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 *

171 related articles for article (PubMed ID: 10662645)

  • 1. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 75(3):246-55. PubMed ID: 17359300
    [TBL] [Abstract][Full Text] [Related]  

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

  • 5. 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; 126(22):4989-96. PubMed ID: 10529417
    [TBL] [Abstract][Full Text] [Related]  

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

  • 7. Orb and a long poly(A) tail are required for efficient oskar translation at the posterior pole of the Drosophila oocyte.
    Castagnetti S; Ephrussi A
    Development; 2003 Mar; 130(5):835-43. PubMed ID: 12538512
    [TBL] [Abstract][Full Text] [Related]  

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

  • 9. 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; 124(3):521-33. PubMed ID: 16469699
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Region-specific activation of oskar mRNA translation by inhibition of Bruno-mediated repression.
    Kim G; Pai CI; Sato K; Person MD; Nakamura A; Macdonald PM
    PLoS Genet; 2015; 11(2):e1004992. PubMed ID: 25723530
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Patterning of the Drosophila oocyte by a sequential translation repression program involving the d4EHP and Belle translational repressors.
    Yarunin A; Harris RE; Ashe MP; Ashe HL
    RNA Biol; 2011; 8(5):904-12. PubMed ID: 21788736
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Translational control of oskar generates short OSK, the isoform that induces pole plasma assembly.
    Markussen FH; Michon AM; Breitwieser W; Ephrussi A
    Development; 1995 Nov; 121(11):3723-32. PubMed ID: 8582284
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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; 154(3):511-23. PubMed ID: 11481346
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Bruno: a double turn-off for Oskar.
    Tekotte H; Davis I
    Dev Cell; 2006 Mar; 10(3):280-1. PubMed ID: 16516832
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Localization-dependent translation requires a functional interaction between the 5' and 3' ends of oskar mRNA.
    Gunkel N; Yano T; Markussen FH; Olsen LC; Ephrussi A
    Genes Dev; 1998 Jun; 12(11):1652-64. PubMed ID: 9620852
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 163(6):1197-204. PubMed ID: 14691132
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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; 11(19):2510-21. PubMed ID: 9334316
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 8(6):1047-60. PubMed ID: 21955496
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Drosophila cup is an eIF4E binding protein that associates with Bruno and regulates oskar mRNA translation in oogenesis.
    Nakamura A; Sato K; Hanyu-Nakamura K
    Dev Cell; 2004 Jan; 6(1):69-78. PubMed ID: 14723848
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Squid is required for efficient posterior localization of oskar mRNA during Drosophila oogenesis.
    Norvell A; Debec A; Finch D; Gibson L; Thoma B
    Dev Genes Evol; 2005 Jul; 215(7):340-9. PubMed ID: 15791421
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.