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Plants (Basel, Switzerland)|August 28, 2021
Environmental Heterogeneity Leads to Spatial Differences in Genetic Diversity and Demographic Structure of <i>Acer caudatifolium</i>Min-Xin Luo, Hsin-Pei Lu, Min-Wei Chai, et al.
Yao Xue Xue Bao = Acta Pharmaceutica Sinica|February 6, 2003
[Synthesis and insecticidal activity of the novel hydroxylbenzenedisulfonanilides compounds]Yu Shi, Ya-xin Jiang, Xue-ping Niu, et al.
Nucleic Acids Research|February 13, 2004
Biochemical characterization of the mitochondrial tRNASer(UCN) T7511C mutation associated with nonsyndromic deafnessXiaoming Li, Nathan Fischel-Ghodsian, Faina Schwartz, et al.
Mitochondrion|December 12, 2017
Leber's hereditary optic neuropathy caused by a mutation in mitochondrial tRNA<sup>Thr</sup> in eight Chinese pedigreesJuanjuan Zhang, Yanchun Ji, Xiaoling Liu, et al.
The Journal of Biological Chemistry|June 5, 2025
Mitochondrial tRNA processing defects reprogram mitochondrial and cellular homeostasisGao Zhu, Yunfan He, Xincheng Li, et al.
Journal of Glaucoma|December 30, 2022
Corneal Biomechanics in Primary Open Angle Glaucoma and Ocular Hypertension: A Systematic Review and Meta-analysisMin-Xin Liu, Miao Zhou, Dan-Lin Li, et al.
World Journal of Gastroenterology|November 18, 2014
GW4064, a farnesoid X receptor agonist, upregulates adipokine expression in preadipocytes and HepG2 cellsXiao-Min Xin, Mu-Xiao Zhong, Gong-Li Yang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 10, 2009
[Association of serotonin transporter gene linked polymorphic region polymorphism with early onset myocardial infarction and platelet membrane glycoprotein I b]Da-sheng Xia, Qian-yu Guo, Yan-qiang Liu, et al.
Huan Jing Ke Xue= Huanjing Kexue|November 2, 2004
[Synergy effect of dissolved oxygen in photodegradation of propisochlor in aqueous solution]Yu Wang, Fa-sheng Li, Min-xin Wang, et al.
American Journal of Medical Genetics. Part A|December 31, 2003
Cosegregation of C-insertion at position 961 with the A1555G mutation of the mitochondrial 12S rRNA gene in a large Chinese family with maternally inherited hearing lossRonghua Li, Guangqian Xing, Ming Yan, et al.
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