Quorum sensing by Streptococcus pyogenes induces global inflammatory suppression in host macrophages

Bile acid receptor FXR promotes intestinal epithelial ferroptosis and subsequent ILC3 dysfunction in neonatal necrotizing enterocolitis [IEC bulk RNA-seq]

Effect of external cues on clock-driven time-of-day specific protection from Influenza A infection

Bile acid receptor FXR promotes intestinal epithelial ferroptosis and subsequent ILC3 dysfunction in neonatal necrotizing enterocolitis [ILC3s bulk RNA-seq]

The liver clock drives circadian rhythms in white adipose tissue [AML12]

The liver clock drives circadian rhythms in white adipose tissue [WTKOLRE]

The liver clock drives circadian rhythms in white adipose tissue [WT_LKO]

Transcriptional profiling of striatum and cortex from a mouse model of Huntington's disease (Q140) crossed with Pms1 heterozygous and homozygous mice

Succinate Dehydrogenase Regulates Homeostasis and Metabolic Integrity of Alveolar Macrophages

An Environmental Toxin-Based Approach to Revealing c-MYC as the Key Regulator of Embryo Compaction

Microenvironmental arginine restriction sensitizes pancreatic cancers to polyunsaturated fatty acids by suppression of lipid synthesis

ATF3 regulates hepatic ApoA4 upon metabolic stress

Bmal1 KO mouse lung versus WT under three ribosomal depletion methods

Impact of ribosomal depletion, PCR ramp rate, and fragment length on RNA-seq

Dysregulation of adipocytokines regulated by hsa-miR-548ay-3p/PPARγ signaling pathway leaded to cardiac fibrosis

RNA-seq analysis of E11.5 and E12.5 Mboat7 KO cortices

H3K36me3 Modification by SETD2 is Essential for Col11a2 and Sema3e Transcription to Maintain Dentinogenesis in Mice

Bile acid receptor FXR promotes intestinal epithelial ferroptosis and subsequent ILC3 dysfunction in neonatal necrotizing enterocolitis [SI bulk RNA-seq]

TDP-43 directly inhibits RNA accumulation in neurites through modulation of RNA stability

Intrapulmonary metastases of non-small cell lung cancer promoted by a hotspot gain-of-function mutation in KMT2C