BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

218 related articles for article (PubMed ID: 9042857)

  • 1. An Egalitarian-BicaudalD complex is essential for oocyte specification and axis determination in Drosophila.
    Mach JM; Lehmann R
    Genes Dev; 1997 Feb; 11(4):423-35. PubMed ID: 9042857
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Egalitarian binds dynein light chain to establish oocyte polarity and maintain oocyte fate.
    Navarro C; Puthalakath H; Adams JM; Strasser A; Lehmann R
    Nat Cell Biol; 2004 May; 6(5):427-35. PubMed ID: 15077115
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Multiple Roles for Egalitarian in Polarization of the Drosophila Egg Chamber.
    Sanghavi P; Liu G; Veeranan-Karmegam R; Navarro C; Gonsalvez GB
    Genetics; 2016 May; 203(1):415-32. PubMed ID: 27017624
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The fusome and microtubules enrich Par-1 in the oocyte, where it effects polarization in conjunction with Par-3, BicD, Egl, and dynein.
    Vaccari T; Ephrussi A
    Curr Biol; 2002 Sep; 12(17):1524-8. PubMed ID: 12225669
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Optimal RNA binding by Egalitarian, a Dynein cargo adaptor, is critical for maintaining oocyte fate in
    Goldman CH; Neiswender H; Baker F; Veeranan-Karmegam R; Misra S; Gonsalvez GB
    RNA Biol; 2021 Dec; 18(12):2376-2389. PubMed ID: 33904382
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clathrin heavy chain plays multiple roles in polarizing the Drosophila oocyte downstream of Bic-D.
    Vazquez-Pianzola P; Adam J; Haldemann D; Hain D; Urlaub H; Suter B
    Development; 2014 May; 141(9):1915-26. PubMed ID: 24718986
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Dynein light chain-dependent dimerization of Egalitarian is essential for maintaining oocyte fate in Drosophila.
    Neiswender H; Goldman CH; Veeranan-Karmegam R; Gonsalvez GB
    Dev Biol; 2021 Oct; 478():76-88. PubMed ID: 34181915
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Conserved signals and machinery for RNA transport in Drosophila oogenesis and embryogenesis.
    Bullock SL; Ish-Horowicz D
    Nature; 2001 Dec; 414(6864):611-6. PubMed ID: 11740552
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The Egalitarian binding partners Dynein light chain and Bicaudal-D act sequentially to link mRNA to the Dynein motor.
    Goldman CH; Neiswender H; Veeranan-Karmegam R; Gonsalvez GB
    Development; 2019 Aug; 146(15):. PubMed ID: 31391195
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The mago nashi gene is required for the polarisation of the oocyte and the formation of perpendicular axes in Drosophila.
    Micklem DR; Dasgupta R; Elliott H; Gergely F; Davidson C; Brand A; González-Reyes A; St Johnston D
    Curr Biol; 1997 Jul; 7(7):468-78. PubMed ID: 9210377
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The role of BicD, Egl, Orb and the microtubules in the restriction of meiosis to the Drosophila oocyte.
    Huynh JR; St Johnston D
    Development; 2000 Jul; 127(13):2785-94. PubMed ID: 10851125
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A spectraplakin is enriched on the fusome and organizes microtubules during oocyte specification in Drosophila.
    Röper K; Brown NH
    Curr Biol; 2004 Jan; 14(2):99-110. PubMed ID: 14738730
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Centrosome migration into the Drosophila oocyte is independent of BicD and egl, and of the organisation of the microtubule cytoskeleton.
    Bolívar J; Huynh JR; López-Schier H; González C; St Johnston D; González-Reyes A
    Development; 2001 May; 128(10):1889-97. PubMed ID: 11311168
    [TBL] [Abstract][Full Text] [Related]  

  • 14. BicD-dependent localization processes: from Drosophilia development to human cell biology.
    Claussen M; Suter B
    Ann Anat; 2005 Nov; 187(5-6):539-53. PubMed ID: 16320833
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Drosophila par-1 is required for oocyte differentiation and microtubule organization.
    Cox DN; Lu B; Sun TQ; Williams LT; Jan YN
    Curr Biol; 2001 Jan; 11(2):75-87. PubMed ID: 11231123
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Bazooka and atypical protein kinase C are required to regulate oocyte differentiation in the Drosophila ovary.
    Cox DN; Seyfried SA; Jan LY; Jan YN
    Proc Natl Acad Sci U S A; 2001 Dec; 98(25):14475-80. PubMed ID: 11734648
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The mRNA transportome of the BicD/Egl transport machinery.
    Vazquez-Pianzola P; Schaller B; Colombo M; Beuchle D; Neuenschwander S; Marcil A; Bruggmann R; Suter B
    RNA Biol; 2017 Jan; 14(1):73-89. PubMed ID: 27801632
    [TBL] [Abstract][Full Text] [Related]  

  • 18. maelstrom is required for an early step in the establishment of Drosophila oocyte polarity: posterior localization of grk mRNA.
    Clegg NJ; Frost DM; Larkin MK; Subrahmanyan L; Bryant Z; Ruohola-Baker H
    Development; 1997 Nov; 124(22):4661-71. PubMed ID: 9409682
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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; 289(5487):2120-2. PubMed ID: 11000113
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Oocyte determination and the origin of polarity in Drosophila: the role of the spindle genes.
    González-Reyes A; Elliott H; St Johnston D
    Development; 1997 Dec; 124(24):4927-37. PubMed ID: 9362456
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.