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Journal Abstract Search

304 related items for PubMed ID: 15130488

  • 1. The Drosophila hnRNPA/B homolog, Hrp48, is specifically required for a distinct step in osk mRNA localization.
    Huynh JR, Munro TP, Smith-Litière K, Lepesant JA, St Johnston D.
    Dev Cell; 2004 May; 6(5):625-35. PubMed ID: 15130488
    [Abstract] [Full Text] [Related]

  • 2. Hrp48, a Drosophila hnRNPA/B homolog, binds and regulates translation of oskar mRNA.
    Yano T, López de Quinto S, Matsui Y, Shevchenko A, Shevchenko A, Ephrussi A.
    Dev Cell; 2004 May; 6(5):637-48. PubMed ID: 15130489
    [Abstract] [Full Text] [Related]

  • 3. Different roles for the adjoining and structurally similar A-rich and poly(A) domains of oskar mRNA: Only the A-rich domain is required for oskar noncoding RNA function, which includes MTOC positioning.
    Kenny A, Morgan MB, Macdonald PM.
    Dev Biol; 2021 Aug; 476():117-127. PubMed ID: 33798537
    [Abstract] [Full Text] [Related]

  • 4. bicoid RNA localization requires specific binding of an endosomal sorting complex.
    Irion U, St Johnston D.
    Nature; 2007 Feb 01; 445(7127):554-8. PubMed ID: 17268469
    [Abstract] [Full Text] [Related]

  • 5. A late phase of germ plasm accumulation during Drosophila oogenesis requires lost and rumpelstiltskin.
    Sinsimer KS, Jain RA, Chatterjee S, Gavis ER.
    Development; 2011 Aug 01; 138(16):3431-40. PubMed ID: 21752933
    [Abstract] [Full Text] [Related]

  • 6. Anterior-posterior axis specification in Drosophila oocytes: identification of novel bicoid and oskar mRNA localization factors.
    Chang CW, Nashchekin D, Wheatley L, Irion U, Dahlgaard K, Montague TG, Hall J, St Johnston D.
    Genetics; 2011 Aug 01; 188(4):883-96. PubMed ID: 21625003
    [Abstract] [Full Text] [Related]

  • 7. Distinct roles of two conserved Staufen domains in oskar mRNA localization and translation.
    Micklem DR, Adams J, Grünert S, St Johnston D.
    EMBO J; 2000 Mar 15; 19(6):1366-77. PubMed ID: 10716936
    [Abstract] [Full Text] [Related]

  • 8. 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 Mar 15; 11(2):e1004992. PubMed ID: 25723530
    [Abstract] [Full Text] [Related]

  • 9. Imp associates with squid and Hrp48 and contributes to localized expression of gurken in the oocyte.
    Geng C, Macdonald PM.
    Mol Cell Biol; 2006 Dec 15; 26(24):9508-16. PubMed ID: 17030623
    [Abstract] [Full Text] [Related]

  • 10. Staufen protein associates with the 3'UTR of bicoid mRNA to form particles that move in a microtubule-dependent manner.
    Ferrandon D, Elphick L, Nüsslein-Volhard C, St Johnston D.
    Cell; 1994 Dec 30; 79(7):1221-32. PubMed ID: 8001156
    [Abstract] [Full Text] [Related]

  • 11. Miranda couples oskar mRNA/Staufen complexes to the bicoid mRNA localization pathway.
    Irion U, Adams J, Chang CW, St Johnston D.
    Dev Biol; 2006 Sep 15; 297(2):522-33. PubMed ID: 16905128
    [Abstract] [Full Text] [Related]

  • 12. The CPEB translational regulator, Orb, functions together with Par proteins to polarize the Drosophila oocyte.
    Barr J, Charania S, Gilmutdinov R, Yakovlev K, Shidlovskii Y, Schedl P.
    PLoS Genet; 2019 Mar 15; 15(3):e1008012. PubMed ID: 30865627
    [Abstract] [Full Text] [Related]

  • 13. Oskar anchoring restricts pole plasm formation to the posterior of the Drosophila oocyte.
    Vanzo NF, Ephrussi A.
    Development; 2002 Aug 15; 129(15):3705-14. PubMed ID: 12117819
    [Abstract] [Full Text] [Related]

  • 14. Drosophila javelin-like encodes a novel microtubule-associated protein and is required for mRNA localization during oogenesis.
    Dubin-Bar D, Bitan A, Bakhrat A, Amsalem S, Abdu U.
    Development; 2011 Nov 15; 138(21):4661-71. PubMed ID: 21989913
    [Abstract] [Full Text] [Related]

  • 15. Localization, anchoring and translational control of oskar, gurken, bicoid and nanos mRNA during Drosophila oogenesis.
    Kugler JM, Lasko P.
    Fly (Austin); 2009 Nov 15; 3(1):15-28. PubMed ID: 19182536
    [Abstract] [Full Text] [Related]

  • 16. A stem-loop structure directs oskar mRNA to microtubule minus ends.
    Jambor H, Mueller S, Bullock SL, Ephrussi A.
    RNA; 2014 Apr 15; 20(4):429-39. PubMed ID: 24572808
    [Abstract] [Full Text] [Related]

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  • 18. 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]

  • 19. Pabp binds to the osk 3'UTR and specifically contributes to osk mRNA stability and oocyte accumulation.
    Vazquez-Pianzola P, Urlaub H, Suter B.
    Dev Biol; 2011 Sep 15; 357(2):404-18. PubMed ID: 21782810
    [Abstract] [Full Text] [Related]

  • 20. In vivo colocalisation of oskar mRNA and trans-acting proteins revealed by quantitative imaging of the Drosophila oocyte.
    Mhlanga MM, Bratu DP, Genovesio A, Rybarska A, Chenouard N, Nehrbass U, Olivo-Marin JC.
    PLoS One; 2009 Jul 14; 4(7):e6241. PubMed ID: 19597554
    [Abstract] [Full Text] [Related]

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