Intervention study of tai chi training on the intestinal flora of college student basketball players

por Kang, Dongyang, Wang, Xiaorong, Wang, Jiahong
Publicado 2023

Clinical and molecular findings in a Chinese family with a de novo mitochondrial A1555G mutation

por Gu, Ping, Wang, Guojian, Gao, Xue, Kang, Dongyang, Dai, Pu, Huang, Shasha
Publicado 2022

A follow‐up study of a Chinese family with Waardenburg syndrome type II caused by a truncating mutation of MITF gene

por Yang, Shuzhi, Wang, Cuicui, Zhou, Chengyong, Kang, DongYang, Zhang, Xin, Yuan, Huijun
Publicado 2020

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

por Huang, Shasha, Gao, Xue, Wang, Yufeng, Kang, Dongyang, Zhang, Xin, Yang, Suyan, Dai, Pu
Publicado 2020

Analysis of the genotype–phenotype correlation of MYO15A variants in Chinese non-syndromic hearing loss patients

por Fu, Ying, Huang, Shasha, Gao, Xue, Han, Mingyu, Wang, Guojian, Kang, Dongyang, Yuan, Yongyi, Dai, Pu
Publicado 2022

Spatial Variations in Vitreous Oxygen Consumption

por Murali, Karthik, Kang, Dongyang, Nazari, Hossein, Scianmarello, Nicholas, Cadenas, Enrique, Tai, Yu-Chong, Kashani, Amir, Humayun, Mark
Publicado 2016

Genetic and Phenotypic Heterogeneity in Chinese Patients with Waardenburg Syndrome Type II

por Yang, Shuzhi, Dai, Pu, Liu, Xin, Kang, Dongyang, Zhang, Xin, Yang, Weiyan, Zhou, Chengyong, Yang, Shiming, Yuan, Huijun
Publicado 2013

KCNJ10 May Not Be a Contributor to Nonsyndromic Enlargement of Vestibular Aqueduct (NSEVA) in Chinese Subjects

por Zhao, Jiandong, Yuan, Yongyi, Huang, Shasha, Huang, Bangqing, Cheng, Jing, Kang, Dongyang, Wang, Guojian, Han, Dongyi, Dai, Pu
Publicado 2014

Extremely discrepant mutation spectrum of SLC26A4 between Chinese patients with isolated Mondini deformity and enlarged vestibular aqueduct

por Huang, Shasha, Han, Dongyi, Yuan, Yongyi, Wang, Guojian, Kang, Dongyang, Zhang, Xin, Yan, Xiaofei, Meng, Xiaoxiao, Dong, Min, Dai, Pu
Publicado 2011

Analysis of the heteroplasmy level and transmitted features in hearing-loss pedigrees with mitochondrial 12S rRNA A1555G mutation

por Zhu, Yuhua, Huang, Shasha, Kang, Dongyang, Han, Mingyu, Wang, Guojian, Yuan, Yongyi, Su, Yu, Yuan, Huijun, Zhai, Suoqiang, Dai, Pu
Publicado 2014

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

por Jiang, Yi, Huang, Shasha, Deng, Tao, Wu, Lihua, Chen, Juan, Kang, Dongyang, Xu, Xiufeng, Li, Ruiyu, Han, Dongyi, Dai, Pu
Publicado 2015

A subunit of V-ATPases, ATP6V1B2, underlies the pathology of intellectual disability

por Zhao, Weihao, Gao, Xue, Qiu, Shiwei, Gao, Bo, Gao, Song, Zhang, Xin, Kang, Dongyang, Han, Weiju, Dai, Pu, Yuan, Yongyi
Publicado 2019

Molecular Etiology of Hearing Impairment in Inner Mongolia: mutations in SLC26A4 gene and relevant phenotype analysis

por Dai, Pu, Yuan, Yongyi, Huang, Deliang, Zhu, Xiuhui, Yu, Fei, Kang, Dongyang, Yuan, Huijun, Wu, Bailin, Han, Dongyi, Wong, Lee-Jun C
Publicado 2008

Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China

por Yuan, Yongyi, You, Yiwen, Huang, Deliang, Cui, Jinghong, Wang, Yong, Wang, Qiang, Yu, Fei, Kang, Dongyang, Yuan, Huijun, Han, Dongyi, Dai, Pu
Publicado 2009

A Rapid Capillary-Pressure Driven Micro-Channel to Demonstrate Newtonian Fluid Behavior of Zebrafish Blood at High Shear Rates

por Lee, Juhyun, Chou, Tzu-Chieh, Kang, Dongyang, Kang, Hanul, Chen, Junjie, Baek, Kyung In, Wang, Wei, Ding, Yichen, Carlo, Dino Di, Tai, Yu-Chong, Hsiai, Tzung K.
Publicado 2017

Comprehensive genetic testing of Chinese SNHL patients and variants interpretation using ACMG guidelines and ethnically matched normal controls

por Yuan, Yongyi, Li, Qi, Su, Yu, Lin, Qiongfen, Gao, Xue, Liu, Hankui, Huang, Shasha, Kang, Dongyang, Todd, N. Wendell, Mattox, Douglas, Zhang, Jianguo, Lin, Xi, Dai, Pu
Publicado 2019

Correction to: Preimplantation genetic testing for hereditary hearing loss in Chinese population

por Bi, Qingling, Huang, Shasha, Wang, Hui, Gao, Xue, Ma, Minyue, Han, Mingyu, Lu, Sijia, Kang, Dongyang, Nourbakhsh, Aida, Yan, Denise, Blanton, Susan, Liu, Xuezhong, Yuan, Yongyi, Yao, Yuanqing, Dai, Pu
Publicado 2023

Preimplantation genetic testing for hereditary hearing loss in Chinese population

por Bi, Qingling, Huang, Shasha, Wang, Hui, Gao, Xue, Ma, Minyue, Han, Mingyu, Lu, Sijia, Kang, Dongyang, Nourbakhsh, Aida, Yan, Denise, Blanton, Susan, Liu, Xuezhong, Yuan, Yongyi, Yao, Yuanqing, Dai, Pu
Publicado 2023

GJB2 mutation spectrum in 2063 Chinese patients with nonsyndromic hearing impairment

por Dai, Pu, Yu, Fei, Han, Bing, Liu, Xuezhong, Wang, Guojian, Li, Qi, Yuan, Yongyi, Liu, Xin, Huang, Deliang, Kang, Dongyang, Zhang, Xin, Yuan, Huijun, Yao, Kun, Hao, Jinsheng, He, Jia, He, Yong, Wang, Youqin, Ye, Qing, Yu, Youjun, Lin, Hongyan, Liu, Lijia, Deng, Wei, Zhu, Xiuhui, You, Yiwen, Cui, Jinghong, Hou, Nongsheng, Xu, Xuehai, Zhang, Jin, Tang, Liang, Song, Rendong, Lin, Yongjun, Sun, Shuanzhu, Zhang, Ruining, Wu, Hao, Ma, Yuebing, Zhu, Shanxiang, Wu, Bai-lin, Han, Dongyi, Wong, Lee-Jun C
Publicado 2009