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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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- [1] . 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, 2019.
- [2] 毛飞. Identification and Functional Analysis of a SLC33A1: c.339T > G (p.Ser113Arg) Variant in the Original SPG42 Family. HUMAN MUTATION, 240-249, 2015.
- [3] 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.
- [4] 马燕燕. Generation of two induced pluripotent stem cell lines from patients with X-linked Alport syndrome. STEM CELL RESEARCH, 53, 2021.
- [5] 段若楠. Smek1 deficiency exacerbates experimental autoimmune encephalomyelitis by activating proinflammatory microglia and suppressing the IDO1-AhR pathway. JOURNAL OF NEUROINFLAMMATION, 18, 2021.
- [6] 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, 2020.
- [7] 李妍. Generation of an induced pluripotent stem cell line SDUBMSi005-A from a patient with double primary gastric and colon carcinoma. STEM CELL RESEARCH, 53, 2021.
- [8] 刘晓林. Establishment of patient-specific induced pluripotent stem cell line SDUBMSi009-A from a patient with X-linked Lowe syndrome. STEM CELL RESEARCH, 51, 2021.
- [9] 马燕燕. Generation and characterization of an integration-free iPSC line SDUBMSi006-A from a patient with Alport syndrome caused by COL4A3 gene mutations. stem cell research, 2021.
- [10] 段若楠. A De Novo Frameshift Mutation in TNFAIP3 Impairs A20 Deubiquitination Function to Cause Neuropsychiatric Systemic Lupus Erythematosus (vol 39, pg 795, 2019). JOURNAL OF CLINICAL IMMUNOLOGY, 40, 1062, 2020.
- [11] 汪小晶. Generation of a human induced pluripotent stem cell line (SDUBMSi001-A) from a hereditary spastic paraplegia patient carrying kif1a c.773C > T missense mutation. STEM CELL RESEARCH, 43, 2020.
- [12] 马燕燕. Generation and characterization of an integration-free iPSC line SDUBMSi006-A from a patient with Alport syndrome caused by COL4A3 gene mutations. STEM CELL RESEARCH, 52, 2021.
- [13] 龙逢. A SMOC2 variant inhibits BMP signaling by competitively binding to BMPR1B and causes growth plate defects. BONE, 142, 2021.
- [14] 刘娉婷. S113R mutation in SLC33A1 leads to neurodegeneration and augmented BMP signaling in a mouse model. Disease Models & Mechanisms, 10, 53, 2017.
- [15] 汪小晶. Generation of a human induced pluripotent stem cell line (SDUMSi001-A) from a hereditary spastic paraplegia patient carrying KIF1A c.773C>T missense mutation. stem cell research, 2020.
- [16] 龚瑶琴. Generation of patient-specific pluripotent induced stem cell line SDUBMSI002-A from a patient with X-linked mental retardation syndrome. stem cell research, 101724, 2020.
- [17] 李曦 , 刘奇迹 , 李江夏 and 袁倩倩. WDFY4 Is Involved in Symptoms of Systemic Lupus Erythematosus by Modulating B Cell Fate via Noncanonical Autophagy. Journal of Immunology, 201, 2570, 2018.
- [18] 王梅天. Nongenetic Optical Modulation of Neural Stem Cell Proliferation and Neuronal/Glial Differentiation. BIOMATERIALS Journal, 225, 119539, 2019.
- [19] 段若楠. A De Novo Frameshift Mutation in TNFAIP3 Impairs A20 Deubiquitination Function to Cause Neuropsychiatric Systemic Lupus Erythematosus. 2019.
- [20] 刘铎 , 刘奇迹 , 李曦 , 刘巧 , 李江夏 , 龚瑶琴 , 杨坤 Exposure to blue light stimulates the proangiogenic capability of exosomes derived from human umbilical cord mesenchymal stem cells. 10, 2019.