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 *

199 related articles for article (PubMed ID: 23948254)

  • 1. Oskar is targeted for degradation by the sequential action of Par-1, GSK-3, and the SCF⁻Slimb ubiquitin ligase.
    Morais-de-Sá E; Vega-Rioja A; Trovisco V; St Johnston D
    Dev Cell; 2013 Aug; 26(3):303-14. PubMed ID: 23948254
    [TBL] [Abstract][Full Text] [Related]  

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

  • 3. Receptor-mediated yolk uptake is required for oskar mRNA localization and cortical anchorage of germ plasm components in the Drosophila oocyte.
    Tanaka T; Tani N; Nakamura A
    PLoS Biol; 2021 Apr; 19(4):e3001183. PubMed ID: 33891588
    [TBL] [Abstract][Full Text] [Related]  

  • 4. An oskar-dependent positive feedback loop maintains the polarity of the Drosophila oocyte.
    Zimyanin V; Lowe N; St Johnston D
    Curr Biol; 2007 Feb; 17(4):353-9. PubMed ID: 17275299
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Slmb antagonises the aPKC/Par-6 complex to control oocyte and epithelial polarity.
    Morais-de-Sá E; Mukherjee A; Lowe N; St Johnston D
    Development; 2014 Aug; 141(15):2984-92. PubMed ID: 25053432
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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(3):e1008012. PubMed ID: 30865627
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The endocytic pathway acts downstream of Oskar in Drosophila germ plasm assembly.
    Tanaka T; Nakamura A
    Development; 2008 Mar; 135(6):1107-17. PubMed ID: 18272590
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 188(4):883-96. PubMed ID: 21625003
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Crumbs promotes expanded recognition and degradation by the SCF(Slimb/β-TrCP) ubiquitin ligase.
    Ribeiro P; Holder M; Frith D; Snijders AP; Tapon N
    Proc Natl Acad Sci U S A; 2014 May; 111(19):E1980-9. PubMed ID: 24778256
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Localization-dependent oskar protein accumulation; control after the initiation of translation.
    Braat AK; Yan N; Arn E; Harrison D; Macdonald PM
    Dev Cell; 2004 Jul; 7(1):125-31. PubMed ID: 15239960
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

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

  • 17. 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]  

  • 18. The SCF Slimb ubiquitin ligase regulates Plk4/Sak levels to block centriole reduplication.
    Rogers GC; Rusan NM; Roberts DM; Peifer M; Rogers SL
    J Cell Biol; 2009 Jan; 184(2):225-39. PubMed ID: 19171756
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Kinesin I-dependent cortical exclusion restricts pole plasm to the oocyte posterior.
    Cha BJ; Serbus LR; Koppetsch BS; Theurkauf WE
    Nat Cell Biol; 2002 Aug; 4(8):592-8. PubMed ID: 12134163
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The SCF ubiquitin ligase Slimb controls Nerfin-1 turnover in Drosophila.
    Lin X; Wang F; Li Y; Zhai C; Wang G; Zhang X; Gao Y; Yi T; Sun D; Wu S
    Biochem Biophys Res Commun; 2018 Jan; 495(1):629-633. PubMed ID: 29154825
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.