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Epigenetic interplay between histone modifications and DNA methylation in gene silencing
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1521-1878(199905)21:5<402::aid-bies7>3.0.co;2-bopenalex-snapshot
Eukaryotic DNA methylation as an evolutionary device
inferredcites →https://doi.org/10.1002/bies.20176openalex-snapshot
Do protein motifs read the histone code?
inferredcites →https://doi.org/10.1007/pl00000895openalex-snapshot
Emerging connections between DNA methylation and histone acetylation
inferredcites →https://doi.org/10.1016/0092-8674(86)90263-1openalex-snapshot
DNA methylation affects the formation of active chromatin
inferredcites →https://doi.org/10.1016/0092-8674(92)90611-fopenalex-snapshot
Targeted mutation of the DNA methyltransferase gene results in embryonic lethality
inferredcites →https://doi.org/10.1016/j.bcp.2005.01.014openalex-snapshot
Curcumin-induced histone hypoacetylation: The role of reactive oxygen species
inferredcites →https://doi.org/10.1016/j.bcp.2006.12.032openalex-snapshot
Histone deacetylase inhibitor Trichostatin A induces global and gene-specific DNA demethylation in human cancer cell lines
inferredcites →https://doi.org/10.1016/s0014-4827(03)00062-4openalex-snapshot
Effects of cadmium on DNA-(Cytosine-5) methyltransferase activity and DNA methylation status during cadmium-induced cellular transformation
inferredcites →https://doi.org/10.1016/s0041-008x(03)00169-8openalex-snapshot
Analysis of specific lysine histone H3 and H4 acetylation and methylation status in clones of cells with a gene silenced by nickel exposure
inferredcites →https://doi.org/10.1016/s0076-6879(03)76018-2openalex-snapshot
Histone Methylation: Recognizing the Methyl Mark
inferredcites →https://doi.org/10.1016/s0092-8674(00)80211-1openalex-snapshot
What's Up and Down with Histone Deacetylation and Transcription?
inferredcites →https://doi.org/10.1016/s0092-8674(00)81532-9openalex-snapshot
Methylation-Induced Repression— Belts, Braces, and Chromatin
inferredcites →https://doi.org/10.1016/s0092-8674(00)81656-6openalex-snapshot
DNA Methyltransferases Dnmt3a and Dnmt3b Are Essential for De Novo Methylation and Mammalian Development
inferredcites →https://doi.org/10.1016/s0092-8674(02)00644-xopenalex-snapshot
Epigenetic Codes for Heterochromatin Formation and Silencing
inferredcites →https://doi.org/10.1016/s0162-0134(00)00009-xopenalex-snapshot
Cadmium carcinogenesis in review
inferredcites →https://doi.org/10.1016/s0190-9622(08)81509-5openalex-snapshot
Nonmelanoma skin cancer in the United States: Incidence
inferredcites →https://doi.org/10.1016/s0190-9622(98)70495-5openalex-snapshot
Graft-versus-host reactions in dermatology
inferredcites →https://doi.org/10.1016/s0960-9822(03)00432-9openalex-snapshot
Suv39h-Mediated Histone H3 Lysine 9 Methylation Directs DNA Methylation to Major Satellite Repeats at Pericentric Heterochromatin
inferredcites →https://doi.org/10.1016/s0960-9822(97)70086-1openalex-snapshot
DNA methylation directs a time-dependent repression of transcription initiation
inferredcites →https://doi.org/10.1016/s0962-8924(01)02125-0openalex-snapshot
Emerging roles for chromatin remodeling in cancer biology
inferredcites →https://doi.org/10.1016/s0968-0004(97)01045-1openalex-snapshot
Mitotic repression of the transcriptional machinery
inferredcites →https://doi.org/10.1016/s1476-5586(03)80039-8openalex-snapshot
Exceptionally High Protection of Photocarcinogenesis by Topical Application of (-)-Epi gal locatechin-3-Gal late in Hydrophilic Cream in SKH-1 Hairless Mouse Model: Relationship to Inhibition of UVB-Induced Global DNA Hypomethylation
inferredcites →https://doi.org/10.1038/12659openalex-snapshot
MBD2 is a transcriptional repressor belonging to the MeCP1 histone deacetylase complex
inferredcites →https://doi.org/10.1038/12664openalex-snapshot
Mi-2 complex couples DNA methylation to chromatin remodelling and histone deacetylation
inferredcites →https://doi.org/10.1038/29680openalex-snapshot
DNA methylation models histone acetylation
inferredcites →https://doi.org/10.1038/30764openalex-snapshot
Transcriptional repression by the methyl-CpG-binding protein MeCP2 involves a histone deacetylase complex
inferredcites →https://doi.org/10.1038/35044127openalex-snapshot
Global histone acetylation and deacetylation in yeast
inferredcites →https://doi.org/10.1038/35104508openalex-snapshot
A histone H3 methyltransferase controls DNA methylation in Neurospora crassa
inferredcites →https://doi.org/10.1038/416552aopenalex-snapshot
DNMT1 and DNMT3b cooperate to silence genes in human cancer cells
inferredcites →https://doi.org/10.1038/561openalex-snapshot
Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription
inferredcites →https://doi.org/10.1038/71750openalex-snapshot
DNA methyltransferase Dnmt1 associates with histone deacetylase activity
inferredcites →https://doi.org/10.1038/77023openalex-snapshot
DNMT1 binds HDAC2 and a new co-repressor, DMAP1, to form a complex at replication foci
inferredcites →https://doi.org/10.1038/bjc.1970.76openalex-snapshot
Cancers of the Lung and Nasal Sinuses in Nickel Workers
inferredcites →https://doi.org/10.1038/bjc.1992.380openalex-snapshot
Cancer potential in liver, lung, bladder and kidney due to ingested inorganic arsenic in drinking water
inferredcites →https://doi.org/10.1038/nature02625openalex-snapshot
Epigenetics in human disease and prospects for epigenetic therapy
inferredcites →https://doi.org/10.1038/nature731openalex-snapshot
Control of CpNpG DNA methylation by the KRYPTONITE histone H3 methyltransferase
inferredcites →https://doi.org/10.1038/ncb1386openalex-snapshot
DNA methyltransferases control telomere length and telomere recombination in mammalian cells
inferredcites →https://doi.org/10.1038/ng1089openalex-snapshot
Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals
inferredcites →https://doi.org/10.1038/nrg1748openalex-snapshot
The epigenetic progenitor origin of human cancer
inferredcites →https://doi.org/10.1038/nrg816openalex-snapshot
The fundamental role of epigenetic events in cancer
inferredcites →https://doi.org/10.1038/sj.emboj.7600013openalex-snapshot
Silencing of transgene transcription precedes methylation of promoter DNA and histone H3 lysine 9
inferredcites →https://doi.org/10.1038/sj.onc.1204322openalex-snapshot
Chromatin remodeling: why it is important in cancer
inferredcites →https://doi.org/10.1073/pnas.0700529104openalex-snapshot
Histone hyperacetylation induces demethylation of reelin and 67-kDa glutamic acid decarboxylase promoters
inferredcites →https://doi.org/10.1073/pnas.84.5.1177openalex-snapshot
Chromatin structure is required to block transcription of the methylated herpes simplex virus thymidine kinase gene.
inferredcites →https://doi.org/10.1073/pnas.94.20.10907openalex-snapshot
Association of arsenic-induced malignant transformation with DNA hypomethylation and aberrant gene expression
inferredcites →https://doi.org/10.1074/jbc.m210256200openalex-snapshot
The Methyl-CpG-binding Protein MeCP2 Links DNA Methylation to Histone Methylation
inferredcites →https://doi.org/10.1074/jbc.r500004200openalex-snapshot
Hyperacetylated Chromatin Domains: Lessons from Heterochromatin
inferredcites →https://doi.org/10.1080/00039896.1979.10667423openalex-snapshot
Lung Cancer among Pesticide Workers Exposed to Inorganic Arsenicais
inferredcites →https://doi.org/10.1086/375041openalex-snapshot
Past Exposure to Densely Ionizing Radiation Leaves a Unique Permanent Signature in the Genome
inferredcites →https://doi.org/10.1093/carcin/23.5.777openalex-snapshot
Sodium arsenite administration via drinking water increases genome-wide and Ha-ras DNA hypomethylation in methyl-deficient C57BL/6J mice
inferredcites →https://doi.org/10.1093/carcin/bgh096openalex-snapshot
Plutonium targets the p16 gene for inactivation by promoter hypermethylation in human lung adenocarcinoma
inferredcites →https://doi.org/10.1093/carcin/bgl167openalex-snapshot
Valproate induces widespread epigenetic reprogramming which involves demethylation of specific genes
inferredcites →https://doi.org/10.1093/emboj/20.10.2536openalex-snapshot
Dnmt3a binds deacetylases and is recruited by a sequence‐specific repressor to silence transcription
inferredcites →https://doi.org/10.1093/genetics/149.1.307openalex-snapshot
A DNA Methyltransferase Homolog With a Chromodomain Exists in Multiple Polymorphic Forms in Arabidopsis
inferredcites →https://doi.org/10.1093/mutage/gel068openalex-snapshot
Epigenetics and cancer: towards an evaluation of the impact of environmental and dietary factors
inferredcites →https://doi.org/10.1093/nar/20.19.5085openalex-snapshot
Characterization of MeCP2, a vertebrate DNA binding protein with affinity for methylated DNA
inferredcites →https://doi.org/10.1093/nar/21.21.4886openalex-snapshot
Dissection of the methyl-CpG binding domain from the chromosomal protein MeCP2
inferredcites →https://doi.org/10.1093/nar/gkg332openalex-snapshot
The DNA methyltransferases associate with HP1 and the SUV39H1 histone methyltransferase
inferredcites →https://doi.org/10.1093/nar/gkh252openalex-snapshot
The diverse superfamily of lysine acetyltransferases and their roles in leukemia and other diseases
inferredcites →https://doi.org/10.1101/gad.11.18.2383openalex-snapshot
DNA methylation inhibits elongation but not initiation of transcription in Neurospora crassa
inferredcites →https://doi.org/10.1101/gad.3.5.612openalex-snapshot
CpG methylation of the cAMP-responsive enhancer/promoter sequence TGACGTCA abolishes specific factor binding as well as transcriptional activation.
inferredcites →https://doi.org/10.1101/gad.905701openalex-snapshot
Arabidopsis cmt3 chromomethylase mutations block non-CG methylation and silencing of an endogenous gene
inferredcites →https://doi.org/10.1101/gad.947102openalex-snapshot
DNA methylation patterns and epigenetic memory
inferredcites →https://doi.org/10.1101/gad.988502openalex-snapshot
The barrier function of an insulator couples high histone acetylation levels with specific protection of promoter DNA from methylation
inferredcites →https://doi.org/10.1105/tpc.010064openalex-snapshot
Maize Chromomethylase Zea methyltransferase2 Is Required for CpNpG Methylation
inferredcites →https://doi.org/10.1111/j.1464-410x.1993.tb15942.xopenalex-snapshot
The Incidence of Bladder Cancer in the Black Foot Disease Endemic Area in Taiwan
inferredcites →https://doi.org/10.1126/science.1059745openalex-snapshot
Requirement of CHROMOMETHYLASE3 for Maintenance of CpXpG Methylation
inferredcites →https://doi.org/10.1126/science.1990442openalex-snapshot
Senescence of Nickel-Transformed Cells by an X Chromosome: Possible Epigenetic Control
inferredcites →https://doi.org/10.1126/science.291.5503.447openalex-snapshot
Insulators and Boundaries: Versatile Regulatory Elements in the Eukaryotic Genome
inferredcites →https://doi.org/10.1128/mcb.15.5.2547openalex-snapshot
Carcinogenic Nickel Silences Gene Expression by Chromatin Condensation and DNA Methylation: a New Model for Epigenetic Carcinogens
inferredcites →https://doi.org/10.1128/mcb.20.24.9103-9112.2000openalex-snapshot
Genomic Targeting of Methylated DNA: Influence of Methylation on Transcription, Replication, Chromatin Structure, and Histone Acetylation
inferredcites →https://doi.org/10.1128/mcb.25.10.3923-3933.2005openalex-snapshot
Chromatin Inactivation Precedes De Novo DNA Methylation during the Progressive Epigenetic Silencing of the RASSF1A Promoter
inferredcites →https://doi.org/10.1146/annurev.genet.32.1.495openalex-snapshot
THE CRITICAL ROLE OF CHROMOSOME TRANSLOCATIONS IN HUMAN LEUKEMIAS
inferredcites →https://doi.org/10.1158/1078-0432.ccr-06-2225openalex-snapshot
Epigenetic Modifications of RASSF1A Gene through Chromatin Remodeling in Prostate Cancer
inferredcites →https://doi.org/10.1242/dev.122.10.3195openalex-snapshot
De novo DNA cytosine methyltransferase activities in mouse embryonic stem cells
inferredcites →https://doi.org/10.4161/cc.4.3.1546openalex-snapshot
Rendez-vous at Mitosis: TRRAPed in the Chromatin
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.3349506openalex-extracted
Association of HOXA9 Promoter Hypomethylation With Colorectal Cancer
inferred← citeshttps://doi.org/10.1002/2211-5463.12659openalex-snapshot
Low expression of WWC1, a tumor suppressor gene, is associated with aggressive breast cancer and poor survival outcome
inferred← citeshttps://doi.org/10.1002/3527600906.mcb.201100009openalex-snapshot
Imprinting and the Epigenetic Asymmetry between Parental Genomes
inferred← citeshttps://doi.org/10.1002/9781118349045.ch17openalex-snapshot
Epigenetic Histone Changes in the Toxicologic Mode of Action of Arsenic
inferred← citeshttps://doi.org/10.1002/9781118907474.ch6openalex-snapshot
Epigenetic regulation of mesenchymal stem/stromal cell growth and multipotentiality
inferred← citeshttps://doi.org/10.1002/9781118924853.ch37openalex-snapshot
Pathogenesis of Microvascular Complications
inferred← citeshttps://doi.org/10.1002/9781119697473.ch42openalex-snapshot
Pathogenesis of Microvascular Complications
inferred← citeshttps://doi.org/10.1002/9781444324808.ch35openalex-snapshot
Pathogenesis of Microvascular Complications
inferred← citeshttps://doi.org/10.1002/biof.70011openalex-snapshot
Molecular and cell phenotype programs in oral epithelial cells directed by co‐exposure to arsenic and smokeless tobacco
inferred← citeshttps://doi.org/10.1002/bit.28013openalex-snapshot
Small molecule epigenetic modulators for enhancing recombinant antibody production in CHO cell cultures
inferred← citeshttps://doi.org/10.1002/btpr.2712openalex-snapshot
Enhancement of transgene expression by nuclear transcription factor Y and CCCTC‐binding factor
inferred← citeshttps://doi.org/10.1002/ece3.7684openalex-snapshot
Expansion of rDNA and pericentromere satellite repeats in the genomes of bank voles Myodes glareolus exposed to environmental radionuclides
inferred← citeshttps://doi.org/10.1002/em.21836openalex-snapshot
Epigenetic regulation: The interface between prenatal and early‐life exposure and asthma susceptibility
inferred← citeshttps://doi.org/10.1002/ijc.27421openalex-snapshot
DNA methylation of the CYP1A1 enhancer is associated with smoking‐induced genetic alterations in human lung
inferred← citeshttps://doi.org/10.1002/jat.2717openalex-snapshot
Epigenetic targets of some toxicologically relevant metals: a review of the literature
inferred← citeshttps://doi.org/10.1002/jcb.22644openalex-snapshot
Role of histone acetylation in the development of diabetic retinopathy and the metabolic memory phenomenon
inferred← citeshttps://doi.org/10.1002/jcb.26126openalex-snapshot
miR‐34a Targets HDAC1‐Regulated H3K9 Acetylation on Lipid Accumulation Induced by Homocysteine in Foam Cells
inferred← citeshttps://doi.org/10.1002/mc.22448openalex-snapshot
The Ezh2 polycomb group protein drives an aggressive phenotype in melanoma cancer stem cells and is a target of diet derived sulforaphane
inferred← citeshttps://doi.org/10.1002/med.21881openalex-snapshot
Epigenetic modification in alcohol‐related liver diseases
inferred← citeshttps://doi.org/10.1002/mrd.23178openalex-snapshot
Enhancement of epigenetic reprogramming status of porcine cloned embryos with zebularine, a DNA methyltransferase inhibitor
inferred← citeshttps://doi.org/10.1002/rmb2.12503openalex-snapshot
How to improve the clinical outcome of round spermatid injection (ROSI) into the oocyte: Correction of epigenetic abnormalities
inferred← citeshttps://doi.org/10.1002/wsbm.125openalex-snapshot
Mechanisms of genetic regulation in gene expression: examples from drug metabolizing enzymes and transporters
inferred← citeshttps://doi.org/10.1007/978-1-4419-0639-7_23openalex-snapshot
Environmental Effects on Age-Associated Epigenetics
inferred← citeshttps://doi.org/10.1007/978-1-4419-7034-3_19openalex-snapshot
The Role of Environmental Obesogens in the Obesity Epidemic
inferred← citeshttps://doi.org/10.1007/978-1-4471-2825-0_11openalex-snapshot
Lung Cancer: Genetic Susceptibility
inferred← citeshttps://doi.org/10.1007/978-1-4899-7678-9_1openalex-snapshot
Epigenetic Mechanisms as an Interface Between the Environment and Genome
inferred← citeshttps://doi.org/10.1007/978-1-60761-580-4_7openalex-snapshot
Introduction to Epigenomics and Epigenome-Wide Analysis
inferred← citeshttps://doi.org/10.1007/978-1-60761-627-6_2openalex-snapshot
Cancer Biology and Nutrigenomics
inferred← citeshttps://doi.org/10.1007/978-1-61779-612-8_12openalex-snapshot
Epigenome and DNA Methylation in Oral Squamous Cell Carcinoma
inferred← citeshttps://doi.org/10.1007/978-1-84882-644-1_11openalex-snapshot
Epigenetics in Psychiatry
inferred← citeshttps://doi.org/10.1007/978-1-84882-644-1_3openalex-snapshot
Mechanisms of Epigenetic Gene Silencing
inferred← citeshttps://doi.org/10.1007/978-3-030-30766-0_14openalex-snapshot
Lung Cancer: Genetic Susceptibility
inferred← citeshttps://doi.org/10.1007/978-3-030-80962-1_31-1openalex-snapshot
Epigenetics and miRNAs in Cancer
inferred← citeshttps://doi.org/10.1007/978-3-030-94475-9_13openalex-snapshot
Epigenetic Epidemiology of Cancer
inferred← citeshttps://doi.org/10.1007/978-3-032-00749-0_31openalex-snapshot
Epigenetics and miRNAs in Cancer
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Genomic Tools for Aquatic Bird Ecology and Conservation—A Comprehensive Overview
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Epigenetics, MicroRNAs and Human Cancer
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Epigenetics of Dental Stem Cells
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Epigenetics: Chromatin Organization and Function
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Current and Future Views on Pulp Exposure Management and Epigenetic Influences
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The Intersection of Genetics and Epigenetics: Reactivation of Mammalian LINE-1 Retrotransposons by Environmental Injury
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Epigenetics, Brain and Behavior
inferred← citeshttps://doi.org/10.1007/978-3-642-27913-3_7openalex-snapshot
The Role of Histone Acetylation in Long-Term Memory Storage
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Einführung in die Genetik
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Role of Epigenetics in Inflammation-Associated Diseases
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Epigenetic Modifiers and Stem Cell Differentiation
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The Emerging Role of Epigenetics
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DNA Methylation and Carcinogenesis: Current and Future Perspectives
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Chromatin-Based Control of Mammalian Sex Determination: Integrating Epigenetic and Metabolic Mechanisms
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The Biology of Cancer: Understanding the Disease and Its Challenges
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Epigenetics and periodontal disease: future perspectives
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Chromatin composition alterations and the critical role of MeCP2 for epigenetic silencing of progesterone receptor-B gene in endometrial cancers
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Epigenomic landscape and epigenetic regulation in maize
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Primary hepatocyte cultures for pharmaco-toxicological studies: at the busy crossroad of various anti-dedifferentiation strategies
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Exposure of pregnant mice to triclosan causes hyperphagic obesity of offspring via the hypermethylation of proopiomelanocortin promoter
inferred← citeshttps://doi.org/10.1007/s00262-012-1340-3openalex-snapshot
DNA methylation at promoter regions of interleukin 1B, interleukin 6, and interleukin 8 in non-small cell lung cancer
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Epigenetic mechanisms underlying extinction of memory and drug-seeking behavior
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Relationship between endometriosis and cancer from current perspective
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Role of oxidative stress in epigenetic modification of MMP-9 promoter in the development of diabetic retinopathy
inferred← citeshttps://doi.org/10.1007/s00438-023-02033-1openalex-snapshot
The transposable element-derived transcript of LIN28B has a placental origin and is not specific to tumours
inferred← citeshttps://doi.org/10.1007/s00441-021-03489-6openalex-snapshot
Epigenetic dysregulation in various types of cells exposed to extremely low-frequency magnetic fields
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Porphyromonas gingivalis LPS stimulation downregulates DNMT1, DNMT3a, and JMJD3 gene expression levels in human HaCaT keratinocytes
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Epigenetic Up-Regulation of Leukemia Inhibitory Factor (LIF) Gene During the Progression to Breast Cancer
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Epigenetic alterations and genetic variations of angiotensin-converting enzyme 2 (ACE2) as a functional receptor for SARS-CoV-2: potential clinical implications
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Interplay among epigenetic alterations and crosstalk between genetic and epigenetic alterations in esophageal squamous cell carcinoma
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Epigenetic approach for angiostatic therapy: promising combinations for cancer treatment
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Expression Profiling of DNA Methylation and Transcriptional Repression Associated Genes in Lens Epithelium Cells of Age-Related Cataract
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The significance of epigenetic alterations in lung carcinogenesis
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UV-mediated Chlamydomonas mutants with enhanced nuclear transgene expression by disruption of DNA methylation-dependent and independent silencing systems
inferred← citeshttps://doi.org/10.1007/s11240-022-02336-yopenalex-snapshot
High temperature and water deficit cause epigenetic changes in somatic plants of Pinus radiata D. Don
inferred← citeshttps://doi.org/10.1007/s11307-010-0300-6openalex-snapshot
Irradiation, Cisplatin, and 5-Azacytidine Upregulate Cytomegalovirus Promoter in Tumors and Muscles: Implementation of Non-invasive Fluorescence Imaging
inferred← citeshttps://doi.org/10.1007/s11596-011-0142-8openalex-snapshot
Effects of DNA methylation and histone modification on differentiation-associated gene expression in ES, NIH3T3, and NIT-1
inferred← citeshttps://doi.org/10.1007/s11748-013-0235-3openalex-snapshot
Epigenetic alterations and their clinical implications in esophageal squamous cell carcinoma
inferred← citeshttps://doi.org/10.1007/s12011-012-9392-yopenalex-snapshot
The Effect of c-Fos Demethylation on Sodium Fluoride-induced Apoptosis in L-02 Cells
inferred← citeshttps://doi.org/10.1007/s12029-019-00338-2openalex-snapshot
Histone Deacetylase Modifications by Probiotics in Colorectal Cancer
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Molecular Genetics and Epigenetics Regulatory Role of miRNAs on Adipogenesis and Intramuscular Fat Development in Beef Cattle: In the Context of Meat Quality
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Hyperacetylation of Histone H3K9 Involved in the Promotion of Abnormally High Transcription of the gdnf Gene in Glioma Cells
inferred← citeshttps://doi.org/10.1007/s12035-019-01843-yopenalex-snapshot
Pre-Exposure to Nicotine with Nocturnal Abstinence Induces Epigenetic Changes that Potentiate Nicotine Preference
inferred← citeshttps://doi.org/10.1007/s12195-011-0199-2openalex-snapshot
Epigenetic Regulation of Vascular Endothelial Biology/Pathobiology and Response to Fluid Shear Stress
inferred← citeshttps://doi.org/10.1007/s12265-026-10820-5openalex-snapshot
The Trajectory of Epigenetic Chromatin Remodeling in Cardiometabolic Disease and its Therapeutic Implications
inferred← citeshttps://doi.org/10.1007/s12640-025-00735-5openalex-snapshot
Protective Effect of myo-Inositol Against Decitabine-Induced Neural Tube Defects in Embryonic Zebrafish
inferred← citeshttps://doi.org/10.1007/s13148-010-0016-0openalex-snapshot
Molecular marks for epigenetic identification of developmental and cancer stem cells
inferred← citeshttps://doi.org/10.1007/s13193-020-01046-1openalex-snapshot
Comparison of Detection of Epidermal Growth Factor Receptor (EFGR) Gene Mutation in Peripheral Blood Plasma (Liquid Biopsy) with Cytological Specimens in Lung Adenocarcinoma Patients
inferred← citeshttps://doi.org/10.1007/s13273-019-0001-4openalex-snapshot
Multi-omics approaches for understanding environmental exposure and human health
inferred← citeshttps://doi.org/10.1007/s13277-014-2618-1openalex-snapshot
Activating transcription factor 3 interferes with p21 activation in histone deacetylase inhibitor-induced growth inhibition of epidermoid carcinoma cells
inferred← citeshttps://doi.org/10.1007/s40199-024-00545-8openalex-snapshot
Cellular and molecular aspects of drug resistance in cancers
inferred← citeshttps://doi.org/10.1007/s40265-015-0461-3openalex-snapshot
Targeting Chromatin-Mediated Transcriptional Control of Gene Expression in Non-Small Cell Lung Cancer Therapy: Preclinical Rationale and Clinical Results
inferred← citeshttps://doi.org/10.1007/s40495-014-0004-8openalex-snapshot
DNA Methylation and Flavonoids in Genitourinary Cancers
inferred← citeshttps://doi.org/10.1016/b978-0-12-375709-8.00002-2openalex-snapshot
Mechanisms of DNA Methylation, Methyl-CpG Recognition, and Demethylation in Mammals
inferred← citeshttps://doi.org/10.1016/b978-0-12-375709-8.00027-7openalex-snapshot
The Effects of Diet on Epigenetic Processes
inferred← citeshttps://doi.org/10.1016/b978-0-12-380864-6.00003-1openalex-snapshot
In Utero Life and Epigenetic Predisposition for Disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-380866-0.60005-8openalex-snapshot
Interplay Between Different Epigenetic Modifications and Mechanisms
inferred← citeshttps://doi.org/10.1016/b978-0-12-380866-0.60012-5openalex-snapshot
DNA Demethylating Agents and Epigenetic Therapy of Cancer
inferred← citeshttps://doi.org/10.1016/b978-0-12-405944-3.00022-2openalex-snapshot
Epigenetic Transgenerational Inheritance of Reproductive Disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-407708-9.00002-9openalex-snapshot
Epigenetic Control of Cytokine Gene Expression
inferred← citeshttps://doi.org/10.1016/b978-0-12-420135-4.00014-0openalex-snapshot
Epigenetics and Personalized Pain Management
inferred← citeshttps://doi.org/10.1016/b978-0-12-800957-4.00016-3openalex-snapshot
Epigenetics of Melanoma
inferred← citeshttps://doi.org/10.1016/b978-0-12-801899-6.00014-0openalex-snapshot
DNA Methylation Alterations as Biomarkers for Prostate Cancer
inferred← citeshttps://doi.org/10.1016/b978-0-12-803239-8.00016-8openalex-snapshot
Epigenetics of Skin Disorders
inferred← citeshttps://doi.org/10.1016/b978-0-12-809552-2.00007-3openalex-snapshot
Epigenetic Modulations in Ovarian Cancer
inferred← citeshttps://doi.org/10.1016/b978-0-12-812215-0.00023-6openalex-snapshot
Translational Aspects of the Endometriosis Epigenome
inferred← citeshttps://doi.org/10.1016/b978-0-12-813035-3.00045-9openalex-snapshot
Effects of Nicotine and Histone Deacetylase Inhibitors on the Brain
inferred← citeshttps://doi.org/10.1016/b978-0-12-813156-5.00011-xopenalex-snapshot
Fetal Alcohol Exposure Impairs the Function of Hypothalamic Proopiomelanocortin Neurons via a Circadian Mechanism
inferred← citeshttps://doi.org/10.1016/b978-0-12-817661-0.00009-3openalex-snapshot
Targeting the Epigenome as a Therapeutic Strategy for Pancreatic Tumors: DNA and Histone Modifying Enzymes
inferred← citeshttps://doi.org/10.1016/b978-0-12-817892-8.00016-7openalex-snapshot
Molecular mechanisms regulating priming and stress memory
inferred← citeshttps://doi.org/10.1016/b978-0-12-817996-3.00004-9openalex-snapshot
Stochastic phenotypic switching in endothelial cell heterogeneity
inferred← citeshttps://doi.org/10.1016/b978-0-12-821514-2.00032-5openalex-snapshot
Epigenetic studies of neurodevelopment in twins
inferred← citeshttps://doi.org/10.1016/b978-0-12-821785-6.00008-6openalex-snapshot
Early life substance abuse and epigenetic programming
inferred← citeshttps://doi.org/10.1016/b978-0-12-823928-5.00011-6openalex-snapshot
Epigenetics of skin disorders
inferred← citeshttps://doi.org/10.1016/b978-0-323-29738-7.00033-2openalex-snapshot
Complications of Diabetes Mellitus
inferred← citeshttps://doi.org/10.1016/b978-0-323-99521-4.00013-1openalex-snapshot
Modulation of epigenetic methylation enzymes by synthetic and natural agents
inferred← citeshttps://doi.org/10.1016/b978-0-443-18661-5.00009-9openalex-snapshot
Epigenetics of diabetes in humans
inferred← citeshttps://doi.org/10.1016/b978-0-443-21863-7.00008-1openalex-snapshot
Translational aspects of the endometriosis epigenome
inferred← citeshttps://doi.org/10.1016/b978-0-443-27765-8.00016-3openalex-snapshot
DNA methylation and histone modification in liver cancer
inferred← citeshttps://doi.org/10.1016/b978-0-443-32888-6.00004-9openalex-snapshot
Phytochemicals and diabetes
inferred← citeshttps://doi.org/10.1016/b978-1-4377-0324-5.00033-xopenalex-snapshot
Complications of Diabetes Mellitus
inferred← citeshttps://doi.org/10.1016/bs.apha.2015.12.001openalex-snapshot
MicroRNA-Based Biomarkers in Pain
inferred← citeshttps://doi.org/10.1016/bs.apha.2023.10.004openalex-snapshot
Epigenetic inheritance of phenotypes associated with parental exposure to cocaine
inferred← citeshttps://doi.org/10.1016/bs.irn.2020.08.003openalex-snapshot
Exposure to drugs of abuse induce effects that persist across generations
inferred← citeshttps://doi.org/10.1016/j.abrep.2024.100569openalex-snapshot
Genomic factors associated with substance use disorder relapse: A critical review
inferred← citeshttps://doi.org/10.1016/j.ajhg.2024.04.017openalex-snapshot
Genome-wide DNA methylation changes in human spermatogenesis
inferred← citeshttps://doi.org/10.1016/j.apsb.2012.01.001openalex-snapshot
Epigenetic regulation of developmental expression of Cyp2d genes in mouse liver
inferred← citeshttps://doi.org/10.1016/j.apsb.2025.09.019openalex-snapshot
How histone modifications influence cellular radiosensitivity: Pharmaceutically targeting epigenetic regulators as a promising avenue to overcome radioresistance
inferred← citeshttps://doi.org/10.1016/j.aquatox.2021.105849openalex-snapshot
Chronic exposure to Bisphenol A resulted in alterations of reproductive functions via immune defense, oxidative damage and disruption DNA/histone methylation in male rare minnow Gobiocypris rarus
inferred← citeshttps://doi.org/10.1016/j.archoralbio.2024.106131openalex-snapshot
MicroRNA expression profiling in the adult offspring of rats with periodontal disease
inferred← citeshttps://doi.org/10.1016/j.atherosclerosis.2019.01.002openalex-snapshot
Endothelial cells of different organs exhibit heterogeneity in von Willebrand factor expression in response to hypoxia
inferred← citeshttps://doi.org/10.1016/j.autrev.2012.09.003openalex-snapshot
Emerging and critical issues in the pathogenesis of lupus
inferred← citeshttps://doi.org/10.1016/j.bbadis.2019.04.002openalex-snapshot
Epigenetic silencing of genes enhanced by collective role of reactive oxygen species and MAPK signaling downstream ERK/Snail axis: Ectopic application of hydrogen peroxide repress CDH1 gene by enhanced DNA methyltransferase activity in human breast cancer
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2017.01.014openalex-snapshot
Epigenetic interplay at the β-globin locus
inferred← citeshttps://doi.org/10.1016/j.bbagrm.2024.195064openalex-snapshot
EBV infection alters DNA methylation in primary human colon cells: A path to inflammation and carcinogenesis?
inferred← citeshttps://doi.org/10.1016/j.bbcan.2025.189261openalex-snapshot
Combating chemoresistance: Current approaches & nanocarrier mediated targeted delivery
inferred← citeshttps://doi.org/10.1016/j.bbr.2014.02.006openalex-snapshot
Learning induced epigenetic modifications in the ventral striatum are necessary for long-term memory
inferred← citeshttps://doi.org/10.1016/j.bbrc.2010.02.020openalex-snapshot
Induced epigenetic modifications of the promoter chromatin silence survivin and inhibit tumor growth
inferred← citeshttps://doi.org/10.1016/j.bbrc.2013.03.074openalex-snapshot
Poly(ADP-ribosylation) regulates chromatin organization through histone H3 modification and DNA methylation of the first cell cycle of mouse embryos
inferred← citeshttps://doi.org/10.1016/j.bcp.2010.07.029openalex-snapshot
Nature or nurture: Let food be your epigenetic medicine in chronic inflammatory disorders
inferred← citeshttps://doi.org/10.1016/j.bcp.2011.05.026openalex-snapshot
Epigenetic regulation of CIITA expression in human T-cells
inferred← citeshttps://doi.org/10.1016/j.biocel.2017.01.019openalex-snapshot
Genomic characterization and dynamic methylation of promoter facilitates transcriptional regulation of H2A variants, H2A.1 and H2A.2 in various pathophysiological states of hepatocyte
inferred← citeshttps://doi.org/10.1016/j.biocel.2018.03.004openalex-snapshot
HDAC inhibitors as epigenetic regulators for cancer immunotherapy
inferred← citeshttps://doi.org/10.1016/j.biochi.2012.05.012openalex-snapshot
Chromatin-modifying agents in anti-cancer therapy
inferred← citeshttps://doi.org/10.1016/j.bioorg.2024.107930openalex-snapshot
Combretastatin A-4 based compounds as potential anticancer agents: A review
inferred← citeshttps://doi.org/10.1016/j.biopha.2017.02.111openalex-snapshot
Repression of DOK7 mediated by DNMT3A promotes the proliferation and invasion of KYSE410 and TE-12 ESCC cells
inferred← citeshttps://doi.org/10.1016/j.biopsych.2012.04.006openalex-snapshot
Male Germline Transmits Fetal Alcohol Adverse Effect on Hypothalamic Proopiomelanocortin Gene Across Generations
inferred← citeshttps://doi.org/10.1016/j.bone.2020.115309openalex-snapshot
Epigenetic mechanisms driving lineage commitment in mesenchymal stem cells
inferred← citeshttps://doi.org/10.1016/j.canlet.2011.12.026openalex-snapshot
Epigenetic biomarkers in urological tumors: A systematic review
inferred← citeshttps://doi.org/10.1016/j.cbi.2013.08.017openalex-snapshot
Carbon disulfide exposure at peri-implantation disrupts embryo implantation by decreasing integrin β3 expression in the uterine tissue of pregnant mice
inferred← citeshttps://doi.org/10.1016/j.cbpb.2012.10.005openalex-snapshot
Do not put all teleosts in one net: Focus on the sox2 and pou2 genes
inferred← citeshttps://doi.org/10.1016/j.cellsig.2014.03.001openalex-snapshot
Re-expression and epigenetic modification of maspin induced apoptosis in MCF-7 cells mediated by myocardin
inferred← citeshttps://doi.org/10.1016/j.celrep.2016.01.008openalex-snapshot
Epigenomic Co-localization and Co-evolution Reveal a Key Role for 5hmC as a Communication Hub in the Chromatin Network of ESCs
inferred← citeshttps://doi.org/10.1016/j.cpb.2024.100408openalex-snapshot
Epigenetic control of plant regeneration: Unraveling the role of histone methylation
inferred← citeshttps://doi.org/10.1016/j.critrevonc.2022.103843openalex-snapshot
P16 gene promoter methylation is associated with oncogenesis and progression of gastric carcinomas: A systematic review and meta-analysis
inferred← citeshttps://doi.org/10.1016/j.ddmod.2009.01.001openalex-snapshot
Epigenetic progenitors in tumor initiation and development
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2026.120805openalex-snapshot
Advances in the mechanisms of histone modification-mediated developmental toxicity induced by organophosphorus pesticides
inferred← citeshttps://doi.org/10.1016/j.ejca.2010.11.029openalex-snapshot
Expression of DNA repair genes in ovarian cancer samples: Biological and clinical considerations
inferred← citeshttps://doi.org/10.1016/j.envint.2021.106693openalex-snapshot
Paternal preconception phthalate exposure alters sperm methylome and embryonic programming
inferred← citeshttps://doi.org/10.1016/j.envpol.2025.125941openalex-snapshot
Exploring the epigenetic impacts of atrazine in zebrafish: Unveiling mechanisms of neurotoxicity, reproductive toxicity, and implications for human health
inferred← citeshttps://doi.org/10.1016/j.envres.2017.11.040openalex-snapshot
Lifetime exposure to ambient air pollution and methylation of tumor suppressor genes in breast tumors
inferred← citeshttps://doi.org/10.1016/j.eururo.2011.06.035openalex-snapshot
Epigenetics in Prostate Cancer: Biologic and Clinical Relevance
inferred← citeshttps://doi.org/10.1016/j.eururo.2022.05.021openalex-snapshot
Proteogenomic, Epigenetic, and Clinical Implications of Recurrent Aberrant Splice Variants in Clear Cell Renal Cell Carcinoma
inferred← citeshttps://doi.org/10.1016/j.exphem.2012.08.003openalex-snapshot
Valproic acid triggers erythro/megakaryocyte lineage decision through induction of GFI1B and MLLT3 expression
inferred← citeshttps://doi.org/10.1016/j.fct.2017.06.034openalex-snapshot
Aflatoxin B1-induced epigenetic alterations: An overview
inferred← citeshttps://doi.org/10.1016/j.fertnstert.2019.07.1324openalex-snapshot
Cross-talk between miR-29c and transforming growth factor-β3 is mediated by an epigenetic mechanism in leiomyoma
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2015.06.013openalex-snapshot
Epigenetic regulation of Keap1-Nrf2 signaling
inferred← citeshttps://doi.org/10.1016/j.fshw.2013.03.002openalex-snapshot
Epigenetic origins of metabolic disease: The impact of the maternal condition to the offspring epigenome and later health consequences
inferred← citeshttps://doi.org/10.1016/j.gene.2013.04.024openalex-snapshot
Oxidative stress causes epigenetic alteration of CDX1 expression in colorectal cancer cells
inferred← citeshttps://doi.org/10.1016/j.gene.2013.10.045openalex-snapshot
The role of DNA methylation in regulation of the murine Lhx3 gene
inferred← citeshttps://doi.org/10.1016/j.ibror.2018.08.003openalex-snapshot
Transcriptional regulation of corticotropin-releasing hormone gene in stress response
inferred← citeshttps://doi.org/10.1016/j.intimp.2020.106262openalex-snapshot
The epigenetic face of lupus: Focus on antigen-presenting cells
inferred← citeshttps://doi.org/10.1016/j.intimp.2023.111227openalex-snapshot
Unlocking the role of EIF5A: A potential diagnostic marker regulating the cell cycle and showing negative correlation with immune infiltration in lung adenocarcinoma
inferred← citeshttps://doi.org/10.1016/j.jddst.2023.105325openalex-snapshot
Deciphering the role of nanocarrier-based nucleic acid delivery to the brain for the management of neurodegenerative disorders
inferred← citeshttps://doi.org/10.1016/j.jhep.2008.11.013openalex-snapshot
HBV protein as a double-barrel shot-gun targets epigenetic landscape in liver cancer
inferred← citeshttps://doi.org/10.1016/j.jmb.2015.10.007openalex-snapshot
HSFs, Stress Sensors and Sculptors of Transcription Compartments and Epigenetic Landscapes
inferred← citeshttps://doi.org/10.1016/j.jmgm.2011.03.003openalex-snapshot
Effect of CpG methylation on DNA binding protein: Molecular dynamics simulations of the homeodomain PITX2 bound to the methylated DNA
inferred← citeshttps://doi.org/10.1016/j.jmii.2012.08.005openalex-snapshot
Lipopolysaccharide extracted from Porphyromonas gingivalis induces DNA hypermethylation of runt-related transcription factor 2 in human periodontal fibroblasts
inferred← citeshttps://doi.org/10.1016/j.jneuroim.2012.03.003openalex-snapshot
Increased promoter methylation of the immune regulatory gene SHP-1 in leukocytes of multiple sclerosis subjects
inferred← citeshttps://doi.org/10.1016/j.mad.2020.111309openalex-snapshot
The role of epigenetics and non-coding RNAs in autophagy: A new perspective for thorough understanding
inferred← citeshttps://doi.org/10.1016/j.mce.2011.10.025openalex-snapshot
The endometrial epigenome and its response to steroid hormones
inferred← citeshttps://doi.org/10.1016/j.mce.2016.07.001openalex-snapshot
Persistent influence of maternal obesity on offspring health: Mechanisms from animal models and clinical studies
inferred← citeshttps://doi.org/10.1016/j.mce.2016.09.032openalex-snapshot
Perinatal exposure to bisphenol A modifies the transcriptional regulation of the β-Casein gene during secretory activation of the rat mammary gland
inferred← citeshttps://doi.org/10.1016/j.mcn.2025.104055openalex-snapshot
Decoding aging through nitrogen containing compounds: A nutrigenomic insight
inferred← citeshttps://doi.org/10.1016/j.metabol.2021.154920openalex-snapshot
Epigenetic modifications in diabetes
inferred← citeshttps://doi.org/10.1016/j.mmr.2026.100024openalex-snapshot
Therapeutic potential of HDAC6 inhibitor Tubastatin A in health and diseases: current perspective and future directions
inferred← citeshttps://doi.org/10.1016/j.molcel.2023.12.021openalex-snapshot
Sequencing of N6-methyl-deoxyadenosine at single-base resolution across the mammalian genome
inferred← citeshttps://doi.org/10.1016/j.molonc.2012.11.004openalex-snapshot
HDAC1‐mSin3a‐NCOR1, Dnmt3b‐HDAC1‐Egr1 and Dnmt1‐PCNA‐UHRF1‐G9a regulate the NY‐ESO1 gene expression
inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2008.07.006openalex-snapshot
Chromatin, cancer and drug therapies
inferred← citeshttps://doi.org/10.1016/j.mrfmmm.2015.03.004openalex-snapshot
MWCNT uptake in Allium cepa root cells induces cytotoxic and genotoxic responses and results in DNA hyper-methylation
inferred← citeshttps://doi.org/10.1016/j.mrrev.2011.04.001openalex-snapshot
Epigenetic mechanisms in hepatocellular carcinoma: How environmental factors influence the epigenome
inferred← citeshttps://doi.org/10.1016/j.msard.2013.08.007openalex-snapshot
The epigenetics of multiple sclerosis and other related disorders
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2021.10.001openalex-snapshot
Implications on hypnotherapy: Neuroplasticity, epigenetics and pain
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2023.105194openalex-snapshot
The epigenetics of animal personality
inferred← citeshttps://doi.org/10.1016/j.nlm.2012.03.007openalex-snapshot
Epigenetic regulation of reelin and brain-derived neurotrophic factor genes in long-term potentiation in rat medial prefrontal cortex
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2014.09.005openalex-snapshot
Epigenetic therapy as a novel approach in hepatocellular carcinoma
inferred← citeshttps://doi.org/10.1016/j.phrs.2016.09.023openalex-snapshot
Epigenetic regulation of active Chinese herbal components for cancer prevention and treatment: A follow-up review
inferred← citeshttps://doi.org/10.1016/j.preteyeres.2024.101318openalex-snapshot
Role of epigenetics in corneal health and disease
inferred← citeshttps://doi.org/10.1016/j.reprotox.2012.10.011openalex-snapshot
Effect of developmental dioxin exposure on methylation and expression of specific imprinted genes in mice
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