Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Lian-hua Sun"'
Publikováno v:
Neurochemical research. 47(5)
The facial nerve is one of the vulnerable nerves in otolaryngology. Repair and recovery of facial nerve injury have a high priority in clinical practice. The proliferation and migration of Schwann cells are considered of great significance in the pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::867d9ecc7c3425aa329404309796600c
https://pubmed.ncbi.nlm.nih.gov/35080688
https://pubmed.ncbi.nlm.nih.gov/35080688
Autor:
Peng Zhang, Helmuth Möhwald, Jie Chen, Lian-Hua Sun, Jilie Kong, Wei Zhao, Huan-Ming Xiong, Ji-Shi Wei
Publikováno v:
ACS Applied Materials & Interfaces. 9:18474-18481
ZnO@polymer core-shell nanoparticles are assembled into novel capsule shells with diameters of about 100 nm to load isotretinoin (ISO) with a capacity as high as 34.6 wt %. Although ISO, a widely used drug for acne treatment, by itself is not suitabl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb75714988f18612a5f0d7b63cb70cbe
https://doi.org/10.1021/acsami.7b02542
https://doi.org/10.1021/acsami.7b02542
Autor:
Lian-hua, Sun, Lei, Li, Xiao-wen, Wang, Ya-zhong, Zhu, Yong-chuan, Chai, Xiao-hua, Li, Hao, Wu, Tao, Yang
Publikováno v:
Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery. 47(12)
To evaluate a microarray-based mutation screening method for genetic deafness and its application in prenatal diagnosis.Mutation screening of common deafness genes was performed in pregnant women and volunteers spouses. Nine common mutations in four
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ffcd0e5431567a531cfa343af8bf1a9e
https://pubmed.ncbi.nlm.nih.gov/23328038
https://pubmed.ncbi.nlm.nih.gov/23328038
Autor:
Wei Huang, Sheng-Di Chen, Jian-Fang Ma, Lian-hua Sun, Fu-ting Sun, Ying Kuang, Wang-Yang Xu, Houbao Zhu, Bao-jun Ji, Lei Huang, Zhugang Wang, Yan Chen, Ming-min Gu, Hong-Xin Zhang, Xiao-lin Wu, Wenting Guo, Wentao Yuan
Publikováno v:
The American Journal of Human Genetics. (6):1088-1094
Charcot-Marie-Tooth (CMT) disease represents a clinically and genetically heterogeneous group of inherited neuropathies. Here, we report a five-generation family of eight affected individuals with CMT disease type 2, CMT2. Genome-wide linkage analysi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a1f63b9885d552f3961ef1f40c477d7
Autor:
Zhen-tao Wang1,2, Ying Chen1,2, Dong-ye Chen1,2, Yong-chuan Chai1,2, Xiu-hong Pang1,2, Lian-hua Sun1,2, Xiao-wen Wang1,2, Tao Yang1,2 yangtfxl@sina.com, Hao Wu1,2 wuhao622@sina.cn
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. Sep2014, Vol. 78 Issue 9, p1513-1516. 4p.