Výsledky vyhledávání - Li, Haichun
- Zobrazuji výsledky 1 - 14 z 14
-
1
-
2
-
3
Angiopep-2-conjugated poly(ethylene glycol)-co- poly(ε-caprolactone) polymersomes for dual-targeting drug delivery to glioma in rats Autor Lu, Fei, Pang, Zhiyong, Zhao, Jingjing, Jin, Kai, Li, Haichun, Pang, Qiang, Zhang, Long, Pang, Zhiqing
Vydáno 2017Text -
4
Engineered superparamagnetic iron oxide nanoparticles (SPIONs) for dual-modality imaging of intracranial glioblastoma via EGFRvIII targeting Autor Liu, Xianping, Du, Chengjuan, Li, Haichun, Jiang, Ting, Luo, Zimiao, Pang, Zhiqing, Geng, Daoying, Zhang, Jun
Vydáno 2019Text -
5
Retro-orbital injection of FITC-dextran combined with isolectin B4 in assessing the retinal neovascularization defect Autor Li, Jizhu, Wu, Yuqing, Liu, Bingqian, Huang, Ying, Wu, Qingxiu, Li, Haichun, Xiao, Sainan, Lin, Ying, Li, Tao
Vydáno 2021Text -
6
Size Dependency of Circulation and Biodistribution of Biomimetic Nanoparticles: Red Blood Cell Membrane-Coated Nanoparticles Autor Li, Haichun, Jin, Kai, Luo, Man, Wang, Xuejun, Zhu, Xiaowen, Liu, Xianping, Jiang, Ting, Zhang, Qin, Wang, Sheng, Pang, Zhiqing
Vydáno 2019Text -
7
Multimodal imaging and genetic analysis of adult-onset best vitelliform macular dystrophy in Chinese patients Autor Lin, Ying, Li, Tao, Liu, Bingqian, Lyu, Cancan, Lian, Yu, Li, Jizhu, Huang, Ying, Li, Haichun, Wu, Qingxiu, Jin, Chenjin, Lu, Lin
Vydáno 2021Text -
8
Targeted next-generation sequencing identifies two novel COL2A1 gene mutations in Stickler syndrome with bilateral retinal detachment Autor Huang, Xinhua, Lin, Ying, Chen, Chuan, Zhu, Yi, Gao, Hongbin, Li, Tao, Liu, Bingqian, Lyu, Cancan, Huang, Ying, Wu, Qingxiu, Li, Haichun, Jin, Chenjin, Liang, Xiaoling, Lu, Lin
Vydáno 2018Text -
9
Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract Autor Lin, Ying, Gao, Hongbin, Zhu, Yi, Chen, Chuan, Li, Tao, Liu, Bingqian, Lyu, Cancan, Huang, Ying, Li, Haichun, Wu, Qingxiu, Jin, Chenjin, Liang, Xiaoling, Huang, Xinhua, Lu, Lin
Vydáno 2018Text -
10
Chaperonin-Containing TCP1 Subunit 5 Protects Against the Effect of Mer Receptor Tyrosine Kinase Knockdown in Retinal Pigment Epithelial Cells by Interacting With Filamentous Actin... Autor Feng, Lujia, Li, Haichun, Du, Yong, Zhang, Ting, Zhu, Yingting, Li, Zhidong, Zhao, Ling, Wang, Xing, Wang, Gongpei, Zhou, Linbin, Jiang, Zhaorong, Liu, Zheng, Ou, Zhancong, Wen, Yuwen, Zhuo, Yehong
Vydáno 2022Text -
11
Two heterozygous mutations identified in one Chinese patient with bilateral macular coloboma Autor Li, Tao, Lin, Ying, Gao, Hongbin, Chen, Chuan, Zhu, Yi, Liu, Bingqian, Lian, Yu, Li, Yonghao, Zhou, Wenli, Jiang, Hongye, Li, Haichun, Wu, Qingxiu, Liang, Xiaoling, Jin, Chenjin, Huang, Xinhua, Lu, Lin
Vydáno 2017Text -
12
Genetic variations in Bestrophin-1 and associated clinical findings in two Chinese patients with juvenile-onset and adult-onset best vitelliform macular dystrophy Autor Lin, Ying, Li, Tao, Ma, Chenghong, Gao, Hongbin, Chen, Chuan, Zhu, Yi, Liu, Bingqian, Lian, Yu, Huang, Ying, Li, Haichun, Wu, Qingxiu, Liang, Xiaoling, Jin, Chenjin, Huang, Xinhua, Ye, Jianhua, Lu, Lin
Vydáno 2018Text -
13
Clinical and next-generation sequencing findings in a Chinese family exhibiting severe familial exudative vitreoretinopathy Autor Lin, Ying, Gao, Hongbin, Chen, Chuan, Zhu, Yi, Li, Tao, Liu, Bingqian, Ma, Chenghong, Jiang, Hongye, Li, Yonghao, Huang, Ying, Wu, Qingxiu, Li, Haichun, Liang, Xiaoling, Jin, Chenjin, Ye, Jianhua, Huang, Xinhua, Lu, Lin
Vydáno 2018Text -
14
FGFR2 mutations and associated clinical observations in two Chinese patients with Crouzon syndrome Autor Lin, Ying, Gao, Hongbin, Ai, Siming, Eswarakumar, Jacob V.P., Zhu, Yi, Chen, Chuan, Li, Tao, Liu, Bingqian, Jiang, Hongye, Liu, Yuhua, Li, Yonghao, Wu, Qingxiu, Li, Haichun, Liang, Xiaoling, Jin, Chenjin, Huang, Xinhua, Lu, Lin
Vydáno 2017Text