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Mitochondrion|September 8, 2014
Leber's hereditary optic neuropathy caused by the homoplasmic ND1 m.3635G>A mutation in nine Han Chinese familiesJuanjuan Zhang, Pingping Jiang, Xiaofen Jin, et al.
JCI Insight|December 3, 2020
Mutations of MAP1B encoding a microtubule-associated phosphoprotein cause sensorineural hearing lossLimei Cui, Jing Zheng, Qiong Zhao, et al.
Journal of Translational Medicine|January 6, 2011
Frequency and spectrum of mitochondrial 12S rRNA variants in 440 Han Chinese hearing impaired pediatric subjects from two otology clinicsZhisen Shen, Jing Zheng, Bobei Chen, et al.
Yi Chuan = Hereditas|April 29, 2010
[Leber's hereditary optic neuropathy may be associated with the mitochondrial tRNAGlu A14693G mutation in three Chinese families]Yong-Mei Zhang, Yan-Chun Ji, Xiao-Ling Liu, et al.
Biochemical and Biophysical Research Communications|September 8, 2009
Leber's hereditary optic neuropathy is associated with mitochondrial ND6 T14502C mutationFuxin Zhao, Minqiang Guan, Xiangtian Zhou, et al.
Scientific Reports|October 27, 2023
Development of machine learning prognostic models for overall survival of prostate cancer patients with lymph node-positiveZi-He Peng, Juan-Hua Tian, Bo-Hong Chen, et al.
Thrombosis and Haemostasis|December 8, 2025
Thrombosis Caused by Factor XI Gly397Ser Mutation with Enhanced Procoagulant ActivityYanyan Shao, Yang Xu, Min Xin, et al.
Molecular Genetics and Metabolism|August 24, 2010
Mitochondrial haplogroup M9a specific variant ND1 T3394C may have a modifying role in the phenotypic expression of the LHON-associated ND4 G11778A mutationMinglian Zhang, Xiangtian Zhou, Chengwu Li, et al.
Yi Chuan = Hereditas|June 16, 2012
[Spectrum and frequency of mitochondrial 12S rRNA variants in the Chinese subjects with nonsynrdomic hearing loss in Zhejiang Province]Bin-Jiao Zheng, Guang-Hua Peng, Bo-Bei Chen, et al.
Biochemical and Biophysical Research Communications|August 10, 2010
Mitochondrial ND6 T14502C variant may modulate the phenotypic expression of LHON-associated G11778A mutation in four Chinese familiesJuanjuan Zhang, Xiangtian Zhou, Jian Zhou, et al.
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