| scholarly article | Q13442814 |
| P50 | author | Geraldine Seydoux | Q5549793 |
| Jennifer T Wang | Q56993329 | ||
| P2860 | cites work | A maternal factor unique to ascidians silences the germline via binding to P-TEFb and RNAP II regulation. | Q54572336 |
| Identification of genes required for cytoplasmic localization in early C. elegans embryos | Q68273724 | ||
| Segregation of germline granules in early embryos of Caenorhabditis elegans: an electron microscopic analysis | Q71233601 | ||
| Transformation of the germ line into muscle in mes-1 mutant embryos of C. elegans | Q71733931 | ||
| DNA replication defects delay cell division and disrupt cell polarity in early Caenorhabditis elegans embryos | Q73286817 | ||
| The Sm proteins regulate germ cell specification during early C. elegans embryogenesis | Q82264705 | ||
| PGL proteins self associate and bind RNPs to mediate germ granule assembly in C. elegans | Q24632882 | ||
| C. elegans PAR proteins function by mobilizing and stabilizing asymmetrically localized protein complexes | Q28265914 | ||
| The embryonic cell lineage of the nematode Caenorhabditis elegans | Q28271877 | ||
| On the control of germ cell development in Caenorhabditis elegans | Q28279917 | ||
| Integrative analysis of the Caenorhabditis elegans genome by the modENCODE project | Q28301622 | ||
| par-1, a gene required for establishing polarity in C. elegans embryos, encodes a putative Ser/Thr kinase that is asymmetrically distributed | Q28301842 | ||
| Asymmetric cell division and axis formation in the embryo | Q29306222 | ||
| Extracellular control of PAR protein localization during asymmetric cell division in the C. elegans embryo | Q30496455 | ||
| Internalization of multiple cells during C. elegans gastrulation depends on common cytoskeletal mechanisms but different cell polarity and cell fate regulators | Q30497921 | ||
| Repression of zygotic gene expression in the Xenopus germline | Q33684273 | ||
| The histone H3K36 methyltransferase MES-4 acts epigenetically to transmit the memory of germline gene expression to progeny. | Q33686906 | ||
| Translational repression: a duet of Nanos and Pumilio | Q33831344 | ||
| Identification of grandchildless loci whose products are required for normal germ-line development in the nematode Caenorhabditis elegans | Q33958810 | ||
| Phenotypic and molecular analysis of mes-3, a maternal-effect gene required for proliferation and viability of the germ line in C. elegans | Q33966270 | ||
| P granule assembly and function in Caenorhabditis elegans germ cells | Q34001356 | ||
| Pathway to totipotency: lessons from germ cells | Q34585032 | ||
| synMuv B proteins antagonize germline fate in the intestine and ensure C. elegans survival | Q34592502 | ||
| Molecular basis of RNA recognition by the embryonic polarity determinant MEX-5. | Q34607717 | ||
| Trans-generational epigenetic regulation of C. elegans primordial germ cells | Q34622455 | ||
| The PGL family proteins associate with germ granules and function redundantly in Caenorhabditis elegans germline development | Q34644841 | ||
| P granules extend the nuclear pore complex environment in the C. elegans germ line | Q34712466 | ||
| A spatial and temporal map of C. elegans gene expression | Q42588671 | ||
| Exclusion of germ plasm proteins from somatic lineages by cullin-dependent degradation | Q42745906 | ||
| SEPA-1 mediates the specific recognition and degradation of P granule components by autophagy in C. elegans. | Q43985030 | ||
| SRC-1 and Wnt signaling act together to specify endoderm and to control cleavage orientation in early C. elegans embryos | Q44057731 | ||
| The pie-1 and mex-1 genes and maternal control of blastomere identity in early C. elegans embryos | Q44058539 | ||
| Differential activation of the DNA replication checkpoint contributes to asynchrony of cell division in C. elegans embryos | Q44441589 | ||
| MEX-5 asymmetry in one-cell C. elegans embryos requires PAR-4- and PAR-1-dependent phosphorylation. | Q45211998 | ||
| C. elegans DAF-18/PTEN mediates nutrient-dependent arrest of cell cycle and growth in the germline. | Q46025317 | ||
| DYRK2 and GSK-3 phosphorylate and promote the timely degradation of OMA-1, a key regulator of the oocyte-to-embryo transition in C. elegans | Q46804755 | ||
| Polo kinases regulate C. elegans embryonic polarity via binding to DYRK2-primed MEX-5 and MEX-6. | Q46805083 | ||
| The MES-2/MES-3/MES-6 complex and regulation of histone H3 methylation in C. elegans | Q47068688 | ||
| Combinatorial RNA interference indicates GLH-4 can compensate for GLH-1; these two P granule components are critical for fertility in C. elegans. | Q47068814 | ||
| nos-1 and nos-2, two genes related to Drosophila nanos, regulate primordial germ cell development and survival in Caenorhabditis elegans | Q47068836 | ||
| PGL-1, a predicted RNA-binding component of germ granules, is essential for fertility in C. elegans | Q47068903 | ||
| pos-1 encodes a cytoplasmic zinc-finger protein essential for germline specification in C. elegans | Q47068917 | ||
| The Conserved Kinases CDK-1, GSK-3, KIN-19, and MBK-2 Promote OMA-1 Destruction to Regulate the Oocyte-to-Embryo Transition in C. elegans | Q47069086 | ||
| MEX-3 is a KH domain protein that regulates blastomere identity in early C. elegans embryos | Q47069183 | ||
| MEX-5 and MEX-6 function to establish soma/germline asymmetry in early C. elegans embryos | Q47069199 | ||
| Soma-germline asymmetry in the distributions of embryonic RNAs in Caenorhabditis elegans | Q47069204 | ||
| Coordinate activation of maternal protein degradation during the egg-to-embryo transition in C. elegans | Q47069248 | ||
| The maternal gene skn-1 encodes a protein that is distributed unequally in early C. elegans embryos | Q47069315 | ||
| MEP-1 and a homolog of the NURD complex component Mi-2 act together to maintain germline-soma distinctions in C. elegans | Q47069337 | ||
| A sex-determining gene, fem-1, required for both male and hermaphrodite development in Caenorhabditis elegans | Q47069368 | ||
| A novel function for the Sm proteins in germ granule localization during C. elegans embryogenesis | Q47069396 | ||
| The C. elegans MEX-1 protein is present in germline blastomeres and is a P granule component | Q47069423 | ||
| The PIE-1 protein and germline specification in C. elegans embryos | Q47069462 | ||
| Processing bodies and germ granules are distinct RNA granules that interact in C. elegans embryos | Q47069466 | ||
| The C. elegans DYRK Kinase MBK-2 Marks Oocyte Proteins for Degradation in Response to Meiotic Maturation | Q47069584 | ||
| Germline P granules are liquid droplets that localize by controlled dissolution/condensation | Q47748097 | ||
| Transcriptionally repressed germ cells lack a subpopulation of phosphorylated RNA polymerase II in early embryos of Caenorhabditis elegans and Drosophila melanogaster. | Q47912453 | ||
| Repression of gene expression in the embryonic germ lineage of C. elegans | Q47915934 | ||
| C. elegans meg-1 and meg-2 differentially interact with nanos family members to either promote or inhibit germ cell proliferation and survival. | Q50546213 | ||
| Translational repression restricts expression of the C. elegans Nanos homolog NOS-2 to the embryonic germline. | Q50652230 | ||
| Multiple RNA-binding proteins function combinatorially to control the soma-restricted expression pattern of the E3 ligase subunit ZIF-1. | Q51822757 | ||
| Epigenetic licensing of germline gene expression by maternal RNA in C. elegans. | Q51855441 | ||
| Ci-Pem-1 localizes to the nucleus and represses somatic gene transcription in the germline of Ciona intestinalis embryos. | Q51863412 | ||
| Somatic misexpression of germline P granules and enhanced RNA interference in retinoblastoma pathway mutants. | Q52043143 | ||
| Composition and dynamics of the Caenorhabditis elegans early embryonic transcriptome. | Q52110050 | ||
| PLK-1 asymmetry contributes to asynchronous cell division of C. elegans embryos. | Q53495600 | ||
| Cytoplasmic partitioning of P granule components is not required to specify the germline in C. elegans | Q34773638 | ||
| PIE-1 is a bifunctional protein that regulates maternal and zygotic gene expression in the embryonic germ line of Caenorhabditis elegans | Q35078092 | ||
| Transcriptional repression by the Caenorhabditis elegans germ-line protein PIE-1. | Q35186960 | ||
| Regulation of the MEX-5 gradient by a spatially segregated kinase/phosphatase cycle | Q35446919 | ||
| The Caenorhabditis elegans maternal-effect sterile proteins, MES-2, MES-3, and MES-6, are associated in a complex in embryos | Q35862584 | ||
| Localization and segregation of lineage-specific cleavage potential in embryos of Caenorhabditis elegans | Q36311940 | ||
| Inhibition of transcription by the Caenorhabditis elegans germline protein PIE-1: genetic evidence for distinct mechanisms targeting initiation and elongation | Q36391813 | ||
| MEG-1 and MEG-2 are embryo-specific P-granule components required for germline development in Caenorhabditis elegans | Q36391837 | ||
| Reversal of cellular polarity and early cell-cell interaction in the embryos of Caenorhabditis elegans | Q36467585 | ||
| PAR proteins direct asymmetry of the cell cycle regulators Polo-like kinase and Cdc25. | Q36491719 | ||
| 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 | ||
| MES-1, a protein required for unequal divisions of the germline in early C. elegans embryos, resembles receptor tyrosine kinases and is localized to the boundary between the germline and gut cells | Q36731904 | ||
| MRG-1, an autosome-associated protein, silences X-linked genes and protects germline immortality in Caenorhabditis elegans | Q36731912 | ||
| Regulation of the different chromatin states of autosomes and X chromosomes in the germ line of C. elegans | Q36731933 | ||
| MES-4: an autosome-associated histone methyltransferase that participates in silencing the X chromosomes in the C. elegans germ line. | Q36731942 | ||
| Germ versus soma decisions: lessons from flies and worms | Q36796578 | ||
| Segregation of germ granules in living Caenorhabditis elegans embryos: cell-type-specific mechanisms for cytoplasmic localisation | Q36797903 | ||
| Multiple maternal proteins coordinate to restrict the translation of C. elegans nanos-2 to primordial germ cells | Q36949298 | ||
| Specification of the germ line | Q37020491 | ||
| Germline genomics | Q37020708 | ||
| Germline chromatin | Q37020713 | ||
| Asymmetric enrichment of PIE-1 in the Caenorhabditis elegans zygote mediated by binary counterdiffusion | Q37124367 | ||
| Less is more: specification of the germline by transcriptional repression | Q37321822 | ||
| An eIF4E-binding protein regulates katanin protein levels in C. elegans embryos | Q37387856 | ||
| MAP kinase signaling antagonizes PAR-1 function during polarization of the early Caenorhabditis elegans embryo | Q37425052 | ||
| Transplantation of posterior polar plasm in Drosophila. Induction of germ cells at the anterior pole of the egg | Q37436465 | ||
| RNA recognition by the embryonic cell fate determinant and germline totipotency factor MEX-3. | Q37453506 | ||
| Translational control in the Caenorhabditis elegans germ line | Q38032806 | ||
| The oocyte-to-embryo transition | Q38032809 | ||
| PAR-2 is asymmetrically distributed and promotes association of P granules and PAR-1 with the cortex in C. elegans embryos | Q39758007 | ||
| Drosophila Pgc protein inhibits P-TEFb recruitment to chromatin in primordial germ cells | Q40024356 | ||
| RNA target specificity of the embryonic cell fate determinant POS-1. | Q41490235 | ||
| A conserved chromatin architecture marks and maintains the restricted germ cell lineage in worms and flies | Q41875362 | ||
| zif-1 translational repression defines a second, mutually exclusive OMA function in germline transcriptional repression | Q41942757 | ||
| Polarization of the C. elegans zygote proceeds via distinct establishment and maintenance phases | Q42149368 | ||
| Global transcriptional repression in C. elegans germline precursors by regulated sequestration of TAF-4 | Q42178390 | ||
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 17-39 | |
| P577 | publication date | 2013-01-01 | |
| P1433 | published in | Advances in Experimental Medicine and Biology | Q4686385 |
| P1476 | title | Germ cell specification | |
| P478 | volume | 757 |
| Q92487276 | A high-content imaging approach to profile C. elegans embryonic development |
| Q37016037 | A twist of fate: How a meiotic protein is providing new perspectives on germ cell development. |
| Q50091958 | Actomyosin contractility regulators stabilize the cytoplasmic bridge between the two primordial germ cells during Caenorhabditis elegans embryogenesis. |
| Q35392744 | Asymmetric transcript discovery by RNA-seq in C. elegans blastomeres identifies neg-1, a gene important for anterior morphogenesis. |
| Q30583153 | C. elegans Anillin proteins regulate intercellular bridge stability and germline syncytial organization |
| Q92740666 | Comparative Proteomics Reveal Me31B's Interactome Dynamics, Expression Regulation, and Assembly Mechanism into Germ Granules during Drosophila Germline Development |
| Q36000713 | Coupling between cytoplasmic concentration gradients through local control of protein mobility in the Caenorhabditis elegans zygote |
| Q38375486 | Cytoplasmic localization and asymmetric division in the early embryo of Caenorhabditis elegans |
| Q54200063 | Distinct chromatin organization in the germ line founder cell of the Caenorhabditis elegans embryo. |
| Q36012704 | Enrichment of H3K9me2 on Unsynapsed Chromatin in Caenorhabditis elegans Does Not Target de Novo Sites |
| Q26830468 | Introduction to germ cell development in Caenorhabditis elegans |
| Q37702564 | LET-418/Mi2 and SPR-5/LSD1 cooperatively prevent somatic reprogramming of C. elegans germline stem cells |
| Q57046164 | PIE-1 Translation in the Germline Lineage Contributes to PIE-1 Asymmetry in the Early Embryo |
| Q64928288 | Rapid diffusion-state switching underlies stable cytoplasmic gradients in the Caenorhabditis elegans zygote. |
| Q39150579 | Regulation of Cell Polarity by PAR-1/MARK Kinase |
| Q52904683 | Restricted distribution of mrg-1 mRNA in C. elegans primordial germ cells through germ granule-independent regulation. |
| Q34025612 | Temporal control over the initiation of cell motility by a regulator of G-protein signaling |
| Q47372758 | The Germline-Specific Factor OEF-1 Facilitates Coordinated Progression Through Germ Cell Development in Caenorhabditis elegans |
| Q27313726 | The specification and global reprogramming of histone epigenetic marks during gamete formation and early embryo development in C. elegans |
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