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The Journal of Biological Chemistry|December 11, 2019
Overexpression of mitochondrial histidyl-tRNA synthetase restores mitochondrial dysfunction caused by a deafness-associated tRNAHis mutationShasha Gong, Xiaoqiong Wang, Feilong Meng, et al.
Infection, Genetics and Evolution : Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases|August 4, 2020
Comparative analysis of mitochondrial DNA datasets indicates that Cylicostephanus minutus represents a species complexYuan Gao, Yang-Yuan Qiu, Xiao-Qing Meng, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|July 4, 2023
Refractive associations with corneal biomechanical properties among young adults: a population-based Corvis ST studyDan-Lin Li, Min-Xin Liu, Zhi-Jian Yin, et al.
American Journal of Medical Genetics. Part A|January 8, 2005
Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutationQiuju Wang, Roughua Li, Hui Zhao, et al.
Eye (London, England)|February 24, 2024
Corneal stress‒strain index in relation to retinal nerve fibre layer thickness among healthy young adultsMin-Xin Liu, Dan-Lin Li, Zhi-Jian Yin, et al.
Molecular Medicine Reports|October 10, 2017
Leber's hereditary optic neuropathy is potentially associated with a novel m.5587T>C mutation in two pedigreesYanchun Ji, Lihua Qiao, Xiaoyang Liang, et al.
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