Limei Cui

Biochemical evidence for a mitochondrial genetic modifier in the phenotypic manifestation of Leber’s hereditary optic neuropathy-associated mitochondrial DNA mutation

Pingping Jiang, Min Liang, Chaofan Zhang et al. · Human Molecular Genetics · 2016 · 42 citations · Full text

Mutations of MAP1B encoding a microtubule-associated phosphoprotein cause sensorineural hearing loss

Limei Cui, Jing Zheng, Qiong Zhao et al. · JCI Insight · 2020 · 39 citations · Full text

Hypertension-associated mitochondrial DNA 4401A>G mutation caused the aberrant processing of tRNAMet, all 8 tRNAs and ND6 mRNA in the light-strand transcript

Xiaoxu Zhao, Limei Cui, Yun Xiao et al. · Nucleic Acids Research · 2019 · 27 citations · Full text

Rna Processing, Mitochondrial Trnamet, Mitochondrial Biogenesis +15

Contribution of a mitochondrial tyrosyl-tRNA synthetase mutation to the phenotypic expression of the deafness-associated tRNASer(UCN) 7511A>G mutation

Wenlu Fan, Jing Zheng, Wanzhong Kong et al. · Journal of Biological Chemistry · 2019 · 25 citations · Full text

miR‐146a enhances regulatory T‐cell differentiation and function in allergic rhinitis by targeting STAT5b

Yu Zhang, Yujuan Yang, Jing Guo et al. · Allergy · 2021 · 25 citations