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 *

136 related articles for article (PubMed ID: 1879554)

  • 21. Nucleotide excision repair of the 5 S ribosomal RNA gene assembled into a nucleosome.
    Liu X; Smerdon MJ
    J Biol Chem; 2000 Aug; 275(31):23729-35. PubMed ID: 10821833
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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; 87(15):5724-8. PubMed ID: 2377610
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Role of histone H1 as an architectural determinant of chromatin structure and as a specific repressor of transcription on Xenopus oocyte 5S rRNA genes.
    Sera T; Wolffe AP
    Mol Cell Biol; 1998 Jul; 18(7):3668-80. PubMed ID: 9632749
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Nucleosomes inhibit both transcriptional initiation and elongation by RNA polymerase III in vitro.
    Morse RH
    EMBO J; 1989 Aug; 8(8):2343-51. PubMed ID: 2792088
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Differential nucleosome positioning on Xenopus oocyte and somatic 5 S RNA genes determines both TFIIIA and H1 binding: a mechanism for selective H1 repression.
    Panetta G; Buttinelli M; Flaus A; Richmond TJ; Rhodes D
    J Mol Biol; 1998 Sep; 282(3):683-97. PubMed ID: 9737930
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Both the 5S rRNA gene and the AT-rich flanks of xenopus laevis oocyte-type 5S rDNA repeat are required for histone H1-dependent repression of transcription of pol III-type genes in in vitro reconstituted chromatin.
    Tomaszewski R; Mogielnicka E; Jerzmanowski A
    Nucleic Acids Res; 1998 Dec; 26(24):5596-601. PubMed ID: 9837988
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Histone-DNA contacts in a nucleosome core containing a Xenopus 5S rRNA gene.
    Pruss D; Wolffe AP
    Biochemistry; 1993 Jul; 32(27):6810-4. PubMed ID: 8334114
    [TBL] [Abstract][Full Text] [Related]  

  • 29. DNA damage induced by bleomycin, neocarzinostatin, and melphalan in a precisely positioned nucleosome. Asymmetry in protection at the periphery of nucleosome-bound DNA.
    Smith BL; Bauer GB; Povirk LF
    J Biol Chem; 1994 Dec; 269(48):30587-94. PubMed ID: 7527033
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Methylation at CpG sequences does not influence histone H1 binding to a nucleosome including a Xenopus borealis 5 S rRNA gene.
    Nightingale K; Wolffe AP
    J Biol Chem; 1995 Mar; 270(9):4197-200. PubMed ID: 7876175
    [TBL] [Abstract][Full Text] [Related]  

  • 31. 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; 299(4):853-8. PubMed ID: 10843841
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Histone contributions to the structure of DNA in the nucleosome.
    Hayes JJ; Clark DJ; Wolffe AP
    Proc Natl Acad Sci U S A; 1991 Aug; 88(15):6829-33. PubMed ID: 1650485
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Quantification of the effect of site-specific histone acetylation on chromatin transcription rate.
    Wakamori M; Okabe K; Ura K; Funatsu T; Takinoue M; Umehara T
    Nucleic Acids Res; 2020 Dec; 48(22):12648-12659. PubMed ID: 33238306
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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; 256(3):458-72. PubMed ID: 8604131
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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; 23(6):1075-82. PubMed ID: 7731795
    [TBL] [Abstract][Full Text] [Related]  

  • 36. DNA sequence-directed nucleosome reconstitution on 5S RNA genes of Xenopus laevis.
    Gottesfeld JM
    Mol Cell Biol; 1987 May; 7(5):1612-22. PubMed ID: 3600640
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Ultraviolet damage and nucleosome folding of the 5S ribosomal RNA gene.
    Liu X; Mann DB; Suquet C; Springer DL; Smerdon MJ
    Biochemistry; 2000 Jan; 39(3):557-66. PubMed ID: 10642180
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The core histone N-terminal tail domains negatively regulate binding of transcription factor IIIA to a nucleosome containing a 5S RNA gene via a novel mechanism.
    Yang Z; Zheng C; Thiriet C; Hayes JJ
    Mol Cell Biol; 2005 Jan; 25(1):241-9. PubMed ID: 15601846
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Enhancement of the transcription potential of nascent chromatin by chromosomal proteins HMG-14/-17 is coupled to nucleosome assembly and not DNA synthesis.
    Weigmann N; Trieschmann L; Bustin M
    DNA Cell Biol; 1997 Oct; 16(10):1207-16. PubMed ID: 9364931
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Acetylation of histone H4 plays a primary role in enhancing transcription factor binding to nucleosomal DNA in vitro.
    Vettese-Dadey M; Grant PA; Hebbes TR; Crane- Robinson C; Allis CD; Workman JL
    EMBO J; 1996 May; 15(10):2508-18. PubMed ID: 8665858
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.