| 1 | Pseudouridine guides germline small RNA transport and epigenetic inheritance | 5.9 | 24 | Citations (PDF) |
| 2 | PhOxi-seq Detects Enzyme-Dependent m
2
G in Multiple RNA Types | 2.5 | 1 | Citations (PDF) |
| 3 | THUMPD3 regulates alternative splicing of ECM transcripts in human lung cancer cells and promotes proliferation and migration | 1.5 | 4 | Citations (PDF) |
| 4 | Predicting genes associated with RNA methylation pathways using machine learning | 3.1 | 12 | Citations (PDF) |
| 5 | Small-molecule inhibition of METTL3 as a strategy against myeloid leukaemia | 31.3 | 1,293 | Citations (PDF) |
| 6 | Identification of SARS-CoV-2–induced pathways reveals drug repurposing strategies | 8.2 | 52 | Citations (PDF) |
| 7 | Targeting the m6A RNA modification pathway blocks SARS-CoV-2 and HCoV-OC43 replication | 2.9 | 142 | Citations (PDF) |
| 8 | Methylation of histone H3 at lysine 37 by Set1 and Set2 prevents spurious DNA replication | 8.7 | 29 | Citations (PDF) |
| 9 | RNA modifications detection by comparative Nanopore direct RNA sequencing | 11.0 | 420 | Citations (PDF) |
| 10 | Further Evidence Supporting N7-Methylation of Guanosine (m7G) in Human MicroRNAs | 8.7 | 24 | Citations (PDF) |
| 11 | Role of RNA modifications in cancer | 33.8 | 1,215 | Citations (PDF) |
| 12 | A computational platform for high-throughput analysis of RNA sequences and modifications by mass spectrometry | 11.0 | 96 | Citations (PDF) |
| 13 | RNA-modifying enzymes and their function in a chromatin context | 5.9 | 34 | Citations (PDF) |
| 14 | Interaction of Sox2 with RNA binding proteins in mouse embryonic stem cells | 2.1 | 12 | Citations (PDF) |
| 15 | METTL1 Promotes let-7 MicroRNA Processing via m7G Methylation | 8.7 | 459 | Citations (PDF) |
| 16 | Citrullination of HP1γ chromodomain affects association with chromatin | 2.2 | 23 | Citations (PDF) |
| 17 | SRPK1 maintains acute myeloid leukemia through effects on isoform usage of epigenetic regulators including BRD4 | 11.0 | 75 | Citations (PDF) |
| 18 | Phosphorylation of Histone H4T80 Triggers DNA Damage Checkpoint Recovery | 8.7 | 29 | Citations (PDF) |
| 19 | DDX3XRNAhelicase affects breast cancer cell cycle progression by regulating expression ofKLF4 | 1.8 | 44 | Citations (PDF) |
| 20 | Inhibition of the acetyltransferase NAT10 normalizes progeric and aging cells by rebalancing the Transportin-1 nuclear import pathway | 3.9 | 104 | Citations (PDF) |
| 21 | Genomic positional conservation identifies topological anchor point RNAs linked to developmental loci | 4.8 | 131 | Citations (PDF) |
| 22 | RNA Binding by Histone Methyltransferases Set1 and Set2 | 1.5 | 37 | Citations (PDF) |
| 23 | Promoter-bound METTL3 maintains myeloid leukaemia by m6A-dependent translation control | 31.3 | 1,107 | Citations (PDF) |
| 24 | A Chemical Probe for the ATAD2 Bromodomain | 0.9 | 10 | Citations (PDF) |
| 25 | A Chemical Probe for the ATAD2 Bromodomain | 11.7 | 74 | Citations (PDF) |
| 26 | Functional interdependence of BRD4 and DOT1L in MLL leukemia | 5.9 | 107 | Citations (PDF) |
| 27 | Discovery of I-BRD9, a Selective Cell Active Chemical Probe for Bromodomain Containing Protein 9 Inhibition | 4.7 | 231 | Citations (PDF) |
| 28 | Post transcriptional control of the epigenetic stem cell regulator PLZF by sirtuin and HDAC deacetylases | 2.2 | 14 | Citations (PDF) |
| 29 | BET inhibitor resistance emerges from leukaemia stem cells | 31.3 | 529 | Citations (PDF) |
| 30 | Generation of a Selective Small Molecule Inhibitor of the CBP/p300 Bromodomain for Leukemia Therapy | 4.2 | 231 | Citations (PDF) |
| 31 | The Breast Cancer Oncogene EMSY Represses Transcription of Antimetastatic microRNA miR-31 | 8.7 | 60 | Citations (PDF) |
| 32 | Citrullination regulates pluripotency and histone H1 binding to chromatin | 31.3 | 420 | Citations (PDF) |
| 33 | Up‐regulation of the interferon‐related genes in BRCA2 knockout epithelial cells | 3.2 | 31 | Citations (PDF) |
| 34 | Histone core modifications regulating nucleosome structure and dynamics | 68.4 | 967 | Citations (PDF) |
| 35 | S6 Kinase 2 Is Bound to Chromatin‐Nuclear Matrix Cellular Fractions and Is Able to Phosphorylate Histone H3 at Threonine 45 In Vitro and In Vivo | 1.9 | 15 | Citations (PDF) |
| 36 | The non-coding snRNA 7SKcontrols transcriptional termination, poising, and bidirectionality in embryonic stem cells | 4.8 | 54 | Citations (PDF) |
| 37 | Glutamine methylation in histone H2A is an RNA-polymerase-I-dedicated modification | 31.3 | 228 | Citations (PDF) |
| 38 | BET protein inhibition shows efficacy against JAK2V617F-driven neoplasms | 3.6 | 76 | Citations (PDF) |
| 39 | Human RNA Methyltransferase BCDIN3D Regulates MicroRNA Processing | 23.8 | 148 | Citations (PDF) |
| 40 | The PHD and Chromo Domains Regulate the ATPase Activity of the Human Chromatin Remodeler CHD4 | 3.0 | 79 | Citations (PDF) |
| 41 | Cancer Epigenetics: From Mechanism to Therapy | 23.8 | 3,029 | Citations (PDF) |
| 42 | Targeting Epigenetic Readers in Cancer | 19.4 | 387 | Citations (PDF) |
| 43 | ALKBH1 is a Histone H2A Dioxygenase Involved in Neural Differentiation | 2.7 | 113 | Citations (PDF) |
| 44 | The S. pombe Histone H2A Dioxygenase Ofd2 Regulates Gene Expression during Hypoxia | 1.5 | 11 | Citations (PDF) |
| 45 | Inhibition of BET recruitment to chromatin as an effective treatment for MLL-fusion leukaemia | 31.3 | 1,497 | Citations (PDF) |
| 46 | Regulation of chromatin by histone modifications | 10.2 | 5,708 | Citations (PDF) |
| 47 | Histone H3 lysine 4 methylation is associated with the transcriptional reprogramming efficiency of somatic nuclei by oocytes | 2.2 | 40 | Citations (PDF) |
| 48 | A chromodomain switch mediated by histone H3 Lys 4 acetylation regulates heterochromatin assembly | 2.9 | 90 | Citations (PDF) |
| 49 | Nucleosome-Interacting Proteins Regulated by DNA and Histone Methylation | 23.8 | 586 | Citations (PDF) |
| 50 | LIF-independent JAK signalling to chromatin in embryonic stem cells uncovered from an adult stem cell disease | 12.8 | 131 | Citations (PDF) |
| 51 | Phosphorylation of Histone H3 Thr-45 Is Linked to Apoptosis | 1.3 | 105 | Citations (PDF) |
| 52 | JAK2 phosphorylates histone H3Y41 and excludes HP1α from chromatin | 31.3 | 603 | Citations (PDF) |
| 53 | An operational definition of epigenetics: Figure 1. | 2.9 | 1,737 | Citations (PDF) |
| 54 | Distinct transcriptional outputs associated with mono- and dimethylated histone H3 arginine 2 | 5.9 | 55 | Citations (PDF) |
| 55 | Heritable Gene Repression through the Action of a Directed DNA Methyltransferase at a Chromosomal Locus | 1.3 | 37 | Citations (PDF) |
| 56 | Histone H3 tail clipping regulates gene expression | 5.9 | 151 | Citations (PDF) |
| 57 | Regulation of Histone H3 Lysine 56 Acetylation in Schizosaccharomyces pombe | 1.3 | 73 | Citations (PDF) |
| 58 | Chromatin Modifications and Their Function | 23.8 | 10,177 | Citations (PDF) |
| 59 | SnapShot: Histone-Modifying EnzymesCell, 2007, 128, 802.e1-802.e2 | 23.8 | 76 | Citations (PDF) |
| 60 | SnapShot: Histone-Modifying EnzymesCell, 2007, 131, 822-822.e1 | 23.8 | 143 | Citations (PDF) |
| 61 | Histone arginine methylation regulates pluripotency in the early mouse embryo | 31.3 | 583 | Citations (PDF) |
| 62 | Arginine methylation at histone H3R2 controls deposition of H3K4 trimethylation | 31.3 | 344 | Citations (PDF) |
| 63 | Genome-Wide Studies of Histone Demethylation Catalysed by the Fission Yeast Homologues of Mammalian LSD1 | 1.5 | 45 | Citations (PDF) |
| 64 | Directed De Novo DNA Methylation of a Genomic Locus Leads to Heritable Transcriptional Repression.Blood, 2007, 110, 343-343 | 3.6 | 0 | Citations (PDF) |
| 65 | Proline Isomerization of Histone H3 Regulates Lysine Methylation and Gene Expression | 23.8 | 283 | Citations (PDF) |
| 66 | Blimp1 associates with Prmt5 and directs histone arginine methylation in mouse germ cells | 12.8 | 438 | Citations (PDF) |
| 67 | Differential expression of selected histone modifier genes in human solid cancers | 2.1 | 219 | Citations (PDF) |
| 68 | p300 is required for orderly G1/S transition in human cancer cells | 5.2 | 54 | Citations (PDF) |
| 69 | Viral oncoproteins target the DNA methyltransferases | 5.2 | 270 | Citations (PDF) |
| 70 | Myc represses transcription through recruitment of DNA methyltransferase corepressor | 5.2 | 402 | Citations (PDF) |
| 71 | Binding of EMSY to HP1β: implications for recruitment of HP1β and BS69 | 3.5 | 31 | Citations (PDF) |
| 72 | Reversing histone methylation | 31.3 | 462 | Citations (PDF) |
| 73 | Spatial Distribution of Di- and Tri-methyl Lysine 36 of Histone H3 at Active Genes | 1.3 | 420 | Citations (PDF) |
| 74 | Human but Not Yeast CHD1 Binds Directly and Selectively to Histone H3 Methylated at Lysine 4 via Its Tandem Chromodomains | 1.3 | 365 | Citations (PDF) |
| 75 | Crystal Structure of the ENT Domain of Human EMSY | 3.0 | 24 | Citations (PDF) |
| 76 | Methylation of H3 Lysine 4 at Euchromatin Promotes Sir3p Association with Heterochromatin | 1.3 | 108 | Citations (PDF) |
| 77 | Direct Binding of INHAT to H3 Tails Disrupted by Modifications | 1.3 | 77 | Citations (PDF) |
| 78 | Histone Deimination Antagonizes Arginine Methylation | 23.8 | 792 | Citations (PDF) |
| 79 | Methylation of Histone H4 Lysine 20 Controls Recruitment of Crb2 to Sites of DNA Damage | 23.8 | 524 | Citations (PDF) |
| 80 | The Tudor domain ‘Royal Family’: Tudor, plant Agenet, Chromo, PWWP and MBT domains | 7.4 | 469 | Citations (PDF) |
| 81 | EMSY Links the BRCA2 Pathway to Sporadic Breast and Ovarian Cancer | 23.8 | 406 | Citations (PDF) |
| 82 | Methylation of Histone H3 K4 Mediates Association of the Isw1p ATPase with Chromatin | 8.7 | 260 | Citations (PDF) |
| 83 | A Novel Human Ada2 Homologue Functions with Gcn5 or Brg1 To Coactivate Transcription | 1.5 | 62 | Citations (PDF) |
| 84 | Mechanisms of P/CAF auto-acetylation | 11.2 | 94 | Citations (PDF) |
| 85 | The Methyl-CpG-binding Protein MeCP2 Links DNA Methylation to Histone Methylation | 1.3 | 919 | Citations (PDF) |
| 86 | Consequences of the depletion of zygotic and embryonic enhancer of zeste 2 during preimplantation mouse development | 2.0 | 308 | Citations (PDF) |
| 87 | The DNA methyltransferases associate with HP1 and the SUV39H1 histone methyltransferase | 11.2 | 669 | Citations (PDF) |
| 88 | Histone H3 lysine 4 methylation patterns in higher eukaryotic genes | 12.8 | 718 | Citations (PDF) |
| 89 | Dnmt3L is a transcriptional repressor that recruits histone deacetylase | 11.2 | 184 | Citations (PDF) |
| 90 | Acetylation of β-Catenin by CREB-binding Protein (CBP) | 1.3 | 177 | Citations (PDF) |
| 91 | Histone H3 Lysine 4 Methylation Disrupts Binding of Nucleosome Remodeling and Deacetylase (NuRD) Repressor Complex | 1.3 | 220 | Citations (PDF) |
| 92 | Mutation analysis of CBP and PCAF reveals rare inactivating mutations in cancer cell lines but not in primary tumours | 4.2 | 62 | Citations (PDF) |
| 93 | Methylation of histone H3 Lys 4 in coding regions of active genes | 5.3 | 711 | Citations (PDF) |
| 94 | Methylation at arginine 17 of histone H3 is linked to gene activation | 3.5 | 302 | Citations (PDF) |
| 95 | Histone Methylation | 23.8 | 505 | Citations (PDF) |
| 96 | Histone methylation in transcriptional control | 2.4 | 863 | Citations (PDF) |
| 97 | DNA methyltransferases get connected to chromatin | 7.6 | 142 | Citations (PDF) |
| 98 | cis-Acting DNA from Fission Yeast Centromeres Mediates Histone H3 Methylation and Recruitment of Silencing Factors and Cohesin to an Ectopic Site | 2.5 | 174 | Citations (PDF) |
| 99 | Crosstalk between CARM1 Methylation and CBP Acetylation on Histone H3 | 2.5 | 276 | Citations (PDF) |
| 100 | Active genes are tri-methylated at K4 of histone H3 | 31.3 | 2,023 | Citations (PDF) |
| 101 | Structure of the HP1 chromodomain bound to histone H3 methylated at lysine 9 | 31.3 | 639 | Citations (PDF) |
| 102 | Human SIR2 deacetylates p53 and antagonizes PML/p53-induced cellular senescence | 5.2 | 795 | Citations (PDF) |
| 103 | The SUMO E3 ligase RanBP2 promotes modification of the HDAC4 deacetylase | 5.2 | 297 | Citations (PDF) |
| 104 | MCM3AP, a novel acetyltransferase that acetylates replication protein MCM3 | 3.5 | 85 | Citations (PDF) |
| 105 | Dnmt3a binds deacetylases and is recruited by a sequence-specific repressor to silence transcription | 5.2 | 516 | Citations (PDF) |
| 106 | High-Throughput Screening for Identification of Small Molecule Inhibitors of Histone Acetyltransferases Using Scintillating Microplates (FlashPlate) | 2.0 | 44 | Citations (PDF) |
| 107 | Selective recognition of methylated lysine 9 on histone H3 by the HP1 chromo domain | 31.3 | 2,770 | Citations (PDF) |
| 108 | Rb targets histone H3 methylation and HP1 to promoters | 31.3 | 860 | Citations (PDF) |
| 109 | Temporal Recruitment of the mSin3A-Histone Deacetylase Corepressor Complex to the ETS Domain Transcription Factor Elk-1 | 1.5 | 127 | Citations (PDF) |
| 110 | Differential localization of HDAC4 orchestrates muscle differentiation | 11.2 | 122 | Citations (PDF) |
| 111 | DNA methyltransferase Dnmt1 associates with histone deacetylase activity | 14.1 | 932 | Citations (PDF) |
| 112 | Mutations truncating the EP300 acetylase in human cancers | 14.1 | 571 | Citations (PDF) |
| 113 | Regulation of E2F1 activity by acetylation | 5.2 | 664 | Citations (PDF) |
| 114 | Acetylation: a regulatory modification to rival phosphorylation? | 5.2 | 1,091 | Citations (PDF) |
| 115 | The Human Cytomegalovirus 86-Kilodalton Major Immediate-Early Protein Interacts Physically and Functionally with Histone Acetyltransferase P/CAF | 2.4 | 59 | Citations (PDF) |
| 116 | The Co-repressor mSin3A Is a Functional Component of the REST-CoREST Repressor Complex | 1.3 | 220 | Citations (PDF) |
| 117 | Acetylation of importin-α nuclear import factors by CBP/p300 | 2.5 | 180 | Citations (PDF) |
| 118 | Nuclear receptor corepressors partner with class II histone deacetylases in a Sin3-independent repression pathway | 2.9 | 291 | Citations (PDF) |
| 119 | Residues phosphorylated by TFIIH are required for E2F-1 degradation during S-phase | 5.2 | 59 | Citations (PDF) |
| 120 | The E7 oncoprotein associates with Mi2 and histone deacetylase activity to promote cell growth | 5.2 | 307 | Citations (PDF) |
| 121 | Retinoblastoma protein meets chromatin | 7.4 | 138 | Citations (PDF) |
| 122 | Histone acetylases and deacetylases in cell proliferation | 2.4 | 584 | Citations (PDF) |
| 123 | CBP/p300 Integrates Raf/Rac-Signaling Pathways in the Transcriptional Induction of NF-ATc during T Cell Activation | 16.6 | 98 | Citations (PDF) |
| 124 | MEF-2 function is modified by a novel co-repressor, MITR | 5.2 | 187 | Citations (PDF) |
| 125 | HDAC4 deacetylase associates with and represses the MEF2 transcription factor | 5.2 | 531 | Citations (PDF) |
| 126 | Characterization of an E1A-CBP Interaction Defines a Novel Transcriptional Adapter Motif (TRAM) in CBP/p300 | 2.4 | 72 | Citations (PDF) |
| 127 | Epstein-Barr Virus Nuclear Antigen 3C Interacts with Histone Deacetylase To Repress Transcription | 2.4 | 140 | Citations (PDF) |
| 128 | Title is missing! | 2.1 | 147 | Citations (PDF) |
| 129 | The acetyltransferase activity of CBP stimulates transcription | 5.2 | 244 | Citations (PDF) |
| 130 | E1A directly binds and regulates the P/CAF acetyltransferase | 5.2 | 115 | Citations (PDF) |
| 131 | Retinoblastoma protein recruits histone deacetylase to repress transcription | 31.3 | 1,209 | Citations (PDF) |
| 132 | Modulation of Fos-mediated AP-1 transcription by the promyelocytic leukemia protein | 5.2 | 49 | Citations (PDF) |
| 133 | Transcription Factors and Cell Differentiation20th Annual Symposium, Burnham Institute, La Jolla, CA, USA, 22 May 1998 | 5.8 | 1 | Citations (PDF) |
| 134 | E2F1-induced apoptosis requires DNA binding but not transactivation and is inhibited by the retinoblastoma protein through direct interaction. | 2.9 | 257 | Citations (PDF) |
| 135 | Transcriptional Repression by the Promyelocytic Leukemia Protein, PML | 2.1 | 45 | Citations (PDF) |
| 136 | RB and hbrm cooperate to repress the activation functions of E2F1 | 5.3 | 286 | Citations (PDF) |
| 137 | The HMG-box transcription factor HBP1 is targeted by the pocket proteins and E1A | 5.2 | 62 | Citations (PDF) |
| 138 | CBP/p300 as a co-factor for the Microphthalmia transcription factor | 5.2 | 183 | Citations (PDF) |
| 139 | An E2F-like repressor of transcription | 31.3 | 118 | Citations (PDF) |
| 140 | Transcriptional activation functions in BRCA2 | 31.3 | 198 | Citations (PDF) |
| 141 | Mechanistic analysis of RNA polymerase III regulation by the retinoblastoma protein | 5.2 | 96 | Citations (PDF) |
| 142 | The TAFII250 Subunit of TFIID Has Histone Acetyltransferase ActivityCell, 1996, 87, 1261-1270 | 23.8 | 692 | Citations (PDF) |
| 143 | E2F1 and E1A(12S) have a homologous activation domain regulated by RB and CBP. | 5.3 | 100 | Citations (PDF) |
| 144 | Repression of RNA polymerase III transcription by the retinoblastoma protein | 31.3 | 207 | Citations (PDF) |
| 145 | The CBP co-activator is a histone acetyltransferase | 31.3 | 1,736 | Citations (PDF) |
| 146 | The CBP co-activator stimulates E2F1/DP1 activity | 11.2 | 108 | Citations (PDF) |
| 147 | Functions of pRb and p53: what's the connection? | 14.2 | 20 | Citations (PDF) |
| 148 | Stimulation of E2F1/DP1 transcriptional activity by MDM2 oncoprotein | 31.3 | 470 | Citations (PDF) |
| 149 | Transcriptional control by the retinoblastoma protein | 10.7 | 64 | Citations (PDF) |
| 150 | An inhibitor domain in c-Fos regulates activation domains containing the HOB1 motif. | 5.2 | 41 | Citations (PDF) |
| 151 | CBP-induced stimulation of c-Fos activity is abrogated by E1A. | 5.2 | 316 | Citations (PDF) |
| 152 | Functional interaction between the HCMV IE2 transactivator and the retinoblastoma protein. | 5.2 | 157 | Citations (PDF) |
| 153 | Evidence for a protein domain superfamily shared by the cyclins, TFIIB and RB/p107 | 11.2 | 74 | Citations (PDF) |
| 154 | Phosphorylation of the c-Fos and c-Jun HOB1 motif stimulates its activation capacity | 11.2 | 35 | Citations (PDF) |
| 155 | c-Fos-Induced Activation of a TATA-Box-Containing Promoter Involves Direct Contact with TATA-Box-Binding Protein | 1.5 | 40 | Citations (PDF) |
| 156 | Transcriptional regulation by the retinoblastoma protein | 14.2 | 19 | Citations (PDF) |
| 157 | The activation domain of transcription factor PU.1 binds the retinoblastoma (RB) protein and the transcription factor TFIID in vitro: RB shows sequence similarity to TFIID and TFIIB. | 5.3 | 318 | Citations (PDF) |
| 158 | c-Jun is phosphorylated by the DNA-dependent protein kinasein vitro; definition of the minimal kinase recognition motif | 11.2 | 113 | Citations (PDF) |
| 159 | The retinoblastoma protein binds E2F residues required for activation in vivo and TBP bindingin vitro | 11.2 | 142 | Citations (PDF) |
| 160 | The human cytomegalovirus 86K immediate early (IE) 2 protein requires the basic region of the TATA-box binding protein (TBP) for binding, and interacts with TBP and transcription factor TFIIB via regions of IE2 required for transcriptional regulation | 1.9 | 162 | Citations (PDF) |
| 161 | Basic peptides enhance protein/ DNA interactionin vitro | 11.2 | 18 | Citations (PDF) |
| 162 | Conserved motifs in Fos and Jun define a new class of activation domain. | 2.9 | 118 | Citations (PDF) |
| 163 | The human cytomegalovirus 80-kilodalton but not the 72-kilodalton immediate-early protein transactivates heterologous promoters in a TATA box-dependent mechanism and interacts directly with TFIID | 2.4 | 229 | Citations (PDF) |
| 164 | Epstein-Barr virus BZLF1 trans-activator specifically binds to a consensus AP-1 site and is related to c-fos. | 5.2 | 309 | Citations (PDF) |
| 165 | Leucine zippers of fos, jun and GCN4 dictate dimerization specificity and thereby control DNA binding | 31.3 | 291 | Citations (PDF) |
| 166 | The role of the leucine zipper in the fos–jun interaction | 31.3 | 862 | Citations (PDF) |
| 167 | Sexist ads | 31.3 | 1 | Citations (PDF) |
| 168 | A lncRNA fine tunes the dynamics of a cell state transition involving Lin28, let-7 and de novo DNA methylation | 1.0 | 46 | Citations (PDF) |
| 169 | Title is missing! 0 | | 2 | Citations (PDF) |
| 170 | Histone methylation defines epigenetic asymmetry in the mouse zygote | 1.1 | 6 | Citations (PDF) |
