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International Journal of Ophthalmology
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February 21, 2022
Combining robot-assisted surgical system and 3D visualization system for teaching minimally invasive vitreoretinal surgery
Yi-Qi Chen, Dan Cheng, Lin Zhu, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
September 26, 2023
The Role of Retinal Dopamine D1 Receptors in Ocular Growth and Myopia Development in Mice
Ziheng Shu, Kaijie Chen, Qiongsi Wang, et al.
Investigative Ophthalmology & Visual Science
|
December 21, 2010
Gene therapy rescues cone structure and function in the 3-month-old rd12 mouse: a model for midcourse RPE65 leber congenital amaurosis
Xia Li, Wensheng Li, Xufeng Dai, et al.
ACS Nano
|
May 14, 2026
Maternal-Derived Polystyrene Nanoplastics Impair Early Retinal Development in Zebrafish (<i>Danio rerio</i>)
Youyuan Zhuang, Dandan Li, Ruting Wang, et al.
Plos One
|
March 11, 2014
Comprehensive molecular diagnosis of Bardet-Biedl syndrome by high-throughput targeted exome sequencing
Dong-Jun Xing, Hong-Xing Zhang, Na Huang, et al.
Acta Ophthalmologica
|
February 13, 2023
One-year myopia control efficacy of cylindrical annular refractive element spectacle lenses
Xinting Liu, Pengqi Wang, Zhu Xie, et al.
Bioactive Materials
|
February 7, 2022
Cyanobacteria-based self-oxygenated photodynamic therapy for anaerobic infection treatment and tissue repair
Bailiang Wang, Liyang Zhou, Yishun Guo, et al.
Ophthalmology
|
January 27, 2009
Extremely low penetrance of Leber's hereditary optic neuropathy in 8 Han Chinese families carrying the ND4 G11778A mutation
Jia Qu, Xiangtian Zhou, Juanjuan Zhang, et al.
Yi Chuan = Hereditas
|
February 24, 2010
[Leber's hereditary optic neuropathy and limbs abnormity claudication may be associated with the mitochondrial ND1 T3866C mutation]
Yan Liu, Shu-Liu Zhuang, Yi Tong, et al.
Plos One
|
June 6, 2013
Targeted exome sequencing identified novel USH2A mutations in Usher syndrome families
Xiu-Feng Huang, Ping Xiang, Jie Chen, et al.
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Showing results (571-580 of 746) with videos related to
Sort By:
Page
of 75
International Journal of Ophthalmology
|
February 21, 2022
Combining robot-assisted surgical system and 3D visualization system for teaching minimally invasive vitreoretinal surgery
Yi-Qi Chen, Dan Cheng, Lin Zhu, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
September 26, 2023
The Role of Retinal Dopamine D1 Receptors in Ocular Growth and Myopia Development in Mice
Ziheng Shu, Kaijie Chen, Qiongsi Wang, et al.
Investigative Ophthalmology & Visual Science
|
December 21, 2010
Gene therapy rescues cone structure and function in the 3-month-old rd12 mouse: a model for midcourse RPE65 leber congenital amaurosis
Xia Li, Wensheng Li, Xufeng Dai, et al.
ACS Nano
|
May 14, 2026
Maternal-Derived Polystyrene Nanoplastics Impair Early Retinal Development in Zebrafish (<i>Danio rerio</i>)
Youyuan Zhuang, Dandan Li, Ruting Wang, et al.
Plos One
|
March 11, 2014
Comprehensive molecular diagnosis of Bardet-Biedl syndrome by high-throughput targeted exome sequencing
Dong-Jun Xing, Hong-Xing Zhang, Na Huang, et al.
Acta Ophthalmologica
|
February 13, 2023
One-year myopia control efficacy of cylindrical annular refractive element spectacle lenses
Xinting Liu, Pengqi Wang, Zhu Xie, et al.
Bioactive Materials
|
February 7, 2022
Cyanobacteria-based self-oxygenated photodynamic therapy for anaerobic infection treatment and tissue repair
Bailiang Wang, Liyang Zhou, Yishun Guo, et al.
Ophthalmology
|
January 27, 2009
Extremely low penetrance of Leber's hereditary optic neuropathy in 8 Han Chinese families carrying the ND4 G11778A mutation
Jia Qu, Xiangtian Zhou, Juanjuan Zhang, et al.
Yi Chuan = Hereditas
|
February 24, 2010
[Leber's hereditary optic neuropathy and limbs abnormity claudication may be associated with the mitochondrial ND1 T3866C mutation]
Yan Liu, Shu-Liu Zhuang, Yi Tong, et al.
Plos One
|
June 6, 2013
Targeted exome sequencing identified novel USH2A mutations in Usher syndrome families
Xiu-Feng Huang, Ping Xiang, Jie Chen, et al.
Page
of 75