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Pu Dai

Showing results (61-70 of 218) with videos related to

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Acta Oto-Laryngologica|November 8, 2014
Mutations in the mitochondrial 12S rRNA gene in elderly Chinese peopleYuhua Zhu, Jiandong Zhao, Bo Feng, et al.
BMC Cancer|May 4, 2006
AIB1 gene amplification and the instability of polyQ encoding sequence in breast cancer cell linesLee-Jun C Wong, Pu Dai, Jyh-Feng Lu, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|January 5, 2013
[Genetic testing and mutation analysis for the cochlear implantation children and their normal auditory phenotype parents]Ming Shi, Yibing Yang, Mei Zhao, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 15, 2010
[Sequencing analysis of whole SLC26A4 gene in severe to profound sensorineural hearing loss patients with IVS7-2A to G mutation of the gene]Qi Li, De-liang Huang, Qing-wen Zhu, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|March 15, 2008
[Mutation analysis of GJB2, GJB3 and GJB6 gene in deaf population from special educational school of Chifeng city]Yongyi Yuan, Deliang Huang, Pu Dai, et al.
International Journal of Pediatric Otorhinolaryngology|December 26, 2012
Sensorineural hearing loss caused by mutations in two alleles of both GJB2 and SLC26A4 genesShasha Huang, Dongyi Han, Guojian Wang, et al.
BMC Genetics|February 3, 2016
Phenotypic Heterogeneity in a DFNA20/26 family segregating a novel ACTG1 mutationYongyi Yuan, Xue Gao, Bangqing Huang, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|September 26, 2012
[Epidemiological studies on mtDNA 12S rRNA A1555G mutation of 10 non syndromic hearing loss families in Yunnan province]Tao Ma, Xijun Xue, Pu Dai, et al.
Biomed Research International|March 2, 2017
Novel Mutations and Mutation Combinations of <i>TMPRSS3</i> Cause Various Phenotypes in One Chinese Family with Autosomal Recessive Hearing ImpairmentXue Gao, Yong-Yi Yuan, Guo-Jian Wang, et al.
Human Gene Therapy|June 26, 2016
Identification of Adeno-Associated Viral Vectors That Target Neonatal and Adult Mammalian Inner Ear Cell SubtypesYilai Shu, Yong Tao, Zhengmin Wang, et al.
Pageof 22

Showing results (61-70 of 218) with videos related to

Sort By:
Pageof 22
Acta Oto-Laryngologica|November 8, 2014
Mutations in the mitochondrial 12S rRNA gene in elderly Chinese peopleYuhua Zhu, Jiandong Zhao, Bo Feng, et al.
BMC Cancer|May 4, 2006
AIB1 gene amplification and the instability of polyQ encoding sequence in breast cancer cell linesLee-Jun C Wong, Pu Dai, Jyh-Feng Lu, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|January 5, 2013
[Genetic testing and mutation analysis for the cochlear implantation children and their normal auditory phenotype parents]Ming Shi, Yibing Yang, Mei Zhao, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 15, 2010
[Sequencing analysis of whole SLC26A4 gene in severe to profound sensorineural hearing loss patients with IVS7-2A to G mutation of the gene]Qi Li, De-liang Huang, Qing-wen Zhu, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|March 15, 2008
[Mutation analysis of GJB2, GJB3 and GJB6 gene in deaf population from special educational school of Chifeng city]Yongyi Yuan, Deliang Huang, Pu Dai, et al.
International Journal of Pediatric Otorhinolaryngology|December 26, 2012
Sensorineural hearing loss caused by mutations in two alleles of both GJB2 and SLC26A4 genesShasha Huang, Dongyi Han, Guojian Wang, et al.
BMC Genetics|February 3, 2016
Phenotypic Heterogeneity in a DFNA20/26 family segregating a novel ACTG1 mutationYongyi Yuan, Xue Gao, Bangqing Huang, et al.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Journal of Clinical Otorhinolaryngology Head and Neck Surgery|September 26, 2012
[Epidemiological studies on mtDNA 12S rRNA A1555G mutation of 10 non syndromic hearing loss families in Yunnan province]Tao Ma, Xijun Xue, Pu Dai, et al.
Biomed Research International|March 2, 2017
Novel Mutations and Mutation Combinations of <i>TMPRSS3</i> Cause Various Phenotypes in One Chinese Family with Autosomal Recessive Hearing ImpairmentXue Gao, Yong-Yi Yuan, Guo-Jian Wang, et al.
Human Gene Therapy|June 26, 2016
Identification of Adeno-Associated Viral Vectors That Target Neonatal and Adult Mammalian Inner Ear Cell SubtypesYilai Shu, Yong Tao, Zhengmin Wang, et al.
Pageof 22