| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/IUB.1264 |
| P8608 | Fatcat ID | release_gcnq7mz5hbf2bkygdkcccnz3si |
| P3181 | OpenCitations bibliographic resource ID | 2049140 |
| P698 | PubMed publication ID | 24706538 |
| P5875 | ResearchGate publication ID | 261409269 |
| P2093 | author name string | Sriharsa Pradhan | |
| Guoqiang Zhang | |||
| P2860 | cites work | Biochemical analysis of histone deacetylase-independent transcriptional repression by MeCP2 | Q36666196 |
| CpG island density and its correlations with genomic features in mammalian genomes | Q36739399 | ||
| DNA methylation and transcriptional noise | Q36811567 | ||
| Co-mutation of histone H2AX S139A with Y142A rescues Y142A-induced ionising radiation sensitivity. | Q36917479 | ||
| Non-CpG methylation is prevalent in embryonic stem cells and may be mediated by DNA methyltransferase 3a. | Q36967574 | ||
| Arginine methylation at a glance | Q37023403 | ||
| DNA methylation presents distinct binding sites for human transcription factors | Q37145633 | ||
| Ten-eleven translocation (Tet) and thymine DNA glycosylase (TDG), components of the demethylation pathway, are direct targets of miRNA-29a | Q37157046 | ||
| Alteration of genic 5-hydroxymethylcytosine patterning in olfactory neurons correlates with changes in gene expression and cell identity | Q37157267 | ||
| DNA hypomethylation restricted to the murine forebrain induces cortical degeneration and impairs postnatal neuronal maturation | Q37252738 | ||
| Charting a dynamic DNA methylation landscape of the human genome | Q37292011 | ||
| Analysis of skewed X-chromosome inactivation in females with rheumatoid arthritis and autoimmune thyroid diseases | Q37350872 | ||
| H4K16 acetylation marks active genes and enhancers of embryonic stem cells, but does not alter chromatin compaction | Q37358012 | ||
| DNMT1-interacting RNAs block gene-specific DNA methylation | Q37408576 | ||
| CRM1 mediates nuclear-cytoplasmic shuttling of mature microRNAs. | Q37454774 | ||
| Histone H3K27 trimethylation inhibits H3 binding and function of SET1-like H3K4 methyltransferase complexes | Q37469434 | ||
| Signals and combinatorial functions of histone modifications | Q37870190 | ||
| Active DNA demethylation by Gadd45 and DNA repair | Q37984958 | ||
| DNA methylation dynamics during the mammalian life cycle | Q38061120 | ||
| Histone H2A mono-ubiquitination is a crucial step to mediate PRC1-dependent repression of developmental genes to maintain ES cell identity | Q38323091 | ||
| A six months exercise intervention influences the genome-wide DNA methylation pattern in human adipose tissue | Q21563356 | ||
| DNA methyltransferases Dnmt3a and Dnmt3b are essential for de novo methylation and mammalian development | Q22010765 | ||
| Translating the Histone Code | Q22065840 | ||
| Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2 | Q22337290 | ||
| JMJD6 is a histone arginine demethylase | Q24298169 | ||
| Reduced histone biotinylation in multiple carboxylase deficiency patients: a nuclear role for holocarboxylase synthetase | Q24299635 | ||
| Hydroxylation of 5-methylcytosine by TET1 promotes active DNA demethylation in the adult brain | Q24299862 | ||
| Methyl-CpG binding domain 1 (MBD1) interacts with the Suv39h1-HP1 heterochromatic complex for DNA methylation-based transcriptional repression | Q24300386 | ||
| Histone H3 lysine 56 methylation regulates DNA replication through its interaction with PCNA | Q24306661 | ||
| WSTF regulates the H2A.X DNA damage response via a novel tyrosine kinase activity | Q24309061 | ||
| Regulation of MBD1-mediated transcriptional repression by SUMO and PIAS proteins | Q24309409 | ||
| YY1 tethers Xist RNA to the inactive X nucleation center | Q24311256 | ||
| Repression of p53 activity by Smyd2-mediated methylation | Q24315991 | ||
| Conversion of 5-methylcytosine to 5-hydroxymethylcytosine in mammalian DNA by MLL partner TET1 | Q24316558 | ||
| Importin 8 is a gene silencing factor that targets argonaute proteins to distinct mRNAs | Q24321397 | ||
| UHRF1 plays a role in maintaining DNA methylation in mammalian cells | Q24336152 | ||
| Methylation of SUV39H1 by SET7/9 results in heterochromatin relaxation and genome instability | Q24336910 | ||
| Co-operation and communication between the human maintenance and de novo DNA (cytosine-5) methyltransferases | Q24534264 | ||
| The replication focus targeting sequence (RFTS) domain is a DNA-competitive inhibitor of Dnmt1 | Q24606880 | ||
| EZH1 and EZH2 cogovern histone H3K27 trimethylation and are essential for hair follicle homeostasis and wound repair | Q24608279 | ||
| Tet proteins can convert 5-methylcytosine to 5-formylcytosine and 5-carboxylcytosine | Q24614582 | ||
| Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss | Q24630545 | ||
| Tet-mediated formation of 5-carboxylcytosine and its excision by TDG in mammalian DNA | Q24632387 | ||
| Association of UHRF1 with methylated H3K9 directs the maintenance of DNA methylation | Q36381487 | ||
| Genome-wide aberrant DNA methylation of microRNA host genes in hepatocellular carcinoma | Q36402751 | ||
| MBD2 and multiple domains of CHD4 are required for transcriptional repression by Mi-2/NuRD complexes | Q36435178 | ||
| Crx activates opsin transcription by recruiting HAT-containing co-activators and promoting histone acetylation | Q36512977 | ||
| Crosstalk between SET7/9-dependent methylation and ARTD1-mediated ADP-ribosylation of histone H1.4. | Q36561147 | ||
| Combined deficiency of Tet1 and Tet2 causes epigenetic abnormalities but is compatible with postnatal development | Q36614856 | ||
| Cytosine methylation prevents binding to DNA of a HeLa cell transcription factor required for optimal expression of the adenovirus major late promoter | Q38346589 | ||
| MicroRNA-143 is downregulated in breast cancer and regulates DNA methyltransferases 3A in breast cancer cells. | Q39064248 | ||
| Uhrf1-dependent H3K23 ubiquitylation couples maintenance DNA methylation and replication | Q39098794 | ||
| Interaction of noncoding RNA with the rDNA promoter mediates recruitment of DNMT3b and silencing of rRNA genes | Q39643251 | ||
| Epigenetic inactivation of the tumor suppressor gene RIZ1 in hepatocellular carcinoma involves both DNA methylation and histone modifications | Q39673131 | ||
| A modified "cross-talk" between histone H2B Lys-120 ubiquitination and H3 Lys-79 methylation. | Q39707641 | ||
| DNA methylation affects nuclear organization, histone modifications, and linker histone binding but not chromatin compaction | Q39753654 | ||
| Complete inactivation of DNMT1 leads to mitotic catastrophe in human cancer cells | Q40166601 | ||
| A profile of methyl-CpG binding domain protein occupancy of hypermethylated promoter CpG islands of tumor suppressor genes in human cancer | Q40236523 | ||
| Dnmt1 deficiency leads to enhanced microsatellite instability in mouse embryonic stem cells | Q40405040 | ||
| RNA interference-mediated knockdown of DNA methyltransferase 1 leads to promoter demethylation and gene re-expression in human lung and breast cancer cells | Q40559173 | ||
| MeCP2 binds to 5hmC enriched within active genes and accessible chromatin in the nervous system. | Q40680118 | ||
| Preferential methylation of unmethylated DNA by Mammalian de novo DNA methyltransferase Dnmt3a. | Q40753457 | ||
| The DNA methyltransferase Dnmt1 directly interacts with the SET and RING finger-associated (SRA) domain of the multifunctional protein Uhrf1 to facilitate accession of the catalytic center to hemi-methylated DNA. | Q41848393 | ||
| Holocarboxylase synthetase is a chromatin protein and interacts directly with histone H3 to mediate biotinylation of K9 and K18 | Q41849919 | ||
| Human TNRC6A is an Argonaute-navigator protein for microRNA-mediated gene silencing in the nucleus | Q42424730 | ||
| Role of ATM and the damage response mediator proteins 53BP1 and MDC1 in the maintenance of G(2)/M checkpoint arrest | Q42738049 | ||
| Isoform-specific phosphorylation of human linker histone H1.4 in mitosis by the kinase Aurora B. | Q42811550 | ||
| Appearance and heterochromatin localization of HP1α in early mouse embryos depends on cytoplasmic clock and H3S10 phosphorylation. | Q42834540 | ||
| Chromatin binding of SRp20 and ASF/SF2 and dissociation from mitotic chromosomes is modulated by histone H3 serine 10 phosphorylation | Q43147112 | ||
| Chromatin 'resetting' during transcription elongation: a central role for methylated H3K36. | Q43158410 | ||
| Learning how to read ADP-ribosylation | Q43266938 | ||
| Control of the hippo pathway by Set7-dependent methylation of Yap. | Q46240754 | ||
| Novel mutation in the replication focus targeting sequence domain of DNMT1 causes hereditary sensory and autonomic neuropathy IE. | Q48114368 | ||
| Histone H1 poly[ADP]-ribosylation regulates the chromatin alterations required for learning consolidation. | Q48179492 | ||
| Methylation-sensitive binding of transcription factor YY1 to an insulator sequence within the paternally expressed imprinted gene, Peg3. | Q48262719 | ||
| Lsh is required for meiotic chromosome synapsis and retrotransposon silencing in female germ cells. | Q50642550 | ||
| Birth of the snoRNPs: the evolution of the modification-guide snoRNAs. | Q51093637 | ||
| Cellular dynamics associated with the genome-wide epigenetic reprogramming in migrating primordial germ cells in mice. | Q51983259 | ||
| Epigenetic reprogramming in mouse primordial germ cells | Q57086629 | ||
| Human DNA methylomes at base resolution show widespread epigenomic differences | Q24633677 | ||
| MeCP2, a key contributor to neurological disease, activates and represses transcription | Q24647533 | ||
| DNA methylation and microRNA dysregulation in cancer | Q26998741 | ||
| Structure of DNMT1-DNA Complex Reveals a Role for Autoinhibition in Maintenance DNA Methylation | Q27666325 | ||
| A methylation and phosphorylation switch between an adjacent lysine and serine determines human DNMT1 stability | Q27666366 | ||
| Structural Basis of the Versatile DNA Recognition Ability of the Methyl-CpG Binding Domain of Methyl-CpG Binding Domain Protein 4 | Q27675890 | ||
| High-resolution profiling of histone methylations in the human genome | Q27860906 | ||
| Histone H3 methylation by Set2 directs deacetylation of coding regions by Rpd3S to suppress spurious intragenic transcription | Q27932406 | ||
| Function and selectivity of bromodomains in anchoring chromatin-modifying complexes to promoter nucleosomes. | Q27934188 | ||
| Targeted mutation of the DNA methyltransferase gene results in embryonic lethality | Q28131773 | ||
| Synergistic coupling of histone H3 phosphorylation and acetylation in response to epidermal growth factor stimulation | Q28141828 | ||
| Suv39h-mediated histone H3 lysine 9 methylation directs DNA methylation to major satellite repeats at pericentric heterochromatin | Q28187783 | ||
| DNA double-strand breaks in heterochromatin elicit fast repair protein recruitment, histone H2AX phosphorylation and relocation to euchromatin | Q28236172 | ||
| UTX and JMJD3 are histone H3K27 demethylases involved in HOX gene regulation and development | Q28241669 | ||
| Genome-wide mapping of HATs and HDACs reveals distinct functions in active and inactive genes | Q28255974 | ||
| Reduced expression of the let-7 microRNAs in human lung cancers in association with shortened postoperative survival | Q28264400 | ||
| Germline DNA demethylation dynamics and imprint erasure through 5-hydroxymethylcytosine | Q28281009 | ||
| Transcriptional repression and heterochromatin formation by MBD1 and MCAF/AM family proteins | Q28305786 | ||
| Essential role for de novo DNA methyltransferase Dnmt3a in paternal and maternal imprinting | Q28508038 | ||
| Reprogramming of the paternal genome upon fertilization involves genome-wide oxidation of 5-methylcytosine | Q28585429 | ||
| HP1 binds specifically to Lys26-methylated histone H1.4, whereas simultaneous Ser27 phosphorylation blocks HP1 binding | Q28587228 | ||
| Dynamics of Dnmt1 interaction with the replication machinery and its role in postreplicative maintenance of DNA methylation | Q28592823 | ||
| Recombinant human DNA (cytosine-5) methyltransferase. I. Expression, purification, and comparison of de novo and maintenance methylation | Q28609169 | ||
| Miwi catalysis is required for piRNA amplification-independent LINE1 transposon silencing | Q28854369 | ||
| Single-cell Hi-C reveals cell-to-cell variability in chromosome structure | Q29397049 | ||
| A targeting sequence directs DNA methyltransferase to sites of DNA replication in mammalian nuclei | Q29616800 | ||
| The Rpd3/Hda1 family of lysine deacetylases: from bacteria and yeast to mice and men | Q29619117 | ||
| On how mammalian transcription factors recognize methylated DNA. | Q30426003 | ||
| DNA methylation-dependent chromatin fiber compaction in vivo and in vitro: requirement for linker histone | Q32041055 | ||
| Maintenance of paternal methylation and repression of the imprinted H19 gene requires MBD3 | Q33294657 | ||
| Regulation of UGT1A1 and HNF1 transcription factor gene expression by DNA methylation in colon cancer cells | Q33526045 | ||
| Visualizing histone modifications in living cells: spatiotemporal dynamics of H3 phosphorylation during interphase | Q33589953 | ||
| Rethinking how DNA methylation patterns are maintained | Q33763852 | ||
| Histone H1 phosphorylation is associated with transcription by RNA polymerases I and II | Q33839979 | ||
| CpG methylation is maintained in human cancer cells lacking DNMT1. | Q33901029 | ||
| Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males | Q34021143 | ||
| Dual-specificity histone demethylase KIAA1718 (KDM7A) regulates neural differentiation through FGF4. | Q34093543 | ||
| Dnmt1 and Dnmt3a maintain DNA methylation and regulate synaptic function in adult forebrain neurons. | Q34103901 | ||
| Dynamic reprogramming of DNA methylation in the early mouse embryo. | Q34108785 | ||
| MicroRNA‐205–directed transcriptional activation of tumor suppressor genes in prostate cancer | Q34133056 | ||
| Selective chemical labeling reveals the genome-wide distribution of 5-hydroxymethylcytosine | Q34154619 | ||
| DNMT1 is required to maintain CpG methylation and aberrant gene silencing in human cancer cells | Q34166536 | ||
| Physical activity and breast cancer survival: an epigenetic link through reduced methylation of a tumor suppressor gene L3MBTL1. | Q34207667 | ||
| Genome-wide erasure of DNA methylation in mouse primordial germ cells is affected by AID deficiency. | Q34249450 | ||
| Dnmt1 overexpression causes genomic hypermethylation, loss of imprinting, and embryonic lethality | Q34276391 | ||
| In vivo control of CpG and non-CpG DNA methylation by DNA methyltransferases | Q34325535 | ||
| The Dnmt1 DNA-(cytosine-C5)-methyltransferase methylates DNA processively with high preference for hemimethylated target sites | Q34344734 | ||
| von Hippel-Lindau partner Jade-1 is a transcriptional co-activator associated with histone acetyltransferase activity. | Q34361522 | ||
| MeCP2-mediated transcription repression in the basolateral amygdala may underlie heightened anxiety in a mouse model of Rett syndrome | Q34420937 | ||
| H3K36 methylation antagonizes PRC2-mediated H3K27 methylation | Q34624209 | ||
| Genome-wide analysis of 5-hydroxymethylcytosine distribution reveals its dual function in transcriptional regulation in mouse embryonic stem cells. | Q34762752 | ||
| Lsh, chromatin remodeling family member, modulates genome-wide cytosine methylation patterns at nonrepeat sequences | Q34804710 | ||
| MicroRNA miR-21 overexpression in human breast cancer is associated with advanced clinical stage, lymph node metastasis and patient poor prognosis | Q34835189 | ||
| De novo DNA methylation by Dnmt3a and Dnmt3b is dispensable for nuclear reprogramming of somatic cells to a pluripotent state | Q34976653 | ||
| Hotspots of transcription factor colocalization in the genome of Drosophila melanogaster | Q35033165 | ||
| Identification of DNMT1 (DNA methyltransferase 1) hypomorphs in somatic knockouts suggests an essential role for DNMT1 in cell survival | Q35080450 | ||
| The inactive X chromosome adopts a unique three-dimensional conformation that is dependent on Xist RNA. | Q35098579 | ||
| Active DNA demethylation mediated by DNA glycosylases | Q35108672 | ||
| Male germ cells express abundant endogenous siRNAs | Q35164762 | ||
| Critical role of monoubiquitination of histone H2AX protein in histone H2AX phosphorylation and DNA damage response | Q35182983 | ||
| H3K4 tri-methylation provides an epigenetic signature of active enhancers | Q35422275 | ||
| DiseaseMeth: a human disease methylation database | Q35631191 | ||
| Haploinsufficiency of Dnmt1 impairs leukemia stem cell function through derepression of bivalent chromatin domains | Q35788928 | ||
| Mouse miRNA-709 directly regulates miRNA-15a/16-1 biogenesis at the posttranscriptional level in the nucleus: evidence for a microRNA hierarchy system | Q35796875 | ||
| On the presence and role of human gene-body DNA methylation. | Q36050706 | ||
| PKM2 phosphorylates histone H3 and promotes gene transcription and tumorigenesis | Q36199783 | ||
| CTCF-mediated functional chromatin interactome in pluripotent cells | Q36218315 | ||
| Spreading of X chromosome inactivation via a hierarchy of defined Polycomb stations | Q36285384 | ||
| Mutations in DNMT1 cause autosomal dominant cerebellar ataxia, deafness and narcolepsy | Q36301666 | ||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 240-56 | |
| P577 | publication date | 2014-04-01 | |
| P1433 | published in | IUBMB Life | Q15764029 |
| P1476 | title | Mammalian epigenetic mechanisms | |
| P478 | volume | 66 |
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