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Temporal and spatial regulation of translation in the mammalian oocyte via the mTOR–eIF4F pathway

https://doi.org/10.1038/ncomms7078
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/j.1460-2075.1992.tb05508.xopenalex-snapshot
mRNAs containing extensive secondary structure in their 5′ non‐coding region translate efficiently in cells overexpressing initiation factor eIF‐4E.
inferredcites →https://doi.org/10.1002/jcp.22171openalex-snapshot
Redistribution of mitochondria leads to bursts of ATP production during spontaneous mouse oocyte maturation
inferredcites →https://doi.org/10.1002/mrd.1080310402openalex-snapshot
U2 small nuclear RNA localization and expression during bovine preimplantation development
inferredcites →https://doi.org/10.1002/mrd.20368openalex-snapshot
Suppression of translation during in vitro maturation of pig oocytes despite enhanced formation of cap-binding protein complex eIF4F and 4E-BP1 hyperphosphorylation
inferredcites →https://doi.org/10.1002/mrd.20913openalex-snapshot
Regulation of cap‐dependent translation initiation in the early stage porcine parthenotes
inferredcites →https://doi.org/10.1006/excr.1999.4683openalex-snapshot
Ribosomal S6 Kinase Signaling and the Control of Translation
inferredcites →https://doi.org/10.1007/978-1-4615-6814-8_12openalex-snapshot
Informational Content of the Echinoderm Egg
inferredcites →https://doi.org/10.1007/978-1-61779-005-8_9openalex-snapshot
Tiny Molecular Beacons for in vivo mRNA Detection
inferredcites →https://doi.org/10.1007/s00412-002-0195-3openalex-snapshot
Simultaneous analysis of chromosomes and chromosome-associated proteins in mammalian oocytes and embryos
inferredcites →https://doi.org/10.1007/s00412-013-0437-6openalex-snapshot
Cell division: control of the chromosomal passenger complex in time and space
inferredcites →https://doi.org/10.1016/0012-1606(88)90135-2openalex-snapshot
Regulation of meiotic metaphase by a cytoplasmic maturation-promoting factor during mouse oocyte maturation
inferredcites →https://doi.org/10.1016/0092-8674(95)90325-9openalex-snapshot
Translational regulation in development
inferredcites →https://doi.org/10.1016/j.biocel.2010.09.018openalex-snapshot
Functions and regulation of the 70 kDa ribosomal S6 kinases
inferredcites →https://doi.org/10.1016/j.cell.2006.11.046openalex-snapshot
Small-Molecule Inhibition of the Interaction between the Translation Initiation Factors eIF4E and eIF4G
inferredcites →https://doi.org/10.1016/j.cell.2007.06.025openalex-snapshot
Self-Organization of MTOCs Replaces Centrosome Function during Acentrosomal Spindle Assembly in Live Mouse Oocytes
inferredcites →https://doi.org/10.1016/j.cell.2007.09.043openalex-snapshot
Splicing Segregation: The Minor Spliceosome Acts outside the Nucleus and Controls Cell Proliferation
inferredcites →https://doi.org/10.1016/j.cmet.2008.04.011openalex-snapshot
Dephosphorylation of Translation Initiation Factor 2α Enhances Glucose Tolerance and Attenuates Hepatosteatosis in Mice
inferredcites →https://doi.org/10.1016/j.devcel.2008.07.010openalex-snapshot
A Subcortical Maternal Complex Essential for Preimplantation Mouse Embryogenesis
inferredcites →https://doi.org/10.1016/j.devcel.2013.06.016openalex-snapshot
REEP3/4 Ensure Endoplasmic Reticulum Clearance from Metaphase Chromatin and Proper Nuclear Envelope Architecture
inferredcites →https://doi.org/10.1016/j.febslet.2008.10.023openalex-snapshot
Nucleophosmin is required for chromosome congression, proper mitotic spindle formation, and kinetochore‐microtubule attachment in HeLa cells
inferredcites →https://doi.org/10.1016/j.gene.2004.02.051openalex-snapshot
Cap-dependent and cap-independent translation in eukaryotic systems
inferredcites →https://doi.org/10.1016/j.tcb.2003.09.008openalex-snapshot
Spindle asymmetry: a compass for the cell
inferredcites →https://doi.org/10.1016/j.ydbio.2004.08.028openalex-snapshot
Major chromatin remodeling in the germinal vesicle (GV) of mammalian oocytes is dispensable for global transcriptional silencing but required for centromeric heterochromatin function
inferredcites →https://doi.org/10.1016/j.ydbio.2005.02.024openalex-snapshot
Oocyte nucleus controls progression through meiotic maturation
inferredcites →https://doi.org/10.1016/j.ydbio.2007.02.006openalex-snapshot
Changes in endoplasmic reticulum structure during mouse oocyte maturation are controlled by the cytoskeleton and cytoplasmic dynein
inferredcites →https://doi.org/10.1016/s0021-9258(18)33716-5openalex-snapshot
The phosphorylation of ribosomal protein S6 in rat tissues following cycloheximide injection, in diabetes, and after denervation of diaphragm. A simple immunological determination of the extent of S6 phosphorylation on protein blots.
inferredcites →https://doi.org/10.1016/s0378-1119(04)00142-8openalex-snapshot
Cap-dependent and cap-independent translation in eukaryotic systems
inferredcites →https://doi.org/10.1016/s0925-4773(97)00185-8openalex-snapshot
Localization of mRNAs to the oocyte is common in Drosophila ovaries
inferredcites →https://doi.org/10.1016/s0960-9822(01)00422-5openalex-snapshot
Cell cycle-dependent phosphorylation of the translational repressor eIF-4E binding protein-1 (4E-BP1)
inferredcites →https://doi.org/10.1016/s0960-9822(98)70152-6openalex-snapshot
Translation control: Connecting mitogens and the ribosome
inferredcites →https://doi.org/10.1017/s1355838201010433openalex-snapshot
IRES interaction with translation initiation factors: Functional characterization of novel RNA contacts with eIF3, eIF4B, and eIF4GII
inferredcites →https://doi.org/10.1038/235211a0openalex-snapshot
Oogenetic Origin of Messenger RNA for Embryonic Synthesis of Microtubule Proteins
inferredcites →https://doi.org/10.1038/nature03205openalex-snapshot
Regulation of cap-dependent translation by eIF4E inhibitory proteins
inferredcites →https://doi.org/10.1038/nature11083openalex-snapshot
A unifying model for mTORC1-mediated regulation of mRNA translation
inferredcites →https://doi.org/10.1038/ncb1183openalex-snapshot
Mammalian TOR complex 2 controls the actin cytoskeleton and is rapamycin insensitive
inferredcites →https://doi.org/10.1038/ncb1735openalex-snapshot
p53-Driven apoptosis limits centrosome amplification and genomic instability downstream of NPM1 phosphorylation
inferredcites →https://doi.org/10.1038/nmeth.1253openalex-snapshot
Imaging individual mRNA molecules using multiple singly labeled probes
inferredcites →https://doi.org/10.1038/nn.2580openalex-snapshot
In situ visualization and dynamics of newly synthesized proteins in rat hippocampal neurons
inferredcites →https://doi.org/10.1042/0264-6021:3440427openalex-snapshot
Mammalian target of rapamycin is a direct target for protein kinase B: identification of a convergence point for opposing effects of insulin and amino-acid deficiency on protein translation
inferredcites →https://doi.org/10.1042/bc20040067openalex-snapshot
Putting RNAs in the right place at the right time: RNA localization in the frog oocyte
inferredcites →https://doi.org/10.1046/j.1432-1033.2002.03291.xopenalex-snapshot
Does phosphorylation of the cap‐binding protein eIF4E play a role in translation initiation?
inferredcites →https://doi.org/10.1046/j.1460-9568.2003.02712.xopenalex-snapshot
Bursts of high‐frequency stimulation trigger rapid delivery of pre‐existing α‐CaMKII mRNA to synapses: a mechanism in dendritic protein synthesis during long‐term potentiation in adult awake rats
inferredcites →https://doi.org/10.1073/pnas.051623398openalex-snapshot
Internal initiation of translation of five dendritically localized neuronal mRNAs
inferredcites →https://doi.org/10.1073/pnas.1219126110openalex-snapshot
Mechanistic basis of infertility of mouse intersubspecific hybrids
inferredcites →https://doi.org/10.1073/pnas.1303781110openalex-snapshot
Human eIF4E promotes mRNA restructuring by stimulating eIF4A helicase activity
inferredcites →https://doi.org/10.1073/pnas.91.16.7668openalex-snapshot
Chromatographic resolution of in vivo phosphorylated and nonphosphorylated eukaryotic translation initiation factor eIF-4E: increased cap affinity of the phosphorylated form.
inferredcites →https://doi.org/10.1074/jbc.270.24.14597openalex-snapshot
Phosphorylation of Eukaryotic Protein Synthesis Initiation Factor 4E at Ser-209
inferredcites →https://doi.org/10.1074/jbc.270.38.22077openalex-snapshot
Regulation of Gene Expression at the Beginning of Mammalian Development
inferredcites →https://doi.org/10.1074/jbc.m300435200openalex-snapshot
Mitotic Regulation of Ribosomal S6 Kinase 1 Involves Ser/Thr, Pro Phosphorylation of Consensus and Non-consensus Sites by Cdc2
inferredcites →https://doi.org/10.1074/jbc.m501707200openalex-snapshot
Phosphorylation of Mammalian Target of Rapamycin (mTOR) at Ser-2448 IsMediated by p70S6 Kinase
inferredcites →https://doi.org/10.1083/jcb.200806118openalex-snapshot
Deconstructing Survivin: comprehensive genetic analysis of Survivin function by conditional knockout in a vertebrate cell line
inferredcites →https://doi.org/10.1083/jcb.201211068openalex-snapshot
Sequential actin-based pushing forces drive meiosis I chromosome migration and symmetry breaking in oocytes
inferredcites →https://doi.org/10.1093/biolreprod/7.3.341openalex-snapshot
Incorporation of Amino Acids During Maturation In Vitro by the Mouse Oocyte: Effect of Puromycin on Protein Synthesis
inferredcites →https://doi.org/10.1093/emboj/16.12.3693openalex-snapshot
Rapamycin suppresses 5′TOP mRNA translation through inhibition of p70s6k
inferredcites →https://doi.org/10.1093/nar/22.24.5255openalex-snapshot
Intron-less RNA injected into the nucleus of Xenopus oocytes accesses a regulated translation control pathway
inferredcites →https://doi.org/10.1093/nar/gkn248openalex-snapshot
Comprehensive detection of human terminal oligo-pyrimidine (TOP) genes and analysis of their characteristics
inferredcites →https://doi.org/10.1095/biolreprod.102.004606openalex-snapshot
Germinal Vesicle Material Is Essential for Nucleus Remodeling after Nuclear Transfer1
inferredcites →https://doi.org/10.1095/biolreprod.109.082057openalex-snapshot
P-Body Loss Is Concomitant with Formation of a Messenger RNA Storage Domain in Mouse Oocytes1
inferredcites →https://doi.org/10.1095/biolreprod66.5.1274openalex-snapshot
Regulation of Translation During In Vitro Maturation of Bovine Oocytes: The Role of MAP Kinase, eIF4E (Cap Binding Protein) Phosphorylation, and eIF4E-BP11
inferredcites →https://doi.org/10.1101/gad.13.11.1422openalex-snapshot
Regulation of 4E-BP1 phosphorylation: a novel two-step mechanism
inferredcites →https://doi.org/10.1101/gad.827500openalex-snapshot
Bub3 gene disruption in mice reveals essential mitotic spindle checkpoint function during early embryogenesis
inferredcites →https://doi.org/10.1101/gad.887201openalex-snapshot
Regulation of translation initiation by FRAP/mTOR
inferredcites →https://doi.org/10.1111/j.1432-1033.1982.tb06565.xopenalex-snapshot
Rapid Alterations in Initiation Rate and Recruitment of Inactive RNA Are Temporally Correlated with S6 Phosphorylation
inferredcites →https://doi.org/10.1126/science.1176488openalex-snapshot
Subcellular mRNA Localization in Animal Cells and Why It Matters
inferredcites →https://doi.org/10.1126/science.1231197openalex-snapshot
Translational Repression and eIF4A2 Activity Are Critical for MicroRNA-Mediated Gene Regulation
inferredcites →https://doi.org/10.1126/science.1236566openalex-snapshot
mTORC1 Phosphorylation Sites Encode Their Sensitivity to Starvation and Rapamycin
inferredcites →https://doi.org/10.1128/mcb.15.9.4990openalex-snapshot
The Translation Initiation Factor eIF-4E Binds to a Common Motif Shared by the Translation Factor eIF-4γ and the Translational Repressors 4E-Binding Proteins
inferredcites →https://doi.org/10.1128/mcb.18.1.334openalex-snapshot
A Novel Functional Human Eukaryotic Translation Initiation Factor 4G
inferredcites →https://doi.org/10.1186/1471-2164-8-39openalex-snapshot
A screen for nuclear transcripts identifies two linked noncoding RNAs associated with SC35 splicing domains
inferredcites →https://doi.org/10.1242/dev.090589openalex-snapshot
Molecular causes of aneuploidy in mammalian eggs
inferredcites →https://doi.org/10.1242/dev.129.2.517openalex-snapshot
Rab11 polarization of theDrosophilaoocyte: a novel link between membrane trafficking, microtubule organization, andoskarmRNA localization and translation
inferredcites →https://doi.org/10.1242/dev.89.supplement.333openalex-snapshot
Inductive interactions in early amphibian development and their general nature
inferredcites →https://doi.org/10.1242/jcs.128744openalex-snapshot
Biased inheritance of mitochondria during asymmetric cell division in the mouse oocyte
inferredcites →https://doi.org/10.1242/jcs.39.1.63openalex-snapshot
Origin and spatial distribution of maternal messenger rna during oogenesis of an insect, Oncopeltus fasciatus
inferredcites →https://doi.org/10.1371/journal.pone.0000242openalex-snapshot
Epigenetic Activation of a Subset of mRNAs by eIF4E Explains Its Effects on Cell Proliferation
inferredcites →https://doi.org/10.1371/journal.pone.0007701openalex-snapshot
Bub3 Is a Spindle Assembly Checkpoint Protein Regulating Chromosome Segregation during Mouse Oocyte Meiosis
inferredcites →https://doi.org/10.1534/genetics.113.154005openalex-snapshot
Association of Maternal mRNA and Phosphorylated EIF4EBP1 Variants With the Spindle in Mouse Oocytes: Localized Translational Control Supporting Female Meiosis in Mammals
inferredcites →https://doi.org/10.4161/cc.21398openalex-snapshot
Lack of response to unaligned chromosomes in mammalian female gametes
inferredcites →https://doi.org/10.4161/cc.21770openalex-snapshot
4E-BP1 participates in maintaining spindle integrity and genomic stability via interacting with PLK1
inferredcites →https://doi.org/10.4161/cc.3.11.1203openalex-snapshot
Distinct Dynamics of Aurora B and Survivin During Mitosis
inferredcites →https://doi.org/10.4161/fly.3.1.7751openalex-snapshot
Localization, anchoring and translational control of oskar , gurken , bicoid and nanos mRNA during Drosophila oogenesis

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4635259openalex-extracted
Spatial Distribution of Maternal Factors in Pig Mature Oocytes
inferred← citeshttps://doi.org/10.1002/1873-3468.13721openalex-snapshot
Cyclin‐dependent kinase 4 inhibits the translational repressor 4E‐BP1 to promote cap‐dependent translation during mitosis–G1 transition
inferred← citeshttps://doi.org/10.1002/1873-3468.70080openalex-snapshot
Molecular insights into RNA recognition by the ZAR1 C‐terminal domain
inferred← citeshttps://doi.org/10.1002/advs.201900295openalex-snapshot
RNA‐Binding Protein IGF2BP2/IMP2 is a Critical Maternal Activator in Early Zygotic Genome Activation
inferred← citeshttps://doi.org/10.1002/advs.202205500openalex-snapshot
Selective Translation of Maternal mRNA by eIF4E1B Controls Oocyte to Embryo Transition
inferred← citeshttps://doi.org/10.1002/aro2.53openalex-snapshot
Roles of sphingosine‐1‐phosphate in follicle development and oocyte maturation
inferred← citeshttps://doi.org/10.1002/cbf.4099openalex-snapshot
Targeting polo‐like kinase 1 to treat kidney diseases
inferred← citeshttps://doi.org/10.1002/mrd.22967openalex-snapshot
Meeting the meiotic challenge: Specializations in mammalian oocyte spindle formation
inferred← citeshttps://doi.org/10.1002/mrd.23676openalex-snapshot
Preimplantation embryo gene expression: 56 years of discovery, and counting
inferred← citeshttps://doi.org/10.1002/wdev.294openalex-snapshot
Regulation of germ cell development by intercellular signaling in the mammalian ovarian follicle
inferred← citeshttps://doi.org/10.1007/978-1-0716-4658-8_5openalex-snapshot
RNA-Fluorescence In Situ Hybridization for the Detection of RNA in Mammalian Oocytes and Embryos
inferred← citeshttps://doi.org/10.1007/978-3-319-60855-6_12openalex-snapshot
Translational Regulation in the Mammalian Oocyte
inferred← citeshttps://doi.org/10.1007/978-3-319-60855-6_2openalex-snapshot
Control of Mammalian Oocyte Development by Interactions with the Maternal Follicular Environment
inferred← citeshttps://doi.org/10.1007/s00018-019-03280-5openalex-snapshot
The CRL4-DCAF13 ubiquitin E3 ligase supports oocyte meiotic resumption by targeting PTEN degradation
inferred← citeshttps://doi.org/10.1007/s00441-015-2269-6openalex-snapshot
Translation in the mammalian oocyte in space and time
inferred← citeshttps://doi.org/10.1007/s10815-016-0788-zopenalex-snapshot
The subcortical maternal complex: multiple functions for one biological structure?
inferred← citeshttps://doi.org/10.1007/s10815-026-03863-9openalex-snapshot
The role of mTOR signaling in regulating the quality of mammalian oocytes
inferred← citeshttps://doi.org/10.1007/s11427-025-3260-6openalex-snapshot
CPEB1 orchestrates cell cycle-dependent translation of maternal factors to coordinate nuclear-cytoplasmic maturation in porcine oocytes
inferred← citeshttps://doi.org/10.1016/b978-0-12-813570-9.00009-7openalex-snapshot
RNA Binding Protein Networks and Translational Regulation in Oocytes
inferred← citeshttps://doi.org/10.1016/b978-0-12-813570-9.00010-3openalex-snapshot
Translational Regulation of Gene Expression During Oogenesis and Preimplantation Embryo Development
inferred← citeshttps://doi.org/10.1016/j.envpol.2020.115382openalex-snapshot
Maternal Bisphenol S exposure affects the reproductive capacity of F1 and F2 offspring in mice
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.138827openalex-snapshot
The GPER is an important factor through which somatic cells regulate oocyte maternal mRNA translation and developmental competence
inferred← citeshttps://doi.org/10.1016/j.jmb.2021.167166openalex-snapshot
Single Molecule RNA Localization and Translation in the Mammalian Oocyte and Embryo
inferred← citeshttps://doi.org/10.1016/j.mad.2025.112129openalex-snapshot
Causes and consequences of chromosomal cohesin loss: Novel insights for mechanisms of aging-related oocyte aneuploidy
inferred← citeshttps://doi.org/10.1016/j.reprotox.2019.12.005openalex-snapshot
Acute low-dose bisphenol S exposure affects mouse oocyte quality
inferred← citeshttps://doi.org/10.1016/j.semcdb.2023.03.003openalex-snapshot
A genome-wide perspective of the maternal mRNA translation program during oocyte development
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2023.06.017openalex-snapshot
Maternal Kdm2a-mediated PI3K/Akt signaling and E-cadherin stimulate the morula-to-blastocyst transition revealing crucial roles in early embryonic development
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2026.117876openalex-snapshot
IP3R1 regulates AMPK-mTOR-mediated mitochondrial function to influence the oocyte-to-embryo transition of porcine
inferred← citeshttps://doi.org/10.1016/j.tibs.2025.05.004openalex-snapshot
Proteostasis in cellular dormancy: lessons from yeast to oocytes
inferred← citeshttps://doi.org/10.1016/j.ydbio.2019.01.008openalex-snapshot
Zebrafish embryogenesis – A framework to study regulatory RNA elements in development and disease
inferred← citeshttps://doi.org/10.1017/s0967199422000478openalex-snapshot
In vivo and in vitro matured bovine oocytes present a distinct pattern of single-cell gene expression
inferred← citeshttps://doi.org/10.1038/s41419-022-05415-2openalex-snapshot
SphK-produced S1P in somatic cells is indispensable for LH-EGFR signaling-induced mouse oocyte maturation
inferred← citeshttps://doi.org/10.1038/s41540-019-0089-0openalex-snapshot
Novel insights into gene expression regulation during meiosis revealed by translation elongation dynamics
inferred← citeshttps://doi.org/10.1038/s41598-017-00570-5openalex-snapshot
Bisphenol S negatively affects the meotic maturation of pig oocytes
inferred← citeshttps://doi.org/10.1038/s41598-018-25187-0openalex-snapshot
CNOT6 regulates a novel pattern of mRNA deadenylation during oocyte meiotic maturation
inferred← citeshttps://doi.org/10.1038/s41598-018-26345-0openalex-snapshot
Using Single Molecule mRNA Fluorescent in Situ Hybridization (RNA-FISH) to Quantify mRNAs in Individual Murine Oocytes and Embryos
inferred← citeshttps://doi.org/10.1038/s41598-019-49483-5openalex-snapshot
Spatio-temporal expression of ANK2 promotes cytokinesis in oocytes
inferred← citeshttps://doi.org/10.1038/s41598-020-61689-6openalex-snapshot
Investigating the role of BCAR4 in ovarian physiology and female fertility by genome editing in rabbit
inferred← citeshttps://doi.org/10.1038/s42003-025-08214-5openalex-snapshot
UBE2V1 governs aging induced protein aggregation and developmental defects in oocytes and embryos
inferred← citeshttps://doi.org/10.1080/10495398.2024.2394692openalex-snapshot
Spatial distribution of maternal factors in pig mature oocytes
inferred← citeshttps://doi.org/10.1080/15384101.2017.1295178openalex-snapshot
Regulation of 4E-BP1 activity in the mammalian oocyte
inferred← citeshttps://doi.org/10.1080/15384101.2017.1304732openalex-snapshot
Translation regulator ballet in meiotic spindle
inferred← citeshttps://doi.org/10.1080/15476286.2021.1880181openalex-snapshot
ncRNA BC1 influences translation in the oocyte
inferred← citeshttps://doi.org/10.1083/jcb.202011153openalex-snapshot
Loss of centromeric RNA activates the spindle assembly checkpoint in mammalian female meiosis I
inferred← citeshttps://doi.org/10.1093/biolre/ioy254openalex-snapshot
Inhibition of Skp1-Cullin-F-box complexes during bovine oocyte maturation and preimplantation development leads to delayed development of embryos†
inferred← citeshttps://doi.org/10.1093/biolre/ioz012openalex-snapshot
A story of birth and death: mRNA translation and clearance at the onset of maternal-to-zygotic transition in mammals†
inferred← citeshttps://doi.org/10.1093/biolre/ioz117openalex-snapshot
Follicle-stimulating hormone administration affects amino acid metabolism in mammalian oocytes†
inferred← citeshttps://doi.org/10.1093/humupd/dmx040openalex-snapshot
Acquisition of oocyte competence to develop as an embryo: integrated nuclear and cytoplasmic events
inferred← citeshttps://doi.org/10.1093/molehr/gaad021openalex-snapshot
Specific processing of meiosis-related transcript is linked to final maturation in human oocytes
inferred← citeshttps://doi.org/10.1093/molehr/gaae023openalex-snapshot
Single-cell proteomics reveals decreased abundance of proteostasis and meiosis proteins in advanced maternal age oocytes
inferred← citeshttps://doi.org/10.1093/nar/gkaa010openalex-snapshot
Genome-wide analysis reveals a switch in the translational program upon oocyte meiotic resumption
inferred← citeshttps://doi.org/10.1093/nar/gkab431openalex-snapshot
Oocyte meiosis-coupled poly(A) polymerase α phosphorylation and activation trigger maternal mRNA translation in mice
inferred← citeshttps://doi.org/10.1093/nar/gkad996openalex-snapshot
The translational oscillation in oocyte and early embryo development
inferred← citeshttps://doi.org/10.1093/nar/gkz1239openalex-snapshot
The most abundant maternal lncRNA Sirena1 acts post-transcriptionally and impacts mitochondrial distribution
inferred← citeshttps://doi.org/10.1093/nar/gkz863openalex-snapshot
ZAR1 and ZAR2 are required for oocyte meiotic maturation by regulating the maternal transcriptome and mRNA translational activation
inferred← citeshttps://doi.org/10.1098/rsob.230081openalex-snapshot
Spatial positioning of preimplantation mouse embryo cells is regulated by mTORC1 and m 7 G-cap-dependent translation at the 8- to 16-cell transition
inferred← citeshttps://doi.org/10.1101/2023.03.07.531473openalex-snapshot
Spatial positioning of preimplantation mouse embryo blastomeres is regulated by mTORC1 and 7mG-cap dependent translation at the 8- to 16-cell transition
inferred← citeshttps://doi.org/10.1101/2024.01.17.575938openalex-snapshot
Multiple intersecting pathways are involved in the phosphorylation of CPEB1 to activate translation during mouse oocyte meiosis
inferred← citeshttps://doi.org/10.1101/2024.03.15.585321openalex-snapshot
N-acetyltransferase 10-mediated mRNA N4-acetylation is Essential for the Translational Regulation During Oocyte Meiotic Maturation in Mice
inferred← citeshttps://doi.org/10.1111/acel.13231openalex-snapshot
Age‐related differences in the translational landscape of mammalian oocytes
inferred← citeshttps://doi.org/10.1111/brv.12937openalex-snapshot
Spatiotemporal regulation of maternal mRNAs during vertebrate oocyte meiotic maturation
inferred← citeshttps://doi.org/10.1126/sciadv.adp5163openalex-snapshot
NAT10-mediated mRNA N 4 -acetylation is essential for the translational regulation during oocyte meiotic maturation in mice
inferred← citeshttps://doi.org/10.1152/ajpcell.00075.2017openalex-snapshot
PLK1 regulates spindle association of phosphorylated eukaryotic translation initiation factor 4E-binding protein and spindle function in mouse oocytes
inferred← citeshttps://doi.org/10.1152/ajpcell.00385.2020openalex-snapshot
mTORC1/2 signaling is downregulated by amino acid-free culture of mouse preimplantation embryos and is only partially restored by amino acid readdition
inferred← citeshttps://doi.org/10.11606/t.74.2023.tde-07122023-103830openalex-snapshot
Estudo sobre os efeitos de diferentes sistemas de maturação >i /i< na progressão meiótica, expressão gênica e comunicação em complexos >i /i<-oócitos bovinos
inferred← citeshttps://doi.org/10.1186/s12958-022-00972-9openalex-snapshot
IGF2 reduces meiotic defects in oocytes from obese mice and improves embryonic developmental competency
inferred← citeshttps://doi.org/10.1186/s12964-024-01976-1openalex-snapshot
PGC7 regulates maternal mRNA translation via AKT1-YBX1 interactions in mouse oocytes
inferred← citeshttps://doi.org/10.1242/dev.190793openalex-snapshot
Regulation of the mammalian maternal-to-embryonic transition by eukaryotic translation initiation factor 4E
inferred← citeshttps://doi.org/10.1242/dev.201572openalex-snapshot
PATL2 regulates mRNA homeostasis in oocytes by interacting with EIF4E and CPEB1
inferred← citeshttps://doi.org/10.1242/jcs.249128openalex-snapshot
Changes in subcellular structures and states of pumilio 1 regulate the translation of target Mad2 and cyclin B1 mRNAs
inferred← citeshttps://doi.org/10.1242/jcs.260787openalex-snapshot
The role of metabolism in cellular quiescence
inferred← citeshttps://doi.org/10.1371/journal.pcbi.1014342openalex-snapshot
Data-driven model reveals increased stability of CAG-expanded huntingtin RNA due to MID1 binding
inferred← citeshttps://doi.org/10.1371/journal.pone.0192544openalex-snapshot
Localization of RNA and translation in the mammalian oocyte and embryo
inferred← citeshttps://doi.org/10.14712/fb2017063010006openalex-snapshot
Dynamics of Lamins B and A/C and Nucleoporin Nup160 during Meiotic Maturation in Mouse Oocytes
inferred← citeshttps://doi.org/10.18632/aging.103126openalex-snapshot
The effect of rapamycin on bovine oocyte maturation success and metaphase telomere length maintenance
inferred← citeshttps://doi.org/10.18632/aging.202214openalex-snapshot
IGF2 improves the developmental competency and meiotic structure of oocytes from aged mice
inferred← citeshttps://doi.org/10.21769/bioprotoc.1666openalex-snapshot
Single Molecule RNA FISH in the Mammalian Oocyte
inferred← citeshttps://doi.org/10.21769/bioprotoc.1729openalex-snapshot
Mouse Oocyte Isolation, Cultivation and RNA Microinjection
inferred← citeshttps://doi.org/10.22074/cellj.2016.4717openalex-snapshot
Effects of Mono-(2-Ethylhexyl) Phthalate and Di-(2-Ethylhexyl) Phthalate Administrations on Oocyte Meiotic Maturation, Apoptosis and Gene Quantification in Mouse Model.
inferred← citeshttps://doi.org/10.3389/fcell.2021.710186openalex-snapshot
The Dynamic Regulation of mRNA Translation and Ribosome Biogenesis During Germ Cell Development and Reproductive Aging
inferred← citeshttps://doi.org/10.3389/fcell.2021.735684openalex-snapshot
Molecular Features of Polycystic Ovary Syndrome Revealed by Transcriptome Analysis of Oocytes and Cumulus Cells
inferred← citeshttps://doi.org/10.3389/fendo.2019.00692openalex-snapshot
Role of mTOR Signaling in Female Reproduction
inferred← citeshttps://doi.org/10.3389/fendo.2021.702446openalex-snapshot
Interplay Between mTOR and Hippo Signaling in the Ovary: Clinical Choice Guidance Between Different Gonadotropin Preparations for Better IVF
inferred← citeshttps://doi.org/10.3390/ani16142125openalex-snapshot
Changes in Ras and Ras-Associated GTPases During Maturation of Porcine Cumulus Cells and Oocytes
inferred← citeshttps://doi.org/10.3390/antiox14081018openalex-snapshot
Peritoneal Fluid Modulates Redox Balance and RNA Integrity in Mouse Oocytes: Insights into Endometriosis-Related Oxidative Stress
inferred← citeshttps://doi.org/10.3390/biomedicines10071689openalex-snapshot
An Interplay between Epigenetics and Translation in Oocyte Maturation and Embryo Development: Assisted Reproduction Perspective
inferred← citeshttps://doi.org/10.3390/cells12010187openalex-snapshot
Multiple Roles of PLK1 in Mitosis and Meiosis
inferred← citeshttps://doi.org/10.3390/cells12141830openalex-snapshot
A Role of PI3K/Akt Signaling in Oocyte Maturation and Early Embryo Development
inferred← citeshttps://doi.org/10.3390/cells13100850openalex-snapshot
CPEB3 Maintains Developmental Competence of the Oocyte
inferred← citeshttps://doi.org/10.3390/cells13221898openalex-snapshot
A Novel Method to Profile Transcripts Encoding SH2 Domains in the Patiria miniata Mature Egg Transcriptome
inferred← citeshttps://doi.org/10.3390/cells9030662openalex-snapshot
Diversity of RNA-Binding Proteins Modulating Post-Transcriptional Regulation of Protein Expression in the Maturing Mammalian Oocyte
inferred← citeshttps://doi.org/10.3390/cells9071568openalex-snapshot
Role of Cyclin-Dependent Kinase 1 in Translational Regulation in the M-Phase
inferred← citeshttps://doi.org/10.3390/ijms19030698openalex-snapshot
Importance of ERK1/2 in Regulation of Protein Translation during Oocyte Meiosis
inferred← citeshttps://doi.org/10.3390/ijms19092841openalex-snapshot
Increased Expression of Maturation Promoting Factor Components Speeds Up Meiosis in Oocytes from Aged Females
inferred← citeshttps://doi.org/10.3390/ijms21041254openalex-snapshot
Identifying the Translatome of Mouse NEBD-Stage Oocytes via SSP-Profiling; A Novel Polysome Fractionation Method
inferred← citeshttps://doi.org/10.3390/ijms26136390openalex-snapshot
Molecular Guardians of Oocyte Maturation: A Systematic Review on TUBB8, KIF11, and CKAP5 in IVF Outcomes
inferred← citeshttps://doi.org/10.3390/ijms27156789openalex-snapshot
Regulation of Translation by PKA Signaling Pathway
inferred← citeshttps://doi.org/10.3724/abbs.2024195openalex-snapshot
Advances in PIWI-piRNA function in female reproduction in mammals
inferred← citeshttps://doi.org/10.5713/ajas.15.0762openalex-snapshot
Rapamycin Influences the Efficiency of In vitro Fertilization and Development in the Mouse: A Role for Autophagic Activation
inferred← citeshttps://doi.org/10.6084/m9.figshare.20317792openalex-snapshot
Additional file 1 of IGF2 reduces meiotic defects in oocytes from obese mice and improves embryonic developmental competency
inferred← citeshttps://doi.org/10.6084/m9.figshare.20317795openalex-snapshot
Additional file 2 of IGF2 reduces meiotic defects in oocytes from obese mice and improves embryonic developmental competency
inferred← citeshttps://doi.org/10.6084/m9.figshare.20317798openalex-snapshot
Additional file 3 of IGF2 reduces meiotic defects in oocytes from obese mice and improves embryonic developmental competency
inferred← citeshttps://doi.org/10.64898/2026.09.29.755503openalex-snapshot
Declining ribosome function limits oocyte longevity
inferred← citeshttps://doi.org/10.70675/50dcbc65z5250z415fz8052z2a6b330aa810openalex-snapshot
Activité traductionnelle et dynamique mitotique induites par la fécondation chez l’oursin
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