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Showing results (681-690 of 746) with videos related to

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Investigative Ophthalmology & Visual Science|July 29, 2015
Prevalence of Mitochondrial ND4 Mutations in 1281 Han Chinese Subjects With Leber's Hereditary Optic NeuropathyPingping Jiang, Min Liang, Juanjuan Zhang, et al.
Science Advances|January 1, 2026
Genome-wide association study reveals genetic architecture and evolution of human retinal pigmentationJian Yuan, Yue Zhang, Yinghao Yao, et al.
Journal of Neuroinflammation|February 27, 2025
Integration and functionality of human iPSC-derived microglia in a chimeric mouse retinal modelChun Tang, Qi-Qi Zhou, Xiu-Feng Huang, et al.
The Plant Cell|June 17, 2008
Targeted degradation of the cyclin-dependent kinase inhibitor ICK4/KRP6 by RING-type E3 ligases is essential for mitotic cell cycle progression during Arabidopsis gametogenesisJingjing Liu, Yiyue Zhang, Genji Qin, et al.
Nucleic Acids Research|October 5, 2017
A 'new lease of life': FnCpf1 possesses DNA cleavage activity for genome editing in human cellsMengjun Tu, Li Lin, Yilu Cheng, et al.
Ophthalmology|December 7, 2010
Leber's hereditary optic neuropathy is associated with the T12338C mutation in mitochondrial ND5 gene in six Han Chinese familiesXiao-Ling Liu, Xiangtian Zhou, Jian Zhou, et al.
Investigative Ophthalmology & Visual Science|January 9, 2014
Frequency and spectrum of mitochondrial ND6 mutations in 1218 Han Chinese subjects with Leber's hereditary optic neuropathyMin Liang, Pingping Jiang, Feng Li, et al.
International Journal of Ophthalmology|September 3, 2016
Novel mutations in PDE6B causing human retinitis pigmentosaLu-Lu Cheng, Ru-Yi Han, Fa-Yu Yang, et al.
Nature Communications|August 7, 2024
Exome-wide association study identifies KDELR3 mutations in extreme myopiaJian Yuan, You-Yuan Zhuang, Xiaoyu Liu, et al.
Patterns (New York, N.Y.)|September 5, 2024
Concepts and applications of digital twins in healthcare and medicineKang Zhang, Hong-Yu Zhou, Daniel T Baptista-Hon, et al.
Pageof 75

Showing results (681-690 of 746) with videos related to

Sort By:
Pageof 75
Investigative Ophthalmology & Visual Science|July 29, 2015
Prevalence of Mitochondrial ND4 Mutations in 1281 Han Chinese Subjects With Leber's Hereditary Optic NeuropathyPingping Jiang, Min Liang, Juanjuan Zhang, et al.
Science Advances|January 1, 2026
Genome-wide association study reveals genetic architecture and evolution of human retinal pigmentationJian Yuan, Yue Zhang, Yinghao Yao, et al.
Journal of Neuroinflammation|February 27, 2025
Integration and functionality of human iPSC-derived microglia in a chimeric mouse retinal modelChun Tang, Qi-Qi Zhou, Xiu-Feng Huang, et al.
The Plant Cell|June 17, 2008
Targeted degradation of the cyclin-dependent kinase inhibitor ICK4/KRP6 by RING-type E3 ligases is essential for mitotic cell cycle progression during Arabidopsis gametogenesisJingjing Liu, Yiyue Zhang, Genji Qin, et al.
Nucleic Acids Research|October 5, 2017
A 'new lease of life': FnCpf1 possesses DNA cleavage activity for genome editing in human cellsMengjun Tu, Li Lin, Yilu Cheng, et al.
Ophthalmology|December 7, 2010
Leber's hereditary optic neuropathy is associated with the T12338C mutation in mitochondrial ND5 gene in six Han Chinese familiesXiao-Ling Liu, Xiangtian Zhou, Jian Zhou, et al.
Investigative Ophthalmology & Visual Science|January 9, 2014
Frequency and spectrum of mitochondrial ND6 mutations in 1218 Han Chinese subjects with Leber's hereditary optic neuropathyMin Liang, Pingping Jiang, Feng Li, et al.
International Journal of Ophthalmology|September 3, 2016
Novel mutations in PDE6B causing human retinitis pigmentosaLu-Lu Cheng, Ru-Yi Han, Fa-Yu Yang, et al.
Nature Communications|August 7, 2024
Exome-wide association study identifies KDELR3 mutations in extreme myopiaJian Yuan, You-Yuan Zhuang, Xiaoyu Liu, et al.
Patterns (New York, N.Y.)|September 5, 2024
Concepts and applications of digital twins in healthcare and medicineKang Zhang, Hong-Yu Zhou, Daniel T Baptista-Hon, et al.
Pageof 75