An Exploratory Study on Integrating Virtual Reality Video into Teaching Chinese as a Second Language on Festival Topics

by Chih-Pu Dai, 戴智璞
Published 2014

The Cultivation and The Aromatherapy of Imported Australia Tea Tree - A case Study of Tribe Nalo

by LUO BA,PU-DAI, 蘿芭‧浦代
Published 2018

The Relationship between the p.V37I Mutation in GJB2 and Hearing Phenotypes in Chinese Individuals.

by Shasha Huang, Bangqing Huang, Guojian Wang, Yongyi Yuan, Pu Dai
Published 2015-01-01

Familial Temperature-Sensitive Auditory Neuropathy: Distinctive Clinical Courses Caused by Variants of the OTOF Gene

by Yi-Ming Zhu, Yi-Ming Zhu, Qi Li, Xue Gao, Yan-Fei Li, You-Li Liu, Pu Dai, Pu Dai, Xiang-Ping Li
Published 2021-10-01

Prelingual Sensorineural Hearing Loss Caused by a Novel GJB2 Dominant Mutation in a Chinese Family

by Shasha Huang, Xue Gao, Yufeng Wang, Dongyang Kang, Xin Zhang, Suyan Yang, Pu Dai
Published 2020-01-01

A novel PIK3CD C896T mutation detected in bilateral sudden sensorineural hearing loss using next generation sequencing: An indication of primary immunodeficiency

by Jing Zou, Xiangqiang Duan, Guiliang Zheng, Zhen Zhao, Shiyue Chen, Pu Dai, Hongliang Zheng
Published 2016-06-01

Novel Mutations and Mutation Combinations of TMPRSS3 Cause Various Phenotypes in One Chinese Family with Autosomal Recessive Hearing Impairment

by Xue Gao, Yong-Yi Yuan, Guo-Jian Wang, Jin-Cao Xu, Yu Su, Xi Lin, Pu Dai
Published 2017-01-01

KCNJ10 may not be a contributor to nonsyndromic enlargement of vestibular aqueduct (NSEVA) in Chinese subjects.

by Jiandong Zhao, Yongyi Yuan, Shasha Huang, Bangqing Huang, Jing Cheng, Dongyang Kang, Guojian Wang, Dongyi Han, Pu Dai
Published 2014-01-01

Genetic and phenotypic heterogeneity in Chinese patients with Waardenburg syndrome type II.

by Shuzhi Yang, Pu Dai, Xin Liu, Dongyang Kang, Xin Zhang, Weiyan Yang, Chengyong Zhou, Shiming Yang, Huijun Yuan
Published 2013-01-01

Generation of a gene corrected human isogenic iPSC line (CPGHi002-A-1) from a DDOD patient with heterozygous c.1516 C>T mutation in the ATP6V1B2 gene

by Xue Gao, Shi–Wei Qiu, Wei-Qian Wang, Dong-Yang Kang, Ning Su, Pu Dai, Yong–Yi Yuan
Published 2021-05-01

A subunit of V-ATPases, ATP6V1B2, underlies the pathology of intellectual disabilityResearch in context

by Weihao Zhao, Xue Gao, Shiwei Qiu, Bo Gao, Song Gao, Xin Zhang, Dongyang Kang, Weiju Han, Pu Dai, Yongyi Yuan
Published 2019-07-01

Mutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, China.

by Yi Jiang, Shasha Huang, Tao Deng, Lihua Wu, Juan Chen, Dongyang Kang, Xiufeng Xu, Ruiyu Li, Dongyi Han, Pu Dai
Published 2015-01-01

Establishment of human induced pluripotent stem cell line (CPGHi002-A) from a 10-month-old female patient with DDOD syndrome carrying a heterozygous c.1516 C > T mutation in ATP6V1...

by Xue Gao, Shi–Wei Qiu, Meng-Long Feng, Sha-Sha Huang, Dong-Yang Kang, Ming-Yu Han, Pu Dai, Yong–Yi Yuan
Published 2020-10-01

Molecular epidemiology and functional assessment of novel allelic variants of SLC26A4 in non-syndromic hearing loss patients with enlarged vestibular aqueduct in China.

by Yongyi Yuan, Weiwei Guo, Jie Tang, Guozheng Zhang, Guojian Wang, Mingyu Han, Xun Zhang, Shiming Yang, David Z Z He, Pu Dai
Published 2012-01-01

Common molecular etiologies are rare in nonsyndromic Tibetan Chinese patients with hearing impairment.

by Yongyi Yuan, Xun Zhang, Shasha Huang, Lujie Zuo, Guozheng Zhang, Yueshuai Song, Guojian Wang, Hongtian Wang, Deliang Huang, Dongyi Han, Pu Dai
Published 2012-01-01

Identification of a Novel TECTA mutation in a Chinese DFNA8/12 family with prelingual progressive sensorineural hearing impairment.

by Zhengyue Li, Yilian Guo, Yu Lu, Jianzhong Li, Zhanguo Jin, Hongbo Li, Yanping Lu, Pu Dai, Dongyi Han, Jing Cheng, Huijun Yuan
Published 2013-01-01

Clinical and molecular characterization of POU3F4 mutations in multiple DFNX2 Chinese families

by Yu Su, Xue Gao, Sha-Sha Huang, Jing-Ning Mao, Bang-Qing Huang, Jian-Dong Zhao, Dong-Yang Kang, Xin Zhang, Pu Dai
Published 2018-09-01

Hearing Phenotypes of Patients with Hearing Loss Homozygous for the GJB2 c.235delc Mutation

by Chang Guo, Sha-Sha Huang, Yong-Yi Yuan, Ying Zhou, Ning Wang, Dong-Yang Kang, Su-Yan Yang, Xin Zhang, Xue Gao, Pu Dai
Published 2020-01-01

Myc and Fgf Are Required for Zebrafish Neuromast Hair Cell Regeneration.

by Sang Goo Lee, Mingqian Huang, Nikolaus D Obholzer, Shan Sun, Wenyan Li, Marco Petrillo, Pu Dai, Yi Zhou, Douglas A Cotanche, Sean G Megason, Huawei Li, Zheng-Yi Chen
Published 2016-01-01

Identification of TMPRSS3 as a Significant Contributor to Autosomal Recessive Hearing Loss in the Chinese Population

by Xue Gao, Sha-Sha Huang, Yong-Yi Yuan, Jin-Cao Xu, Ping Gu, Dan Bai, Dong-Yang Kang, Ming-Yu Han, Guo-Jian Wang, Mei-Guang Zhang, Jia Li, Pu Dai
Published 2017-01-01