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 *

152 related articles for article (PubMed ID: 10415352)

  • 1. The actin cytoskeleton is required for maintenance of posterior pole plasm components in the Drosophila embryo.
    Lantz VA; Clemens SE; Miller KG
    Mech Dev; 1999 Jul; 85(1-2):111-22. PubMed ID: 10415352
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. A class VI unconventional myosin is associated with a homologue of a microtubule-binding protein, cytoplasmic linker protein-170, in neurons and at the posterior pole of Drosophila embryos.
    Lantz VA; Miller KG
    J Cell Biol; 1998 Feb; 140(4):897-910. PubMed ID: 9472041
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mutations in the Drosophila gene bullwinkle cause the formation of abnormal eggshell structures and bicaudal embryos.
    Rittenhouse KR; Berg CA
    Development; 1995 Sep; 121(9):3023-33. PubMed ID: 7555728
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Distinct mechanisms for mRNA localization during embryonic axis specification in the wasp Nasonia.
    Olesnicky EC; Desplan C
    Dev Biol; 2007 Jun; 306(1):134-42. PubMed ID: 17434472
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Live imaging of endogenous RNA reveals a diffusion and entrapment mechanism for nanos mRNA localization in Drosophila.
    Forrest KM; Gavis ER
    Curr Biol; 2003 Jul; 13(14):1159-68. PubMed ID: 12867026
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Dynamic Hsp83 RNA localization during Drosophila oogenesis and embryogenesis.
    Ding D; Parkhurst SM; Halsell SR; Lipshitz HD
    Mol Cell Biol; 1993 Jun; 13(6):3773-81. PubMed ID: 7684502
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Bazooka regulates microtubule organization and spatial restriction of germ plasm assembly in the Drosophila oocyte.
    Becalska AN; Gavis ER
    Dev Biol; 2010 Apr; 340(2):528-38. PubMed ID: 20152826
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Different genetic requirements for anterior RNA localization revealed by the distribution of Adducin-like transcripts during Drosophila oogenesis.
    Ding D; Parkhurst SM; Lipshitz HD
    Proc Natl Acad Sci U S A; 1993 Mar; 90(6):2512-6. PubMed ID: 7681599
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The molecular chaperone Hsp90 is required for mRNA localization in Drosophila melanogaster embryos.
    Song Y; Fee L; Lee TH; Wharton RP
    Genetics; 2007 Aug; 176(4):2213-22. PubMed ID: 17565952
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Oskar organizes the germ plasm and directs localization of the posterior determinant nanos.
    Ephrussi A; Dickinson LK; Lehmann R
    Cell; 1991 Jul; 66(1):37-50. PubMed ID: 2070417
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. Drosophila Mon2 couples Oskar-induced endocytosis with actin remodeling for cortical anchorage of the germ plasm.
    Tanaka T; Kato Y; Matsuda K; Hanyu-Nakamura K; Nakamura A
    Development; 2011 Jun; 138(12):2523-32. PubMed ID: 21610029
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Role of Adducin-like (hu-li tai shao) mRNA and protein localization in regulating cytoskeletal structure and function during Drosophila Oogenesis and early embryogenesis.
    Zaccai M; Lipshitz HD
    Dev Genet; 1996; 19(3):249-57. PubMed ID: 8952067
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The translational repressor Cup is required for germ cell development in Drosophila.
    Ottone C; Gigliotti S; Giangrande A; Graziani F; Verrotti di Pianella A
    J Cell Sci; 2012 Jul; 125(Pt 13):3114-23. PubMed ID: 22454519
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.