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姚俊
joelyao@njmu.edu.cn
中文, 英语
江苏
南京医科大学
Basic Medical Sciences
  • 1997-2001 学士:南京工业大学,材料科学与工程学院
  • 2001-2004 硕士:南京工业大学,生命科学与制药学院,生物化工专业
  • 2004-2008 博士:南京工业大学,生命科学与制药学院,生物化工专业
  • 主持国家自然科学基金项目2项
  • 以第一或通讯作者发表科研论文20余篇
  • 获国家发明专利授权2项
  • 2008-2017 - 南京医科大学,基础医学院生物技术系 - 讲师
  • 2018-至今 - 南京医科大学,基础医学院医学遗传系 - 副教授
  • 2017年:南京医科大学赵息保青年教师奖教金
  • 2020年:南京医科大学优秀本科生导师
遗传性耳聋的分子发病机制
生物医用材料
  • Mutations in OSBPL2 cause hearing loss associated with primary cilia defects via Sonic Hedgehog signaling., Hairong Shi, Hongshun Wang, Cheng Zhang, Yajie Lu, Jun Yao, Zhibin Chen, Guangqian Xing, Qinjun Wei, Xin Cao, 2022
  • Disruption of Gprasp2 down-regulates Hedgehog signaling and leads to apoptosis in auditory cells., Yajie Lu, Min Zhang, Qinjun Wei, Zhibin Chen, Guangqian Xing, Jun Yao, Xin Cao, 2021
  • OSBPL2-disrupted pigs recapitulate dual features of human hearing loss and hypercholesterolaemia., Jun Yao, Huasha Zeng, Min Zhang, Qinjun Wei, Ying Wang, Haiyuan Yang, Yajie Lu, Rongfeng Li, Qiang Xiong, Lining Zhang, Zhibin Chen, Guangqian Xing, Xin Cao, Yifan Dai, 2019
  • Deletion of OSBPL2 in auditory cells increases cholesterol biosynthesis and drives reactive oxygen species production by inhibiting AMPK activity., Hongshun Wang, Changsong Lin, Jun Yao, Hairong Shi, Cui Zhang, Qinjun Wei, Yajie Lu, Zhibin Chen, Guangqian Xing, Xin Cao, 2019
  • Spatial and temporal expression patterns of Osbpl2a and Osbpl2b during zebrafish embryonic development., Chunyu Liu, Jun Yao, Qinjun Wei, Guangqian Xing, Xin Cao, 2016
  • GPRASP2, a novel causative gene mutated in an X-linked recessive syndromic hearing loss., Guangqian Xing, Jun Yao, Chunyu Liu, Qinjun Wei, Xuli Qian, Lingxin Wu, Yajie Lu, Xin Cao, 2017
  • Genetic analysis of CLDN14 in the Chinese population affected with non-syndromic hearing loss., Yajie Lu, Jun Yao, Qinjun Wei, Jin Xu, Guangqian Xing, Xin Cao, 2018
  • Identification of OSBPL2 as a novel causative gene of progressive nonsyndromic hearing loss by exome sequencing., Guangqian Xing, Jun Yao, Bin Wu, Tingting Liu, Qinjun Wei, Cheng Liu, Yajie Lu, Zhibin Chen, Heng Zheng, Xiaonan Yang, Xin Cao, 2015
  • Probing the effect of two heterozygous mutations in codon 723 of SLC26A4 on deafness phenotype based on molecular dynamics simulations., Jun Yao, Xuli Qian, Jingxiao Bao, Qinjun Wei, Yajie Lu, Heng Zheng, Guangqian Xing, Xin Cao, 2015
  • 大鼠耳蜗前体细胞的体外培养与分化鉴定., 姚俊, 王帅, 魏钦俊, 鲁雅洁, 邢光前, 曹新, 2015
  • FGF信号通路在内耳发育调控和毛细胞再生中的作用., 杨志, 姚俊, 曹新, 2018
  • 胆甾醇基γ-聚谷氨酸载紫杉醇自组装纳米胶束的制备与性能., 胡凡, 肖港, 王育川, 姚俊, 曹新, 2018
  • 胆甾醇基γ-聚谷氨酸负载阿霉素纳米胶束的制备与体内外释药性能评价., 姚俊, 肖港, 徐宁, 曹新, 徐虹, 2017
  • γ-聚谷氨酸胆甾醇基衍生物自组装纳米胶束的制备与表征., 李睿, 阮文辉, 姚俊, 陈宽婷, 魏钦俊, 鲁雅洁, 曹新, 2014
遗传性耳聋 分子发病机制 基因突变 听觉细胞 生物医用材料 纳米颗粒 药物递送 基因治疗 细胞信号 听力损失

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