220 related articles for article (PubMed ID: 19597554)
21. 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]
22. Myosin-V regulates oskar mRNA localization in the Drosophila oocyte.
Krauss J; López de Quinto S; Nüsslein-Volhard C; Ephrussi A
Curr Biol; 2009 Jun; 19(12):1058-63. PubMed ID: 19481457
[TBL] [Abstract][Full Text] [Related]
23. 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]
24. 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]
25. 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]
26. Dimerization of oskar 3' UTRs promotes hitchhiking for RNA localization in the Drosophila oocyte.
Jambor H; Brunel C; Ephrussi A
RNA; 2011 Dec; 17(12):2049-57. PubMed ID: 22028360
[TBL] [Abstract][Full Text] [Related]
27. Ooplasmic flow cooperates with transport and anchorage in
Lu W; Lakonishok M; Serpinskaya AS; Kirchenbüechler D; Ling SC; Gelfand VI
J Cell Biol; 2018 Oct; 217(10):3497-3511. PubMed ID: 30037924
[TBL] [Abstract][Full Text] [Related]
28. 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
[TBL] [Abstract][Full Text] [Related]
29. BREs mediate both repression and activation of oskar mRNA translation and act in trans.
Reveal B; Yan N; Snee MJ; Pai CI; Gim Y; Macdonald PM
Dev Cell; 2010 Mar; 18(3):496-502. PubMed ID: 20230756
[TBL] [Abstract][Full Text] [Related]
30. Dynein-dependent transport of nanos RNA in Drosophila sensory neurons requires Rumpelstiltskin and the germ plasm organizer Oskar.
Xu X; Brechbiel JL; Gavis ER
J Neurosci; 2013 Sep; 33(37):14791-800. PubMed ID: 24027279
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. 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]
33. Isolation of a ribonucleoprotein complex involved in mRNA localization in Drosophila oocytes.
Wilhelm JE; Mansfield J; Hom-Booher N; Wang S; Turck CW; Hazelrigg T; Vale RD
J Cell Biol; 2000 Feb; 148(3):427-40. PubMed ID: 10662770
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. 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]
36. Requirement for Drosophila cytoplasmic tropomyosin in oskar mRNA localization.
Erdélyi M; Michon AM; Guichet A; Glotzer JB; Ephrussi A
Nature; 1995 Oct; 377(6549):524-7. PubMed ID: 7566149
[TBL] [Abstract][Full Text] [Related]
37. 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; 79(7):1221-32. PubMed ID: 8001156
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. Comparative analysis of the kinetics and dynamics of K10, bicoid, and oskar mRNA localization in the Drosophila oocyte.
Karlin-Mcginness M; Serano TL; Cohen RS
Dev Genet; 1996; 19(3):238-48. PubMed ID: 8952066
[TBL] [Abstract][Full Text] [Related]
40. An interaction type of genetic screen reveals a role of the Rab11 gene in oskar mRNA localization in the developing Drosophila melanogaster oocyte.
Jankovics F; Sinka R; Erdélyi M
Genetics; 2001 Jul; 158(3):1177-88. PubMed ID: 11454766
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]