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European Journal of Human Genetics : EJHG|February 10, 2012
The 12S rRNA A1555G mutation in the mitochondrial haplogroup D5a is responsible for maternally inherited hypertension and hearing loss in two Chinese pedigreesHong Chen, Jing Zheng, Ling Xue, et al.
The Journal of Biological Chemistry|July 10, 2025
Leber's hereditary optic neuropathy-associated ND1 3733G>C mutation ameliorates the mitochondrial quality control and cellular homeostasisMeiheriayi Yasheng, Yanchun Ji, Yunfan He, et al.
International Journal of Pediatric Otorhinolaryngology|November 9, 2010
Homoplasmy of the G7444A mtDNA and heterozygosity of the GJB2 c.35delG mutations in a family with hearing lossHaris Kokotas, Maria Grigoriadou, Li Yang, et al.
Glia|September 9, 2021
Increasing astrogenesis in the developing hippocampus induces autistic-like behavior in mice via enhancing inhibitory synaptic transmissionJuan Chen, Xiao-Lin Ma, Hui Zhao, et al.
Mitochondrion|August 22, 2016
Mitochondrial tRNA mutations in 2070 Chinese Han subjects with hypertensionLing Xue, Meng Wang, Haiying Li, et al.
The Journal of Biological Chemistry|November 6, 2019
Contribution of a mitochondrial tyrosyl-tRNA synthetase mutation to the phenotypic expression of the deafness-associated tRNASer(UCN) 7511A>G mutationWenlu Fan, Jing Zheng, Wanzhong Kong, et al.
Circulation Research|April 2, 2011
Maternally inherited essential hypertension is associated with the novel 4263A>G mutation in the mitochondrial tRNAIle gene in a large Han Chinese familyShiwen Wang, Ronghua Li, Andrea Fettermann, et al.
Biochemical and Biophysical Research Communications|August 19, 2007
Coexistence of mitochondrial 12S rRNA C1494T and CO1/tRNA(Ser(UCN)) G7444A mutations in two Han Chinese pedigrees with aminoglycoside-induced and non-syndromic hearing lossHuijun Yuan, Jing Chen, Xin Liu, et al.
Plos One|February 3, 2017
Cytokeratin-14 contributes to collective invasion of salivary adenoid cystic carcinomaXiao-Lei Gao, Jia-Shun Wu, Min-Xin Cao, et al.
Yi Chuan = Hereditas|April 12, 2013
[Prevalence of common genetic mutations and clinical characteristics analysis in patients at different ages with nonsyndromic hearing impairment]Chu-Qin Zhang, Bo-Bei Chen, Ying-Ying Chen, et al.
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