Paper Publications

• [1]  马燕燕. CUL4B mutations impair human cortical neurogenesis through PP2A-dependent inhibition of AKT and ERK.  Cell Death & Disease,  15,  2024. 
• [2]  . Near-infrared light induces neurogenesis and modulates anxiety-like behavior.  Stem Cell Research and Therapy,  1,  494, 2024. 
• [3]  田文坦. 在生物医药创新升级背景下模式动物研究中心的发展.  医学动物防制,  2024. 
• [4]  田文坦. 在生物医药创新升级背景下模式动物研究中心的发展.  医学动物防制,  40,  2024. 
• [5]  . Ablation of ORMDL3 impairs adipose tissue thermogenesis and insulin sensitivity by increasing ceramide generation.  MOLECULAR METABOLISM,  56,  101423, 2022. 
• [6]  刘奇迹. A functional polymorphism in the SPINK5 gene is associated with asthma in a Chinese Han Population.  BMC Medical Genetics,  10,  2009. 
• [7]  . 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. 
• [8]  龚瑶琴. Ablation of ORMDL3 impairs adipose tissue thermogenesis and insulin sensitivity by increasing ceramide generation..  MOLECULAR METABOLISM,  101423, 2022. 
• [9]  赵晓晗. Zebrafish cul4a, but not cul4b, modulates cardiac and forelimb development by upregulating tbx5a expression.  Human Molecular Genetics,  24,  853-864, 2015. 
• [10]  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. 
• [11]  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. 
• [12]  段若楠. Smek1 deficiency exacerbates experimental autoimmune encephalomyelitis by activating proinflammatory microglia and suppressing the IDO1-AhR pathway.  JOURNAL OF NEUROINFLAMMATION,  18,  2021. 
• [13]  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. 
• [14]  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. 
• [15]  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.