Area of research
Molecular Biology · Cardiology and Cardiovascular Medicine
Research interest
Research interests include Muscle Physiology and Disorders, Cardiomyopathy and Myosin Studies, RNA Research and Splicing, and Amyotrophic Lateral Sclerosis Research.
L-NAME improves the morphology and necrosis of skeletal muscle by activating PINK1-PARKIN mediated mitophagy in mdx mice
Clinical, pathological and genetic characteristics of GNE myopathy: a single-center observational study
Research hotspots and trends for Duchenne muscular dystrophy: a machine learning bibliometric analysis from 2004 to 2023
Comprehensive analysis of m6A regulators characterized by the immune microenvironment in Duchenne muscular dystrophy
Additional file 7 of Comprehensive analysis of m6A regulators characterized by the immune microenvironment in Duchenne muscular dystrophy
Identification of Auxiliary Biomarkers and Description of the Immune Microenvironmental Characteristics in Duchenne Muscular Dystrophy by Bioinformatical Analysis and Experiment
The clinical, myopathological, and molecular characteristics of 26 Chinese patients with dysferlinopathy: a high proportion of misdiagnosis and novel variants
The clinical, pathological, and genetic characteristics of lipid storage myopathy in northern China
NOTCH2NLC-related oculopharyngodistal myopathy type 3 complicated with focal segmental glomerular sclerosis: a case report
Case Report: A Novel Splice-Site Mutation in DNAJB6 Associated With Juvenile-Onset Proximal–Distal Myopathy in a Chinese Patient
Correction: NOTCH2NLC-related oculopharyngodistal myopathy type 3 complicated with focal segmental glomerular sclerosis: a case report
Clinical heterogeneity and molecular characteristics in a group of Chinese patients with dysferlinopathy
Activation of the Notch Signaling Pathway and Cellular Localization of Notch Signaling Molecules in the Spinal Cord of SOD1-G93A ALS Model Mice
Effect of AAV9-hIGF-1 on inflammatory reaction in mdx mice and its mechanism.
PubMed 2020cited by 6position: middle
Golgi apparatus fragmentation participates in oxidized low‐density lipoprotein‐induced endothelial cell injury
Adolescent Hyperuricemia with Lipid Storage Myopathy: A Clinical Study
Identification of a novel <i>SGCA</i> missense mutation in a case of limb‐girdle muscular dystrophy 2D with the absence of four sarcoglycan proteins
A novel mutation in the DYSF gene in a patient with a presumed inflammatory myopathy
A novel DMD splicing mutation found in a family responsible for X-linked dilated cardiomyopathy with hyper-CKemia
Adeno-associated virus serotype 9 mediated vascular endothelial growth factor gene overexpression in mdx mice