孙文杰
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Paper Publications
- [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.
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