DNA methylation drug

Aliases

CpG methylation, DNA methylation, DNA methylation changes, DNA methylation marks, DNA methylation pattern, DNA methylation patterns, X chromosome DNA methylation, cytosine methylation, hypomethylation, methylated DNA, methylated cytosine, methylation, promoter DNA methylation

External links

DrugBank · PubChem

Related entities (9)

Mentioned in (71)

Papers in which this entity is mentioned.

• Integrative epigenetics and transcriptomics identify aging genes in human blood. (2026)
• Consortium profile: the methylation, imaging and NeuroDevelopment (MIND) consortium. (2026)
• Advancing regulatory variant effect prediction with AlphaGenome. (2026)
• Investigation of a global mouse methylome atlas reveals subtype-specific copy number alterations in pediatric cancer models. (2026)
• LINE-1 retrotransposons mediate cis-acting transcriptional control in human pluripotent stem cells and regulate early brain development. (2025)
• Multi-omic quantitative trait loci link tandem repeat size variation to gene regulation in human brain. (2025)
• Rapid brain tumor classification from sparse epigenomic data. (2025)
• Chromosomal instability as a driver of cancer progression. (2025)
• Three-dimensional genome landscape of primary human cancers. (2025)
• Synchronized long-read genome, methylome, epigenome and transcriptome profiling resolve a Mendelian condition. (2025)
• Alcohol Exposure May Increase Prenatal Choline Needs Through Redirection of Choline into Lipid Synthesis Rather than Methyl Donation. (2025)
• Foundation models in bioinformatics. (2025)
• Transcription start sites experience a high influx of heritable variants fueled by early development. (2025)
• Predicting fetal alcohol spectrum disorders in preschool-aged children from early life factors. (2024)
• Machine learning approaches to the identification of children affected by prenatal alcohol exposure: A narrative review. (2024)
• Consortium Profile: The Methylation, Imaging and NeuroDevelopment (MIND) Consortium. (2024)
• The Application of Long-Read Sequencing to Cancer. (2024)
• A DNA methylation atlas of normal human cell types. (2023)
• Predicting Fetal Alcohol Spectrum Disorders Using Machine Learning Techniques: Multisite Retrospective Cohort Study. (2023)
• Single-molecule methylation profiles of cell-free DNA in cancer with nanopore sequencing. (2023)
• RNA splicing dysregulation and the hallmarks of cancer. (2023)
• Nucleosome footprinting in plasma cell-free DNA for the pre-surgical diagnosis of ovarian cancer. (2022)
• At the dawn: cell-free DNA fragmentomics and gene regulation. (2022)
• Epigenetic analysis of cell-free DNA by fragmentomic profiling. (2022)
• Nanopore sequencing of RNA and cDNA molecules in . (2022)
• Cell-free DNA technologies for the analysis of brain cancer. (2022)
• Detecting cell-of-origin and cancer-specific methylation features of cell-free DNA from Nanopore sequencing. (2022)
• Large-scale collaboration in ENIGMA-EEG: A perspective on the meta-analytic approach to link neurological and psychiatric liability genes to electrophysiological brain activity. (2021)
• Prenatal Adversity Alters the Epigenetic Profile of the Prefrontal Cortex: Sexually Dimorphic Effects of Prenatal Alcohol Exposure and Food-Related Stress. (2021)
• Evaluating the transcriptional fidelity of cancer models. (2021)
• Programmed suppression of oxidative phosphorylation and mitochondrial function by gestational alcohol exposure correlate with widespread increases in H3K9me2 that do not suppress transcription. (2021)
• Therapeutic Implications of Germline Testing in Patients With Advanced Cancers. (2021)
• Hypermethylation of Proopiomelanocortin and Period 2 Genes in Blood Are Associated with Greater Subjective and Behavioral Motivation for Alcohol in Humans. (2019)
• Super-enhancers: critical roles and therapeutic targets in hematologic malignancies. (2019)
• The mutational constraint spectrum quantified from variation in 141,456 humans (2019)
• Persistent Changes in Stress-Regulatory Genes in Pregnant Women or Children Exposed Prenatally to Alcohol. (2019)
• Ventral striatal regulation of CREM mediates impulsive action and drug addiction vulnerability. (2018)
• The Human Transcription Factors. (2018)
• The Immune Landscape of Cancer. (2018)
• Nanopore sequencing and assembly of a human genome with ultra-long reads. (2018)
• HRDetect is a predictor of BRCA1 and BRCA2 deficiency based on mutational signatures. (2017)
• Integrative clustering of multi-level 'omic data based on non-negative matrix factorization algorithm. (2017)
• Epigenetics studies of fetal alcohol spectrum disorder: where are we now? (2017)
• Cell-free DNA Comprises an In Vivo Nucleosome Footprint that Informs Its Tissues-Of-Origin. (2016)
• Association of germline variants in the APOBEC3 region with cancer risk and enrichment with APOBEC-signature mutations in tumors. (2016)
• Landscape of somatic mutations in 560 breast cancer whole-genome sequences. (2016)
• Divergent clonal evolution of castration-resistant neuroendocrine prostate cancer. (2016)
• Comprehensive analyses of tumor immunity: implications for cancer immunotherapy. (2016)
• The PsychENCODE project. (2015)
• Recurrent somatic mutations in regulatory regions of human cancer genomes. (2015)
• CTCF as a multifunctional protein in genome regulation and gene expression. (2015)
• The impact of micronutrient supplementation in alcohol-exposed pregnancies on information processing skills in Ukrainian infants. (2015)
• Advances in Diagnosis and Treatment of Fetal Alcohol Spectrum Disorders: From Animal Models to Human Studies. (2015)
• Reconstructing A/B compartments as revealed by Hi-C using long-range correlations in epigenetic data. (2015)
• MBASED: allele-specific expression detection in cancer tissues and cell lines. (2014)
• Involvement of p53 in the repair of DNA double strand breaks: multifaceted Roles of p53 in homologous recombination repair (HRR) and non-homologous end joining (NHEJ). (2014)
• Cancer genome landscapes. (2013)
• Integrative analysis of complex cancer genomics and clinical profiles using the cBioPortal. (2013)
• Emerging landscape of oncogenic signatures across human cancers. (2013)
• Pan-cancer patterns of somatic copy number alteration. (2013)
• Integrative analysis reveals relationships of genetic and epigenetic alterations in osteosarcoma. (2012)
• Mutational processes molding the genomes of 21 breast cancers. (2012)
• An integrated encyclopedia of DNA elements in the human genome. (2012)
• Differential expression in RNA-seq: a matter of depth. (2011)
• Fetal alcohol spectrum disorders: research challenges and opportunities. (2011)
• Gene-environment interaction in psychological traits and disorders. (2011)
• Transcriptional and epigenetic mechanisms of addiction. (2011)
• Comparison of Beta-value and M-value methods for quantifying methylation levels by microarray analysis. (2010)
• Structural, metabolic, and functional brain abnormalities as a result of prenatal exposure to drugs of abuse: evidence from neuroimaging. (2010)
• Maternal ethanol consumption alters the epigenotype and the phenotype of offspring in a mouse model. (2010)
• RNA-seq: an assessment of technical reproducibility and comparison with gene expression arrays. (2008)

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