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Journal Abstract Search

162 related items for PubMed ID: 10021333

  • 1. Apontic binds the translational repressor Bruno and is implicated in regulation of oskar mRNA translation.
    Lie YS, Macdonald PM.
    Development; 1999 Mar; 126(6):1129-38. PubMed ID: 10021333
    [Abstract] [Full Text] [Related]

  • 2. Control of oskar mRNA translation by Bruno in a novel cell-free system from Drosophila ovaries.
    Castagnetti S, Hentze MW, Ephrussi A, Gebauer F.
    Development; 2000 Mar; 127(5):1063-8. PubMed ID: 10662645
    [Abstract] [Full Text] [Related]

  • 3. Bruno acts as a dual repressor of oskar translation, promoting mRNA oligomerization and formation of silencing particles.
    Chekulaeva M, Hentze MW, Ephrussi A.
    Cell; 2006 Feb 10; 124(3):521-33. PubMed ID: 16469699
    [Abstract] [Full Text] [Related]

  • 4. Bruno regulates gurken during Drosophila oogenesis.
    Filardo P, Ephrussi A.
    Mech Dev; 2003 Mar 10; 120(3):289-97. PubMed ID: 12591598
    [Abstract] [Full Text] [Related]

  • 5. Translational regulation of oskar mRNA by bruno, an ovarian RNA-binding protein, is essential.
    Kim-Ha J, Kerr K, Macdonald PM.
    Cell; 1995 May 05; 81(3):403-12. PubMed ID: 7736592
    [Abstract] [Full Text] [Related]

  • 6. Translational repressor bruno plays multiple roles in development and is widely conserved.
    Webster PJ, Liang L, Berg CA, Lasko P, Macdonald PM.
    Genes Dev; 1997 Oct 01; 11(19):2510-21. PubMed ID: 9334316
    [Abstract] [Full Text] [Related]

  • 7. A late phase of Oskar accumulation is crucial for posterior patterning of the Drosophila embryo, and is blocked by ectopic expression of Bruno.
    Snee MJ, Harrison D, Yan N, Macdonald PM.
    Differentiation; 2007 Mar 01; 75(3):246-55. PubMed ID: 17359300
    [Abstract] [Full Text] [Related]

  • 8. Multiple RNA binding domains of Bruno confer recognition of diverse binding sites for translational repression.
    Reveal B, Garcia C, Ellington A, Macdonald PM.
    RNA Biol; 2011 Mar 01; 8(6):1047-60. PubMed ID: 21955496
    [Abstract] [Full Text] [Related]

  • 9. Two distinct domains of Bruno bind specifically to the oskar mRNA.
    Snee M, Benz D, Jen J, Macdonald PM.
    RNA Biol; 2008 Mar 01; 5(1):1-9. PubMed ID: 18388491
    [Abstract] [Full Text] [Related]

  • 10. Translational regulation of oskar mRNA occurs independent of the cap and poly(A) tail in Drosophila ovarian extracts.
    Lie YS, Macdonald PM.
    Development; 1999 Nov 01; 126(22):4989-96. PubMed ID: 10529417
    [Abstract] [Full Text] [Related]

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  • 14. BrunoL1 regulates endoderm proliferation through translational enhancement of cyclin A2 mRNA.
    Horb LD, Horb ME.
    Dev Biol; 2010 Sep 15; 345(2):156-69. PubMed ID: 20633547
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  • 15. Bruno negatively regulates germ cell-less expression in a BRE-independent manner.
    Moore J, Han H, Lasko P.
    Mech Dev; 2009 Jul 15; 126(7):503-16. PubMed ID: 19393317
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  • 18. Cup is an eIF4E binding protein required for both the translational repression of oskar and the recruitment of Barentsz.
    Wilhelm JE, Hilton M, Amos Q, Henzel WJ.
    J Cell Biol; 2003 Dec 22; 163(6):1197-204. PubMed ID: 14691132
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  • 19. A co-repressor assembly nucleated by Sex-lethal in the 3'UTR mediates translational control of Drosophila msl-2 mRNA.
    Grskovic M, Hentze MW, Gebauer F.
    EMBO J; 2003 Oct 15; 22(20):5571-81. PubMed ID: 14532129
    [Abstract] [Full Text] [Related]

  • 20. Barentsz is essential for the posterior localization of oskar mRNA and colocalizes with it to the posterior pole.
    van Eeden FJ, Palacios IM, Petronczki M, Weston MJ, St Johnston D.
    J Cell Biol; 2001 Aug 06; 154(3):511-23. PubMed ID: 11481346
    [Abstract] [Full Text] [Related]

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