Tao Yang
14PUBLICATIONS
19CO-AUTHORS
Get your video featured.
Publish with JoVEGet your video featured.
Publish with JoVE
Publications (14)
Sort by Publication Date:
|Oct 14, 2024
The p. S178L mutation in Tbc1d24 disrupts endosome-mediated synaptic vesicle trafficking of cochlear hair cells and leads to hearing impairment in mice.Penghui Chen, Shule Hou, Gen Li
|May 12, 2021
Next-Generation Sequencing Identifies Pathogenic Variants in HGF, POU3F4, TECTA, and MYO7A in Consanguineous Pakistani Deaf Families.Xueshuang Mei, Yaqi Zhou, Muhammad Amjad
|Aug 18, 2020
Compound Heterozygous Mutations in TMC1 and MYO15A Are Associated with Autosomal Recessive Nonsyndromic Hearing Loss in Two Chinese Han Families.Pengcheng Xu, Jun Xu, Hu Peng
|Aug 11, 2020
THOC1 deficiency leads to late-onset nonsyndromic hearing loss through p53-mediated hair cell apoptosis.Luping Zhang, Yu Gao, Ru Zhang
|Jul 04, 2020
Targeted Next-Generation Sequencing Identified Compound Heterozygous Mutations in MYO15A as the Probable Cause of Nonsyndromic Deafness in a Chinese Han Family.Longhao Wang, Lin Zhao, Hu Peng
|Jan 30, 2020
Molecular epidemiology of Chinese Han deaf patients with bi-allelic and mono-allelic GJB2 mutations.Xiaoyu Yu, Yun Lin, Jun Xu
Pageof 3
