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Frontiers in Psychiatry|January 12, 2026
Parental control and depressive symptoms in college freshmen with myopia: the mediating role of vision-related quality of lifeGang Liang, Xing-Xuan Dong, Dan-Lin Li, et al.
Yi Chuan = Hereditas|March 4, 2014
[Research progress in heritable dyslipidemia]Yi-Qun He, Mei-Fen Xu, Han Yu, et al.
Yi Chuan = Hereditas|April 13, 2011
[The mitochondrial ND5 T12338C mutation may be associated with Leber's hereditary optic neuropathy in two Chinese families]Yan-Chun Ji, Xiao-Ling Liu, Fu-Xin Zhao, et al.
Biochemical and Biophysical Research Communications|March 3, 2012
A novel OPA1 mutation in a Chinese family with autosomal dominant optic atrophyJuanjuan Zhang, Yimin Yuan, Bing Lin, et al.
Investigative Ophthalmology & Visual Science|May 4, 2010
Leber's hereditary optic neuropathy affects only female matrilineal relatives in two Chinese familiesJia Qu, Ying Wang, Yi Tong, et al.
American Journal of Medical Genetics. Part A|September 7, 2006
Variants in mitochondrial tRNAGlu, tRNAArg, and tRNAThr may influence the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese families with hearing lossWie-Yen Young, Lidong Zhao, Yaping Qian, et al.
Investigative Ophthalmology & Visual Science|July 26, 2021
Assocation Between Leber's Hereditary Optic Neuropathy and MT-ND1 3460G>A Mutation-Induced Alterations in Mitochondrial Function, Apoptosis, and MitophagyJuanjuan Zhang, Yanchun Ji, Jie Chen, et al.
World Journal of Gastroenterology|October 11, 2012
CpG island methylator phenotype and Helicobacter pylori infection associated with gastric cancerJi-Bin Liu, Xu-Ming Wu, Jin Cai, et al.
Biochemical and Biophysical Research Communications|December 21, 2005
Leber's hereditary optic neuropathy is associated with the mitochondrial ND4 G11696A mutation in five Chinese familiesXiangtian Zhou, Qiping Wei, Li Yang, et al.
Biochemical and Biophysical Research Communications|April 17, 2007
The mitochondrial tRNA(Glu) A14693G mutation may influence the phenotypic manifestation of ND1 G3460A mutation in a Chinese family with Leber's hereditary optic neuropathyYi Tong, Yijian Mao, Xiangtian Zhou, et al.
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