Area of research
Molecular Biology · Cancer Research
Research interest
Research focused on Slug and Haematopoiesis, with related work in Gene knockdown, Cell biology, FOXM1. Notable publications include 'Activation of Wnt/β-Catenin Protein Signaling Induces Mitochondria-mediated Apoptosis in Hematopoietic Progenitor Cells', 'The transcription factor Foxm1 is essential for the quiescence and maintenance of hematopoietic stem cells', and 'The transcription factor Slug represses p16Ink4a and regulates murine muscle stem cell aging'.
Hepatic Snai1 and Snai2 promote liver regeneration and suppress liver fibrosis in mice
ZBTB7C m6A modification incurred by METTL3 aberration promotes osteosarcoma progression
miR-30e-5p regulates leukemia stem cell self-renewal through the Cyb561/ROS signaling pathway
Long noncoding RNA TUG1 promotes malignant progression of osteosarcoma by enhancing ZBTB7C expression
Hepatic Slug epigenetically promotes liver lipogenesis, fatty liver disease, and type 2 diabetes
A Cdh1–FoxM1–Apc axis controls muscle development and regeneration
The transcription factor Slug represses p16Ink4a and regulates murine muscle stem cell aging
Inhibition of Slug effectively targets leukemia stem cells via the Slc13a3/ROS signaling pathway
The transcription factor Foxm1 is essential for the quiescence and maintenance of hematopoietic stem cells
Sodium Butyrate Facilitates Reprogramming by Derepressing OCT4 Transactivity at the Promoter of Embryonic Stem Cell–Specific miR-302/367 Cluster
Activation of Wnt/β-Catenin Protein Signaling Induces Mitochondria-mediated Apoptosis in Hematopoietic Progenitor Cells