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These results suggest that TRPV4 mediates ER stress and inflammation pathways, contributing to the loss of dopamine (DA) neurons in the SN and movement deficits in PD mice. Moreover, this study provides a new perspective on molecular targets and gene therapies for the treatment of PD in the future.
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Na Liu
Liping Bai
Zhipeng Lu
SHILAP Revista de lepidopterología
Journal of Neuroinflammation
Kunming University of Science and Technology
Kunming Medical University
First People's Hospital of Yunnan Province
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Liu et al. (Sat,) studied this question.
synapsesocial.com/papers/69dd66ff80eea7d3f699c824 — DOI: https://doi.org/10.1186/s12974-022-02382-5