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Sister-chromatid separation at anaphase onset is promoted by cleavage of the cohesin subunit Scc1
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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/elps.11501401133openalex-snapshot
Structural characterization of blotting membranes and the influence of membrane parameters for electroblotting and subsequent amino acid sequence analysis of proteins
inferredcites →https://doi.org/10.1002/j.1460-2075.1996.tb01052.xopenalex-snapshot
Fission yeast Cut1 and Cut2 are essential for sister chromatid separation, concentrate along the metaphase spindle and form large complexes.
inferredcites →https://doi.org/10.1016/0092-8674(90)90266-hopenalex-snapshot
The fission yeast cut1+ gene regulates spindle pole body duplication and has homology to the budding yeast ESP1 gene
inferredcites →https://doi.org/10.1016/0378-1119(88)90185-0openalex-snapshot
New yeast-Escherichia coli shuttle vectors constructed with in vitro mutagenized yeast genes lacking six-base pair restriction sites
inferredcites →https://doi.org/10.1016/s0021-9258(19)49597-5openalex-snapshot
The bimB3 mutation of Aspergillus nidulans uncouples DNA replication from the completion of mitosis.
inferredcites →https://doi.org/10.1016/s0092-8674(00)80914-9openalex-snapshot
An Anaphase Calcium Signal Controls Chromosome Disjunction in Early Sea Urchin Embryos
inferredcites →https://doi.org/10.1016/s0092-8674(00)81211-8openalex-snapshot
An ESP1/PDS1 Complex Regulates Loss of Sister Chromatid Cohesion at the Metaphase to Anaphase Transition in Yeast
inferredcites →https://doi.org/10.1016/s0092-8674(01)80007-6openalex-snapshot
Cohesins: Chromosomal Proteins that Prevent Premature Separation of Sister Chromatids
inferredcites →https://doi.org/10.1016/s0092-8674(01)80008-8openalex-snapshot
A Direct Link between Sister Chromatid Cohesion and Chromosome Condensation Revealed through the Analysis of MCD1 in S. cerevisiae
inferredcites →https://doi.org/10.1016/s0955-0674(96)80077-9openalex-snapshot
The spindle assembly checkpoint
inferredcites →https://doi.org/10.1016/s0955-0674(98)80119-1openalex-snapshot
SCF and APC: the Yin and Yang of cell cycle regulated proteolysis
inferredcites →https://doi.org/10.1016/s0960-9822(98)70088-0openalex-snapshot
Cdc20 is essential for the cyclosome-mediated proteolysis of both Pds1 and Clb2 during M phase in budding yeast
inferredcites →https://doi.org/10.1016/s0960-9822(98)70250-7openalex-snapshot
Cut1 is loaded onto the spindle by binding to Cut2 and promotes anaphase spindle movement upon Cut2 proteolysis
inferredcites →https://doi.org/10.1016/s0960-9822(98)70463-4openalex-snapshot
Cohesion between sister chromatids must be established during DNA replication
inferredcites →https://doi.org/10.1016/s0962-8924(98)01299-9openalex-snapshot
The vertebrate cell kinetochore and its roles during mitosis
inferredcites →https://doi.org/10.1016/s0968-0004(99)01358-4openalex-snapshot
Separating sister chromatids
inferredcites →https://doi.org/10.1038/381438a0openalex-snapshot
Cut2 proteolysis required for sister-chromatid separation in fission yeast
inferredcites →https://doi.org/10.1074/jbc.270.13.7703openalex-snapshot
The rad21 Gene Product of Schizosaccharomyces pombe Is a Nuclear, Cell Cycle-regulated Phosphoprotein
inferredcites →https://doi.org/10.1074/jbc.273.37.24088openalex-snapshot
Structural Maintenance of Chromosomes Protein C-terminal Domains Bind Preferentially to DNA with Secondary Structure
inferredcites →https://doi.org/10.1083/jcb.131.1.7openalex-snapshot
A postprophase topoisomerase II-dependent chromatid core separation step in the formation of metaphase chromosomes.
inferredcites →https://doi.org/10.1083/jcb.133.1.99openalex-snapshot
Pds1p, an inhibitor of anaphase in budding yeast, plays a critical role in the APC and checkpoint pathway(s).
inferredcites →https://doi.org/10.1083/jcb.142.6.1595openalex-snapshot
The Symmetrical Structure of Structural Maintenance of Chromosomes (SMC) and MukB Proteins: Long, Antiparallel Coiled Coils, Folded at a Flexible Hinge
inferredcites →https://doi.org/10.1091/mbc.3.12.1443openalex-snapshot
Requirement for ESP1 in the nuclear division of Saccharomyces cerevisiae.
inferredcites →https://doi.org/10.1093/dnares/1.5.223openalex-snapshot
Prediction of the Coding Sequences of Unidentified Human Genes. II. The Coding Sequences of 40 New Genes (KIAA0041-KIAA0080) Deduced by Analysis of cDNA Clones from Human Cell Line KG-1
inferredcites →https://doi.org/10.1093/dnares/3.1.17openalex-snapshot
Prediction of the Coding Sequences of Unidentified Human Genes. V. The Coding Sequences of 40 New Genes (KIAA0161-KIAA0200) Deduced by Analysis of cDNA Clones from Human Cell Line KG-1
inferredcites →https://doi.org/10.1093/emboj/18.10.2707openalex-snapshot
Sister chromatid separation and chromosome re‐duplication are regulated by different mechanisms in response to spindle damage
inferredcites →https://doi.org/10.1093/genetics/132.1.75openalex-snapshot
Meiotically induced rec7 and rec8 genes of Schizosaccharomyces pombe.
inferredcites →https://doi.org/10.1093/genetics/141.1.61openalex-snapshot
The rec8 gene of Schizosaccharomyces pombe is involved in linear element formation, chromosome pairing and sister-chromatid cohesion during meiosis.
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.11.24.3375openalex-snapshot
Persistent initiation of DNA replication and chromatin-bound MCM proteins during the cell cycle in cdc6 mutants
inferredcites →https://doi.org/10.1101/gad.12.13.1986openalex-snapshot
Identification of Xenopus SMC protein complexes required for sister chromatid cohesion
inferredcites →https://doi.org/10.1101/gad.13.3.307openalex-snapshot
Ctf7p is essential for sister chromatid cohesion and links mitotic chromosome structure to the DNA replication machinery
inferredcites →https://doi.org/10.1101/gad.13.3.320openalex-snapshot
Yeast Cohesin complex requires a conserved protein, Eco1p(Ctf7), to establish cohesion between sister chromatids during DNA replication
inferredcites →https://doi.org/10.1146/annurev.bb.17.060188.002243openalex-snapshot
The Forces that Move Chromosomes in Mitosis
inferredcites →https://doi.org/10.1146/annurev.ge.28.120194.001123openalex-snapshot
SISTER-CHROMATID COHESION IN MITOSIS AND MEIOSIS
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/(sici)1521-1878(200004)22:4<351::aid-bies5>3.0.co;2-wopenalex-snapshot
Checkpoints controlling mitosis
inferred← citeshttps://doi.org/10.1002/0471684228.egp11627openalex-snapshot
Sister Chromatid Cohesion
inferred← citeshttps://doi.org/10.1002/1873-3468.14949openalex-snapshot
Cohesin — bridging the gap among gene transcription, genome stability, and human diseases
inferred← citeshttps://doi.org/10.1002/9780470015902.a0005917.pub2openalex-snapshot
Mitosis and Meiosis: Molecular Control of Chromosome Separation
inferred← citeshttps://doi.org/10.1002/9780470015902.a0022413.pub2openalex-snapshot
Sister Chromatid Cohesion, Chromosome Instability ( CIN ) and Diseases
inferred← citeshttps://doi.org/10.1002/advs.202411988openalex-snapshot
Nuclear Overexpression of SAMHD1 Induces M Phase Stalling in Hepatoma Cells and Suppresses HCC Progression by Interacting with the Cohesin Complex
inferred← citeshttps://doi.org/10.1002/bies.10361openalex-snapshot
Building and breaking bridges between sister chromatids
inferred← citeshttps://doi.org/10.1002/bies.1133openalex-snapshot
Shaping the metaphase chromosome: coordination of cohesion and condensation
inferred← citeshttps://doi.org/10.1002/bies.201800182openalex-snapshot
Are SMC Complexes Loop Extruding Factors? Linking Theory With Fact
inferred← citeshttps://doi.org/10.1002/cbin.70220openalex-snapshot
Sister Chromatid Cohesion: A Multilayered Regulatory Network Beyond the Cohesin Ring
inferred← citeshttps://doi.org/10.1002/cm.20072openalex-snapshot
SAC‐ing mitotic errors: How the spindle assembly checkpoint (SAC) plays defense against chromosome mis‐segregation
inferred← citeshttps://doi.org/10.1002/cm.20118openalex-snapshot
Temporal change in local forces and total force all over the surface of the sea urchin egg during cytokinesis
inferred← citeshttps://doi.org/10.1002/em.20412openalex-snapshot
Faulty spindle checkpoint and cohesion protein activities predispose oocytes to premature chromosome separation and aneuploidy
inferred← citeshttps://doi.org/10.1002/jcb.10324openalex-snapshot
Establishment of dependence relationships between genome replication and mitosis
inferred← citeshttps://doi.org/10.1002/jcb.25835openalex-snapshot
Separase: Function Beyond Cohesion Cleavage and an Emerging Oncogene
inferred← citeshttps://doi.org/10.1002/jcp.21086openalex-snapshot
Separase, securin and Rad21 in neural cell growth
inferred← citeshttps://doi.org/10.1002/pro.3030openalex-snapshot
Structural aspects of HDAC8 mechanism and dysfunction in Cornelia de Lange syndrome spectrum disorders
inferred← citeshttps://doi.org/10.1002/prot.10060openalex-snapshot
Classification of the caspase–hemoglobinase fold: Detection of new families and implications for the origin of the eukaryotic separins
inferred← citeshttps://doi.org/10.1002/sstr.202400203openalex-snapshot
Rethinking Models of DNA Organization in Micrometer‐Sized Chromosomes from the Perspective of the Nanoproperties of Chromatin Favoring a Multilayer Structure
inferred← citeshttps://doi.org/10.1002/wdev.190openalex-snapshot
Etiology and pathogenesis of the cohesinopathies
inferred← citeshttps://doi.org/10.1002/yea.1410openalex-snapshot
The fission yeast spindle orientation checkpoint: a model that generates tension?
inferred← citeshttps://doi.org/10.1002/yea.761openalex-snapshot
Genetic analysis of TAF68/61 reveals links to cell cycle regulators
inferred← citeshttps://doi.org/10.1002/yea.803openalex-snapshot
SRC1: an intron‐containing yeast gene involved in sister chromatid segregation
inferred← citeshttps://doi.org/10.1006/cbir.2002.0867openalex-snapshot
DNA PLASMID TRANSMISSION IN YEAST IS ASSOCIATED WITH SPECIFIC SUB‐NUCLEAR LOCALISATION DURING CELL DIVISION
inferred← citeshttps://doi.org/10.1006/excr.1999.4651openalex-snapshot
Chromosome Segregation and Cancer
inferred← citeshttps://doi.org/10.1006/geno.2001.6474openalex-snapshot
Disruption of Apc10/Doc1 in Three Alleles of Oligosyndactylism
inferred← citeshttps://doi.org/10.1006/jsbi.2000.4255openalex-snapshot
Review: SMCs in the World of Chromosome Biology— From Prokaryotes to Higher Eukaryotes
inferred← citeshttps://doi.org/10.1007/1-4020-3764-3_10openalex-snapshot
The Dream of Every Chromosome: Equal Segregation for a Healthy Life of the Host
inferred← citeshttps://doi.org/10.1007/978-0-387-69076-6_2openalex-snapshot
The Basics of Chromosome Segregation
inferred← citeshttps://doi.org/10.1007/978-1-4419-6448-9_11openalex-snapshot
Cornelia de Lange Syndrome
inferred← citeshttps://doi.org/10.1007/978-1-4614-1683-8_11openalex-snapshot
Cohesin and Human Diseases
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/10.1007/978-1-4939-0888-2_4openalex-snapshot
Cell Cycle Regulation by Protein Degradation
inferred← citeshttps://doi.org/10.1007/978-1-4939-0888-2_5openalex-snapshot
Linking Chromosome Duplication and Segregation via Sister Chromatid Cohesion
inferred← citeshttps://doi.org/10.1007/978-1-4939-6502-1_4openalex-snapshot
Determination of Cell Cycle Stage and Mitotic Exit Through the Quantification of the Protein Levels of Known Mitotic Regulators
inferred← citeshttps://doi.org/10.1007/978-1-4939-6545-8_4openalex-snapshot
Detection of Cohesin SUMOylation In Vivo
inferred← citeshttps://doi.org/10.1007/978-1-4939-7306-4_32openalex-snapshot
Imaging of DNA Ultrafine Bridges in Budding Yeast
inferred← citeshttps://doi.org/10.1007/978-3-030-23173-6_18openalex-snapshot
Centrosome Amplification and Tumorigenesis: Cause or Effect?
inferred← citeshttps://doi.org/10.1007/978-3-030-28151-9_18openalex-snapshot
The Anaphase Promoting Complex/Cyclosome (APC/C): A Versatile E3 Ubiquitin Ligase
inferred← citeshttps://doi.org/10.1007/978-3-030-58532-7_15openalex-snapshot
Cell Cycle, DNA Replication, Centrosomes, Centrioles and Cell Division
inferred← citeshttps://doi.org/10.1007/978-3-030-58971-4_4openalex-snapshot
Structure and Function of the Separase-Securin Complex
inferred← citeshttps://doi.org/10.1007/978-3-031-06573-6_12openalex-snapshot
Epigenetic-Mediated Regulation of Gene Expression for Biological Control and Cancer: Cell and Tissue Structure, Function, and Phenotype
inferred← citeshttps://doi.org/10.1007/978-3-031-06573-6_13openalex-snapshot
Epigenetic-Mediated Regulation of Gene Expression for Biological Control and Cancer: Fidelity of Mechanisms Governing the Cell Cycle
inferred← citeshttps://doi.org/10.1007/978-3-319-58592-5_20openalex-snapshot
Centromeric Cohesin: Molecular Glue and Much More
inferred← citeshttps://doi.org/10.1007/978-3-642-55747-7_4openalex-snapshot
SMC Protein Complexes and the Maintenance of Chromosome Integrity
inferred← citeshttps://doi.org/10.1007/978-4-431-88663-1_17openalex-snapshot
Expression of Rad21 Cleaved Products in Oral Epithelium
inferred← citeshttps://doi.org/10.1007/b136681openalex-snapshot
The ubiquitin-proteasome pathway in cell cycle control
inferred← citeshttps://doi.org/10.1007/bf02703338openalex-snapshot
Stable propagation of ‘selfish’ genetic elements
inferred← citeshttps://doi.org/10.1007/s00018-007-6443-1openalex-snapshot
Mitotic regulation of the anaphase-promoting complex
inferred← citeshttps://doi.org/10.1007/s00018-008-8479-2openalex-snapshot
Mid-anaphase arrest in S. cerevisiae cells eliminated for the function of Cin8 and dynein
inferred← citeshttps://doi.org/10.1007/s00018-009-0004-8openalex-snapshot
Cohesins: chromatin architects in chromosome segregation, control of gene expression and much more
inferred← citeshttps://doi.org/10.1007/s00018-024-05122-5openalex-snapshot
Role of chromosomal cohesion and separation in aneuploidy and tumorigenesis
inferred← citeshttps://doi.org/10.1007/s00294-016-0634-yopenalex-snapshot
A role for the spindle assembly checkpoint in the DNA damage response
inferred← citeshttps://doi.org/10.1007/s00294-017-0723-6openalex-snapshot
New insights into cohesin loading
inferred← citeshttps://doi.org/10.1007/s00294-017-0727-2openalex-snapshot
Functions and regulation of the Polo-like kinase Cdc5 in the absence and presence of DNA damage
inferred← citeshttps://doi.org/10.1007/s00294-018-0824-xopenalex-snapshot
Cohesin dynamic association to chromatin and interfacing with replication forks in genome integrity maintenance
inferred← citeshttps://doi.org/10.1007/s00294-018-0852-6openalex-snapshot
Chromatin mobility upon DNA damage: state of the art and remaining questions
inferred← citeshttps://doi.org/10.1007/s00412-005-0331-yopenalex-snapshot
Rephrasing anaphase: separase FEARs shugoshin
inferred← citeshttps://doi.org/10.1007/s00412-006-0072-6openalex-snapshot
Roles of the sister chromatid cohesion apparatus in gene expression, development, and human syndromes
inferred← citeshttps://doi.org/10.1007/s00412-007-0104-xopenalex-snapshot
Cohesin regulation: fashionable ways to wear a ring
inferred← citeshttps://doi.org/10.1007/s00412-007-0139-zopenalex-snapshot
The Suv39h–HP1 histone methylation pathway is dispensable for enrichment and protection of cohesin at centromeres in mammalian cells
inferred← citeshttps://doi.org/10.1007/s00412-009-0244-2openalex-snapshot
Re-examination of siRNA specificity questions role of PICH and Tao1 in the spindle checkpoint and identifies Mad2 as a sensitive target for small RNAs
inferred← citeshttps://doi.org/10.1007/s00412-013-0396-yopenalex-snapshot
An Eco1-independent sister chromatid cohesion establishment pathway in S. cerevisiae
inferred← citeshttps://doi.org/10.1007/s00412-013-0434-9openalex-snapshot
Cohesin removal precedes topoisomerase IIα-dependent decatenation at centromeres in male mammalian meiosis II
inferred← citeshttps://doi.org/10.1007/s00412-014-0474-9openalex-snapshot
Functional interplay between cohesin and Smc5/6 complexes
inferred← citeshttps://doi.org/10.1007/s00412-025-00829-1openalex-snapshot
Tetraploidy in normal tissues and diseases: mechanisms and consequences
inferred← citeshttps://doi.org/10.1007/s004120050408openalex-snapshot
Sister chromatid cohesion and recombination in meiosis
inferred← citeshttps://doi.org/10.1007/s00428-005-0132-yopenalex-snapshot
Correlation of invasion and metastasis of cancer cells, and expression of the RAD21 gene in oral squamous cell carcinoma
inferred← citeshttps://doi.org/10.1007/s00432-005-0035-yopenalex-snapshot
Jun activation domain-binding protein 1 is required for mitotic checkpoint activation via its involvement in hyperphosphorylation of 53BP1
inferred← citeshttps://doi.org/10.1007/s00438-008-0358-xopenalex-snapshot
Identification and characterisation of structural maintenance of chromosome 1 (smc1) mutants of Coprinopsis cinerea
inferred← citeshttps://doi.org/10.1007/s10577-007-1146-xopenalex-snapshot
Meiotic recombination in Caenorhabditis elegans
inferred← citeshttps://doi.org/10.1007/s10577-008-9015-9openalex-snapshot
Lampbrush chromosomes enable study of cohesin dynamics
inferred← citeshttps://doi.org/10.1007/s10577-013-9400-xopenalex-snapshot
CDK11p58 kinase activity is required to protect sister chromatid cohesion at centromeres in mitosis
inferred← citeshttps://doi.org/10.1007/s11177-005-0001-4openalex-snapshot
Mitosis: Regulation and organization of cell division
inferred← citeshttps://doi.org/10.1007/s11177-005-0051-7openalex-snapshot
Interphase cytogenetics in estimation of genomic mutations in somatic cells
inferred← citeshttps://doi.org/10.1007/s11373-007-9157-3openalex-snapshot
Dual inhibition of Cdc20 by the spindle checkpoint
inferred← citeshttps://doi.org/10.1007/s11427-015-4956-7openalex-snapshot
Regulation of sister chromatid cohesion during the mitotic cell cycle
inferred← citeshttps://doi.org/10.1007/s11515-014-1334-yopenalex-snapshot
Comparative analysis of chromosome segregation in human, yeasts and trypanosome
inferred← citeshttps://doi.org/10.1007/s11684-016-0458-7openalex-snapshot
Physiological functions and clinical implications of the N-end rule pathway
inferred← citeshttps://doi.org/10.1007/s12551-024-01235-0openalex-snapshot
Force generation and resistance in human mitosis
inferred← citeshttps://doi.org/10.1007/s13346-013-0141-3openalex-snapshot
Liposomally encapsulated CDC20 siRNA inhibits both solid melanoma tumor growth and spontaneous growth of intravenously injected melanoma cells on mouse lung
inferred← citeshttps://doi.org/10.1007/springerreference_106117openalex-snapshot
Sister Chromatid Cohesion
inferred← citeshttps://doi.org/10.1007/springerreference_36779openalex-snapshot
Sister Chromatid Cohesion
inferred← citeshttps://doi.org/10.1016/b978-0-12-369441-6.00011-8openalex-snapshot
Growth factors: Setting the Framework
inferred← citeshttps://doi.org/10.1016/b978-0-12-382219-2.00685-2openalex-snapshot
Ssy5 Peptidase: A Chymotrypsin-Like Signaling Protease in Yeast
inferred← citeshttps://doi.org/10.1016/b978-0-12-383834-6.00173-7openalex-snapshot
Pathways—Cohesinopathies
inferred← citeshttps://doi.org/10.1016/b978-0-12-387688-1.00003-xopenalex-snapshot
How Mitotic Errors Contribute to Karyotypic Diversity in Cancer
inferred← citeshttps://doi.org/10.1016/b978-0-12-397175-3.00004-1openalex-snapshot
Fertilization in Mammals
inferred← citeshttps://doi.org/10.1016/b978-0-12-416024-8.00001-5openalex-snapshot
Cohesin in Gametogenesis
inferred← citeshttps://doi.org/10.1016/b978-012515400-0/50007-5openalex-snapshot
Fertilization in Mammals
inferred← citeshttps://doi.org/10.1016/b978-1-4557-4066-6.00011-1openalex-snapshot
Regulation of the Cell Cycle
inferred← citeshttps://doi.org/10.1016/b978-141603703-3.10013-5openalex-snapshot
Regulation of the Cell Cycle
inferred← citeshttps://doi.org/10.1016/bs.apcsb.2023.02.001openalex-snapshot
Cyclin-dependent kinases in cancer: Role, regulation, and therapeutic targeting
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2022.04.007openalex-snapshot
Checkpoint control in meiotic prophase: Idiosyncratic demands require unique characteristics
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2022.06.003openalex-snapshot
Emerging mechanisms and roles of meiotic crossover repression at centromeres
inferred← citeshttps://doi.org/10.1016/j.ab.2009.05.046openalex-snapshot
Development and validation of a fluorogenic assay to measure separase enzyme activity
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.bbcan.2016.05.002openalex-snapshot
Cohesin mutations in human cancer
inferred← citeshttps://doi.org/10.1016/j.bbrc.2022.06.056openalex-snapshot
Identification of a novel substrate motif of yeast separase and deciphering the recognition specificity using AlphaFold2 and molecular dynamics simulation
inferred← citeshttps://doi.org/10.1016/j.bcp.2019.03.028openalex-snapshot
Mitotic functions of poly(ADP-ribose) polymerases
inferred← citeshttps://doi.org/10.1016/j.biolcel.2004.04.011openalex-snapshot
Drosophila cohesins DSA1 and Drad21 persist and colocalize along the centromeric heterochromatin during mitosis
inferred← citeshttps://doi.org/10.1016/j.bpj.2010.06.006openalex-snapshot
Mechanism of Cohesin Loading onto Chromosomes: A Conformational Dynamics Study
inferred← citeshttps://doi.org/10.1016/j.ceb.2016.02.018openalex-snapshot
Cell cycle control of DNA joint molecule resolution
inferred← citeshttps://doi.org/10.1016/j.ceb.2020.12.004openalex-snapshot
Nuclear envelope remodelling during mitosis
inferred← citeshttps://doi.org/10.1016/j.cell.2005.01.032openalex-snapshot
The Yeast APC/C Subunit Mnd2 Prevents Premature Sister Chromatid Separation Triggered by the Meiosis-Specific APC/C-Ama1
inferred← citeshttps://doi.org/10.1016/j.cell.2005.07.018openalex-snapshot
A Topological Interaction between Cohesin Rings and a Circular Minichromosome
inferred← citeshttps://doi.org/10.1016/j.cell.2006.03.038openalex-snapshot
Downregulation of PP2ACdc55 Phosphatase by Separase Initiates Mitotic Exit in Budding Yeast
inferred← citeshttps://doi.org/10.1016/j.cell.2011.09.047openalex-snapshot
A Quantitative Model for Ordered Cdk Substrate Dephosphorylation during Mitotic Exit
inferred← citeshttps://doi.org/10.1016/j.cell.2012.07.028openalex-snapshot
Cohesin’s DNA Exit Gate Is Distinct from Its Entrance Gate and Is Regulated by Acetylation
inferred← citeshttps://doi.org/10.1016/j.cell.2018.04.015openalex-snapshot
The Cohesin Ring Uses Its Hinge to Organize DNA Using Non-topological as well as Topological Mechanisms
inferred← citeshttps://doi.org/10.1016/j.cellsig.2017.02.003openalex-snapshot
Transcriptional and post-transcriptional regulation of Cdc20 during the spindle assembly checkpoint in S. cerevisiae
inferred← citeshttps://doi.org/10.1016/j.cellsig.2022.110303openalex-snapshot
Roles and regulation of Haspin kinase and its impact on carcinogenesis
inferred← citeshttps://doi.org/10.1016/j.celrep.2016.02.020openalex-snapshot
Crystal Structure of the Cohesin Gatekeeper Pds5 and in Complex with Kleisin Scc1
inferred← citeshttps://doi.org/10.1016/j.celrep.2017.08.092openalex-snapshot
Cohesin Can Remain Associated with Chromosomes during DNA Replication
inferred← citeshttps://doi.org/10.1016/j.celrep.2019.10.041openalex-snapshot
Cdc14 and PP2A Phosphatases Cooperate to Shape Phosphoproteome Dynamics during Mitotic Exit
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.111723openalex-snapshot
Autocleavage of Separase Suppresses its Premature Activation by Promoting Binding to Cyclin B1
inferred← citeshttps://doi.org/10.1016/j.chembiol.2014.11.005openalex-snapshot
Pregnenolone Functions in Centriole Cohesion during Mitosis
inferred← citeshttps://doi.org/10.1016/j.coisb.2018.02.004openalex-snapshot
Genome stability during cell proliferation: A systems analysis of the molecular mechanisms controlling progression through the eukaryotic cell cycle
inferred← citeshttps://doi.org/10.1016/j.critrevonc.2008.12.002openalex-snapshot
Road to the crossroads of life and death: Linking sister chromatid cohesion and separation to aneuploidy, apoptosis and cancer
inferred← citeshttps://doi.org/10.1016/j.cryobiol.2021.07.008openalex-snapshot
Melatonin promotes in vitro maturation of vitrified-warmed mouse GV oocytes potentially by modulating MAD2 protein expression of SAC component through MTRs
inferred← citeshttps://doi.org/10.1016/j.cub.2003.10.030openalex-snapshot
A Model for ATP Hydrolysis-Dependent Binding of Cohesin to DNA
inferred← citeshttps://doi.org/10.1016/j.cub.2003.10.036openalex-snapshot
ATP Hydrolysis Is Required for Cohesin's Association with Chromosomes
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.cub.2004.11.020openalex-snapshot
DNA Repair: Keeping It Together
inferred← citeshttps://doi.org/10.1016/j.cub.2005.12.028openalex-snapshot
Experimental Evolution of Mating Discrimination in Budding Yeast
inferred← citeshttps://doi.org/10.1016/j.cub.2007.12.019openalex-snapshot
Pericentric Chromatin Is Organized into an Intramolecular Loop in Mitosis
inferred← citeshttps://doi.org/10.1016/j.cub.2009.12.059openalex-snapshot
Both Interaction Surfaces within Cohesin's Hinge Domain Are Essential for Its Stable Chromosomal Association
inferred← citeshttps://doi.org/10.1016/j.cub.2012.06.045openalex-snapshot
SUMOylation of the α-Kleisin Subunit of Cohesin Is Required for DNA Damage-Induced Cohesion
inferred← citeshttps://doi.org/10.1016/j.cub.2012.10.023openalex-snapshot
Condensin, Chromatin Crossbarring and Chromosome Condensation
inferred← citeshttps://doi.org/10.1016/j.cub.2013.09.003openalex-snapshot
WAPL-Mediated Removal of Cohesin Protects against Segregation Errors and Aneuploidy
inferred← citeshttps://doi.org/10.1016/j.cub.2013.12.038openalex-snapshot
Pds5 Prevents the PolySUMO-Dependent Separation of Sister Chromatids
inferred← citeshttps://doi.org/10.1016/j.cub.2015.07.025openalex-snapshot
The Deubiquitinase USP37 Regulates Chromosome Cohesion and Mitotic Progression
inferred← citeshttps://doi.org/10.1016/j.cub.2015.12.073openalex-snapshot
Chromosome Cohesion Established by Rec8-Cohesin in Fetal Oocytes Is Maintained without Detectable Turnover in Oocytes Arrested for Months in Mice
inferred← citeshttps://doi.org/10.1016/j.cub.2017.02.019openalex-snapshot
The N-Terminal Non-Kinase-Domain-Mediated Binding of Haspin to Pds5B Protects Centromeric Cohesion in Mitosis
inferred← citeshttps://doi.org/10.1016/j.cub.2017.04.023openalex-snapshot
APC/CCdh1 Enables Removal of Shugoshin-2 from the Arms of Bivalent Chromosomes by Moderating Cyclin-Dependent Kinase Activity
inferred← citeshttps://doi.org/10.1016/j.cub.2018.03.056openalex-snapshot
Chromosome Biology: The Smc–Kleisin Enzymology Finally Comes of Age
inferred← citeshttps://doi.org/10.1016/j.cub.2018.06.062openalex-snapshot
Absence of the Spindle Assembly Checkpoint Restores Mitotic Fidelity upon Loss of Sister Chromatid Cohesion
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.2010.07.013openalex-snapshot
Condensins Promote Chromosome Recoiling during Early Anaphase to Complete Sister Chromatid Separation
inferred← citeshttps://doi.org/10.1016/j.devcel.2012.06.007openalex-snapshot
Separase Biosensor Reveals that Cohesin Cleavage Timing Depends on Phosphatase PP2ACdc55 Regulation
inferred← citeshttps://doi.org/10.1016/j.devcel.2012.06.015openalex-snapshot
Separase Sensor Reveals Dual Roles for Separase Coordinating Cohesin Cleavage and Cdk1 Inhibition
inferred← citeshttps://doi.org/10.1016/j.devcel.2013.10.018openalex-snapshot
Entrapment of Chromosomes by Condensin Rings Prevents Their Breakage during Cytokinesis
inferred← citeshttps://doi.org/10.1016/j.devcel.2014.09.010openalex-snapshot
Cohesin and Its Regulation: On the Logic of X-Shaped Chromosomes
inferred← citeshttps://doi.org/10.1016/j.devcel.2016.11.021openalex-snapshot
Casein Kinase 1 Coordinates Cohesin Cleavage, Gametogenesis, and Exit from M Phase in Meiosis II
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.diff.2018.01.002openalex-snapshot
Stretching, scrambling, piercing and entangling: Challenges for telomeres in mitotic and meiotic chromosome segregation
inferred← citeshttps://doi.org/10.1016/j.dnarep.2015.01.006openalex-snapshot
Mec1-dependent phosphorylation of Mms21 modulates its SUMO ligase activity
inferred← citeshttps://doi.org/10.1016/j.dnarep.2025.103871openalex-snapshot
Synthetic cytotoxicity profiling of cohesin mutants highlights recombination-based dependencies
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2004.05.006openalex-snapshot
The RING-H2–finger protein APC11 as a target of hydrogen peroxide
inferred← citeshttps://doi.org/10.1016/j.gde.2011.11.003openalex-snapshot
Cohesin and chromatin organisation
inferred← citeshttps://doi.org/10.1016/j.gene.2013.12.045openalex-snapshot
Two novel RAD21 mutations in patients with mild Cornelia de Lange syndrome-like presentation and report of the first familial case
inferred← citeshttps://doi.org/10.1016/j.gene.2020.144966openalex-snapshot
Cohesin subunit RAD21: From biology to disease
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.142189openalex-snapshot
Balance of polo-like kinase Plo1 and monopolar attachment protein 1 (Moa1) regulates fission yeast meiosis
inferred← citeshttps://doi.org/10.1016/j.isci.2023.108011openalex-snapshot
A Haspin-ARHGAP11A axis regulates epithelial morphogenesis through Rho-ROCK dependent modulation of LIMK1-Cofilin
inferred← citeshttps://doi.org/10.1016/j.jgg.2013.11.006openalex-snapshot
Expression of Epitope-Tagged SYN3 Cohesin Proteins Can Disrupt Meiosis in Arabidopsis
inferred← citeshttps://doi.org/10.1016/j.jmb.2006.09.010openalex-snapshot
Serpin1 of Arabidopsis thaliana is a Suicide Inhibitor for Metacaspase 9
inferred← citeshttps://doi.org/10.1016/j.jsb.2008.11.004openalex-snapshot
Organization of human replicon: Singles or zipping couples?
inferred← citeshttps://doi.org/10.1016/j.jsb.2019.08.010openalex-snapshot
Quantification of the dynamic behaviour of ribosomal DNA genes and nucleolus during yeast Saccharomyces cerevisiae cell cycle
inferred← citeshttps://doi.org/10.1016/j.jsbmb.2010.02.019openalex-snapshot
In vitro effects of 2-methoxyestradiol on morphology, cell cycle progression, cell death and gene expression changes in the tumorigenic MCF-7 breast epithelial cell line
inferred← citeshttps://doi.org/10.1016/j.lfs.2014.04.011openalex-snapshot
Chk1 is required for the metaphase–anaphase transition via regulating the expression and localization of Cdc20 and Mad2
inferred← citeshttps://doi.org/10.1016/j.mad.2016.07.006openalex-snapshot
Cell-cycle involvement in autophagy and apoptosis in yeast
inferred← citeshttps://doi.org/10.1016/j.molcel.2004.08.030openalex-snapshot
Structure and Stability of Cohesin's Smc1-Kleisin Interaction
inferred← citeshttps://doi.org/10.1016/j.molcel.2004.11.026openalex-snapshot
Postreplicative Recruitment of Cohesin to Double-Strand Breaks Is Required for DNA Repair
inferred← citeshttps://doi.org/10.1016/j.molcel.2005.03.017openalex-snapshot
Sororin, a Substrate of the Anaphase- Promoting Complex, Is Required for Sister Chromatid Cohesion in Vertebrates
inferred← citeshttps://doi.org/10.1016/j.molcel.2006.05.019openalex-snapshot
A Branched Pathway Governing the Activation of a Developmental Transcription Factor by Regulated Intramembrane Proteolysis
inferred← citeshttps://doi.org/10.1016/j.molcel.2006.08.018openalex-snapshot
Establishment of Sister Chromatid Cohesion at the S. cerevisiae Replication Fork
inferred← citeshttps://doi.org/10.1016/j.molcel.2006.11.005openalex-snapshot
ChlR1 Is Required for Loading Papillomavirus E2 onto Mitotic Chromosomes and Viral Genome Maintenance
inferred← citeshttps://doi.org/10.1016/j.molcel.2007.07.002openalex-snapshot
A Physical Assay for Sister Chromatid Cohesion In Vitro
inferred← citeshttps://doi.org/10.1016/j.molcel.2010.08.008openalex-snapshot
An Smc3 Acetylation Cycle Is Essential for Establishment of Sister Chromatid Cohesion
inferred← citeshttps://doi.org/10.1016/j.molcel.2010.08.009openalex-snapshot
Hos1 Deacetylates Smc3 to Close the Cohesin Acetylation Cycle
inferred← citeshttps://doi.org/10.1016/j.molcel.2011.07.034openalex-snapshot
Cohesin's Concatenation of Sister DNAs Maintains Their Intertwining
inferred← citeshttps://doi.org/10.1016/j.molcel.2012.07.004openalex-snapshot
Cohesin Association to Replication Sites Depends on Rad50 and Promotes Fork Restart
inferred← citeshttps://doi.org/10.1016/j.molcel.2014.12.038openalex-snapshot
Error-Free DNA Damage Tolerance and Sister Chromatid Proximity during DNA Replication Rely on the Polα/Primase/Ctf4 Complex
inferred← citeshttps://doi.org/10.1016/j.molcel.2016.01.026openalex-snapshot
Releasing Activity Disengages Cohesin’s Smc3/Scc1 Interface in a Process Blocked by Acetylation
inferred← citeshttps://doi.org/10.1016/j.molcel.2016.05.036openalex-snapshot
Ctf4 Links DNA Replication with Sister Chromatid Cohesion Establishment by Recruiting the Chl1 Helicase to the Replisome
inferred← citeshttps://doi.org/10.1016/j.molcel.2016.10.032openalex-snapshot
RPA Mediates Recruitment of MRX to Forks and Double-Strand Breaks to Hold Sister Chromatids Together
inferred← citeshttps://doi.org/10.1016/j.molcel.2017.10.009openalex-snapshot
Smc3 Deacetylation by Hos1 Facilitates Efficient Dissolution of Sister Chromatid Cohesion during Early Anaphase
inferred← citeshttps://doi.org/10.1016/j.molcel.2019.10.029openalex-snapshot
MRX Increases Chromatin Accessibility at Stalled Replication Forks to Promote Nascent DNA Resection and Cohesin Loading
inferred← citeshttps://doi.org/10.1016/j.molcel.2020.01.019openalex-snapshot
Regulation of Cohesin-Mediated Chromosome Folding by Eco1 and Other Partners
inferred← citeshttps://doi.org/10.1016/j.molcel.2024.07.022openalex-snapshot
A liquid-like coat mediates chromosome clustering during mitotic exit
inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2008.08.010openalex-snapshot
Cohesinopathies: One ring, many obligations
inferred← citeshttps://doi.org/10.1016/j.mrrev.2011.07.004openalex-snapshot
The dark side of cohesin: The carcinogenic point of view
inferred← citeshttps://doi.org/10.1016/j.plasmid.2004.02.005openalex-snapshot
Segregation of the yeast plasmid: similarities and contrasts with bacterial plasmid partitioning
inferred← citeshttps://doi.org/10.1016/j.protis.2007.07.004openalex-snapshot
Asymmetric Cell Division as a Route to Reduction in Cell Length and Change in Cell Morphology in Trypanosomes
inferred← citeshttps://doi.org/10.1016/j.sbi.2018.01.012openalex-snapshot
Structural biology of the separase–securin complex with crucial roles in chromosome segregation
inferred← citeshttps://doi.org/10.1016/j.scienta.2022.111777openalex-snapshot
A transcriptomic study of ‘Granny Smith’ apple fruit response to x-ray irradiation using RNA-Seq
inferred← citeshttps://doi.org/10.1016/j.semcancer.2018.04.005openalex-snapshot
DNA replication stress and its impact on chromosome segregation and tumorigenesis
inferred← citeshttps://doi.org/10.1016/j.semcdb.2011.03.002openalex-snapshot
Aneuploidy and tumorigenesis
inferred← citeshttps://doi.org/10.1016/j.semcdb.2011.03.013openalex-snapshot
The sister bonding of duplicated chromosomes
inferred← citeshttps://doi.org/10.1016/j.semcdb.2021.06.014openalex-snapshot
Mitosis under the macroscope
inferred← citeshttps://doi.org/10.1016/j.soc.2008.08.001openalex-snapshot
Family Cancer Syndromes: Inherited Deficiencies in Systems for the Maintenance of Genomic Integrity
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