Zobrazeno 1 - 10
of 130
pro vyhledávání: '"Dong–yi, Han"'
Autor:
Lang Zhang, Jin-Yuan Yang, Qiu-Quan Wang, Xue Gao, Guo-Jian Wang, Ming-Yu Han, Dong-Yang Kang, Dong-Yi Han, Sha-Sha Huang, Yong-Yi Yuan
Publikováno v:
BMC Medical Genomics, Vol 17, Iss 1, Pp 1-10 (2024)
Abstract Background Mutations in MPZL2, the characteristic genetic etiology of autosomal recessive deafness loci 111 (DFNB111), cause non-syndromic and moderate sensorineural hearing loss. Methods In this study, we analyzed the phenotype and genotype
Externí odkaz:
https://doaj.org/article/9056a91342b84ef7b12cc530b53a6390
Autor:
Jiang, Yu1 (AUTHOR), Dong, Yi-han2 (AUTHOR), Zhao, Shi-wei1 (AUTHOR), Liu, Dong-yu3 (AUTHOR), Zhang, Ji-yang3 (AUTHOR), Xu, Xiao-ya3 (AUTHOR), Chen, Hao4 (AUTHOR) hao.chen@jmdna.com, Jin, Jia-bin1 (AUTHOR) jjb11501@rjh.com.cn
Publikováno v:
Cell Communication & Signaling. 3/6/2024, Vol. 22 Issue 1, p1-17. 17p.
Autor:
Jiang, Yu1 (AUTHOR), Dong, Yi-han2 (AUTHOR), Zhao, Shi-wei1 (AUTHOR), Liu, Dong-yu3 (AUTHOR), Zhang, Ji-yang3 (AUTHOR), Xu, Xiao-ya3 (AUTHOR), Chen, Hao1,4 (AUTHOR) hao.chen@jmdna.com, Jin, Jia-bin1 (AUTHOR) jjb11501@rjh.com.cn
Publikováno v:
Cell Communication & Signaling. 3/14/2024, Vol. 22 Issue 1, p1-1. 1p.
Autor:
Wang, Qiu–ju *, Shao–qi, Rao, Yu–fen, Guo, Qing–zhong, Li, Hui, Zhao, Li–dong, Zhao, Hu, Yuan, Liang, Zong, Qiong, Liu, Ya–li, Zhao, Da–yong, Wang, Ming–kun, Han, Yu–bin, Ji, Jian–qiang, Li, Lan, Lan, Wei–yan, Yang, Yan, Shen, Dong–yi, Han *
Publikováno v:
In Journal of Otology December 2009 4(2):98-105
Publikováno v:
In Journal of Otology December 2009 4(2):119-123
Publikováno v:
In Journal of Otology December 2009 4(2):115-118
Publikováno v:
In Journal of Otology June 2009 4(1):44-49
Publikováno v:
In Journal of Otology June 2009 4(1):50-54
Autor:
Yu Su, Wen-Xue Tang, Xue Gao, Fei Yu, Zhi-Yao Dai, Jian-Dong Zhao, Yu Lu, Fei Ji, Sha-Sha Huang, Yong-Yi Yuan, Ming-Yu Han, Yue-Shuai Song, Yu-Hua Zhu, Dong-Yang Kang, Dong-Yi Han, Pu Dai
Publikováno v:
PLoS ONE, Vol 9, Iss 2, p e89240 (2014)
TECTA-related deafness can be inherited as autosomal-dominant nonsyndromic deafness (designated DFNA) or as the autosomal-recessive version. The α-tectorin protein, which is encoded by the TECTA gene, is one of the major components of the tectorial
Externí odkaz:
https://doaj.org/article/7fee7500339447a884b2422b630fba8a
Autor:
Dong, Yi-Han, Ding, Yi-Ming, Guo, Wei, Huang, Jun-Wei, Yang, Zheng, Zhang, Yang, Chen, Xiao-Hong
Publikováno v:
OncoTargets & Therapy. Oct2018, Vol. 11, p7053-7059. 7p.