| scholarly article | Q13442814 |
| P50 | author | Paul Lasko | Q41780113 |
| P2093 | author name string | Oona Johnstone | |
| P433 | issue | 17 | |
| P407 | language of work or name | English | Q1860 |
| P1104 | number of pages | 12 | |
| P304 | page(s) | 4167-4178 | |
| P577 | publication date | 2004-07-27 | |
| P1433 | published in | Development | Q3025404 |
| P1476 | title | Interaction with eIF5B is essential for Vasa function during development. | |
| P478 | volume | 131 |
| Q48502782 | ---Pleiotropic Functions of the Chromodomain-Containing Protein Hat-trick During Oogenesis in Drosophila melanogaster. |
| Q34342503 | A conserved germline multipotency program |
| Q35128008 | A late phase of germ plasm accumulation during Drosophila oogenesis requires lost and rumpelstiltskin |
| Q43129108 | A strawberry notch homolog, let-765/nsh-1, positively regulates lin-3/egf expression to promote RAS-dependent vulval induction in C. elegans |
| Q36993929 | An unregulated regulator: Vasa expression in the development of somatic cells and in tumorigenesis |
| Q35775944 | Arginine methylation of RNA-binding proteins regulates cell function and differentiation |
| Q33707074 | Arginine methylation of vasa protein is conserved across phyla |
| Q47071418 | Belle is a Drosophila DEAD-box protein required for viability and in the germ line |
| Q34087911 | Building RNA-protein granules: insight from the germline |
| Q48090281 | C-terminal residues specific to Vasa among DEAD-box helicases are required for its functions in piRNA biogenesis and embryonic patterning |
| Q38208676 | DDX6 and its orthologs as modulators of cellular and viral RNA expression |
| Q24671865 | Dead-box proteins: a family affair--active and passive players in RNP-remodeling |
| Q36400263 | Drosophila RNA binding proteins. |
| Q91487558 | Drosophila pericentrin-like protein promotes the formation of primordial germ cells |
| Q47072339 | Drosophila tudor is essential for polar granule assembly and pole cell specification, but not for posterior patterning |
| Q42596663 | Eukaryotic translation initiation factor 5B activity regulates larval growth rate and germline development in Caenorhabditis elegans |
| Q36930579 | Evidence against a germ plasm in the milkweed bug Oncopeltus fasciatus, a hemimetabolous insect |
| Q35845505 | Gene expression analysis at the onset of sex differentiation in turbot (Scophthalmus maximus). |
| Q35907579 | Genome-wide analysis of the maternal-to-zygotic transition in Drosophila primordial germ cells |
| Q28072709 | Germ Plasm Biogenesis--An Oskar-Centric Perspective |
| Q34124431 | Germ cell specification and ovary structure in the rotifer Brachionus plicatilis |
| Q46447503 | Germ cell survival in C. elegans and C. remanei is affected when the DEAD box RNA helicases VBH-1 or Cre-VBH-1 are silenced |
| Q30586613 | Germ plasm anchoring is a dynamic state that requires persistent trafficking |
| Q36106690 | Germ plasm localisation of the HELICc of Vasa in Drosophila: analysis of domain sufficiency and amino acids critical for localisation |
| Q90044018 | Germline Maintenance Through the Multifaceted Activities of GLH/Vasa in Caenorhabditis elegans P Granules |
| Q39291698 | Human immunodeficiency virus type 1 Gag polyprotein modulates its own translation |
| Q35453337 | In vivo mapping of the functional regions of the DEAD-box helicase Vasa |
| Q30646761 | Independent and coordinate trafficking of single Drosophila germ plasm mRNAs |
| Q90622906 | Insights into Germline Development and Differentiation in Molluscs and Reptiles: The Use of Molecular Markers in the Study of Non-model Animals |
| Q52684479 | Investigating translation initiation using Drosophila molecular genetics. |
| Q36944982 | Isolation of new polar granule components in Drosophila reveals P body and ER associated proteins |
| Q36439815 | Long-term and short-term evolutionary impacts of transposable elements on Drosophila |
| Q36068739 | Mechanisms of translational regulation in Drosophila |
| Q35912441 | Modulation of gurken translation by insulin and TOR signaling in Drosophila |
| Q42680218 | Molecular cloning of vasa gene and the effects of LHRH-A on its expression in blue tilapia Oreochromis aureus |
| Q47988457 | Multiple Functions of the DEAD-Box Helicase Vasa in Drosophila Oogenesis |
| Q37419321 | New insights into the regulation of RNP granule assembly in oocytes |
| Q37940424 | Posttranscriptional regulation in Drosophila oocytes and early embryos |
| Q35578422 | RNA granules in germ cells |
| Q27025517 | RNA helicase proteins as chaperones and remodelers |
| Q33725475 | Regulation of Drosophila vasa in vivo through paralogous cullin-RING E3 ligase specificity receptors |
| Q28111696 | Regulation of translation initiation in eukaryotes: mechanisms and biological targets |
| Q34341796 | Repression of Gurken translation by a meiotic checkpoint in Drosophila oogenesis is suppressed by a reduction in the dose of eIF1A. |
| Q37548069 | Role of Eukaryotic Initiation Factors during Cellular Stress and Cancer Progression |
| Q36807747 | Roles of helicases in translation initiation: a mechanistic view |
| Q33576305 | The C. elegans sex determination gene laf-1 encodes a putative DEAD-box RNA helicase |
| Q33638256 | The DEAD Box RNA helicase VBH-1 is a new player in the stress response in C. elegans |
| Q47069323 | The DEAD box RNA helicase VBH-1 is required for germ cell function in C. elegans |
| Q33763607 | The LOTUS domain is a conserved DEAD-box RNA helicase regulator essential for the recruitment of Vasa to the germ plasm and nuage |
| Q27932287 | The highly conserved eukaryotic DRG factors are required for efficient translation in a manner redundant with the putative RNA helicase Slh1 |
| Q29547270 | The mechanism of eukaryotic translation initiation and principles of its regulation |
| Q35945702 | The molecular chaperone Hsp90 is required for mRNA localization in Drosophila melanogaster embryos |
| Q38850747 | The multiple functions of RNA helicases as drivers and regulators of gene expression. |
| Q37913259 | The multiple hats of Vasa: its functions in the germline and in cell cycle progression |
| Q34168375 | Translation initiation on mammalian mRNAs with structured 5'UTRs requires DExH-box protein DHX29. |
| Q42040692 | Translation of ASH1 mRNA is repressed by Puf6p-Fun12p/eIF5B interaction and released by CK2 phosphorylation |
| Q37726452 | Translational control during early development |
| Q38008495 | Translational control in cellular and developmental processes |
| Q35234622 | Translational control in oocyte development |
| Q36109314 | Tudor and its domains: germ cell formation from a Tudor perspective |
| Q48766537 | UAP56 RNA helicase is required for axis specification and cytoplasmic mRNA localization in Drosophila |
| Q36404136 | UAP56 couples piRNA clusters to the perinuclear transposon silencing machinery |
| Q47908672 | Vasa and the germ line lineage in a colonial urochordate |
| Q34960707 | Vasa genes: emerging roles in the germ line and in multipotent cells |
| Q37457970 | Vasa promotes Drosophila germline stem cell differentiation by activating mei-P26 translation by directly interacting with a (U)-rich motif in its 3' UTR. |
| Q37217595 | Vasa protein expression is restricted to the small micromeres of the sea urchin, but is inducible in other lineages early in development |
| Q34345035 | Zebrafish vasa is required for germ-cell differentiation and maintenance |
| Q37856199 | mRNA helicases: the tacticians of translational control |
| Q36329472 | mRNA localization and translational control in Drosophila oogenesis |
| Q36425494 | vasa is expressed in somatic cells of the embryonic gonad in a sex-specific manner in Drosophila melanogaster |
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