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Gene|April 21, 2006
The mitochondrial tRNA(Thr) A15951G mutation may influence the phenotypic expression of the LHON-associated ND4 G11778A mutation in a Chinese familyRonghua Li, Jia Qu, Xiangtian Zhou, et al.
AI Zheng = Aizheng = Chinese Journal of Cancer|March 13, 2008
[Serum proteomic spectra of esophageal squamous cell carcinoma patients analyzed with IMAC3 protein chip]Cha-Zhen Liu, Pei-Yun Zhu, Min-Xin Shi, et al.
Nucleic Acids Research|August 19, 2016
A deafness-associated tRNAAsp mutation alters the m1G37 modification, aminoacylation and stability of tRNAAsp and mitochondrial functionMeng Wang, Yanyan Peng, Jing Zheng, et al.
Mitochondrion|February 16, 2007
Cosegregation of the ND4 G11696A mutation with the LHON-associated ND4 G11778A mutation in a four generation Chinese familyJia Qu, Ronghua Li, Xiangtian Zhou, et al.
Investigative Ophthalmology & Visual Science|January 25, 2006
The novel A4435G mutation in the mitochondrial tRNAMet may modulate the phenotypic expression of the LHON-associated ND4 G11778A mutationJia Qu, Ronghua Li, Xiangtian Zhou, et al.
Journal of Cardiothoracic Surgery|April 21, 2021
Research on clinical characteristics and prognostic analysis of heparin-induced thrombocytopenia after surgery for acute type a aortic dissectionChu-Zhi Zhou, Dong-Jie Feng, Yuan Fang, et al.
Biochemical and Biophysical Research Communications|September 20, 2005
Clinical evaluation and mitochondrial DNA sequence analysis in two Chinese families with aminoglycoside-induced and non-syndromic hearing lossLidong Zhao, Qiuju Wang, Yaping Qian, et al.
Biochemical and Biophysical Research Communications|August 1, 2006
Maternally transmitted diabetes mellitus associated with the mitochondrial tRNA(Leu(UUR)) A3243G mutation in a four-generation Han Chinese familyJianxin Lu, Dawang Wang, Ronghua Li, et al.
Botanical Studies|September 29, 2025
Margins of adaptation at the desert frontier: genetic responses of Ammopiptanthus mongolicus in arid northwestern ChinaYong-Zhi Yang, De-Ming Gao, Pei-Wei Sun, et al.
Human Molecular Genetics|January 7, 2023
Nuclear modifier YARS2 allele correction restored retinal ganglion cells-specific deficiencies in Leber's hereditary optic neuropathyJia-Rong Chen, Chao Chen, Jie Chen, et al.
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