Zobrazeno 1 - 10
of 225
pro vyhledávání: '"Yuan Yongyi"'
Autor:
Gao, Bo, Jiang, Yi, Han, Mingyu, Ji, Xiaowen, Zhang, Dejun, Wu, Lihua, Gao, Xue, Huang, Shasha, Zhao, Chaoyue, Su, Yu, Yang, Suyan, Zhang, Xin, Liu, Na, Han, Lu, Wang, Lihai, Ren, Lina, Yang, Jinyuan, Wu, Jian, Yuan, Yongyi, Dai, Pu
Publikováno v:
In The Journal of Molecular Diagnostics July 2024 26(7):638-651
Autor:
Zhang, Dejun, Wu, Jie, Yuan, Yongyi, Li, Xiaohong, Gao, Xue, Kang, Dongyang, Zhang, Xin, Huang, Sha-sha, Dai, Pu
Publikováno v:
In Heliyon 30 March 2024 10(6)
Akademický článek
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Publikováno v:
Journal of Translational Medicine, Vol 10, Iss 1, p 82 (2012)
Abstract Background Many patients with enlarged vestibular aqueduct (EVA) have either only one allelic mutant of the SLC26A4 gene or lack any detectable mutation. In this study, multiplex ligation-dependent probe amplification (MLPA) was used to scre
Externí odkaz:
https://doaj.org/article/01386c1c1ac64818810e53167b95e334
Autor:
Yan Xiaofei, Zhang Xin, Kang Dongyang, Wang Guojian, Yuan Yongyi, Han Dongyi, Huang Shasha, Meng Xiaoxiao, Dong Min, Dai Pu
Publikováno v:
Journal of Translational Medicine, Vol 9, Iss 1, p 167 (2011)
Abstract Background Mutations in SLC26A4 cause Pendred syndrome (hearing loss with goiter) or DFNB4 (non-syndromic hearing loss with inner ear malformation, such as enlarged vestibular aqueduct or Mondini deformity). The relationship between mutation
Externí odkaz:
https://doaj.org/article/696075a6682341c2a3414fa41f064462
Autor:
Zhang Xin, Yu Ruili, Huang Shasha, Wang Guojian, Yu Fei, Yuan Yongyi, Huang Deliang, Han Dongyi, Dai Pu
Publikováno v:
Journal of Translational Medicine, Vol 8, Iss 1, p 127 (2010)
Abstract Background Mutations in the GJB2 gene are the most common cause of nonsyndromic recessive hearing loss in China. In about 6% of Chinese patients with severe to profound sensorineural hearing impairment, only monoallelic GJB2 mutations known
Externí odkaz:
https://doaj.org/article/ff92ab9b40ed4b58a29baff8878d57f2
Autor:
Kang Dongyang, Yu Fei, Wang Qiang, Wang Yong, Cui Jinghong, Huang Deliang, You Yiwen, Yuan Yongyi, Yuan Huijun, Han Dongyi, Dai Pu
Publikováno v:
Journal of Translational Medicine, Vol 7, Iss 1, p 79 (2009)
Abstract Background Every year, 30,000 babies are born with congenital hearing impairment in China. The molecular etiology of hearing impairment in the Chinese population has not been investigated thoroughly. To provide appropriate genetic testing an
Externí odkaz:
https://doaj.org/article/07fc2c2cac314686a3383b67427b1ab7
Autor:
Tang Liang, Zhang Jin, Xu Xuehai, Hou Nongsheng, Cui Jinghong, You Yiwen, Zhu Xiuhui, Deng Wei, Liu Lijia, Lin Hongyan, Yu Youjun, Ye Qing, Wang Youqin, He Yong, He Jia, Hao Jinsheng, Yao Kun, Yuan Huijun, Zhang Xin, Kang Dongyang, Huang Deliang, Liu Xin, Yuan Yongyi, Li Qi, Wang Guojian, Liu Xuezhong, Han Bing, Yu Fei, Dai Pu, Song Rendong, Lin Yongjun, Sun Shuanzhu, Zhang Ruining, Wu Hao, Ma Yuebing, Zhu Shanxiang, Wu Bai-lin, Han Dongyi, Wong Lee-Jun C
Publikováno v:
Journal of Translational Medicine, Vol 7, Iss 1, p 26 (2009)
Abstract Background Mutations in GJB2 are the most common molecular defects responsible for autosomal recessive nonsyndromic hearing impairment (NSHI). The mutation spectra of this gene vary among different ethnic groups. Methods In order to understa
Externí odkaz:
https://doaj.org/article/05c6bc3b9b4e41d4b1f10e2d89c19cae
Autor:
Wu Bailin, Yuan Huijun, Kang Dongyang, Yu Fei, Zhu Xiuhui, Huang Deliang, Yuan Yongyi, Dai Pu, Han Dongyi, Wong Lee-Jun C
Publikováno v:
Journal of Translational Medicine, Vol 6, Iss 1, p 74 (2008)
Abstract Background The molecular etiology of hearing impairment in Chinese has not been thoroughly investigated. Study of GJB2 gene revealed that 30.4% of the patients with hearing loss in Inner Mongolia carried GJB2 mutations. The SLC26A4 gene muta
Externí odkaz:
https://doaj.org/article/66743125babb4452995120519daf3f14
Akademický článek
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