BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

450 related articles for article (PubMed ID: 9499577)

  • 1. Linker histone transitions during mammalian oogenesis and embryogenesis.
    Clarke HJ; McLay DW; Mohamed OA
    Dev Genet; 1998; 22(1):17-30. PubMed ID: 9499577
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Assembly of somatic histone H1 onto chromatin during bovine early embryogenesis.
    Smith LC; Meirelles FV; Bustin M; Clarke HJ
    J Exp Zool; 1995 Nov; 273(4):317-26. PubMed ID: 8530913
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Chromatin modifications during oogenesis in the mouse: removal of somatic subtypes of histone H1 from oocyte chromatin occurs post-natally through a post-transcriptional mechanism.
    Clarke HJ; Bustin M; Oblin C
    J Cell Sci; 1997 Feb; 110 ( Pt 4)():477-87. PubMed ID: 9067599
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Factors controlling the loss of immunoreactive somatic histone H1 from blastomere nuclei in oocyte cytoplasm: a potential marker of nuclear reprogramming.
    Bordignon V; Clarke HJ; Smith LC
    Dev Biol; 2001 May; 233(1):192-203. PubMed ID: 11319868
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mouse oocytes and early embryos express multiple histone H1 subtypes.
    Fu G; Ghadam P; Sirotkin A; Khochbin S; Skoultchi AI; Clarke HJ
    Biol Reprod; 2003 May; 68(5):1569-76. PubMed ID: 12606334
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Absence of somatic histone H1 in oocytes and preblastula embryos of Xenopus laevis.
    Hock R; Moorman A; Fischer D; Scheer U
    Dev Biol; 1993 Aug; 158(2):510-22. PubMed ID: 8344467
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Somatic linker histones cause loss of mesodermal competence in Xenopus.
    Steinbach OC; Wolffe AP; Rupp RA
    Nature; 1997 Sep; 389(6649):395-9. PubMed ID: 9311783
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Somatic histone H1 microinjected into fertilized mouse eggs is transported into the pronuclei but does not disrupt subsequent preimplantation development.
    Lin P; Clarke HJ
    Mol Reprod Dev; 1996 Jun; 44(2):185-92. PubMed ID: 9115716
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Remodeling somatic nuclei in Xenopus laevis egg extracts: molecular mechanisms for the selective release of histones H1 and H1(0) from chromatin and the acquisition of transcriptional competence.
    Dimitrov S; Wolffe AP
    EMBO J; 1996 Nov; 15(21):5897-906. PubMed ID: 8918467
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Analysis of TATA-binding protein 2 (TBP2) and TBP expression suggests different roles for the two proteins in regulation of gene expression during oogenesis and early mouse development.
    Gazdag E; Rajkovic A; Torres-Padilla ME; Tora L
    Reproduction; 2007 Jul; 134(1):51-62. PubMed ID: 17641088
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Chromatin in early mammalian embryos: achieving the pluripotent state.
    Fulka H; St John JC; Fulka J; Hozák P
    Differentiation; 2008 Jan; 76(1):3-14. PubMed ID: 18093226
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A conserved element in the protein-coding sequence is required for normal expression of replication-dependent histone genes in developing Xenopus embryos.
    Ficzycz A; Kaludov NK; Lele Z; Hurt MM; Ovsenek N
    Dev Biol; 1997 Feb; 182(1):21-32. PubMed ID: 9073440
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Characterization of linker histone H1FOO during bovine in vitro embryo development.
    McGraw S; Vigneault C; Tremblay K; Sirard MA
    Mol Reprod Dev; 2006 Jun; 73(6):692-9. PubMed ID: 16470586
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The maternal histone H1 variant, H1M (B4 protein), is the predominant H1 histone in Xenopus pregastrula embryos.
    Dworkin-Rastl E; Kandolf H; Smith RC
    Dev Biol; 1994 Feb; 161(2):425-39. PubMed ID: 8313993
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Messenger RNA expression patterns of histone-associated genes in bovine preimplantation embryos derived from different origins.
    Nowak-Imialek M; Wrenzycki C; Herrmann D; Lucas-Hahn A; Lagutina I; Lemme E; Lazzari G; Galli C; Niemann H
    Mol Reprod Dev; 2008 May; 75(5):731-43. PubMed ID: 18058811
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Initiation of a chromatin-based transcriptionally repressive state in the preimplantation mouse embryo: lack of a primary role for expression of somatic histone H1.
    Stein P; Schultz RM
    Mol Reprod Dev; 2000 Mar; 55(3):241-8. PubMed ID: 10657042
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Accumulation of histone H1(0) during early Xenopus laevis development.
    Grunwald D; Lawrence JJ; Khochbin S
    Exp Cell Res; 1995 Jun; 218(2):586-95. PubMed ID: 7796895
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Changes in global histone acetylation pattern in somatic cell nuclei after their transfer into oocytes at different stages of maturation.
    Fulka H
    Mol Reprod Dev; 2008 Mar; 75(3):556-64. PubMed ID: 17926342
    [TBL] [Abstract][Full Text] [Related]  

  • 19. DNA hypomethylation circuit of the mouse oocyte-specific histone H1foo gene in female germ cell lineage.
    Maeda C; Sato S; Hattori N; Tanaka S; Yagi S; Shiota K
    Biol Reprod; 2008 May; 78(5):816-21. PubMed ID: 18184919
    [TBL] [Abstract][Full Text] [Related]  

  • 20. How do linker histones mediate differential gene expression?
    Crane-Robinson C
    Bioessays; 1999 May; 21(5):367-71. PubMed ID: 10376007
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 23.