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Recombinational DNA double-strand breaks in mice precede synapsis

https://doi.org/10.1038/85830
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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/j.1460-2075.1994.tb06239.xopenalex-snapshot
The meiosis‐specific Xmr gene product is homologous to the lymphocyte Xlr protein and is a component of the XY body.
inferredcites →https://doi.org/10.1006/excr.1996.0315openalex-snapshot
Change of Karyoskeleton during Mammalian Spermatogenesis: Expression Pattern of Nuclear Lamin C2 and Its Regulation
inferredcites →https://doi.org/10.1007/978-3-540-48461-5_6openalex-snapshot
An Integration of Old and New Perspectives of Mammalian Meiotic Sterility
inferredcites →https://doi.org/10.1007/bf00285846openalex-snapshot
Synaptonemal complex analysis of mouse chromosomal rearrangements
inferredcites →https://doi.org/10.1007/bf00285847openalex-snapshot
Synaptonemal complex analysis of mouse chromosomal rearrangements
inferredcites →https://doi.org/10.1007/bf00327371openalex-snapshot
Univalent sex chromosomes in spermatocytes of Sxr-carrying mice
inferredcites →https://doi.org/10.1007/bf00328227openalex-snapshot
Identification of a family of human centromere proteins using autoimmune sera from patients with scleroderma
inferredcites →https://doi.org/10.1007/bf00356023openalex-snapshot
Sex chromosomes, recombination, and chromatin conformation
inferredcites →https://doi.org/10.1007/s004120000075openalex-snapshot
XMR is associated with the asynapsed segments of sex chromosomes in the XY body of mouse primary spermatocytes
inferredcites →https://doi.org/10.1007/s004120050241openalex-snapshot
Rad51 immunocytology in rat and mouse spermatocytes and oocytes
inferredcites →https://doi.org/10.1007/s004120050420openalex-snapshot
Localisation of RAD50 and MRE11 in spermatocyte nuclei of mouse and rat
inferredcites →https://doi.org/10.1016/0092-8674(95)90318-6openalex-snapshot
Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis
inferredcites →https://doi.org/10.1016/s0092-8674(00)81481-6openalex-snapshot
Meiotic Recombination in C. elegans Initiates by a Conserved Mechanism and Is Dispensable for Homologous Chromosome Synapsis
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/s1097-2765(00)00097-6openalex-snapshot
The Mouse Spo11 Gene Is Required for Meiotic Chromosome Synapsis
inferredcites →https://doi.org/10.1016/s1097-2765(00)00098-8openalex-snapshot
Chromosome Synapsis Defects and Sexually Dimorphic Meiotic Progression in Mice Lacking Spo11
inferredcites →https://doi.org/10.1016/s1097-2765(00)80069-6openalex-snapshot
Meiotic Prophase Arrest with Failure of Chromosome Synapsis in Mice Deficient for Dmc1 , a Germline-Specific RecA Homolog
inferredcites →https://doi.org/10.1016/s1097-2765(00)80070-2openalex-snapshot
The Mouse RecA-like Gene Dmc1 Is Required for Homologous Chromosome Synapsis during Meiosis
inferredcites →https://doi.org/10.1023/a:1009209628300openalex-snapshot
Squash Procedure for Protein Immunolocalization in Meiotic Cells
inferredcites →https://doi.org/10.1023/a:1018445520117openalex-snapshot
SHORT COMMUNICATIONS A drying-down technique for the spreading of mammalian meiocytes from the male and female germline
inferredcites →https://doi.org/10.1023/b:chro.0000038762.60086.efopenalex-snapshot
Meiosis in Carriers of Heteromorphic Bivalents: Sex Differences and Implications for Male Fertility
inferredcites →https://doi.org/10.1038/5075openalex-snapshot
Mammalian MutS homologue 5 is required for chromosome pairing in meiosis
inferredcites →https://doi.org/10.1073/pnas.93.12.5920openalex-snapshot
Presynaptic association of Rad51 protein with selected sites in meiotic chromatin.
inferredcites →https://doi.org/10.1073/pnas.96.5.1921openalex-snapshot
Nuclear foci of mammalian recombination proteins are located at single-stranded DNA regions formed after DNA damage
inferredcites →https://doi.org/10.1074/jbc.273.10.5858openalex-snapshot
DNA Double-stranded Breaks Induce Histone H2AX Phosphorylation on Serine 139
inferredcites →https://doi.org/10.1083/jcb.146.5.905openalex-snapshot
Megabase Chromatin Domains Involved in DNA Double-Strand Breaks in Vivo
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/10.1093/emboj/16.17.5207openalex-snapshot
Distribution of the Rad51 recombinase in human and mouse spermatocytes
inferredcites →https://doi.org/10.1101/gad.11.20.2600openalex-snapshot
Meiotic chromosomes: it takes two to tango
inferredcites →https://doi.org/10.1101/gad.12.14.2208openalex-snapshot
Rad52 associates with RPA and functions with Rad55 and Rad57 to assemble meiotic recombination complexes
inferredcites →https://doi.org/10.1101/gad.13.5.523openalex-snapshot
Mouse MutS-like protein Msh5 is required for proper chromosome synapsis in male and female meiosis
inferredcites →https://doi.org/10.1101/gad.14.9.1085openalex-snapshot
MutS homolog 4 localization to meiotic chromosomes is required for chromosome pairing during meiosis in male and female mice
inferredcites →https://doi.org/10.1126/science.279.5352.876openalex-snapshot
Meiotic Synapsis in the Absence of Recombination
inferredcites →https://doi.org/10.1128/mcb.14.2.1137openalex-snapshot
The Gene Encoding a Major Component of the Lateral Elements of Synaptonemal Complexes of the Rat Is Related to X-Linked Lymphocyte-Regulated Genes
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

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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EWSR1 Regulates PRDM9-Dependent Histone 3 Methylation and Links Recombination Hotspots With the Chromosomal Axis
inferred← citeshttps://doi.org/10.2139/ssrn.3971109openalex-extracted
inferred← citeshttps://doi.org/10.1002/0470868732openalex-snapshot
The Genetics and Biology of Sex Determination
inferred← citeshttps://doi.org/10.1002/1521-4141(200202)32:2<316::aid-immu316>3.0.co;2-popenalex-snapshot
Mice deficient for the type II topoisomerase-like DNA transesterase Spo11 show normal immunoglobulin somatic hypermutation and class switching
inferred← citeshttps://doi.org/10.1002/3527600906.mcb.200400163openalex-snapshot
Recombination and Genome Rearrangements
inferred← citeshttps://doi.org/10.1002/9780470015902.a0001359.pub3openalex-snapshot
Meiosis
inferred← citeshttps://doi.org/10.1002/9780470015902.a0022109openalex-snapshot
Meiotic Sex Chromosome Inactivation
inferred← citeshttps://doi.org/10.1002/9780470687970.ch5openalex-snapshot
Homologous Chromosome Pairing and Synapsis during Oogenesis
inferred← citeshttps://doi.org/10.1002/9780470687970.ch6openalex-snapshot
Meiotic Recombination in Mammals
inferred← citeshttps://doi.org/10.1002/ar.24187openalex-snapshot
Histochemical Study of the Emergence of Apoptosis and Altered SYCP3 Protein Distribution During the First Spermatogenic Wave in Wistar Rats
inferred← citeshttps://doi.org/10.1002/bies.20264openalex-snapshot
The evolution of meiosis: Recruitment and modification of somatic DNA-repair proteins
inferred← citeshttps://doi.org/10.1002/bies.20349openalex-snapshot
Molecular features of meiotic recombination hot spots
inferred← citeshttps://doi.org/10.1002/bies.20639openalex-snapshot
The management of DNA double‐strand breaks in mitotic G2, and in mammalian meiosis viewed from a mitotic G2 perspective
inferred← citeshttps://doi.org/10.1002/cbf.1375openalex-snapshot
Homologous recombination‐mediated double‐strand break repair in mouse testicular extracts and comparison with different germ cell stages
inferred← citeshttps://doi.org/10.1002/cyto.a.24539openalex-snapshot
Dual DNA staining enables isolation of multiple sub‐types of post‐replicative mouse male germ cells
inferred← citeshttps://doi.org/10.1002/dvdy.20083openalex-snapshot
Retinoic acid receptor α is required for synchronization of spermatogenic cycles and its absence results in progressive breakdown of the spermatogenic process
inferred← citeshttps://doi.org/10.1002/dvdy.22661openalex-snapshot
Isolation and cytogenetic characterization of zebrafish meiotic prophase I mutants
inferred← citeshttps://doi.org/10.1002/em.20358openalex-snapshot
The γ‐H2A.X: Is it just a surrogate marker of double‐strand breaks or much more?
inferred← citeshttps://doi.org/10.1002/em.22401openalex-snapshot
ATR signaling in mammalian meiosis: From upstream scaffolds to downstream signaling
inferred← citeshttps://doi.org/10.1002/ijc.21782openalex-snapshot
Assessing the likelihood of severe side effects in radiotherapy
inferred← citeshttps://doi.org/10.1002/jcb.21067openalex-snapshot
The cellular control of DNA double‐strand breaks
inferred← citeshttps://doi.org/10.1002/jcp.24172openalex-snapshot
Retinoic acid derived from the fetal ovary initiates meiosis in mouse germ cells
inferred← citeshttps://doi.org/10.1002/jemt.20730openalex-snapshot
γH2AX marks the main events of the spermatogenic process
inferred← citeshttps://doi.org/10.1002/mrd.20430openalex-snapshot
Timing of entry of meiosis depends on a mark generated by DNA methyltransferase 3a in testis
inferred← citeshttps://doi.org/10.1002/mrd.20508openalex-snapshot
Spermatocyte responses in vitro to induced DNA damage
inferred← citeshttps://doi.org/10.1002/mrd.21369openalex-snapshot
Heteromorphic sex chromosomes: Navigating meiosis without a homologous partner
inferred← citeshttps://doi.org/10.1002/mrd.22314openalex-snapshot
Dynamics of radiation induced γH2AX foci in chromatin subcompartments of mouse pachytene spermatocytes and round spermatids
inferred← citeshttps://doi.org/10.1002/path.6292openalex-snapshot
Multiplex imaging reveals spatially resolved DNA ‐damage response neighborhoods in TP53 ‐mutated myelodysplastic neoplasms
inferred← citeshttps://doi.org/10.1006/dbio.2001.0535openalex-snapshot
The Mouse Meiotic Mutation mei1 Disrupts Chromosome Synapsis with Sexually Dimorphic Consequences for Meiotic Progression
inferred← citeshttps://doi.org/10.1006/dbio.2002.0663openalex-snapshot
Disruption of Testis Cords by Cyclopamine or Forskolin Reveals Independent Cellular Pathways in Testis Organogenesis
inferred← citeshttps://doi.org/10.1006/geno.2002.6817openalex-snapshot
Molecular Characterization of the Pb Recombination Hotspot in the Mouse Major Histocompatibility Complex Class II Region
inferred← citeshttps://doi.org/10.1007/3-540-27310-7_3openalex-snapshot
How to Pack the Genome for a Safe Trip
inferred← citeshttps://doi.org/10.1007/7050_2007_024openalex-snapshot
Meiosis in Arabidopis thaliana: Recombination, Chromosome Organization and Meiotic Progression
inferred← citeshttps://doi.org/10.1007/7050_2007_026openalex-snapshot
Spo11 and the Formation of DNA Double-Strand Breaks in Meiosis
inferred← citeshttps://doi.org/10.1007/7050_2007_035openalex-snapshot
Synaptic and Recombination Nodules in Mammals: Structural Continuity with Shifting Protein Composition
inferred← citeshttps://doi.org/10.1007/978-0-387-88186-7_27openalex-snapshot
The Molecular Landscape of Spermatogonial Stem Cell Renewal, Meiotic Sex Chromosome Inactivation, and Spermatic Head Shaping
inferred← citeshttps://doi.org/10.1007/978-1-4020-9187-2_17openalex-snapshot
Meiotic Silencing, Infertility and X Chromosome Evolution
inferred← citeshttps://doi.org/10.1007/978-1-4419-6857-9_17openalex-snapshot
Sperm Epigenetic Profile
inferred← citeshttps://doi.org/10.1007/978-1-4614-6558-4_8openalex-snapshot
Organization of Chromosomes in Human Sperm Nucleus
inferred← citeshttps://doi.org/10.1007/978-1-4614-8459-2_20openalex-snapshot
Sperm Epigenetic Profile
inferred← citeshttps://doi.org/10.1007/978-1-4614-8624-4_10openalex-snapshot
Properties and Functions of Histone Variants
inferred← citeshttps://doi.org/10.1007/978-1-4939-2474-5_18openalex-snapshot
Detecting ATM-Dependent Chromatin Modification in DNA Damage Response
inferred← citeshttps://doi.org/10.1007/978-1-59745-190-1_26openalex-snapshot
Detecting ATM-Dependent Chromatin Modification in DNA Damage and Heat Shock Response
inferred← citeshttps://doi.org/10.1007/978-1-60761-103-5_22openalex-snapshot
Analysis of Telomere Dynamics in Mouse Spermatogenesis
inferred← citeshttps://doi.org/10.1007/978-1-62703-529-3_15openalex-snapshot
γ-H2AX Detection in Somatic and Germ Cells of Mice
inferred← citeshttps://doi.org/10.1007/978-3-030-21664-1_1openalex-snapshot
Genetic Factors Affecting Sperm Chromatin Structure
inferred← citeshttps://doi.org/10.1007/978-3-030-77779-1_11openalex-snapshot
Destruction or Reconstruction: A Subtle Liaison between the Proteolytic and Signaling Role of Protein Ubiquitination in Spermatogenesis
inferred← citeshttps://doi.org/10.1007/978-3-319-25325-1_4openalex-snapshot
The Epigenetic Biomarker γH2AX: From Bench to Clinical Trials
inferred← citeshttps://doi.org/10.1007/978-3-642-14773-9_6openalex-snapshot
Epigenetic Factors and Regulation of Meiotic Recombination in Mammals
inferred← citeshttps://doi.org/10.1007/978-3-642-14773-9_7openalex-snapshot
Meiotic Pairing of Homologous Chromosomes and Silencing of Heterologous Regions
inferred← citeshttps://doi.org/10.1007/978-3-642-14773-9_8openalex-snapshot
Histone Variants during Gametogenesis and Early Development
inferred← citeshttps://doi.org/10.1007/978-4-431-55873-6_6openalex-snapshot
Homologous Recombination During Meiosis
inferred← citeshttps://doi.org/10.1007/978-90-481-9023-2_10openalex-snapshot
Marsupial Sex Chromosome Behaviour During Male Meiosis
inferred← citeshttps://doi.org/10.1007/978-90-481-9023-2_9openalex-snapshot
Gene Content of the Mammalian X Chromosome
inferred← citeshttps://doi.org/10.1007/978-94-017-1033-6_13openalex-snapshot
Interphase Cytogenetics in Understanding Chromosome and Telomere Dynamics During Prophase I: Implications for Meiotic Telomere Movements
inferred← citeshttps://doi.org/10.1007/978-94-017-7417-8_6openalex-snapshot
Non-coding RNA in Spermatogenesis and Epididymal Maturation
inferred← citeshttps://doi.org/10.1007/s00018-006-6463-2openalex-snapshot
Telomeres and meiosis in health and disease
inferred← citeshttps://doi.org/10.1007/s00018-012-0941-5openalex-snapshot
Sex chromosome inactivation in germ cells: emerging roles of DNA damage response pathways
inferred← citeshttps://doi.org/10.1007/s00018-023-04744-5openalex-snapshot
The RNA-binding protein FUS/TLS interacts with SPO11 and PRDM9 and localize at meiotic recombination hotspots
inferred← citeshttps://doi.org/10.1007/s00018-023-04912-7openalex-snapshot
The proper interplay between the expression of Spo11 splice isoforms and the structure of the pseudoautosomal region promotes XY chromosomes recombination
inferred← citeshttps://doi.org/10.1007/s00018-024-05216-0openalex-snapshot
Recent advances in mechanisms ensuring the pairing, synapsis and segregation of XY chromosomes in mice and humans
inferred← citeshttps://doi.org/10.1007/s00204-026-04371-6openalex-snapshot
Prenatal exposure to polystyrene nanoplastics impairs offspring fertility in mice by disrupting meiotic recombination and chromatin accessibility in oocytes
inferred← citeshttps://doi.org/10.1007/s00335-016-9630-2openalex-snapshot
Robertsonian translocations modify genomic distribution of γH2AFX and H3.3 in mouse germ cells
inferred← citeshttps://doi.org/10.1007/s00412-002-0223-3openalex-snapshot
Mammalian meiosis involves DNA double-strand breaks with 3′ overhangs
inferred← citeshttps://doi.org/10.1007/s00412-003-0237-5openalex-snapshot
Genetic and cytological characterization of the recombination protein RAD-51 in Caenorhabditis elegans
inferred← citeshttps://doi.org/10.1007/s00412-003-0242-8openalex-snapshot
Improper chromosome synapsis is associated with elongated RAD51 structures in the maize desynaptic2 mutant
inferred← citeshttps://doi.org/10.1007/s00412-004-0277-5openalex-snapshot
TopBP1 localises to centrosomes in mitosis and to chromosome cores in meiosis
inferred← citeshttps://doi.org/10.1007/s00412-004-0290-8openalex-snapshot
Female-specific features of recombinational double-stranded DNA repair in relation to synapsis and telomere dynamics in human oocytes
inferred← citeshttps://doi.org/10.1007/s00412-004-0311-7openalex-snapshot
SUMO modified proteins localize to the XY body of pachytene spermatocytes
inferred← citeshttps://doi.org/10.1007/s00412-005-0344-6openalex-snapshot
Poly(ADP-ribosyl)ation during chromatin remodeling steps in rat spermiogenesis
inferred← citeshttps://doi.org/10.1007/s00412-005-0346-4openalex-snapshot
Mei1 is epistatic to Dmc1 during mouse meiosis
inferred← citeshttps://doi.org/10.1007/s00412-006-0057-5openalex-snapshot
The diverse roles of transverse filaments of synaptonemal complexes in meiosis
inferred← citeshttps://doi.org/10.1007/s00412-009-0204-xopenalex-snapshot
Relationship between incomplete synapsis and chiasma localization
inferred← citeshttps://doi.org/10.1007/s00412-009-0218-4openalex-snapshot
Cohesin axis maturation and presence of RAD51 during first meiotic prophase in a true bug
inferred← citeshttps://doi.org/10.1007/s00412-009-0223-7openalex-snapshot
Synaptonemal complex assembly and H3K4Me3 demethylation determine DIDO3 localization in meiosis
inferred← citeshttps://doi.org/10.1007/s00412-010-0258-9openalex-snapshot
Meiotic silencing and fragmentation of the male germline restricted chromosome in zebra finch
inferred← citeshttps://doi.org/10.1007/s00412-010-0260-2openalex-snapshot
Heterochromatin and histone modifications in the germline-restricted chromosome of the zebra finch undergoing elimination during spermatogenesis
inferred← citeshttps://doi.org/10.1007/s00412-010-0274-9openalex-snapshot
MRE11 and COM1/SAE2 are required for double-strand break repair and efficient chromosome pairing during meiosis of the protist Tetrahymena
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/s00412-010-0295-4openalex-snapshot
Rap1-independent telomere attachment and bouquet formation in mammalian meiosis
inferred← citeshttps://doi.org/10.1007/s00412-010-0306-5openalex-snapshot
Chromatin configuration and epigenetic landscape at the sex chromosome bivalent during equine spermatogenesis
inferred← citeshttps://doi.org/10.1007/s00412-011-0336-7openalex-snapshot
The template choice decision in meiosis: is the sister important?
inferred← citeshttps://doi.org/10.1007/s00412-011-0346-5openalex-snapshot
Genetically enhanced asynapsis of autosomal chromatin promotes transcriptional dysregulation and meiotic failure
inferred← citeshttps://doi.org/10.1007/s00412-012-0364-yopenalex-snapshot
Inactivation or non-reactivation: what accounts better for the silence of sex chromosomes during mammalian male meiosis?
inferred← citeshttps://doi.org/10.1007/s00412-012-0394-5openalex-snapshot
Presence of an extra chromosome alters meiotic double-stranded break repair dynamics and MLH1 foci distribution in human oocytes
inferred← citeshttps://doi.org/10.1007/s00412-013-0415-zopenalex-snapshot
Oocyte heterogeneity with respect to the meiotic silencing of unsynapsed X chromosomes in the XY female mouse
inferred← citeshttps://doi.org/10.1007/s00412-014-0475-8openalex-snapshot
High histone variant H3.3 content in mouse prospermatogonia suggests a role in epigenetic reformatting
inferred← citeshttps://doi.org/10.1007/s00412-014-0479-4openalex-snapshot
Contrasting behavior of heterochromatic and euchromatic chromosome portions and pericentric genome separation in pre-bouquet spermatocytes of hybrid mice
inferred← citeshttps://doi.org/10.1007/s00412-015-0511-3openalex-snapshot
Nuclear localization of PRDM9 and its role in meiotic chromatin modifications and homologous synapsis
inferred← citeshttps://doi.org/10.1007/s00412-015-0533-xopenalex-snapshot
Effect of species-specific differences in chromosome morphology on chromatin compaction and the frequency and distribution of RAD51 and MLH1 foci in two bovid species: cattle (Bos taurus) and the common eland (Taurotragus oryx)
inferred← citeshttps://doi.org/10.1007/s00412-015-0549-2openalex-snapshot
FancJ (Brip1) loss-of-function allele results in spermatogonial cell depletion during embryogenesis and altered processing of crossover sites during meiotic prophase I in mice
inferred← citeshttps://doi.org/10.1007/s00412-015-0558-1openalex-snapshot
Male meiosis in Crustacea: synapsis, recombination, epigenetics and fertility in Daphnia magna
inferred← citeshttps://doi.org/10.1007/s00412-015-0564-3openalex-snapshot
E-type cyclins modulate telomere integrity in mammalian male meiosis
inferred← citeshttps://doi.org/10.1007/s00412-016-0577-6openalex-snapshot
Transcription reactivation during the first meiotic prophase in bugs is not dependent on synapsis
inferred← citeshttps://doi.org/10.1007/s00412-016-0622-5openalex-snapshot
Homoeologous recombination in the presence of Ph1 gene in wheat
inferred← citeshttps://doi.org/10.1007/s00412-017-0658-1openalex-snapshot
Main steps in DNA double-strand break repair: an introduction to homologous recombination and related processes
inferred← citeshttps://doi.org/10.1007/s00412-018-0674-9openalex-snapshot
Defects in meiotic recombination delay progression through pachytene in Tex19.1−/− mouse spermatocytes
inferred← citeshttps://doi.org/10.1007/s00412-019-00713-9openalex-snapshot
SIRT7 promotes chromosome synapsis during prophase I of female meiosis
inferred← citeshttps://doi.org/10.1007/s00412-019-00725-5openalex-snapshot
Cyclin B3 is dispensable for mouse spermatogenesis
inferred← citeshttps://doi.org/10.1007/s00412-020-00735-8openalex-snapshot
shani mutation in mouse affects splicing of Spata22 and leads to impaired meiotic recombination
inferred← citeshttps://doi.org/10.1007/s00412-021-00755-yopenalex-snapshot
Sex differences in the meiotic behavior of an XX sex chromosome pair in males and females of the mole vole Ellobius tancrei: turning an X into a Y chromosome?
inferred← citeshttps://doi.org/10.1007/s00412-023-00803-9openalex-snapshot
Casting histone variants during mammalian reproduction
inferred← citeshttps://doi.org/10.1007/s00441-013-1723-6openalex-snapshot
Bisphenol A exposure at an environmentally relevant dose induces meiotic abnormalities in adult male rats
inferred← citeshttps://doi.org/10.1007/s00497-022-00444-5openalex-snapshot
The meiotic topoisomerase VI B subunit (MTOPVIB) is essential for meiotic DNA double-strand break formation in barley (Hordeum vulgare L.)
inferred← citeshttps://doi.org/10.1007/s00709-006-0192-0openalex-snapshot
Phosphorylation of H2AX histones in response to double-strand breaks and induction of premature chromatin condensation in hydroxyurea-treated root meristem cells of Raphanus sativus, Vicia faba, and Allium porrum
inferred← citeshttps://doi.org/10.1007/s10330-008-0093-0openalex-snapshot
Analysis of cell cycle’s correlation of γ-H2AX
inferred← citeshttps://doi.org/10.1007/s10528-024-10963-7openalex-snapshot
Evaluation of circANKLE2 & circL3MBTL4 -RNAs Expression in Fertile and Infertile Men
inferred← citeshttps://doi.org/10.1007/s10577-007-1140-3openalex-snapshot
Regulating double-stranded DNA break repair towards crossover or non-crossover during mammalian meiosis
inferred← citeshttps://doi.org/10.1007/s10577-007-1143-0openalex-snapshot
Meiotic silencing and the epigenetics of sex
inferred← citeshttps://doi.org/10.1007/s10577-007-1144-zopenalex-snapshot
Small RNAs and RNAi pathways in meiotic prophase I
inferred← citeshttps://doi.org/10.1007/s10577-007-1150-1openalex-snapshot
ZMM proteins during meiosis: Crossover artists at work
inferred← citeshttps://doi.org/10.1007/s10577-007-1165-7openalex-snapshot
Protein immunolocalization supports the presence of identical mechanisms of XY body formation in eutherians and marsupials
inferred← citeshttps://doi.org/10.1007/s10577-007-1183-5openalex-snapshot
The DNA-repair Ku70 protein is located in the nucleus and tail of elongating spermatids in grasshoppers
inferred← citeshttps://doi.org/10.1007/s10577-008-1225-7openalex-snapshot
In human pachytene spermatocytes, SUMO protein is restricted to the constitutive heterochromatin
inferred← citeshttps://doi.org/10.1007/s10577-008-9006-xopenalex-snapshot
Sumoylation precedes accumulation of phosphorylated H2AX on sex chromosomes during their meiotic inactivation
inferred← citeshttps://doi.org/10.1007/s10577-010-9169-0openalex-snapshot
Many functions of the meiotic cohesin
inferred← citeshttps://doi.org/10.1007/s10577-015-9465-9openalex-snapshot
Decreased XY recombination and disturbed meiotic prophase I progression in an infertile 48, XYY, +sSMC man
inferred← citeshttps://doi.org/10.1007/s10577-016-9524-xopenalex-snapshot
Meiotic behaviour of evolutionary sex-autosome translocations in Bovidae
inferred← citeshttps://doi.org/10.1007/s10577-022-09699-0openalex-snapshot
Meiotic pairing and double-strand break formation along the heteromorphic threespine stickleback sex chromosomes
inferred← citeshttps://doi.org/10.1007/s10709-017-9997-3openalex-snapshot
Sequence requirement of the ade6-4095 meiotic recombination hotspot in Schizosaccharomyces pombe
inferred← citeshttps://doi.org/10.1007/s11255-023-03601-5openalex-snapshot
Improving effects of telmisartan on spermatogenic disorder induced by fractionated low-dose irradiation in mice
inferred← citeshttps://doi.org/10.1007/s11427-025-3314-1openalex-snapshot
Docosahexaenoic acid alleviates Ornidazole toxicity related to spermatogenic dysfunction by modulating PPARγ-dependent ER-mitochondrial uncoupling
inferred← citeshttps://doi.org/10.1007/s11515-011-1127-5openalex-snapshot
Histone variants: making structurally and functionally divergent nucleosomes and linkers in chromatin
inferred← citeshttps://doi.org/10.1007/s12015-022-10412-1openalex-snapshot
A Comprehensive Review on the Role of ZSCAN4 in Embryonic Development, Stem Cells, and Cancer
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/b978-0-12-386041-5.00006-6openalex-snapshot
Roles of Small Ubiquitin-Related Modifiers in Male Reproductive Function
inferred← citeshttps://doi.org/10.1016/b978-0-12-397175-3.00001-6openalex-snapshot
Mammalian Meiosis
inferred← citeshttps://doi.org/10.1016/b978-012124546-7/50646-xopenalex-snapshot
Multiple Signaling Routes to Histone Phosphorylation
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2019.01.009openalex-snapshot
Evolution and meiotic organization of heteromorphic sex chromosomes
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2024.740787openalex-snapshot
Examination of the effects of impaired spermatogenesis on sterility in triploid oysters (Crassostrea gigas), and implications for commercial aquaculture
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2026.744103openalex-snapshot
Identification of late histone h2a.2.2 (lhh2a.2.2) as a novel marker highly expressed in mitotically active spermatogonia in teleost fish large yellow croaker
inferred← citeshttps://doi.org/10.1016/j.aquatox.2013.01.020openalex-snapshot
Generation of intracellular reactive oxygen species and genotoxicity effect to exposure of nanosized polyamidoamine (PAMAM) dendrimers in PLHC-1 cells in vitro
inferred← citeshttps://doi.org/10.1016/j.bbadis.2012.02.008openalex-snapshot
Molecular control of rodent spermatogenesis
inferred← citeshttps://doi.org/10.1016/j.bbadis.2014.01.016openalex-snapshot
ARF tumor suppression in the nucleolus
inferred← citeshttps://doi.org/10.1016/j.bbrc.2005.06.097openalex-snapshot
ARF and ATM/ATR cooperate in p53-mediated apoptosis upon oncogenic stress
inferred← citeshttps://doi.org/10.1016/j.bbrc.2021.02.143openalex-snapshot
MRNIP is essential for meiotic progression and spermatogenesis in mice
inferred← citeshttps://doi.org/10.1016/j.bbrc.2026.154058openalex-snapshot
RBM46 promotes meiotic initiation during oogenesis
inferred← citeshttps://doi.org/10.1016/j.biochi.2004.11.017openalex-snapshot
Tails and cuts: the role of histone post-translational modifications in the formation of programmed double-strand breaks
inferred← citeshttps://doi.org/10.1016/j.canlet.2005.07.016openalex-snapshot
Does γH2AX foci formation depend on the presence of DNA double strand breaks?
inferred← citeshttps://doi.org/10.1016/j.ceb.2006.02.008openalex-snapshot
Histone post-translational modifications and the response to DNA double-strand breaks
inferred← citeshttps://doi.org/10.1016/j.ceb.2007.04.015openalex-snapshot
Germline histone dynamics and epigenetics
inferred← citeshttps://doi.org/10.1016/j.cell.2010.11.015openalex-snapshot
Sister Cohesion and Structural Axis Components Mediate Homolog Bias of Meiotic Recombination
inferred← citeshttps://doi.org/10.1016/j.cellsig.2010.07.007openalex-snapshot
Both ERK1 and ERK2 kinases promote G2/M arrest in etoposide-treated MCF7 cells by facilitating ATM activation
inferred← citeshttps://doi.org/10.1016/j.celrep.2017.06.033openalex-snapshot
Emi2 Is Essential for Mouse Spermatogenesis
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.107686openalex-snapshot
Meiosis-Specific C19orf57/4930432K21Rik/BRME1 Modulates Localization of RAD51 and DMC1 to DSBs in Mouse Meiotic Recombination
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.108575openalex-snapshot
The Essential Function of SETDB1 in Homologous Chromosome Pairing and Synapsis during Meiosis
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.112953openalex-snapshot
ATF7IP2, a meiosis-specific partner of SETDB1, is required for proper chromosome remodeling and crossover formation during spermatogenesis
inferred← citeshttps://doi.org/10.1016/j.cub.2004.04.030openalex-snapshot
Mnd1 Is Required for Meiotic Interhomolog Repair
inferred← citeshttps://doi.org/10.1016/j.cub.2004.11.032openalex-snapshot
BRCA1, Histone H2AX Phosphorylation, and Male Meiotic Sex Chromosome Inactivation
inferred← citeshttps://doi.org/10.1016/j.cub.2006.01.066openalex-snapshot
Postmeiotic Sex Chromatin in the Male Germline of Mice
inferred← citeshttps://doi.org/10.1016/j.cub.2006.03.009openalex-snapshot
Checking Your Breaks: Surveillance Mechanisms of Meiotic Recombination
inferred← citeshttps://doi.org/10.1016/j.cub.2006.12.048openalex-snapshot
The Mre11 Complex Influences DNA Repair, Synapsis, and Crossing Over in Murine Meiosis
inferred← citeshttps://doi.org/10.1016/j.cub.2009.07.001openalex-snapshot
Meiosis: Making a Synaptonemal Complex Just Got Easier
inferred← citeshttps://doi.org/10.1016/j.cub.2009.07.041openalex-snapshot
Key Features of the X Inactivation Process Are Conserved between Marsupials and Eutherians
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.2019.11.064openalex-snapshot
The Initiation of Meiotic Sex Chromosome Inactivation Sequesters DNA Damage Signaling from Autosomes in Mouse Spermatogenesis
inferred← citeshttps://doi.org/10.1016/j.devcel.2006.02.009openalex-snapshot
Pachytene Asynapsis Drives Meiotic Sex Chromosome Inactivation and Leads to Substantial Postmeiotic Repression in Spermatids
inferred← citeshttps://doi.org/10.1016/j.devcel.2007.03.001openalex-snapshot
MIWI2 Is Essential for Spermatogenesis and Repression of Transposons in the Mouse Male Germline
inferred← citeshttps://doi.org/10.1016/j.devcel.2008.05.015openalex-snapshot
Mouse Maelstrom, a Component of Nuage, Is Essential for Spermatogenesis and Transposon Repression in Meiosis
inferred← citeshttps://doi.org/10.1016/j.devcel.2010.10.014openalex-snapshot
Histone Variants in Metazoan Development
inferred← citeshttps://doi.org/10.1016/j.devcel.2020.07.018openalex-snapshot
Single-Cell RNA Sequencing of the Cynomolgus Macaque Testis Reveals Conserved Transcriptional Profiles during Mammalian Spermatogenesis
inferred← citeshttps://doi.org/10.1016/j.devcel.2025.06.008openalex-snapshot
Generation of germinal-vesicle oocytes from mouse embryonic stem cells under an ovarian soma-free condition
inferred← citeshttps://doi.org/10.1016/j.devcel.2025.08.017openalex-snapshot
Maternal CENP-C restores centromere symmetry in mammalian zygotes to ensure proper chromosome segregation
inferred← citeshttps://doi.org/10.1016/j.dnarep.2004.03.024openalex-snapshot
H2AX: the histone guardian of the genome
inferred← citeshttps://doi.org/10.1016/j.dnarep.2004.05.007openalex-snapshot
The role of the DNA double-strand break response network in meiosis
inferred← citeshttps://doi.org/10.1016/j.dnarep.2006.05.043openalex-snapshot
γH2AX signalling during sperm chromatin remodelling in the mouse zygote
inferred← citeshttps://doi.org/10.1016/j.dnarep.2007.02.011openalex-snapshot
Differences in DNA double strand breaks repair in male germ cell types: Lessons learned from a differential expression of Mdc1 and 53BP1
inferred← citeshttps://doi.org/10.1016/j.dnarep.2008.10.008openalex-snapshot
Dynamic localization of human RAD18 during the cell cycle and a functional connection with DNA double-strand break repair
inferred← citeshttps://doi.org/10.1016/j.dnarep.2010.10.007openalex-snapshot
Protecting the heritable genome: DNA damage response mechanisms in spermatogonial stem cells
inferred← citeshttps://doi.org/10.1016/j.dnarep.2011.07.007openalex-snapshot
The DNA damage checkpoint allows recombination between divergent DNA sequences in budding yeast
inferred← citeshttps://doi.org/10.1016/j.febslet.2006.10.016openalex-snapshot
Oxidative stress induces H2AX phosphorylation in human spermatozoa
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2003.05.021openalex-snapshot
Meiosis I arrest and azoospermia in an infertile male explained by failure of formation of a component of the synaptonemal complex
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2005.11.072openalex-snapshot
Use of sex chromosome bivalent pairing in spermatocytes of nonobstructive azoospermic men for the prediction of successful sperm retrieval
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2013.07.1995openalex-snapshot
rs189037, a functional variant in ATM gene promoter, is associated with idiopathic nonobstructive azoospermia
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2019.08.004openalex-snapshot
Meiotic arrest occurs most frequently at metaphase and is often incomplete in azoospermic men
inferred← citeshttps://doi.org/10.1016/j.gene.2004.12.004openalex-snapshot
Establishment of male-specific epigenetic information
inferred← citeshttps://doi.org/10.1016/j.gyobfe.2004.07.003openalex-snapshot
Organisation nucléaire du spermatozoïde
inferred← citeshttps://doi.org/10.1016/j.ijrobp.2009.07.1722openalex-snapshot
Poly(ADP-Ribose) Polymerase-1 and DNA-Dependent Protein Kinase Have Equivalent Roles in Double Strand Break Repair Following Ionizing Radiation
inferred← citeshttps://doi.org/10.1016/j.isci.2022.104008openalex-snapshot
FBXO47 is essential for preventing the synaptonemal complex from premature disassembly in mouse male meiosis
inferred← citeshttps://doi.org/10.1016/j.jgg.2014.01.003openalex-snapshot
The Role of Chromatin Modifications in Progression through Mouse Meiotic Prophase
inferred← citeshttps://doi.org/10.1016/j.mce.2007.11.025openalex-snapshot
Sexual dimorphism in parental imprint ontogeny and contribution to embryonic development
inferred← citeshttps://doi.org/10.1016/j.mce.2011.09.029openalex-snapshot
Mammalian ovary differentiation – A focus on female meiosis
inferred← citeshttps://doi.org/10.1016/j.mce.2020.110964openalex-snapshot
Paternal epigenetics: Mammalian sperm provide much more than DNA at fertilization
inferred← citeshttps://doi.org/10.1016/j.molcel.2005.09.021openalex-snapshot
Crossover and Noncrossover Pathways in Mouse Meiosis
inferred← citeshttps://doi.org/10.1016/j.molcel.2013.04.026openalex-snapshot
Multiple Epigenetic Mechanisms and the piRNA Pathway Enforce LINE1 Silencing during Adult Spermatogenesis
inferred← citeshttps://doi.org/10.1016/j.molcel.2016.10.017openalex-snapshot
Phosphorylated CtIP Functions as a Co-factor of the MRE11-RAD50-NBS1 Endonuclease in DNA End Resection
inferred← citeshttps://doi.org/10.1016/j.molcel.2018.01.033openalex-snapshot
PRDM9 Methyltransferase Activity Is Essential for Meiotic DNA Double-Strand Break Formation at Its Binding Sites
inferred← citeshttps://doi.org/10.1016/j.molcel.2018.08.031openalex-snapshot
Impeding DNA Break Repair Enables Oocyte Quality Control
inferred← citeshttps://doi.org/10.1016/j.molcel.2019.03.023openalex-snapshot
REC114 Partner ANKRD31 Controls Number, Timing, and Location of Meiotic DNA Breaks
inferred← citeshttps://doi.org/10.1016/j.molcel.2024.10.001openalex-snapshot
ZC3H14 facilitates backsplicing by binding to exon-intron boundary and 3′ UTR
inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2006.11.020openalex-snapshot
Effect of ATM heterozygosity on heritable DNA damage in mice following paternal F0 germline irradiation
inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2009.06.010openalex-snapshot
DNA double-strand breaks: Their production, recognition, and repair in eukaryotes
inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2009.10.011openalex-snapshot
Parp1–XRCC1 and the repair of DNA double strand breaks in mouse round spermatids
inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2010.02.004openalex-snapshot
Genetic probing of homologous recombination and non-homologous end joining during meiotic prophase in irradiated mouse spermatocytes
inferred← citeshttps://doi.org/10.1016/j.mrrev.2008.08.003openalex-snapshot
Role of H2AX in DNA damage response and human cancers
inferred← citeshttps://doi.org/10.1016/j.mrrev.2016.07.004openalex-snapshot
Consequences of irradiation on adult spermatogenesis: Between infertility and hereditary risk
inferred← citeshttps://doi.org/10.1016/j.rbmo.2017.12.017openalex-snapshot
Analysis of CDK2 mutations in Chinese men with non-obstructive azoospermia who underwent testis biopsy
inferred← citeshttps://doi.org/10.1016/j.reprotox.2015.01.009openalex-snapshot
2,2′,4,4′-Tetrabromodiphenyl ether disrupts spermatogenesis, impairs mitochondrial function and induces apoptosis of early leptotene spermatocytes in rats
inferred← citeshttps://doi.org/10.1016/j.scr.2013.12.007openalex-snapshot
Generation of male germ cells from mouse induced pluripotent stem cells in vitro
inferred← citeshttps://doi.org/10.1016/j.semcdb.2016.01.026openalex-snapshot
Atypical ploidy cycles, Spo11, and the evolution of meiosis
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