Area of research
Cancer Research · Molecular Biology
Research interest
Research focused on Cancer research and Wnt signaling pathway, with related work in Protein kinase B, Stroke (engine), Cell biology. Notable publications include 'The lncRNA NEAT1 activates Wnt/β-catenin signaling and promotes colorectal cancer progression via interacting with DDX5', 'FTO-dependent m6A modification of Plpp3 in circSCMH1-regulated vascular repair and functional recovery following stroke', and 'Integrating spatial and single-cell transcriptomics to characterize the molecular and cellular architecture of the ischemic mouse brain'.
FAP upregulates PD-L1 expression in cancer-associated fibroblasts to exacerbate T cells dysfunction and suppress anti-tumor immunity
Integrating spatial and single-cell transcriptomics to characterize the molecular and cellular architecture of the ischemic mouse brain
Correction: Li et al. Preliminary Evaluation of Protective Efficacy of Inactivated Senecavirus A on Pigs. Life 2021, 11, 157
FTO-dependent m6A modification of Plpp3 in circSCMH1-regulated vascular repair and functional recovery following stroke
Systems pharmacology-based mechanism exploration of Acanthopanax senticosusin for Alzheimer's disease using UPLC-Q-TOF-MS, network analysis, and experimental validation
Systems and breakdown of self-incompatibility
The effects of probiotics plus dietary fiber on antipsychotic-induced weight gain: a randomized clinical trial
Preliminary Evaluation of Protective Efficacy of Inactivated Senecavirus A on Pigs
RPS15A promotes gastric cancer progression via activation of the Akt/IKK‐β/NF‐κB signalling pathway
Myotubularin related protein 7 is essential for the spermatogonial stem cell homeostasis via PI3K/AKT signaling
The lncRNA NEAT1 activates Wnt/β-catenin signaling and promotes colorectal cancer progression via interacting with DDX5
Pim1 supports human colorectal cancer growth during glucose deprivation by enhancing the Warburg effect
Strawberry Notch 1 (SBNO1) promotes proliferation of spermatogonial stem cells via the noncanonical Wnt pathway in mice