Author

L.-F.-R. Qi

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Pharmacology & Toxicology· 1

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Approach:biophysical modeling· 1 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:drug response / drug discovery· 1 Approach:experimental assay· 1 Organism:human· 1 Assay:metabolomics· 1 Organism:mouse· 1

Frequent Co-Authors

C. Peng· 1 shared C. Qian· 1 shared M. Zhang· 1 shared P. Li· 1 shared P. Wu· 1 shared P. Yang· 1 shared S. Liu· 1 shared X. Xu· 1 shared

Activity by Year

2021-2021 · peak 1/yr

Co-Author Collaboration Network

8 top collaborators · 28 mutual co-author links

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1 shared paperPharmacology & Toxicology

C. Peng

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1 paper

Recent·Most cited

Discovery of a molecular glue that enhances UPRmt to restore proteostasis via TRKA-GRB2-EVI1-CRLS1 axis

L.-F.-R. Qi, C. Qian, S. Liu, C. Peng, M. Zhang, P. Yang, P. Wu, P. Li, X. Xu

This study identifies ginsenoside Rg3 as a molecular glue that enhances mitochondrial UPR via the TRKA-GRB2-EVI1-CRLS1 axis to restore proteostasis in Parkinson's disease.

bioRxiv · Feb 17, 2021 · PreprintPharmacology & Toxicology