Author

Nhu Nguyen

Stanford MedicinePrimary ORCID profile (0000-0001-8276-7042 · 2 papers)Unclaimed ORCID profile · follow to get notified of new preprints

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

Same name, identified by ORCID

Nhu NguyeniD2 papers · University of Hawaiʻi at Mānoa

Biology Disciplines

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Pathology· 1 Synthetic Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Organism:human· 1 Organism:mouse· 1

Frequent Co-Authors

Alexandre de Fraipont· 1 shared Andrew Richardson· 1 shared Antonios ChronopoulosiD· 1 shared Clement T. Y. ChaniD· 1 shared Fateme EsmailieiD· 1 shared Gregory W. CharvilleiD· 1 shared Koshi Kunimoto· 1 shared L. Joseph Su· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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Curved chords = mutual co-authorship

1 shared paperPathology

Alexandre de Fraipont

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Author profile →

2 papers

Recent·Most cited

Hyaluronan and CD44 targeting reverses early matrix changes, proinflammatory signals and fibrosis in primary sclerosing cholangitis

Vidushi Bansal, Lóránd Váncza, Weiguo Fan, Koshi Kunimoto, Tzu Han Lo, Nhu Nguyen, Andrew Richardson, Antonios Chronopoulos, Rui Chen, Xingcai Zhang, Alexandre de Fraipont, Yuan Li, Yi Wei, Gregory W. Charville, Shuang Li, , Natalie Julia Torok

This study identifies HA and CD44 as mediators of matrix changes and fibrosis in PSC, showing their targeting can reverse disease progression.

bioRxiv · Jul 24, 2026 · PreprintPathology

Engineered probiotics that sequester arsenite in a mouse gastrointestinal system

Nhu Nguyen, Miaomiao Wang, Sithembio S Msibi, Vincenzo Kennedy, Fateme Esmailie, L. Joseph Su, Lin Li, Clement T. Y. Chan

This paper engineers probiotics to sequester arsenite in the mouse gut, reducing its systemic absorption and demonstrating the feasibility of using living therapeutics for environmental toxin interception.

bioRxiv · Jan 21, 2026 · PreprintSynthetic Biology