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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.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.Mitochondrion|May 14, 2013
Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated m.14484T>C (MT-ND6) mutation in Chinese familiesJuanjuan Zhang, Fuxin Zhao, Qun Fu, et al.Journal of Hepatology|November 3, 2024
Blood markers for type-1, -2, and -3 inflammation are associated with severity of acutely decompensated cirrhosisZhujun Cao, Yujing Yao, Minghao Cai, et al.The Journal of Clinical Investigation|June 10, 2020
PRICKLE3 linked to ATPase biogenesis manifested Leber's hereditary optic neuropathyJialing Yu, Xiaoyang Liang, Yanchun Ji, et al.Blood Advances|January 15, 2025
α-Actinin-1 deficiency in megakaryocytes causes low platelet count, platelet dysfunction, and mitochondrial impairmentXiangjie Lin, Hanchen Gao, Min Xin, et al.Journal of Medical Genetics|September 21, 2011
Maternally transmitted late-onset non-syndromic deafness is associated with the novel heteroplasmic T12201C mutation in the mitochondrial tRNAHis geneXukun Yan, Xinjian Wang, Zhengmin Wang, et al.Mitochondrion|October 13, 2009
Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutationJianxin Lu, Yaping Qian, Zhiyuan Li, et al.JCI Insight|April 26, 2022
Heteroplasmic and homoplasmic m.616T>C in mitochondria tRNAPhe promote isolated chronic kidney disease and hyperuricemiaChengxian Xu, Lingxiao Tong, Jia Rao, et al.Pageof 37