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个人信息Personal Information
副教授 硕士生导师
性别：女
学历：博士研究生毕业
学位：理学博士学位
在职信息：在职
所在单位：基础医学院
入职时间：2009-07-16
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- . Generation of an iPSC line (SDQLCHi015-A) from peripheral blood mononuclear cells of a patient with mental retardation type 15 carrying c.1007_1011del, p.(Ile336fs) in CUL4B gene. 41, 2023.
- 毛飞. Identification and Functional Analysis of a SLC33A1: c.339T > G (p.Ser113Arg) Variant in the Original SPG42 Family. HUMAN MUTATION, 240-249, 2022.
- 龙逢. An iPS cell line SDUBMSi0011-A from a multiple epiphyseal dysplasia patient carrying c. 1076T > G mutation in the SMOC2 gene. STEM CELL RESEARCH, 53, 2021.
- 马燕燕. Generation of two induced pluripotent stem cell lines from patients with X-linked Alport syndrome. STEM CELL RESEARCH, 53, 2021.
- 段若楠. Smek1 deficiency exacerbates experimental autoimmune encephalomyelitis by activating proinflammatory microglia and suppressing the IDO1-AhR pathway. JOURNAL OF NEUROINFLAMMATION, 18, 2021.
- 刘晓林. Generation of patient-specific pluripotent induced stem cell line SDUBMSI002-A from a patient with X-linked mental retardation syndrome. STEM CELL RESEARCH, 43, 2021.
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- 遗传性痉挛性截瘫特异的诱导性多潜能干细胞库的建立及质量控制, 2019/07/08-2021/12/31
- 神经肌肉病的转化医学研究---转化医学专题, 2016/11/01-2019/12/01
- 抑郁症新药发现与鉴定的合作研究, 2013/04/01-2016/12/31
- 利用Cul4b基因敲除小鼠模型研究CUL4B在脂肪分化中的作用及其分子机制, 2014/08/15-2017/12/31
- 乙酰辅酶A转运蛋白SLC33A1在遗传性痉挛性截瘫发生中的作用机制研究, 2017/08/17-2021/12/31
- SLC33A1通过BMP信号通路介导遗传性痉挛性截瘫发生的作用机制研究, 2016/10/29-2019/06/30
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