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 *

176 related articles for article (PubMed ID: 17151014)

  • 1. Oskar controls morphology of polar granules and nuclear bodies in Drosophila.
    Jones JR; Macdonald PM
    Development; 2007 Jan; 134(2):233-6. PubMed ID: 17151014
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 117(Pt 10):2109-20. PubMed ID: 15090597
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 42(7):112723. PubMed ID: 37384531
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Compartmentalized
    Eichler CE; Hakes AC; Hull B; Gavis ER
    Elife; 2020 Jan; 9():. PubMed ID: 31909715
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Drosophila tudor is essential for polar granule assembly and pole cell specification, but not for posterior patterning.
    Thomson T; Lasko P
    Genesis; 2004 Nov; 40(3):164-70. PubMed ID: 15495201
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Oskar protein interaction with Vasa represents an essential step in polar granule assembly.
    Breitwieser W; Markussen FH; Horstmann H; Ephrussi A
    Genes Dev; 1996 Sep; 10(17):2179-88. PubMed ID: 8804312
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Phase transitioned nuclear Oskar promotes cell division of
    Kistler KE; Trcek T; Hurd TR; Chen R; Liang FX; Sall J; Kato M; Lehmann R
    Elife; 2018 Sep; 7():. PubMed ID: 30260314
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Isolation of new polar granule components in Drosophila reveals P body and ER associated proteins.
    Thomson T; Liu N; Arkov A; Lehmann R; Lasko P
    Mech Dev; 2008; 125(9-10):865-73. PubMed ID: 18590813
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 185(8):1308-1324.e23. PubMed ID: 35325593
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Interspecific transplantation of polar plasm between Drosophila embryos.
    Mahowald AP; Illmensee K; Turner FR
    J Cell Biol; 1976 Aug; 70(2 pt 1):358-73. PubMed ID: 820700
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Targeting and anchoring Tudor in the pole plasm of the Drosophila oocyte.
    Anne J
    PLoS One; 2010 Dec; 5(12):e14362. PubMed ID: 21179512
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 129(14):3469-78. PubMed ID: 12091316
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 12(4):543-55. PubMed ID: 17419993
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mitochondrially encoded 16S large ribosomal RNA is concentrated in the posterior polar plasm of early Drosophila embryos but is not required for pole cell formation.
    Ding D; Whittaker KL; Lipshitz HD
    Dev Biol; 1994 Jun; 163(2):503-15. PubMed ID: 7515364
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 136(1):95-105. PubMed ID: 19036801
    [TBL] [Abstract][Full Text] [Related]  

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

  • 17. Aubergine encodes a Drosophila polar granule component required for pole cell formation and related to eIF2C.
    Harris AN; Macdonald PM
    Development; 2001 Jul; 128(14):2823-32. PubMed ID: 11526087
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 138(16):3431-40. PubMed ID: 21752933
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 444(1):98-103. PubMed ID: 24440702
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 17(5):558-68. PubMed ID: 25848747
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.