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 *

165 related articles for article (PubMed ID: 20724388)

  • 1. Telomere position effect is regulated by heterochromatin-associated proteins and NkuA in Aspergillus nidulans.
    Palmer JM; Mallaredy S; Perry DW; Sanchez JF; Theisen JM; Szewczyk E; Oakley BR; Wang CCC; Keller NP; Mirabito PM
    Microbiology (Reading); 2010 Dec; 156(Pt 12):3522-3531. PubMed ID: 20724388
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Telomerase, Ku, and telomeric silencing in Saccharomyces cerevisiae.
    Evans SK; Sistrunk ML; Nugent CI; Lundblad V
    Chromosoma; 1998 Dec; 107(6-7):352-8. PubMed ID: 9914366
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A versatile and efficient gene-targeting system for Aspergillus nidulans.
    Nayak T; Szewczyk E; Oakley CE; Osmani A; Ukil L; Murray SL; Hynes MJ; Osmani SA; Oakley BR
    Genetics; 2006 Mar; 172(3):1557-66. PubMed ID: 16387870
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Yeast Ku protein plays a direct role in telomeric silencing and counteracts inhibition by rif proteins.
    Mishra K; Shore D
    Curr Biol; 1999 Oct; 9(19):1123-6. PubMed ID: 10531008
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Fission yeast Rhp51 is required for the maintenance of telomere structure in the absence of the Ku heterodimer.
    Kibe T; Tomita K; Matsuura A; Izawa D; Kodaira T; Ushimaru T; Uritani M; Ueno M
    Nucleic Acids Res; 2003 Sep; 31(17):5054-63. PubMed ID: 12930956
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Functional characterization of the putative Aspergillus nidulans DNA damage binding protein homologue DdbA.
    Lima JF; Malavazi I; da Silva Ferreira ME; Savoldi M; Mota AO; Capellaro JL; de Souza Goldman MH; Goldman GH
    Mol Genet Genomics; 2008 Mar; 279(3):239-53. PubMed ID: 18060432
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Ku-deficient yeast strains exhibit alternative states of silencing competence.
    Maillet L; Gaden F; Brevet V; Fourel G; Martin SG; Dubrana K; Gasser SM; Gilson E
    EMBO Rep; 2001 Mar; 2(3):203-10. PubMed ID: 11266361
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Heterochromatic marks are associated with the repression of secondary metabolism clusters in Aspergillus nidulans.
    Reyes-Dominguez Y; Bok JW; Berger H; Shwab EK; Basheer A; Gallmetzer A; Scazzocchio C; Keller N; Strauss J
    Mol Microbiol; 2010 Jun; 76(6):1376-86. PubMed ID: 20132440
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Expanding heterochromatin reveals discrete subtelomeric domains delimited by chromatin landscape transitions.
    Hocher A; Ruault M; Kaferle P; Descrimes M; Garnier M; Morillon A; Taddei A
    Genome Res; 2018 Dec; 28(12):1867-1881. PubMed ID: 30355601
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutation of yeast Ku genes disrupts the subnuclear organization of telomeres.
    Laroche T; Martin SG; Gotta M; Gorham HC; Pryde FE; Louis EJ; Gasser SM
    Curr Biol; 1998 May; 8(11):653-6. PubMed ID: 9635192
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A means to a DNA end: the many roles of Ku.
    Downs JA; Jackson SP
    Nat Rev Mol Cell Biol; 2004 May; 5(5):367-78. PubMed ID: 15122350
    [No Abstract]   [Full Text] [Related]  

  • 12. 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]  

  • 13. RNA silencing in Aspergillus nidulans is independent of RNA-dependent RNA polymerases.
    Hammond TM; Keller NP
    Genetics; 2005 Feb; 169(2):607-17. PubMed ID: 15545645
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Involvement of replicative polymerases, Tel1p, Mec1p, Cdc13p, and the Ku complex in telomere-telomere recombination.
    Tsai YL; Tseng SF; Chang SH; Lin CC; Teng SC
    Mol Cell Biol; 2002 Aug; 22(16):5679-87. PubMed ID: 12138180
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The TamA protein fused to a DNA-binding domain can recruit AreA, the major nitrogen regulatory protein, to activate gene expression in Aspergillus nidulans.
    Small AJ; Hynes MJ; Davis MA
    Genetics; 1999 Sep; 153(1):95-105. PubMed ID: 10471703
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Ku interacts with telomerase RNA to promote telomere addition at native and broken chromosome ends.
    Stellwagen AE; Haimberger ZW; Veatch JR; Gottschling DE
    Genes Dev; 2003 Oct; 17(19):2384-95. PubMed ID: 12975323
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Role for cohesin in the formation of a heterochromatic domain at fission yeast subtelomeres.
    Dheur S; Saupe SJ; Genier S; Vazquez S; Javerzat JP
    Mol Cell Biol; 2011 Mar; 31(5):1088-97. PubMed ID: 21189291
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Telomeric position effect--a third silencing mechanism in eukaryotes.
    Doheny JG; Mottus R; Grigliatti TA
    PLoS One; 2008; 3(12):e3864. PubMed ID: 19057646
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hush, hush: the origin of telomeric silence.
    Eggleston A
    Nat Cell Biol; 2000 Feb; 2(2):E27. PubMed ID: 10655599
    [No Abstract]   [Full Text] [Related]  

  • 20. Subtelomeric silencing of the MTL3 locus of Candida glabrata requires yKu70, yKu80, and Rif1 proteins.
    Ramírez-Zavaleta CY; Salas-Delgado GE; De Las Peñas A; Castaño I
    Eukaryot Cell; 2010 Oct; 9(10):1602-11. PubMed ID: 20675581
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.