scholarly article | Q13442814 |
P50 | author | X. Johne Liu | Q71069162 |
P2093 | author name string | X Johné Liu | |
P2860 | cites work | Asymmetric cell division in B. subtilis involves a spiral-like intermediate of the cytokinetic protein FtsZ | Q74083515 |
Development of cortical polarity in mouse eggs: involvement of the meiotic apparatus | Q93606230 | ||
The chromosomal passenger complex is required for chromatin-induced microtubule stabilization and spindle assembly | Q24299655 | ||
Spire-type actin nucleators cooperate with Formin-2 to drive asymmetric oocyte division | Q24304847 | ||
Asymmetric CLASP-dependent nucleation of noncentrosomal microtubules at the trans-Golgi network | Q24307694 | ||
Aurora B regulates MCAK at the mitotic centromere | Q24307822 | ||
An ECT2-centralspindlin complex regulates the localization and function of RhoA | Q24315633 | ||
APC15 drives the turnover of MCC-CDC20 to make the spindle assembly checkpoint responsive to kinetochore attachment | Q24338143 | ||
Biphasic activation of Aurora-A kinase during the meiosis I- meiosis II transition in Xenopus oocytes | Q24554325 | ||
Zona pellucida glycoproteins | Q24655051 | ||
Human ECT2 is an exchange factor for Rho GTPases, phosphorylated in G2/M phases, and involved in cytokinesis | Q24681007 | ||
Ca(2+)(cyt) negatively regulates the initiation of oocyte maturation | Q24811316 | ||
The spindle-assembly checkpoint in space and time | Q27860766 | ||
Golgi-localized GAP for Cdc42 functions downstream of ARF1 to control Arp2/3 complex and F-actin dynamics | Q28241896 | ||
GM130, a cis-Golgi protein, regulates meiotic spindle assembly and asymmetric division in mouse oocyte | Q28507061 | ||
Formin-2, polyploidy, hypofertility and positioning of the meiotic spindle in mouse oocytes | Q28507117 | ||
The meiosis I-to-meiosis II transition in mouse oocytes requires separase activity | Q28507209 | ||
Arp2/3 complex regulates asymmetric division and cytokinesis in mouse oocytes | Q28508733 | ||
PAR-3 defines a central subdomain of the cortical actin cap in mouse eggs | Q28509592 | ||
In germ cells of mouse embryonic ovaries, the decision to enter meiosis precedes premeiotic DNA replication | Q28513959 | ||
Dynamic maintenance of asymmetric meiotic spindle position through Arp2/3-complex-driven cytoplasmic streaming in mouse oocytes | Q28589717 | ||
The Mos/mitogen-activated protein kinase (MAPK) pathway regulates the size and degradation of the first polar body in maturing mouse oocytes | Q28590245 | ||
Differential expression and functions of cortical myosin IIA and IIB isotypes during meiotic maturation, fertilization, and mitosis in mouse oocytes and embryos | Q28590998 | ||
Calcium/calmodulin-dependent protein kinase II and calmodulin: regulators of the meiotic spindle in mouse eggs | Q28594045 | ||
Human cyclins A and B1 are differentially located in the cell and undergo cell cycle-dependent nuclear transport | Q28612313 | ||
Lateral microtubule bundles promote chromosome alignment during acentrosomal oocyte meiosis | Q28750580 | ||
Self-organization of microtubules into bipolar spindles around artificial chromosomes in Xenopus egg extracts | Q29616137 | ||
To err (meiotically) is human: the genesis of human aneuploidy | Q29618613 | ||
Evidence that the Ipl1-Sli15 (Aurora kinase-INCENP) complex promotes chromosome bi-orientation by altering kinetochore-spindle pole connections | Q29619579 | ||
Self-perpetuating states in signal transduction: positive feedback, double-negative feedback and bistability | Q29619706 | ||
The biochemical basis of an all-or-none cell fate switch in Xenopus oocytes | Q29619826 | ||
Chromosomal passengers: conducting cell division | Q29620468 | ||
Aurora B phosphorylates centromeric MCAK and regulates its localization and microtubule depolymerization activity | Q30312108 | ||
Midzone activation of aurora B in anaphase produces an intracellular phosphorylation gradient | Q30438972 | ||
Regulation of cytokinesis by Rho GTPase flux | Q30439337 | ||
A centriole- and RanGTP-independent spindle assembly pathway in meiosis I of vertebrate oocytes | Q30480417 | ||
Regional variation of microtubule flux reveals microtubule organization in the metaphase meiotic spindle | Q30483135 | ||
Op18 reveals the contribution of nonkinetochore microtubules to the dynamic organization of the vertebrate meiotic spindle | Q30490092 | ||
Aurora-C kinase deficiency causes cytokinesis failure in meiosis I and production of large polyploid oocytes in mice | Q30495481 | ||
Polar body emission requires a RhoA contractile ring and Cdc42-mediated membrane protrusion | Q30532695 | ||
The APC is dispensable for first meiotic anaphase in Xenopus oocytes. | Q31808529 | ||
Concentric zones of active RhoA and Cdc42 around single cell wounds | Q33211372 | ||
Sperm chromatin-induced ectopic polar body extrusion in mouse eggs after ICSI and delayed egg activation | Q33507267 | ||
MCAK is present at centromeres, midspindle and chiasmata and involved in silencing of the spindle assembly checkpoint in mammalian oocytes | Q33560603 | ||
Action at a distance during cytokinesis | Q33589990 | ||
Understanding cytokinesis: lessons from fission yeast | Q33641901 | ||
Mad2 prevents aneuploidy and premature proteolysis of cyclin B and securin during meiosis I in mouse oocytes | Q33763645 | ||
Aurora kinase inhibitor ZM447439 blocks chromosome-induced spindle assembly, the completion of chromosome condensation, and the establishment of the spindle integrity checkpoint in Xenopus egg extracts | Q33914085 | ||
The Golgi complex is a microtubule-organizing organelle | Q33937465 | ||
A novel regulatory element determines the timing of Mos mRNA translation during Xenopus oocyte maturation | Q34079032 | ||
A single bivalent efficiently inhibits cyclin B1 degradation and polar body extrusion in mouse oocytes indicating robust SAC during female meiosis I. | Q34085727 | ||
Differential mRNA translation and meiotic progression require Cdc2-mediated CPEB destruction | Q34086318 | ||
Cortical mechanics and meiosis II completion in mammalian oocytes are mediated by myosin-II and Ezrin-Radixin-Moesin (ERM) proteins | Q34123394 | ||
Evidence that weakened centromere cohesion is a leading cause of age-related aneuploidy in oocytes. | Q34126610 | ||
Oocyte Cohesin Expression Restricted to Predictyate Stages Provides Full Fertility and Prevents Aneuploidy | Q34153758 | ||
Anaphase B precedes anaphase A in the mouse egg. | Q34255126 | ||
Asymmetric cell division during animal development | Q34286348 | ||
Rec8-containing cohesin maintains bivalents without turnover during the growing phase of mouse oocytes | Q34289002 | ||
Germline stem cells and follicular renewal in the postnatal mammalian ovary | Q34304906 | ||
Centrosome reduction during gametogenesis and its significance | Q34350796 | ||
The chromosome passenger complex is required for fidelity of chromosome transmission and cytokinesis in meiosis of mouse oocytes | Q34371416 | ||
The molecular requirements for cytokinesis | Q34404139 | ||
Oocyte generation in adult mammalian ovaries by putative germ cells in bone marrow and peripheral blood | Q34437923 | ||
HURP permits MTOC sorting for robust meiotic spindle bipolarity, similar to extra centrosome clustering in cancer cells. | Q34439699 | ||
Determining the position of the cell division plane | Q44540743 | ||
Formation and function of the polar body contractile ring in Spisula | Q44863925 | ||
Fertilization and InsP3-induced Ca2+ release stimulate a persistent increase in the rate of degradation of cyclin B1 specifically in mature mouse oocytes | Q44970229 | ||
Age-Related Meiotic Segregation Errors in Mammalian Oocytes Are Preceded by Depletion of Cohesin and Sgo2 | Q46305683 | ||
Spindle positioning in mouse oocytes relies on a dynamic meshwork of actin filaments. | Q46321191 | ||
A model system for increased meiotic nondisjunction in older oocytes | Q46378427 | ||
Spatial coordination of spindle assembly by chromosome-mediated signaling gradients | Q46670028 | ||
Involvement of calcium/calmodulin-dependent protein kinase II (CaMKII) in meiotic maturation and activation of pig oocytes | Q46744328 | ||
Mad2 is required for inhibiting securin and cyclin B degradation following spindle depolymerisation in meiosis I mouse oocytes. | Q46831372 | ||
Ca(2+)-promoted cyclin B1 degradation in mouse oocytes requires the establishment of a metaphase arrest | Q47774194 | ||
Two PAR6 proteins become asymmetrically localized during establishment of polarity in mouse oocytes | Q47885081 | ||
Assembly mechanism of the contractile ring for cytokinesis by fission yeast | Q48026763 | ||
Symmetrical division of mouse oocytes during meiotic maturation can lead to the development of twin embryos that amalgamate to form a chimeric hermaphrodite | Q48659647 | ||
Mini Golgi stacks participate in spindle assembly in acentrosomal mouse oocytes? | Q48666913 | ||
The small GTPase Cdc42 promotes membrane protrusion during polar body emission via ARP2-nucleated actin polymerization | Q48675311 | ||
Actomyosin tube formation in polar body cytokinesis requires Anillin in C. elegans | Q48686905 | ||
Epithelial cell transforming protein 2 (ECT2) depletion blocks polar body extrusion and generates mouse oocytes containing two metaphase II spindles | Q48709137 | ||
A new model for asymmetric spindle positioning in mouse oocytes | Q48732518 | ||
ADP-ribosylation factor 1 regulates asymmetric cell division in female meiosis in the mouse. | Q48735272 | ||
Cdc42 protein acts upstream of IQGAP1 and regulates cytokinesis in mouse oocytes and embryos | Q48743265 | ||
Brefeldin A disrupts asymmetric spindle positioning in mouse oocytes | Q48771441 | ||
Self-organization of MTOCs replaces centrosome function during acentrosomal spindle assembly in live mouse oocytes | Q48785884 | ||
Inhibition of MEK or cdc2 kinase parthenogenetically activates mouse eggs and yields the same phenotypes as Mos(-/-) parthenogenotes. | Q48857930 | ||
Evidence that multifunctional calcium/calmodulin-dependent protein kinase II (CaM KII) participates in the meiotic maturation of mouse oocytes | Q48866101 | ||
Activation of the anaphase-promoting complex and degradation of cyclin B is not required for progression from Meiosis I to II in Xenopus oocytes | Q48884009 | ||
Fertilisability and developmental ability of mouse oocytes with reduced amounts of cytoplasm. | Q48924762 | ||
Consequences of non-extrusion of the first polar body and control of the sequential segregation of homologues and chromatids in mammalian oocytes | Q49040675 | ||
Ectopic spindle assembly during maturation of Xenopus oocytes: evidence for functional polarization of the oocyte cortex | Q49134418 | ||
Rac activity is polarized and regulates meiotic spindle stability and anchoring in mammalian oocytes. | Q50639505 | ||
The Ran GTPase mediates chromatin signaling to control cortical polarity during polar body extrusion in mouse oocytes. | Q50639510 | ||
Formin-2 is required for spindle migration and for the late steps of cytokinesis in mouse oocytes. | Q50644638 | ||
Interactions of the meiotic spindle with mitotic chromosomes in GV mouse oocytes. | Q50646260 | ||
Loss of Rec8 from chromosome arm and centromere region is required for homologous chromosome separation and sister chromatid separation, respectively, in mammalian meiosis. | Q50646910 | ||
Resolution of chiasmata in oocytes requires separase-mediated proteolysis. | Q50647080 | ||
Ovulated oocytes in adult mice derive from non-circulating germ cells. | Q50647633 | ||
Asymmetric positioning and organization of the meiotic spindle of mouse oocytes requires CDC42 function. | Q50647964 | ||
SMC1beta-deficient female mice provide evidence that cohesins are a missing link in age-related nondisjunction. | Q50656030 | ||
Calmodulin-dependent protein kinase II, and not protein kinase C, is sufficient for triggering cell-cycle resumption in mammalian eggs. | Q50658761 | ||
Small GTPase RhoA is required for ooplasmic segregation and spindle rotation, but not for spindle organization and chromosome separation during mouse oocyte maturation, fertilization, and early cleavage. | Q50664486 | ||
Asymmetric division in mouse oocytes: with or without Mos. | Q50721646 | ||
Bipolar meiotic spindle formation without chromatin. | Q50742045 | ||
Microtubule organization during maturation of Xenopus oocytes: assembly and rotation of the meiotic spindles. | Q50792222 | ||
A microtubule-binding myosin required for nuclear anchoring and spindle assembly. | Q52560093 | ||
Nonredundant functions of Kinesin-13s during meiotic spindle assembly. | Q53552320 | ||
Germline stem cells and neo-oogenesis in the adult human ovary. | Q53560094 | ||
Counting cytokinesis proteins globally and locally in fission yeast. | Q53653661 | ||
Polo-like Kinase 1 Triggers the Initiation of Cytokinesis in Human Cells by Promoting Recruitment of the RhoGEF Ect2 to the Central Spindle | Q56157380 | ||
Cohesion between sister chromatids must be established during DNA replication | Q57270146 | ||
Cell Cleavage in Polar Body Formation | Q58994851 | ||
Regulation of the cell cycle during early Xenopus development | Q70367519 | ||
Aurora B is required for mitotic chromatin-induced phosphorylation of Op18/Stathmin | Q34448311 | ||
Lack of checkpoint control at the metaphase/anaphase transition: a mechanism of meiotic nondisjunction in mammalian females | Q34450618 | ||
Animal cytokinesis: from parts list to mechanisms | Q34535176 | ||
A kinetochore-independent mechanism drives anaphase chromosome separation during acentrosomal meiosis | Q34643436 | ||
Exit from mitosis in Drosophila syncytial embryos requires proteolysis and cyclin degradation, and is associated with localized dephosphorylation | Q35200340 | ||
Cdc42 activation couples spindle positioning to first polar body formation in oocyte maturation. | Q35230006 | ||
The spatial and mechanical challenges of female meiosis | Q35387829 | ||
Oocyte-specific differences in cell-cycle control create an innate susceptibility to meiotic errors | Q35576326 | ||
Aurora kinases link chromosome segregation and cell division to cancer susceptibility | Q35756009 | ||
Translation of incenp during oocyte maturation is required for embryonic development in Xenopus laevis. | Q35779093 | ||
Calcium influx-mediated signaling is required for complete mouse egg activation | Q35837015 | ||
A new method reveals microtubule minus ends throughout the meiotic spindle | Q36118983 | ||
Shugoshin protects cohesin complexes at centromeres | Q36129356 | ||
Role of spindle microtubules in the control of cell cycle timing | Q36200472 | ||
Cell cycle dynamics of an M-phase-specific cytoplasmic factor in Xenopus laevis oocytes and eggs | Q36210628 | ||
Non-spindle microtubule organizing centers in metaphase II-arrested mouse oocytes | Q36213721 | ||
A microtubule-dependent zone of active RhoA during cleavage plane specification | Q36320722 | ||
Mammalian egg activation: from Ca2+ spiking to cell cycle progression | Q36328662 | ||
Start me up: cell signaling and the journey from oocyte to embryo in C. elegans | Q36350349 | ||
A cytoplasmic clock with the same period as the division cycle in Xenopus eggs | Q36352644 | ||
Kinetochore fibers are not involved in the formation of the first meiotic spindle in mouse oocytes, but control the exit from the first meiotic M phase | Q36382101 | ||
Role of calcium signals in early development | Q36437318 | ||
Meiosis, egg activation, and nuclear envelope breakdown are differentially reliant on Ca2+, whereas germinal vesicle breakdown is Ca2+ independent in the mouse oocyte | Q36531395 | ||
Cell polarization during monopolar cytokinesis | Q36562880 | ||
Regulation of the Aurora B chromosome passenger protein complex during oocyte maturation in Xenopus laevis | Q36710819 | ||
Mature Drosophila meiosis I spindles comprise microtubules of mixed polarity. | Q37239312 | ||
Mitosis in the Drosophila embryo--in and out of control | Q37778070 | ||
Protein-DNA interactions at a drug-responsive element of the human apolipoprotein A-I gene | Q38352112 | ||
Dominoes and clocks: the union of two views of the cell cycle | Q38718174 | ||
Kinetics of spermatogenesis in mammals: seminiferous epithelium cycle and spermatogonial renewal | Q39955364 | ||
MCAK regulates chromosome alignment but is not necessary for preventing aneuploidy in mouse oocyte meiosis I. | Q40928235 | ||
Actin-driven chromosomal motility leads to symmetry breaking in mammalian meiotic oocytes | Q42695317 | ||
Chromosomal enrichment and activation of the aurora B pathway are coupled to spatially regulate spindle assembly | Q42745909 | ||
Schizosaccharomyces pombe Pxl1 is a paxillin homologue that modulates Rho1 activity and participates in cytokinesis | Q43110524 | ||
Aurora kinase B, epigenetic state of centromeric heterochromatin and chiasma resolution in oocytes | Q43271914 | ||
Involvement of Aurora A kinase during meiosis I-II transition in Xenopus oocytes | Q44212497 | ||
P433 | issue | 10 | |
P304 | page(s) | 670-685 | |
P577 | publication date | 2012-06-21 | |
P1433 | published in | Cytoskeleton | Q2196987 |
P1476 | title | Polar body emission | |
P478 | volume | 69 |
Q57048871 | Cdk1 inactivation induces post-anaphase-onset spindle migration and membrane protrusion required for extreme asymmetry in mouse oocytes |
Q37347136 | LIMK1/2 inhibitor LIMKi 3 suppresses porcine oocyte maturation |
Q39062611 | Mechanics and regulation of cytokinesis in budding yeast |
Q33728945 | Meiosis I in Xenopus oocytes is not error-prone despite lacking spindle assembly checkpoint |
Q38050708 | Rho GTPases in animal cell cytokinesis: an occupation by the one percent |
Q37204583 | Symmetry breaking and polarity establishment during mouse oocyte maturation |
Q35860862 | The Majority of Resorptions in Old Mice Are Euploid. |
Q37694071 | The nuclear F-actin interactome of Xenopus oocytes reveals an actin-bundling kinesin that is essential for meiotic cytokinesis. |
Q27304958 | Unique spatiotemporal activation pattern of Cdc42 by Gef1 and Scd1 promotes different events during cytokinesis. |
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