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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

158 related articles for article (PubMed ID: 22876257)

  • 1. Effects of Perinuclear Chromosome Tethers in the Telomeric URA3/5FOA System Reflect Changes to Gene Silencing and not Nucleotide Metabolism.
    Poon BP; Mekhail K
    Front Genet; 2012; 3():144. PubMed ID: 22876257
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A common telomeric gene silencing assay is affected by nucleotide metabolism.
    Rossmann MP; Luo W; Tsaponina O; Chabes A; Stillman B
    Mol Cell; 2011 Apr; 42(1):127-36. PubMed ID: 21474074
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Perinuclear cohibin complexes maintain replicative life span via roles at distinct silent chromatin domains.
    Chan JN; Poon BP; Salvi J; Olsen JB; Emili A; Mekhail K
    Dev Cell; 2011 Jun; 20(6):867-79. PubMed ID: 21664583
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Subtelomeric elements influence but do not determine silencing levels at Saccharomyces cerevisiae telomeres.
    Mondoux MA; Zakian VA
    Genetics; 2007 Dec; 177(4):2541-6. PubMed ID: 18073447
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Telomere folding is required for the stable maintenance of telomere position effects in yeast.
    de Bruin D; Kantrow SM; Liberatore RA; Zakian VA
    Mol Cell Biol; 2000 Nov; 20(21):7991-8000. PubMed ID: 11027269
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Factors influencing the recombinational expansion and spread of telomeric tandem arrays in Kluyveromyces lactis.
    Natarajan S; Groff-Vindman C; McEachern MJ
    Eukaryot Cell; 2003 Oct; 2(5):1115-27. PubMed ID: 14555494
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Silent domains are assembled continuously from the telomere and are defined by promoter distance and strength, and by SIR3 dosage.
    Renauld H; Aparicio OM; Zierath PD; Billington BL; Chhablani SK; Gottschling DE
    Genes Dev; 1993 Jul; 7(7A):1133-45. PubMed ID: 8319906
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Components of the Ku-dependent non-homologous end-joining pathway are involved in telomeric length maintenance and telomeric silencing.
    Boulton SJ; Jackson SP
    EMBO J; 1998 Mar; 17(6):1819-28. PubMed ID: 9501103
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A SIR-independent role for cohesin in subtelomeric silencing and organization.
    Kothiwal D; Laloraya S
    Proc Natl Acad Sci U S A; 2019 Mar; 116(12):5659-5664. PubMed ID: 30842278
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Yeast telomerase and the SUN domain protein Mps3 anchor telomeres and repress subtelomeric recombination.
    Schober H; Ferreira H; Kalck V; Gehlen LR; Gasser SM
    Genes Dev; 2009 Apr; 23(8):928-38. PubMed ID: 19390087
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Differential nuclear localization does not determine the silencing status of Saccharomyces cerevisiae telomeres.
    Mondoux MA; Scaife JG; Zakian VA
    Genetics; 2007 Dec; 177(4):2019-29. PubMed ID: 18073421
    [TBL] [Abstract][Full Text] [Related]  

  • 12.
    Liu J; Mosser L; Botanch C; François JM; Capp JP
    G3 (Bethesda); 2020 Sep; 10(9):3435-3443. PubMed ID: 32727919
    [TBL] [Abstract][Full Text] [Related]  

  • 13. SIRT6 is required for maintenance of telomere position effect in human cells.
    Tennen RI; Bua DJ; Wright WE; Chua KF
    Nat Commun; 2011 Aug; 2():433. PubMed ID: 21847107
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Epistatic interaction between the K-homology domain protein HEK2 and SIR1 at HMR and telomeres in yeast.
    Denisenko O; Bomsztyk K
    J Mol Biol; 2008 Jan; 375(4):1178-87. PubMed ID: 18067921
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Limitations of silencing at native yeast telomeres.
    Pryde FE; Louis EJ
    EMBO J; 1999 May; 18(9):2538-50. PubMed ID: 10228167
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Dot1 and histone H3K79 methylation in natural telomeric and HM silencing.
    Takahashi YH; Schulze JM; Jackson J; Hentrich T; Seidel C; Jaspersen SL; Kobor MS; Shilatifard A
    Mol Cell; 2011 Apr; 42(1):118-26. PubMed ID: 21474073
    [TBL] [Abstract][Full Text] [Related]  

  • 17. yKu70/yKu80 and Rif1 regulate silencing differentially at telomeres in Candida glabrata.
    Rosas-Hernández LL; Juárez-Reyes A; Arroyo-Helguera OE; De Las Peñas A; Pan SJ; Cormack BP; Castaño I
    Eukaryot Cell; 2008 Dec; 7(12):2168-78. PubMed ID: 18836091
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Extra telomeres, but not internal tracts of telomeric DNA, reduce transcriptional repression at Saccharomyces telomeres.
    Wiley EA; Zakian VA
    Genetics; 1995 Jan; 139(1):67-79. PubMed ID: 7705652
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Overcoming telomeric silencing: a trans-activator competes to establish gene expression in a cell cycle-dependent way.
    Aparicio OM; Gottschling DE
    Genes Dev; 1994 May; 8(10):1133-46. PubMed ID: 7926719
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The functional importance of telomere clustering: global changes in gene expression result from SIR factor dispersion.
    Taddei A; Van Houwe G; Nagai S; Erb I; van Nimwegen E; Gasser SM
    Genome Res; 2009 Apr; 19(4):611-25. PubMed ID: 19179643
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.