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Microtubule and chromatin behavior follow MAP kinase activity but not MPF activity during meiosis in mouse oocytes
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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.1460-2075.1991.tb07809.xopenalex-snapshot
Xenopus M phase MAP kinase: isolation of its cDNA and activation by MPF.
inferredcites →https://doi.org/10.1002/j.1460-2075.1991.tb08021.xopenalex-snapshot
Identification of the regulatory phosphorylation sites in pp42/mitogen‐activated protein kinase (MAP kinase).
inferredcites →https://doi.org/10.1002/j.1460-2075.1992.tb05136.xopenalex-snapshot
Xenopus MAP kinase activator: identification and function as a key intermediate in the phosphorylation cascade.
inferredcites →https://doi.org/10.1002/j.1460-2075.1992.tb05271.xopenalex-snapshot
MAP kinase activator from insulin‐stimulated skeletal muscle is a protein threonine/tyrosine kinase.
inferredcites →https://doi.org/10.1002/j.1460-2075.1992.tb05490.xopenalex-snapshot
Activation of p42 MAP kinase and the release of oocytes from cell cycle arrest.
inferredcites →https://doi.org/10.1002/j.1460-2075.1993.tb05847.xopenalex-snapshot
The c‐mos proto‐oncogene protein kinase turns on and maintains the activity of MAP kinase, but not MPF, in cell‐free extracts of Xenopus oocytes and eggs.
inferredcites →https://doi.org/10.1002/jez.1401770202openalex-snapshot
Cytoplasmic control of nuclear behavior during meiotic maturation of frog oocytes
inferredcites →https://doi.org/10.1002/jez.1402260217openalex-snapshot
Parthenogenetic activation of mouse oocytes in vitro with ethanol and benzyl alcohol
inferredcites →https://doi.org/10.1006/dbio.1993.1192openalex-snapshot
MAP Kinase Becomes Stably Activated at Metaphase and Is Associated with Microtubule-Organizing Centers during Meiotic Maturation of Mouse Oocytes
inferredcites →https://doi.org/10.1016/0012-1606(89)90279-0openalex-snapshot
Mouse oocytes gradually develop the capacity for activation during the metaphase II arrest
inferredcites →https://doi.org/10.1016/0014-4827(88)90121-8openalex-snapshot
6-Dimethylaminopurine blocks starfish oocyte maturation by inhibiting a relevant protein kinase activity
inferredcites →https://doi.org/10.1016/0092-8674(89)90509-6openalex-snapshot
A putative protein kinase overcomes pheromone-induced arrest of cell cycling in S. cerevisiae
inferredcites →https://doi.org/10.1016/0092-8674(90)90668-5openalex-snapshot
FUS3 encodes a cdc2+/CDC28-related kinase required for the transition from mitosis into conjugation
inferredcites →https://doi.org/10.1016/0092-8674(91)90098-jopenalex-snapshot
ERKs: A family of protein-serine/threonine kinases that are activated and tyrosine phosphorylated in response to insulin and NGF
inferredcites →https://doi.org/10.1016/0955-0674(93)90104-xopenalex-snapshot
MAP kinase and the activation of quiescent cells
inferredcites →https://doi.org/10.1016/0955-0674(93)90112-4openalex-snapshot
A conserved kinase cascade for MAP kinase activation in yeast
inferredcites →https://doi.org/10.1016/s0021-9258(19)49722-6openalex-snapshot
Purification and characterization of mitogen-activated protein kinase activator(s) from epidermal growth factor-stimulated A431 cells.
inferredcites →https://doi.org/10.1038/227680a0openalex-snapshot
Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
inferredcites →https://doi.org/10.1038/342512a0openalex-snapshot
The c-mos proto-oncogene product is a cytostatic factor responsible for meiotic arrest in vertebrate eggs
inferredcites →https://doi.org/10.1038/343233a0openalex-snapshot
Regulation of microtubule dynamics by cdc2 protein kinase in cell-free extracts of Xenopus eggs
inferredcites →https://doi.org/10.1038/343651a0openalex-snapshot
Requirement for integration of signals from two distinct phosphorylation pathways for activation of MAP kinase
inferredcites →https://doi.org/10.1038/349251a0openalex-snapshot
In vitro effects on microtubule dynamics of purified Xenopus M phase-activated MAP kinase
inferredcites →https://doi.org/10.1073/pnas.88.14.6142openalex-snapshot
Microtubule-associated protein 2 kinases, ERK1 and ERK2, undergo autophosphorylation on both tyrosine and threonine residues: implications for their mechanism of activation.
inferredcites →https://doi.org/10.1083/jcb.118.5.1097openalex-snapshot
Control of microtubule dynamics and length by cyclin A- and cyclin B-dependent kinases in Xenopus egg extracts.
inferredcites →https://doi.org/10.1091/mbc.2.12.965openalex-snapshot
Extracellular signal-regulated kinases: ERKs in progress.
inferredcites →https://doi.org/10.1111/j.1440-169x.1991.00543.xopenalex-snapshot
The Role of “Cytostatic Factor (CSF)” in the Control of Oocyte Cell Cycles: A Summary of 20 Years of Study
inferredcites →https://doi.org/10.1126/science.1313186openalex-snapshot
Requirements for Phosphorylation of Map Kinase During Meiosis in Xenopus Oocytes
inferredcites →https://doi.org/10.1126/science.2164259openalex-snapshot
An Insulin-Stimulated Protein Kinase Similar to Yeast Kinases Involved in Cell Cycle Control
inferredcites →https://doi.org/10.1126/science.8235656openalex-snapshot
Induction of metaphase arrest in cleaving Xenopus embryos by MAP kinase
inferredcites →https://doi.org/10.1128/mcb.11.4.1965openalex-snapshot
Cell cycle tyrosine phosphorylation of p34cdc2 and a microtubule-associated protein kinase homolog in Xenopus oocytes and eggs.
inferredcites →https://doi.org/10.1128/mcb.11.5.2517openalex-snapshot
Tyrosine Phosphorylation and Activation of Homologous Protein Kinases during Oocyte Maturation and Mitogenic Activation of Fibroblasts
inferredcites →https://doi.org/10.1128/mcb.13.4.2546openalex-snapshot
Mos stimulates MAP kinase in Xenopus oocytes and activates a MAP kinase kinase in vitro.
inferredcites →https://doi.org/10.1128/mcb.13.5.3067openalex-snapshot
A Yeast Mitogen-Activated Protein Kinase Homolog (Mpk1p) Mediates Signalling by Protein Kinase C
inferredcites →https://doi.org/10.1242/jcs.102.3.457openalex-snapshot
Cell cycle modification during the transitions between meiotic M-phases in mouse oocytes
inferredcites →https://doi.org/10.1242/jcs.104.3.861openalex-snapshot
Inhibition of protein kinases by 6-dimethylaminopurine accelerates the transition to interphase in activated mouse oocytes
inferredcites →https://doi.org/10.1387/ijdb.8398674openalex-snapshot
Full activation of the rat oocyte by protein synthesis inhibition requires protein phosphatase activity
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.4137330openalex-extracted
Cloning and Functional Analysis of Mapkapk2 in Hyriopsis Cumingii
inferred← citeshttps://doi.org/10.1002/(sici)1097-010x(19991015)285:3<226::aid-jez5>3.0.co;2-zopenalex-snapshot
The ins and outs of meiosis
inferred← citeshttps://doi.org/10.1002/(sici)1098-2795(199602)43:2<248::aid-mrd14>3.0.co;2-#openalex-snapshot
Microtubule and microfilament dynamics in porcine oocytes during meiotic maturation
inferred← citeshttps://doi.org/10.1002/(sici)1098-2795(199608)44:4<486::aid-mrd8>3.0.co;2-hopenalex-snapshot
Synchronization of cell division in eight-cell bovine embryos produced in vitro: Effects of nocodazole
inferred← citeshttps://doi.org/10.1002/(sici)1098-2795(199611)45:3<351::aid-mrd12>3.0.co;2-1openalex-snapshot
Mitogen-activated protein kinase activity during goat oocyte maturation and the acquisition of meiotic competence
inferred← citeshttps://doi.org/10.1002/(sici)1098-2795(199703)46:3<325::aid-mrd11>3.0.co;2-yopenalex-snapshot
In vivo aging of oocytes influences the behavior of nuclei transferred to enucleated rabbit oocytes
inferred← citeshttps://doi.org/10.1002/(sici)1098-2795(199711)48:3<397::aid-mrd14>3.0.co;2-topenalex-snapshot
On cyclins, oocytes, and eggs
inferred← citeshttps://doi.org/10.1002/(sici)1098-2795(199802)49:2<176::aid-mrd8>3.0.co;2-mopenalex-snapshot
Tyrosyl-phosphorylated proteins are involved in regulation of meiosis in the rat egg
inferred← citeshttps://doi.org/10.1002/(sici)1098-2795(199806)50:2<221::aid-mrd13>3.0.co;2-9openalex-snapshot
Microtubule and chromatin organization during the first cell-cycle following intracytoplasmic injection of round spermatid into porcine oocytes
inferred← citeshttps://doi.org/10.1002/(sici)1098-2795(199807)50:3<251::aid-mrd1>3.0.co;2-iopenalex-snapshot
p34cdc2 expression and meiotic competence in growing goat oocytes
inferred← citeshttps://doi.org/10.1002/(sici)1098-2795(199903)52:3<310::aid-mrd9>3.0.co;2-copenalex-snapshot
MAP kinase activity is downregulated by phorbol ester during mouse oocyte maturation and egg activation in vitro
inferred← citeshttps://doi.org/10.1002/(sici)1098-2795(200006)56:2<155::aid-mrd6>3.0.co;2-1openalex-snapshot
Interaction of cell cycle kinases, microtubules, and chromatin in ascidian oocytes during meiosis
inferred← citeshttps://doi.org/10.1002/(sici)1521-1878(199910)21:10<833::aid-bies5>3.0.co;2-popenalex-snapshot
Xenopus oocyte maturation: new lessons from a good egg
inferred← citeshttps://doi.org/10.1002/(sici)1521-1878(200001)22:1<57::aid-bies10>3.0.co;2-lopenalex-snapshot
Egg timers: how is developmental time measured in the early vertebrate embryo?
inferred← citeshttps://doi.org/10.1002/1098-2795(200012)57:4<353::aid-mrd7>3.0.co;2-ropenalex-snapshot
Low oxygen tension during in vitro maturation is beneficial for supporting the subsequent development of bovine cumulus-oocyte complexes
inferred← citeshttps://doi.org/10.1002/1098-2795(200101)58:1<101::aid-mrd13>3.0.co;2-jopenalex-snapshot
Protein kinase C and meiotic regulation in isolated mouse oocytes
inferred← citeshttps://doi.org/10.1002/1098-2795(200101)58:1<69::aid-mrd10>3.0.co;2-oopenalex-snapshot
Colocalization of CaM KII and MAP kinase on architectural elements of the mouse egg: Potentiation of MAP kinase activity by CaM KII
inferred← citeshttps://doi.org/10.1002/3527600906.mcb.200300099openalex-snapshot
Cellular Interactions
inferred← citeshttps://doi.org/10.1002/9780470687970.ch12openalex-snapshot
The Control of the Metaphase‐to‐Anaphase Transition in Meiosis I
inferred← citeshttps://doi.org/10.1002/9780470687970.ch3openalex-snapshot
Clytia hemisphaerica: A Cnidarian Model for Studying Oogenesis
inferred← citeshttps://doi.org/10.1002/bies.950190106openalex-snapshot
Synthesis and function of mos: The control switch of vertebrate oocyte meiosis
inferred← citeshttps://doi.org/10.1002/bies.950190107openalex-snapshot
PKC ‐ A pivotal regulator of early development
inferred← citeshttps://doi.org/10.1002/jcb.26184openalex-snapshot
Role of Mitogen Activated Protein Kinase and Maturation Promoting Factor During the Achievement of Meiotic Competency in Mammalian Oocytes
inferred← citeshttps://doi.org/10.1002/jcp.22108openalex-snapshot
Meiotic cell cycle arrest in mammalian oocytes
inferred← citeshttps://doi.org/10.1002/mrd.10072openalex-snapshot
Association of MPF, MAPK, and nuclear progression dynamics during activation of young and aged bovine oocytes*
inferred← citeshttps://doi.org/10.1002/mrd.1012openalex-snapshot
Mitogen activated protein kinase plays a significant role in metaphase II arrest, spindle morphology, and maintenance of maturation promoting factor activity in bovine oocytes
inferred← citeshttps://doi.org/10.1002/mrd.10163openalex-snapshot
Effects of β‐endorphin and Naloxone on in vitro maturation of bovine oocytes
inferred← citeshttps://doi.org/10.1002/mrd.10176openalex-snapshot
Chromosome condensation in pig oocytes: Lack of a requirement for either cdc2 kinase or MAP kinase activity
inferred← citeshttps://doi.org/10.1002/mrd.1022openalex-snapshot
Cytoplasmic changes in relation to nuclear maturation and early embryo developmental potential of porcine oocytes: Effects of gonadotropins, cumulus cells, follicular size, and protein synthesis inhibition*
inferred← citeshttps://doi.org/10.1002/mrd.10233openalex-snapshot
Chromatin configuration and transcriptional control in human and mouse oocytes
inferred← citeshttps://doi.org/10.1002/mrd.10285openalex-snapshot
Asynchronous cytoplast and karyoplast transplantation reveals that the cytoplasm determines the developmental fate of the nucleus in mouse oocytes
inferred← citeshttps://doi.org/10.1002/mrd.1080410106openalex-snapshot
Mitogen‐activated protein (MAP) kinase during the acquisition of meiotic competence by growing oocytes of the mouse
inferred← citeshttps://doi.org/10.1002/mrd.1080410212openalex-snapshot
Cytoskeletal organization in the oocyte, zygote, and early cleaving embryo of the stripe‐faced dunnart (Sminthopsis macroura)
inferred← citeshttps://doi.org/10.1002/mrd.1086openalex-snapshot
Organisation of the cytoskeleton during in vitro maturation of horse oocytes
inferred← citeshttps://doi.org/10.1002/mrd.1113openalex-snapshot
Microtubule assembly after treatment of pig oocytes with taxol: Correlation with chromosomes, γ‐tubulin, and MAP kinase*
inferred← citeshttps://doi.org/10.1002/mrd.20062openalex-snapshot
Chromatin, microtubules, and kinases activities during meiotic resumption in bitch oocytes
inferred← citeshttps://doi.org/10.1002/mrd.20216openalex-snapshot
Meiotic maternal chromosomes introduced to the late mouse zygote are recruited to later embryonic divisions
inferred← citeshttps://doi.org/10.1002/mrd.20232openalex-snapshot
Effects of MAP kinase pathway and other factors on meiosis ofUrechis unicinctus eggs
inferred← citeshttps://doi.org/10.1002/mrd.20267openalex-snapshot
Effects of duration, concentration, and timing of ionomycin and 6‐dimethylaminopurine (6‐DMAP) treatment on activation of goat oocytes
inferred← citeshttps://doi.org/10.1002/mrd.20332openalex-snapshot
Parthenogenetic and nuclear transfer rabbit embryo development and apoptosis after activation treatments
inferred← citeshttps://doi.org/10.1002/mrd.20432openalex-snapshot
Effect of maturation stage at cryopreservation on post‐thaw cytoskeleton quality and fertilizability of equine oocytes
inferred← citeshttps://doi.org/10.1002/mrd.20725openalex-snapshot
Effects of pre‐treating in vitro‐matured bovine oocytes with the cytoskeleton stabilizing agent taxol prior to vitrification
inferred← citeshttps://doi.org/10.1002/mrd.20891openalex-snapshot
MEK1/2 is a critical regulator of microtubule assembly and spindle organization during rat oocyte meiotic maturation
inferred← citeshttps://doi.org/10.1002/mrd.21385openalex-snapshot
Rat eggs cannot wait: Spontaneous exit from meiotic metaphase‐II arrest
inferred← citeshttps://doi.org/10.1002/mrd.23045openalex-snapshot
Stress‐induced alterations in oocyte transcripts are further expressed in the developing blastocyst
inferred← citeshttps://doi.org/10.1002/mrd.23637openalex-snapshot
Regulation of oocyte maturation: Role of conserved ERK signaling
inferred← citeshttps://doi.org/10.1002/smll.202500221openalex-snapshot
Atomic Force Microscopy Reveals Differences In Mechanical Properties Linked To Cortical Structure In Mouse And Human Oocytes
inferred← citeshttps://doi.org/10.1006/bbrc.2000.3052openalex-snapshot
The Role of RhoA in the Germinal Vesicle Breakdown of Mouse Oocytes
inferred← citeshttps://doi.org/10.1006/bbrc.2001.5381openalex-snapshot
The Role of Tissue Transglutaminase in the Germinal Vesicle Breakdown of Mouse Oocytes
inferred← citeshttps://doi.org/10.1006/dbio.1998.8930openalex-snapshot
Cytostatic Activity Develops during Meiosis I in Oocytes of LT/Sv Mice
inferred← citeshttps://doi.org/10.1006/dbio.1998.8981openalex-snapshot
MAP Kinase Inactivation Is Required Only for G2–M Phase Transition in Early Embryogenesis Cell Cycles of the StarfishesMarthasterias glacialisandAstropecten aranciacus
inferred← citeshttps://doi.org/10.1006/dbio.1998.9109openalex-snapshot
On the Control of Oocyte Meiotic Maturation and Ovulation inCaenorhabditis elegans
inferred← citeshttps://doi.org/10.1006/dbio.1999.9468openalex-snapshot
MAP Kinase, Meiosis, and Sperm Centrosome Suppression in Urechis caupo
inferred← citeshttps://doi.org/10.1006/dbio.2000.9656openalex-snapshot
Characterization of Polo-like Kinase 1 during Meiotic Maturation of the Mouse Oocyte
inferred← citeshttps://doi.org/10.1006/dbio.2000.9669openalex-snapshot
The Control of Cyclin B1 mRNA Translation during Mouse Oocyte Maturation
inferred← citeshttps://doi.org/10.1006/dbio.2000.9762openalex-snapshot
Functional and Molecular Reorganization of the Nucleolar Apparatus in Maturing Mouse Oocytes
inferred← citeshttps://doi.org/10.1006/dbio.2001.0188openalex-snapshot
Meiotic Maturation of the Mouse Oocyte Requires an Equilibrium between Cyclin B Synthesis and Degradation
inferred← citeshttps://doi.org/10.1006/dbio.2001.0311openalex-snapshot
Evidence That Protein Kinase C (PKC) Participates in the Meiosis I to Meiosis II Transition in Mouse Oocytes
inferred← citeshttps://doi.org/10.1006/dbio.2002.0601openalex-snapshot
Interaction of the Essential Drosophila Nuclear Protein YA with P0/AP3 in the Cytoplasm and in Vitro: Implications for Developmental Regulation of YA's Subcellular Location
inferred← citeshttps://doi.org/10.1006/dbio.2002.0680openalex-snapshot
Inhibition of MEK or cdc2 Kinase Parthenogenetically Activates Mouse Eggs and Yields the Same Phenotypes as Mos−/− Parthenogenotes
inferred← citeshttps://doi.org/10.1006/dbio.2002.0853openalex-snapshot
Discrimination of the Roles of MPF and MAP Kinase in Morphological Changes That Occur during Oocyte Maturation
inferred← citeshttps://doi.org/10.1007/978-1-4419-1436-1_44openalex-snapshot
Evaluation and Selection of Preimplantation Embryos for Transfer
inferred← citeshttps://doi.org/10.1007/978-1-4419-8955-0_13openalex-snapshot
The Biological Basis of Oocyte and Embryo Competence: Morphodynamic Criteria for Embryo Selection in In-Vitro Fertilization
inferred← citeshttps://doi.org/10.1007/978-1-4419-8955-0_8openalex-snapshot
Maternal Age and Oocyte Competence
inferred← citeshttps://doi.org/10.1007/978-1-4615-0273-9_17openalex-snapshot
Activation of Mammalian Oocytes: Principles and Practice
inferred← citeshttps://doi.org/10.1007/978-1-4615-1809-9_23openalex-snapshot
The MAP kinase cascade: Its role in Xenopus oocytes, eggs and embryos
inferred← citeshttps://doi.org/10.1007/978-1-4615-1809-9_24openalex-snapshot
The oocyte metaphase arrest
inferred← citeshttps://doi.org/10.1007/978-1-4939-8603-3_15openalex-snapshot
Photoactivation of Actin in Mouse Oocyte
inferred← citeshttps://doi.org/10.1007/978-1-59259-369-9_3openalex-snapshot
Control of Oocyte Nuclear and Cytoplasmic Maturation
inferred← citeshttps://doi.org/10.1007/978-1-59745-285-4_54openalex-snapshot
Animal Models for Investigating the Causes and Mechanisms of Mammalian Germ Cell Aneuploidy
inferred← citeshttps://doi.org/10.1007/978-1-62703-191-2_5openalex-snapshot
Protein Kinase Assays for Measuring MPF and MAPK Activities in Mouse and Rat Oocytes and Early Embryos
inferred← citeshttps://doi.org/10.1007/978-3-0348-8705-2_14openalex-snapshot
The Multiple Roles of Mos during Meiosis
inferred← citeshttps://doi.org/10.1007/978-3-319-53150-2_13openalex-snapshot
Asymmetries and Symmetries in the Mouse Oocyte and Zygote
inferred← citeshttps://doi.org/10.1007/978-3-540-49166-8_8openalex-snapshot
Regulation of Cell Division and the Cytoskeleton by Mitogen-Activated Protein Kinases in Higher Plants
inferred← citeshttps://doi.org/10.1007/978-3-642-19065-0_14openalex-snapshot
Protein Kinases and Protein Phosphatases that Regulate Meiotic Maturation in Mouse Oocytes
inferred← citeshttps://doi.org/10.1007/978-3-642-19065-0_2openalex-snapshot
Evolution of Bet-Hedging Mechanisms in Cell Cycle and Embryo Development Stimulated by Weak Linkage of Stochastic Processes
inferred← citeshttps://doi.org/10.1007/978-3-642-30406-4_4openalex-snapshot
Cyclin B in Mouse Oocytes and Embryos: Importance for Human Reproduction and Aneuploidy
inferred← citeshttps://doi.org/10.1007/978-3-642-61180-3_6openalex-snapshot
Mos, Meiosis and Cellular Transformation
inferred← citeshttps://doi.org/10.1007/978-3-662-03671-6_13openalex-snapshot
Role of c-kit in Egg Activation
inferred← citeshttps://doi.org/10.1007/978-3-662-04960-0_8openalex-snapshot
Ageing and Aneuploidy in Oocytes
inferred← citeshttps://doi.org/10.1007/bf00357761openalex-snapshot
Reorganisation of microtubule arrays in the telotrophic ovaries of hemipteran insects: Correlation with meiotic reinitiation
inferred← citeshttps://doi.org/10.1007/bf02907599openalex-snapshot
Roles of MAP kinase signaling pathway in oocyte meiosis
inferred← citeshttps://doi.org/10.1007/s004120050327openalex-snapshot
Mouse polo-like kinase 1 associates with the acentriolar spindle poles, meiotic chromosomes and spindle midzone during oocyte maturation
inferred← citeshttps://doi.org/10.1007/s11626-014-9749-yopenalex-snapshot
RyR channel-mediated increase of cytosolic free calcium level signals cyclin B1 degradation during abortive spontaneous egg activation in rat
inferred← citeshttps://doi.org/10.1007/s12374-013-0123-5openalex-snapshot
ASYMMETRIC LEAVES1 is phosphorylated by MPK3/6 in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s12522-014-0177-1openalex-snapshot
Effect of single‐oocyte culture system on in vitro maturation and developmental competence in mice
inferred← citeshttps://doi.org/10.1007/s43032-019-00004-9openalex-snapshot
Exogenous Ganglioside GT1b Enhances Porcine Oocyte Maturation, Including the Cumulus Cell Expansion and Activation of EGFR and ERK1/2 Signaling
inferred← citeshttps://doi.org/10.1016/1043-2760(95)00079-wopenalex-snapshot
Molecular control of meiosis
inferred← citeshttps://doi.org/10.1016/b978-0-12-386541-0.00012-6openalex-snapshot
Cell Cycle Regulation in Cloning
inferred← citeshttps://doi.org/10.1016/b978-0-12-394306-4.00014-9openalex-snapshot
Role of Store-Operated Calcium Entry During Meiotic Progression and Fertilization of Mammalian Oocytes
inferred← citeshttps://doi.org/10.1016/b978-0-12-397175-3.00004-1openalex-snapshot
Fertilization in Mammals
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.64452-5openalex-snapshot
Polar Body Extrusion and Ovulation
inferred← citeshttps://doi.org/10.1016/b978-0-12-813209-8.00011-xopenalex-snapshot
Regulation of Mammalian Oocyte Maturation
inferred← citeshttps://doi.org/10.1016/b978-0-443-21477-6.00437-5openalex-snapshot
Polar Body Extrusion and Ovulation
inferred← citeshttps://doi.org/10.1016/b978-012174597-4.50022-3openalex-snapshot
Cell Cycle Regulation in Cloning
inferred← citeshttps://doi.org/10.1016/b978-012444562-8/50008-2openalex-snapshot
Regulation of Mammalian Oocyte Maturation
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2006.05.020openalex-snapshot
In vitro production of llama (Lama glama) embryos by intracytoplasmic sperm injection: Effect of chemical activation treatments and culture conditions
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2006.10.004openalex-snapshot
Oocyte biology and challenges in developing in vitro maturation systems in the domestic dog
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2006.12.018openalex-snapshot
Total RNA and protein content, Cyclin B1 expression and developmental competence of prepubertal goat oocytes
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2008.03.002openalex-snapshot
Effect of inhibition of synthesis of inducible nitric oxide synthase-derived nitric oxide by aminoguanidine on the in vitro maturation of oocyte–cumulus complexes of cattle
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2012.07.009openalex-snapshot
In vivo vs. in vitro models for studying the effects of elevated temperature on the GV-stage oocyte, subsequent developmental competence and gene expression
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2008.12.003openalex-snapshot
Regulation of inositol 1,4,5-trisphosphate-induced Ca2+ release by reversible phosphorylation and dephosphorylation
inferred← citeshttps://doi.org/10.1016/j.bpj.2018.02.009openalex-snapshot
Active Mechanics Reveal Molecular-Scale Force Kinetics in Living Oocytes
inferred← citeshttps://doi.org/10.1016/j.ceca.2012.11.007openalex-snapshot
Ca2+ mobilization in cumulus cells: Role in oocyte maturation and acrosome reaction
inferred← citeshttps://doi.org/10.1016/j.cub.2008.08.044openalex-snapshot
Spindle Positioning in Mouse Oocytes Relies on a Dynamic Meshwork of Actin Filaments
inferred← citeshttps://doi.org/10.1016/j.devcel.2019.09.010openalex-snapshot
Active Fluctuations of the Nuclear Envelope Shape the Transcriptional Dynamics in Oocytes
inferred← citeshttps://doi.org/10.1016/j.devcel.2022.09.005openalex-snapshot
Cyclin B3 implements timely vertebrate oocyte arrest for fertilization
inferred← citeshttps://doi.org/10.1016/j.envpol.2019.113843openalex-snapshot
Microcystin-LR promotes zebrafish (Danio rerio) oocyte (in vivo) maturation by activating ERK1/2-MPF signaling pathways, and cAMP is involved in this process
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2003.06.033openalex-snapshot
Dynamic changes in microtubular cytoskeleton of human postmature oocytes revert after ooplasm transfer
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2004.07.983openalex-snapshot
Noninvasive imaging of spindle dynamics during mammalian oocyte activation
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.131417openalex-snapshot
Bone morphogenetic protein 15 gene disruption affects the in vitro maturation of porcine oocytes by impairing spindle assembly and organelle function
inferred← citeshttps://doi.org/10.1016/j.jgg.2015.07.004openalex-snapshot
ERK1/2 Activities Are Dispensable for Oocyte Growth but Are Required for Meiotic Maturation and Pronuclear Formation in Mouse
inferred← citeshttps://doi.org/10.1016/j.mce.2007.11.023openalex-snapshot
Temporal regulation of the first mitosis in Xenopus and mouse embryos
inferred← citeshttps://doi.org/10.1016/j.mce.2014.06.008openalex-snapshot
High cAMP attenuation of insulin-stimulated meiotic G2-M1 transition in zebrafish oocytes: Interaction between the cAMP-dependent protein kinase (PKA) and the MAPK3/1 pathways
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2004.08.005openalex-snapshot
Formation of mammalian oocytes and their growth, differentiation and maturation within ovarian follicles
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2006.09.003openalex-snapshot
Effect of oocyte diameter on meiotic competence, embryo development, p34 (cdc2) expression and MPF activity in prepubertal goat oocytes
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2007.04.044openalex-snapshot
Changes in MPF and MAPK activities in porcine oocytes activated by different methods
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2007.11.011openalex-snapshot
Chemical activation of in vitro matured dromedary camel (Camelus dromedarius) oocytes: Optimization of protocols
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2020.06.037openalex-snapshot
Regulation of the aryl hydrocarbon receptor activity in bovine cumulus-oocyte complexes during in vitro maturation: The role of EGFR and post-EGFR ERK1/2 signaling cascade
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2022.04.031openalex-snapshot
TPX2 deficiency leads to spindle abnormity and meiotic impairment in porcine oocytes
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2025.117614openalex-snapshot
The Src family kinases contribute to MII arrest maintenance in aging porcine oocytes
inferred← citeshttps://doi.org/10.1016/j.tiv.2009.08.025openalex-snapshot
The effect of glucocorticoids on mouse oocyte in vitro maturation and subsequent fertilization and embryo development
inferred← citeshttps://doi.org/10.1016/j.ydbio.2004.04.012openalex-snapshot
Fertilization and InsP3-induced Ca2+ release stimulate a persistent increase in the rate of degradation of cyclin B1 specifically in mature mouse oocytes
inferred← citeshttps://doi.org/10.1016/j.ydbio.2005.04.031openalex-snapshot
Differential roles of p39Mos–Xp42Mpk1 cascade proteins on Raf1 phosphorylation and spindle morphogenesis in Xenopus oocytes
inferred← citeshttps://doi.org/10.1016/j.ydbio.2005.06.028openalex-snapshot
Differences in regulation of the first two M-phases in Xenopus laevis embryo cell-free extracts
inferred← citeshttps://doi.org/10.1016/j.ydbio.2005.12.052openalex-snapshot
Germinal vesicle material drives meiotic cell cycle of mouse oocyte through the 3′UTR-dependent control of cyclin B1 synthesis
inferred← citeshttps://doi.org/10.1016/j.ydbio.2006.02.005openalex-snapshot
Intracellular Ca2+ increase induces post-fertilization events via MAP kinase dephosphorylation in eggs of the hydrozoan jellyfish Cladonema pacificum
inferred← citeshttps://doi.org/10.1016/j.ydbio.2006.06.051openalex-snapshot
Transmission of modified nucleosomes from the mouse male germline to the zygote and subsequent remodeling of paternal chromatin
inferred← citeshttps://doi.org/10.1016/j.ydbio.2006.10.034openalex-snapshot
The presence of X- and Y-chromosomes in oocytes leads to impairment in the progression of the second meiotic division
inferred← citeshttps://doi.org/10.1016/j.ydbio.2007.03.029openalex-snapshot
The MEK inhibitor, U0126, alters fertilization-induced [Ca2+]i oscillation parameters and secretion: Differential effects associated with in vivo and in vitro meiotic maturation
inferred← citeshttps://doi.org/10.1016/j.ydbio.2007.10.009openalex-snapshot
Brefeldin A disrupts asymmetric spindle positioning in mouse oocytes
inferred← citeshttps://doi.org/10.1016/j.ydbio.2008.05.548openalex-snapshot
Inositol 1,4,5-trisphosphate receptor 1, a widespread Ca2+ channel, is a novel substrate of polo-like kinase 1 in eggs
inferred← citeshttps://doi.org/10.1016/j.ydbio.2008.06.016openalex-snapshot
CDC2A (CDK1)-mediated phosphorylation of MSY2 triggers maternal mRNA degradation during mouse oocyte maturation
inferred← citeshttps://doi.org/10.1016/s0012-1606(02)00049-0openalex-snapshot
Maturation-associated increase in IP3 receptor type 1: role in conferring increased IP3 sensitivity and Ca2+ oscillatory behavior in mouse eggs
inferred← citeshttps://doi.org/10.1016/s0070-2153(08)60179-9openalex-snapshot
10 Sexual Dimorphism in the Regulation of Mammalian Meiosis
inferred← citeshttps://doi.org/10.1016/s0070-2153(08)60563-3openalex-snapshot
2 Molecular Basis of Mammalian Egg Activation
inferred← citeshttps://doi.org/10.1016/s0074-7696(01)07006-1openalex-snapshot
Molecular and biochemical regulation of early mammalian development
inferred← citeshttps://doi.org/10.1016/s0076-6879(97)83046-7openalex-snapshot
Mechanisms of Xenopus oocyte maturation
inferred← citeshttps://doi.org/10.1016/s0092-8674(00)81037-5openalex-snapshot
Identification of a Protein That Interacts with Tubulin Dimers and Increases the Catastrophe Rate of Microtubules
inferred← citeshttps://doi.org/10.1016/s0093-691x(01)00451-4openalex-snapshot
Dynamics of meiosis and protein kinase activities in bovine oocytes correlated to prolactin treatment and follicle size
inferred← citeshttps://doi.org/10.1016/s0093-691x(97)00418-4openalex-snapshot
Interplay between CDC2 kinase and MAP kinase pathway during maturation of mammalian oocytes
inferred← citeshttps://doi.org/10.1016/s0171-9335(99)80092-2openalex-snapshot
Caulerpenyne blocks MBP kinase activation controlling mitosis in sea urchin eggs
inferred← citeshttps://doi.org/10.1016/s0248-4900(00)88528-7openalex-snapshot
Transient reactivation of CSF in parthenogenetic one-cell mouse embryos
inferred← citeshttps://doi.org/10.1016/s0248-4900(03)00088-1openalex-snapshot
Effect of taxol and okadaic acid on microtubule dynamics in thimerosal‐arrested primary mouse oocytes: a confocal study
inferred← citeshttps://doi.org/10.1016/s0248-4900(97)80037-8openalex-snapshot
Stability of cyclin B protein during meiotic maturation and the first mitotic cell division in mouse oocytes
inferred← citeshttps://doi.org/10.1016/s0248-4900(99)80040-9openalex-snapshot
Changes in the activity of type 2A protein phosphatases during meiotic maturation and the first mitotic cell cycle in mouse oocytes
inferred← citeshttps://doi.org/10.1016/s0301-4622(98)00131-8openalex-snapshot
Link between fertilization-induced Ca2+ oscillations and relief from metaphase II arrest in mammalian eggs: a model based on calmodulin-dependent kinase II activation
inferred← citeshttps://doi.org/10.1016/s0303-7207(01)00691-8openalex-snapshot
Signalling in mammalian egg activation: role of protein kinases
inferred← citeshttps://doi.org/10.1016/s0378-4320(01)00094-xopenalex-snapshot
Kinetics of meiotic progression, M-phase promoting factor (MPF) and mitogen-activated protein kinase (MAP kinase) activities during in vitro maturation of porcine and bovine oocytes: species specific differences in the length of the meiotic stages
inferred← citeshttps://doi.org/10.1016/s0378-4320(98)00084-0openalex-snapshot
Differential effects of kinase inhibitor and electrical stimulus on activation and histone H1 kinase activity in pig oocytes
inferred← citeshttps://doi.org/10.1016/s0959-437x(97)80105-0openalex-snapshot
Stopping and starting the meiotic cell cycle
inferred← citeshttps://doi.org/10.1016/s0960-9822(00)00753-3openalex-snapshot
Asymmetric division in mouse oocytes: with or without Mos
inferred← citeshttps://doi.org/10.1016/s1472-6483(10)60497-xopenalex-snapshot
Spindles, mitochondria and redox potential in ageing oocytes
inferred← citeshttps://doi.org/10.1017/s0967199400000794openalex-snapshot
The distribution and requirements of microtubules and microfilaments in bovine oocytes during in vitro maturation
inferred← citeshttps://doi.org/10.1017/s0967199400000939openalex-snapshot
Degradation of pig cyclin B1 molecules precedes MAP kinase dephosphorylation during fertilisation of the oocytes
inferred← citeshttps://doi.org/10.1017/s0967199400002665openalex-snapshot
Activation of mitogen-activated protein kinase during meiotic maturation in porcine oocytes
inferred← citeshttps://doi.org/10.1017/s0967199400003105openalex-snapshot
Mitogen-activated protein kinase activity and microtuble organisation are altered by protein synthesis inhibition in maturing porcine oocytes
inferred← citeshttps://doi.org/10.1017/s0967199400003166openalex-snapshot
Co-culture with pig membrana granulosa cells modulates the activity of cdc2 and MAP kinase in maturing cattle oocytes
inferred← citeshttps://doi.org/10.1017/s0967199400003580openalex-snapshot
Calcium- and meiotic-spindle-independent activation of pig oocytes by the inhibition of staurosporine-sensitive protein kinases
inferred← citeshttps://doi.org/10.1017/s0967199400003671openalex-snapshot
Fertilisation competence of bovine normally matured or aged oocytes derived from different antral follicles: morphology, protein synthesis, H1 and MBP kinase activity
inferred← citeshttps://doi.org/10.1017/s0967199400003841openalex-snapshot
Transformation of sperm nuclei into metaphase chromosomes in maturing pig oocytes penetratedin vitro
inferred← citeshttps://doi.org/10.1017/s0967199402002344openalex-snapshot
Acquisition of meiotic competence in growing pig oocytes correlates with their ability to activate Cdc2 kinase and MAP kinase
inferred← citeshttps://doi.org/10.1017/s0967199403001084openalex-snapshot
The effect of PD98059 on MAPK regulation in cumulus-enclosed and cumulus-free mouse oocytes
inferred← citeshttps://doi.org/10.1017/s096719940400276xopenalex-snapshot
Somatic nucleus remodelling in immature and mature Rassir oocyte cytoplasm
inferred← citeshttps://doi.org/10.1017/s0967199407004170openalex-snapshot
Phosphorylation pattern of the p90rskand mitogen-activated protein kinase (MAPK) molecule: comparison ofin vitroandin vivomatured porcine oocytes
inferred← citeshttps://doi.org/10.1017/s0967199407004285openalex-snapshot
Parthenogenetic activation of bovine oocytes using single and combined strontium, ionomycin and 6-dimethylaminopurine treatments
inferred← citeshttps://doi.org/10.1017/s0967199411000219openalex-snapshot
Regulation of fusion of the nucleolar precursor bodies following activation of mouse oocytes: roles of the maturation-promoting factors and mitogen-activated protein kinases
inferred← citeshttps://doi.org/10.1017/s096719941700003xopenalex-snapshot
Effects of ghrelin on activation of Akt1 and ERK1/2 pathways duringin vitromaturation of bovine oocytes
inferred← citeshttps://doi.org/10.1017/s0967199499000556openalex-snapshot
Mitogen-activated protein kinase in human eggs
inferred← citeshttps://doi.org/10.1017/s0967199499000696openalex-snapshot
Control of duration of the first two mitoses in a mouse embryo
inferred← citeshttps://doi.org/10.1017/s1431927611012773openalex-snapshot
Reliability of Hoechst 33342 Staining under Wide-Field Microscopy for Evaluation of the Nuclear Status of Living Dog Oocytes
inferred← citeshttps://doi.org/10.1038/ncb2799openalex-snapshot
A soft cortex is essential for asymmetric spindle positioning in mouse oocytes
inferred← citeshttps://doi.org/10.1038/ncb3131openalex-snapshot
Active diffusion positions the nucleus in mouse oocytes
inferred← citeshttps://doi.org/10.1038/ncomms10253openalex-snapshot
F-actin mechanics control spindle centring in the mouse zygote
inferred← citeshttps://doi.org/10.1038/ncomms7027openalex-snapshot
A narrow window of cortical tension guides asymmetric spindle positioning in the mouse oocyte
inferred← citeshttps://doi.org/10.1038/s41467-020-15470-yopenalex-snapshot
Artificially decreasing cortical tension generates aneuploidy in mouse oocytes
inferred← citeshttps://doi.org/10.1038/s41467-022-32675-5openalex-snapshot
Cytoplasmic forces functionally reorganize nuclear condensates in oocytes
inferred← citeshttps://doi.org/10.1038/s43587-024-00769-yopenalex-snapshot
Hallmarks of female reproductive aging in physiologic aging mice
inferred← citeshttps://doi.org/10.1038/sj.cr.7290183openalex-snapshot
Effects of MEK inhibitor U0126 on meiotic progression in mouse oocytes: microtuble organization, asymmetric division and metaphase II arrest
inferred← citeshttps://doi.org/10.1038/sj.onc.1202683openalex-snapshot
Differential signaling by alternative HGF isoforms through c-Met: activation of both MAP kinase and PI 3-kinase pathways is insufficient for mitogenesis
inferred← citeshttps://doi.org/10.1038/sj.onc.1204814openalex-snapshot
Protection against chemotherapy-induced cytotoxicity by cyclin-dependent kinase inhibitors (CKI) in CKI-responsive cells compared with CKI-unresponsive cells
inferred← citeshttps://doi.org/10.1042/bc20050020openalex-snapshot
PKB/AKT is involved in resumption of meiosis in mouse oocytes
inferred← citeshttps://doi.org/10.1042/bst20170493openalex-snapshot
Regulation of the meiotic divisions of mammalian oocytes and eggs
inferred← citeshttps://doi.org/10.1046/j.1440-169x.1996.t01-4-00008.xopenalex-snapshot
Bovine embryo cloning: Characterization of the recipient cytoplasts by phosphorylation patterns and kinase activities
inferred← citeshttps://doi.org/10.1046/j.1440-169x.2002.00644.xopenalex-snapshot
Studies on fertilization in the teleost IV. Effects of aphidicolin and camptothecin on chromosome formation in fertilized medaka eggs
inferred← citeshttps://doi.org/10.1051/medsci/2002182169openalex-snapshot
Cellules souches embryonnaires et clonage thérapeutique
inferred← citeshttps://doi.org/10.1051/rnd:19950608openalex-snapshot
Microtubule rearrangement during in vitro maturation of pig oocytes. Effect of cycloheximide
inferred← citeshttps://doi.org/10.1071/rd00104openalex-snapshot
Antioxidants stimulate meiosis resumption, but inhibit mitogen-activated protein kinase phosphorylation and further cell cycle progression in porcine oocytes
inferred← citeshttps://doi.org/10.1071/rd06026openalex-snapshot
Chromatin, microtubule and microfilament configurations in the canine oocyte
inferred← citeshttps://doi.org/10.1071/rd08268openalex-snapshot
Enhanced developmental potential of heat-shocked porcine parthenogenetic embryos is related to accelerated mitogen-activated protein kinase dephosphorylation
inferred← citeshttps://doi.org/10.1071/rd11033openalex-snapshot
The conformation and activation of Fyn kinase in the oocyte determine its localisation to the spindle poles and cleavage furrow
inferred← citeshttps://doi.org/10.1071/rd12242openalex-snapshot
Molecular participants in regulation of the meiotic cell cycle in mammalian oocytes
inferred← citeshttps://doi.org/10.1073/pnas.92.19.8881openalex-snapshot
Association of mitogen-activated protein kinase with the microtubule cytoskeleton.
inferred← citeshttps://doi.org/10.1073/pnas.92.8.3430openalex-snapshot
Mos overexpression in Swiss 3T3 cells induces meiotic-like alterations of the mitotic spindle.
inferred← citeshttps://doi.org/10.1073/pnas.93.10.4730openalex-snapshot
Mos/mitogen-activated protein kinase can induce early meiotic phenotypes in the absence of maturation-promoting factor: a novel system for analyzing spindle formation during meiosis I.
inferred← citeshttps://doi.org/10.1073/pnas.93.14.7032openalex-snapshot
The Mos/mitogen-activated protein kinase (MAPK) pathway regulates the size and degradation of the first polar body in maturing mouse oocytes.
inferred← citeshttps://doi.org/10.1074/jbc.274.47.33571openalex-snapshot
Activation of the Mitogen-activated Protein Kinase ERK1 during Meiotic Progression of Mouse Pachytene Spermatocytes
inferred← citeshttps://doi.org/10.1074/jbc.m117.803080openalex-snapshot
Betaine is accumulated via transient choline dehydrogenase activation during mouse oocyte meiotic maturation
inferred← citeshttps://doi.org/10.1074/jbc.m414437200openalex-snapshot
Inhibiting MAP Kinase Activity Prevents Calcium Transients and Mitosis Entry in Early Sea Urchin Embryos
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