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Journal Abstract Search

660 related items for PubMed ID: 9778352

  • 1. Linker histones stabilize the intrinsic salt-dependent folding of nucleosomal arrays: mechanistic ramifications for higher-order chromatin folding.
    Carruthers LM, Bednar J, Woodcock CL, Hansen JC.
    Biochemistry; 1998 Oct 20; 37(42):14776-87. PubMed ID: 9778352
    [Abstract] [Full Text] [Related]

  • 2. Hybrid trypsinized nucleosomal arrays: identification of multiple functional roles of the H2A/H2B and H3/H4 N-termini in chromatin fiber compaction.
    Tse C, Hansen JC.
    Biochemistry; 1997 Sep 23; 36(38):11381-8. PubMed ID: 9298957
    [Abstract] [Full Text] [Related]

  • 3. A method for the in vitro reconstitution of a defined "30 nm" chromatin fibre containing stoichiometric amounts of the linker histone.
    Huynh VA, Robinson PJ, Rhodes D.
    J Mol Biol; 2005 Feb 04; 345(5):957-68. PubMed ID: 15644197
    [Abstract] [Full Text] [Related]

  • 4. Reversible oligonucleosome self-association: dependence on divalent cations and core histone tail domains.
    Schwarz PM, Felthauser A, Fletcher TM, Hansen JC.
    Biochemistry; 1996 Apr 02; 35(13):4009-15. PubMed ID: 8672434
    [Abstract] [Full Text] [Related]

  • 5. Disruption of higher-order folding by core histone acetylation dramatically enhances transcription of nucleosomal arrays by RNA polymerase III.
    Tse C, Sera T, Wolffe AP, Hansen JC.
    Mol Cell Biol; 1998 Aug 02; 18(8):4629-38. PubMed ID: 9671473
    [Abstract] [Full Text] [Related]

  • 6. Removal of histone tails from nucleosome dissects the physical mechanisms of salt-induced aggregation, linker histone H1-induced compaction, and 30-nm fiber formation of the nucleosome array.
    Hizume K, Nakai T, Araki S, Prieto E, Yoshikawa K, Takeyasu K.
    Ultramicroscopy; 2009 Jul 02; 109(8):868-73. PubMed ID: 19328628
    [Abstract] [Full Text] [Related]

  • 7. The core histone N termini function independently of linker histones during chromatin condensation.
    Carruthers LM, Hansen JC.
    J Biol Chem; 2000 Nov 24; 275(47):37285-90. PubMed ID: 10970897
    [Abstract] [Full Text] [Related]

  • 8. Linker histone H1 per se can induce three-dimensional folding of chromatin fiber.
    Hizume K, Yoshimura SH, Takeyasu K.
    Biochemistry; 2005 Oct 04; 44(39):12978-89. PubMed ID: 16185066
    [Abstract] [Full Text] [Related]

  • 9. Chromatin dynamics of unfolding and refolding controlled by the nucleosome repeat length and the linker and core histones.
    Kobori T, Iwamoto S, Takeyasu K, Ohtani T.
    Biopolymers; 2007 Mar 04; 85(4):295-307. PubMed ID: 17211885
    [Abstract] [Full Text] [Related]

  • 10. Detection of interactions between nucleosome arrays mediated by specific core histone tail domains.
    Kan PY, Hayes JJ.
    Methods; 2007 Mar 04; 41(3):278-85. PubMed ID: 17309837
    [Abstract] [Full Text] [Related]

  • 11. Major role of the histones H3-H4 in the folding of the chromatin fiber.
    Moore SC, Ausió J.
    Biochem Biophys Res Commun; 1997 Jan 03; 230(1):136-9. PubMed ID: 9020030
    [Abstract] [Full Text] [Related]

  • 12. [The type of interaction of histone H5 wo ith DNA changes significantly at various stages of chromatin condensation].
    Pruss DV, Ebralidze KK, Mirzabekov AD.
    Mol Biol (Mosk); 1988 Jan 03; 22(4):1108-18. PubMed ID: 3185531
    [Abstract] [Full Text] [Related]

  • 13. Chromatin compaction at the mononucleosome level.
    Tóth K, Brun N, Langowski J.
    Biochemistry; 2006 Feb 14; 45(6):1591-8. PubMed ID: 16460006
    [Abstract] [Full Text] [Related]

  • 14. Two DNA-binding sites on the globular domain of histone H5 are required for binding to both bulk and 5 S reconstituted nucleosomes.
    Duggan MM, Thomas JO.
    J Mol Biol; 2000 Nov 17; 304(1):21-33. PubMed ID: 11071807
    [Abstract] [Full Text] [Related]

  • 15. Nucleosomal arrays can be salt-reconstituted on a single-copy MMTV promoter DNA template: their properties differ in several ways from those of comparable 5S concatameric arrays.
    Bash R, Wang H, Yodh J, Hager G, Lindsay SM, Lohr D.
    Biochemistry; 2003 Apr 29; 42(16):4681-90. PubMed ID: 12705831
    [Abstract] [Full Text] [Related]

  • 16. The essential histone variant H2A.Z regulates the equilibrium between different chromatin conformational states.
    Fan JY, Gordon F, Luger K, Hansen JC, Tremethick DJ.
    Nat Struct Biol; 2002 Mar 29; 9(3):172-6. PubMed ID: 11850638
    [Abstract] [Full Text] [Related]

  • 17. [Features of the chromatin structure of erythrocytes depending on the properties of lysine-rich histones].
    Kostyleva EI, Selivanova GV, Zalenskaia IA.
    Mol Biol (Mosk); 1989 Mar 29; 23(1):73-9. PubMed ID: 2544799
    [Abstract] [Full Text] [Related]

  • 18. H2A.Z and H3.3 histone variants affect nucleosome structure: biochemical and biophysical studies.
    Thakar A, Gupta P, Ishibashi T, Finn R, Silva-Moreno B, Uchiyama S, Fukui K, Tomschik M, Ausio J, Zlatanova J.
    Biochemistry; 2009 Nov 24; 48(46):10852-7. PubMed ID: 19856965
    [Abstract] [Full Text] [Related]

  • 19. Formation and stability of higher order chromatin structures. Contributions of the histone octamer.
    Schwarz PM, Hansen JC.
    J Biol Chem; 1994 Jun 10; 269(23):16284-9. PubMed ID: 8206934
    [Abstract] [Full Text] [Related]

  • 20. Chromatin superstructure-dependent crosslinking with DNA of the histone H5 residues Thr1, His25 and His62.
    Mirzabekov AD, Pruss DV, Ebralidse KK.
    J Mol Biol; 1990 Jan 20; 211(2):479-91. PubMed ID: 2106584
    [Abstract] [Full Text] [Related]

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