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Items: 1 to 20 of 125

1.

In vivo imaging of oskar mRNA transport reveals the mechanism of posterior localization.

Zimyanin VL, Belaya K, Pecreaux J, Gilchrist MJ, Clark A, Davis I, St Johnston D.

Cell. 2008 Sep 5;134(5):843-53. doi: 10.1016/j.cell.2008.06.053.

2.

Assembly of endogenous oskar mRNA particles for motor-dependent transport in the Drosophila oocyte.

Trucco A, Gaspar I, Ephrussi A.

Cell. 2009 Nov 25;139(5):983-98. doi: 10.1016/j.cell.2009.10.012. Retraction in: Trucco A, Gaspar I, Ephrussi A. Cell. 2010 Oct 29;143(3):485.

3.

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 6;154(3):511-23. Epub 2001 Jul 30.

4.
5.

An eIF4AIII-containing complex required for mRNA localization and nonsense-mediated mRNA decay.

Palacios IM, Gatfield D, St Johnston D, Izaurralde E.

Nature. 2004 Feb 19;427(6976):753-7.

PMID:
14973490
6.

Control of RNP motility and localization by a splicing-dependent structure in oskar mRNA.

Ghosh S, Marchand V, Gáspár I, Ephrussi A.

Nat Struct Mol Biol. 2012 Mar 18;19(4):441-9. doi: 10.1038/nsmb.2257.

PMID:
22426546
7.
8.

A function for kinesin I in the posterior transport of oskar mRNA and Staufen protein.

Brendza RP, Serbus LR, Duffy JB, Saxton WM.

Science. 2000 Sep 22;289(5487):2120-2.

9.

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. doi: 10.1261/rna.041566.113. Epub 2014 Feb 26.

10.

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.

PMID:
12134163
11.
12.

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 23;19(12):1058-63. doi: 10.1016/j.cub.2009.04.062. Epub 2009 May 28.

13.

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. doi: 10.1371/journal.pone.0006241.

14.

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. doi: 10.1242/dev.065029. Epub 2011 Jul 13.

16.

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.

17.

Dynein associates with oskar mRNPs and is required for their efficient net plus-end localization in Drosophila oocytes.

Sanghavi P, Laxani S, Li X, Bullock SL, Gonsalvez GB.

PLoS One. 2013 Nov 11;8(11):e80605. doi: 10.1371/journal.pone.0080605. eCollection 2013. Erratum in: PLoS One. 2014;9(1). doi:10.1371/annotation/1d5f32a4-54f6-4633-a8b4-f0fae0627507.

19.

Requirement for Drosophila cytoplasmic tropomyosin in oskar mRNA localization.

Erdélyi M, Michon AM, Guichet A, Glotzer JB, Ephrussi A.

Nature. 1995 Oct 12;377(6549):524-7.

PMID:
7566149
20.

Splicing of oskar RNA in the nucleus is coupled to its cytoplasmic localization.

Hachet O, Ephrussi A.

Nature. 2004 Apr 29;428(6986):959-63.

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