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Epigenetic Transitions in Germ Cell Development and Meiosis
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/dvg.20438openalex-snapshot
De novo DNA methylation independent establishment of maternal imprint on X chromosome in mouse oocytes
inferredcites →https://doi.org/10.1007/s00412-009-0214-8openalex-snapshot
Epigenetic marks for chromosome imprinting during spermatogenesis in coccids
inferredcites →https://doi.org/10.1007/s10577-007-1143-0openalex-snapshot
Meiotic silencing and the epigenetics of sex
inferredcites →https://doi.org/10.1007/s10815-008-9270-xopenalex-snapshot
Two single nucleotide polymorphisms in PRDM9 (MEISETZ) gene may be a genetic risk factor for Japanese patients with azoospermia by meiotic arrest
inferredcites →https://doi.org/10.1016/j.cell.2004.11.011openalex-snapshot
Generation of Pluripotent Stem Cells from Neonatal Mouse Testis
inferredcites →https://doi.org/10.1016/j.cell.2008.11.042openalex-snapshot
DNA Demethylation in Zebrafish Involves the Coupling of a Deaminase, a Glycosylase, and Gadd45
inferredcites →https://doi.org/10.1016/j.cell.2009.02.015openalex-snapshot
A C. elegans LSD1 Demethylase Contributes to Germline Immortality by Reprogramming Epigenetic Memory
inferredcites →https://doi.org/10.1016/j.cub.2004.08.062openalex-snapshot
The MES-2/MES-3/MES-6 Complex and Regulation of Histone H3 Methylation in C. elegans
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.2009.07.041openalex-snapshot
Key Features of the X Inactivation Process Are Conserved between Marsupials and Eutherians
inferredcites →https://doi.org/10.1016/j.devcel.2006.05.010openalex-snapshot
In Vitro-Differentiated Embryonic Stem Cells Give Rise to Male Gametes that Can Generate Offspring Mice
inferredcites →https://doi.org/10.1016/j.devcel.2007.03.001openalex-snapshot
MIWI2 Is Essential for Spermatogenesis and Repression of Transposons in the Mouse Male Germline
inferredcites →https://doi.org/10.1016/j.devcel.2010.01.010openalex-snapshot
RNF8-Dependent Histone Modifications Regulate Nucleosome Removal during Spermatogenesis
inferredcites →https://doi.org/10.1016/j.ejcb.2009.09.001openalex-snapshot
Distinct functions of Mst77F and protamines in nuclear shaping and chromatin condensation during Drosophila spermiogenesis
inferredcites →https://doi.org/10.1016/j.gde.2009.03.003openalex-snapshot
Xist gene regulation at the onset of X inactivation
inferredcites →https://doi.org/10.1016/j.molcel.2007.02.025openalex-snapshot
Heterochromatin Formation in Drosophila Is Initiated through Active Removal of H3K4 Methylation by the LSD1 Homolog SU(VAR)3-3
inferredcites →https://doi.org/10.1016/j.tcb.2009.03.001openalex-snapshot
Crosstalk between histone modifications during the DNA damage response
inferredcites →https://doi.org/10.1016/j.ydbio.2004.11.025openalex-snapshot
Extensive and orderly reprogramming of genome-wide chromatin modifications associated with specification and early development of germ cells in mice
inferredcites →https://doi.org/10.1016/s0092-8674(00)80154-3openalex-snapshot
Inactivation of the HR6B Ubiquitin-Conjugating DNA Repair Enzyme in Mice Causes Male Sterility Associated with Chromatin Modification
inferredcites →https://doi.org/10.1016/s0092-8674(01)00542-6openalex-snapshot
Loss of the Suv39h Histone Methyltransferases Impairs Mammalian Heterochromatin and Genome Stability
inferredcites →https://doi.org/10.1016/s0092-8674(01)00609-2openalex-snapshot
Meiotic Silencing by Unpaired DNA
inferredcites →https://doi.org/10.1016/s0925-4773(02)00181-8openalex-snapshot
Epigenetic reprogramming in mouse primordial germ cells
inferredcites →https://doi.org/10.1016/s1534-5807(02)00165-xopenalex-snapshot
miwi, a Murine Homolog of piwi, Encodes a Cytoplasmic Protein Essential for Spermatogenesis
inferredcites →https://doi.org/10.1038/85927openalex-snapshot
Maternal methylation imprints on human chromosome 15 are established during or after fertilization
inferredcites →https://doi.org/10.1038/emboj.2008.257openalex-snapshot
Histone H3 lysine 4 trimethylation marks meiotic recombination initiation sites
inferredcites →https://doi.org/10.1038/emboj.2009.207openalex-snapshot
Distinct histone modifications define initiation and repair of meiotic recombination in the mouse
inferredcites →https://doi.org/10.1038/emboj.2010.80openalex-snapshot
Dynamic link of DNA demethylation, DNA strand breaks and repair in mouse zygotes
inferredcites →https://doi.org/10.1038/nature02222openalex-snapshot
Inheritance of a pre-inactivated paternal X chromosome in early mouse embryos
inferredcites →https://doi.org/10.1038/nature02633openalex-snapshot
Essential role for de novo DNA methyltransferase Dnmt3a in paternal and maternal imprinting
inferredcites →https://doi.org/10.1038/nature02886openalex-snapshot
Meiotic catastrophe and retrotransposon reactivation in male germ cells lacking Dnmt3L
inferredcites →https://doi.org/10.1038/nature03368openalex-snapshot
Chromatin remodelling and epigenetic features of germ cells
inferredcites →https://doi.org/10.1038/nature03813openalex-snapshot
Blimp1 is a critical determinant of the germ cell lineage in mice
inferredcites →https://doi.org/10.1038/nature04112openalex-snapshot
A histone H3 methyltransferase controls epigenetic events required for meiotic prophase
inferredcites →https://doi.org/10.1038/nature04155openalex-snapshot
Evidence for de novo imprinted X-chromosome inactivation independent of meiotic inactivation in mice
inferredcites →https://doi.org/10.1038/nature05918openalex-snapshot
Stability and flexibility of epigenetic gene regulation in mammalian development
inferredcites →https://doi.org/10.1038/nature05987openalex-snapshot
DNMT3L connects unmethylated lysine 4 of histone H3 to de novo methylation of DNA
inferredcites →https://doi.org/10.1038/nature06236openalex-snapshot
Histone demethylase JHDM2A is critical for Tnp1 and Prm1 transcription and spermatogenesis
inferredcites →https://doi.org/10.1038/nature06714openalex-snapshot
Chromatin dynamics during epigenetic reprogramming in the mouse germ line
inferredcites →https://doi.org/10.1038/nature08161openalex-snapshot
Evidence of Xist RNA-independent initiation of mouse imprinted X-chromosome inactivation
inferredcites →https://doi.org/10.1038/nature08162openalex-snapshot
Distinctive chromatin in human sperm packages genes for embryo development
inferredcites →https://doi.org/10.1038/nature08315openalex-snapshot
KDM1B is a histone H3K4 demethylase required to establish maternal genomic imprints
inferredcites →https://doi.org/10.1038/nature08397openalex-snapshot
Cooperative binding of two acetylation marks on a histone tail by a single bromodomain
inferredcites →https://doi.org/10.1038/nature08829openalex-snapshot
Genome-wide erasure of DNA methylation in mouse primordial germ cells is affected by AID deficiency
inferredcites →https://doi.org/10.1038/ncb1413openalex-snapshot
Blimp1 associates with Prmt5 and directs histone arginine methylation in mouse germ cells
inferredcites →https://doi.org/10.1038/ncb1513openalex-snapshot
Lsh is required for meiotic chromosome synapsis and retrotransposon silencing in female germ cells
inferredcites →https://doi.org/10.1038/ng.268openalex-snapshot
The lysine demethylase LSD1 (KDM1) is required for maintenance of global DNA methylation
inferredcites →https://doi.org/10.1038/ng1283openalex-snapshot
Meiotic pairing and imprinted X chromatin assembly in Caenorhabditis elegans
inferredcites →https://doi.org/10.1038/ng1484openalex-snapshot
Silencing of unsynapsed meiotic chromosomes in the mouse
inferredcites →https://doi.org/10.1038/ng1949openalex-snapshot
Chromosome-wide nucleosome replacement and H3.3 incorporation during mammalian meiotic sex chromosome inactivation
inferredcites →https://doi.org/10.1038/nrg2295openalex-snapshot
Epigenetic events in mammalian germ-cell development: reprogramming and beyond
inferredcites →https://doi.org/10.1038/nrg2505openalex-snapshot
The consequences of asynapsis for mammalian meiosis
inferredcites →https://doi.org/10.1038/nsmb.1821openalex-snapshot
Repressive and active histone methylation mark distinct promoters in human and mouse spermatozoa
inferredcites →https://doi.org/10.1038/sj.emboj.7601513openalex-snapshot
Differential histone modifications mark mouse imprinting control regions during spermatogenesis
inferredcites →https://doi.org/10.1038/sj.emboj.7601767openalex-snapshot
Functional dynamics of H3K9 methylation during meiotic prophase progression
inferredcites →https://doi.org/10.1073/pnas.0902087106openalex-snapshot
Protein-binding elements establish in the oocyte the primary imprint of the Prader-Willi/Angelman syndromes domain
inferredcites →https://doi.org/10.1073/pnas.0910267107openalex-snapshot
UBR2 mediates transcriptional silencing during spermatogenesis via histone ubiquitination
inferredcites →https://doi.org/10.1074/jbc.m304545200openalex-snapshot
The Structural Organization of Sperm Chromatin
inferredcites →https://doi.org/10.1078/0171-9335-00123openalex-snapshot
Regulated hyperacetylation of core histones during mouse spermatogenesis: involvement of histone-deacetylases
inferredcites →https://doi.org/10.1083/jcb.200604141openalex-snapshot
Pericentric heterochromatin reprogramming by new histone variants during mouse spermiogenesis
inferredcites →https://doi.org/10.1093/hmg/ddg315openalex-snapshot
Methylation imprints of the imprint control region of the SNRPN-gene in human gametes and preimplantation embryos
inferredcites →https://doi.org/10.1093/hmg/ddm179openalex-snapshot
Role of the Dnmt3 family in de novo methylation of imprinted and repetitive sequences during male germ cell development in the mouse
inferredcites →https://doi.org/10.1093/hmg/ddp277openalex-snapshot
Histone methylation is mechanistically linked to DNA methylation at imprinting control regions in mammals
inferredcites →https://doi.org/10.1093/humrep/dem365openalex-snapshot
Incomplete nuclear transformation of human spermatozoa in oligo-astheno-teratospermia: characterization by indirect immunofluorescence of chromatin and thiol status
inferredcites →https://doi.org/10.1093/mp/ssp027openalex-snapshot
An Epigenetic Perspective on Developmental Regulation of Seed Genes
inferredcites →https://doi.org/10.1095/biolreprod.104.028191openalex-snapshot
Nucleoprotein Transitions During Spermiogenesis in Mice with Transition Nuclear Protein Tnp1 and Tnp2 Mutations1
inferredcites →https://doi.org/10.1101/gad.1649908openalex-snapshot
Complex genome-wide transcription dynamics orchestrated by Blimp1 for the specification of the germ cell lineage in mice
inferredcites →https://doi.org/10.1101/gad.495809openalex-snapshot
Transcription is required for establishment of germline methylation marks at imprinted genes
inferredcites →https://doi.org/10.1111/j.1365-2443.2008.01193.xopenalex-snapshot
Spermatogenesis‐specific association of SMCY and MSH5
inferredcites →https://doi.org/10.1111/j.1742-4658.2009.07504.xopenalex-snapshot
From meiosis to postmeiotic events: The secrets of histone disappearance
inferredcites →https://doi.org/10.1126/science.1065848openalex-snapshot
Dnmt3L and the Establishment of Maternal Genomic Imprints
inferredcites →https://doi.org/10.1126/science.1092727openalex-snapshot
Epigenetic Dynamics of Imprinted X Inactivation During Early Mouse Development
inferredcites →https://doi.org/10.1126/science.1126316openalex-snapshot
The Xist RNA Gene Evolved in Eutherians by Pseudogenization of a Protein-Coding Gene
inferredcites →https://doi.org/10.1126/science.1140846openalex-snapshot
Germ Versus Soma Decisions: Lessons from Flies and Worms
inferredcites →https://doi.org/10.1126/science.1142612openalex-snapshot
Developmentally Regulated piRNA Clusters Implicate MILI in Transposon Control
inferredcites →https://doi.org/10.1126/science.1181495openalex-snapshot
Prdm9 Controls Activation of Mammalian Recombination Hotspots
inferredcites →https://doi.org/10.1126/science.1182363openalex-snapshot
Drive Against Hotspot Motifs in Primates Implicates the PRDM9 Gene in Meiotic Recombination
inferredcites →https://doi.org/10.1126/science.1183439openalex-snapshot
PRDM9 Is a Major Determinant of Meiotic Recombination Hotspots in Humans and Mice
inferredcites →https://doi.org/10.1126/science.1187945openalex-snapshot
Genome-Wide Reprogramming in the Mouse Germ Line Entails the Base Excision Repair Pathway
inferredcites →https://doi.org/10.1126/science.1190830openalex-snapshot
High-Resolution Analysis of Parent-of-Origin Allelic Expression in the Mouse Brain
inferredcites →https://doi.org/10.1128/mcb.00275-09openalex-snapshot
A Randomly Integrated Transgenic H19 Imprinting Control Region Acquires Methylation Imprinting Independently of Its Establishment in Germ Cells
inferredcites →https://doi.org/10.1128/mcb.00679-09openalex-snapshot
Loss of YY1 Impacts the Heterochromatic State and Meiotic Double-Strand Breaks during Mouse Spermatogenesis
inferredcites →https://doi.org/10.1128/mcb.18.6.3350openalex-snapshot
Histone- and Protamine-DNA Association: Conservation of Different Patterns within the β-Globin Domain in Human Sperm
inferredcites →https://doi.org/10.1128/mcb.23.15.5354-5365.2003openalex-snapshot
Acetylation-Dependent Chromatin Reorganization by BRDT, a Testis-Specific Bromodomain-Containing Protein
inferredcites →https://doi.org/10.1128/mcb.25.3.1041-1053.2005openalex-snapshot
Silencing of Unpaired Chromatin and Histone H2A Ubiquitination in Mammalian Meiosis
inferredcites →https://doi.org/10.1146/annurev.cellbio.24.110707.175327openalex-snapshot
The Biogenesis and Function of PIWI Proteins and piRNAs: Progress and Prospect
inferredcites →https://doi.org/10.1159/000090814openalex-snapshot
Genomic imprinting in the mealybugs
inferredcites →https://doi.org/10.1159/000185175openalex-snapshot
The Y Chromosome Region Essential for Spermatogenesis
inferredcites →https://doi.org/10.1186/1471-213x-8-34openalex-snapshot
Sperm-derived histones contribute to zygotic chromatin in humans
inferredcites →https://doi.org/10.1186/1756-8935-2-5openalex-snapshot
The histone 3 lysine 4 methyltransferase, Mll2, is only required briefly in development and spermatogenesis
inferredcites →https://doi.org/10.1186/1756-8935-3-9openalex-snapshot
HP1γ function is required for male germ cell survival and spermatogenesis
inferredcites →https://doi.org/10.1242/dev.004481openalex-snapshot
The first bromodomain of Brdt, a testis-specific member of the BET sub-family of double-bromodomain-containing proteins, is essential for male germ cell differentiation
inferredcites →https://doi.org/10.1242/dev.004770openalex-snapshot
The testis-specific proteasome subunit Prosα6T of D. melanogaster is required for individualization and nuclear maturation during spermatogenesis
inferredcites →https://doi.org/10.1242/dev.005611openalex-snapshot
Cellular dynamics associated with the genome-wide epigenetic reprogramming in migrating primordial germ cells in mice
inferredcites →https://doi.org/10.1242/dev.020966openalex-snapshot
Developmental roles of the histone lysine demethylases
inferredcites →https://doi.org/10.1242/dev.02584openalex-snapshot
MES-4: an autosome-associated histone methyltransferase that participates in silencing the X chromosomes in theC. elegansgerm line
inferredcites →https://doi.org/10.1242/dev.030403openalex-snapshot
The function of non-coding RNAs in genomic imprinting
inferredcites →https://doi.org/10.1242/dev.125.17.3353openalex-snapshot
Tetraploid embryos rescue embryonic lethality caused by an additional maternally inherited X chromosome in the mouse
inferredcites →https://doi.org/10.1242/jcs.03279openalex-snapshot
Methylation of histone H3 at Lys4 differs between paternal and maternal chromosomes inSciara ocellarisgermline development
inferredcites →https://doi.org/10.3109/19396360903490790openalex-snapshot
Histone H4 Acetylation is Essential to Proceed from a Histone- to a Protamine-based Chromatin Structure in Spermatid Nuclei ofDrosophila melanogaster
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.4834779openalex-extracted
Meiosis Achieves Epigenetic Reprogramming Independently of Gametogenesis and Fertilization
inferred← citeshttps://doi.org/10.1002/3527600906.mcb.200300031.pub2openalex-snapshot
Molecular Genetics of Genomic Imprinting
inferred← citeshttps://doi.org/10.1002/9781118538074.ch7openalex-snapshot
Epigenetic Modifications during Mammalian Oocyte Growth and Meiotic Progression
inferred← citeshttps://doi.org/10.1002/9781118782392.ch15openalex-snapshot
Bioinformatics Analysis of Epigenetics
inferred← citeshttps://doi.org/10.1002/9781118881286.ch18openalex-snapshot
Alterations of the Epigenome Induced by the Environment in Reproduction
inferred← citeshttps://doi.org/10.1002/9781394372683.ch2openalex-snapshot
Molecular Players of Epigenetic Information
inferred← citeshttps://doi.org/10.1002/adma.201905309openalex-snapshot
Supercharged Proteins and Polypeptides
inferred← citeshttps://doi.org/10.1002/bies.201100141openalex-snapshot
Histone crotonylation specifically marks the haploid male germ cell gene expression program
inferred← citeshttps://doi.org/10.1002/dvdy.23924openalex-snapshot
Epigenetics of sex determination and gonadogenesis
inferred← citeshttps://doi.org/10.1002/jcp.31201openalex-snapshot
Balanced spatiotemporal arrangements of histone H3 and H4 posttranslational modifications are necessary for meiotic prophase I chromosome organization
inferred← citeshttps://doi.org/10.1002/jemt.22880openalex-snapshot
Bones Morphogenic Protein‐4 and retinoic acid combined treatment comparative analysis for in vitro differentiation potential of murine mesenchymal stem cells derived from bone marrow and adipose tissue into germ cells
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.22151openalex-snapshot
Lessons for inductive germline determination
inferred← citeshttps://doi.org/10.1002/mrd.22951openalex-snapshot
The effects of superovulation and reproductive aging on the epigenome of the oocyte and embryo
inferred← citeshttps://doi.org/10.1002/mrd.23449openalex-snapshot
Genome‐wide chromatin occupancy of BRDT and gene expression analysis suggest transcriptional partners and specific epigenetic landscapes that regulate gene expression during spermatogenesis
inferred← citeshttps://doi.org/10.1007/978-1-4614-8078-5_1openalex-snapshot
Epigenetic Reprogramming in the Mammalian Germline
inferred← citeshttps://doi.org/10.1007/978-1-4939-0706-9_1openalex-snapshot
Epigenetics in Childhood Health and Disease
inferred← citeshttps://doi.org/10.1007/978-1-4939-0820-2_6openalex-snapshot
The Epigenetic Basis of Adaptation and Responses to Environmental Change: Perspective on Human Reproduction
inferred← citeshttps://doi.org/10.1007/978-1-4939-3070-8_3openalex-snapshot
piRNAs-Transposon Silencing and Germ Line Development
inferred← citeshttps://doi.org/10.1007/978-1-62703-011-3_19openalex-snapshot
Nonmammalian Parent-of-Origin Effects
inferred← citeshttps://doi.org/10.1007/978-3-030-21664-1_4openalex-snapshot
Epigenetic Transgenerational Inheritance
inferred← citeshttps://doi.org/10.1007/978-3-031-80973-6_14openalex-snapshot
Application of Machine Learning in Cancer Epigenetics: A Deeper Look into the Epigenome
inferred← citeshttps://doi.org/10.1007/978-3-319-27186-6_2openalex-snapshot
Noncoding RNAs and Chromatin Modifications in the Developmental Control of Imprinted Genes
inferred← citeshttps://doi.org/10.1007/978-3-642-23380-7_4openalex-snapshot
Complex Phenotypes: Epigenetic Manifestation of Environmental Exposures
inferred← citeshttps://doi.org/10.1007/978-94-007-2495-2_6openalex-snapshot
Epigenome Changes During Development
inferred← citeshttps://doi.org/10.1007/978-94-007-4525-4_6openalex-snapshot
Epigenetic Regulation of Male Germ Cell Differentiation
inferred← citeshttps://doi.org/10.1007/978-94-007-7772-9_1openalex-snapshot
Physiology of Gametogenesis
inferred← citeshttps://doi.org/10.1007/978-981-10-5203-3_6openalex-snapshot
Long Noncoding RNAs in Mammalian Development and Diseases
inferred← citeshttps://doi.org/10.1007/s00204-019-02529-zopenalex-snapshot
Effects of 2,3′,4,4′5-pentachlorobiphenyl exposure during pregnancy on epigenetic imprinting and maturation of offspring’s oocytes in mice
inferred← citeshttps://doi.org/10.1007/s00204-024-03713-6openalex-snapshot
Future in the past: paternal reprogramming of offspring phenotype and the epigenetic mechanisms
inferred← citeshttps://doi.org/10.1007/s00249-023-01679-4openalex-snapshot
MIL-CELL: a tool for multi-scale simulation of yeast replication and prion transmission
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/s00412-013-0415-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/s00412-016-0577-6openalex-snapshot
Transcription reactivation during the first meiotic prophase in bugs is not dependent on synapsis
inferred← citeshttps://doi.org/10.1007/s00412-017-0656-3openalex-snapshot
Telomere chromatin establishment and its maintenance during mammalian development
inferred← citeshttps://doi.org/10.1007/s00439-018-1888-xopenalex-snapshot
Pronounced maternal parent-of-origin bias for type-1 NF1 microdeletions
inferred← citeshttps://doi.org/10.1007/s12032-023-02028-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12033-012-9560-5openalex-snapshot
Gene Expression and DNA Methylation Status of Chicken Primordial Germ Cells
inferred← citeshttps://doi.org/10.1007/s12035-014-9040-yopenalex-snapshot
Epigenetics of Stress, Addiction, and Resilience: Therapeutic Implications
inferred← citeshttps://doi.org/10.1007/s13744-020-00777-8openalex-snapshot
Epigenetic Molecular Mechanisms in Insects
inferred← citeshttps://doi.org/10.1016/b978-0-12-374984-0.01278-xopenalex-snapshot
Recombination Hot Spots, Mouse
inferred← citeshttps://doi.org/10.1016/b978-0-12-405944-3.00005-2openalex-snapshot
Epigenetic Changes in the Paternal Germline
inferred← citeshttps://doi.org/10.1016/b978-0-12-416027-9.00009-7openalex-snapshot
Parental Epigenetic Asymmetry in Mammals
inferred← citeshttps://doi.org/10.1016/b978-0-12-800957-4.00003-5openalex-snapshot
Keratinocyte Differentiation and Epigenetics
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Histones and variants
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Maternal epigenetic inheritance
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Long noncoding RNA and epigenetic inheritance
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Epigenetics of major depressive disorder
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Getting Ready for Pregnancy
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Role of epigenetic molecular mechanisms in insect evolutionary innovations
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Getting Ready for Pregnancy
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Gametogenesis: A journey from inception to conception
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2022.10.002openalex-snapshot
Transgenerational inheritance and its modulation by environmental cues
inferred← citeshttps://doi.org/10.1016/j.ajhg.2015.11.019openalex-snapshot
Correlations between Synaptic Initiation and Meiotic Recombination: A Study of Humans and Mice
inferred← citeshttps://doi.org/10.1016/j.anireprosci.2015.05.018openalex-snapshot
Perspectives on mammalian chromatoid body research
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Thyroid hormone potentiates androgen-induced sex reversal during early gonadal differentiation in orange-spotted grouper, Epinephelus coioides
inferred← citeshttps://doi.org/10.1016/j.bbadis.2023.166742openalex-snapshot
Oxidative stress-induced apoptosis and autophagy: Balancing the contrary forces in spermatogenesis
inferred← citeshttps://doi.org/10.1016/j.bbcan.2025.189437openalex-snapshot
Testicular germ cell tumors and infertility: Exploring epigenetic dysregulation in the journey of the male germ cell towards new biomarkers and therapeutics
inferred← citeshttps://doi.org/10.1016/j.bbrc.2015.01.122openalex-snapshot
Physical interaction between MPP8 and PRC1 complex and its implication for regulation of spermatogenesis
inferred← citeshttps://doi.org/10.1016/j.biocel.2015.04.004openalex-snapshot
Chromatin mechanisms in the developmental control of imprinted gene expression
inferred← citeshttps://doi.org/10.1016/j.cell.2014.04.042openalex-snapshot
Polar Body Genome Transfer for Preventing the Transmission of Inherited Mitochondrial Diseases
inferred← citeshttps://doi.org/10.1016/j.celrep.2015.10.066openalex-snapshot
Exogenous Expression of Human Protamine 1 (hPrm1) Remodels Fibroblast Nuclei into Spermatid-like Structures
inferred← citeshttps://doi.org/10.1016/j.celrep.2017.01.074openalex-snapshot
Sirt1 Regulates DNA Methylation and Differentiation Potential of Embryonic Stem Cells by Antagonizing Dnmt3l
inferred← citeshttps://doi.org/10.1016/j.cotox.2024.100465openalex-snapshot
Inter- and trans-generational impacts of environmental exposures on the germline resolved at the single-cell level
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.2015.01.014openalex-snapshot
SCML2 Establishes the Male Germline Epigenome through Regulation of Histone H2A Ubiquitination
inferred← citeshttps://doi.org/10.1016/j.devcel.2022.03.006openalex-snapshot
Znhit1 controls meiotic initiation in male germ cells by coordinating with Stra8 to activate meiotic gene expression
inferred← citeshttps://doi.org/10.1016/j.ejmech.2020.113120openalex-snapshot
Single-step fluorescent probes to detect decrotonylation activity of HDACs through intramolecular reactions
inferred← citeshttps://doi.org/10.1016/j.gendis.2022.05.012openalex-snapshot
Clinical heterogeneity of NLRP12-associated autoinflammatory diseases
inferred← citeshttps://doi.org/10.1016/j.gene.2011.11.062openalex-snapshot
Gender-specific methylation differences in relation to prenatal exposure to cigarette smoke
inferred← citeshttps://doi.org/10.1016/j.heliyon.2021.e06029openalex-snapshot
Transposable elements, contributors in the evolution of organisms (from an arms race to a source of raw materials)
inferred← citeshttps://doi.org/10.1016/j.jmb.2017.02.008openalex-snapshot
Dynamics and Context-Dependent Roles of DNA Methylation
inferred← citeshttps://doi.org/10.1016/j.mam.2024.101321openalex-snapshot
Physiological and pathological aspects of epididymal sperm maturation
inferred← citeshttps://doi.org/10.1016/j.pbiomolbio.2012.08.014openalex-snapshot
Epigenetic inheritance and plasticity: The responsive germline
inferred← citeshttps://doi.org/10.1016/j.pbiomolbio.2017.08.009openalex-snapshot
From cholesterol to consciousness
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2018.08.063openalex-snapshot
Can epigenetics translate environmental cues into phenotypes?
inferred← citeshttps://doi.org/10.1016/j.semcdb.2019.09.002openalex-snapshot
Gaps and barriers: Gap junctions as a channel of communication between the soma and the germline
inferred← citeshttps://doi.org/10.1016/j.tig.2012.01.005openalex-snapshot
Parallel mechanisms of epigenetic reprogramming in the germline
inferred← citeshttps://doi.org/10.1016/j.tox.2017.08.010openalex-snapshot
Gender-specific association of exposure to non-dioxin-like polychlorinated biphenyls during pregnancy with methylation levels of H19 and long interspersed nuclear element-1 in cord blood in the Hokkaido study
inferred← citeshttps://doi.org/10.1016/j.tox.2021.152780openalex-snapshot
Environmental pollutants exposure and male reproductive toxicity: The role of epigenetic modifications
inferred← citeshttps://doi.org/10.1017/cbo9781139540742.003openalex-snapshot
Germ-cell differentiation from pluripotent cells
inferred← citeshttps://doi.org/10.1017/s0029665111000851openalex-snapshot
The potential role of epigenetic responses to diet in ageing
inferred← citeshttps://doi.org/10.1038/nature11709openalex-snapshot
Tet1 controls meiosis by regulating meiotic gene expression
inferred← citeshttps://doi.org/10.1038/ncomms10116openalex-snapshot
LSD1 is essential for oocyte meiotic progression by regulating CDC25B expression in mice
inferred← citeshttps://doi.org/10.1038/ncomms13387openalex-snapshot
Reader domain specificity and lysine demethylase-4 family function
inferred← citeshttps://doi.org/10.1038/npre.2011.6507.1openalex-snapshot
Transcriptional memory emerges from cooperative histone modifications
inferred← citeshttps://doi.org/10.1038/nrg3142openalex-snapshot
Epigenetics and the environment: emerging patterns and implications
inferred← citeshttps://doi.org/10.1038/nrg3685openalex-snapshot
Epigenetic reprogramming in plant sexual reproduction
inferred← citeshttps://doi.org/10.1038/pr.2013.106openalex-snapshot
Postweaning exposure to a high-fat diet is associated with alterations to the hepatic histone code in Japanese macaques
inferred← citeshttps://doi.org/10.1038/s41398-023-02620-1openalex-snapshot
Epigenome-wide association studies of prenatal maternal mental health and infant epigenetic profiles: a systematic review
inferred← citeshttps://doi.org/10.1038/s41419-020-2333-3openalex-snapshot
UHRF1-repressed 5’-hydroxymethylcytosine is essential for the male meiotic prophase I
inferred← citeshttps://doi.org/10.1038/s41419-025-08158-yopenalex-snapshot
Somatic Kitl promotes mTOR to facilitate prophase I of meiosis in female embryonic gonads
inferred← citeshttps://doi.org/10.1038/s41467-021-23378-4openalex-snapshot
Meiosis-specific ZFP541 repressor complex promotes developmental progression of meiotic prophase towards completion during mouse spermatogenesis
inferred← citeshttps://doi.org/10.1038/s41467-026-72540-3openalex-snapshot
SIRT7 links H3K36ac epigenetic regulation with genome maintenance in the mouse testis
inferred← citeshttps://doi.org/10.1038/s41588-023-01329-7openalex-snapshot
Distinct chromatin signatures in the Arabidopsis male gametophyte
inferred← citeshttps://doi.org/10.1038/s42003-023-05335-7openalex-snapshot
The localization of centromere protein A is conserved among tissues
inferred← citeshttps://doi.org/10.1038/srep25089openalex-snapshot
Dynamics of histone H2A, H4 and HS1ph during spermatogenesis with a focus on chromatin condensation and maturity of spermatozoa
inferred← citeshttps://doi.org/10.1039/d3cp05957jopenalex-snapshot
Probing the hierarchical dynamics of DNA-sperm nuclear transition protein complexes through fuzzy interaction and mesoscale condensation
inferred← citeshttps://doi.org/10.1051/medsci/2011275002openalex-snapshot
Quand l’environnement du père influence l’expression génique chez l’enfant
inferred← citeshttps://doi.org/10.1055/s-0032-1331795openalex-snapshot
In Vitro–Derived Gametes from Stem Cells
inferred← citeshttps://doi.org/10.1071/rd14167openalex-snapshot
Epigenetic processes in the male germline
inferred← citeshttps://doi.org/10.1073/pnas.1611995113openalex-snapshot
MRG15 is required for pre-mRNA splicing and spermatogenesis
inferred← citeshttps://doi.org/10.1073/pnas.1711229114openalex-snapshot
Parallel epigenetic modifications induced by hatchery rearing in a Pacific salmon
inferred← citeshttps://doi.org/10.1073/pnas.1804512115openalex-snapshot
Polycomb protein SCML2 facilitates H3K27me3 to establish bivalent domains in the male germline
inferred← citeshttps://doi.org/10.1073/pnas.1817675116openalex-snapshot
OsAGO2 controls ROS production and the initiation of tapetal PCD by epigenetically regulating OsHXK1 expression in rice anthers
inferred← citeshttps://doi.org/10.1073/pnas.2412185121openalex-snapshot
Imprinted X chromosome inactivation in marsupials: The paternal X arrives at the egg with a silent DNA methylation profile
inferred← citeshttps://doi.org/10.1074/jbc.m114.626697openalex-snapshot
Non-germ Line Restoration of Genomic Imprinting for a Small Subset of Imprinted Genes in Ubiquitin-like PHD and RING Finger Domain-Containing 1 (Uhrf1) Null Mouse Embryonic Stem Cells
inferred← citeshttps://doi.org/10.1083/jcb.201903125openalex-snapshot
CDK2 regulates the NRF1/Ehmt1 axis during meiotic prophase I
inferred← citeshttps://doi.org/10.1088/1478-3975/10/2/026006openalex-snapshot
Transcriptional regulation by histone modifications: towards a theory of chromatin re-organization during stem cell differentiation
inferred← citeshttps://doi.org/10.1089/cell.2019.0041openalex-snapshot
DNA Methylation of the Insulin-Like Growth Factor 2-Imprinted Gene in Trophoblast Cells of Elongated Bovine Embryo: Effects of the In Vitro Culture
inferred← citeshttps://doi.org/10.1089/scd.2015.0230openalex-snapshot
In Vitro Gamete Differentiation from Pluripotent Stem Cells as a Promising Therapy for Infertility
inferred← citeshttps://doi.org/10.1093/bfgp/els018openalex-snapshot
Proteins involved in establishment and maintenance of imprinted methylation marks
inferred← citeshttps://doi.org/10.1093/bib/bbw007openalex-snapshot
GED: a manually curated comprehensive resource for epigenetic modification of gametogenesis
inferred← citeshttps://doi.org/10.1093/biolre/ioab085openalex-snapshot
Epigenetic transgenerational inheritance, gametogenesis and germline development†
inferred← citeshttps://doi.org/10.1093/biolre/ioab114openalex-snapshot
Aging and oxidative stress alter DNA repair mechanisms in male germ cells of superoxide dismutase-1 null mice
inferred← citeshttps://doi.org/10.1093/biolre/ioab158openalex-snapshot
Exposures during the prepuberty period and future offspring’s health: evidence from human cohort studies†
inferred← citeshttps://doi.org/10.1093/biolre/ioac051openalex-snapshot
Environmental epigenetic interaction of gametes and early embryos
inferred← citeshttps://doi.org/10.1093/biolre/ioy181openalex-snapshot
A rapidly evolved domain, the SCML2 DNA-binding repeats, contributes to chromatin binding of mouse SCML2†
inferred← citeshttps://doi.org/10.1093/eep/dvaa002openalex-snapshot
Cannabis use and the sperm epigenome: a budding concern?
inferred← citeshttps://doi.org/10.1093/humupd/dmz017openalex-snapshot
Transgenerational inheritance: how impacts to the epigenetic and genetic information of parents affect offspring health
inferred← citeshttps://doi.org/10.1093/ije/dys016openalex-snapshot
Epigenesis for epidemiologists: does evo-devo have implications for population health research and practice?
inferred← citeshttps://doi.org/10.1093/jn/nxac184openalex-snapshot
Maternal Periconceptional Folic Acid Supplementation and DNA Methylation Patterns in Adolescent Offspring
inferred← citeshttps://doi.org/10.1093/molehr/gar077openalex-snapshot
Changes in histone H4 acetylation during in vivo versus in vitro maturation of equine oocytes
inferred← citeshttps://doi.org/10.1093/molehr/gat027openalex-snapshot
The dormant and the fully competent oocyte: comparing the transcriptome of human oocytes from primordial follicles and in metaphase II
inferred← citeshttps://doi.org/10.1093/nar/gkt884openalex-snapshot
PRMT5-mediated histone H4 arginine-3 symmetrical dimethylation marks chromatin at G + C-rich regions of the mouse genome
inferred← citeshttps://doi.org/10.1093/nar/gkx1052openalex-snapshot
Dynamic reorganization of open chromatin underlies diverse transcriptomes during spermatogenesis
inferred← citeshttps://doi.org/10.1093/reprod/xaag066openalex-snapshot
The role of heterogeneous nuclear ribonucleoproteins in mammalian spermatogenesis: mechanisms and clinical implications
inferred← citeshttps://doi.org/10.1095/biolreprod.111.095463openalex-snapshot
Male Germline Control of Transposable Elements1
inferred← citeshttps://doi.org/10.1095/biolreprod.111.097097openalex-snapshot
Essential Roles of the Chromatin Remodeling Factor Brg1 in Spermatogenesis in Mice1
inferred← citeshttps://doi.org/10.1095/biolreprod.115.135988openalex-snapshot
The Histone Demethylase FBXL10 Regulates the Proliferation of Spermatogonia and Ensures Long-Term Sustainable Spermatogenesis in Mice1
inferred← citeshttps://doi.org/10.1095/biolreprod.115.137802openalex-snapshot
The Effects of Chemotherapeutic Agents, Bleomycin, Etoposide, and Cisplatin, on Chromatin Remodeling in Male Rat Germ Cells1
inferred← citeshttps://doi.org/10.1098/rstb.2011.0336openalex-snapshot
New insights into establishment and maintenance of DNA methylation imprints in mammals
inferred← citeshttps://doi.org/10.1101/2021.01.15.426901openalex-snapshot
Meiosis-specific ZFP541 repressor complex promotes meiotic prophase exit during spermatogenesis
inferred← citeshttps://doi.org/10.1101/2022.06.17.496537openalex-snapshot
The Prmt5-Vasa module is essential for dichotomous spermatogenesis in Bombyx mori
inferred← citeshttps://doi.org/10.1101/2023.02.14.528413openalex-snapshot
Probing the hierarchical dynamics of DNA-sperm nuclear transition protein complex through fuzzy interaction and mesoscale condensation
inferred← citeshttps://doi.org/10.1101/2023.04.12.536672openalex-snapshot
A novel mouse allele of the DNA/RNA helicase senataxin ( Setx spcar3 ) causing meiotic arrest of spermatocytes and male infertility
inferred← citeshttps://doi.org/10.1101/2023.05.17.541143openalex-snapshot
Epigenetic reprogramming of imprinting at meiosis
inferred← citeshttps://doi.org/10.1101/2024.06.04.597381openalex-snapshot
The protamines of the noble false widow spider Steatoda nobilis provide an example of liquid-liquid phase separation chromatin transitions during spermiogenesis
inferred← citeshttps://doi.org/10.1101/2024.06.06.597721openalex-snapshot
ZNHIT1-dependent H2A.Z deposition at meiotic prophase I underlies pachytene gene expression and meiotic progression during male meiosis
inferred← citeshttps://doi.org/10.1101/223685openalex-snapshot
A non-genetic meiotic repair program inferred from spore survival values in fission yeast wild isolates: a clue for an epigenetic ratchet-like model of ageing?
inferred← citeshttps://doi.org/10.1101/gad.234294.113openalex-snapshot
DNA methylation dynamics during epigenetic reprogramming in the germline and preimplantation embryos
inferred← citeshttps://doi.org/10.1101/gad.265215.115openalex-snapshot
RNF17 blocks promiscuous activity of PIWI proteins in mouse testes
inferred← citeshttps://doi.org/10.1111/cge.12882openalex-snapshot
The biology of germ cell tumors in disorders of sex development
inferred← citeshttps://doi.org/10.1111/cpr.12106openalex-snapshot
Epigenetic regulation of the Igf2/H19 gene cluster
inferred← citeshttps://doi.org/10.1111/gcb.14882openalex-snapshot
Limitations of cross‐ and multigenerational plasticity for marine invertebrates faced with global climate change
inferred← citeshttps://doi.org/10.1111/imb.12010openalex-snapshot
Evidence of a conserved functional role for DNA methylation in termites
inferred← citeshttps://doi.org/10.1111/mpp.13091openalex-snapshot
ARGONAUTE 2 increases rice susceptibility to rice black‐streaked dwarf virus infection by epigenetically regulating HEXOKINASE 1 expression
inferred← citeshttps://doi.org/10.1126/sciadv.aed5708openalex-snapshot
PUM1 and PUM2 promote translation of chromatin regulators to ensure mammalian spermatogenesis
inferred← citeshttps://doi.org/10.1128/mcb.00235-14openalex-snapshot
Insertion of an Imprinted Insulator into the IgH Locus Reveals Developmentally Regulated, Transcription-Dependent Control of V(D)J Recombination
inferred← citeshttps://doi.org/10.1128/mcb.00282-12openalex-snapshot
The Linker Histone Plays a Dual Role during Gametogenesis in Saccharomyces cerevisiae
inferred← citeshttps://doi.org/10.1128/mcb.00942-15openalex-snapshot
Functional Roles of Acetylated Histone Marks at Mouse Meiotic Recombination Hot Spots
inferred← citeshttps://doi.org/10.1134/s2079059713050079openalex-snapshot
Population epigenetics, ecotoxicology, and human diseases
inferred← citeshttps://doi.org/10.1139/g2012-056openalex-snapshot
DNA methyltransferase 1 ( Dnmt1 ) mutation affects Snrpn imprinting in the mouse male germ line
inferred← citeshttps://doi.org/10.1146/annurev-genet-021920-102037openalex-snapshot
What Has a Century of Quantitative Genetics Taught Us About Nature's Genetic Tool Kit?
inferred← citeshttps://doi.org/10.1146/annurev-marine-010318-095114openalex-snapshot
Marine Environmental Epigenetics
inferred← citeshttps://doi.org/10.1159/000520683openalex-snapshot
Retrotransposons in the Mammalian Male Germline
inferred← citeshttps://doi.org/10.11606/d.41.2012.tde-11072012-075646openalex-snapshot
Estabilidade do controle epigenético em células humanas normais e transformadas
inferred← citeshttps://doi.org/10.1177/1099800417742967openalex-snapshot
Primer in Genetics and Genomics, Article 6: Basics of Epigenetic Control
inferred← citeshttps://doi.org/10.1186/1471-2164-14-412openalex-snapshot
Comparative transcriptome analysis of obligately asexual and cyclically sexual rotifers reveals genes with putative functions in sexual reproduction, dormancy, and asexual egg production
inferred← citeshttps://doi.org/10.1186/1745-6150-6-19openalex-snapshot
The struggle for life of the genome's selfish architects
inferred← citeshttps://doi.org/10.1186/2051-4190-24-6openalex-snapshot
Recent knowledge concerning mammalian sperm chromatin organization and its potential weaknesses when facing oxidative challenge
inferred← citeshttps://doi.org/10.1186/s12610-016-0044-5openalex-snapshot
Mammalian sperm nuclear organization: resiliencies and vulnerabilities
inferred← citeshttps://doi.org/10.1186/s12864-025-11340-3openalex-snapshot
The effect of induced molting on the testicular physiological remodeling in no-semen roosters
inferred← citeshttps://doi.org/10.1186/s12885-015-1006-6openalex-snapshot
Clinical observations on chemotherapy curable malignancies: unique genetic events, frozen development and enduring apoptotic potential
inferred← citeshttps://doi.org/10.1186/s12958-015-0074-4openalex-snapshot
A functional variant in the UBE2B gene promoter is associated with idiopathic azoospermia
inferred← citeshttps://doi.org/10.1186/s13059-017-1383-zopenalex-snapshot
Extensive epigenetic reprogramming during the life cycle of Marchantia polymorpha
inferred← citeshttps://doi.org/10.1186/s13072-019-0276-7openalex-snapshot
Ovarian dysfunction following prenatal exposure to an insecticide, chlordecone, associates with altered epigenetic features
inferred← citeshttps://doi.org/10.1186/s13072-021-00413-8openalex-snapshot
Histone deacetylase inhibition leads to regulatory histone mark alterations and impairs meiosis in oocytes
inferred← citeshttps://doi.org/10.1186/s13072-021-00433-4openalex-snapshot
Chromatin alterations during the epididymal maturation of mouse sperm refine the paternally inherited epigenome
inferred← citeshttps://doi.org/10.1186/s13072-025-00605-6openalex-snapshot
Molecular mechanisms and biological functions of active DNA demethylation in plants
inferred← citeshttps://doi.org/10.1186/s13148-025-01984-zopenalex-snapshot
An epigenetic perspective on neonatal encephalopathy with suspected hypoxic ischaemic encephalopathy
inferred← citeshttps://doi.org/10.1186/s43043-026-00320-6openalex-snapshot
The role of meiotic genes in primary ovarian insufficiency and non-obstructive azoospermia: a genetic perspective
inferred← citeshttps://doi.org/10.1242/bio.060029openalex-snapshot
Chromosomal organization of multigene families and meiotic analysis in species of Loricariidae (Siluriformes) from Brazilian Amazon, with description of a new cytotype for genus Spatuloricaria
inferred← citeshttps://doi.org/10.1242/dev.070771openalex-snapshot
Tet family proteins and 5-hydroxymethylcytosine in development and disease
inferred← citeshttps://doi.org/10.1242/dev.073478openalex-snapshot
An essential role for a mammalian SWI/SNF chromatin-remodeling complex during male meiosis
inferred← citeshttps://doi.org/10.1242/dev.118927openalex-snapshot
ATRX contributes to epigenetic asymmetry and silencing of major satellite transcripts in the maternal genome of the mouse embryo
inferred← citeshttps://doi.org/10.1242/dev.200089openalex-snapshot
INO80 requires a polycomb subunit to regulate the establishment of poised chromatin in murine spermatocytes
inferred← citeshttps://doi.org/10.1242/dev.203134openalex-snapshot
The protamines of the spider Steatoda sp. provide an example of liquid–liquid phase separation chromatin transitions during spermiogenesis
inferred← citeshttps://doi.org/10.1242/dev.204630openalex-snapshot
The KMT2 complex protein ASH2L is required for meiotic prophase progression but dispensable for mitosis in differentiated spermatogonia
inferred← citeshttps://doi.org/10.1242/jcs.259196openalex-snapshot
ADAD2 regulates heterochromatin in meiotic and post-meiotic male germ cells via translation of MDC1
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/10.1360/n972016-00790openalex-snapshot
Sperm epigenome and its potential role in transgenerational inheritance
inferred← citeshttps://doi.org/10.1371/journal.pgen.1005970openalex-snapshot
Maternal Setdb1 Is Required for Meiotic Progression and Preimplantation Development in Mouse
inferred← citeshttps://doi.org/10.1371/journal.pgen.1006128openalex-snapshot
TAF4b Regulates Oocyte-Specific Genes Essential for Meiosis
inferred← citeshttps://doi.org/10.1371/journal.pgen.1007209openalex-snapshot
BRDT is an essential epigenetic regulator for proper chromatin organization, silencing of sex chromosomes and crossover formation in male meiosis
inferred← citeshttps://doi.org/10.1371/journal.pgen.1010600openalex-snapshot
The Prmt5-Vasa module is essential for spermatogenesis in Bombyx mori
inferred← citeshttps://doi.org/10.1371/journal.pone.0042695openalex-snapshot
Circadian Proteins CLOCK and BMAL1 in the Chromatoid Body, a RNA Processing Granule of Male Germ Cells
inferred← citeshttps://doi.org/10.1371/journal.pone.0045819openalex-snapshot
GAGE Cancer-Germline Antigens Are Recruited to the Nuclear Envelope by Germ Cell-Less (GCL)
inferred← citeshttps://doi.org/10.1371/journal.pone.0085075openalex-snapshot
Cytological Studies of Human Meiosis: Sex-Specific Differences in Recombination Originate at, or Prior to, Establishment of Double-Strand Breaks
inferred← citeshttps://doi.org/10.1371/journal.pone.0212043openalex-snapshot
Epigenome-wide analysis of sperm cells identifies IL22 as a possible germ line risk locus for psoriatic arthritis
inferred← citeshttps://doi.org/10.1387/ijdb.120246rdopenalex-snapshot
Histone hyperacetylation during meiosis interferes with large-scale chromatin remodeling, axial chromatid condensation and sister chromatid separation in the mammalian oocyte
inferred← citeshttps://doi.org/10.1530/rep-22-0206openalex-snapshot
OXIDATIVE STRESS AND REPRODUCTIVE FUNCTION: Oxidative stress and in vitro ageing of the post-ovulatory oocyte: an update on recent advances in the field
inferred← citeshttps://doi.org/10.1530/rep-23-0166openalex-snapshot
New allele of mouse DNA/RNA helicase senataxin causes meiotic arrest and infertility
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