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Rec8 phosphorylation and recombination promote the step-wise loss of cohesins in meiosis
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/0092-8674(90)90524-iopenalex-snapshot
Analysis of wild-type and rad50 mutants of yeast suggests an intimate relationship between meiotic chromosome synapsis and recombination
inferredcites →https://doi.org/10.1016/0092-8674(92)90446-jopenalex-snapshot
DMC1: A meiosis-specific yeast homolog of E. coli recA required for recombination, synaptonemal complex formation, and cell cycle progression
inferredcites →https://doi.org/10.1016/0092-8674(95)90166-3openalex-snapshot
Mei-S332, a drosophila protein required for sister-chromatid cohesion, can localize to meiotic centromere regions
inferredcites →https://doi.org/10.1016/j.cell.2005.09.014openalex-snapshot
Chromosome Morphogenesis: Condensin-Dependent Cohesin Removal during Meiosis
inferredcites →https://doi.org/10.1016/j.cub.2003.10.057openalex-snapshot
Spindle Checkpoint Component Mad2 Contributes to Biorientation of Homologous Chromosomes
inferredcites →https://doi.org/10.1016/j.cub.2004.03.001openalex-snapshot
Maintenance of Cohesin at Centromeres after Meiosis I in Budding Yeast Requires a Kinetochore-Associated Protein Related to MEI-S332
inferredcites →https://doi.org/10.1016/s0092-8674(00)00131-8openalex-snapshot
Disjunction of Homologous Chromosomes in Meiosis I Depends on Proteolytic Cleavage of the Meiotic Cohesin Rec8 by Separin
inferredcites →https://doi.org/10.1016/s0092-8674(00)00217-8openalex-snapshot
Functional Genomics Identifies Monopolin
inferredcites →https://doi.org/10.1016/s0092-8674(00)80609-1openalex-snapshot
A Central Role for Cohesins in Sister Chromatid Cohesion, Formation of Axial Elements, and Recombination during Yeast Meiosis
inferredcites →https://doi.org/10.1016/s0092-8674(00)81876-0openalex-snapshot
Meiosis-Specific DNA Double-Strand Breaks Are Catalyzed by Spo11, a Member of a Widely Conserved Protein Family
inferredcites →https://doi.org/10.1016/s0092-8674(01)00362-2openalex-snapshot
Phosphorylation of the Cohesin Subunit Scc1 by Polo/Cdc5 Kinase Regulates Sister Chromatid Separation in Yeast
inferredcites →https://doi.org/10.1016/s1097-2765(00)80286-5openalex-snapshot
The Phosphatase Cdc14 Triggers Mitotic Exit by Reversal of Cdk-Dependent Phosphorylation
inferredcites →https://doi.org/10.1016/s1534-5807(03)00129-1openalex-snapshot
Division of the Nucleolus and Its Release of CDC14 during Anaphase of Meiosis I Depends on Separase, SPO12, and SLK19
inferredcites →https://doi.org/10.1038/386414a0openalex-snapshot
An atypical topoisomerase II from archaea with implications for meiotic recombination
inferredcites →https://doi.org/10.1038/nature02312openalex-snapshot
The conserved kinetochore protein shugoshin protects centromeric cohesion during meiosis
inferredcites →https://doi.org/10.1038/nature04663openalex-snapshot
Shugoshin collaborates with protein phosphatase 2A to protect cohesin
inferredcites →https://doi.org/10.1038/nature04664openalex-snapshot
Protein phosphatase 2A protects centromeric sister chromatid cohesion during meiosis I
inferredcites →https://doi.org/10.1038/ncb977openalex-snapshot
Polo-like kinase Cdc5 promotes chiasmata formation and cosegregation of sister centromeres at meiosis I
inferredcites →https://doi.org/10.1038/nrm1526openalex-snapshot
Meiosis: cell-cycle controls shuffle and deal
inferredcites →https://doi.org/10.1038/sj.emboj.7600303openalex-snapshot
Preferential cleavage of chromatin‐bound cohesin after targeted phosphorylation by Polo‐like kinase
inferredcites →https://doi.org/10.1101/gad.10.24.3081openalex-snapshot
Anaphase initiation in Saccharomyces cerevisiae is controlled by the APC-dependent degradation of the anaphase inhibitor Pds1p.
inferredcites →https://doi.org/10.1101/gad.11.17.2272openalex-snapshot
mre11S—a yeast mutation that blocks double-strand-break processing and permits nonhomologous synapsis in meiosis
inferredcites →https://doi.org/10.1101/gad.12.24.3843openalex-snapshot
Maintenance of sister-chromatid cohesion at the centromere by the Drosophila MEI-S332 protein
inferredcites →https://doi.org/10.1101/gad.1373005openalex-snapshot
The core centromere and Sgo1 establish a 50-kb cohesin-protected domain around centromeres during meiosis I
inferredcites →https://doi.org/10.1126/science.1081846openalex-snapshot
Role of Polo-like Kinase CDC5 in Programming Meiosis I Chromosome Segregation
inferredcites →https://doi.org/10.1126/science.1094220openalex-snapshot
A Genome-Wide Screen Identifies Genes Required for Centromeric Cohesion
inferredcites →https://doi.org/10.1126/science.289.5477.300openalex-snapshot
Requirement of the Spindle Checkpoint for Proper Chromosome Segregation in Budding Yeast Meiosis
inferredcites →https://doi.org/10.1146/annurev.biochem.74.082803.133219openalex-snapshot
THE STRUCTURE AND FUNCTION OF SMC AND KLEISIN COMPLEXES
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.3155549openalex-extracted
EWSR1 Regulates PRDM9-Dependent Histone 3 Methylation and Links Recombination Hotspots With the Chromosomal Axis
inferred← citeshttps://doi.org/10.1002/bies.202000018openalex-snapshot
Meiosis I Kinase Regulators: Conserved Orchestrators of Reductional Chromosome Segregation
inferred← citeshttps://doi.org/10.1002/bies.20448openalex-snapshot
Shugoshin and PP2A, shared duties at the centromere
inferred← citeshttps://doi.org/10.1002/pmic.201400072openalex-snapshot
Proteomic and phosphoproteomic analyses of chromatin‐associated proteins from Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1002/pmic.201400073openalex-snapshot
Phosphorylation‐dependent regulation of plant chromatin and chromatin‐associated proteins
inferred← citeshttps://doi.org/10.1007/978-0-387-69076-6_13openalex-snapshot
Roles of Centromeres and Kinetochores in Meiosis
inferred← citeshttps://doi.org/10.1007/978-0-387-69076-6_6openalex-snapshot
Kinetochore Composition, Formation, and Organization
inferred← citeshttps://doi.org/10.1007/978-1-4939-0888-2_11openalex-snapshot
The Roles of Cohesins in Mitosis, Meiosis, and Human Health and Disease
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/s00018-012-0974-9openalex-snapshot
How to halve ploidy: lessons from budding yeast meiosis
inferred← citeshttps://doi.org/10.1007/s00294-018-0832-xopenalex-snapshot
An interplay between Shugoshin and Spo13 for centromeric cohesin protection and sister kinetochore mono-orientation during meiosis I in Saccharomyces cerevisiae
inferred← citeshttps://doi.org/10.1007/s00294-019-00959-xopenalex-snapshot
Meiotic prophase-like pathway for cleavage-independent removal of cohesin for chromosome morphogenesis
inferred← citeshttps://doi.org/10.1007/s00412-008-0190-4openalex-snapshot
Shugoshin regulates cohesion by driving relocalization of PP2A in Xenopus extracts
inferred← citeshttps://doi.org/10.1007/s00412-010-0284-7openalex-snapshot
OsSPO11-1 is essential for both homologous chromosome pairing and crossover formation in rice
inferred← citeshttps://doi.org/10.1007/s00412-013-0439-4openalex-snapshot
Couples, pairs, and clusters: mechanisms and implications of centromere associations in meiosis
inferred← citeshttps://doi.org/10.1007/s10577-008-9013-yopenalex-snapshot
Studies of meiosis disclose distinct roles of cohesion in the core centromere and pericentromeric regions
inferred← citeshttps://doi.org/10.1007/s10577-008-9015-9openalex-snapshot
Lampbrush chromosomes enable study of cohesin dynamics
inferred← citeshttps://doi.org/10.1007/s12043-008-0187-9openalex-snapshot
Magnetic field dependence of vortex activation energy: A comparison between MgB2, NbSe2 and Bi2Sr2Ca2Cu3O10 superconductors
inferred← citeshttps://doi.org/10.1007/s12275-019-8541-9openalex-snapshot
The nature of meiotic chromosome dynamics and recombination in budding yeast
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2012.05.027openalex-snapshot
Cohesin: A guardian of genome integrity
inferred← citeshttps://doi.org/10.1016/j.ceb.2009.08.003openalex-snapshot
Protein phosphatases take the mitotic stage
inferred← citeshttps://doi.org/10.1016/j.ceb.2013.07.009openalex-snapshot
Meiosis I: when chromosomes undergo extreme makeover
inferred← citeshttps://doi.org/10.1016/j.chembiol.2007.09.011openalex-snapshot
A Coupled Chemical-Genetic and Bioinformatic Approach to Polo-like Kinase Pathway Exploration
inferred← citeshttps://doi.org/10.1016/j.cub.2013.02.028openalex-snapshot
Chromosome Segregation: Disarming the Protector
inferred← citeshttps://doi.org/10.1016/j.cub.2023.11.061openalex-snapshot
Age-dependent loss of cohesion protection in human oocytes
inferred← citeshttps://doi.org/10.1016/j.cub.2025.08.019openalex-snapshot
Crossover designation recruits condensin to reorganize the meiotic chromosome axis
inferred← citeshttps://doi.org/10.1016/j.devcel.2009.07.015openalex-snapshot
Polo Kinase and Separase Regulate the Mitotic Licensing of Centriole Duplication in Human Cells
inferred← citeshttps://doi.org/10.1016/j.devcel.2010.01.014openalex-snapshot
Rec8 Phosphorylation by Casein Kinase 1 and Cdc7-Dbf4 Kinase Regulates Cohesin Cleavage by Separase during Meiosis
inferred← citeshttps://doi.org/10.1016/j.devcel.2019.04.003openalex-snapshot
Reductional Meiosis I Chromosome Segregation Is Established by Coordination of Key Meiotic Kinases
inferred← citeshttps://doi.org/10.1016/j.devcel.2021.06.019openalex-snapshot
Separase cleaves the kinetochore protein Meikin at the meiosis I/II transition
inferred← citeshttps://doi.org/10.1016/j.devcel.2021.10.017openalex-snapshot
Loss of sister kinetochore co-orientation and peri-centromeric cohesin protection after meiosis I depends on cleavage of centromeric REC8
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2021.12.023openalex-snapshot
Whole exome sequencing in a cohort of familial premature ovarian insufficiency cases reveals a broad array of pathogenic or likely pathogenic variants in 50% of families
inferred← citeshttps://doi.org/10.1016/j.molcel.2009.04.013openalex-snapshot
Polo Kinase Regulates Mitotic Chromosome Condensation by Hyperactivation of Condensin DNA Supercoiling Activity
inferred← citeshttps://doi.org/10.1016/j.molcel.2009.06.031openalex-snapshot
Structure and Function of the PP2A-Shugoshin Interaction
inferred← citeshttps://doi.org/10.1016/j.tig.2012.03.003openalex-snapshot
Shugoshins: from protectors of cohesion to versatile adaptors at the centromere
inferred← citeshttps://doi.org/10.1016/j.tig.2017.03.005openalex-snapshot
Specialize and Divide (Twice): Functions of Three Aurora Kinase Homologs in Mammalian Oocyte Meiotic Maturation
inferred← citeshttps://doi.org/10.1016/j.yexcr.2009.05.011openalex-snapshot
The role of meiotic cohesin REC8 in chromosome segregation in γ irradiation-induced endopolyploid tumour cells
inferred← citeshttps://doi.org/10.1038/emboj.2011.187openalex-snapshot
Shugoshin is a Mad1/Cdc20‐like interactor of Mad2
inferred← citeshttps://doi.org/10.1038/ncb1667openalex-snapshot
Unified mode of centromeric protection by shugoshin in mammalian oocytes and somatic cells
inferred← citeshttps://doi.org/10.1038/ncb2052openalex-snapshot
Shugoshin–PP2A counteracts casein-kinase-1-dependent cleavage of Rec8 by separase
inferred← citeshttps://doi.org/10.1038/nrg2454openalex-snapshot
Emerging roles for centromeres in meiosis I chromosome segregation
inferred← citeshttps://doi.org/10.1038/nrm3349openalex-snapshot
Geometry and force behind kinetochore orientation: lessons from meiosis
inferred← citeshttps://doi.org/10.1038/s41477-021-00889-yopenalex-snapshot
HIGH CROSSOVER RATE1 encodes PROTEIN PHOSPHATASE X1 and restricts meiotic crossovers in Arabidopsis
inferred← citeshttps://doi.org/10.1038/s41580-025-00933-1openalex-snapshot
Organization of replicated chromosomes by DNA loops and sister chromatid cohesion
inferred← citeshttps://doi.org/10.1038/sj.emboj.7601683openalex-snapshot
Proteomic screen defines the Polo‐box domain interactome and identifies Rock2 as a Plk1 substrate
inferred← citeshttps://doi.org/10.1042/bj20100151openalex-snapshot
Cohesin: a regulator of genome integrity and gene expression
inferred← citeshttps://doi.org/10.1073/pnas.1311845110openalex-snapshot
Polo kinase Cdc5 is a central regulator of meiosis I
inferred← citeshttps://doi.org/10.1073/pnas.2312820121openalex-snapshot
Absence of chromosome axis protein recruitment prevents meiotic recombination chromosome-wide in the budding yeast Lachancea kluyveri
inferred← citeshttps://doi.org/10.1073/pnas.2414426122openalex-snapshot
Yeast centrosomes act as organizing centers to promote Polo kinase–mediated adaptation to persistent DNA damage
inferred← citeshttps://doi.org/10.1074/jbc.m116.727438openalex-snapshot
Physical Association of Saccharomyces cerevisiae Polo-like Kinase Cdc5 with Chromosomal Cohesin Facilitates DNA Damage Response
inferred← citeshttps://doi.org/10.1074/mcp.m110.004457openalex-snapshot
The Plk1-dependent Phosphoproteome of the Early Mitotic Spindle
inferred← citeshttps://doi.org/10.1080/15384101.2015.1100770openalex-snapshot
Unique subcellular distribution of phosphorylated Plk1 (Ser137 and Thr210) in mouse oocytes during meiotic division and pPlk1Ser137involvement in spindle formation and REC8 cleavage
inferred← citeshttps://doi.org/10.1083/jcb.202006094openalex-snapshot
Spatial and temporal control of targeting Polo-like kinase during meiotic prophase
inferred← citeshttps://doi.org/10.1091/mbc.e07-06-0584openalex-snapshot
Shugoshin Promotes Sister Kinetochore Biorientation inSaccharomyces cerevisiae
inferred← citeshttps://doi.org/10.1091/mbc.e08-06-0637openalex-snapshot
The Multiple Roles of Cohesin in Meiotic Chromosome Morphogenesis and Pairing
inferred← citeshttps://doi.org/10.1091/mbc.e16-01-0004openalex-snapshot
Polo kinase Cdc5 associates with centromeres to facilitate the removal of centromeric cohesin during mitosis
inferred← citeshttps://doi.org/10.1091/mbc.e17-02-0101openalex-snapshot
Destabilization of the replication fork protection complex disrupts meiotic chromosome segregation
inferred← citeshttps://doi.org/10.1091/mbc.e20-09-0604openalex-snapshot
EWSR1 affects PRDM9-dependent histone 3 methylation and provides a link between recombination hotspots and the chromosome axis protein REC8
inferred← citeshttps://doi.org/10.1093/biolre/ioag086openalex-snapshot
Molecular basis of chromosome segregation and age-associated errors in oocyte meiosis I
inferred← citeshttps://doi.org/10.1093/biolre/ioag134openalex-snapshot
Meiosis-specific cohesin in mammalian germ cells
inferred← citeshttps://doi.org/10.1093/nar/gkac640openalex-snapshot
The S. cerevisiae m6A-reader Pho92 promotes timely meiotic recombination by controlling key methylated transcripts
inferred← citeshttps://doi.org/10.1093/nar/gkw682openalex-snapshot
Meiotic prophase roles of Rec8 in crossover recombination and chromosome structure
inferred← citeshttps://doi.org/10.1093/nar/gkw715openalex-snapshot
The interplay between chromosome stability and cell cycle control explored through gene–gene interaction and computational simulation
inferred← citeshttps://doi.org/10.1093/nar/gkz903openalex-snapshot
Recruitment of Rec8, Pds5 and Rad61/Wapl to meiotic homolog pairing, recombination, axis formation and S-phase
inferred← citeshttps://doi.org/10.1093/plcell/koab257openalex-snapshot
Heat stress reveals a specialized variant of the pachytene checkpoint in meiosis of Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1096/fasebj.23.1_supplement.656.1openalex-snapshot
Regulation of meiotic recombination by a multifunctional ATF/CREB protein
inferred← citeshttps://doi.org/10.1101/2024.06.13.598907openalex-snapshot
Centrosomes act as organizing centers to promote Polo kinase-mediated adaptation to persistent DNA damage
inferred← citeshttps://doi.org/10.1101/250589openalex-snapshot
Meiosis-specific prophase-like pathway controls cleavage-independent release of cohesin by Wapl phosphorylation
inferred← citeshttps://doi.org/10.1101/gad.1626608openalex-snapshot
Cdc7-dependent phosphorylation of Mer2 facilitates initiation of yeast meiotic recombination
inferred← citeshttps://doi.org/10.1101/gad.1711408openalex-snapshot
Polo-like kinase Cdc5 drives exit from pachytene during budding yeast meiosis
inferred← citeshttps://doi.org/10.1101/gad.1724308openalex-snapshot
The cohesin complex and its roles in chromosome biology
inferred← citeshttps://doi.org/10.1101/gad.240291.114openalex-snapshot
Tension-dependent removal of pericentromeric shugoshin is an indicator of sister chromosome biorientation
inferred← citeshttps://doi.org/10.1101/gad.255554.114openalex-snapshot
From equator to pole: splitting chromosomes in mitosis and meiosis
inferred← citeshttps://doi.org/10.1101/gad.459308openalex-snapshot
Coupling meiotic chromosome axis integrity to recombination
inferred← citeshttps://doi.org/10.1101/gad.507509openalex-snapshot
Shugoshin prevents cohesin cleavage by PP2ACdc55-dependent inhibition of separase
inferred← citeshttps://doi.org/10.1104/pp.18.01320openalex-snapshot
Protein Phosphatase 2A B'α and B'β Protect Centromeric Cohesion during Meiosis I
inferred← citeshttps://doi.org/10.1111/gtc.12652openalex-snapshot
The cohesin complex in mammalian meiosis
inferred← citeshttps://doi.org/10.1111/gtc.12653openalex-snapshot
Meiosis‐specific cohesin component, Rec8, promotes the localization of Mps3 SUN domain protein on the nuclear envelope
inferred← citeshttps://doi.org/10.1111/gtc.13081openalex-snapshot
DNA double‐strand breaks regulate the cleavage‐independent release of Rec8‐cohesin during yeast meiosis
inferred← citeshttps://doi.org/10.1111/j.1600-0463.2008.00983.xopenalex-snapshot
Maternal Epstein‐Barr virus and cytomegalovirus infections and risk of testicular cancer in the offspring: a nested case‐control study
inferred← citeshttps://doi.org/10.1111/j.1742-4658.2009.07502.xopenalex-snapshot
From meiosis to postmeiotic events: Homologous recombination is obligatory but flexible
inferred← citeshttps://doi.org/10.1111/jipb.13872openalex-snapshot
Somatic variations in the meiosis‐specific gene CrMER3 confer seedlessness in a citrus bud sport
inferred← citeshttps://doi.org/10.1111/tpj.13019openalex-snapshot
Proteomic and phosphoproteomic analyses reveal extensive phosphorylation of regulatory proteins in developing rice anthers
inferred← citeshttps://doi.org/10.1111/tpj.13752openalex-snapshot
Affinity proteomics reveals extensive phosphorylation of the Brassica chromosome axis protein ASY 1 and a network of associated proteins at prophase I of meiosis
inferred← citeshttps://doi.org/10.1126/scisignal.2001796openalex-snapshot
Spatial Exclusivity Combined with Positive and Negative Selection of Phosphorylation Motifs Is the Basis for Context-Dependent Mitotic Signaling
inferred← citeshttps://doi.org/10.1126/scisignal.2002010openalex-snapshot
Large-Scale Discovery of ERK2 Substrates Identifies ERK-Mediated Transcriptional Regulation by ETV3
inferred← citeshttps://doi.org/10.1128/mcb.00279-09openalex-snapshot
Mcl-1 Integrates the Opposing Actions of Signaling Pathways That Mediate Survival and Apoptosis
inferred← citeshttps://doi.org/10.1128/mcb.01176-14openalex-snapshot
Shugoshins: Tension-Sensitive Pericentromeric Adaptors Safeguarding Chromosome Segregation
inferred← citeshttps://doi.org/10.1146/annurev-biochem-061708-092640openalex-snapshot
Regulators of the Cohesin Network
inferred← citeshttps://doi.org/10.1146/annurev-genet-102108-134233openalex-snapshot
Cohesin: Its Roles and Mechanisms
inferred← citeshttps://doi.org/10.1155/2009/726728openalex-snapshot
Integrative Decomposition Procedure and Kappa Statistics for the Distinguished Single Molecular Network Construction and Analysis
inferred← citeshttps://doi.org/10.1159/000323793openalex-snapshot
The Role of Shugoshin in Meiotic Chromosome Segregation
inferred← citeshttps://doi.org/10.1242/jcs.03324openalex-snapshot
Chromosome cohesion in mitosis and meiosis
inferred← citeshttps://doi.org/10.1242/jcs.035287openalex-snapshot
Role of cleavage by separase of the Rec8 kleisin subunit of cohesin during mammalian meiosis I
inferred← citeshttps://doi.org/10.1242/jcs.161273openalex-snapshot
Sgo1 recruits PP2A to chromosomes to ensure sister chromatid bi-orientation in mitosis
inferred← citeshttps://doi.org/10.12688/wellcomeopenres.15066.1openalex-snapshot
Spo13 prevents premature cohesin cleavage during meiosis
inferred← citeshttps://doi.org/10.1371/journal.pgen.1005225openalex-snapshot
Casein Kinase 1 and Phosphorylation of Cohesin Subunit Rec11 (SA3) Promote Meiotic Recombination through Linear Element Formation
inferred← citeshttps://doi.org/10.1371/journal.pgen.1007851openalex-snapshot
Meiosis-specific prophase-like pathway controls cleavage-independent release of cohesin by Wapl phosphorylation
inferred← citeshttps://doi.org/10.1371/journal.pone.0155931openalex-snapshot
Identification of Putative Mek1 Substrates during Meiosis in Saccharomyces cerevisiae Using Quantitative Phosphoproteomics
inferred← citeshttps://doi.org/10.15252/embr.201541060openalex-snapshot
Sororin loads to the synaptonemal complex central region independently of meiotic cohesin complexes
inferred← citeshttps://doi.org/10.15252/embr.202052295openalex-snapshot
A highly conserved pocket on PP2A-B56 is required for hSgo1 binding and cohesion protection during mitosis
inferred← citeshttps://doi.org/10.1534/g3.114.013888openalex-snapshot
A Method for Sporulating Budding Yeast Cells That Allows for Unbiased Identification of Kinase Substrates Using Stable Isotope Labeling by Amino Acids in Cell Culture
inferred← citeshttps://doi.org/10.1534/genetics.112.145144openalex-snapshot
Chromosome Segregation in Budding Yeast: Sister Chromatid Cohesion and Related Mechanisms
inferred← citeshttps://doi.org/10.1534/genetics.117.199703openalex-snapshot
Coordination of Double Strand Break Repair and Meiotic Progression in Yeast by a Mek1-Ndt80 Negative Feedback Loop
inferred← citeshttps://doi.org/10.17077/etd.pxn6py62openalex-snapshot
The signal between the initiation of recombination and the first division of meiosis in Saccharomyces cervisiae
inferred← citeshttps://doi.org/10.3389/fcell.2017.00109openalex-snapshot
Multiple Duties for Spindle Assembly Checkpoint Kinases in Meiosis
inferred← citeshttps://doi.org/10.3389/fcell.2021.667073openalex-snapshot
Phospho-Regulation of Meiotic Prophase
inferred← citeshttps://doi.org/10.3389/fpls.2014.00167openalex-snapshot
OsRAD51C is essential for double-strand break repair in rice meiosis
inferred← citeshttps://doi.org/10.3389/fpls.2018.00829openalex-snapshot
Tackling Plant Meiosis: From Model Research to Crop Improvement
inferred← citeshttps://doi.org/10.3390/genes13030546openalex-snapshot
Loss, Gain, and Retention: Mechanisms Driving Late Prophase I Chromosome Remodeling for Accurate Meiotic Chromosome Segregation
inferred← citeshttps://doi.org/10.3390/genes2010260openalex-snapshot
NEK1 Facilitates Cohesin Removal during Mammalian Spermatogenesis
inferred← citeshttps://doi.org/10.4014/jmb.1501.01081openalex-snapshot
Mitotic Cohesin Subunit Mcd1 Regulates the Progression of Meiotic Recombination in Budding Yeast
inferred← citeshttps://doi.org/10.4161/cc.10.6.15032openalex-snapshot
Sgo1 is required for co-segregation of sister chromatids during achiasmate meiosis I
inferred← citeshttps://doi.org/10.4161/cc.20633openalex-snapshot
Shugoshins function as a guardian for chromosomal stability in nuclear division
inferred← citeshttps://doi.org/10.4161/cc.7.2.5325openalex-snapshot
What makes centromeric cohesion resistant to separase cleavage during meiosis I but not during meiosis II?
inferred← citeshttps://doi.org/10.4161/cc.9.13.12146openalex-snapshot
Casein kinase 1 is required for efficient removal of Rec8 during meiosis I
inferred← citeshttps://doi.org/10.4161/cc.9.6.11068openalex-snapshot
Analysis of Polo-like kinase Cdc5 in the meiosis recombination checkpoint
inferred← citeshttps://doi.org/10.4236/ojgen.2012.21001openalex-snapshot
Irr1/Scc3 cohesin interacts with Rec8 in meiotic prophase of Saccharomyces cerevisiae
inferred← citeshttps://doi.org/10.70675/040b3488z29f5z484fz8d84z5da8d7354a16openalex-snapshot
Exploring the phosphoproteome landscape at the transition from the first to the second meiotic division
inferred← citeshttps://doi.org/10.70675/551b43b1zd937z4c11z920dzf3963c9bf07bopenalex-snapshot
Role of the protein kinase MPS1 in the regulation of chromosome segregation in budding yeast mitosis
inferred← citeshttps://doi.org/10.70675/88aa41c7z2926z475bzad55z97961883fb55openalex-snapshot
Interplay between meiotic crossing-overs and chromosome architecture : role of the meiosis specific complex Zip2-Zip4-Spo16
inferred← citeshttps://doi.org/10.7554/elife.00117openalex-snapshot
Meiosis I chromosome segregation is established through regulation of microtubule–kinetochore interactions
inferred← citeshttps://doi.org/10.7554/elife.23437openalex-snapshot
Polo-like kinase-dependent phosphorylation of the synaptonemal complex protein SYP-4 regulates double-strand break formation through a negative feedback loop.
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