The murine bleomycin (BLM)-induced fibrosis model is the most widely used in systemic sclerosis (SSc) studies. It has been reported that systemic delivery of BLM via continuous diffusion from subcutan
10x multiome data on E15.5 and E18.5 mouse lungs from ctrl, Tbx4-rtTa;Tet-Cre;Snai1f/f;Snai2f/f, Tbx4-rtTa;Tet-Cre;Yap1f/f;Wwtr1f/f and Tbx4-rtTa;Tet-Cre;Stk3f/f;Stk4f/f (Mst12) mice induced from E9.5
Gene expression data from bioprinted liver tissues comprising primary human hepatocytes (HCs), hepatic stellate cells (HSCs), and human umbilical vein endothelial cells (HUVECs) with and without Kupff
A mouse model of bleomycin (BLM)-induced pulmonary fibrosis was established. IMRC-EVs were infused via the tracheal or intravenous route. By accurately measuring the transcripts provided by RNA-seq te
