Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Ming–kun, Han"'
Autor:
Wan Du, Ming-Kun Han, Da-Yong Wang, Bing Han, Liang Zong, Lan Lan, Ju Yang, Qi Shen, Lin-Yi Xie, Lan Yu, Jing Guan, Qiu-Ju Wang
Publikováno v:
Chinese Medical Journal, Vol 130, Iss 1, Pp 88-92 (2017)
Background: The molecular genetic research showed the association between X-linked hearing loss and mutations in POU3F4. This research aimed to identify a POU3F4 mutation in a nonsyndromic X-linked recessive hearing loss family. Methods: A series of
Externí odkaz:
https://doaj.org/article/4b05e8b75cba437f9ab42aa3b42811a2
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
Autor:
Ming-kun, Han, Dong-yi, Han, Yu-fen, Guo, Qing-zhong, Li, Ya-li, Zhao, Shao-qi, Rao, Hu, Yuan, Liang, Zong, Jing, Guan, Bai-cheng, Xu, Da-yong, Wang *, lan, Lan, Qiu-ju, Wang
Publikováno v:
In Journal of Otology June 2007 2(1):18-22
Autor:
Ning Yu, Liwei Chen, Shiming Yang, Yan Lu, Wei Sun, Daishi Chen, Ming-Kun Han, Xuejun Sun, Suoqiang Zhai
Publikováno v:
Acta Oto-Laryngologica. 137:1063-1068
This study aimed to explore the molecular mechanism of the protective effects of hydrogen-saturated saline on NIHL.Guinea pigs were divided into three groups: hydrogen-saturated saline; normal saline; and control. For saline administration, the guine
Autor:
Qi Shen, Wan Du, Lan Yu, Qiuju Wang, Liang Zong, Linyi Xie, Ju Yang, Jing Guan, Dayong Wang, Ming-Kun Han, Bing Han, Lan Lan
Publikováno v:
Chinese Medical Journal, Vol 130, Iss 1, Pp 88-92 (2017)
Background: The molecular genetic research showed the association between X-linked hearing loss and mutations in POU3F4. This research aimed to identify a POU3F4 mutation in a nonsyndromic X-linked recessive hearing loss family. Methods: A series of
Autor:
Wan, Du, Ming-Kun, Han, Da-Yong, Wang, Bing, Han, Liang, Zong, Lan, Lan, Ju, Yang, Qi, Shen, Lin-Yi, Xie, Lan, Yu, Jing, Guan, Qiu-Ju, Wang
Publikováno v:
Chinese Medical Journal
Background: The molecular genetic research showed the association between X-linked hearing loss and mutations in POU3F4. This research aimed to identify a POU3F4 mutation in a nonsyndromic X-linked recessive hearing loss family. Methods: A series of
Autor:
Yu-Bin Ji, Qiu-Ju Wang, Dong-yi Han, Ya-Li Zhao, Da-Yong Wang, Qian Li, Lan Lan, Shaoqi Rao, Ming-Kun Han, Feifan Zhao
Publikováno v:
Genetic Testing and Molecular Biomarkers. 15:619-625
The connexin 26 coding gene (GJB2) is the primary causative gene for nonsyndromic sensorineural hearing impairment (NSSHI). More than 100 mutations in this gene have been reported to be linked to hearing impairment (HI), from mild to profound hearing
Autor:
Lan, Lan, Dong-Yi, Han, Wei, Shi, Ming-Kun, Han, Qiong, Liu, Hai-Na, Ding, Zhi-Hui, Chen, Da-Yong, Wang, Shan-Hong, Li, Ming-Li, Guo, Shao-Qi, Rao, Qiu-Ju, Wang
Publikováno v:
Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery. 43(5)
To estimate correlation between phonetically balanced maximum (PB max) and pure tone auditory threshold in auditory neuropathy (AN) patients.One hundred and six AN patients were identified using multiple criteria including PB max, a metric for speech
Autor:
Weiyan Yang, Qiuju Wang, Liang Zong, Dongyi Han, Yali Zhao, Qing-Jie Liu, Shao-Qi Rao, Ming-Kun Han
Publikováno v:
Acta oto-laryngologica. 129(6)
The DFNY1 phenotypes shared many characteristics with some autosomal dominant hearing loss, in the aspects of age of onset, severity and audiometric configuration. However, the typical, outstanding feature of this trait was its remarkable pattern of
Publikováno v:
Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery. 42(11)
To discuss and analyze the feasibility and strategy for perform the newborn gene screening in the process of newborn hearing screening in order to supply the defects or limitation in the hearing screening.Four hundreds and sixty newborn babies from D