere elongation.
    Chung I; Leonhardt H; Rippe K
    J Cell Sci; 2011 Nov; 124(Pt 21):3603-18. PubMed ID: 22045732
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The SMC5/6 complex maintains telomere length in ALT cancer cells through SUMOylation of telomere-binding proteins.
    Potts PR; Yu H
    Nat Struct Mol Biol; 2007 Jul; 14(7):581-90. PubMed ID: 17589526
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Alternative lengthening of telomeres is a self-perpetuating process in ALT-associated PML bodies.
    Zhang JM; Genois MM; Ouyang J; Lan L; Zou L
    Mol Cell; 2021 Mar; 81(5):1027-1042.e4. PubMed ID: 33453166
    [TBL] [Abstract][Full Text] [Related]  

  • 11. DNA damage induces alternative lengthening of telomeres (ALT) associated promyelocytic leukemia bodies that preferentially associate with linear telomeric DNA.
    Fasching CL; Neumann AA; Muntoni A; Yeager TR; Reddel RR
    Cancer Res; 2007 Aug; 67(15):7072-7. PubMed ID: 17652140
    [TBL] [Abstract][Full Text] [Related]  

  • 12. PML induces compaction, TRF2 depletion and DNA damage signaling at telomeres and promotes their alternative lengthening.
    Osterwald S; Deeg KI; Chung I; Parisotto D; Wörz S; Rohr K; Erfle H; Rippe K
    J Cell Sci; 2015 May; 128(10):1887-900. PubMed ID: 25908860
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Telomere length heterogeneity in ALT cells is maintained by PML-dependent localization of the BTR complex to telomeres.
    Loe TK; Li JSZ; Zhang Y; Azeroglu B; Boddy MN; Denchi EL
    Genes Dev; 2020 May; 34(9-10):650-662. PubMed ID: 32217664
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Telomerase suppresses formation of ALT-associated single-stranded telomeric C-circles.
    Plantinga MJ; Pascarelli KM; Merkel AS; Lazar AJ; von Mehren M; Lev D; Broccoli D
    Mol Cancer Res; 2013 Jun; 11(6):557-67. PubMed ID: 23505069
    [TBL] [Abstract][Full Text] [Related]  

  • 15. ATM regulates proteasome-dependent subnuclear localization of TRF1, which is important for telomere maintenance.
    McKerlie M; Lin S; Zhu XD
    Nucleic Acids Res; 2012 May; 40(9):3975-89. PubMed ID: 22266654
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Nucleostemin prevents telomere damage by promoting PML-IV recruitment to SUMOylated TRF1.
    Hsu JK; Lin T; Tsai RY
    J Cell Biol; 2012 May; 197(5):613-24. PubMed ID: 22641345
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cyclin B-dependent kinase 1 regulates human TRF1 to modulate the resolution of sister telomeres.
    McKerlie M; Zhu XD
    Nat Commun; 2011 Jun; 2():371. PubMed ID: 21712819
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The telomere-associated homeobox-containing protein TAH1/HMBOX1 participates in telomere maintenance in ALT cells.
    Feng X; Luo Z; Jiang S; Li F; Han X; Hu Y; Wang D; Zhao Y; Ma W; Liu D; Huang J; Songyang Z
    J Cell Sci; 2013 Sep; 126(Pt 17):3982-9. PubMed ID: 23813958
    [TBL] [Abstract][Full Text] [Related]  

  • 19. WRN loss induces switching of telomerase-independent mechanisms of telomere elongation.
    Gocha AR; Acharya S; Groden J
    PLoS One; 2014; 9(4):e93991. PubMed ID: 24709898
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Probing PML body function in ALT cells reveals spatiotemporal requirements for telomere recombination.
    Draskovic I; Arnoult N; Steiner V; Bacchetti S; Lomonte P; Londoño-Vallejo A
    Proc Natl Acad Sci U S A; 2009 Sep; 106(37):15726-31. PubMed ID: 19717459
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.