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Shouqing Luo

Researcher at University of Plymouth

Publications -  52
Citations -  13730

Shouqing Luo is an academic researcher from University of Plymouth. The author has contributed to research in topics: Autophagy & Programmed cell death. The author has an hindex of 29, co-authored 50 publications receiving 11554 citations. Previous affiliations of Shouqing Luo include Peking Union Medical College & University of Cambridge.

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α Pix enhances mutant huntingtin aggregation

TL;DR: Using immunoprecipitation experiments, it is shown that alpha Pix binds to both the N-terminal of wild-type htt (wthtt) and mutant htt (muthtt), which suggests thatalpha Pix plays an important role in muthtt aggregation.
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The formation of autophagosomes during lysosomal defect: A new source of cytotoxicity.

TL;DR: This study suggests that production/accumulation of autophagosomes during lysosomal defect directly induces cellular toxicity, and this process may be implicated in the pathological conditions where lyssomes are defective.
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Local anesthetics induce autophagy in young permanent tooth pulp cells

TL;DR: Using pig model and human young permanent tooth pulp cells, this research has identified that the local anesthetics commonly used in clinics can affect cell proliferation and molecular pathway profiling suggested that LC3II is one of the earliest molecules induced by the agents and p62 is the only common downstream target identified for all the drugs tested.
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Enhanced lysosomal function is critical for paclitaxel resistance in cancer cells: reversed by artesunate.

TL;DR: The results suggest that artesunate or other inhibitors of lysosomal function would be potential in the treatment of cancer cells with drug resistance caused by the enhanced lysOSomal function.
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Bim contributes to the progression of Huntington's disease-associated phenotypes.

TL;DR: It is shown that the levels of Bim, a BH3-only protein, are significantly increased in HD human post-mortem and HD mouse striata, correlating with neuronal death, which could contribute to the progression of HD.