| P2093 | author name string | Laura S Salinas | |
| | Rosa E Navarro | |
| | Ernesto Maldonado | |
| | Ari Franco-Cea | |
| | Emmanuel Villanueva-Chimal | |
| | Laura I Láscarez-Lagunas | |
| P2860 | cites work | Ingestion of bacterially expressed dsRNAs can produce specific and potent genetic interference in Caenorhabditis elegans | Q29618535 |
| | Apoptosis maintains oocyte quality in aging Caenorhabditis elegans females | Q33389871 |
| | The C. elegans sex determination gene laf-1 encodes a putative DEAD-box RNA helicase | Q33576305 |
| | Perinuclear P granules are the principal sites of mRNA export in adult C. elegans germ cells | Q33761242 |
| | P granule assembly and function in Caenorhabditis elegans germ cells | Q34001356 |
| | Pathway to totipotency: lessons from germ cells | Q34585032 |
| | The PGL family proteins associate with germ granules and function redundantly in Caenorhabditis elegans germline development | Q34644841 |
| | Cytoplasmic partitioning of P granule components is not required to specify the germline in C. elegans | Q34773638 |
| | Multiple potential germ-line helicases are components of the germ-line-specific P granules of Caenorhabditis elegans | Q35932460 |
| | Immunofluorescence visualization of germ-line-specific cytoplasmic granules in embryos, larvae, and adults of Caenorhabditis elegans | Q36285245 |
| | Genetic analysis of the Caenorhabditis elegans GLH family of P-granule proteins | Q36571751 |
| | glh-1, a germ-line putative RNA helicase from Caenorhabditis, has four zinc fingers | Q36585340 |
| | Protection of specific maternal messenger RNAs by the P body protein CGH-1 (Dhh1/RCK) during Caenorhabditis elegans oogenesis | Q36817904 |
| | Maternal mRNAs are regulated by diverse P body-related mRNP granules during early Caenorhabditis elegans development | Q36817913 |
| | CGH-1 and the control of maternal mRNAs | Q37343239 |
| | The multiple hats of Vasa: its functions in the germline and in cell cycle progression | Q37913259 |
| | A comparative study of sperm morphology, cytology and activation in Caenorhabditis elegans, Caenorhabditis remanei and Caenorhabditis briggsae | Q40360679 |
| | Initiation of spermiogenesis in C. elegans: a pharmacological and genetic analysis | Q43618762 |
| | The unc-86 gene product couples cell lineage and cell identity in C. elegans | Q45300411 |
| | PGL-1, a predicted RNA-binding component of germ granules, is essential for fertility in C. elegans | Q47068903 |
| | The DEAD box RNA helicase VBH-1 is required for germ cell function in C. elegans | Q47069323 |
| | CED-1 is a transmembrane receptor that mediates cell corpse engulfment in C. elegans | Q47069350 |
| | Posterior localization of vasa protein correlates with, but is not sufficient for, pole cell development | Q47072288 |
| | Repression of gene expression in the embryonic germ lineage of C. elegans | Q47915934 |
| | Mutations in two independent pathways are sufficient to create hermaphroditic nematodes | Q48709223 |
| | Analyses of reproductive interactions that occur after heterospecific matings within the genus Caenorhabditis. | Q50717569 |
| | Interaction with eIF5B is essential for Vasa function during development. | Q50797471 |
| | Vesicle fusion, pseudopod extension and amoeboid motility are induced in nematode spermatids by the ionophore monensin | Q71140415 |
| | P granules in the germ cells of Caenorhabditis elegans adults are associated with clusters of nuclear pores and contain RNA | Q73492327 |
| | Stress-induced germ cell apoptosis by a p53 independent pathway in Caenorhabditis elegans | Q83855433 |
| | Bioinformatic analysis of P granule-related proteins: insights into germ granule evolution in nematodes | Q84373032 |
| P433 | issue | 11 | |
| P921 | main subject | Caenorhabditis elegans | Q91703 |
| P304 | page(s) | 801-818 | |
| P577 | publication date | 2012-07-11 | |
| P1433 | published in | Genesis | Q5532784 |
| P1476 | title | 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 | |
| P478 | volume | 50 | |