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Pu Dai

Showing results (101-110 of 218) with videos related to

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Journal of Translational Medicine|October 4, 2011
Extremely discrepant mutation spectrum of SLC26A4 between Chinese patients with isolated Mondini deformity and enlarged vestibular aqueductShasha Huang, Dongyi Han, Yongyi Yuan, 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
[Analysis of positive rate of common genetic mutations in 1448 cases with different hearing phenotype]Guojian Wang, Yongyi Yuan, Rong Li, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|June 23, 2022
Surgical management of endolymphatic sac tumor: classification, outcomes and strategy. A single institution's experienceNan Wu, Xiaoyan Ma, Weidong Shen, et al.
Zhonghua Yi Xue Za Zhi|February 12, 2008
[Prevalence of GJB2 mutations in Uigur and Han ethnic populations with deafness in Xinjiang region of China]Qi Li, Pu Dai, De-Liang Huang, et al.
International Journal of Pediatric Otorhinolaryngology|February 8, 2014
Hearing loss associated with an unusual mutation combination in the gap junction beta 2 (GJB2) gene in a Chinese familyAiping Huang, Yongyi Yuan, Naichao Duan, et al.
Zhonghua Yi Xue Za Zhi|July 15, 2009
[Genetic counseling and instruction of marriage for deaf young people: study of 115 cases]Bing Han, Pu Dai, Guo-Jian Wang, et al.
Ebiomedicine|July 2, 2019
A subunit of V-ATPases, ATP6V1B2, underlies the pathology of intellectual disabilityWeihao Zhao, Xue Gao, Shiwei Qiu, et al.
Mitochondrion|August 18, 2009
Mitochondrial haplotype and phenotype of 13 Chinese families may suggest multi-original evolution of mitochondrial C1494T mutationYuhua Zhu, Qi Li, Zhengyi Chen, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|September 30, 2009
Mutation analysis of SLC26A4 in mainland Chinese patients with enlarged vestibular aqueductSamuel Reyes, Guojian Wang, Xiaomei Ouyang, et al.
Stem Cell Research|June 12, 2022
Establishment of an iPSC line (CPGHi005-A) from a patient with Waardenburg syndrome carrying a heterozygous SVA-F retrotransposon insertion into SOX10Xiaohong Li, Xue Gao, Shasha Huang, et al.
Pageof 22

Showing results (101-110 of 218) with videos related to

Sort By:
Pageof 22
Journal of Translational Medicine|October 4, 2011
Extremely discrepant mutation spectrum of SLC26A4 between Chinese patients with isolated Mondini deformity and enlarged vestibular aqueductShasha Huang, Dongyi Han, Yongyi Yuan, 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
[Analysis of positive rate of common genetic mutations in 1448 cases with different hearing phenotype]Guojian Wang, Yongyi Yuan, Rong Li, et al.
European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : Affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery|June 23, 2022
Surgical management of endolymphatic sac tumor: classification, outcomes and strategy. A single institution's experienceNan Wu, Xiaoyan Ma, Weidong Shen, et al.
Zhonghua Yi Xue Za Zhi|February 12, 2008
[Prevalence of GJB2 mutations in Uigur and Han ethnic populations with deafness in Xinjiang region of China]Qi Li, Pu Dai, De-Liang Huang, et al.
International Journal of Pediatric Otorhinolaryngology|February 8, 2014
Hearing loss associated with an unusual mutation combination in the gap junction beta 2 (GJB2) gene in a Chinese familyAiping Huang, Yongyi Yuan, Naichao Duan, et al.
Zhonghua Yi Xue Za Zhi|July 15, 2009
[Genetic counseling and instruction of marriage for deaf young people: study of 115 cases]Bing Han, Pu Dai, Guo-Jian Wang, et al.
Ebiomedicine|July 2, 2019
A subunit of V-ATPases, ATP6V1B2, underlies the pathology of intellectual disabilityWeihao Zhao, Xue Gao, Shiwei Qiu, et al.
Mitochondrion|August 18, 2009
Mitochondrial haplotype and phenotype of 13 Chinese families may suggest multi-original evolution of mitochondrial C1494T mutationYuhua Zhu, Qi Li, Zhengyi Chen, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|September 30, 2009
Mutation analysis of SLC26A4 in mainland Chinese patients with enlarged vestibular aqueductSamuel Reyes, Guojian Wang, Xiaomei Ouyang, et al.
Stem Cell Research|June 12, 2022
Establishment of an iPSC line (CPGHi005-A) from a patient with Waardenburg syndrome carrying a heterozygous SVA-F retrotransposon insertion into SOX10Xiaohong Li, Xue Gao, Shasha Huang, et al.
Pageof 22