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Biomolecules|June 28, 2023
Mitochondrial Diabetes Is Associated with the ND4 G11696A MutationYu Ding, Shunrong Zhang, Qinxian Guo, et al.Genes|October 27, 2022
Mitochondrial tRNAGln 4394C>T Mutation May Contribute to the Clinical Expression of 1555A>G-Induced DeafnessYu Ding, Yaoshu Teng, Qinxian Guo, et al.Peerj|February 8, 2021
Leber's Hereditary Optic Neuropathy: the roles of mitochondrial transfer RNA variantsYu Ding, Guangchao Zhuo, Qinxian Guo, et al.Diabetes, Metabolic Syndrome and Obesity : Targets and Therapy|June 10, 2022
Mitochondrial Diabetes is Associated with tRNALeu(UUR) A3243G and ND6 T14502C MutationsYu Ding, Shunrong Zhang, Qinxian Guo, et al.Journal of Clinical Laboratory Analysis|November 23, 2021
Late onset of type 2 diabetes is associated with mitochondrial tRNATrp A5514G and tRNASer(AGY) C12237T mutationsLiuchun Yang, Qinxian Guo, Jianhang Leng, et al.The Journal of Gene Medicine|February 24, 2021
Molecular characterization of two Chinese pedigrees with maternally inherited hypertensionYu Ding, Jinfang Yu, Qinxian Guo, et al.Pharmacogenomics and Personalized Medicine|April 2, 2024
The Association Between Mitochondrial tRNAGlu Variants and Hearing Loss: A Case-Control StudyXuejiao Yu, Sheng Li, Qinxian Guo, et al.Clinical Laboratory|February 27, 2018
Lesch-Nyhan Syndrome in a Chinese Family with Mutation in the Hypoxanthine-Guanine Phosphoribosyltransferase GeneJiao Huang, Chu Zhang, Qinxian Guo, et al.Pageof 1