Area of research
Sensory Systems · Renewable Energy, Sustainability and the Environment
Research interest
Research interests include Hearing loss, Chemistry, Catalysis, Biology, Genetics, and Cochlea.
Alleviating O-Intermediates Adsorption Strength over PdRhCu Ternary Metallene via Ligand Effect for Enhanced Oxygen Reduction in Practical PEMFCs
Expediting the Volmer Step of Alkaline Hydrogen Oxidation with High-Efficiency and CO-Tolerance by Ru–O–Eu Bridge
Manipulation of Electronic States of Pt Sites via d-Band Center Tuning for Enhanced Oxygen Reduction Reaction in Proton Exchange Membrane Fuel Cells
Weakening O-Intermediates Adsorption Strength Over the Pd Metallene via Lewis-Acidic Site Modulation for Enhanced Oxygen Reduction
Ligand Effect-Induced Electronic Structure Manipulation of Media-Entropy Alloy for Remarkable Stability over 50,000 Cycles in Oxygen Reduction
A novel variant in GAS2 is associated with autosomal dominant nonsyndromic hearing impairment in a Chinese family
Stub1 promotes degradation of the activated Diaph3: A negative feedback regulatory mechanism of the actin nucleator
Tailoring the Chemisorption Manner of Fe d‐Band Center with La<sub>2</sub>O<sub>3</sub> for Enhanced Oxygen Reduction in Anion Exchange Membrane Fuel Cells
Facilitating Reconstruction of the Heterointerface Electronic Structure by the Enriched Oxygen Vacancy for the Oxygen Evolution Reaction
Novel biallelic variants in the PLEC gene are associated with severe hearing loss
Precise detection of CRISPR-Cas9 editing in hair cells in the treatment of autosomal dominant hearing loss
A humanized murine model, demonstrating dominant progressive hearing loss caused by a novel <scp>KCNQ4</scp> mutation (p. <scp>G228D</scp> ) from a large Chinese family
Combination of tea polyphenols and proanthocyanidins prevents menopause-related memory decline in rats via increased hippocampal synaptic plasticity by inhibiting p38 MAPK and TNF-α pathway
Transcriptome analysis of molecular mechanisms underlying facial nerve injury repair in rats
THOC1 deficiency leads to late-onset nonsyndromic hearing loss through p53-mediated hair cell apoptosis
Clinical and genetic study of 12 Chinese Han families with nonsyndromic deafness
Inhibitive Effect of Resveratrol on the Inflammation in Cultured Astrocytes and Microglia Induced by Aβ1–42
Genetic Etiology Study of Ten Chinese Families with Nonsyndromic Hearing Loss
Akt and cAMP response element binding protein mediate 17β-estradiol regulation of glucose transporter 3 expression in human SH-SY5Y neuroblastoma cell line
A Dominant Mutation in the Stereocilia-Expressing Gene<i>TBC1D24</i>is a Probable Cause for Nonsyndromic Hearing Impairment