一、个人简介

毕业于浙江大学遗传研究所，硕博连读。2022年12月入职山东第一医科大学科技创新中心。现主要通过动物模型研究老年性耳聋的发病机制，共发表SCI论文7篇。主持国自然青年基金1项，已结题；主持国自然面上项目1项，在研。

二、代表论著

1. Zhao X, Cui L, Xiao Y, Mao Q, Aishanjiang M, Kong W, Liu Y, Chen H, Hong F, Jia Z, Wang M, Jiang P, Guan MX. Hypertension-associated mitochondrial DNA 4401A>G mutation caused the aberrant processing of tRNA^Met, all 8 tRNAs and ND6 mRNA in the light-strand transcript. Nucleic Acids Res. 2019 Nov 4;47(19):10340-10356.

2. Zhao X, Han J, Zhu L, Xiao Y, Wang C, Hong F, Jiang P, Guan MX. Overexpression of human mitochondrial alanyl-tRNA synthetase suppresses biochemical defects of the mt-tRNA^Ala mutation in cybrids. Int J Biol Sci. 2018 Aug 6;14(11):1437-1444.

3. Yu J, Liang X, Ji Y, Ai C, Liu J, Zhu L, Nie Z, Jin X, Wang C, Zhang J, Zhao F, Mei S, Zhao X, Zhou X, Zhang M, Wang M, Huang T, Jiang P, Guan MX. PRICKLE3 linked to ATPase biogenesis manifested Leber's hereditary optic neuropathy. J Clin Invest. 2020 Sep 1;130(9):4935-4946.

4. Jiang P, Liang M, Zhang C, Zhao X, He Q, Cui L, Liu X, Sun YH, Fu Q, Ji Y, Bai Y, Huang T, Guan MX. Biochemical evidence for a mitochondrial genetic modifier in the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation. Hum Mol Genet. 2016 Aug 15;25(16):3613-3625.

三、招生要求

学术型：偏向生物化学与分子生物学方向

专业型：偏向医学检验技术方向