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Investigative Ophthalmology & Visual Science|May 14, 2016
Mitochondrial ND1 Variants in 1281 Chinese Subjects With Leber's Hereditary Optic NeuropathyYanchun Ji, Min Liang, Juanjuan Zhang, et al.
Scientific Reports|July 20, 2017
A novel ADOA-associated OPA1 mutation alters the mitochondrial function, membrane potential, ROS production and apoptosisJuanjuan Zhang, Xiaoling Liu, Xiaoyang Liang, et al.
Biochimica Et Biophysica Acta|September 8, 2009
Low penetrance of Leber's hereditary optic neuropathy in ten Han Chinese families carrying the ND6 T11484C mutationJia Qu, Xiangtian Zhou, Fuxin Zhao, et al.
Molecular Genetics and Metabolism|February 16, 2010
Maternally inherited hearing loss is associated with the novel mitochondrial tRNA Ser(UCN) 7505T>C mutation in a Han Chinese familyXiaowen Tang, Ronghua Li, Jing Zheng, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|February 11, 2014
[Hearing loss may be associated with the novel mitochondrial tRNA(Asp) A7551G mutation in a Chinese family]Yue Wu, Ling-zhi Liang, Hong-li Xiao, et al.
Nature Communications|October 23, 2024
SpliceTransformer predicts tissue-specific splicing linked to human diseasesNingyuan You, Chang Liu, Yuxin Gu, et al.
BMC Medical Education|August 5, 2025
Exploring the integration of OFST and IPE in cross-regional physiology teaching-a novel approachTing-Huai Wang, Xiao-Dan Xu, Zhi-Yuan Long, et al.
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