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Journal Abstract Search
309 related items for PubMed ID: 19036801
21. Drosophila tudor is essential for polar granule assembly and pole cell specification, but not for posterior patterning. Thomson T, Lasko P. Genesis; 2004 Nov; 40(3):164-70. PubMed ID: 15495201 [Abstract] [Full Text] [Related]
22. 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 [Abstract] [Full Text] [Related]
23. PKA-R1 spatially restricts Oskar expression for Drosophila embryonic patterning. Yoshida S, Müller HA, Wodarz A, Ephrussi A. Development; 2004 Mar; 131(6):1401-10. PubMed ID: 14993189 [Abstract] [Full Text] [Related]
25. Oskar is targeted for degradation by the sequential action of Par-1, GSK-3, and the SCF⁻Slimb ubiquitin ligase. Morais-de-Sá E, Vega-Rioja A, Trovisco V, St Johnston D. Dev Cell; 2013 Aug 12; 26(3):303-14. PubMed ID: 23948254 [Abstract] [Full Text] [Related]
33. Cup regulates oskar mRNA stability during oogenesis. Broyer RM, Monfort E, Wilhelm JE. Dev Biol; 2017 Jan 01; 421(1):77-85. PubMed ID: 27554167 [Abstract] [Full Text] [Related]
34. 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 01; 158(3):1177-88. PubMed ID: 11454766 [Abstract] [Full Text] [Related]
37. Mitochondrially encoded 16S large ribosomal RNA is concentrated in the posterior polar plasm of early Drosophila embryos but is not required for pole cell formation. Ding D, Whittaker KL, Lipshitz HD. Dev Biol; 1994 Jun 01; 163(2):503-15. PubMed ID: 7515364 [Abstract] [Full Text] [Related]