To gain a deeper insight into dynamic changes of H3K9cr and H3K9ac during cell fate commitment, ChIP-seq was performed to analyze the genome-wide changes of H3K9cr and H3K9ac during neuroectodermal di
H3K27me3 was enhanced in the gene loci related to the inflammatory pathway. Overall design: MAT2Ai (10 mg/kg BW) was injected into intraperitoneal cavity of SGLT2 MT mice with prior exposure to HFD fo
H3K4 methylation is a conserved histone modification crucial for gene regulation, yet the post-translational modifications of the Set1-COMPASS complex remain largely unexplored. This study elucidates
