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. A novelMYH14mutation in a Chinese family with autosomal dominant nonsyndromic hearing loss. BMC MEDICAL GENETICS, 21, 2024.
李明. Lamivudine improves cognitive decline in SAMP8 mice: Integrating in vivo pharmacological evaluation and network pharmacology. journal of cellular and molecular medicine, 25, 8490, 2021.
白晓卉. Five Novel Mutations in LOXHD1 Gene Were Identified to Cause Autosomal Recessive Nonsyndromic Hearing Loss in Four Chinese Families (vol 2020, pg 9, 2020). BioMed Research International, 2020, 2021.
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致聋基因新突变致非综合征性耳聋的致病机制研究, 2021-10-10-2024-10-10
基于2个常染色体显性遗传耳聋家系致聋基因新突变的机制研究, 2021-05-31-2024-05-31
4-辛基衣康酸激活Nrf2信号通路在修复骨关节炎软骨损伤中的作用及机制研究, 2019-08-16-2023-12-31
利用CRISPR-Cas9技术研究POU4F3基因在斑马鱼听觉系统中的功能及机制, 2016-08-17-2020-12-31
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