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Biochemical and Biophysical Research Communications|March 28, 2009
Leber's hereditary optic neuropathy is associated with mitochondrial ND1 T3394C mutationMin Liang, Minqiang Guan, Fuxing Zhao, et al.
Plos One|December 5, 2014
Aminoglycoside stress together with the 12S rRNA 1494C>T mutation leads to mitophagyJialing Yu, Jing Zheng, Xiaoxu Zhao, et al.
Nucleic Acids Research|August 26, 2022
Human TRUB1 is a highly conserved pseudouridine synthase responsible for the formation of Ψ55 in mitochondrial tRNAAsn, tRNAGln, tRNAGlu and tRNAProZidong Jia, Feilong Meng, Hui Chen, et al.
Nucleic Acids Research|September 11, 2019
Hypertension-associated mitochondrial DNA 4401A>G mutation caused the aberrant processing of tRNAMet, all 8 tRNAs and ND6 mRNA in the light-strand transcriptXiaoxu Zhao, Limei Cui, Yun Xiao, et al.
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi = Chinese Journal of Otorhinolaryngology Head and Neck Surgery|February 11, 2014
[Analysis of genotype-phenotype correlation for GJB2 in 221 non-syndromic deafness probands and their pedigrees]Xiao Yu, Bo-bei Chen, Hai-jie Xiang, et al.
Haematologica|May 30, 2024
The role of PALLD-STAT3 interaction in megakaryocyte differentiation and thrombocytopenia treatmentGuoming Li, Haojie Jiang, Lingbin Wang, et al.
Investigative Ophthalmology & Visual Science|May 12, 2012
Leber's hereditary optic neuropathy is associated with the T3866C mutation in mitochondrial ND1 gene in three Han Chinese FamiliesXiangtian Zhou, Yaping Qian, Juanjuan Zhang, et al.
Human Molecular Genetics|July 19, 2016
Biochemical evidence for a mitochondrial genetic modifier in the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutationPingping Jiang, Min Liang, Chaofan Zhang, et al.
Biomaterials Science|May 5, 2020
ZBTB20-mediated titanium particle-induced peri-implant osteolysis by promoting macrophage inflammatory responsesJunxiong Qiu, Peng Peng, Min Xin, et al.
Biochemical and Biophysical Research Communications|February 28, 2006
Aminoglycoside-induced and non-syndromic hearing loss is associated with the G7444A mutation in the mitochondrial COI/tRNASer(UCN) genes in two Chinese familiesYi Zhu, Yaping Qian, Xiaowen Tang, et al.
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