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Journal Abstract Search


424 related items for PubMed ID: 7731795

  • 1. Deposition of histone H1 onto reconstituted nucleosome arrays inhibits both initiation and elongation of transcripts by T7 RNA polymerase.
    O'Neill TE, Meersseman G, Pennings S, Bradbury EM.
    Nucleic Acids Res; 1995 Mar 25; 23(6):1075-82. PubMed ID: 7731795
    [Abstract] [Full Text] [Related]

  • 2. Nucleosome arrays inhibit both initiation and elongation of transcripts by bacteriophage T7 RNA polymerase.
    O'Neill TE, Roberge M, Bradbury EM.
    J Mol Biol; 1992 Jan 05; 223(1):67-78. PubMed ID: 1731087
    [Abstract] [Full Text] [Related]

  • 3. Histone octamer dissociation is not required for transcript elongation through arrays of nucleosome cores by phage T7 RNA polymerase in vitro.
    O'Neill TE, Smith JG, Bradbury EM.
    Proc Natl Acad Sci U S A; 1993 Jul 01; 90(13):6203-7. PubMed ID: 8327500
    [Abstract] [Full Text] [Related]

  • 4. Nucleosome transcription studied in a real-time synchronous system: test of the lexosome model and direct measurement of effects due to histone octamer.
    Protacio RU, Widom J.
    J Mol Biol; 1996 Mar 01; 256(3):458-72. PubMed ID: 8604131
    [Abstract] [Full Text] [Related]

  • 5. Binding of the RNA polymerase I transcription complex to its promoter can modify positioning of downstream nucleosomes assembled in vitro.
    Georgel P, Demeler B, Terpening C, Paule MR, van Holde KE.
    J Biol Chem; 1993 Jan 25; 268(3):1947-54. PubMed ID: 8420969
    [Abstract] [Full Text] [Related]

  • 6. Mechanism of nucleosome dissociation produced by transcription elongation in a short chromatin template.
    Gallego F, Fernandez-Busquets X, Daban JR.
    Biochemistry; 1995 May 23; 34(20):6711-9. PubMed ID: 7756302
    [Abstract] [Full Text] [Related]

  • 7. Transcription of DNA templates associated with histone (H3 x H4)(2) tetramers.
    Chirinos M, Hernández F, Palacián E.
    Arch Biochem Biophys; 1999 Oct 15; 370(2):222-30. PubMed ID: 10510281
    [Abstract] [Full Text] [Related]

  • 8. Repressive effect on oligonucleosome transcription of the core histone tail domains.
    Chirinos M, Hernández F, Palacián E.
    Biochemistry; 1998 May 19; 37(20):7251-9. PubMed ID: 9585538
    [Abstract] [Full Text] [Related]

  • 9. Blocking transcription through a nucleosome with synthetic DNA ligands.
    Gottesfeld JM, Belitsky JM, Melander C, Dervan PB, Luger K.
    J Mol Biol; 2002 Aug 09; 321(2):249-63. PubMed ID: 12144782
    [Abstract] [Full Text] [Related]

  • 10. DNA and protein determinants of nucleosome positioning on sea urchin 5S rRNA gene sequences in vitro.
    Dong F, Hansen JC, van Holde KE.
    Proc Natl Acad Sci U S A; 1990 Aug 09; 87(15):5724-8. PubMed ID: 2377610
    [Abstract] [Full Text] [Related]

  • 11. Homogeneous reconstituted oligonucleosomes, evidence for salt-dependent folding in the absence of histone H1.
    Hansen JC, Ausio J, Stanik VH, van Holde KE.
    Biochemistry; 1989 Nov 14; 28(23):9129-36. PubMed ID: 2605246
    [Abstract] [Full Text] [Related]

  • 12. Atomic force microscopy sees nucleosome positioning and histone H1-induced compaction in reconstituted chromatin.
    Sato MH, Ura K, Hohmura KI, Tokumasu F, Yoshimura SH, Hanaoka F, Takeyasu K.
    FEBS Lett; 1999 Jun 11; 452(3):267-71. PubMed ID: 10386604
    [Abstract] [Full Text] [Related]

  • 13. Folding of chromatin in the presence of heterogeneous histone H1 binding to nucleosomes.
    Howe L, Iskandar M, Ausió J.
    J Biol Chem; 1998 May 08; 273(19):11625-9. PubMed ID: 9565581
    [Abstract] [Full Text] [Related]

  • 14. A bacteriophage RNA polymerase transcribes in vitro through a nucleosome core without displacing it.
    Losa R, Brown DD.
    Cell; 1987 Aug 28; 50(5):801-8. PubMed ID: 3621345
    [Abstract] [Full Text] [Related]

  • 15. The mechanism of nucleosome assembly onto oligomers of the sea urchin 5 S DNA positioning sequence.
    Hansen JC, van Holde KE, Lohr D.
    J Biol Chem; 1991 Mar 05; 266(7):4276-82. PubMed ID: 1900288
    [Abstract] [Full Text] [Related]

  • 16. An immuno-electron microscopical analysis of transcribing multinucleosomal templates: what happens to the histones?
    ten Heggeler-Bordier B, Muller S, Monestier M, Wahli W.
    J Mol Biol; 2000 Jun 16; 299(4):853-8. PubMed ID: 10843841
    [Abstract] [Full Text] [Related]

  • 17. The AT-rich flanks of the oocyte-type 5S RNA gene of Xenopus laevis act as a strong local signal for histone H1-mediated chromatin reorganization in vitro.
    Tomaszewski R, Jerzmanowski A.
    Nucleic Acids Res; 1997 Feb 01; 25(3):458-66. PubMed ID: 9016582
    [Abstract] [Full Text] [Related]

  • 18. Transcriptional repression by nucleosomes but not H1 in reconstituted preblastoderm Drosophila chromatin.
    Sandaltzopoulos R, Blank T, Becker PB.
    EMBO J; 1994 Jan 15; 13(2):373-9. PubMed ID: 8313882
    [Abstract] [Full Text] [Related]

  • 19. A positive role for nucleosome mobility in the transcriptional activity of chromatin templates: restriction by linker histones.
    Ura K, Hayes JJ, Wolffe AP.
    EMBO J; 1995 Aug 01; 14(15):3752-65. PubMed ID: 7641694
    [Abstract] [Full Text] [Related]

  • 20. Studies on the interaction of T7 RNA polymerase with a DNA template containing a site-specifically placed psoralen cross-link. I. Characterization of elongation complexes.
    Sastry SS, Hearst JE.
    J Mol Biol; 1991 Oct 20; 221(4):1091-110. PubMed ID: 1942044
    [Abstract] [Full Text] [Related]


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