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PUBMED FOR HANDHELDS

Journal Abstract Search


178 related items for PubMed ID: 17151014

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  • 2. Live imaging of nuage and polar granules: evidence against a precursor-product relationship and a novel role for Oskar in stabilization of polar granule components.
    Snee MJ, Macdonald PM.
    J Cell Sci; 2004 Apr 15; 117(Pt 10):2109-20. PubMed ID: 15090597
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  • 3. Proteins rather than mRNAs regulate nucleation and persistence of Oskar germ granules in Drosophila.
    Curnutte HA, Lan X, Sargen M, Ao Ieong SM, Campbell D, Kim H, Liao Y, Lazar SB, Trcek T.
    Cell Rep; 2023 Jul 25; 42(7):112723. PubMed ID: 37384531
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  • 4. Compartmentalized oskar degradation in the germ plasm safeguards germline development.
    Eichler CE, Hakes AC, Hull B, Gavis ER.
    Elife; 2020 Jan 07; 9():. PubMed ID: 31909715
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  • 7. Phase transitioned nuclear Oskar promotes cell division of Drosophila primordial germ cells.
    Kistler KE, Trcek T, Hurd TR, Chen R, Liang FX, Sall J, Kato M, Lehmann R.
    Elife; 2018 Sep 27; 7():. PubMed ID: 30260314
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  • 9. Liquid-to-solid phase transition of oskar ribonucleoprotein granules is essential for their function in Drosophila embryonic development.
    Bose M, Lampe M, Mahamid J, Ephrussi A.
    Cell; 2022 Apr 14; 185(8):1308-1324.e23. PubMed ID: 35325593
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  • 12. poirot, a new regulatory gene of Drosophila oskar acts at the level of the short Oskar protein isoform.
    Sinka R, Jankovics F, Somogyi K, Szlanka T, Lukácsovich T, Erdélyi M.
    Development; 2002 Jul 14; 129(14):3469-78. PubMed ID: 12091316
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  • 13. Stimulation of endocytosis and actin dynamics by Oskar polarizes the Drosophila oocyte.
    Vanzo N, Oprins A, Xanthakis D, Ephrussi A, Rabouille C.
    Dev Cell; 2007 Apr 14; 12(4):543-55. PubMed ID: 17419993
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  • 15. The actin-binding protein Lasp promotes Oskar accumulation at the posterior pole of the Drosophila embryo.
    Suyama R, Jenny A, Curado S, Pellis-van Berkel W, Ephrussi A.
    Development; 2009 Jan 14; 136(1):95-105. PubMed ID: 19036801
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  • 16. 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 14; 75(3):246-55. PubMed ID: 17359300
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  • 17. Aubergine encodes a Drosophila polar granule component required for pole cell formation and related to eIF2C.
    Harris AN, Macdonald PM.
    Development; 2001 Jul 14; 128(14):2823-32. PubMed ID: 11526087
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  • 18. 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 14; 138(16):3431-40. PubMed ID: 21752933
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  • 19. Phylogenetic comparison of oskar mRNA localization signals.
    Kim J, Lee J, Lee S, Lee B, Kim-Ha J.
    Biochem Biophys Res Commun; 2014 Jan 31; 444(1):98-103. PubMed ID: 24440702
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  • 20. Independent and coordinate trafficking of single Drosophila germ plasm mRNAs.
    Little SC, Sinsimer KS, Lee JJ, Wieschaus EF, Gavis ER.
    Nat Cell Biol; 2015 May 31; 17(5):558-68. PubMed ID: 25848747
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