Area of research
Molecular Biology · Cellular and Molecular Neuroscience
Research interest
Research interests include RNA modifications and cancer, Genetic Neurodegenerative Diseases, Cancer-related gene regulation, and Amyotrophic Lateral Sclerosis Research.
uN2CpolyG-mediated p65 nuclear sequestration suppresses the NF-κB-NLRP3 pathway in neuronal intranuclear inclusion disease
Metabolic inflexibility promotes mitochondrial health during liver regeneration
Deep learning assists detection of esophageal cancer and precursor lesions in a prospective, randomized controlled study
The association between prenatal bisphenol F exposure and infant neurodevelopment: The mediating role of placental estradiol
Encephalitis-like episodes with cortical edema and enhancement in patients with neuronal intranuclear inclusion disease
Cerebral involvement in sitosterolemia
The relationship between circulating metabolites and prostate hyperplasia: a Mendelian randomization study
FUS Mutation Causes Disordered Lipid Metabolism in Skeletal Muscle Associated with ALS
Genetic spectrum in a cohort of patients with distal hereditary motor neuropathy
Subclinical peripheral neuropathy is common in neuronal intranuclear inclusion disease with dominant encephalopathy
Diverse myopathological features in the congenital myasthenia syndrome with GFPT1 mutation
Additional file 3 of The relationship between menopausal syndrome and gut microbes
Additional file 4 of The relationship between menopausal syndrome and gut microbes
The GGC repeat expansion in<i>NOTCH2NLC</i>is associated with oculopharyngodistal myopathy type 3
Genetic origin of sporadic cases and RNA toxicity in neuronal intranuclear inclusion disease
Matricellular Protein Cilp1 Promotes Myocardial Fibrosis in Response to Myocardial Infarction
GGC repeat expansions in NOTCH2NLC causing a phenotype of distal motor neuropathy and myopathy
Expansion of GGC Repeat in GIPC1 Is Associated with Oculopharyngodistal Myopathy
Repeat expansion scanning of the <i>NOTCH2NLC</i> gene in patients with multiple system atrophy
Clinical and pathological features in adult-onset NIID patients with cortical enhancement
<i>FUS</i> P525L mutation causing amyotrophic lateral sclerosis and movement disorders
Fatty Acid Metabolites Combine with Reduced β Oxidation to Activate Th17 Inflammation in Human Type 2 Diabetes
Long-read sequencing identified repeat expansions in the 5′UTR of the <i>NOTCH2NLC</i> gene from Chinese patients with neuronal intranuclear inclusion disease
Clinical and muscle magnetic resonance image findings in patients with late-onset multiple acyl-CoA dehydrogenase deficiency
Beclin-1-Dependent Autophagy Protects the Heart During Sepsis
Novel <b><i>ABCD1</i></b> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum
Arid1a Has Context-Dependent Oncogenic and Tumor Suppressor Functions in Liver Cancer
Phenotype variability and histopathological findings in patients with a novel <i>DNM2</i> mutation
Th17 cytokines differentiate obesity from obesity‐associated type 2 diabetes and promote <scp>TNF</scp>α production
Up-regulation of Tim-3 is associated with poor prognosis of patients with colon cancer.
PubMed 2015cited by 86position: middle