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A histone H3 methyltransferase controls epigenetic events required for meiotic prophase
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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/mrd.1080330312openalex-snapshot
Characterization of male meiotic germ cell‐specific antigen (Meg 1) by monoclonal antibody TRA 369 in mice
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/s0968-0004(99)01503-0openalex-snapshot
GHKL, an emergent ATPase/kinase superfamily
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/10.1016/s1097-2765(01)00405-1openalex-snapshot
Purification and Functional Characterization of a Histone H3-Lysine 4-Specific Methyltransferase
inferredcites →https://doi.org/10.1016/s1097-2765(02)00740-2openalex-snapshot
ALL-1 Is a Histone Methyltransferase that Assembles a Supercomplex of Proteins Involved in Transcriptional Regulation
inferredcites →https://doi.org/10.1016/s1097-2765(02)00741-4openalex-snapshot
MLL Targets SET Domain Methyltransferase Activity to Hox Gene Promoters
inferredcites →https://doi.org/10.1038/35020506openalex-snapshot
Regulation of chromatin structure by site-specific histone H3 methyltransferases
inferredcites →https://doi.org/10.1038/85830openalex-snapshot
Recombinational DNA double-strand breaks in mice precede synapsis
inferredcites →https://doi.org/10.1038/nature01080openalex-snapshot
Active genes are tri-methylated at K4 of histone H3
inferredcites →https://doi.org/10.1038/ncb1076openalex-snapshot
Histone H3 lysine 4 methylation patterns in higher eukaryotic genes
inferredcites →https://doi.org/10.1038/ng1484openalex-snapshot
Silencing of unsynapsed meiotic chromosomes in the mouse
inferredcites →https://doi.org/10.1073/pnas.082249499openalex-snapshot
Methylation of histone H3 Lys 4 in coding regions of active genes
inferredcites →https://doi.org/10.1073/pnas.231473398openalex-snapshot
COMPASS: A complex of proteins associated with a trithorax-related SET domain protein
inferredcites →https://doi.org/10.1074/jbc.m101914200openalex-snapshot
SET Domain-containing Protein, G9a, Is a Novel Lysine-preferring Mammalian Histone Methyltransferase with Hyperactivity and Specific Selectivity to Lysines 9 and 27 of Histone H3
inferredcites →https://doi.org/10.1083/jcb.74.1.68openalex-snapshot
Spermatogenic cells of the prepuberal mouse: isolation and morphological characterization
inferredcites →https://doi.org/10.1093/emboj/20.24.7137openalex-snapshot
The Saccharomyces cerevisiae Set1 complex includes an Ash2 homologue and methylates histone 3 lysine 4
inferredcites →https://doi.org/10.1101/gad.252103openalex-snapshot
Human Sin3 deacetylase and trithorax-related Set1/Ash2 histone H3-K4 methyltransferase are tethered together selectively by the cell-proliferation factor HCF-1
inferredcites →https://doi.org/10.1101/gad.927301openalex-snapshot
Transcription regulation by histone methylation: interplay between different covalent modifications of the core histone tails
inferredcites →https://doi.org/10.1101/gad.967202openalex-snapshot
Set9, a novel histone H3 methyltransferase that facilitates transcription by precluding histone tail modifications required for heterochromatin formation
inferredcites →https://doi.org/10.1126/science.1064150openalex-snapshot
Transitions in Distinct Histone H3 Methylation Patterns at the Heterochromatin Domain Boundaries
inferredcites →https://doi.org/10.1128/mcb.20.24.9423-9433.2000openalex-snapshot
Isolation and Characterization of Suv39h2 , a Second Histone H3 Methyltransferase Gene That Displays Testis-Specific Expression
inferredcites →https://doi.org/10.1128/mcb.23.1.140-149.2003openalex-snapshot
Activating Signal Cointegrator 2 Belongs to a Novel Steady-State Complex That Contains a Subset of Trithorax Group Proteins
inferredcites →https://doi.org/10.1128/mcb.25.3.1041-1053.2005openalex-snapshot
Silencing of Unpaired Chromatin and Histone H2A Ubiquitination in Mammalian Meiosis
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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SET domain protein lysine methyltransferases: Structure, specificity and catalysis
inferred← citeshttps://doi.org/10.1007/s00018-006-6281-6openalex-snapshot
Epigenetic regulation for the induction of meiosis
inferred← citeshttps://doi.org/10.1007/s00018-008-8303-zopenalex-snapshot
Dynamic protein methylation in chromatin biology
inferred← citeshttps://doi.org/10.1007/s00018-010-0456-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00018-025-05831-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00335-011-9388-5openalex-snapshot
ENU mutagenesis in mice identifies candidate genes for hypogonadism
inferred← citeshttps://doi.org/10.1007/s00335-022-09954-zopenalex-snapshot
Prdm9 deficiency of rat oocytes causes synapsis among non-homologous chromosomes and aneuploidy
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/s00412-011-0346-5openalex-snapshot
Genetically enhanced asynapsis of autosomal chromatin promotes transcriptional dysregulation and meiotic failure
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/s00412-017-0631-zopenalex-snapshot
The PRDM9 KRAB domain is required for meiosis and involved in protein interactions
inferred← citeshttps://doi.org/10.1007/s00412-019-00730-8openalex-snapshot
Copy-number variation introduced by long transgenes compromises mouse male fertility independently of pachytene checkpoints
inferred← citeshttps://doi.org/10.1007/s00438-016-1260-6openalex-snapshot
Evolutionary dynamics of meiotic recombination hotspots regulator PRDM9 in bovids
inferred← citeshttps://doi.org/10.1007/s00439-012-1180-4openalex-snapshot
Evaluation of PRDM9 variation as a risk factor for recurrent genomic disorders and chromosomal non-disjunction
inferred← citeshttps://doi.org/10.1007/s00894-015-2673-6openalex-snapshot
How Y357F, Y276F mutants affect the methylation activity of PRDM9: QM/MM MD and free energy simulations
inferred← citeshttps://doi.org/10.1007/s10577-017-9552-1openalex-snapshot
The long zinc finger domain of PRDM9 forms a highly stable and long-lived complex with its DNA recognition sequence
inferred← citeshttps://doi.org/10.1007/s10616-014-9838-5openalex-snapshot
Histone methyltransferase SMYD3 regulates the expression of transcriptional factors during bovine oocyte maturation and early embryonic development
inferred← citeshttps://doi.org/10.1007/s10616-015-9846-0openalex-snapshot
Spatiotemporal expression of Prdm genes during Xenopus development
inferred← citeshttps://doi.org/10.1007/s10695-021-00986-xopenalex-snapshot
Sexual dimorphism of DNA and histone methylation profiles in the gonads of the olive flounder Paralichthys olivaceus
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1007/s10815-011-9576-yopenalex-snapshot
Single nucleotide polymorphism in the UBR2 gene may be a genetic risk factor for Japanese patients with azoospermia by meiotic arrest
inferred← citeshttps://doi.org/10.1007/s10815-011-9679-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10815-012-9715-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11427-018-9346-6openalex-snapshot
Characterization of H3 methylation in regulating oocyte development in cyprinid fish
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Insights into Ovarian Cancer: Unraveling the Role of DNA Double-strand Break-related Genes in Pathogenesis and Therapeutic Avenues
inferred← citeshttps://doi.org/10.1016/b978-0-12-394309-5.00005-5openalex-snapshot
Genetics of Meiosis and Recombination in Mice
inferred← citeshttps://doi.org/10.1016/b978-0-12-800049-6.00183-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-813570-9.00003-6openalex-snapshot
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The evolutionary modern synthesis, t-haplotypes in the wild, and reproductive isolation
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inferred← citeshttps://doi.org/10.1016/bs.mie.2016.01.011openalex-snapshot
Chemical Biology Approaches for Characterization of Epigenetic Regulators
inferred← citeshttps://doi.org/10.1016/bs.mie.2017.11.037openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/bs.pmbts.2023.01.010openalex-snapshot
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PRDM14, a putative histone methyl-transferase, interacts with and decreases the stability and activity of the HOXA1 transcription factor
inferred← citeshttps://doi.org/10.1016/j.bbrc.2007.12.189openalex-snapshot
PRDM14 suppresses expression of differentiation marker genes in human embryonic stem cells
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inferred← citeshttps://doi.org/10.1016/j.febslet.2006.10.066openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.gde.2006.02.015openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.gde.2012.12.002openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.gene.2021.146123openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.gep.2009.07.005openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.ibmb.2016.06.010openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.isci.2024.110276openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jbc.2023.104651openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jgg.2012.02.004openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.livsci.2013.12.017openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.mce.2024.112194openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.molcel.2006.12.014openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.molcel.2018.01.033openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.molcel.2019.03.022openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.molcel.2024.04.001openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.neuron.2011.09.035openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.phrs.2018.12.003openalex-snapshot
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DNA methylation and histone post-translational modifications in the mouse germline following in-vitro maturation of fresh or cryopreserved prepubertal testicular tissue
inferred← citeshttps://doi.org/10.1016/j.scib.2017.04.002openalex-snapshot
A novel male-specific SET domain-containing gene setdm identified from extra microchromosomes of gibel carp males
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2019.02.393openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.semcdb.2016.03.001openalex-snapshot
Multiple LINEs of retrotransposon silencing mechanisms in the mammalian germline
inferred← citeshttps://doi.org/10.1016/j.tcb.2013.01.001openalex-snapshot
Transposable elements as genetic regulatory substrates in early development
inferred← citeshttps://doi.org/10.1016/j.tem.2015.11.005openalex-snapshot
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The expression of histone methyltransferases and distribution of selected histone methylations in testes of yak and cattle-yak hybrid
inferred← citeshttps://doi.org/10.1016/j.theriogenology.2023.08.017openalex-snapshot
The chromatin remodeling protein BPTF mediates cell cycle, proliferation and apoptosis in porcine ovarian granulosa cells
inferred← citeshttps://doi.org/10.1016/j.tibs.2022.10.003openalex-snapshot
To incise or not and where: SET-domain methyltransferases know
inferred← citeshttps://doi.org/10.1016/j.tig.2011.02.001openalex-snapshot
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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.tig.2012.11.007openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tig.2017.12.017openalex-snapshot
PRDM9 and Its Role in Genetic Recombination
inferred← citeshttps://doi.org/10.1016/j.toxlet.2016.04.004openalex-snapshot
G9a-mediated histone methylation regulates cadmium-induced male fertility damage in pubertal mice
inferred← citeshttps://doi.org/10.1016/j.ydbio.2007.03.006openalex-snapshot
Germline stem cells and neo-oogenesis in the adult human ovary
inferred← citeshttps://doi.org/10.1016/j.ydbio.2012.10.006openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s1877-1173(09)87010-5openalex-snapshot
Chapter 10 Roles of Histone H3‐Lysine 4 Methyltransferase Complexes in NR‐Mediated Gene Transcription
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inferred← citeshttps://doi.org/10.1017/cbo9781139044547.019openalex-snapshot
The role of the X chromosome in house mouse speciation
inferred← citeshttps://doi.org/10.1017/cbo9781139044547.021openalex-snapshot
Hybrid male sterility genes in the mouse subspecific crosses
inferred← citeshttps://doi.org/10.1021/acs.biochem.5b01129openalex-snapshot
Protein Methyltransferases: A Distinct, Diverse, and Dynamic Family of Enzymes
inferred← citeshttps://doi.org/10.1038/aja.2010.101openalex-snapshot
Mouse models in male fertility research
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Conditional inactivation of Miwi2 reveals that MIWI2 is only essential for prospermatogonial development in mice
inferred← citeshttps://doi.org/10.1038/cr.2012.109openalex-snapshot
Meiotic DSBs and the control of mammalian recombination
inferred← citeshttps://doi.org/10.1038/emboj.2009.207openalex-snapshot
Distinct histone modifications define initiation and repair of meiotic recombination in the mouse
inferred← citeshttps://doi.org/10.1038/hdy.2010.49openalex-snapshot
Epigenetic regulation of development by histone lysine methylation
inferred← citeshttps://doi.org/10.1038/nature09429openalex-snapshot
xnd-1 regulates the global recombination landscape in Caenorhabditis elegans
inferred← citeshttps://doi.org/10.1038/nature11089openalex-snapshot
Genetic recombination is directed away from functional genomic elements in mice
inferred← citeshttps://doi.org/10.1038/nature11709openalex-snapshot
Tet1 controls meiosis by regulating meiotic gene expression
inferred← citeshttps://doi.org/10.1038/nature16931openalex-snapshot
Re-engineering the zinc fingers of PRDM9 reverses hybrid sterility in mice
inferred← citeshttps://doi.org/10.1038/ncb1513openalex-snapshot
Lsh is required for meiotic chromosome synapsis and retrotransposon silencing in female germ cells
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/ncomms5370openalex-snapshot
Primate evolution of the recombination regulator PRDM9
inferred← citeshttps://doi.org/10.1038/ng.2766openalex-snapshot
Arabidopsis meiotic crossover hot spots overlap with H2A.Z nucleosomes at gene promoters
inferred← citeshttps://doi.org/10.1038/ng.658openalex-snapshot
PRDM9 variation strongly influences recombination hot-spot activity and meiotic instability in humans
inferred← citeshttps://doi.org/10.1038/nrg2295openalex-snapshot
Epigenetic events in mammalian germ-cell development: reprogramming and beyond
inferred← citeshttps://doi.org/10.1038/nrg2712openalex-snapshot
Mammalian recombination hot spots: properties, control and evolution
inferred← citeshttps://doi.org/10.1038/nrg3173openalex-snapshot
Histone methylation: a dynamic mark in health, disease and inheritance
inferred← citeshttps://doi.org/10.1038/nrg3573openalex-snapshot
Meiotic recombination in mammals: localization and regulation
inferred← citeshttps://doi.org/10.1038/nrm2849openalex-snapshot
Genome destabilization by homologous recombination in the germ line
inferred← citeshttps://doi.org/10.1038/nsmb.3201openalex-snapshot
X marks the spot: PRDM9 rescues hybrid sterility by finding hidden treasure in the genome
inferred← citeshttps://doi.org/10.1038/onc.2011.12openalex-snapshot
Prdm14 initiates lymphoblastic leukemia after expanding a population of cells resembling common lymphoid progenitors
inferred← citeshttps://doi.org/10.1038/s41392-019-0095-0openalex-snapshot
Targeting epigenetic regulators for cancer therapy: mechanisms and advances in clinical trials
inferred← citeshttps://doi.org/10.1038/s41436-021-01266-yopenalex-snapshot
Pathogenic variants of meiotic double strand break (DSB) formation genes PRDM9 and ANKRD31 in premature ovarian insufficiency
inferred← citeshttps://doi.org/10.1038/s41467-019-13652-xopenalex-snapshot
Discovery of a chemical probe for PRDM9
inferred← citeshttps://doi.org/10.1038/s41467-025-56991-8openalex-snapshot
Maternal PRDM10 activates essential genes for oocyte-to-embryo transition
inferred← citeshttps://doi.org/10.1038/s41467-025-65888-5openalex-snapshot
Histone methyltransferase PRDM9 promotes survival of drug-tolerant persister cells in glioblastoma
inferred← citeshttps://doi.org/10.1038/s41586-025-09540-8openalex-snapshot
The formation and propagation of human Robertsonian chromosomes
inferred← citeshttps://doi.org/10.1038/s41598-020-65986-yopenalex-snapshot
Reverse genetics reveals single gene of every candidate on Hybrid sterility, X Chromosome QTL 2 (Hstx2) are dispensable for spermatogenesis
inferred← citeshttps://doi.org/10.1038/s44319-025-00500-xopenalex-snapshot
Insights from human NF-κB knockouts
inferred← citeshttps://doi.org/10.1038/sj.emboj.7601767openalex-snapshot
Functional dynamics of H3K9 methylation during meiotic prophase progression
inferred← citeshttps://doi.org/10.1038/sj.emboj.7601967openalex-snapshot
Dynamic histone H3 methylation during gene induction: HYPB/Setd2 mediates all H3K36 trimethylation
inferred← citeshttps://doi.org/10.1038/srep24228openalex-snapshot
Chromatin architecture may dictate the target site for DMC1, but not for RAD51, during homologous pairing
inferred← citeshttps://doi.org/10.1038/srep32932openalex-snapshot
Selective de-repression of germ cell-specific genes in mouse embryonic fibroblasts in a permissive epigenetic environment
inferred← citeshttps://doi.org/10.1038/srep34618openalex-snapshot
The pioneering role of PRDM9 indel mutations in tarsier evolution
inferred← citeshttps://doi.org/10.1038/tp.2015.177openalex-snapshot
Brain-specific epigenetic markers of schizophrenia
inferred← citeshttps://doi.org/10.1039/d1cb00196eopenalex-snapshot
Lysine methyltransferase inhibitors: where we are now
inferred← citeshttps://doi.org/10.1042/bcj20161067openalex-snapshot
Discovery and characterisation of the automethylation properties of PRDM9
inferred← citeshttps://doi.org/10.1042/bj20140374openalex-snapshot
Characterization of the histone methyltransferase PRDM9 using biochemical, biophysical and chemical biology techniques
inferred← citeshttps://doi.org/10.1051/medsci/2010265468openalex-snapshot
Identification d’une protéine-clé pour le contrôle des sites de recombinaison méiotique
inferred← citeshttps://doi.org/10.1051/medsci/20112712005openalex-snapshot
Comment sont choisis les sites d’échanges entre chromosomes lors de la méiose ?
inferred← citeshttps://doi.org/10.1051/medsci/201127163openalex-snapshot
Déterminants de la carte génétique
inferred← citeshttps://doi.org/10.1071/rd12116openalex-snapshot
Mouse oocyte meiosis is disturbed by knockdown of Suv4-20h
inferred← citeshttps://doi.org/10.1073/pnas.0607521104openalex-snapshot
A unique configuration of genome-wide DNA methylation patterns in the testis
inferred← citeshttps://doi.org/10.1073/pnas.0903197106openalex-snapshot
Sustained activation of XBP1 splicing leads to endothelial apoptosis and atherosclerosis development in response to disturbed flow
inferred← citeshttps://doi.org/10.1073/pnas.0908664107openalex-snapshot
NANOS2 interacts with the CCR4-NOT deadenylation complex and leads to suppression of specific RNAs
inferred← citeshttps://doi.org/10.1073/pnas.1220813110openalex-snapshot
Recombination regulator PRDM9 influences the instability of its own coding sequence in humans
inferred← citeshttps://doi.org/10.1073/pnas.2208441119openalex-snapshot
DNA polymerase epsilon interacts with SUVH2/9 to repress the expression of genes associated with meiotic DSB hotspot in Arabidopsis
inferred← citeshttps://doi.org/10.1074/jbc.m109.066845openalex-snapshot
Jmjd1a Demethylase-regulated Histone Modification Is Essential for cAMP-response Element Modulator-regulated Gene Expression and Spermatogenesis
inferred← citeshttps://doi.org/10.1074/jbc.m113.523183openalex-snapshot
Trimethylation of Histone H3 Lysine 36 by Human Methyltransferase PRDM9 Protein
inferred← citeshttps://doi.org/10.1074/jbc.m116.721472openalex-snapshot
PR Domain-containing Protein 7 (PRDM7) Is a Histone 3 Lysine 4 Trimethyltransferase
inferred← citeshttps://doi.org/10.1074/jbc.m117.805754openalex-snapshot
Structural basis of human PR/SET domain 9 (PRDM9) allele C–specific recognition of its cognate DNA sequence
inferred← citeshttps://doi.org/10.1074/jbc.ra118.002851openalex-snapshot
The histone methyltransferase SETD2 is required for expression of acrosin-binding protein 1 and protamines and essential for spermiogenesis in mice
inferred← citeshttps://doi.org/10.1080/15384101.2018.1464847openalex-snapshot
Control of meiotic double-strand-break formation by ATM: local and global views
inferred← citeshttps://doi.org/10.1080/15592294.2017.1382786openalex-snapshot
Estrogen, through estrogen receptor 1, regulates histone modifications and chromatin remodeling during spermatogenesis in adult rats
inferred← citeshttps://doi.org/10.1083/jcb.201903125openalex-snapshot
CDK2 regulates the NRF1/Ehmt1 axis during meiotic prophase I
inferred← citeshttps://doi.org/10.1089/cell.2009.0106openalex-snapshot
Optimization of Culture Conditions to Support Undifferentiated Growth of Human Embryonic Stem Cells
inferred← citeshttps://doi.org/10.1091/mbc.e16-09-0686openalex-snapshot
PRDM9 interactions with other proteins provide a link between recombination hotspots and the chromosomal axis in meiosis
inferred← citeshttps://doi.org/10.1091/mbc.e18-10-0681openalex-snapshot
Uncoupling of transcriptomic and cytological differentiation in mouse spermatocytes with impaired meiosis
inferred← citeshttps://doi.org/10.1091/mbc.e20-09-0604openalex-snapshot
EWSR1 affects PRDM9-dependent histone 3 methylation and provides a link between recombination hotspots and the chromosome axis protein REC8
inferred← citeshttps://doi.org/10.1093/bioinformatics/btl498openalex-snapshot
Meisetz and the birth of the KRAB motif
inferred← citeshttps://doi.org/10.1093/biolinnean/bly035openalex-snapshot
The chromosomal basis of species initiation: Prdm9 as an anti-speciation gene
inferred← citeshttps://doi.org/10.1093/biolre/ioaa207openalex-snapshot
Male hybrid sterility in the cattle-yak and other bovines: a review
inferred← citeshttps://doi.org/10.1093/biolre/ioab085openalex-snapshot
Epigenetic transgenerational inheritance, gametogenesis and germline development†
inferred← citeshttps://doi.org/10.1093/biolre/ioag102openalex-snapshot
ssDNA dynamics during mammalian meiotic recombination
inferred← citeshttps://doi.org/10.1093/dnares/dst059openalex-snapshot
Prdm9 Polymorphism Unveils Mouse Evolutionary Tracks
inferred← citeshttps://doi.org/10.1093/evolut/qpae044openalex-snapshot
Do genetic loci that cause reproductive isolation in the lab inhibit gene flow in nature?
inferred← citeshttps://doi.org/10.1093/gbe/evu230openalex-snapshot
Specific Modifications of Histone Tails, but Not DNA Methylation, Mirror the Temporal Variation of Mammalian Recombination Hotspots
inferred← citeshttps://doi.org/10.1093/gbe/evv182openalex-snapshot
Recombining without Hotspots: A Comprehensive Evolutionary Portrait of Recombination in Two Closely Related Species of Drosophila
inferred← citeshttps://doi.org/10.1093/gbe/evz090openalex-snapshot
Divergent Fine-Scale Recombination Landscapes between a Freshwater and Marine Population of Threespine Stickleback Fish
inferred← citeshttps://doi.org/10.1093/gbe/evz101openalex-snapshot
Parallel Molecular Evolution in Pathways, Genes, and Sites in High-Elevation Hummingbirds Revealed by Comparative Transcriptomics
inferred← citeshttps://doi.org/10.1093/genetics/iyab172openalex-snapshot
Differential effects of two catalytic mutations on full-length PRDM9 and its isolated PR/SET domain reveal a case of pseudomodularity
inferred← citeshttps://doi.org/10.1093/genetics/iyae004openalex-snapshot
Natural variation in the zinc-finger-encoding exon of Prdm9 affects hybrid sterility phenotypes in mice
inferred← citeshttps://doi.org/10.1093/humrep/der334openalex-snapshot
Mouse germ cells go through typical epigenetic modifications after intratesticular tissue grafting
inferred← citeshttps://doi.org/10.1093/humrep/des395openalex-snapshot
Haploinsufficiency of the paternal-effect gene Dnmt3L results in transient DNA hypomethylation in progenitor cells of the male germline
inferred← citeshttps://doi.org/10.1093/humupd/dmp001openalex-snapshot
Differentiation of germ cells and gametes from stem cells
inferred← citeshttps://doi.org/10.1093/jb/mvt054openalex-snapshot
Initiation of meiotic recombination in chromatin structure
inferred← citeshttps://doi.org/10.1093/jxb/erq421openalex-snapshot
Have a break: determinants of meiotic DNA double strand break (DSB) formation and processing in plants
inferred← citeshttps://doi.org/10.1093/molbev/msaa003openalex-snapshot
Snake Recombination Landscapes Are Concentrated in Functional Regions despite PRDM9
inferred← citeshttps://doi.org/10.1093/molbev/msq348openalex-snapshot
Extraordinary Sequence Divergence at Tsga8, an X-linked Gene Involved in Mouse Spermiogenesis
inferred← citeshttps://doi.org/10.1093/mp/ssn030openalex-snapshot
SWI1 Is Required for Meiotic Chromosome Remodeling Events
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