Author

Andrea R. Argouarch

University of California, San FranciscoORCID 0000-0002-0970-4894Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Neuroscience· 2

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:C. elegans· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Organism:mouse· 1 Research Focus:protein structure prediction· 1 Assay:proteomics· 1 Approach:statistical model· 1

Frequent Co-Authors

Aimee W. KaoiD· 2 shared Alma L. BurlingameiD· 2 shared Ana María CuervoiD· 2 shared Bruce L. MilleriD· 2 shared Aurora ScrivoiD· 1 shared Benjamin Caballero· 1 shared Beth A. DombroskiiD· 1 shared Carolina AlquézariD· 1 shared

Activity by Year

2018-2020 · peak 1/yr

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10 top collaborators · 40 mutual co-author links

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2 shared papersNeuroscience

Aimee W. KaoORCID

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2 papers

Recent·Most cited

NeurosciencebioRxivPreprintNov 8, 2020

TSC1 loss-of-function increases risk for tauopathy by inducing tau acetylation and preventing autophagy-mediated tau clearance

Carolina Alquézar, Kathleen M. Schoch, Ethan G. Geier…·Aimee W. Kao

This study identifies TSC1 loss-of-function as a risk factor for tauopathies by promoting tau acetylation and impairing autophagy-mediated tau clearance.

1 citation

mouseproteomics

𝕏 PostBluesky

NeurosciencebioRxivPreprintNov 17, 2018

C. elegans granulins promote an age-associated decline in protein homeostasis via lysosomal protease inhibition

Victoria J. Butler, Wilian Augusto Cortopassi, Andrea R. Argouarch…·Aimee W. Kao

This study identifies granulins as regulators of lysosomal protease activity in C. elegans, showing their role in age-related protein homeostasis decline.

1 citation

C. elegansexperimental assay

𝕏 PostBluesky