A single dose of dexamethasone encapsulated in polyethylene glycol-coated polylactic acid nanoparticles attenuates cisplatin-induced hearing loss following round window membrane administration

Dehong Yu, Hao Wu, Changling Sun, +5

International Journal of Nanomedicine

Inner ear delivery of dexamethasone using injectable silk-polyethylene glycol (PEG) hydrogel

Dehong Yu, Changling Sun, Zhaozhu Zheng, +5

International Journal of Pharmaceutics

Tissue EngineeringHydrogelsBiopolymer GelEngineeringPolymer Science +5

Dexamethasone loaded nanoparticles exert protective effects against Cisplatin-induced hearing loss by systemic administration

Changling Sun, Xueling Wang, Dongye Chen, +3

Neuroscience Letters

NanomedicineNanotherapeuticsTherapeutic NanomaterialsMedicineSystemic Administration +6

A dominant variant in DMXL2 is linked to nonsyndromic hearing loss

Dongye Chen, Xingfeng Liu, Xiaojiang Lin, +13

Genetics in Medicine

Genetic DisorderGeneticsAudiologyPathologyNonsyndromic Hearing Loss +6

Targeted Next-Generation Sequencing in Uyghur Families with Non-Syndromic Sensorineural Hearing Loss

Ying Chen, Zhentao Wang, Zhaoyan Wang, +7

PLoS ONE

Uyghur FamiliesGeneticsPathologyMolecular GeneticsDisease Gene Identification +19

A novel splice site mutation in DFNA5 causes late-onset progressive non-syndromic hearing loss in a Chinese family

Yongchuan Chai, Dongye Chen, Xiaowen Wang, +2

International Journal of Pediatric Otorhinolaryngology

Chinese FamilyDevelopmental BiologyGenetic DisorderGeneticsAudiology +8

Effects of long-term salicylate administration on synaptic ultrastructure and metabolic activity in the rat CNS

Bin Yi, Shousen Hu, Chuantao Zuo, +9

Scientific Reports

Characterization of Spectrum, de novo Rate and Genotype-Phenotype Correlation of Dominant GJB2 Mutations in Chinese Hans

Xiuhong Pang, Yongchuan Chai, Lianhua Sun, +5

PLoS ONE

EngineeringFamily MembersGeneticsMolecular BiologyMolecular Genetics +14

Clinical characterization of a novel COCH mutation G87V in a Chinese DFNA9 family

Dongye Chen, Yongchuan Chai, Tao Yang, +1

International Journal of Pediatric Otorhinolaryngology

Chinese Dfna9 FamilyMendelian DisorderGenetic DisorderMedicineGenetics +5

High Prevalence of the Connexin 26 (GJB2) Mutation in Chinese Cochlear Implant Recipients

Dongye Chen, Xiaowei Chen, Keli Cao, +4

ORL