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Shaoyang Sun

Showing results (31-40 of 46) with videos related to

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Frontiers in Neurology|February 25, 2022
Efficacy and Safety of Tirofiban in Clinical Patients With Acute Ischemic StrokeBin Han, Teng Ma, Zhendong Liu, et al.
Human Molecular Genetics|December 26, 2016
SLC44A4 mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing lossZhaoxin Ma, Wenjun Xia, Fei Liu, et al.
The International Journal of Developmental Biology|October 28, 2015
Down-regulation of msrb3 and destruction of normal auditory system development through hair cell apoptosis in zebrafishXiaofang Shen, Fei Liu, Yingzhi Wang, et al.
Plos One|September 17, 2015
Solute Carrier Family 26 Member a2 (slc26a2) Regulates Otic Development and Hair Cell Survival in ZebrafishFei Liu, Wenjun Xia, Jiongjiong Hu, et al.
DNA and Cell Biology|January 4, 2017
Disruption of the gaa Gene in Zebrafish Fails to Generate the Phenotype of Classical Pompe DiseaseJing Wu, Yi Yang, Chengjun Sun, et al.
BMC Neurology|December 21, 2014
Comparison of clinical characteristics between neuromyelitis optica spectrum disorders with and without spinal cord atrophyYanqiang Wang, Aimin Wu, Xiaoyu Chen, et al.
Human Mutation|July 6, 2017
New role of LRP5, associated with nonsyndromic autosomal-recessive hereditary hearing lossWenjun Xia, Jiongjiong Hu, Fei Liu, et al.
Biology Open|December 5, 2019
Combinatorial genetic replenishments in myocardial and outflow tract tissues restore heart function in <i>tnnt2</i> mutant zebrafishLian Liu, Fei Fei, Ranran Zhang, et al.
Genes & Diseases|July 2, 2025
Haplotype-resolved assemblies of the MHC region in five widely used tumor cell linesHaozhe Yuan, Mengping Jiang, Xingyu Xu, et al.
Disease Models & Mechanisms|July 30, 2017
Screening in larval zebrafish reveals tissue-specific distribution of fifteen fluorescent compoundsYuxiao Yao, Shaoyang Sun, Fei Fei, et al.
Pageof 5

Showing results (31-40 of 46) with videos related to

Sort By:
Pageof 5
Frontiers in Neurology|February 25, 2022
Efficacy and Safety of Tirofiban in Clinical Patients With Acute Ischemic StrokeBin Han, Teng Ma, Zhendong Liu, et al.
Human Molecular Genetics|December 26, 2016
SLC44A4 mutation causes autosomal dominant hereditary postlingual non-syndromic mid-frequency hearing lossZhaoxin Ma, Wenjun Xia, Fei Liu, et al.
The International Journal of Developmental Biology|October 28, 2015
Down-regulation of msrb3 and destruction of normal auditory system development through hair cell apoptosis in zebrafishXiaofang Shen, Fei Liu, Yingzhi Wang, et al.
Plos One|September 17, 2015
Solute Carrier Family 26 Member a2 (slc26a2) Regulates Otic Development and Hair Cell Survival in ZebrafishFei Liu, Wenjun Xia, Jiongjiong Hu, et al.
DNA and Cell Biology|January 4, 2017
Disruption of the gaa Gene in Zebrafish Fails to Generate the Phenotype of Classical Pompe DiseaseJing Wu, Yi Yang, Chengjun Sun, et al.
BMC Neurology|December 21, 2014
Comparison of clinical characteristics between neuromyelitis optica spectrum disorders with and without spinal cord atrophyYanqiang Wang, Aimin Wu, Xiaoyu Chen, et al.
Human Mutation|July 6, 2017
New role of LRP5, associated with nonsyndromic autosomal-recessive hereditary hearing lossWenjun Xia, Jiongjiong Hu, Fei Liu, et al.
Biology Open|December 5, 2019
Combinatorial genetic replenishments in myocardial and outflow tract tissues restore heart function in <i>tnnt2</i> mutant zebrafishLian Liu, Fei Fei, Ranran Zhang, et al.
Genes & Diseases|July 2, 2025
Haplotype-resolved assemblies of the MHC region in five widely used tumor cell linesHaozhe Yuan, Mengping Jiang, Xingyu Xu, et al.
Disease Models & Mechanisms|July 30, 2017
Screening in larval zebrafish reveals tissue-specific distribution of fifteen fluorescent compoundsYuxiao Yao, Shaoyang Sun, Fei Fei, et al.
Pageof 5