Area of research
Cancer Research · Cell Biology
Research interest
Research focused on Neointima and Vascular smooth muscle, with related work in Cell biology, Myocardin, Long non-coding RNA. Notable publications include 'Long noncoding RNA NEAT1 (nuclear paraspeckle assembly transcript 1) is critical for phenotypic switching of vascular smooth muscle cells', 'TEAD1 (TEA Domain Transcription Factor 1) Promotes Smooth Muscle Cell Proliferation Through Upregulating SLC1A5 (Solute Carrier Family 1 Member 5)-Mediated Glutamine Uptake', and 'Transcription factor TEAD1 is essential for vascular development by promoting vascular smooth muscle differentiation'.
[Evaluation of severity and prognosis of acute pancreatitis by CT severity index and modified CT severity index].
YAP1/TEAD1 upregulate platelet-derived growth factor receptor beta to promote vascular smooth muscle cell proliferation and neointima formation
YY1 directly interacts with myocardin to repress the triad myocardin/SRF/CArG box-mediated smooth muscle gene transcription during smooth muscle phenotypic modulation
TEAD1 (TEA Domain Transcription Factor 1) Promotes Smooth Muscle Cell Proliferation Through Upregulating SLC1A5 (Solute Carrier Family 1 Member 5)-Mediated Glutamine Uptake
Transcription factor TEAD1 is essential for vascular development by promoting vascular smooth muscle differentiation
Long noncoding RNA <i>NEAT1</i> (nuclear paraspeckle assembly transcript 1) is critical for phenotypic switching of vascular smooth muscle cells
Long noncoding RNA NEAT1 (nuclear paraspeckle assembly transcript 1) is critical for phenotypic switching of vascular smooth muscle cells
PMC 2018cited by 16position: middle