Showing results (111-120 of 167) with videos related to

Sort By:
Pageof 17
Nanoscale|December 10, 2015
Gd-based upconversion nanocarriers with yolk-shell structure for dual-modal imaging and enhanced chemotherapy to overcome multidrug resistance in breast cancerYuanwei Pan, Ling'e Zhang, Leyong Zeng, et al.
Experimental Eye Research|July 5, 2016
Molecular genetics of Leber congenital amaurosis in Chinese: New data from 66 probands and mutation overview of 159 probandsYan Xu, Xueshan Xiao, Shiqiang Li, et al.
Frontiers in Cell and Developmental Biology|July 12, 2021
An Early Diagnostic Clue for COL18A1- and LAMA1-Associated Diseases: High Myopia With Alopecia Areata in the Cranial MidlinePanfeng Wang, Xiaoyun Jia, Xueshan Xiao, et al.
Investigative Ophthalmology & Visual Science|September 14, 2011
Replication study supports CTNND2 as a susceptibility gene for high myopiaBoyu Lu, Dan Jiang, Panfeng Wang, et al.
Investigative Ophthalmology & Visual Science|May 19, 2021
Characterization of PROM1 p.Arg373Cys Variant in a Cohort of Chinese Patients: Macular Dystrophy Plus Peripheral Bone-Spicule DegenerationYingwei Wang, Panfeng Wang, Shiqiang Li, et al.
Investigative Ophthalmology & Visual Science|May 17, 2022
Autosomal Dominant Retinitis Pigmentosa-Associated TOPORS Protein Truncating Variants Are Exclusively Located in the Region of Amino Acid Residues 807 to 867Junwen Wang, Yingwei Wang, Yi Jiang, et al.
Molecular Medicine Reports|November 8, 2014
Mutation analysis of Leber congenital amaurosis‑associated genes in patients with retinitis pigmentosaTao Shen, Liping Guan, Shiqiang Li, et al.
Molecular Vision|September 6, 2018
Phenotypic characterization of patients with early-onset high myopia due to mutations in COL2A1 or COL11A1: Why not Stickler syndrome?Lin Zhou, Xueshan Xiao, Shiqiang Li, et al.
Investigative Ophthalmology & Visual Science|September 30, 2025
Pigmentation Pattern of Iris and Fundus in 75 Chinese Families With GPR143-Associated Ocular AlbinismShuowei Chen, Zhen Yi, Yuxi Zheng, et al.
The British Journal of Ophthalmology|February 12, 2024
Variant and clinical landscape of Leber hereditary optic neuropathy based on 1516 families with mtDNA variants in a tertiary centreYuxi Zheng, Yingwei Wang, Yi Jiang, et al.
Pageof 17