近5年内发表的代表性论文/专著
1. Ye Y, Jin B, Zhang HW, Sheng N*. Strategies for Dissecting the Genetic Driving of Conserved Noncoding-Elements for Evolutionary Development of the Corpus Callosum. Neuroscience Bulletin (2024) 40(7):1025-1027.
2. Li Y, Wan LP, Song NN, Ding YQ, Zhao S, Niu J, Mao B*, Sheng N*, Ma P*. RNF220-mediated K63-linked polyubiquitination stabilizes Olig proteins during oligodendroglial development and myelination. Science Advances (2024) 10(6):eadk3931.
3. Zhuang XL#, Zhang JJ#, Shao Y#, Ye Y#, Chen CY#, Zhou L#, Wang ZB#, Luo X, Su B, Yao YG, Cooper DN, Hu BX, Wang L, Qi XG, Lin J, Zhang GJ*, Wang W*, Sheng N*, Wu DD*. Integrative omics reveals rapidly evolving regulatory sequences driving primate brain evolution. Molecular Biology and Evolution (2023) 40(8):msad173.
4. Ma P#, Wan LP#, Li Y#, He CH#, Song NN, Zhao S, Wang H, Ding YQ*, Mao B*, Sheng N*. RNF220 is an E3 ubiquitin ligase for AMPA receptors to regulate synaptic transmission. Science Advances (2022) 8(39):eabq4736.
其他代表性论文/专著
1. Duan GF, Ye Y, Xu S, Tao W, Zhao S, Jin T, Nicoll RA, Shi YS*, Sheng N*. Signal peptide represses GluK1 surface and synaptic trafficking through binding to amino-terminal domain. Nature Communications (2018) 9(1):4879.
2. Sheng N*, Bemben MA, Díaz-Alonso J, Tao W, Shi YS, Nicoll RA*. LTP requires postsynaptic PDZ-domain interactions with glutamate receptor/auxiliary protein complexes. PNAS (2018) 115(15):3948-3953.
3. Sheng N, Shi YS, Nicoll RA*. Amino-terminal domains of kainate receptors determine the differential dependence on Neto auxiliary subunits for trafficking. PNAS (2017) 114(5):1159-1164.
4. Sheng N, Shi YS, Lomash RM, Roche KW, Nicoll RA*. Neto auxiliary proteins control both the trafficking and biophysical properties of the kainate receptor GluK1. Elife (2015) 3:e11682.
5. Sheng N, Xie Z, Wang C, Bai G, Zhang K, Zhu Q, Song J, Guillemot F, Chen YG, Lin A, Jing N*. Retinoic acid regulates bone morphogenic protein signal duration by promoting the degradation of phosphorylated Smad1. PNAS (2010) 107(44):18886-18891.