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 *

182 related articles for article (PubMed ID: 9155034)

  • 1. Effects of Sin- versions of histone H4 on yeast chromatin structure and function.
    Wechser MA; Kladde MP; Alfieri JA; Peterson CL
    EMBO J; 1997 Apr; 16(8):2086-95. PubMed ID: 9155034
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Sin mutations of histone H3: influence on nucleosome core structure and function.
    Kurumizaka H; Wolffe AP
    Mol Cell Biol; 1997 Dec; 17(12):6953-69. PubMed ID: 9372928
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Amino acid substitutions in the structured domains of histones H3 and H4 partially relieve the requirement of the yeast SWI/SNF complex for transcription.
    Kruger W; Peterson CL; Sil A; Coburn C; Arents G; Moudrianakis EN; Herskowitz I
    Genes Dev; 1995 Nov; 9(22):2770-9. PubMed ID: 7590252
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The SIN domain of the histone octamer is essential for intramolecular folding of nucleosomal arrays.
    Horn PJ; Crowley KA; Carruthers LM; Hansen JC; Peterson CL
    Nat Struct Biol; 2002 Mar; 9(3):167-71. PubMed ID: 11836537
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Depletion of histone H4 and nucleosomes activates the PHO5 gene in Saccharomyces cerevisiae.
    Han M; Kim UJ; Kayne P; Grunstein M
    EMBO J; 1988 Jul; 7(7):2221-8. PubMed ID: 3046934
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Yeast histone H3 and H4 amino termini are important for nucleosome assembly in vivo and in vitro: redundant and position-independent functions in assembly but not in gene regulation.
    Ling X; Harkness TA; Schultz MC; Fisher-Adams G; Grunstein M
    Genes Dev; 1996 Mar; 10(6):686-99. PubMed ID: 8598296
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Partial depletion of histone H4 increases homologous recombination-mediated genetic instability.
    Prado F; Aguilera A
    Mol Cell Biol; 2005 Feb; 25(4):1526-36. PubMed ID: 15684401
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Yeast histone H4 and H3 N-termini have different effects on the chromatin structure of the GAL1 promoter.
    Fisher-Adams G; Grunstein M
    EMBO J; 1995 Apr; 14(7):1468-77. PubMed ID: 7729422
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The LRS and SIN domains: two structurally equivalent but functionally distinct nucleosomal surfaces required for transcriptional silencing.
    Fry CJ; Norris A; Cosgrove M; Boeke JD; Peterson CL
    Mol Cell Biol; 2006 Dec; 26(23):9045-59. PubMed ID: 17015465
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A core nucleosome surface crucial for transcriptional silencing.
    Park JH; Cosgrove MS; Youngman E; Wolberger C; Boeke JD
    Nat Genet; 2002 Oct; 32(2):273-9. PubMed ID: 12244315
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Non-conservative mutations are well tolerated in the globular region of yeast histone H4.
    Agarwal S; Behe MJ
    J Mol Biol; 1996 Jan; 255(3):401-11. PubMed ID: 8568885
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutations in both the structured domain and N-terminus of histone H2B bypass the requirement for Swi-Snf in yeast.
    Recht J; Osley MA
    EMBO J; 1999 Jan; 18(1):229-40. PubMed ID: 9878065
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Histone octamer function in vivo: mutations in the dimer-tetramer interfaces disrupt both gene activation and repression.
    Santisteban MS; Arents G; Moudrianakis EN; Smith MM
    EMBO J; 1997 May; 16(9):2493-506. PubMed ID: 9171362
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A single amino acid change in histone H4 enhances UV survival and DNA repair in yeast.
    Nag R; Gong F; Fahy D; Smerdon MJ
    Nucleic Acids Res; 2008 Jun; 36(11):3857-66. PubMed ID: 18508805
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Comprehensive structural analysis of mutant nucleosomes containing lysine to glutamine (KQ) substitutions in the H3 and H4 histone-fold domains.
    Iwasaki W; Tachiwana H; Kawaguchi K; Shibata T; Kagawa W; Kurumizaka H
    Biochemistry; 2011 Sep; 50(36):7822-32. PubMed ID: 21812398
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Differential contributions of histone H3 and H4 residues to heterochromatin structure.
    Yu Q; Olsen L; Zhang X; Boeke JD; Bi X
    Genetics; 2011 Jun; 188(2):291-308. PubMed ID: 21441216
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Increasing the rate of chromatin remodeling and gene activation--a novel role for the histone acetyltransferase Gcn5.
    Barbaric S; Walker J; Schmid A; Svejstrup JQ; Hörz W
    EMBO J; 2001 Sep; 20(17):4944-51. PubMed ID: 11532958
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The mouse mammary tumour virus promoter positioned on a tetramer of histones H3 and H4 binds nuclear factor 1 and OTF1.
    Spangenberg C; Eisfeld K; Stünkel W; Luger K; Flaus A; Richmond TJ; Truss M; Beato M
    J Mol Biol; 1998 May; 278(4):725-39. PubMed ID: 9614938
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Sin mutations alter inherent nucleosome mobility.
    Flaus A; Rencurel C; Ferreira H; Wiechens N; Owen-Hughes T
    EMBO J; 2004 Jan; 23(2):343-53. PubMed ID: 14726954
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Antagonistic remodelling by Swi-Snf and Tup1-Ssn6 of an extensive chromatin region forms the background for FLO1 gene regulation.
    Fleming AB; Pennings S
    EMBO J; 2001 Sep; 20(18):5219-31. PubMed ID: 11566885
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.