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RAD21L, a novel cohesin subunit implicated in linking homologous chromosomes in mammalian meiosis

https://doi.org/10.1083/jcb.201008005
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What this work says

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

inferredcites →https://doi.org/10.1002/j.1460-2075.1992.tb05616.xopenalex-snapshot
A coiled‐coil related protein specific for synapsed regions of meiotic prophase chromosomes.
inferredcites →https://doi.org/10.1002/jemt.20730openalex-snapshot
γH2AX marks the main events of the spermatogenic process
inferredcites →https://doi.org/10.1007/bf02484408openalex-snapshot
Expression of the mouse testicular histone gene H1t during spermatogenesis
inferredcites →https://doi.org/10.1007/s00412-004-0305-5openalex-snapshot
The Drosophila meiotic kleisin C(2)M functions before the meiotic divisions
inferredcites →https://doi.org/10.1007/s00412-006-0057-5openalex-snapshot
The diverse roles of transverse filaments of synaptonemal complexes in meiosis
inferredcites →https://doi.org/10.1016/j.cell.2006.09.040openalex-snapshot
Wapl Controls the Dynamic Association of Cohesin with Chromatin
inferredcites →https://doi.org/10.1016/j.cub.2004.11.032openalex-snapshot
BRCA1, Histone H2AX Phosphorylation, and Male Meiotic Sex Chromosome Inactivation
inferredcites →https://doi.org/10.1016/j.cub.2006.10.061openalex-snapshot
Human Wapl Is a Cohesin-Binding Protein that Promotes Sister-Chromatid Resolution in Mitotic Prophase
inferredcites →https://doi.org/10.1016/j.devcel.2005.03.018openalex-snapshot
Absence of Mouse REC8 Cohesin Promotes Synapsis of Sister Chromatids in Meiosis
inferredcites →https://doi.org/10.1016/j.febslet.2004.11.070openalex-snapshot
A dioxin sensitive gene, mammalian WAPL, is implicated in spermatogenesis
inferredcites →https://doi.org/10.1016/j.molcel.2005.09.021openalex-snapshot
Crossover and Noncrossover Pathways in Mouse Meiosis
inferredcites →https://doi.org/10.1016/j.yexcr.2009.08.007openalex-snapshot
A novel mammalian HORMA domain-containing protein, HORMAD1, preferentially associates with unsynapsed meiotic chromosomes
inferredcites →https://doi.org/10.1016/s0070-2153(01)52008-6openalex-snapshot
Mechanism and control of meiotic recombination initiation
inferredcites →https://doi.org/10.1016/s0092-8674(00)80378-5openalex-snapshot
Interhomolog Bias during Meiotic Recombination: Meiotic Functions Promote a Highly Differentiated Interhomolog-Only Pathway
inferredcites →https://doi.org/10.1016/s0092-8674(01)00430-5openalex-snapshot
The Single-End Invasion
inferredcites →https://doi.org/10.1016/s0092-8674(03)00083-7openalex-snapshot
Un Ménage à Quatre
inferredcites →https://doi.org/10.1016/s0168-9525(00)02080-1openalex-snapshot
The pachytene checkpoint
inferredcites →https://doi.org/10.1016/s0960-9822(03)00050-2openalex-snapshot
The Synaptonemal Complex Component C(2)M Regulates Meiotic Crossing over in Drosophila
inferredcites →https://doi.org/10.1016/s1097-2765(00)80404-9openalex-snapshot
The Murine SCP3 Gene Is Required for Synaptonemal Complex Assembly, Chromosome Synapsis, and Male Fertility
inferredcites →https://doi.org/10.1016/s1097-2765(02)00473-2openalex-snapshot
The Dissociation of Cohesin from Chromosomes in Prophase Is Regulated by Polo-like Kinase
inferredcites →https://doi.org/10.1016/s1097-2765(03)00108-4openalex-snapshot
Kleisins: A Superfamily of Bacterial and Eukaryotic SMC Protein Partners
inferredcites →https://doi.org/10.1023/b:chro.0000021945.83198.0eopenalex-snapshot
Cohesin component dynamics during meiotic prophase I in mammalian oocytes
inferredcites →https://doi.org/10.1038/35087082openalex-snapshot
Mammalian STAG3 is a cohesin specific to sister chromatid arms in meiosis I
inferredcites →https://doi.org/10.1038/85830openalex-snapshot
Recombinational DNA double-strand breaks in mice precede synapsis
inferredcites →https://doi.org/10.1038/nature06967openalex-snapshot
The amphioxus genome and the evolution of the chordate karyotype
inferredcites →https://doi.org/10.1038/ncb1135openalex-snapshot
Cohesin SMC1β is required for meiotic chromosome dynamics, sister chromatid cohesion and DNA recombination
inferredcites →https://doi.org/10.1038/ncb1667openalex-snapshot
Unified mode of centromeric protection by shugoshin in mammalian oocytes and somatic cells
inferredcites →https://doi.org/10.1038/ng1672openalex-snapshot
SMC1β-deficient female mice provide evidence that cohesins are a missing link in age-related nondisjunction
inferredcites →https://doi.org/10.1038/nrm1909openalex-snapshot
At the heart of the chromosome: SMC proteins in action
inferredcites →https://doi.org/10.1038/sj.embor.7400121openalex-snapshot
A new role for the mitotic RAD21/SCC1 cohesin in meiotic chromosome cohesion and segregation in the mouse
inferredcites →https://doi.org/10.1073/pnas.0500172102openalex-snapshot
Juxtaposition of C(2)M and the transverse filament protein C(3)G within the central region of Drosophila synaptonemal complex
inferredcites →https://doi.org/10.1083/jcb.105.4.1549openalex-snapshot
Existence of two populations of cyclin/proliferating cell nuclear antigen during the cell cycle: association with DNA replication sites.
inferredcites →https://doi.org/10.1083/jcb.147.2.207openalex-snapshot
Rad51 and Dmc1 Form Mixed Complexes Associated with Mouse Meiotic Chromosome Cores and Synaptonemal Complexes
inferredcites →https://doi.org/10.1083/jcb.150.3.405openalex-snapshot
Identification and Characterization of Sa/Scc3p Subunits in the Xenopus and Human Cohesin Complexes
inferredcites →https://doi.org/10.1083/jcb.200212080openalex-snapshot
Meiotic cohesin REC8 marks the axial elements of rat synaptonemal complexes before cohesins SMC1β and SMC3
inferredcites →https://doi.org/10.1083/jcb.200310077openalex-snapshot
The cohesion protein ORD is required for homologue bias during meiotic recombination
inferredcites →https://doi.org/10.1083/jcb.200603063openalex-snapshot
Mouse SYCP2 is required for synaptonemal complex assembly and chromosomal synapsis during male meiosis
inferredcites →https://doi.org/10.1083/jcb.200904040openalex-snapshot
SOLO: a meiotic protein required for centromere cohesion, coorientation, and SMC1 localization in Drosophila melanogaster
inferredcites →https://doi.org/10.1093/embo-reports/kvf108openalex-snapshot
STAG2 and Rad21 mammalian mitotic cohesins are implicated in meiosis
inferredcites →https://doi.org/10.1093/genetics/151.4.1569openalex-snapshot
Distribution of Crossing Over on Mouse Synaptonemal Complexes Using Immunofluorescent Localization of MLH1 Protein
inferredcites →https://doi.org/10.1093/nar/26.11.2572openalex-snapshot
SCP2: a major protein component of the axial elements of synaptonemal complexes of the rat
inferredcites →https://doi.org/10.1096/fj.14.11.1539openalex-snapshot
MSH4 acts in conjunction with MLH1 during mammalian meiosis
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.1808809openalex-snapshot
The axial element protein HTP-3 promotes cohesin loading and meiotic axis assembly in C. elegans to implement the meiotic program of chromosome segregation
inferredcites →https://doi.org/10.1101/gad.1844309openalex-snapshot
Releasing cohesin from chromosome arms in early mitosis: opposing actions of Wapl–Pds5 and Sgo1
inferredcites →https://doi.org/10.1101/gad.249202openalex-snapshot
Cohesin release is required for sister chromatid resolution, but not for condensin-mediated compaction, at the onset of mitosis
inferredcites →https://doi.org/10.1101/gad.329705openalex-snapshot
Mouse Sycp1 functions in synaptonemal complex assembly, meiotic recombination, and XY body formation
inferredcites →https://doi.org/10.1128/mcb.21.16.5667-5677.2001openalex-snapshot
A Meiotic Chromosomal Core Consisting of Cohesin Complex Proteins Recruits DNA Recombination Proteins and Promotes Synapsis in the Absence of an Axial Element in Mammalian Meiotic Cells
inferredcites →https://doi.org/10.1128/mcb.21.20.6984-6998.2001openalex-snapshot
Novel Meiosis-Specific Isoform of Mammalian SMC1
inferredcites →https://doi.org/10.1128/mcb.25.16.7203-7215.2005openalex-snapshot
Surveillance of Different Recombination Defects in Mouse Spermatocytes Yields Distinct Responses despite Elimination at an Identical Developmental Stage
inferredcites →https://doi.org/10.1146/annurev-genet-102108-134233openalex-snapshot
Cohesin: Its Roles and Mechanisms
inferredcites →https://doi.org/10.1146/annurev.cellbio.19.111301.155141openalex-snapshot
THE GENETICS AND MOLECULAR BIOLOGY OF THE SYNAPTONEMAL COMPLEX
inferredcites →https://doi.org/10.1146/annurev.cellbio.23.090506.123245openalex-snapshot
Prelude to a Division
inferredcites →https://doi.org/10.1146/annurev.ge.28.120194.001123openalex-snapshot
SISTER-CHROMATID COHESION IN MITOSIS AND MEIOSIS
inferredcites →https://doi.org/10.1159/000166622openalex-snapshot
Cohesin Complexes and Sister Chromatid Cohesion in Mammalian Meiosis
inferredcites →https://doi.org/10.1242/dev.000018openalex-snapshot
Meiotic sex chromosome inactivation
inferredcites →https://doi.org/10.1242/jcs.004945openalex-snapshot
Characterization ofSpo11-dependent and independent phospho-H2AX foci during meiotic prophase I in the male mouse
inferredcites →https://doi.org/10.1242/jcs.00495openalex-snapshot
Temporally and spatially selective loss of Rec8 protein from meiotic chromosomes during mammalian meiosis
inferredcites →https://doi.org/10.1242/jcs.02466openalex-snapshot
SPO11 is required for sex-body formation, and Spo11 heterozygosity rescues the prophase arrest ofAtm-/- spermatocytes
inferredcites →https://doi.org/10.1242/jcs.107.10.2749openalex-snapshot
Synaptonemal complex proteins: occurrence, epitope mapping and chromosome disjunction
inferredcites →https://doi.org/10.1242/jcs.111.4.413openalex-snapshot
Changes in protein composition of meiotic nodules during mammalian meiosis
inferredcites →https://doi.org/10.1242/jcs.113.4.673openalex-snapshot
Association of mammalian SMC1 and SMC3 proteins with meiotic chromosomes and synaptonemal complexes
inferredcites →https://doi.org/10.1371/journal.pbio.0030069openalex-snapshot
Dissociation of Cohesin from Chromosome Arms and Loss of Arm Cohesion during Early Mitosis Depends on Phosphorylation of SA2
inferredcites →https://doi.org/10.1371/journal.pgen.1000702openalex-snapshot
Mouse HORMAD1 and HORMAD2, Two Conserved Meiotic Chromosomal Proteins, Are Depleted from Synapsed Chromosome Axes with the Help of TRIP13 AAA-ATPase
inferredcites →https://doi.org/10.1371/journal.pgen.1001006openalex-snapshot
Cohesin Is Limiting for the Suppression of DNA Damage–Induced Recombination between Homologous Chromosomes
inferredcites →https://doi.org/10.2108/zsj.19.539openalex-snapshot
Analyses of mRNA Expression Patterns of Cohesin Subunits Rad21 and Rec8 in Mice: Germ Cell-Specific Expression ofrec8mRNA in Both Male and Female Mice

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/embj.201387329openalex-snapshot
STAG3‐mediated stabilization of REC8 cohesin complexes promotes chromosome synapsis during meiosis
inferred← citeshttps://doi.org/10.1002/embj.201387330openalex-snapshot
Meiotic cohesin STAG3 is required for chromosome axis formation and sister chromatid cohesion
inferred← citeshttps://doi.org/10.1002/jcb.25835openalex-snapshot
Separase: Function Beyond Cohesion Cleavage and an Emerging Oncogene
inferred← citeshttps://doi.org/10.1002/rmb2.12299openalex-snapshot
Is age‐related increase of chromosome segregation errors in mammalian oocytes caused by cohesin deterioration?
inferred← citeshttps://doi.org/10.1007/978-1-4614-1683-8_11openalex-snapshot
Cohesin and Human Diseases
inferred← citeshttps://doi.org/10.1007/978-1-4614-4015-4_6openalex-snapshot
Meiotic Development in Caenorhabditis elegans
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/10.1007/978-1-4939-6545-8_5openalex-snapshot
Analysis of Meiotic Sister Chromatid Cohesion in Caenorhabditis elegans
inferred← citeshttps://doi.org/10.1007/978-1-62703-191-2_3openalex-snapshot
Studying Meiosis-Specific Cohesins in Mouse Embryonic Oocytes
inferred← citeshttps://doi.org/10.1007/978-3-031-97173-0_8openalex-snapshot
Aurora Kinases: A Summary of Mouse Genetic Models Used to Distinguish Their Roles in Oocyte Meiosis and Female Fertility
inferred← citeshttps://doi.org/10.1007/978-3-319-44820-6_5openalex-snapshot
Prophase I: Preparing Chromosomes for Segregation in the Developing Oocyte
inferred← citeshttps://doi.org/10.1007/978-3-319-60855-6_15openalex-snapshot
The Regulation and Function of Cohesin and Condensin in Mammalian Oocytes and Spermatocytes
inferred← citeshttps://doi.org/10.1007/978-981-92-1439-6_5openalex-snapshot
Chromosome Architecture Defined by the Meiosis-Specific Cohesin in Mammalian Germ Cells
inferred← citeshttps://doi.org/10.1007/s00294-016-0570-xopenalex-snapshot
A cohesin-based structural platform supporting homologous chromosome pairing in meiosis
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/s00412-012-0363-zopenalex-snapshot
Altered distribution of MLH1 foci is associated with changes in cohesins and chromosome axis compaction in an asynaptic mutant of tomato
inferred← citeshttps://doi.org/10.1007/s00412-012-0393-6openalex-snapshot
Dynamics of cohesin subunits in grasshopper meiotic divisions
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/s00412-015-0551-8openalex-snapshot
Meiotic cohesin-based chromosome structure is essential for homologous chromosome pairing in Schizosaccharomyces pombe
inferred← citeshttps://doi.org/10.1007/s10577-016-9529-5openalex-snapshot
The distribution of α-kleisin during meiosis in the holocentromeric plant Luzula elegans
inferred← citeshttps://doi.org/10.1007/s10577-016-9542-8openalex-snapshot
Sororin is enriched at the central region of synapsed meiotic chromosomes
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/s12551-013-0116-0openalex-snapshot
Application of advanced fluorescence microscopy to the structure of meiotic chromosomes
inferred← citeshttps://doi.org/10.1007/s13237-012-0054-4openalex-snapshot
Evolutionary origin of chromatin remodeling for dosage compensation: Lessons from epigenetic modifications of X chromosomes in germ cells of Drosophila, C.elegans and Mammals
inferred← citeshttps://doi.org/10.1016/b978-0-12-416024-8.00001-5openalex-snapshot
Cohesin in Gametogenesis
inferred← citeshttps://doi.org/10.1016/b978-0-12-813570-9.00003-6openalex-snapshot
Genetics of Meiotic Chromosome Dynamics and Fertility
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2015.11.031openalex-snapshot
Oocyte Meiotic Spindle Assembly and Function
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2022.04.005openalex-snapshot
Mechanism of initiation of meiosis in mouse germ cells
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2026.01.014openalex-snapshot
Synaptonemal complex: The structural basis for meiosis I
inferred← citeshttps://doi.org/10.1016/j.bbadis.2012.02.008openalex-snapshot
Molecular control of rodent spermatogenesis
inferred← citeshttps://doi.org/10.1016/j.bbrc.2015.01.099openalex-snapshot
Dynamics of histone H3 phosphorylation at threonine 3 during meiotic maturation in mouse oocytes
inferred← citeshttps://doi.org/10.1016/j.cub.2011.10.005openalex-snapshot
A Pathway for Synapsis Initiation during Zygotene in Drosophila Oocytes
inferred← citeshttps://doi.org/10.1016/j.cub.2016.05.006openalex-snapshot
Dynamic and Stable Cohesins Regulate Synaptonemal Complex Assembly and Chromosome Segregation
inferred← citeshttps://doi.org/10.1016/j.cub.2017.12.020openalex-snapshot
SMC1α Substitutes for Many Meiotic Functions of SMC1β but Cannot Protect Telomeres from Damage
inferred← citeshttps://doi.org/10.1016/j.cub.2019.02.007openalex-snapshot
Prdm9 and Meiotic Cohesin Proteins Cooperatively Promote DNA Double-Strand Break Formation in Mammalian Spermatocytes
inferred← citeshttps://doi.org/10.1016/j.cub.2024.04.008openalex-snapshot
Centromere pairing enables correct segregation of meiotic chromosomes
inferred← citeshttps://doi.org/10.1016/j.devcel.2020.01.010openalex-snapshot
MEIOSIN Directs the Switch from Mitosis to Meiosis in Mammalian Germ Cells
inferred← citeshttps://doi.org/10.1016/j.dnarep.2018.01.007openalex-snapshot
Repair of exogenous DNA double-strand breaks promotes chromosome synapsis in SPO11-mutant mouse meiocytes, and is altered in the absence of HORMAD1
inferred← citeshttps://doi.org/10.1016/j.dnarep.2026.103963openalex-snapshot
Meiotic recombination proteins in cancer
inferred← citeshttps://doi.org/10.1016/j.febslet.2013.06.035openalex-snapshot
Cohesin: Functions beyond sister chromatid cohesion
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.gene.2022.146281openalex-snapshot
Novel STAG3 variant associated with primary ovarian insufficiency and non-obstructive azoospermia in an Iranian consanguineous family
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.mad.2025.112129openalex-snapshot
Causes and consequences of chromosomal cohesin loss: Novel insights for mechanisms of aging-related oocyte aneuploidy
inferred← citeshttps://doi.org/10.1016/j.tig.2012.03.003openalex-snapshot
Shugoshins: from protectors of cohesion to versatile adaptors at the centromere
inferred← citeshttps://doi.org/10.1016/j.yexcr.2012.02.012openalex-snapshot
Chromosomal, metabolic, environmental, and hormonal origins of aneuploidy in mammalian oocytes
inferred← citeshttps://doi.org/10.1016/j.yexcr.2012.03.016openalex-snapshot
Cohesin in determining chromosome architecture
inferred← citeshttps://doi.org/10.1016/j.yexcr.2016.03.025openalex-snapshot
The width of the lateral element of the synaptonemal complex is determined by a multilayered organization of its components
inferred← citeshttps://doi.org/10.1016/j.ygcen.2019.113230openalex-snapshot
Expression of GnRH receptor and 3βHSD during meiosis and foliculogénesis in Columba livia (Aves: Columbiformes): Histological and immunohistochemical analysis
inferred← citeshttps://doi.org/10.1038/emboj.2011.222openalex-snapshot
The cohesin subunit RAD21L functions in meiotic synapsis and exhibits sexual dimorphism in fertility
inferred← citeshttps://doi.org/10.1038/embor.2011.24openalex-snapshot
Cohesin subunit Rad21L, the new kid on the block has new ideas
inferred← citeshttps://doi.org/10.1038/ncomms11428openalex-snapshot
A genetic basis for the variation in the vulnerability of cancer to DNA damage
inferred← citeshttps://doi.org/10.1038/ng.2833openalex-snapshot
Common and low-frequency variants associated with genome-wide recombination rate
inferred← citeshttps://doi.org/10.1038/nrm3349openalex-snapshot
Geometry and force behind kinetochore orientation: lessons from meiosis
inferred← citeshttps://doi.org/10.1038/s41419-025-07442-1openalex-snapshot
Single-cell RNA-seq and pathological phenotype reveal the functional atlas and precise roles of Sox30 in testicular cell development and differentiation
inferred← citeshttps://doi.org/10.1038/s41467-026-73644-6openalex-snapshot
High-resolution chromatin mapping reveals that CTCF anchors meiotic loops to the chromosome axis
inferred← citeshttps://doi.org/10.1038/s41598-017-04560-5openalex-snapshot
Differential cohesin loading marks paired and unpaired regions of platypus sex chromosomes at prophase I
inferred← citeshttps://doi.org/10.1038/s42003-020-01265-wopenalex-snapshot
Micromanipulation of prophase I chromosomes from mouse spermatocytes reveals high stiffness and gel-like chromatin organization
inferred← citeshttps://doi.org/10.1038/srep28355openalex-snapshot
CTCF contributes in a critical way to spermatogenesis and male fertility
inferred← citeshttps://doi.org/10.1042/bcj20180512openalex-snapshot
Large-scale chromatin organisation in interphase, mitosis and meiosis
inferred← citeshttps://doi.org/10.1073/pnas.2204071119openalex-snapshot
Ectopic expression of meiotic cohesin generates chromosome instability in cancer cell line
inferred← citeshttps://doi.org/10.1074/jbc.m116.714964openalex-snapshot
Degradation of the Separase-cleaved Rec8, a Meiotic Cohesin Subunit, by the N-end Rule Pathway
inferred← citeshttps://doi.org/10.1080/14647273.2017.1292004openalex-snapshot
Single-nucleotide polymorphisms in the human RAD21L gene may be a genetic risk factor for Japanese patients with azoospermia caused by meiotic arrest and Sertoli cell-only syndrome
inferred← citeshttps://doi.org/10.1083/jcb.201201100openalex-snapshot
Meiotic cohesin complexes are essential for the formation of the axial element in mice
inferred← citeshttps://doi.org/10.1083/jcb.201906100openalex-snapshot
Wapl releases Scc1-cohesin and regulates chromosome structure and segregation in mouse oocytes
inferred← citeshttps://doi.org/10.1093/biolre/ioac040openalex-snapshot
Meiotic chromosome organization and crossover patterns
inferred← citeshttps://doi.org/10.1093/biolre/ioag092openalex-snapshot
The synaptonemal complex: structure, function, and clinical implications
inferred← citeshttps://doi.org/10.1093/biolre/ioag134openalex-snapshot
Meiosis-specific cohesin in mammalian germ cells
inferred← citeshttps://doi.org/10.1093/genetics/iyag159openalex-snapshot
A dynamic meiotic cohesin complex regulates synaptonemal complex assembly in Drosophila oocytes
inferred← citeshttps://doi.org/10.1093/hmg/ddu051openalex-snapshot
STAG3 is a strong candidate gene for male infertility
inferred← citeshttps://doi.org/10.1093/humupd/dmac024openalex-snapshot
Meiotic recombination: insights into its mechanisms and its role in human reproduction with a special focus on non-obstructive azoospermia
inferred← citeshttps://doi.org/10.1093/nar/gkw034openalex-snapshot
Rad61/Wpl1 (Wapl), a cohesin regulator, controls chromosome compaction during meiosis
inferred← citeshttps://doi.org/10.1093/nar/gkz754openalex-snapshot
Conserved HORMA domain-containing protein Hop1 stabilizes interaction between proteins of meiotic DNA break hotspots and chromosome axis
inferred← citeshttps://doi.org/10.1093/nargab/lqac085openalex-snapshot
Mapping separase-mediated cleavage in situ
inferred← citeshttps://doi.org/10.1093/procel/pwac040openalex-snapshot
RBM46 is essential for gametogenesis and functions in post-transcriptional roles affecting meiotic cohesin subunits
inferred← citeshttps://doi.org/10.1101/2022.06.20.496767openalex-snapshot
The cohesin subunit RAD21.2 functions as a recombination silencer of ribosomal DNA arrays
inferred← citeshttps://doi.org/10.1101/2022.12.19.520819openalex-snapshot
Centromere Pairing in Prophase Allows Partner Chromosomes to Orient on the Meiosis I Spindle
inferred← citeshttps://doi.org/10.1101/2025.04.21.649846openalex-snapshot
Exploring the C(2)M Cohesin Complex: Structure, Dynamics, and Ability to Facilitate Assembly of the Synaptonemal Complex
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/cshperspect.a017970openalex-snapshot
Meiosis and Maternal Aging: Insights from Aneuploid Oocytes and Trisomy Births
inferred← citeshttps://doi.org/10.1101/cshperspect.a041705openalex-snapshot
Chromosome Ends in Motion: Telomeres as Hazards and Hubs in Meiosis
inferred← citeshttps://doi.org/10.1101/gad.237313.113openalex-snapshot
Meiosis-specific cohesin mediates homolog recognition in mouse spermatocytes
inferred← citeshttps://doi.org/10.1101/gr.275358.121openalex-snapshot
Genome-wide variability in recombination activity is associated with meiotic chromatin organization
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/acel.13343openalex-snapshot
Identification of SRY‐box 30 as an age‐related essential gatekeeper for male germ‐cell meiosis and differentiation
inferred← citeshttps://doi.org/10.1111/cpr.70003openalex-snapshot
Testis‐Specific PDHA2 Is Required for Proper Meiotic Recombination and Chromosome Organisation During Spermatogenesis
inferred← citeshttps://doi.org/10.1111/dgd.12410openalex-snapshot
Mechanisms of kinetochore‐microtubule attachment errors in mammalian oocytes
inferred← citeshttps://doi.org/10.1111/evo.13850openalex-snapshot
Molecular evolution of the meiotic recombination pathway in mammals
inferred← citeshttps://doi.org/10.1111/febs.13301openalex-snapshot
Complex elaboration: making sense of meiotic cohesin dynamics
inferred← citeshttps://doi.org/10.1111/gtc.12652openalex-snapshot
The cohesin complex in mammalian meiosis
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.1365-313x.2012.04979.xopenalex-snapshot
The Arabidopsis SYN3 cohesin protein is important for early meiotic events
inferred← citeshttps://doi.org/10.1126/sciadv.adv2283openalex-snapshot
Meiotic cohesin RAD21L shapes 3D genome structure and transcription in the male germline
inferred← citeshttps://doi.org/10.1134/s102279541712002xopenalex-snapshot
Noncanonical meiosis in the nematode Caenorhabditis elegans as a model for studying the molecular bases of the homologous chromosome synapsis, crossing over, and segregation
inferred← citeshttps://doi.org/10.1146/annurev-genet-071719-020235openalex-snapshot
Architecture and Dynamics of Meiotic Chromosomes
inferred← citeshttps://doi.org/10.1146/annurev-genom-110122-090239openalex-snapshot
Meiotic Chromosome Structure, the Synaptonemal Complex, and Infertility
inferred← citeshttps://doi.org/10.1159/000520682openalex-snapshot
Sexually Dimorphic Properties in Meiotic Chromosome
inferred← citeshttps://doi.org/10.1186/1747-1028-8-12openalex-snapshot
Cohesin loading factor Nipbl localizes to chromosome axes during mammalian meiotic prophase
inferred← citeshttps://doi.org/10.1186/1755-8166-6-1openalex-snapshot
A specific family of interspersed repeats (SINEs) facilitates meiotic synapsis in mammals
inferred← citeshttps://doi.org/10.1186/2045-9769-2-4openalex-snapshot
Cohesin complexes with a potential to link mammalian meiosis to cancer
inferred← citeshttps://doi.org/10.1186/s12876-022-02400-zopenalex-snapshot
The upregulation of stromal antigen 3 expression suppresses the phenotypic hallmarks of hepatocellular carcinoma through the Smad3-CDK4/CDK6-cyclin D1 and CXCR4/RhoA pathways
inferred← citeshttps://doi.org/10.1186/s13048-023-01221-2openalex-snapshot
DNA double-strand break genetic variants in patients with premature ovarian insufficiency
inferred← citeshttps://doi.org/10.1186/s13059-022-02632-yopenalex-snapshot
Meiosis-specific cohesin complexes display essential and distinct roles in mitotic embryonic stem cell chromosomes
inferred← citeshttps://doi.org/10.1242/bio.035626openalex-snapshot
Retinoic acid-induced CYP51 nuclear translocation promotes meiosis prophase I process and is correlated to the expression of REC8 and STAG3 in mice
inferred← citeshttps://doi.org/10.1242/dev.121830openalex-snapshot
Disruption ofTh2aandTh2bgenes causes defects in spermatogenesis
inferred← citeshttps://doi.org/10.1242/dev.204227openalex-snapshot
BMP and STRA8 act collaboratively to ensure correct mitotic-to-meiotic transition in the fetal mouse ovary
inferred← citeshttps://doi.org/10.1242/jcs.212100openalex-snapshot
Studying meiotic cohesin in somatic cells reveals that Rec8-containing cohesin requires Stag3 to function and is regulated by Wapl and sororin
inferred← citeshttps://doi.org/10.1262/jrd.2013-068openalex-snapshot
Roles of Cohesin and Condensin in Chromosome Dynamics During Mammalian Meiosis
inferred← citeshttps://doi.org/10.1262/jrd.2016-127openalex-snapshot
Meiotic cohesin subunits RAD21L and REC8 are positioned at distinct regions between lateral elements and transverse filaments in the synaptonemal complex of mouse spermatocytes
inferred← citeshttps://doi.org/10.1262/jrd.2016-171openalex-snapshot
Ectopic expression of meiotic cohesin RAD21L promotes adjacency of homologous chromosomes in somatic cells
inferred← citeshttps://doi.org/10.1262/jrd.2022-075openalex-snapshot
Analysis of absolute amounts of two meiotic cohesin subunits, RAD21L and REC8, in mouse spermatocytes
inferred← citeshttps://doi.org/10.1262/jrd.2024-077openalex-snapshot
CpG site methylation regulates mouse Rec8 gene promoter activity
inferred← citeshttps://doi.org/10.1266/ggs.21-00054openalex-snapshot
MEIOSIN directs initiation of meiosis and subsequent meiotic prophase program during spermatogenesis
inferred← citeshttps://doi.org/10.1371/journal.pgen.1002485openalex-snapshot
Phosphorylation of Chromosome Core Components May Serve as Axis Marks for the Status of Chromosomal Events during Mammalian Meiosis
inferred← citeshttps://doi.org/10.1371/journal.pgen.1002790openalex-snapshot
Interplay between Synaptonemal Complex, Homologous Recombination, and Centromeres during Mammalian Meiosis
inferred← citeshttps://doi.org/10.1371/journal.pgen.1003985openalex-snapshot
Meiotic Cohesin SMC1β Provides Prophase I Centromeric Cohesion and Is Required for Multiple Synapsis-Associated Functions
inferred← citeshttps://doi.org/10.1371/journal.pgen.1004413openalex-snapshot
Meiosis-Specific Cohesin Component, Stag3 Is Essential for Maintaining Centromere Chromatid Cohesion, and Required for DNA Repair and Synapsis between Homologous Chromosomes
inferred← citeshttps://doi.org/10.1371/journal.pgen.1004540openalex-snapshot
The Cohesin Subunit Rad21 Is Required for Synaptonemal Complex Maintenance, but Not Sister Chromatid Cohesion, during Drosophila Female Meiosis
inferred← citeshttps://doi.org/10.1371/journal.pgen.1004821openalex-snapshot
The Dissection of Meiotic Chromosome Movement in Mice Using an In Vivo Electroporation Technique
inferred← citeshttps://doi.org/10.1371/journal.pgen.1006389openalex-snapshot
Distinct Roles of Meiosis-Specific Cohesin Complexes in Mammalian Spermatogenesis
inferred← citeshttps://doi.org/10.1371/journal.pgen.1007382openalex-snapshot
Condensin I protects meiotic cohesin from WAPL-1 mediated removal
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.pgen.1008414openalex-snapshot
A candidate gene analysis and GWAS for genes associated with maternal nondisjunction of chromosome 21
inferred← citeshttps://doi.org/10.1371/journal.pgen.1009048openalex-snapshot
Meiotic cohesins mediate initial loading of HORMAD1 to the chromosomes and coordinate SC formation during meiotic prophase
inferred← citeshttps://doi.org/10.1371/journal.pgen.1009127openalex-snapshot
Rad21l1 cohesin subunit is dispensable for spermatogenesis but not oogenesis in zebrafish
inferred← citeshttps://doi.org/10.1371/journal.pgen.1009773openalex-snapshot
Transcriptional progression during meiotic prophase I reveals sex-specific features and X chromosome dynamics in human fetal female germline
inferred← citeshttps://doi.org/10.1371/journal.pgen.1010822openalex-snapshot
Building the synaptonemal complex: Molecular interactions between the axis and the central region
inferred← citeshttps://doi.org/10.15252/embj.2020105002openalex-snapshot
A small RNA system ensures accurate homologous pairing and unpaired silencing of meiotic chromosomes
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.201642030openalex-snapshot
High density of REC8 constrains sister chromatid axes and prevents illegitimate synaptonemal complex formation
inferred← citeshttps://doi.org/10.15252/embr.201642544openalex-snapshot
The cohesin REC8 prevents illegitimate inter‐sister synaptonemal complex assembly
inferred← citeshttps://doi.org/10.1534/g3.116.029462openalex-snapshot
Genetic Interactions Between the Meiosis-Specific Cohesin Components, STAG3, REC8, and RAD21L
inferred← citeshttps://doi.org/10.18632/oncotarget.580openalex-snapshot
Meta-analysis of clinical data using human meiotic genes identifies a novel cohort of highly restricted cancer-specific marker genes
inferred← citeshttps://doi.org/10.3389/fcell.2021.688878openalex-snapshot
Chromosome Organization in Early Meiotic Prophase
inferred← citeshttps://doi.org/10.3389/fcell.2021.710033openalex-snapshot
Meiotic Cohesin and Variants Associated With Human Reproductive Aging and Disease
inferred← citeshttps://doi.org/10.3389/fcell.2021.757445openalex-snapshot
Meiotic Chromosome Dynamics in Zebrafish
inferred← citeshttps://doi.org/10.3389/fcell.2022.1097446openalex-snapshot
Chromosome architecture and homologous recombination in meiosis
inferred← citeshttps://doi.org/10.3389/fpls.2015.01034openalex-snapshot
Involvement of the Cohesin Cofactor PDS5 (SPO76) During Meiosis and DNA Repair in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3390/cells15201859openalex-snapshot
Transcriptional Regulation of the Meiotic Cohesin Subunit RAD21L by Methylation of Two CpG Islands in Its Promoter and Characterization of Its Interactions with Histones
inferred← citeshttps://doi.org/10.3390/ijms17060890openalex-snapshot
Ectopic Expression of Testis Germ Cell Proteins in Cancer and Its Potential Role in Genomic Instability
inferred← citeshttps://doi.org/10.3390/ijms24055017openalex-snapshot
Function and Evolution of the Loop Extrusion Machinery in Animals
inferred← citeshttps://doi.org/10.4161/cc.10.12.15688openalex-snapshot
Chagas disease
inferred← citeshttps://doi.org/10.4161/cc.10.12.15691openalex-snapshot
RAD21L is a novel kleisin subunit of the cohesin complex
inferred← citeshttps://doi.org/10.4161/cc.10.9.15515openalex-snapshot
Identification and molecular characterization of the mammalian α-kleisin RAD21L
inferred← citeshttps://doi.org/10.4161/cc.29350openalex-snapshot
The meiosis-specific modification of mammalian telomeres
inferred← citeshttps://doi.org/10.5483/bmbrep.2022-0106openalex-snapshot
α-Kleisin subunit of cohesin preserves the genome integrity of embryonic stem cells
inferred← citeshttps://doi.org/10.5772/31553openalex-snapshot
Cohesins and Cohesin-Regulators in Meiosis
inferred← citeshttps://doi.org/10.6084/m9.figshare.20452892openalex-snapshot
Additional file 1 of The upregulation of stromal antigen 3 expression suppresses the phenotypic hallmarks of hepatocellular carcinoma through the Smad3-CDK4/CDK6-cyclin D1 and CXCR4/RhoA pathways
inferred← citeshttps://doi.org/10.6084/m9.figshare.20452895openalex-snapshot
Additional file 2 of The upregulation of stromal antigen 3 expression suppresses the phenotypic hallmarks of hepatocellular carcinoma through the Smad3-CDK4/CDK6-cyclin D1 and CXCR4/RhoA pathways
inferred← citeshttps://doi.org/10.64898/2026.05.26.727825openalex-snapshot
Molecular mechanism for the functional divergence between cohesin paralogs during meiosis
inferred← citeshttps://doi.org/10.70675/8449c2e5z2818z4a05z978dz5e9f84c9c83bopenalex-snapshot
Organisation du chromosome bactérien d'Escherichia coli : analyse fonctionnelle de la condensine MukBEF
inferred← citeshttps://doi.org/10.70675/b9afe47czb451z4b8fz9aa0z31eb4db88f97openalex-snapshot
La recombinaison méiotique dans le contexte de l’organisation des chromosomes chez la souris
inferred← citeshttps://doi.org/10.70675/eb921333z2b62z4270z9720zd65f15cb9a8fopenalex-snapshot
Control of meiotic divisions in oocytes : a novel role for cyclin B3
inferred← citeshttps://doi.org/10.7282/t39g5qp8openalex-snapshot
The role of meiosis-specific cohesins in accurate chromosome segregation
inferred← citeshttps://doi.org/10.7554/elife.03467openalex-snapshot
Divergent kleisin subunits of cohesin specify mechanisms to tether and release meiotic chromosomes
inferred← citeshttps://doi.org/10.7554/elife.10851openalex-snapshot
Cohesin-interacting protein WAPL-1 regulates meiotic chromosome structure and cohesion by antagonizing specific cohesin complexes
inferred← citeshttps://doi.org/10.7554/elife.84138openalex-snapshot
The kleisin subunit controls the function of C. elegans meiotic cohesins by determining the mode of DNA binding and differential regulation by SCC-2 and WAPL-1
inferred← citeshttps://doi.org/10.7868/s0016675817120025openalex-snapshot
Неканонический мейоз у нематоды Caenorhabditis elegans как модель для изучения молекулярных основ синапсиса, кроссинговера и сегрегации гомологичных хромосом, "Генетика"
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.