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Pu Dai

Showing results (131-140 of 218) with videos related to

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Frontiers in Cell and Developmental Biology|November 8, 2021
Syndromic Deafness Gene <i>ATP6V1B2</i> Controls Degeneration of Spiral Ganglion Neurons Through Modulating Proton FluxShiwei Qiu, Weihao Zhao, Xue Gao, et al.
Plos One|March 6, 2012
Common molecular etiologies are rare in nonsyndromic Tibetan Chinese patients with hearing impairmentYongyi Yuan, Xun Zhang, Shasha Huang, et al.
American Journal of Medical Genetics. Part A|September 7, 2006
Variants in mitochondrial tRNAGlu, tRNAArg, and tRNAThr may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese families with hearing lossWie-Yen Young, Lidong Zhao, Yaping Qian, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|May 10, 2024
Clinical Application of the 4K-3D Exoscope System in Cochlear ImplantationHonglei Zhang, Guojian Wang, Xin Zhang, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|December 4, 2009
[Clinical analysis of adenoid cystic carcinoma of external auditory canal]Fei-fan Zhao, Jia-ling Wang, Wen-ming Wu, et al.
Zhonghua Yi Xue Za Zhi|July 2, 2009
[Mutation of Gap junction protein beta 2 gene and treatment outcome of cochlear implantation in cochlear implantation recipients]Jun Liu, Fei Yu, Pu Dai, et al.
Zhonghua Yi Xue Za Zhi|February 14, 2008
[Mutation screening of the COCH gene in familial and sporadic patients with late onset nonsyndromic sensorineural hearing loss among Chinese population]Qing Sun, Shu-Zhi Yang, Dong-Yang Kang, et al.
Acta Oto-Laryngologica|February 19, 2019
Cochlear implantation in patients with canal wall down mastoidectomy cavitiesSong Gao, Yi Jiang, Guo-Jian Wang, et al.
BMC Medical Genetics|September 5, 2018
Clinical and molecular characterization of POU3F4 mutations in multiple DFNX2 Chinese familiesYu Su, Xue Gao, Sha-Sha Huang, et al.
Zhonghua Yi Xue Za Zhi|December 11, 2007
[Sequencing of SLC26A4 exons 7 and 8 and hot spot mutation analysis in 1552 moderate to profound sensorineural hearing loss patients in China]Pu Dai, Yong-Yi Yuan, Dong-Yang Kang, et al.
Pageof 22

Showing results (131-140 of 218) with videos related to

Sort By:
Pageof 22
Frontiers in Cell and Developmental Biology|November 8, 2021
Syndromic Deafness Gene <i>ATP6V1B2</i> Controls Degeneration of Spiral Ganglion Neurons Through Modulating Proton FluxShiwei Qiu, Weihao Zhao, Xue Gao, et al.
Plos One|March 6, 2012
Common molecular etiologies are rare in nonsyndromic Tibetan Chinese patients with hearing impairmentYongyi Yuan, Xun Zhang, Shasha Huang, et al.
American Journal of Medical Genetics. Part A|September 7, 2006
Variants in mitochondrial tRNAGlu, tRNAArg, and tRNAThr may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese families with hearing lossWie-Yen Young, Lidong Zhao, Yaping Qian, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|May 10, 2024
Clinical Application of the 4K-3D Exoscope System in Cochlear ImplantationHonglei Zhang, Guojian Wang, Xin Zhang, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|December 4, 2009
[Clinical analysis of adenoid cystic carcinoma of external auditory canal]Fei-fan Zhao, Jia-ling Wang, Wen-ming Wu, et al.
Zhonghua Yi Xue Za Zhi|July 2, 2009
[Mutation of Gap junction protein beta 2 gene and treatment outcome of cochlear implantation in cochlear implantation recipients]Jun Liu, Fei Yu, Pu Dai, et al.
Zhonghua Yi Xue Za Zhi|February 14, 2008
[Mutation screening of the COCH gene in familial and sporadic patients with late onset nonsyndromic sensorineural hearing loss among Chinese population]Qing Sun, Shu-Zhi Yang, Dong-Yang Kang, et al.
Acta Oto-Laryngologica|February 19, 2019
Cochlear implantation in patients with canal wall down mastoidectomy cavitiesSong Gao, Yi Jiang, Guo-Jian Wang, et al.
BMC Medical Genetics|September 5, 2018
Clinical and molecular characterization of POU3F4 mutations in multiple DFNX2 Chinese familiesYu Su, Xue Gao, Sha-Sha Huang, et al.
Zhonghua Yi Xue Za Zhi|December 11, 2007
[Sequencing of SLC26A4 exons 7 and 8 and hot spot mutation analysis in 1552 moderate to profound sensorineural hearing loss patients in China]Pu Dai, Yong-Yi Yuan, Dong-Yang Kang, et al.
Pageof 22