Quiescence Enables Unrestricted Cell Fate in Naive Embryonic Stem Cells

Quiescence Enables Unrestricted Cell Fate in Naive Embryonic Stem Cells

Quiescence Enables Unrestricted Cell Fate in Naive Embryonic Stem Cells

Profiling histone post-translational modifications in mouse adult hepatocytes, biliary epithelial cells and biliary reprogrammed cells from hepatocytes.

Quiescence Enables Unrestricted Cell Fate in Naive Embryonic Stem Cells

Endocrine disruptor-induced epimutagenesis in vitro: Insight into molecular mechanisms [EM-Seq]

Endocrine disruptor-induced epimutagenesis in vitro: Insight into molecular mechanisms

Myocardial KLF15 epigenomic changes with single ZT0 prednisone pulse

Maternal Exercise Prior to and During Gestation Induces Sex-Specific Alterations in the Mouse Placenta

Maternal Western Diet Programs Cardiometabolic Dysfunction and Hypothalamic Inflammation via Epigenetic Mechanisms Predominantly in the Male Offspring [Methyl-seq]

Maternal Western Diet Programs Cardiometabolic Dysfunction and Hypothalamic Inflammation via Epigenetic Mechanisms Predominantly in the Male Offspring

Acute gastrointestinal permeability after traumatic brain injury in mice precedes a bloom in Akkermansia muciniphila supported by intestinal hypoxia

TRAIL deletion in myeloid cells augments cholestatic liver injury

Maternal Western Diet Programs Cardiometabolic Dysfunction and Hypothalamic Inflammation via Epigenetic Mechanisms Predominantly in the Male Offspring [RNA-seq]

The R1441C-LRRK2 mutation induces myeloid immune cell exhaustion in an age- and sex-dependent manner

Lysine tRNA fragments and miR-194-5p co-regulate hepatic steatosis via β-Klotho and Perilipin 2 (small RNA I)

Lysine tRNA fragments and miR-194-5p co-regulate hepatic steatosis via β-Klotho and Perilipin 2 (small RNA II)

Nanopore long-read RNA sequencing shows region-specific sex differences in wild-type mouse brain mRNA isoform expression and usage

4E-BP1-dependent translation in microglia controls mechanical hypersensitivity

Maintenance of hematopoietic stem cells by tyrosine-unphosphorylated STAT5 and JAK inhibition