Biblio

Author Title [ Type(Desc)] Year
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Journal Article
Jang SEun, Qiu L, Cai X, Lee JWei Ling, Zhang W, Tan E-K, Liu B, Zeng L. Aggregation-induced emission (AIE) nanoparticles labeled human embryonic stem cells (hESCs)-derived neurons for transplantation. Biomaterials. 2021;271:120747.
Zhang Z-W, Tu H, Jiang M, Vanan S, Chia SYoong, Jang S-E, Saw W-T, Ong Z-W, Ma D-R, Zhou Z-D, et al. The APP intracellular domain promotes expression to enable feed-forward neurodegenerative mechanisms in Parkinson's disease. Sci Signal. 2022;15(748):eabk3411.
Jiang M, Tu H-T, Zhang K, Zhang W, Yu W-P, Xu J, Tan E-K, Guo K-H, Zeng L. Impaired neurogenesis in the hippocampus of an adult VPS35 mutant mouse model of Parkinson's disease through interaction with APP. Neurobiol Dis. 2021:105313.
Wu D, Dou J, Chai X, Bellis C, Wilm A, Shih CChuan, Soon WWei Jia, Bertin N, Lin CBitong, Khor CChuen, et al. Large-Scale Whole-Genome Sequencing of Three Diverse Asian Populations in Singapore. Cell. 2019;179(3):736-749.e15.
Lim S-Y, Closas AMarl FDy, Tan AHuey, Lim JLun, Tan YJayne, Vijayanathan Y, Tay YWen, Khalid RBinti Abdu, Ng WKeong, Kanesalingam R, et al. New insights from a multi-ethnic Asian progressive supranuclear palsy cohort. Parkinsonism Relat Disord. 2023;108:105296.
Chen BL, Yang W, Luo Y, Tan E-K, Wang Q. Non-pharmacological and drug treatment of autonomic dysfunction in multiple system atrophy: current status and future directions. J Neurol. 2023.
Zhou W, Ma D, Sun AXuyang, Tran H-D, Ma D-L, Singh BK, Zhou J, Zhang J, Wang D, Zhao Y, et al. PD-linked CHCHD2 mutations impair CHCHD10 and MICOS complex leading to mitochondria dysfunction. Hum Mol Genet. 2018.