A DNMT3A PWWP mutation leads to methylation of bivalent chromatin and postnatal growth retardation in mice

A Molecular Signature Defining Exercise Adaptation and In Vivo Reprogramming in Skeletal Muscle

A maternal-effect Padi6 variant causes nuclear and cytoplasmic abnormalities in oocytes as well 2 as failure of epigenetic reprogramming and zygotic genome activation in embryos

A novel role of Tet1/2 proteins in cell cycle progression of trophoblast stem cells

AMAR-seq: automated multimodal sequencing of DNA methylation, chromatin accessibility, and RNA expression with single-cell resolution

Ablation of DNA-methyltransferase 3A in skeletal muscle does not affect energy metabolism or exercise capacity

Activation of neuronal genes via LINE-1 elements upon global DNA demethylation in human neural progenitors

Age-associated cryptic transcription in mammalian stem cells is linked to permissive chromatin at cryptic promoters

Ageing affects DNA methylation and transcriptional cell-to-cell variability in muscle stem cells

Aging imparts cell-autonomous dysfunction to regulatory T cells during recovery from influenza pneumonia

An engineered Sox17 induces somatic to neural stem cell fate transition independently from pluripotency reprogramming

Astrocyte Reactivity and Cognitive Decline Follow Chronic Heterochromatin Loss in Neurons

Astrocyte-produced HB-EGF limits autoimmune CNS pathology

CATACOMB: an endogenous inducible gene that antagonizes H3K27 methylation activity of Polycomb Repressive complex 2 via a H3K27M-like mechanism

Cancer prevention by phenethyl isothiocyanate (PEITC) in transgenic adenocarcinoma of the mouse prostate (TRAMP) mice

Cancer-associated DNA Hypermethylation of Polycomb Targets Requires DNMT3A Dual Recognition of histone H2AK119 Ubiquitination and the Nucleosome Acidic Patch

Cancer-specific CTCF binding facilitates oncogenic transcriptional dysregulation

Cell type purification by single-cell transcriptome-trained sorting

Cell-type specific DNA methylome signatures reveal epigenetic mechanisms for neuronal diversity and neurodevelopmental disorder

ChIP-seq, RNA-seq and BS-seq for WT and osino80