Ming Lei
The Affiliated Yongchuan Hospital of Chongqing Medical University(CN)Chongqing Medical University(CN)
Publications by Year
Research Areas
Hereditary Neurological Disorders, Cancer-related molecular mechanisms research, RNA Research and Splicing, Neurological diseases and metabolism, Endoplasmic Reticulum Stress and Disease
Most-Cited Works
- → A long noncoding RNA maintains active chromatin to coordinate homeotic gene expression(2011)2,015 cited
- → Mutations in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia(2001)359 cited
- → Neuropathy Target Esterase Gene Mutations Cause Motor Neuron Disease(2008)243 cited
- → Essential role of lncRNA binding for WDR5 maintenance of active chromatin and embryonic stem cell pluripotency(2014)202 cited
- Mutations in a novel GTPase cause autosomal dominant hereditary spastic paraplegia.(2001)
- → miR-361-3p overexpression promotes apoptosis and inflammation by regulating the USP49/IκBα/NF-κB pathway to aggravate sepsis-induced myocardial injury(2024)2 cited
- → Author response: Essential role of lncRNA binding for WDR5 maintenance of active chromatin and embryonic stem cell pluripotency(2013)
- → Hereditary spastic paraplegia with simultaneous mutations of Atlastin and Nipa1 genes in one family(2008)
- The mechanism for PKA-mediated facilitation of Cav1.2 channel: a new model(2017)
- → Abstract 2117: GenSciP107, a MICA/B-directed and Fc-enhanced antibody, potently inhibits tumor growth via ADCC and stimulation of immune response(2025)