review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1016/S0955-0674(00)00208-8 |
P698 | PubMed publication ID | 11343896 |
P2093 | author name string | Allis CD | |
Rice JC | |||
P2860 | cites work | Analysis of the NuRD subunits reveals a histone deacetylase core complex and a connection with DNA methylation | Q22003769 |
Functional mammalian homologues of the Drosophila PEV-modifier Su(var)3-9 encode centromere-associated proteins which complex with the heterochromatin component M31 | Q22009388 | ||
Structure and ligand of a histone acetyltransferase bromodomain | Q22009928 | ||
Crystal structure of the nucleosome core particle at 2.8 A resolution | Q22122355 | ||
Regulation of chromatin structure by site-specific histone H3 methyltransferases | Q24290115 | ||
Nucleosomal DNA regulates the core-histone-binding subunit of the human Hat1 acetyltransferase | Q24320001 | ||
Physical association between the histone acetyl transferase CBP and a histone methyl transferase | Q24522491 | ||
Acetylation of histones and transcription-related factors | Q24548503 | ||
The structural basis for the recognition of acetylated histone H4 by the bromodomain of histone acetyltransferase gcn5p | Q24596953 | ||
Structure and function of a human TAFII250 double bromodomain module | Q27622657 | ||
Methylation of histone H3 lysine 9 creates a binding site for HP1 proteins | Q27860456 | ||
Selective recognition of methylated lysine 9 on histone H3 by the HP1 chromo domain | Q27860477 | ||
The language of covalent histone modifications | Q27860931 | ||
Tetrahymena histone acetyltransferase A: a homolog to yeast Gcn5p linking histone acetylation to gene activation | Q27937778 | ||
Use of selectively trypsinized nucleosome core particles to analyze the role of the histone "tails" in the stabilization of the nucleosome | Q41307889 | ||
Changes in the methylation pattern of core histones during heat-shock in Drosophila cells. | Q41320571 | ||
Time out: developmental regulation of heterochromatic silencing in Drosophila | Q41714816 | ||
Overcoming telomeric silencing: a trans-activator competes to establish gene expression in a cell cycle-dependent way. | Q42491877 | ||
In vivo turnover and distribution of radio-N-methyl in arginine-rich histones from rat tissues | Q44406484 | ||
Phosphorylation and methylation of chromatin proteins from mouse brain nuclei | Q44980121 | ||
Histone acetylation reduces nucleosome core particle linking number change | Q46129118 | ||
The histone deacetylase RPD3 counteracts genomic silencing in Drosophila and yeast | Q47072158 | ||
The histone tails of the nucleosome | Q48018656 | ||
The Drosophila Fab-7 chromosomal element conveys epigenetic inheritance during mitosis and meiosis | Q48032990 | ||
In vivo methylation and turnover of rat brain histones | Q48526775 | ||
Beyond the nucleosome: epigenetic aspects of position-effect variegation in Drosophila. | Q52563488 | ||
Propagating epigenetic states through meiosis: where Mendel's gene is more than a DNA moiety. | Q52565504 | ||
NuRD and SIN3 | Q55884279 | ||
Intercalating agents as probes of the spatial relationship between chromatin components | Q66921227 | ||
Kinetics of Histone Methylation in vivo and Its Relation to the Cell Cycle in Ehrlich Ascites Tumor Cells | Q66956608 | ||
The distribution and turnover of labeled methyl groups in histone fractions of cultured mammalian cells | Q70456628 | ||
A positive role for histone acetylation in transcription factor access to nucleosomal DNA | Q70535287 | ||
Methylation of lysine residues of histone fractions in synchronized mommalian cells | Q70563923 | ||
Chromosomal inheritance of epigenetic states in fission yeast during mitosis and meiosis | Q71214328 | ||
Relationship between methylation and acetylation of arginine-rich histones in cycling and arrested HeLa cells | Q72638509 | ||
Characterization of nucleosome core particles containing histone proteins made in bacteria | Q73770026 | ||
Acetylation increases the alpha-helical content of the histone tails of the nucleosome | Q74152760 | ||
THE OCCURRENCE OF EPSILON-N-METHYL LYSINE IN HISTONES | Q76706209 | ||
Structure and function of the core histone N-termini: more than meets the eye | Q77917240 | ||
Regulation of transcription by a protein methyltransferase | Q28138085 | ||
The bromodomain: a chromatin-targeting module? | Q28139513 | ||
Synergistic coupling of histone H3 phosphorylation and acetylation in response to epidermal growth factor stimulation | Q28141828 | ||
Mi-2 complex couples DNA methylation to chromatin remodelling and histone deacetylation | Q28143634 | ||
Mammalian chromodomain proteins: their role in genome organisation and expression | Q28143752 | ||
A mammalian histone deacetylase related to the yeast transcriptional regulator Rpd3p | Q28276243 | ||
The chromo superfamily: new members, duplication of the chromo domain and possible role in delivering transcription regulators to chromatin | Q28285261 | ||
The dermatomyositis-specific autoantigen Mi2 is a component of a complex containing histone deacetylase and nucleosome remodeling activities | Q28286772 | ||
Heterochromatin Dynamics in Mouse Cells | Q29012057 | ||
Histone acetyltransferases | Q29547823 | ||
Role of histone H3 lysine 9 methylation in epigenetic control of heterochromatin assembly | Q29614718 | ||
Synergy of demethylation and histone deacetylase inhibition in the re-expression of genes silenced in cancer | Q29615066 | ||
Alteration of nucleosome structure as a mechanism of transcriptional regulation | Q29620047 | ||
Methylation of histone H3 at lysine 4 is highly conserved and correlates with transcriptionally active nuclei in Tetrahymena | Q30304568 | ||
Heterochromatin | Q33592042 | ||
Functional interaction between the coactivator Drosophila CREB-binding protein and ASH1, a member of the trithorax group of chromatin modifiers | Q33606495 | ||
Chromatin-modifying and -remodeling complexes | Q33632339 | ||
Signaling to chromatin through histone modifications: how clear is the signal? | Q33671512 | ||
Role of covalent modifications of histones in regulating gene expression | Q33775005 | ||
The HP1 protein family: getting a grip on chromatin | Q33885013 | ||
Review: chromatin structural features and targets that regulate transcription | Q33915685 | ||
Synergistic enhancement of nuclear receptor function by p160 coactivators and two coactivators with protein methyltransferase activities | Q33922863 | ||
Histone H4 acetylation of euchromatin and heterochromatin is cell cycle dependent and correlated with replication rather than with transcription | Q33926085 | ||
25 years after the nucleosome model: chromatin modifications | Q34104537 | ||
Role of protein methylation in chromatin remodeling and transcriptional regulation | Q34290239 | ||
SET domain proteins modulate chromatin domains in eu- and heterochromatin. | Q34458687 | ||
Conservation of deposition-related acetylation sites in newly synthesized histones H3 and H4. | Q34709355 | ||
Position effect variegation and chromatin proteins | Q35284118 | ||
Acetylation of histone H4 plays a primary role in enhancing transcription factor binding to nucleosomal DNA in vitro. | Q35850301 | ||
Efficient transcriptional silencing in Saccharomyces cerevisiae requires a heterochromatin histone acetylation pattern | Q36561489 | ||
Quantitative features of chromatin structure in the prognosis of breast cancer | Q39243708 | ||
A truncated form of the human CAF-1 p150 subunit impairs the maintenance of transcriptional gene silencing in mammalian cells | Q39458267 | ||
Chromatin disruption and modification | Q39726920 | ||
Heterochromatin polymorphism and human cancer | Q40315929 | ||
Position-effect variegation and the new biology of heterochromatin | Q40672449 | ||
Functional analysis of the chromo domain of HP1 | Q40789118 | ||
Co-operation between protein-acetylating and protein-methylating co-activators in transcriptional activation | Q40858644 | ||
Heterochromatin and gene regulation in Drosophila | Q41044078 | ||
Acetylation and methylation of histones H3 and H4 in chicken immature erythrocytes are not directly coupled | Q41122296 | ||
Histone acetylation and chromatin assembly: a single escort, multiple dances? | Q41152817 | ||
Dynamically acetylated histones of chicken erythrocytes are selectively methylated | Q41178669 | ||
P433 | issue | 3 | |
P921 | main subject | histone acetylation | Q14908264 |
P304 | page(s) | 263-273 | |
P577 | publication date | 2001-06-01 | |
P1433 | published in | Current Opinion in Cell Biology | Q13505682 |
P1476 | title | Histone methylation versus histone acetylation: new insights into epigenetic regulation | |
P478 | volume | 13 |
Q34734091 | (-)-Epigallocatechin-3-gallate reactivates silenced tumor suppressor genes, Cip1/p21 and p16INK4a, by reducing DNA methylation and increasing histones acetylation in human skin cancer cells |
Q57884146 | 6 Structure of SET domain protein lysine methyltransferases |
Q41914545 | A HAT for sleep?: epigenetic regulation of sleep by Tip60 in Drosophila |
Q42029829 | A Neuronal Activity-Dependent Dual Function Chromatin-Modifying Complex Regulates Arc Expression(1,2,3). |
Q35148553 | A chemical proteomics approach for global analysis of lysine monomethylome profiling. |
Q33757634 | A heterochromatin protein 1 homologue in Caenorhabditis elegans acts in germline and vulval development |
Q41534451 | A method to distinguish between lysine acetylation and lysine ubiquitination with feature selection and analysis. |
Q37825723 | A new regulator of the cell cycle: the PR-Set7 histone methyltransferase |
Q31118612 | A nonenzymatic modification of the amino-terminal domain of histone H3 by bile acid acyl adenylate. |
Q24594322 | A novel docking site on Mediator is critical for activation by VP16 in mammalian cells |
Q34210889 | A role for repressive histone methylation in cocaine-induced vulnerability to stress |
Q34563310 | A second catalytic domain in the Elp3 histone acetyltransferases: a candidate for histone demethylase activity? |
Q46009407 | A trans-tail histone code defined by monomethylated H4 Lys-20 and H3 Lys-9 demarcates distinct regions of silent chromatin. |
Q34616104 | A unique class of conditional sir2 mutants displays distinct silencing defects in Saccharomyces cerevisiae. |
Q36951565 | Acetate reduces PGE2 release and modulates phospholipase and cyclooxygenase levels in neuroglia stimulated with lipopolysaccharide |
Q36319571 | Acetate reduces microglia inflammatory signaling in vitro |
Q35027641 | Acetylation in hormone signaling and the cell cycle |
Q33952737 | Acetylation-dependent nuclear arrangement and recruitment of BMI1 protein to UV-damaged chromatin |
Q24336785 | Activating signal cointegrator 2 belongs to a novel steady-state complex that contains a subset of trithorax group proteins |
Q50611631 | Activation of facultatively silenced Drosophila loci associates with increased acetylation of histone H2AvD. |
Q35639785 | Alternative mRNA splicing of corepressors generates variants that play opposing roles in adipocyte differentiation. |
Q34309185 | An epigenetic perspective on the free radical theory of development |
Q38050404 | Analysing the sperm epigenome: roles in early embryogenesis and assisted reproduction. |
Q33185238 | Analysis of core histones by liquid chromatography-mass spectrometry and peptide mapping |
Q39214234 | Anticancer Natural Compounds as Epigenetic Modulators of Gene Expression |
Q36161311 | Antigen receptor loci poised for V(D)J rearrangement are broadly associated with BRG1 and flanked by peaks of histone H3 dimethylated at lysine 4 |
Q30768842 | Arrangements of macro- and microchromosomes in chicken cells |
Q34154556 | Association of the histone methyltransferase Set2 with RNA polymerase II plays a role in transcription elongation |
Q43587769 | Attomole detection of in vivo protein targets of benzene in mice: evidence for a highly reactive metabolite |
Q41094049 | BRD3 and BRD4 BET Bromodomain Proteins Differentially Regulate Skeletal Myogenesis. |
Q49667498 | Beyond the genetic code in leaf senescence |
Q34997981 | Bookmarking the genome: maintenance of epigenetic information. |
Q35230823 | Buffalo embryos produced by handmade cloning from oocytes selected using brilliant cresyl blue staining have better developmental competence and quality and are closer to embryos produced by in vitro fertilization in terms of their epigenetic status |
Q34522955 | Catalytic roles for carbon-oxygen hydrogen bonding in SET domain lysine methyltransferases |
Q39756065 | Centromeric chromatin pliability and memory at a human neocentromere. |
Q34508481 | Chemical genomics in the global study of protein functions |
Q37097824 | Chemical mechanisms of histone lysine and arginine modifications |
Q30492487 | Choline deficiency alters global histone methylation and epigenetic marking at the Re1 site of the calbindin 1 gene |
Q61041700 | Chromatin Fiber Folding: Requirement for the Histone H4 N-terminal Tail |
Q36813011 | Chromatin as a target for the DNA-binding anticancer drugs. |
Q34977174 | Chromatin dynamics in plants |
Q34869782 | Chromatin landscape defined by repressive histone methylation during oligodendrocyte differentiation. |
Q28504868 | Chromatin remodeling complex interacts with ADD1/SREBP1c to mediate insulin-dependent regulation of gene expression |
Q36511855 | Chromatin remodeling in cancer: a gateway to regulate gene transcription |
Q79522492 | Chromatin supraorganization and extensibility in mouse hepatocytes with development and aging |
Q37073231 | Chromatin, cancer and drug therapies |
Q38337531 | Chromatin-level regulation of the IL10 gene in T cells. |
Q52659538 | CoA synthase regulates mitotic fidelity via CBP-mediated acetylation. |
Q36378300 | Coactivator recruitment is enhanced by thyroid hormone receptor trimers |
Q35101485 | Coactivator-associated arginine methyltransferase 1 enhances transcriptional activity of the human T-cell lymphotropic virus type 1 long terminal repeat through direct interaction with Tax. |
Q38258716 | Cocaine triggers epigenetic alterations in the corticostriatal circuit |
Q59088503 | Code of silence |
Q90576377 | Codependency of Metabolism and Epigenetics Drives Cancer Progression: A Review |
Q24531547 | Common pathways in circadian and cell cycle clocks: light-dependent activation of Fos/AP-1 in zebrafish controls CRY-1a and WEE-1 |
Q24810685 | Comparative analysis of expression of histone H2a genes in mouse |
Q92889807 | Comprehensive analysis of histone modification-associated genes on differential gene expression and prognosis in gastric cancer |
Q44079501 | Connecting the DOTs: covalent histone modifications and the formation of silent chromatin |
Q52571236 | Constitutive expression exposes functional redundancy between the Arabidopsis histone H2A gene HTA1 and other H2A gene family members. |
Q35641906 | Coordinated recruitment of histone methyltransferase G9a and other chromatin-modifying enzymes in SHP-mediated regulation of hepatic bile acid metabolism |
Q37152573 | Critical role of p38 and GATA3 in natural helper cell function |
Q36833884 | DNA and Flavonoids Leach out from Active Nuclei of Taxus and Tsuga after Extreme Climate Stresses |
Q34361252 | DNA methylation controls histone H3 lysine 9 methylation and heterochromatin assembly in Arabidopsis. |
Q33632861 | DNA replication components as regulators of epigenetic inheritance--lesson from fission yeast centromere |
Q91647449 | Demethylation of the Protein Phosphatase PP2A Promotes Demethylation of Histones to Enable Their Function as a Methyl Group Sink |
Q33569694 | Development of homogeneous luminescence assays for histone demethylase catalysis and binding. |
Q38868449 | Developmental origins of male subfertility: role of infection, inflammation, and environmental factors. |
Q41915130 | Di-methyl H4 lysine 20 targets the checkpoint protein Crb2 to sites of DNA damage |
Q38818485 | Dietary phytochemicals as epigenetic modifiers in cancer: Promise and challenges |
Q40596783 | Differences in stability of repressor complexes at promoters underlie distinct roles for Rb family members |
Q33526991 | Differential localization and independent acquisition of the H3K9me2 and H3K9me3 chromatin modifications in the Caenorhabditis elegans adult germ line |
Q43820588 | Differentially methylated forms of histone H3 show unique association patterns with inactive human X chromosomes |
Q40186303 | Differentiation-specific association of HP1alpha and HP1beta with chromocentres is correlated with clustering of TIF1beta at these sites |
Q42590205 | Dimethylation of histone H3 at lysine 36 demarcates regulatory and nonregulatory chromatin genome-wide |
Q35253001 | Discriminating between lysine sumoylation and lysine acetylation using mRMR feature selection and analysis |
Q34675849 | Dissecting long-range transcriptional mechanisms by chromatin immunoprecipitation |
Q37492667 | During lytic infection herpes simplex virus type 1 is associated with histones bearing modifications that correlate with active transcription. |
Q40337035 | Dynamic changes in histone H3 lysine 9 methylations: identification of a mitosis-specific function for dynamic methylation in chromosome congression and segregation |
Q51920475 | Dynamic landscapes of four histone modifications during deetiolation in Arabidopsis. |
Q33988138 | Dynamic methylation of histone H3 at lysine 4 in transcriptional regulation by the androgen receptor. |
Q39657214 | Dynamic regulation of histone H3K9 is linked to the switch between replication and transcription at the Dbf4 origin-promoter locus |
Q53314416 | Effect of cryopreservation and in vitro culture of bovine fibroblasts on histone acetylation levels and in vitro development of hand-made cloned embryos. |
Q43541112 | Effect of varicocelectomy on sperm functional characteristics and DNA methylation. |
Q47380191 | Effects of Arsenic Trioxide on INF-gamma Gene Expression in MRL/lpr Mice and Human Lupus. |
Q40153283 | Effects of KNK437 on heat-induced methylation of histone H3 in human oral squamous cell carcinoma cells |
Q34093642 | Effects of acetylation of histone H4 at lysines 8 and 16 on activity of the Hat1 histone acetyltransferase |
Q50536825 | Emerging Trends in Epigenetic Regulation of Nutrient Deficiency Response in Plants. |
Q60955063 | Enhancing the Anticancer Efficacy of Immunotherapy through Combination with Histone Modification Inhibitors |
Q54356522 | Enrichment of (pro)renin receptor promoter with activating histone codes in the kidneys of spontaneously hypertensive rats. |
Q35782828 | Epigenetic alterations in ultraviolet radiation-induced skin carcinogenesis: interaction of bioactive dietary components on epigenetic targets |
Q38051195 | Epigenetic aspects of MDS and its molecular targeted therapy |
Q33767309 | Epigenetic changes in the myelodysplastic syndrome. |
Q34120020 | Epigenetic codes for heterochromatin formation and silencing: rounding up the usual suspects |
Q38260030 | Epigenetic dynamics: role of epimarks and underlying machinery in plants exposed to abiotic stress |
Q44858633 | Epigenetic histone methylation regulates transforming growth factor β-1 expression following bile duct ligation in rats. |
Q42166729 | Epigenetic marking correlates with developmental potential in cloned bovine preimplantation embryos. |
Q34302493 | Epigenetic mechanisms of depression and antidepressant action |
Q39836698 | Epigenetic modulation of gene expression from quiescent herpes simplex virus genomes |
Q46504209 | Epigenetic modulation on cat-cow interspecies somatic cell nuclear transfer embryos by treatment with trichostatin A. |
Q35012703 | Epigenetic regulation in alcoholic liver disease. |
Q39369985 | Epigenetic regulation of GATA4 expression by histone modification in AFP-producing gastric adenocarcinoma |
Q50629929 | Epigenetic regulation of cardiac myofibril gene expression during heart development. |
Q37480728 | Epigenetic regulation of caspase-3 gene expression in rat brain development |
Q37130484 | Epigenetic regulation of mammalian stem cells |
Q35459817 | Epigenetic regulation of pericentromeric heterochromatin during mammalian meiosis |
Q33742171 | Epigenetic remodeling of chromatin architecture: exploring tumor differentiation therapies in mesenchymal stem cells and sarcomas |
Q35201463 | Epigenetic silencing of RNA polymerase I transcription |
Q36299715 | Epigenetically downregulated Semaphorin 3E contributes to gastric cancer |
Q37096807 | Epigenetics and chromatin plasticity in embryonic stem cells |
Q26829156 | Epigenetics and psychostimulant addiction |
Q35021339 | Epigenetics in cancer: implications for early detection and prevention |
Q38941751 | Epigenetics in male reproduction: effect of paternal diet on sperm quality and offspring health |
Q33620204 | Epigenetics in the placenta |
Q38040133 | Epigenetics of psychoactive drugs |
Q39921148 | Epigenome and chromatin structure in human embryonic stem cells undergoing differentiation |
Q38009566 | Epigenomic regulation of bile acid metabolism: emerging role of transcriptional cofactors |
Q34703672 | Epigenomic reprogramming of the developing reproductive tract and disease susceptibility in adulthood |
Q37130888 | Evaluating epigenetic landmarks in the brain of multiple sclerosis patients: a contribution to the current debate on disease pathogenesis |
Q50110257 | Evaluation of Possible Proximate Mechanisms Underlying the Kinship Theory of Intragenomic Conflict in Social Insects |
Q36384014 | Exercise during pregnancy protects adult mouse offspring from diet-induced obesity |
Q21131237 | Exploiting tumor epigenetics to improve oncolytic virotherapy |
Q39434016 | Expression of DNA methyltransferases in breast cancer patients and to analyze the effect of natural compounds on DNA methyltransferases and associated proteins |
Q50765322 | Expression of Sox4 and Sox11 is regulated by multiple mechanisms during retinal development. |
Q40686709 | Expression of foot and mouth disease virus non-structural polypeptide 3ABC induces histone H3 cleavage in BHK21 cells |
Q24535523 | Footprinting of mammalian promoters: use of a CpG DNA methyltransferase revealing nucleosome positions at a single molecule level |
Q91745335 | Force-induced gene up-regulation does not follow the weak power law but depends on H3K9 demethylation |
Q42685039 | Functional analysis of H2B-Lys-123 ubiquitination in regulation of H3-Lys-4 methylation and recruitment of RNA polymerase II at the coding sequences of several active genes in vivo |
Q36410811 | G-CSF-activated STAT3 enhances production of the chemokine MIP-2 in bone marrow neutrophils |
Q95277612 | Generation of Transgenic Cloned Buffalo Embryos Harboring the EGFP Gene in the Y Chromosome Using CRISPR/Cas9-Mediated Targeted Integration |
Q37422466 | Genes related to mitochondrial functions, protein degradation, and chromatin folding are differentially expressed in lymphomonocytes of Rett syndrome patients |
Q37025333 | Genetic and epigenetic alterations in breast cancer: what are the perspectives for clinical practice? |
Q60544121 | Genetic and epigenetic aspects of somaclonal variation: flower colour bud sports in azalea, a case study |
Q38681940 | Genetics and epigenetics of varicocele pathophysiology: an overview |
Q36083462 | Genomic imprinting: cis-acting sequences and regional control |
Q37600561 | Global analysis of transcript and protein levels across the Plasmodium falciparum life cycle |
Q30452353 | Global and specific transcriptional repression by the histone H3 amino terminus in yeast |
Q36124032 | Grape seed proanthocyanidins reactivate silenced tumor suppressor genes in human skin cancer cells by targeting epigenetic regulators |
Q37737514 | HP1: heterochromatin binding proteins working the genome |
Q58114460 | Habitual sleep quality, plasma metabolites and risk of coronary heart disease in post-menopausal women |
Q43890842 | Higher-order structure in pericentric heterochromatin involves a distinct pattern of histone modification and an RNA component |
Q55360907 | Histone Deacetylase-3 Modification of MicroRNA-31 Promotes Cell Proliferation and Aerobic Glycolysis in Breast Cancer and Is Predictive of Poor Prognosis. |
Q43868725 | Histone H1 is phosphorylated in non-replicating and infective forms of Trypanosoma cruzi |
Q82862568 | Histone H3 acetylated at lysine 9 in promoter is associated with low nucleosome density in the vicinity of transcription start site in human cell |
Q28343956 | Histone H3 lysine 4 methylation is mediated by Set1 and required for cell growth and rDNA silencing in Saccharomyces cerevisiae |
Q35577727 | Histone H3K9 modifications are a local chromatin event involved in ethanol-induced neuroadaptation of the NR2B gene |
Q40509434 | Histone H4 hyperacetylation precludes histone H4 lysine 20 trimethylation. |
Q37797706 | Histone Modification Therapy of Cancer |
Q30850198 | Histone acetylation and deacetylation: identification of acetylation and methylation sites of HeLa histone H4 by mass spectrometry |
Q34554335 | Histone acetylation: a switch between repressive and permissive chromatin. Second in review series on chromatin dynamics. |
Q28245651 | Histone acetyltransferase proteins contribute to transcriptional processes at multiple levels |
Q39690407 | Histone deacetylase inhibition suppresses the transforming growth factor beta1-induced epithelial-to-mesenchymal transition in hepatocytes |
Q37118947 | Histone deacetylase inhibitors in lymphoma and solid malignancies |
Q28569252 | Histone deacetylase-2 is a key regulator of diabetes- and transforming growth factor-beta1-induced renal injury |
Q24336747 | Histone demethylation mediated by the nuclear amine oxidase homolog LSD1 |
Q45354425 | Histone gene complement, variant expression, and mRNA processing in a urochordate Oikopleura dioica that undergoes extensive polyploidization |
Q37605090 | Histone hypomethylation is an indicator of epigenetic plasticity in quiescent lymphocytes |
Q46744669 | Histone lysine methylation patterns in human cell types are arranged in distinct three-dimensional nuclear zones |
Q24632499 | Histone methylation regulates memory formation. |
Q28609779 | Histone methyltransferases direct different degrees of methylation to define distinct chromatin domains |
Q34322087 | Histone modification enzymes: novel targets for cancer drugs |
Q35012707 | Histone modifications and alcohol-induced liver disease: are altered nutrients the missing link? |
Q34596416 | Histone modifications in the male germ line of Drosophila |
Q40293973 | Histone modifications silence the GATA transcription factor genes in ovarian cancer |
Q26829142 | Histone regulation in the CNS: basic principles of epigenetic plasticity |
Q35229609 | Histones: at the crossroads of peptide and protein chemistry |
Q28609765 | Hormone-dependent, CARM1-directed, arginine-specific methylation of histone H3 on a steroid-regulated promoter |
Q35075758 | How the ubiquitin-proteasome system controls transcription |
Q64063180 | Increased Extracellular Matrix Protein Production in Chronic Diabetic Complications: Implications of Non-Coding RNAs |
Q34090472 | Influence of sequential guanidinium methylation on the energetics of the guanidinium...guanine dimer and guanidinium...guanine...cytosine trimer: implications for the control of protein...DNA interactions by arginine methyltransferases |
Q54253099 | Influenza A virus nucleoprotein is acetylated by histone acetyltransferases PCAF and GCN5. |
Q39576488 | Inhibition of metastasis-associated gene 1 expression affects proliferation and osteogenic differentiation of immortalized human mesenchymal stem cells |
Q37305070 | Instructing an embryonic stem cell-derived oocyte fate: lessons from endogenous oogenesis |
Q89707294 | Invited Reviews Epigenetics in neurodevelopment |
Q57404742 | Iron-Catalyzed Acylative Dealkylation ofN-Alkylsulfoximines |
Q57568062 | Is the “Histone Code” an Organic Code? |
Q34889102 | Isotype-restricted corepressor recruitment: a constitutively closed helix 12 conformation in retinoic acid receptors beta and gamma interferes with corepressor recruitment and prevents transcriptional repression |
Q27675574 | LSD2/KDM1B and Its Cofactor NPAC/GLYR1 Endow a Structural and Molecular Model for Regulation of H3K4 Demethylation |
Q35838075 | Linking epigenetics to human disease and Rett syndrome: the emerging novel and challenging concepts in MeCP2 research |
Q35670206 | Linking the epigenetic 'language' of covalent histone modifications to cancer |
Q51464359 | Lysine deacetylase inhibition attenuates hypertension and is accompanied by acetylation of mineralocorticoid receptor instead of histone acetylation in spontaneously hypertensive rats. |
Q29615368 | MLL translocations, histone modifications and leukaemia stem-cell development |
Q24541393 | Maintenance of open chromatin and selective genomic occupancy at the cell cycle-regulated histone H4 promoter during differentiation of HL-60 promyelocytic leukemia cells |
Q53570517 | Markers of oxidative stress in obese men with and without hypertension. |
Q33222019 | Mass spectrometric analysis of histone posttranslational modifications |
Q99587019 | Mechanical properties of nucleoprotein complexes determined by nanoindentation spectroscopy |
Q27641462 | Mechanism of multiple lysine methylation by the SET domain enzyme Rubisco LSMT |
Q34688357 | Mechanisms of chromatin assembly and transcription |
Q33810523 | Mechanisms of epigenetic memory |
Q27003300 | Mechanisms of transgenerational inheritance of addictive-like behaviors |
Q37347306 | Menin, histone h3 methyltransferases, and regulation of cell proliferation: current knowledge and perspective |
Q37442063 | Metabolic defects provide a spark for the epigenetic switch in cancer |
Q34037729 | Methods for Activity Analysis of the Proteins that Regulate Histone Methylation |
Q24291436 | Methylation of histone H4 at arginine 3 occurs in vivo and is mediated by the nuclear receptor coactivator PRMT1 |
Q40110203 | Methylation: lost in hydroxylation? |
Q60302688 | MicroRNAs derived from the insect virus HzNV-1 promote lytic infection by suppressing histone methylation |
Q36012679 | Mitochondrial regulation of epigenetics and its role in human diseases |
Q24671073 | Mitotic-specific methylation of histone H4 Lys 20 follows increased PR-Set7 expression and its localization to mitotic chromosomes |
Q36654889 | Modulation of inflammatory cytokines and mitogen-activated protein kinases by acetate in primary astrocytes |
Q33887080 | Molecular cloning and functional characterization of genes associated with flowering in citrus using an early-flowering trifoliate orange (Poncirus trifoliata L. Raf.) mutant |
Q36322196 | Mouse centric and pericentric satellite repeats form distinct functional heterochromatin |
Q39632417 | Mutant Genetic Background Affects the Functional Rearrangement and Kinetic Properties of JMJD2b Histone Demethylase |
Q93079009 | Mutation of the gene encoding the circadian clock component PERIOD2 in oncogenic cells confers chemoresistance by up-regulating the Aldh3a1 gene |
Q38819556 | Mycobacteria modulate host epigenetic machinery by Rv1988 methylation of a non-tail arginine of histone H3. |
Q36449308 | Neural stem cell self-renewal |
Q90101961 | Neuroepigenetic mechanisms underlying fear extinction: emerging concepts |
Q38060713 | Neuroplasticity in addiction: cellular and transcriptional perspectives. |
Q35647685 | Neurotrophin-mediated degradation of histone methyltransferase by S-nitrosylation cascade regulates neuronal differentiation |
Q86816730 | Not low hanging but still sweet: Metabolic proteomes in cardiovascular disease |
Q34029662 | NuRD-mediated deacetylation of H3K27 facilitates recruitment of Polycomb Repressive Complex 2 to direct gene repression |
Q36480533 | Nuclear architecture in the light of gene expression and cell differentiation studies |
Q35217761 | Nuclear microenvironments support physiological control of gene expression |
Q35758130 | Nuclear organisation and subnuclear bodies. |
Q34347197 | Nuclear phosphoproteins HMGA and their relationship with chromatin structure and cancer |
Q28266740 | Nuclear receptor coactivators: the key to unlock chromatin |
Q34621596 | Nuclear receptor-dependent transcription with chromatin. Is it all about enzymes? |
Q37310211 | Nucleoside analogs: molecular mechanisms signaling cell death. |
Q54291064 | Nucleosome Positioning. |
Q34259740 | PLMLA: prediction of lysine methylation and lysine acetylation by combining multiple features |
Q24312030 | PR-Set7 establishes a repressive trans-tail histone code that regulates differentiation |
Q29614513 | Partitioning and plasticity of repressive histone methylation states in mammalian chromatin |
Q37630418 | Pharmacogenetics and pharmacoepigenetics of gemcitabine |
Q45397285 | Physical activity in the prevention of human diseases: role of epigenetic modifications. |
Q38283093 | Polycomb group proteins--epigenetic repressors with emerging roles in melanocytes and melanoma |
Q41161231 | Post-Translational Modifications of Histones in Human Sperm. |
Q34584859 | Post-translational modifications of nucleosomal histones in oligodendrocyte lineage cells in development and disease |
Q40713614 | Postsynthetic trimethylation of histone H4 at lysine 20 in mammalian tissues is associated with aging. |
Q38441683 | Posttranslational Modifications of Chloroplast Proteins: An Emerging Field. |
Q53188659 | Preventing N- and O-formylation of proteins when incubated in concentrated formic acid. |
Q36230208 | Proenkephalin mediates the enduring effects of adolescent cannabis exposure associated with adult opiate vulnerability |
Q37815537 | Prognostic markers for competent human spermatozoa: fertilizing capacity and contribution to the embryo |
Q28829460 | Prostate cancer epigenetics and its clinical implications |
Q33832710 | Protein complex of Drosophila ATRX/XNP and HP1a is required for the formation of pericentric beta-heterochromatin in vivo |
Q41970805 | Proteomic Analysis of a Fraction with Intact Eyespots of Chlamydomonas reinhardtii and Assignment of Protein Methylation |
Q28363122 | Reconstitution of recombinant chromatin establishes a requirement for histone-tail modifications during chromatin assembly and transcription |
Q33885097 | Redox signaling, alkylation (carbonylation) of conserved cysteines inactivates class I histone deacetylases 1, 2, and 3 and antagonizes their transcriptional repressor function |
Q38315887 | Regulation of CD4 T-cell differentiation and inflammation by repressive histone methylation. |
Q42777824 | Regulation of Chromatin Assembly and Cell Transformation by Formaldehyde Exposure in Human Cells |
Q33638415 | Regulation of chromatin structure and function by HMGN proteins |
Q24556492 | Regulation of coactivator complex assembly and function by protein arginine methylation and demethylimination |
Q37189609 | Regulation of demethylation and re-expression of RASSF1A gene in gastric cancer cell lines by combined treatment of 5-Aza-CdR and NaB |
Q92709516 | Regulation of gene expression by altered promoter methylation using a CRISPR/Cas9-mediated epigenetic editing system |
Q53627307 | Repression of Biotin-Related Proteins by Benzo[a]Pyrene-Induced Epigenetic Modifications in Human Bronchial Epithelial Cells. |
Q44679410 | Resetting the histone code at CDKN2A in HNSCC by inhibition of DNA methylation |
Q37175201 | Response of SMRT (silencing mediator of retinoic acid and thyroid hormone receptor) and N-CoR (nuclear receptor corepressor) corepressors to mitogen-activated protein kinase kinase kinase cascades is determined by alternative mRNA splicing |
Q36459959 | Role of DNA methyltransferases in regulation of human ribosomal RNA gene transcription |
Q34712569 | Role of nucleosomal occupancy in the epigenetic silencing of the MLH1 CpG island. |
Q92542928 | Roles for Non-coding RNAs in Spatial Genome Organization |
Q30440069 | SMRT and N-CoR corepressors are regulated by distinct kinase signaling pathways |
Q37294669 | Selenite reactivates silenced genes by modifying DNA methylation and histones in prostate cancer cells |
Q24537640 | Set2 is a nucleosomal histone H3-selective methyltransferase that mediates transcriptional repression. |
Q41673156 | Simultaneous transcriptome analysis of Colletotrichum gloeosporioides and tomato fruit pathosystem reveals novel fungal pathogenicity and fruit defense strategies |
Q35266388 | Single-stranded noncoding RNAs mediate local epigenetic alterations at gene promoters in rat cell lines. |
Q44012132 | Site-specific loss of acetylation upon phosphorylation of histone H3. |
Q90683560 | Skin wound healing triggers epigenetic modifications of histone H4 |
Q41848329 | Small-molecule inhibition of MLL activity by disruption of its interaction with WDR5 |
Q37306191 | Smyd1b is required for skeletal and cardiac muscle function in zebrafish |
Q35740604 | Smyd2 controls cytoplasmic lysine methylation of Hsp90 and myofilament organization |
Q48238395 | Somatic mutations in murine models of leukemia and lymphoma: Disease specificity and clinical relevance. |
Q34230157 | Spatial organization of gene expression: the active chromatin hub. |
Q30307942 | Specificity of the HP1 chromo domain for the methylated N-terminus of histone H3. |
Q26862533 | Sperm nuclear proteome and its epigenetic potential |
Q38958761 | Stable isotope dimethyl labelling for quantitative proteomics and beyond. |
Q34463095 | Stable transmission of reversible modifications: maintenance of epigenetic information through the cell cycle |
Q34531990 | Step out of the groove: epigenetic gene control systems and engineered transcription factors |
Q38443809 | Stepping inside the realm of epigenetic modifiers. |
Q56654756 | Stress related epigenetic changes may explain opportunistic success in biological invasions in Antipode mussels |
Q27658848 | Structural Basis for Acetylated Histone H4 Recognition by the Human BRD2 Bromodomain |
Q33803135 | Structure and epigenetics of nucleoli in comparison with non-nucleolar compartments |
Q27704244 | Substituted 2-(2-aminopyrimidin-4-yl)pyridine-4-carboxylates as potent inhibitors of JumonjiC domain-containing histone demethylases |
Q40390762 | Supramolecular Ligands for Histone Tails by Employing a Multivalent Display of Trisulfonated Calix[4]arenes. |
Q46705645 | Surrogate alcohols and their metabolites modify histone H3 acetylation: involvement of histone acetyl transferase and histone deacetylase |
Q34280124 | Synergy among nuclear receptor coactivators: selective requirement for protein methyltransferase and acetyltransferase activities |
Q50111962 | T(H) cell differentiation is accompanied by dynamic changes in histone acetylation of cytokine genes |
Q37880676 | TGF-β signal transduction spreading to a wider field: a broad variety of mechanisms for context-dependent effects of TGF-β. |
Q38212160 | Targeted therapy of epigenomic regulatory mechanisms controlling the epithelial to mesenchymal transition during tumor progression. |
Q38290243 | Targeting chromatin to improve radiation response |
Q36515754 | The Caenorhabditis elegans ekl (enhancer of ksr-1 lethality) genes include putative components of a germline small RNA pathway |
Q26746703 | The Impact of External Factors on the Epigenome: In Utero and over Lifetime |
Q35730122 | The cloning and characterization of the histone acetyltransferase human homolog Dmel\TIP60 in Drosophila melanogaster: Dmel\TIP60 is essential for multicellular development |
Q35023253 | The effect of N-acetylation and N-methylation of lysine residue of Tat peptide on its interaction with HIV-1 TAR RNA. |
Q37594007 | The emerging therapeutic potential of histone methyltransferase and demethylase inhibitors |
Q24624411 | The epigenetic landscape of addiction |
Q38823331 | The expanding footprint of CRISPR/Cas9 in the plant sciences |
Q37120599 | The glial or neuronal fate choice of oligodendrocyte progenitors is modulated by their ability to acquire an epigenetic memory |
Q24796904 | The histone deacetylase inhibitor Trichostatin A modulates CD4+ T cell responses |
Q37480775 | The histone demethylase Dmel\Kdm4A controls genes required for life span and male-specific sex determination in Drosophila |
Q28207378 | The human beta-globin locus control region |
Q27931919 | The identification of protein-protein interactions of the nuclear pore complex of Saccharomyces cerevisiae using high throughput matrix-assisted laser desorption ionization time-of-flight tandem mass spectrometry |
Q34688382 | The many faces of histone lysine methylation |
Q33947040 | The maternal effect gene, abnormal oocyte (abo), of Drosophila melanogaster encodes a specific negative regulator of histones |
Q28508771 | The nucleolar remodeling complex NoRC mediates heterochromatin formation and silencing of ribosomal gene transcription |
Q34363968 | The rest is silence. |
Q35133494 | The synthesis and evaluation of N1-(4-(2-[18F]-fluoroethyl)phenyl)-N8-hydroxyoctanediamide ([18F]-FESAHA), a PET radiotracer designed for the delineation of histone deacetylase expression in cancer. |
Q24564544 | Tissue-specific and imprinted epigenetic modifications of the human NDN gene |
Q44324363 | Transcriptional activation of the enterocyte differentiation marker intestinal alkaline phosphatase is associated with changes in the acetylation state of histone H3 at a specific site within its promoter region in vitro |
Q35625721 | Transcriptional regulation: a genomic overview |
Q27000542 | Trials with 'epigenetic' drugs: an update |
Q33662557 | Trichostatin A and 5-azacytidine both cause an increase in global histone H4 acetylation and a decrease in global DNA and H3K9 methylation during mitosis in maize. |
Q42443365 | Trichostatin A and structurally related histone deacetylase inhibitors induce 5-lipoxygenase promoter activity |
Q36916497 | Two essential MYST-family proteins display distinct roles in histone H4K10 acetylation and telomeric silencing in trypanosomes. |
Q89454193 | Two faces of bivalent domain regulate VEGFA responsiveness and angiogenesis |
Q42222766 | Ubp8p, a histone deubiquitinase whose association with SAGA is mediated by Sgf11p, differentially regulates lysine 4 methylation of histone H3 in vivo |
Q43154267 | Unraveling the histone's potential: a proteomics perspective |
Q37122090 | Unravelling the hidden DNA structural/physical code provides novel insights on promoter location |
Q33321264 | VILIP-1 downregulation in non-small cell lung carcinomas: mechanisms and prediction of survival |
Q35862781 | Valproic acid improves the in vitro development competence of bovine somatic cell nuclear transfer embryos |
Search more.