| review article | Q7318358 |
| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1009881946 |
| P356 | DOI | 10.1038/NRM4029 |
| P698 | PubMed publication ID | 26204160 |
| P50 | author | Chiara Mozzetta | Q57306807 |
| Yekaterina Boyarchuk | Q79810593 | ||
| P2093 | author name string | Slimane Ait-Si-Ali | |
| Julien Pontis | |||
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| EZH1 mediates methylation on histone H3 lysine 27 and complements EZH2 in maintaining stem cell identity and executing pluripotency | Q24645960 | ||
| Mitotic-specific methylation of histone H4 Lys 20 follows increased PR-Set7 expression and its localization to mitotic chromosomes | Q24671073 | ||
| Functional demarcation of active and silent chromatin domains in human HOX loci by noncoding RNAs | Q24673619 | ||
| G9a histone methyltransferase plays a dominant role in euchromatic histone H3 lysine 9 methylation and is essential for early embryogenesis | Q24673923 | ||
| Direct interaction between DNMT1 and G9a coordinates DNA and histone methylation during replication | Q24675218 | ||
| SETDB1: a novel KAP-1-associated histone H3, lysine 9-specific methyltransferase that contributes to HP1-mediated silencing of euchromatic genes by KRAB zinc-finger proteins | Q24685694 | ||
| A chromosomal memory triggered by Xist regulates histone methylation in X inactivation | Q24802695 | ||
| Protein methylation at the surface and buried deep: thinking outside the histone box | Q27025874 | ||
| Structure of the catalytic domain of human DOT1L, a non-SET domain nucleosomal histone methyltransferase | Q27640679 | ||
| The ankyrin repeats of G9a and GLP histone methyltransferases are mono- and dimethyllysine binding modules | Q27649828 | ||
| Role of the polycomb protein EED in the propagation of repressive histone marks | Q27657483 | ||
| Histone methylation by PRC2 is inhibited by active chromatin marks | Q27667743 | ||
| SET domain proteins modulate chromatin domains in eu- and heterochromatin. | Q34458687 | ||
| PTMs on H3 variants before chromatin assembly potentiate their final epigenetic state | Q34575324 | ||
| Telomere length regulates the epigenetic status of mammalian telomeres and subtelomeres | Q34604352 | ||
| The histone H3K4 demethylase SMCX links REST target genes to X-linked mental retardation. | Q34624060 | ||
| Endogenous retroviruses and neighboring genes are coordinately repressed by LSD1/KDM1A. | Q34691326 | ||
| AGO2 and SETDB1 cooperate in promoter-targeted transcriptional silencing of the androgen receptor gene | Q34712114 | ||
| Lysine methyltransferase G9a is required for de novo DNA methylation and the establishment, but not the maintenance, of proviral silencing | Q34804800 | ||
| AEBP2 as a potential targeting protein for Polycomb Repression Complex PRC2. | Q34964097 | ||
| Specificity, propagation, and memory of pericentric heterochromatin | Q34986658 | ||
| CBP-mediated acetylation of histone H3 lysine 27 antagonizes Drosophila Polycomb silencing. | Q34998982 | ||
| Recognition of H3K9 methylation by GLP is required for efficient establishment of H3K9 methylation, rapid target gene repression, and mouse viability | Q35104153 | ||
| The zinc finger proteins ZNF644 and WIZ regulate the G9a/GLP complex for gene repression | Q35194348 | ||
| Functional Crosstalk Between Lysine Methyltransferases on Histone Substrates: The Case of G9A/GLP and Polycomb Repressive Complex 2 | Q35609473 | ||
| Functional Proteomic Analysis of Repressive Histone Methyltransferase Complexes Reveals ZNF518B as a G9A Regulator | Q35692081 | ||
| Lysine methyltransferase G9a methylates the transcription factor MyoD and regulates skeletal muscle differentiation | Q35735009 | ||
| The transcriptional and epigenomic foundations of ground state pluripotency. | Q36100410 | ||
| AS1DHRS4, a head-to-head natural antisense transcript, silences the DHRS4 gene cluster in cis and trans | Q36212913 | ||
| Asymmetrically modified nucleosomes | Q36401114 | ||
| Maintenance of gene silencing by the coordinate action of the H3K9 methyltransferase G9a/KMT1C and the H3K4 demethylase Jarid1a/KDM5A | Q36414731 | ||
| G9a mediates Sharp-1-dependent inhibition of skeletal muscle differentiation | Q36465083 | ||
| KDM2B links the Polycomb Repressive Complex 1 (PRC1) to recognition of CpG islands. | Q36474376 | ||
| The control of histone lysine methylation in epigenetic regulation | Q36571342 | ||
| H2A.Z facilitates access of active and repressive complexes to chromatin in embryonic stem cell self-renewal and differentiation. | Q36604868 | ||
| Ezh1 and Ezh2 maintain repressive chromatin through different mechanisms | Q36810306 | ||
| PR-SET7 and SUV4-20H regulate H4 lysine-20 methylation at imprinting control regions in the mouse. | Q36851813 | ||
| Chromatin connections to pluripotency and cellular reprogramming | Q36874359 | ||
| Polycomb associates genome-wide with a specific RNA polymerase II variant, and regulates metabolic genes in ESCs | Q36927892 | ||
| De novo DNA methylation of endogenous retroviruses is shaped by KRAB-ZFPs/KAP1 and ESET. | Q36966957 | ||
| De novo DNA methylation promoted by G9a prevents reprogramming of embryonically silenced genes | Q36968883 | ||
| Chromodomain-mediated oligomerization of HP1 suggests a nucleosome-bridging mechanism for heterochromatin assembly. | Q37118383 | ||
| Monomethylation of histone H4-lysine 20 is involved in chromosome structure and stability and is essential for mouse development | Q37145387 | ||
| Modulation of lysine methylation in myocyte enhancer factor 2 during skeletal muscle cell differentiation. | Q37417041 | ||
| SetDB1 contributes to repression of genes encoding developmental regulators and maintenance of ES cell state | Q37426752 | ||
| Methylation of histone H3 lysine 9 creates a binding site for HP1 proteins | Q27860456 | ||
| High-resolution profiling of histone methylations in the human genome | Q27860906 | ||
| A bivalent chromatin structure marks key developmental genes in embryonic stem cells | Q27860977 | ||
| Suv39h-mediated histone H3 lysine 9 methylation directs DNA methylation to major satellite repeats at pericentric heterochromatin | Q28187783 | ||
| SUV39H1 interacts with AML1 and abrogates AML1 transactivity. AML1 is methylated in vivo | Q28201653 | ||
| mAM facilitates conversion by ESET of dimethyl to trimethyl lysine 9 of histone H3 to cause transcriptional repression | Q28208422 | ||
| 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 | Q28214048 | ||
| Molecular cloning of ESET, a novel histone H3-specific methyltransferase that interacts with ERG transcription factor | Q28215563 | ||
| Control of developmental regulators by Polycomb in human embryonic stem cells | Q28235841 | ||
| A PHD finger of NURF couples histone H3 lysine 4 trimethylation with chromatin remodelling | Q28242453 | ||
| Histone methylation: a dynamic mark in health, disease and inheritance | Q28263573 | ||
| Domain organization of human chromosomes revealed by mapping of nuclear lamina interactions | Q28279406 | ||
| Coordinated regulation of transcriptional repression by the RBP2 H3K4 demethylase and Polycomb-Repressive Complex 2 | Q28280326 | ||
| A chromatin-wide transition to H4K20 monomethylation impairs genome integrity and programmed DNA rearrangements in the mouse | Q28289637 | ||
| Histone H1 and its isoforms: contribution to chromatin structure and function | Q28303037 | ||
| Physical and functional association of SU(VAR)3-9 and HDAC1 in Drosophila | Q28360331 | ||
| The histone H3K79 methyltransferase Dot1L is essential for mammalian development and heterochromatin structure | Q28473586 | ||
| Polycomb EZH2 controls self-renewal and safeguards the transcriptional identity of skeletal muscle stem cells | Q28506827 | ||
| The Air noncoding RNA epigenetically silences transcription by targeting G9a to chromatin | Q28506981 | ||
| The Polycomb Ezh2 methyltransferase regulates muscle gene expression and skeletal muscle differentiation | Q28508225 | ||
| Jarid2/Jumonji coordinates control of PRC2 enzymatic activity and target gene occupancy in pluripotent cells | Q28585926 | ||
| HP1 binds specifically to Lys26-methylated histone H1.4, whereas simultaneous Ser27 phosphorylation blocks HP1 binding | Q28587228 | ||
| Histone methyltransferase Suv39h1 represses MyoD-stimulated myogenic differentiation | Q28588561 | ||
| An interspecies analysis reveals a key role for unmethylated CpG dinucleotides in vertebrate Polycomb complex recruitment | Q28593101 | ||
| NSD1 is essential for early post-implantation development and has a catalytically active SET domain | Q28593118 | ||
| Prdm16 is required for the maintenance of brown adipocyte identity and function in adult mice | Q28593617 | ||
| Histone methyltransferases G9a and GLP form heteromeric complexes and are both crucial for methylation of euchromatin at H3-K9 | Q28594945 | ||
| Histone methyltransferases direct different degrees of methylation to define distinct chromatin domains | Q28609779 | ||
| PR-Set7 is a nucleosome-specific methyltransferase that modifies lysine 20 of histone H4 and is associated with silent chromatin | Q28647369 | ||
| Distinct roles of KAP1, HP1 and G9a/GLP in silencing of the two-cell-specific retrotransposon MERVL in mouse ES cells | Q28681397 | ||
| Polycomb complexes repress developmental regulators in murine embryonic stem cells | Q29547274 | ||
| The Polycomb complex PRC2 and its mark in life | Q29547358 | ||
| Polycomb proteins targeted by a short repeat RNA to the mouse X chromosome | Q29547359 | ||
| Kcnq1ot1 antisense noncoding RNA mediates lineage-specific transcriptional silencing through chromatin-level regulation | Q29614333 | ||
| Partitioning and plasticity of repressive histone methylation states in mammalian chromatin | Q29614513 | ||
| Nonprocessive methylation by Dot1 leads to functional redundancy of histone H3K79 methylation states | Q46567995 | ||
| Step-wise methylation of histone H3K9 positions heterochromatin at the nuclear periphery. | Q47068818 | ||
| The chromo and SET domains of the Clr4 protein are essential for silencing in fission yeast | Q47991804 | ||
| Gene silencing triggers polycomb repressive complex 2 recruitment to CpG islands genome wide. | Q50650644 | ||
| Epigenetic regulation of telomere length in mammalian cells by the Suv39h1 and Suv39h2 histone methyltransferases. | Q51598430 | ||
| Structural differences in centromeric heterochromatin are spatially reconciled on fertilisation in the mouse zygote. | Q51756263 | ||
| Polycomb protein Ezh1 promotes RNA polymerase II elongation. | Q51832730 | ||
| Silencing of endogenous retroviruses: when and why do histone marks predominate? | Q51834987 | ||
| Lineage-specific polycomb targets and de novo DNA methylation define restriction and potential of neuronal progenitors. | Q51956004 | ||
| RUNX1 associates with histone deacetylases and SUV39H1 to repress transcription. | Q52570374 | ||
| The SENP7 SUMO-Protease Presents a Module of Two HP1 Interaction Motifs that Locks HP1 Protein at Pericentric Heterochromatin. | Q52969109 | ||
| SUMOylation promotes de novo targeting of HP1α to pericentric heterochromatin | Q57549485 | ||
| A transcription factor–based mechanism for mouse heterochromatin formation | Q64387285 | ||
| Histone methylation is mechanistically linked to DNA methylation at imprinting control regions in mammals | Q84042482 | ||
| Multivalent engagement of chromatin modifications by linked binding modules | Q29617236 | ||
| Loss of the Suv39h histone methyltransferases impairs mammalian heterochromatin and genome stability | Q29620365 | ||
| Rb targets histone H3 methylation and HP1 to promoters | Q29620452 | ||
| Reversal of H3K9me2 by a small-molecule inhibitor for the G9a histone methyltransferase | Q33272939 | ||
| Family expansion and gene rearrangements contributed to the functional specialization of PRDM genes in vertebrates. | Q33301582 | ||
| The target of the NSD family of histone lysine methyltransferases depends on the nature of the substrate | Q33553524 | ||
| Active and repressive chromatin are interspersed without spreading in an imprinted gene cluster in the mammalian genome. | Q33760054 | ||
| GC-rich sequence elements recruit PRC2 in mammalian ES cells | Q33775517 | ||
| The central role of EED in the orchestration of polycomb group complexes. | Q33815083 | ||
| Distinct epigenomic landscapes of pluripotent and lineage-committed human cells. | Q33842527 | ||
| DZNep is a global histone methylation inhibitor that reactivates developmental genes not silenced by DNA methylation. | Q34017960 | ||
| Ring1B and Suv39h1 delineate distinct chromatin states at bivalent genes during early mouse lineage commitment | Q34022860 | ||
| The histone H3 lysine 9 methyltransferases G9a and GLP regulate polycomb repressive complex 2-mediated gene silencing | Q34039506 | ||
| The Xist lncRNA interacts directly with SHARP to silence transcription through HDAC3. | Q34043853 | ||
| Human LSD2/KDM1b/AOF1 regulates gene transcription by modulating intragenic H3K4me2 methylation. | Q34128674 | ||
| The histone H4 Lys 20 methyltransferase PR-Set7 regulates replication origins in mammalian cells. | Q34144213 | ||
| TNF/p38α/polycomb signaling to Pax7 locus in satellite cells links inflammation to the epigenetic control of muscle regeneration. | Q34181742 | ||
| Setdb1 is required for germline development and silencing of H3K9me3-marked endogenous retroviruses in primordial germ cells | Q34235670 | ||
| The MSX1 homeoprotein recruits G9a methyltransferase to repressed target genes in myoblast cells | Q34282108 | ||
| An epigenetic silencing pathway controlling T helper 2 cell lineage commitment | Q34286068 | ||
| EHMT1 controls brown adipose cell fate and thermogenesis through the PRDM16 complex. | Q34382953 | ||
| Polycomb-dependent H3K27me1 and H3K27me2 regulate active transcription and enhancer fidelity | Q34388755 | ||
| Identification and characterization of a novel human histone H3 lysine 36-specific methyltransferase | Q34445102 | ||
| Eset partners with Oct4 to restrict extraembryonic trophoblast lineage potential in embryonic stem cells | Q37426774 | ||
| G9a selectively represses a class of late-replicating genes at the nuclear periphery. | Q37428891 | ||
| Chromatin signatures in multipotent human hematopoietic stem cells indicate the fate of bivalent genes during differentiation | Q37449132 | ||
| A conformational switch in HP1 releases auto-inhibition to drive heterochromatin assembly | Q37533718 | ||
| ESET methylates UBF at K232/254 and regulates nucleolar heterochromatin plasticity and rDNA transcription. | Q37574135 | ||
| Histone H3 lysine 4 (H3K4) methylation in development and differentiation | Q37585674 | ||
| SET for life: biochemical activities and biological functions of SET domain-containing proteins | Q37615671 | ||
| A dual role for the histone methyltransferase PR-SET7/SETD8 and histone H4 lysine 20 monomethylation in the local regulation of RNA polymerase II pausing | Q37635773 | ||
| Understanding the language of Lys36 methylation at histone H3. | Q37672319 | ||
| Decoding the histone H4 lysine 20 methylation mark | Q37782080 | ||
| The diverse functions of Dot1 and H3K79 methylation. | Q37897061 | ||
| Polycomb group proteins: repression in 3D. | Q37906862 | ||
| The COMPASS family of histone H3K4 methylases: mechanisms of regulation in development and disease pathogenesis | Q38015891 | ||
| The Prdm family: expanding roles in stem cells and development | Q38016394 | ||
| Emerging roles for chromatin as a signal integration and storage platform | Q38092575 | ||
| Transcriptional regulation by Polycomb group proteins | Q38149730 | ||
| Histone lysine demethylases as targets for anticancer therapy | Q38162717 | ||
| Polycomb silencing: from linear chromatin domains to 3D chromosome folding | Q38179206 | ||
| R-loops induce repressive chromatin marks over mammalian gene terminators | Q38949719 | ||
| Single-cell dynamics of genome-nuclear lamina interactions | Q39176932 | ||
| Control of proinflammatory gene programs by regulated trimethylation and demethylation of histone H4K20. | Q39291348 | ||
| Ring1B compacts chromatin structure and represses gene expression independent of histone ubiquitination | Q39703639 | ||
| Proviral silencing in embryonic stem cells requires the histone methyltransferase ESET. | Q39737989 | ||
| Ezh2 requires PHF1 to efficiently catalyze H3 lysine 27 trimethylation in vivo. | Q40011376 | ||
| Methylation of a histone mimic within the histone methyltransferase G9a regulates protein complex assembly | Q40091979 | ||
| Variant PRC1 complex-dependent H2A ubiquitylation drives PRC2 recruitment and polycomb domain formation. | Q40406465 | ||
| Histone methylation by the Drosophila epigenetic transcriptional regulator Ash1. | Q40694593 | ||
| PR-Set7-dependent methylation of histone H4 Lys 20 functions in repression of gene expression and is essential for mitosis | Q41078460 | ||
| The Msx1 Homeoprotein Recruits Polycomb to the Nuclear Periphery during Development | Q41578287 | ||
| Large histone H3 lysine 9 dimethylated chromatin blocks distinguish differentiated from embryonic stem cells | Q41868578 | ||
| Genome-wide regulation of 5hmC, 5mC, and gene expression by Tet1 hydroxylase in mouse embryonic stem cells | Q41960997 | ||
| Trimethylation of histone H3 lysine 4 impairs methylation of histone H3 lysine 9: regulation of lysine methyltransferases by physical interaction with their substrates. | Q41970615 | ||
| H3K27me3 forms BLOCs over silent genes and intergenic regions and specifies a histone banding pattern on a mouse autosomal chromosome | Q42076431 | ||
| Suv39h-dependent H3K9me3 marks intact retrotransposons and silences LINE elements in mouse embryonic stem cells. | Q42209064 | ||
| Molecular maps of the reorganization of genome-nuclear lamina interactions during differentiation | Q42472280 | ||
| Quiescence-induced LncRNAs trigger H4K20 trimethylation and transcriptional silencing | Q42803505 | ||
| G9a co-suppresses LINE1 elements in spermatogonia. | Q42918668 | ||
| Histone methyltransferase G9a contributes to H3K27 methylation in vivo | Q42939574 | ||
| A subset of the histone H3 lysine 9 methyltransferases Suv39h1, G9a, GLP, and SETDB1 participate in a multimeric complex. | Q43175284 | ||
| Polycomb repressive complex 2 is dispensable for maintenance of embryonic stem cell pluripotency | Q43194593 | ||
| Reassessing the abundance of H3K9me2 chromatin domains in embryonic stem cells | Q43206621 | ||
| Prdm3 and Prdm16 are H3K9me1 methyltransferases required for mammalian heterochromatin integrity. | Q45262911 | ||
| FSHD muscular dystrophy region gene 1 binds Suv4-20h1 histone methyltransferase and impairs myogenesis. | Q45290619 | ||
| Argonaute proteins couple chromatin silencing to alternative splicing. | Q45345567 | ||
| P433 | issue | 8 | |
| P304 | page(s) | 499-513 | |
| P577 | publication date | 2015-08-01 | |
| P1433 | published in | Nature Reviews Molecular Cell Biology | Q1573120 |
| P1476 | title | Sound of silence: the properties and functions of repressive Lys methyltransferases | |
| P478 | volume | 16 |
| Q36283537 | A Role for Widely Interspaced Zinc Finger (WIZ) in Retention of the G9a Methyltransferase on Chromatin |
| Q38738529 | A cross-talk between DNA methylation and H3 lysine 9 dimethylation at the KvDMR1 region controls the induction of Cdkn1c in muscle cells. |
| Q39096411 | A drive in SUVs: From development to disease |
| Q60908127 | ANKHD1 is required for SMYD3 to promote tumor metastasis in hepatocellular carcinoma |
| Q90430696 | ATF7IP regulates SETDB1 nuclear localization and increases its ubiquitination |
| Q39298989 | ATF7IP-Mediated Stabilization of the Histone Methyltransferase SETDB1 Is Essential for Heterochromatin Formation by the HUSH Complex |
| Q47157361 | Allele-Specific DNA Methylation and Its Interplay with Repressive Histone Marks at Promoter-Mutant TERT Genes. |
| Q36956991 | Anaplasma phagocytophilum increases the levels of histone modifying enzymes to inhibit cell apoptosis and facilitate pathogen infection in the tick vector Ixodes scapularis. |
| Q64111220 | Antigen receptor control of methionine metabolism in T cells |
| Q42172387 | Application of dual reading domains as novel reagents in chromatin biology reveals a new H3K9me3 and H3K36me2/3 bivalent chromatin state. |
| Q38803790 | Association of ORCA/LRWD1 with repressive histone methyl transferases mediates heterochromatin organization |
| Q91651372 | Cockayne syndrome group B deficiency reduces H3K9me3 chromatin remodeler SETDB1 and exacerbates cellular aging |
| Q46288028 | Computational characterization of substrate and product specificities, and functionality of S-adenosylmethionine binding pocket in histone lysine methyltransferases from Arabidopsis, rice and maize |
| Q54116646 | Contrasting epigenetic states of heterochromatin in the different types of mouse pluripotent stem cells. |
| Q60922662 | DOT1L inhibition blocks multiple myeloma cell proliferation by suppressing IRF4-MYC signaling |
| Q48298211 | Discovery of Potent and Selective Inhibitors for G9a-Like Protein (GLP) Lysine Methyltransferase. |
| Q92410964 | Epigenetic Regulation of Chromatin in Prostate Cancer |
| Q33764436 | Epigenetic regulation of epithelial-mesenchymal transition |
| Q90430690 | Essential roles of Windei and nuclear monoubiquitination of Eggless/SETDB1 in transposon silencing |
| Q42158675 | Establishment of expression-state boundaries by Rif1 and Taz1 in fission yeast |
| Q92528246 | Expression of the Major and Pro-Oncogenic H3K9 Lysine Methyltransferase SETDB1 in Non-Small Cell Lung Cancer |
| Q58745588 | G9a Correlates with VLA-4 Integrin and Influences the Migration of Childhood Acute Lymphoblastic Leukemia Cells |
| Q37126598 | Generalized nucleation and looping model for epigenetic memory of histone modifications |
| Q47139599 | H3K14ac is linked to methylation of H3K9 by the triple Tudor domain of SETDB1. |
| Q64070328 | Histone 4 Lysine 20 Methylation: A Case for Neurodevelopmental Disease |
| Q50072349 | How Communication Between Nucleosomes Enables Spreading and Epigenetic Memory of Histone Modifications |
| Q64092199 | Identification of human silencers by correlating cross-tissue epigenetic profiles and gene expression |
| Q26775369 | Insights into epigenetic landscape of recombination-free regions |
| Q39768084 | Investigation of H2AX methylation by the SUV39H2 protein lysine methyltransferase |
| Q90610454 | KDM2A/B lysine demethylases and their alternative isoforms in development and disease |
| Q64252282 | KDM4B: A Nail for Every Hammer? |
| Q64101984 | KMT1 family methyltransferases regulate heterochromatin-nuclear periphery tethering via histone and non-histone protein methylation |
| Q57799763 | LncRNA HOTAIR regulates lipopolysaccharide-induced cytokine expression and inflammatory response in macrophages |
| Q90013973 | Lung Cancer Therapy Targeting Histone Methylation: Opportunities and Challenges |
| Q64101463 | Lysine methylation of transcription factors in cancer |
| Q27309192 | Mechanisms underlying epigenetic and transcriptional heterogeneity in Chinese hamster ovary (CHO) cell lines |
| Q88669970 | Metabolic regulation of chromatin modifications and gene expression |
| Q39440781 | Orchestration of H3K27 methylation: mechanisms and therapeutic implication |
| Q38725574 | Position-effect variegation revisited: HUSHing up heterochromatin in human cells. |
| Q38861640 | Protein and Genetic Composition of Four Chromatin Types in Drosophila melanogaster Cell Lines |
| Q39212312 | Protein arginine methylation: a prominent modification and its demethylation |
| Q52095907 | Regulation of USP37 Expression by REST-Associated G9a-Dependent Histone Methylation. |
| Q41863682 | Relating protein functional diversity to cell type number identifies genes that determine dynamic aspects of chromatin organisation as potential contributors to organismal complexity. |
| Q31157515 | Retrieving Chromatin Patterns from Deep Sequencing Data Using Correlation Functions. |
| Q58596731 | SETDB1 Links the Meiotic DNA Damage Response to Sex Chromosome Silencing in Mice |
| Q36115303 | SETDB2 Links Glucocorticoid to Lipid Metabolism through Insig2a Regulation |
| Q52871562 | SIRT6: a new guardian of mitosis. |
| Q55002950 | Silencing of transposable elements may not be a major driver of regulatory evolution in primate iPSCs. |
| Q64107073 | Somatic Embryogenesis Induction in Woody Species: The Future After OMICs Data Assessment |
| Q36648714 | Suppression of F1 Male-Specific Lethality in Caenorhabditis Hybrids by cbr-him-8. |
| Q59357685 | Switching roles for DNA and histone methylation depend on evolutionary ages of human endogenous retroviruses |
| Q64092144 | Synergistic lethality between BRCA1 and H3K9me2 loss reflects satellite derepression |
| Q64961640 | TSPYL2 Regulates the Expression of EZH2 Target Genes in Neurons. |
| Q96304809 | The Emerging Roles of Heterochromatin in Cell Migration |
| Q90311780 | The H3K9 Methylation Writer SETDB1 and its Reader MPP8 Cooperate to Silence Satellite DNA Repeats in Mouse Embryonic Stem Cells |
| Q59793161 | The Heterochromatin Landscape in Migrating Cells and the Importance of H3K27me3 for Associated Transcriptome Alterations |
| Q58718492 | The biological significance of histone modifiers in multiple myeloma: clinical applications |
| Q92376610 | The roles of homologous recombination and the immune system in the genomic evolution of cancer |
| Q97544686 | Trait-associated noncoding variant regions affect TBX3 regulation and cardiac conduction |
| Q57026544 | Tri-methylation of ATF7IP by G9a/GLP recruits the chromodomain protein MPP8 |
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