Peng Jiang

Affiliations: 
University of California, Davis, Davis, CA 
Area:
Ion channels, embryonic and induce pluripotent stem cells, oligodendrocytes
Google:
"Peng Jiang"
Mean distance: 17.13 (cluster 11)
 
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Publications

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Zhang YN, Chen XL, Guo LY, et al. (2023) Downregulation of peripheral luteinizing hormone rescues ovariectomy-associated cognitive deficits in APP/PS1 mice. Neurobiology of Aging. 135: 60-69
Boreland AJ, Stillitano AC, Lin HC, et al. (2023) Dysregulated neuroimmune interactions and sustained type I interferon signaling after human immunodeficiency virus type 1 infection of human iPSC derived microglia and cerebral organoids. Biorxiv : the Preprint Server For Biology
Wang L, Mirabella VR, Dai R, et al. (2022) Analyses of the autism-associated neuroligin-3 R451C mutation in human neurons reveal a gain-of-function synaptic mechanism. Molecular Psychiatry
Jin M, Xu R, Wang L, et al. (2022) Type-I-interferon signaling drives microglial dysfunction and senescence in human iPSC models of Down syndrome and Alzheimer's disease. Cell Stem Cell. 29: 1135-1153.e8
Xu R, Boreland AJ, Li X, et al. (2021) Developing human pluripotent stem cell-based cerebral organoids with a controllable microglia ratio for modeling brain development and pathology. Stem Cell Reports
Jiang P, Turkalj L, Xu R. (2020) High-Fidelity Modeling of Human Microglia with Pluripotent Stem Cells. Cell Stem Cell. 26: 629-631
Xu R, Li X, Boreland AJ, et al. (2020) Human iPSC-derived mature microglia retain their identity and functionally integrate in the chimeric mouse brain. Nature Communications. 11: 1577
Chen C, Jiang P, Xue H, et al. (2020) Author Correction: Role of astroglia in Down's syndrome revealed by patient-derived human-induced pluripotent stem cells. Nature Communications. 11: 1070
Biswas S, Chung SH, Jiang P, et al. (2019) Development of glial restricted human neural stem cells for oligodendrocyte differentiation in vitro and in vivo. Scientific Reports. 9: 9013
Xu R, Brawner AT, Li S, et al. (2019) OLIG2 Drives Abnormal Neurodevelopmental Phenotypes in Human iPSC-Based Organoid and Chimeric Mouse Models of Down Syndrome. Cell Stem Cell
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