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Paper Publications
- [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] gongyaoqin. 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.
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