| scholarly article | Q13442814 |
| P50 | author | Richard A. Young | Q21230104 |
| Garrett M Frampton | Q30502367 | ||
| P2093 | author name string | Peter B Rahl | |
| Steve Bilodeau | |||
| Michael H Kagey | |||
| P2860 | cites work | Formation of pluripotent stem cells in the mammalian embryo depends on the POU transcription factor Oct4 | Q22008002 |
| Embryonic stem cell differentiation: emergence of a new era in biology and medicine | Q22065783 | ||
| The HP1alpha-CAF1-SetDB1-containing complex provides H3K9me1 for Suv39-mediated K9me3 in pericentric heterochromatin | Q24317426 | ||
| Core transcriptional regulatory circuitry in human embryonic stem cells | Q24322016 | ||
| Ronin is essential for embryogenesis and the pluripotency of mouse embryonic stem cells | Q24336456 | ||
| Self-renewal of pluripotent embryonic stem cells is mediated via activation of STAT3 | Q24600230 | ||
| Genome-wide maps of chromatin state in pluripotent and lineage-committed cells | Q24632506 | ||
| Combinatorial patterns of histone acetylations and methylations in the human genome | Q24647290 | ||
| ES cells derived from cloned embryos in monkey--a jump toward human therapeutic cloning | Q40036419 | ||
| A core Klf circuitry regulates self-renewal of embryonic stem cells. | Q51964604 | ||
| Ring1-mediated ubiquitination of H2A restrains poised RNA polymerase II at bivalent genes in mouse ES cells | Q56813076 | ||
| Regulated recruitment of HP1 to a euchromatic gene induces mitotically heritable, epigenetic gene silencing: a mammalian cell culture model of gene variegation | Q24671965 | ||
| 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 bivalent chromatin structure marks key developmental genes in embryonic stem cells | Q27860977 | ||
| Embryonic stem cell lines derived from human blastocysts | Q27861010 | ||
| Chromatin modifications and their function | Q27861067 | ||
| mAM facilitates conversion by ESET of dimethyl to trimethyl lysine 9 of histone H3 to cause transcriptional repression | Q28208422 | ||
| Control of developmental regulators by Polycomb in human embryonic stem cells | Q28235841 | ||
| Nuclear reprogramming and pluripotency | Q28249466 | ||
| An extended transcriptional network for pluripotency of embryonic stem cells | Q28273615 | ||
| Genome regulation by polycomb and trithorax proteins | Q28289984 | ||
| T-cell factor 3 regulates embryonic stem cell pluripotency and self-renewal by the transcriptional control of multiple lineage pathways | Q28506950 | ||
| Histone H3-K9 methyltransferase ESET is essential for early development | Q28513000 | ||
| Repression of Nanog gene transcription by Tcf3 limits embryonic stem cell self-renewal | Q28586947 | ||
| Tcf3 is an integral component of the core regulatory circuitry of embryonic stem cells | Q28587342 | ||
| The Oct4 and Nanog transcription network regulates pluripotency in mouse embryonic stem cells | Q28593119 | ||
| Integration of external signaling pathways with the core transcriptional network in embryonic stem cells | Q29547179 | ||
| A chromatin landmark and transcription initiation at most promoters in human cells | Q29547180 | ||
| Polycomb complexes repress developmental regulators in murine embryonic stem cells | Q29547274 | ||
| Divergent transcription from active promoters | Q29614332 | ||
| Stem cells, the molecular circuitry of pluripotency and nuclear reprogramming | Q29614416 | ||
| A high-resolution map of active promoters in the human genome | Q29614431 | ||
| Genome-wide mapping of Polycomb target genes unravels their roles in cell fate transitions | Q29614512 | ||
| Chromatin signatures of pluripotent cell lines | Q29614675 | ||
| A lentiviral RNAi library for human and mouse genes applied to an arrayed viral high-content screen | Q29615061 | ||
| Connecting microRNA genes to the core transcriptional regulatory circuitry of embryonic stem cells | Q29615089 | ||
| Embryonic stem cell lines from human blastocysts: somatic differentiation in vitro | Q29617383 | ||
| Differentiation of embryonic stem cells to clinically relevant populations: lessons from embryonic development | Q29617978 | ||
| Ubiquitin E3 ligase Ring1b/Rnf2 of polycomb repressive complex 1 contributes to stable maintenance of mouse embryonic stem cells | Q33336429 | ||
| The polycomb group protein Suz12 is required for embryonic stem cell differentiation | Q35856936 | ||
| Human embryonic stem cells: prospects for development | Q35930345 | ||
| Nucleosome displacement in transcription | Q36554288 | ||
| Genetic and epigenetic regulators of pluripotency | Q36744480 | ||
| Aberrant chromatin at genes encoding stem cell regulators in human mixed-lineage leukemia | Q37023597 | ||
| Gene regulation in the postgenomic era: technology takes the wheel | Q37033127 | ||
| Oct-4 knockdown induces similar patterns of endoderm and trophoblast differentiation markers in human and mouse embryonic stem cells | Q38344261 | ||
| P433 | issue | 21 | |
| P921 | main subject | embryonic stem cell | Q1151519 |
| P304 | page(s) | 2484-2489 | |
| P577 | publication date | 2009-11-01 | |
| P1433 | published in | Genes & Development | Q1524533 |
| P1476 | title | SetDB1 contributes to repression of genes encoding developmental regulators and maintenance of ES cell state | |
| P478 | volume | 23 |
| Q48118039 | A Histone Methyltransferase ESET Is Critical for T Cell Development. |
| Q42435861 | A central role for TFIID in the pluripotent transcription circuitry |
| Q42022480 | A chemical method for labeling lysine methyltransferase substrates. |
| Q26823816 | A double take on bivalent promoters |
| Q33574854 | A team of heterochromatin factors collaborates with small RNA pathways to combat repetitive elements and germline stress |
| Q34712114 | AGO2 and SETDB1 cooperate in promoter-targeted transcriptional silencing of the androgen receptor gene |
| Q38266057 | An H3K9/S10 methyl-phospho switch modulates Polycomb and Pol II binding at repressed genes during differentiation |
| Q47136073 | An efficient method for generation of bi-allelic null mutant mouse embryonic stem cells and its application for investigating epigenetic modifiers |
| Q37583341 | An epigenetic switch induced by Shh signalling regulates gene activation during development and medulloblastoma growth. |
| Q35950995 | Anteroposterior Limb Skeletal Patterning Requires the Bifunctional Action of SWI/SNF Chromatin Remodeling Complex in Hedgehog Pathway |
| Q60912253 | Arrayed functional genetic screenings in pluripotency reprogramming and differentiation |
| Q34574808 | Bayesian inference of spatial organizations of chromosomes |
| Q27003156 | Bivalent histone modifications in early embryogenesis |
| Q28660713 | CR Cistrome: a ChIP-Seq database for chromatin regulators and histone modification linkages in human and mouse |
| Q27336177 | Caenorhabditis elegans histone methyltransferase MET-2 shields the male X chromosome from checkpoint machinery and mediates meiotic sex chromosome inactivation |
| Q37345655 | Canonical Wnt signalling regulates nuclear export of Setdb1 during skeletal muscle terminal differentiation |
| Q57785571 | Canonical and single-cell Hi-C reveal distinct chromatin interaction sub-networks of mammalian transcription factors |
| Q35144895 | Chromatin landscapes of retroviral and transposon integration profiles |
| Q34394111 | Chromatin modifiers and remodellers: regulators of cellular differentiation |
| Q37811021 | Chromatin regulation landscape of embryonic stem cell identity |
| Q34903800 | Chromatin regulatory mechanisms in pluripotency |
| Q27691396 | Chromatin structure of pluripotent stem cells and induced pluripotent stem cells. |
| Q64110381 | Combined analysis of dissimilar promoter accessibility and gene expression profiles identifies tissue-specific genes and actively repressed networks |
| Q34625297 | Comparative RNA-seq analysis in the unsequenced axolotl: the oncogene burst highlights early gene expression in the blastema. |
| Q34486035 | Comparative analysis of metazoan chromatin organization |
| Q48172698 | Connected Gene Communities Underlie Transcriptional Changes in Cornelia de Lange Syndrome. |
| Q36985728 | Continual removal of H3K9 promoter methylation by Jmjd2 demethylases is vital for ESC self-renewal and early development |
| Q29614793 | Control of the embryonic stem cell state |
| Q47445776 | Critical roles of protein methyltransferases and demethylases in the regulation of embryonic stem cell fate |
| Q42826399 | DNA methylation and SETDB1/H3K9me3 regulate predominantly distinct sets of genes, retroelements, and chimeric transcripts in mESCs |
| Q58601814 | DNMTs and SETDB1 function as co-repressors in MAX-mediated repression of germ cell-related genes in mouse embryonic stem cells |
| Q33842527 | Distinct epigenomic landscapes of pluripotent and lineage-committed human cells. |
| Q33934698 | Distinct histone modifications in stem cell lines and tissue lineages from the early mouse embryo |
| Q38166840 | Dynamic changes of the epigenetic landscape during cellular differentiation. |
| Q38706933 | Dynamic chromatin states in human ES cells reveal potential regulatory sequences and genes involved in pluripotency. |
| Q37830853 | Dynamic control of endogenous retroviruses during development. |
| Q41940196 | Dynamics and memory of heterochromatin in living cells. |
| Q36170703 | Dynamics of inherently bounded histone modification domains |
| Q40730252 | E3-Independent Constitutive Monoubiquitination Complements Histone Methyltransferase Activity of SETDB1. |
| Q24633489 | Embryonic stem cell and induced pluripotent stem cell: an epigenetic perspective |
| Q38958989 | Enhancers and their dynamics during hematopoietic differentiation and emerging strategies for therapeutic action |
| Q36277309 | Epigenetic control of cell cycle-dependent histone gene expression is a principal component of the abbreviated pluripotent cell cycle. |
| Q37756526 | Epigenetic control of neural precursor cell fate during development |
| Q30540197 | Epigenetic marks define the lineage and differentiation potential of two distinct neural crest-derived intermediate odontogenic progenitor populations |
| Q35066333 | Epigenetic mechanisms of induced pluripotency |
| Q34143430 | Epigenetic modifications in pluripotent and differentiated cells |
| Q37801811 | Epigenetic regulation of reprogramming factors towards pluripotency in mouse preimplantation development |
| Q28084849 | Epigenetic regulation of the intestinal epithelium |
| Q64119402 | Epigenetic signatures associated with imprinted paternally expressed genes in the Arabidopsis endosperm |
| Q35145499 | Epigenetic signatures distinguish multiple classes of enhancers with distinct cellular functions |
| Q33750227 | Epigenetic silencing of spermatocyte-specific and neuronal genes by SUMO modification of the transcription factor Sp3. |
| Q92528246 | Expression of the Major and Pro-Oncogenic H3K9 Lysine Methyltransferase SETDB1 in Non-Small Cell Lung Cancer |
| Q41462593 | FOXA and master transcription factors recruit Mediator and Cohesin to the core transcriptional regulatory circuitry of cancer cells |
| Q35609473 | Functional Crosstalk Between Lysine Methyltransferases on Histone Substrates: The Case of G9A/GLP and Polycomb Repressive Complex 2 |
| Q28818311 | GC Content Heterogeneity Transition of Conserved Noncoding Sequences Occurred at the Emergence of Vertebrates |
| Q33652528 | Gene amplification of the histone methyltransferase SETDB1 contributes to human lung tumorigenesis |
| Q34806568 | Genome-wide identification of chromatin transitional regions reveals diverse mechanisms defining the boundary of facultative heterochromatin |
| Q35633661 | Genomic binding of Pol III transcription machinery and relationship with TFIIS transcription factor distribution in mouse embryonic stem cells |
| Q47139599 | H3K14ac is linked to methylation of H3K9 by the triple Tudor domain of SETDB1. |
| Q38671298 | H3K9me3-Dependent Heterochromatin: Barrier to Cell Fate Changes. |
| Q39038126 | Heterochromatin and the molecular mechanisms of 'parent-of-origin' effects in animals. |
| Q36340201 | Heterochromatin components in germline stem cell maintenance |
| Q38273698 | High-wire act: the poised genome and cellular memory. |
| Q34474887 | Histone H3.3 is required for endogenous retroviral element silencing in embryonic stem cells |
| Q34116874 | Histone H3K9 trimethylase Eggless controls germline stem cell maintenance and differentiation |
| Q55269967 | Histone deacetylation promotes transcriptional silencing at facultative heterochromatin. |
| Q41852966 | Histone demethylase LSD1 regulates adipogenesis |
| Q27318351 | Histone methylation restrains the expression of subtype-specific genes during terminal neuronal differentiation in Caenorhabditis elegans |
| Q27014505 | Histone methylations in heart development, congenital and adult heart diseases |
| Q55006254 | Histone methyltransferase SETDB1 promotes cells proliferation and migration by interacting withTiam1 in hepatocellular carcinoma. |
| Q33663060 | Histone methyltransferase SETDB1 regulates liver cancer cell growth through methylation of p53 |
| Q33767860 | How does the royal family of Tudor rule the PIWI-interacting RNA pathway? |
| Q29305058 | IDH mutation impairs histone demethylation and results in a block to cell differentiation |
| Q35534127 | In embryonic stem cells, ZFP57/KAP1 recognize a methylated hexanucleotide to affect chromatin and DNA methylation of imprinting control regions |
| Q90975535 | Inducible histone K-to-M mutations are dynamic tools to probe the physiological role of site-specific histone methylation in vitro and in vivo |
| Q62478086 | Inferring Spatial Organization of Individual Topologically Associated Domains via Piecewise Helical Model |
| Q38831555 | Inhibition of EHMT2 Induces a Robust Antiviral Response Against Foot-and-Mouth Disease and Vesicular Stomatitis Virus Infections in Bovine Cells. |
| Q37725232 | Integrative framework for identification of key cell identity genes uncovers determinants of ES cell identity and homeostasis |
| Q36155124 | KDM3B is the H3K9 demethylase involved in transcriptional activation of lmo2 in leukemia |
| Q33834910 | Kdm2b maintains murine embryonic stem cell status by recruiting PRC1 complex to CpG islands of developmental genes. |
| Q34434347 | LIF-independent JAK signalling to chromatin in embryonic stem cells uncovered from an adult stem cell disease |
| Q30717456 | Large-scale quality analysis of published ChIP-seq data |
| Q34626174 | Long noncoding RNAs: an emerging link between gene regulation and nuclear organization |
| Q26765418 | Maintaining memory of silencing at imprinted differentially methylated regions |
| Q35987178 | Maternal Setdb1 Is Required for Meiotic Progression and Preimplantation Development in Mouse |
| Q59314000 | Mining Massive Amounts of Genomic Data: A Semiparametric Topic Modeling Approach |
| Q39268159 | Modulation of gene expression dynamics by co-transcriptional histone methylations. |
| Q38736146 | Molecular features of cellular reprogramming and development |
| Q36001860 | Molecular marks for epigenetic identification of developmental and cancer stem cells |
| Q37344597 | Multiple structural maintenance of chromosome complexes at transcriptional regulatory elements. |
| Q48630874 | NEUROG1 Regulates CDK2 to Promote Proliferation in Otic Progenitors. |
| Q35848560 | New and novel intrinsic host repressive factors against HIV-1: PAF1 complex, HERC5 and others |
| Q91644556 | On the relations of phase separation and Hi-C maps to epigenetics |
| Q55039489 | PAF1 complex interactions with SETDB1 mediate promoter H3K9 methylation and transcriptional repression of Hoxa9 and Meis1 in acute myeloid leukemia. |
| Q37874803 | Paused RNA polymerase II as a developmental checkpoint |
| Q47402982 | Polycomb repression complex 2 is required for the maintenance of retinal progenitor cells and balanced retinal differentiation |
| Q34297995 | Polycomb repressive complex 2 and H3K27me3 cooperate with H3K9 methylation to maintain heterochromatin protein 1α at chromatin |
| Q26770764 | Post-Translational Modifications of Histones in Vertebrate Neurogenesis |
| Q41290879 | Posttranslational modifications of the histone 3 tail and their impact on the activity of histone lysine demethylases in vitro |
| Q41193415 | Prmt5 is essential for early mouse development and acts in the cytoplasm to maintain ES cell pluripotency |
| Q35002456 | Product binding enforces the genomic specificity of a yeast polycomb repressive complex |
| Q37071550 | Proteomic and genomic approaches reveal critical functions of H3K9 methylation and heterochromatin protein-1γ in reprogramming to pluripotency |
| Q35784896 | Reactivation of maternal SNORD116 cluster via SETDB1 knockdown in Prader-Willi syndrome iPSCs |
| Q27665584 | Recognition and Specificity Determinants of the Human Cbx Chromodomains |
| Q24299712 | Recognition of multivalent histone states associated with heterochromatin by UHRF1 protein |
| Q37106147 | Recruitment and biological consequences of histone modification of H3K27me3 and H3K9me3. |
| Q36432067 | Regulation of the imprinted Dlk1-Dio3 locus by allele-specific enhancer activity |
| Q38023496 | Reprogramming chromatin |
| Q36742802 | Resources for methylome analysis suitable for gene knockout studies of potential epigenome modifiers |
| Q33816360 | Responsiveness of genes to manipulation of transcription factors in ES cells is associated with histone modifications and tissue specificity |
| Q47104740 | Rif1 promotes a repressive chromatin state to safeguard against endogenous retrovirus activation. |
| Q34022860 | Ring1B and Suv39h1 delineate distinct chromatin states at bivalent genes during early mouse lineage commitment |
| Q24309465 | SETD6 monomethylates H2AZ on lysine 7 and is required for the maintenance of embryonic stem cell self-renewal |
| Q35097426 | SETDB1 accelerates tumourigenesis by regulating the WNT signalling pathway |
| Q90317043 | SETDB1 mediated histone H3 lysine 9 methylation suppresses MLL-fusion target expression and leukemic transformation |
| Q36032490 | SETDB1 modulates PRC2 activity at developmental genes independently of H3K9 trimethylation in mouse ES cells |
| Q33785287 | SMARCAD1 Contributes to the Regulation of Naive Pluripotency by Interacting with Histone Citrullination |
| Q34597982 | SOX2 co-occupies distal enhancer elements with distinct POU factors in ESCs and NPCs to specify cell state |
| Q39283917 | Sequence features and chromatin structure around the genomic regions bound by 119 human transcription factors |
| Q34464546 | Setdb1 is required for myogenic differentiation of C2C12 myoblast cells via maintenance of MyoD expression |
| Q36911257 | Setdb1-mediated H3K9 methylation is enriched on the inactive X and plays a role in its epigenetic silencing |
| Q55002950 | Silencing of transposable elements may not be a major driver of regulatory evolution in primate iPSCs. |
| Q38552741 | Sound of silence: the properties and functions of repressive Lys methyltransferases. |
| Q34027077 | Stem cells and reprogramming: breaking the epigenetic barrier? |
| Q90039542 | TAF5L and TAF6L Maintain Self-Renewal of Embryonic Stem Cells via the MYC Regulatory Network |
| Q39097023 | TGF-β Family Signaling in Embryonic and Somatic Stem-Cell Renewal and Differentiation |
| Q36660136 | TRIM28 repression of retrotransposon-based enhancers is necessary to preserve transcriptional dynamics in embryonic stem cells |
| Q90311780 | The H3K9 Methylation Writer SETDB1 and its Reader MPP8 Cooperate to Silence Satellite DNA Repeats in Mouse Embryonic Stem Cells |
| Q64898475 | The Polycomb protein Ezl1 mediates H3K9 and H3K27 methylation to repress transposable elements in Paramecium. |
| Q36886887 | The abbreviated pluripotent cell cycle. |
| Q36225648 | The chromatin fingerprint of gene enhancer elements |
| Q90196318 | The control of gene expression and cell identity by H3K9 trimethylation |
| Q38704904 | The dynamic genome: transposons and environmental adaptation in the nervous system |
| Q37381685 | The epigenomics of embryonic stem cell differentiation |
| Q24625220 | The histone methyltransferase SETDB1 is recurrently amplified in melanoma and accelerates its onset |
| Q26782196 | The interplay of histone modifications - writers that read |
| Q26866571 | The transcriptional regulation of pluripotency |
| Q36620852 | The trithorax group protein Ash2l is essential for pluripotency and maintaining open chromatin in embryonic stem cells |
| Q28264221 | Topological domains in mammalian genomes identified by analysis of chromatin interactions |
| Q37186218 | Transcriptional activation by Oct4 is sufficient for the maintenance and induction of pluripotency |
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| Q41834088 | Transient Downregulation of Nanog and Oct4 Induced by DETA/NO Exposure in Mouse Embryonic Stem Cells Leads to Mesodermal/Endodermal Lineage Differentiation |
| Q36977328 | Transposable Elements and Their KRAB-ZFP Controllers Regulate Gene Expression in Adult Tissues |
| Q35617265 | Treatment of breast cancer cells with DNA demethylating agents leads to a release of Pol II stalling at genes with DNA-hypermethylated regions upstream of TSS. |
| Q41970615 | Trimethylation of histone H3 lysine 4 impairs methylation of histone H3 lysine 9: regulation of lysine methyltransferases by physical interaction with their substrates. |
| Q53306403 | Up-regulation of histone methyltransferase SETDB1 by multiple mechanisms in hepatocellular carcinoma promotes cancer metastasis. |
| Q28513471 | Wdr5 mediates self-renewal and reprogramming via the embryonic stem cell core transcriptional network |
| Q24318366 | ZNF274 recruits the histone methyltransferase SETDB1 to the 3' ends of ZNF genes |
| Q24629119 | c-Myc regulates transcriptional pause release |
| Q35163529 | esBAF facilitates pluripotency by conditioning the genome for LIF/STAT3 signalling and by regulating polycomb function |
| Q28543055 | hnRNP K coordinates transcriptional silencing by SETDB1 in embryonic stem cells |
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