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Fuxin Zhao

Showing results (1-10 of 50) with videos related to

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Frontiers in Psychology|May 16, 2022
Comparative Study on Online and Offline Teaching for Creative Idea GenerationJing Zhang, Ying Dai, Fuxin Zhao
Materials (Basel, Switzerland)|August 10, 2024
Direct Ink Writing of SiCN/RuO<sub>2</sub>/TiB<sub>2</sub> Composite Ceramic Ink for High-Temperature Thin-Film SensorsYusen Wang, Lida Xu, Xiong Zhou, et al.
Human Molecular Genetics|August 10, 2022
Abnormal morphology and function in retinal ganglion cells derived from patients-specific iPSCs generated from individuals with Leber's hereditary optic neuropathyZhipeng Nie, Chenghui Wang, Jiarong Chen, et al.
Human Genetics|April 13, 2013
Exome sequencing reveals CCDC111 mutation associated with high myopiaFuxin Zhao, Jinyu Wu, Anquan Xue, et al.
Experimental Eye Research|March 3, 2022
Form-deprivation myopia downregulates calcium levels in retinal horizontal cells in miceQihang Li, He Zhu, Miaomiao Fan, et al.
Frontiers in Microbiology|June 6, 2018
The Kynurenine 3-Monooxygenase Encoding Gene, <i>BcKMO</i>, Is Involved in the Growth, Development, and Pathogenicity of <i>Botrytis cinerea</i>Kang Zhang, Xuemei Yuan, Jinping Zang, et al.
Molecular Genetics and Metabolism|January 8, 2010
Very low penetrance of Leber's hereditary optic neuropathy in five Han Chinese families carrying the ND1 G3460A mutationYi Tong, Yan-Hong Sun, Xiangtian Zhou, et al.
Frontiers in Cellular Neuroscience|June 18, 2020
Increased Connexin36 Phosphorylation in AII Amacrine Cell Coupling of the Mouse Myopic RetinaSeema Banerjee, Qin Wang, Fuxin Zhao, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 8, 2015
[A novel mutation T8821G in mitochondrial DNA may be associated with Leber's hereditary optic neuropathy]Min Gao, Sai Zhang, Zengjun Zhang, et al.
International Journal of Molecular Sciences|February 15, 2022
Genetic Interaction between <i>Mfrp</i> and <i>Adipor1</i> Mutations Affect Retinal Disease PhenotypesNavdeep Gogna, Sonia Weatherly, Fuxin Zhao, et al.
Pageof 5

Showing results (1-10 of 50) with videos related to

Sort By:
Pageof 5
Frontiers in Psychology|May 16, 2022
Comparative Study on Online and Offline Teaching for Creative Idea GenerationJing Zhang, Ying Dai, Fuxin Zhao
Materials (Basel, Switzerland)|August 10, 2024
Direct Ink Writing of SiCN/RuO<sub>2</sub>/TiB<sub>2</sub> Composite Ceramic Ink for High-Temperature Thin-Film SensorsYusen Wang, Lida Xu, Xiong Zhou, et al.
Human Molecular Genetics|August 10, 2022
Abnormal morphology and function in retinal ganglion cells derived from patients-specific iPSCs generated from individuals with Leber's hereditary optic neuropathyZhipeng Nie, Chenghui Wang, Jiarong Chen, et al.
Human Genetics|April 13, 2013
Exome sequencing reveals CCDC111 mutation associated with high myopiaFuxin Zhao, Jinyu Wu, Anquan Xue, et al.
Experimental Eye Research|March 3, 2022
Form-deprivation myopia downregulates calcium levels in retinal horizontal cells in miceQihang Li, He Zhu, Miaomiao Fan, et al.
Frontiers in Microbiology|June 6, 2018
The Kynurenine 3-Monooxygenase Encoding Gene, <i>BcKMO</i>, Is Involved in the Growth, Development, and Pathogenicity of <i>Botrytis cinerea</i>Kang Zhang, Xuemei Yuan, Jinping Zang, et al.
Molecular Genetics and Metabolism|January 8, 2010
Very low penetrance of Leber's hereditary optic neuropathy in five Han Chinese families carrying the ND1 G3460A mutationYi Tong, Yan-Hong Sun, Xiangtian Zhou, et al.
Frontiers in Cellular Neuroscience|June 18, 2020
Increased Connexin36 Phosphorylation in AII Amacrine Cell Coupling of the Mouse Myopic RetinaSeema Banerjee, Qin Wang, Fuxin Zhao, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 8, 2015
[A novel mutation T8821G in mitochondrial DNA may be associated with Leber's hereditary optic neuropathy]Min Gao, Sai Zhang, Zengjun Zhang, et al.
International Journal of Molecular Sciences|February 15, 2022
Genetic Interaction between <i>Mfrp</i> and <i>Adipor1</i> Mutations Affect Retinal Disease PhenotypesNavdeep Gogna, Sonia Weatherly, Fuxin Zhao, et al.
Pageof 5