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YuShan Tu

Researcher at University of Toronto

Publications -  6
Citations -  313

YuShan Tu is an academic researcher from University of Toronto. The author has contributed to research in topics: Hyperalgesia & Proto-oncogene tyrosine-protein kinase Src. The author has an hindex of 6, co-authored 6 publications receiving 213 citations.

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Microglial P2X4R-evoked pain hypersensitivity is sexually dimorphic in rats.

TL;DR: The findings demonstrate the existence of sexually dimorphic pain signalling in rats, suggesting that this sex difference is evolutionarily conserved, at least across rodent species.
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Circulating NOD1 Activators and Hematopoietic NOD1 Contribute to Metabolic Inflammation and Insulin Resistance

TL;DR: It is shown that circulating activators of NOD1, a receptor for bacterial peptidoglycan, increase with high fat feeding in mice, suggesting that N OD1 could be a critical sensor leading to metabolic inflammation.
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Priming of Adult Incision Response by Early-Life Injury: Neonatal Microglial Inhibition Has Persistent But Sexually Dimorphic Effects in Adult Rats

TL;DR: Neonatal microglial inhibition with systemic minocycline or intrathecal SB203580 at the time of neonatal incision revealed sex-dependent effects: the persistent mechanical and thermal hyperalgesia following reincision in adulthood was prevented in males but unaffected in females, emphasizing the importance of evaluating sex- dependent differences at all ages in preclinical studies.
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Control of Long-Term Synaptic Potentiation and Learning by Alternative Splicing of the NMDA Receptor Subunit GluN1.

TL;DR: Alternative splicing of GluN1 is a mechanism for controlling physiological long-lasting synaptic potentiation, learning, and memory and in human iPSC-derived neurons in autism spectrum disorder NMDARs show characteristics of N1-lacking GLUN1.
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Fyn Kinase regulates GluN2B subunit-dominant NMDA receptors in human induced pluripotent stem cell-derived neurons

TL;DR: These findings provide a basis for utilizing human iPSC-derived neurons in screening for drugs targeting NMDARs in neurological disorders, and are the first evidence that tyrosine phosphorylation regulates the function of NMD ARs in human i PSCs.