Author

L. M. Rich

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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Immunology· 2 Biochemistry· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:host-pathogen & immune response· 2 Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:drug response / drug discovery· 1 Organism:mouse· 1 Assay:protein structure· 1

Frequent Co-Authors

J. S. Debley· 3 shared E. R. Vanderwall· 2 shared K. A. Barrow· 2 shared A. Barilli· 1 shared A. Sali· 1 shared B. T. Chait· 1 shared C. Fung· 1 shared C. Trapnell· 1 shared

Activity by Year

2021-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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Curved chords = mutual co-authorship

3 shared papersImmunology

J. S. Debley

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

ImmunologybioRxivPreprintMar 17, 2023

Tuft cell-derived acetylcholine regulates epithelial fluid secretion

T. E. Billipp, C. Fung, L. M. Webeck…·J. von Moltke

This study shows that tuft cell-derived acetylcholine in the intestine triggers immediate fluid secretion, distinct from its role in immune responses, and is involved in Type 2 inflammation and helminth clearance.

DOI 10.1101/2023.03.17.533208

mouseexperimental assay

𝕏 PostBluesky

ImmunologybioRxivNov 20, 2021

Airway epithelial interferon response to SARS-CoV-2 is inferior to rhinovirus and heterologous rhinovirus infection suppresses SARS-CoV-2 replication

E. R. Vanderwall, K. A. Barrow, L. M. Rich…·J. S. Debley

The paper compares the IFN response to SARS-CoV-2 and HRV-16 in airway epithelial cells and shows that HRV-16 induces a stronger IFN response and reduces SARS-CoV-2 replication.

DOI 10.1038/s41598-022-10763-2

humanbulk RNA-seq

𝕏 PostBluesky

BiochemistrybioRxivApr 8, 2021

Nanobody Repertoires for Exposing Vulnerabilities of SARS-CoV-2

F. D. Mast, P. C. Fridy, N. E. Ketaren…·M. P. Rout

This paper presents a large repertoire of high-affinity nanobodies against SARS-CoV-2 Spike protein with potent neutralization properties and resistance to viral variants.

DOI 10.7554/elife.73027

humanprotein structure

𝕏 PostBluesky