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Pu Dai

Showing results (181-190 of 218) with videos related to

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Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|September 25, 2007
[Genetic counseling and instruction for deaf couples directed by genetic testing]Bing Han, Pu Dai, Guo-jian Wang, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|August 4, 2011
[Cochlear implantation with pericanal electrode insertion technique]Tingting Cui, Hong Jiang, Xiaowei Chen, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|March 11, 2025
Single Administration of AAV-mAtp6v1b2 Gene Therapy Rescues Hearing and Vestibular Disorders Caused by Atp6v1b2-Induced Lysosomal Dysfunction in Hair CellsGege Wei, Shiwei Qiu, Xue Gao, et al.
Yi Chuan = Hereditas|December 2, 2006
[Mapping of gene underlying autosomal dominant non-syndromic hearing loss(DFNA)]Han-Jun Sun, Ran Tao, Jing Cheng, et al.
Journal of Human Genetics|August 18, 2022
Molecular diagnose of a large hearing loss population from China by targeted genome sequencingJie Wu, Zongfu Cao, Yu Su, et al.
Biomed Research International|June 1, 2018
A Missense Mutation in <i>POU4F3</i> Causes Midfrequency Hearing Loss in a Chinese ADNSHL FamilyXue Gao, Jin-Cao Xu, Wei-Qian Wang, et al.
Journal of Translational Medicine|November 12, 2013
Novel compound heterozygous mutations in the MYO15A gene in autosomal recessive hearing loss identified by whole-exome sequencingXue Gao, Qing-yan Zhu, Yue-Shuai Song, et al.
Plos One|May 22, 2013
Novel compound heterozygous TMC1 mutations associated with autosomal recessive hearing loss in a Chinese familyXue Gao, Yu Su, Li-Ping Guan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 3, 2006
Molecular bases of hearing loss in multi-systemic mitochondrial cytopathyFernando Scaglia, Chang-Hung Hsu, Haeyoung Kwon, et al.
Zhonghua Yi Xue Za Zhi|June 27, 2006
[Large-scale screening of mtDNA A1555G mutation in China and its significance in prevention of aminoglycoside antibiotic induced deafness]Xin Liu, Pu Dai, De-liang Huang, et al.
Pageof 22

Showing results (181-190 of 218) with videos related to

Sort By:
Pageof 22
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|September 25, 2007
[Genetic counseling and instruction for deaf couples directed by genetic testing]Bing Han, Pu Dai, Guo-jian Wang, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|August 4, 2011
[Cochlear implantation with pericanal electrode insertion technique]Tingting Cui, Hong Jiang, Xiaowei Chen, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|March 11, 2025
Single Administration of AAV-mAtp6v1b2 Gene Therapy Rescues Hearing and Vestibular Disorders Caused by Atp6v1b2-Induced Lysosomal Dysfunction in Hair CellsGege Wei, Shiwei Qiu, Xue Gao, et al.
Yi Chuan = Hereditas|December 2, 2006
[Mapping of gene underlying autosomal dominant non-syndromic hearing loss(DFNA)]Han-Jun Sun, Ran Tao, Jing Cheng, et al.
Journal of Human Genetics|August 18, 2022
Molecular diagnose of a large hearing loss population from China by targeted genome sequencingJie Wu, Zongfu Cao, Yu Su, et al.
Biomed Research International|June 1, 2018
A Missense Mutation in <i>POU4F3</i> Causes Midfrequency Hearing Loss in a Chinese ADNSHL FamilyXue Gao, Jin-Cao Xu, Wei-Qian Wang, et al.
Journal of Translational Medicine|November 12, 2013
Novel compound heterozygous mutations in the MYO15A gene in autosomal recessive hearing loss identified by whole-exome sequencingXue Gao, Qing-yan Zhu, Yue-Shuai Song, et al.
Plos One|May 22, 2013
Novel compound heterozygous TMC1 mutations associated with autosomal recessive hearing loss in a Chinese familyXue Gao, Yu Su, Li-Ping Guan, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 3, 2006
Molecular bases of hearing loss in multi-systemic mitochondrial cytopathyFernando Scaglia, Chang-Hung Hsu, Haeyoung Kwon, et al.
Zhonghua Yi Xue Za Zhi|June 27, 2006
[Large-scale screening of mtDNA A1555G mutation in China and its significance in prevention of aminoglycoside antibiotic induced deafness]Xin Liu, Pu Dai, De-liang Huang, et al.
Pageof 22