BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

201 related articles for article (PubMed ID: 38345426)

  • 41. orb is required for anteroposterior and dorsoventral patterning during Drosophila oogenesis.
    Christerson LB; McKearin DM
    Genes Dev; 1994 Mar; 8(5):614-28. PubMed ID: 7926753
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Rtnl1 is enriched in a specialized germline ER that associates with ribonucleoprotein granule components.
    Röper K
    J Cell Sci; 2007 Mar; 120(Pt 6):1081-92. PubMed ID: 17327273
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Localized Translation of gurken/TGF-α mRNA during Axis Specification Is Controlled by Access to Orb/CPEB on Processing Bodies.
    Davidson A; Parton RM; Rabouille C; Weil TT; Davis I
    Cell Rep; 2016 Mar; 14(10):2451-62. PubMed ID: 26947065
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Microtubules are a general component of mRNA localization systems in Drosophila oocytes.
    Pokrywka NJ; Stephenson EC
    Dev Biol; 1995 Jan; 167(1):363-70. PubMed ID: 7851657
    [TBL] [Abstract][Full Text] [Related]  

  • 45. 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]  

  • 46. Competition between kinesin-1 and myosin-V defines
    Lu W; Lakonishok M; Liu R; Billington N; Rich A; Glotzer M; Sellers JR; Gelfand VI
    Elife; 2020 Feb; 9():. PubMed ID: 32057294
    [TBL] [Abstract][Full Text] [Related]  

  • 47. 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]  

  • 48. Subcellular localization of Bic-D::GFP is linked to an asymmetric oocyte nucleus.
    Paré C; Suter B
    J Cell Sci; 2000 Jun; 113 ( Pt 12)():2119-27. PubMed ID: 10825285
    [TBL] [Abstract][Full Text] [Related]  

  • 49. 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]  

  • 50. Multiple cis-acting targeting sequences are required for orb mRNA localization during Drosophila oogenesis.
    Lantz V; Schedl P
    Mol Cell Biol; 1994 Apr; 14(4):2235-42. PubMed ID: 8139529
    [TBL] [Abstract][Full Text] [Related]  

  • 51. The Drosophila CPEB homolog, orb, is required for oskar protein expression in oocytes.
    Chang JS; Tan L; Schedl P
    Dev Biol; 1999 Nov; 215(1):91-106. PubMed ID: 10525352
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Physical interactions of Dmnk with Orb: implications in the regulated localization of Orb by Dmnk during oogenesis and embryogenesis.
    Iwai K; Oishi I; Xu XZ; Minami Y; Yamamura H
    Biochem Biophys Res Commun; 2002 Jan; 290(1):225-9. PubMed ID: 11779157
    [TBL] [Abstract][Full Text] [Related]  

  • 53. The Ovhts polyprotein is cleaved to produce fusome and ring canal proteins required for Drosophila oogenesis.
    Petrella LN; Smith-Leiker T; Cooley L
    Development; 2007 Feb; 134(4):703-12. PubMed ID: 17215303
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Drosophila javelin-like encodes a novel microtubule-associated protein and is required for mRNA localization during oogenesis.
    Dubin-Bar D; Bitan A; Bakhrat A; Amsalem S; Abdu U
    Development; 2011 Nov; 138(21):4661-71. PubMed ID: 21989913
    [TBL] [Abstract][Full Text] [Related]  

  • 55. 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]  

  • 56. A small predicted stem-loop structure mediates oocyte localization of Drosophila K10 mRNA.
    Serano TL; Cohen RS
    Development; 1995 Nov; 121(11):3809-18. PubMed ID: 8582290
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Mago Nashi, Tsunagi/Y14, and Ranshi form a complex that influences oocyte differentiation in Drosophila melanogaster.
    Lewandowski JP; Sheehan KB; Bennett PE; Boswell RE
    Dev Biol; 2010 Mar; 339(2):307-19. PubMed ID: 20045686
    [TBL] [Abstract][Full Text] [Related]  

  • 58. 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]  

  • 59. asunder is required for dynein localization and dorsal fate determination during Drosophila oogenesis.
    Sitaram P; Merkle JA; Lee E; Lee LA
    Dev Biol; 2014 Feb; 386(1):42-52. PubMed ID: 24333177
    [TBL] [Abstract][Full Text] [Related]  

  • 60. 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]  

    [Previous]   [Next]    [New Search]
    of 11.