Author

B. Dickey

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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Cell Biology· 1 Pharmacology & Toxicology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Research Focus:cell signaling & trafficking· 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 Assay:proteomics· 1

Frequent Co-Authors

A. T. Brunger· 1 shared B. Czako· 1 shared J. Cross· 1 shared J. Dickinson· 1 shared J. J. Peters· 1 shared J. Leitz· 1 shared J. Sweeter· 1 shared K. Hunt· 1 shared

Activity by Year

2020-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperPharmacology & Toxicology

A. T. Brunger

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2 papers

Recent·Most cited

Screening of hydrocarbon-stapled peptides for inhibition of calcium-triggered exocytosis

Y. Lai, M. Tuvim, J. Leitz, J. J. Peters, R. Pfuetzner, L. Esquivies, Q. Zhou, B. Czako, J. Cross, P. Jones, B. Dickey, A. T. Brunger

The paper screens hydrocarbon-stapled peptides targeting the SNARE-Syt1 primary interface to inhibit Ca2+-triggered exocytosis and mucus hypersecretion.

bioRxiv · Mar 21, 2022Pharmacology & Toxicology

Mucin granules are degraded in the autophagosome-lysosome pathway as a means of resolving airway mucous cell metaplasia

J. Sweeter, K. Kudrna, K. Hunt, P. Thomes, B. Dickey, S. L. Brody, J. Dickinson

This study shows that autophagy degrades mucin granules in airway mucous cells during resolution of mucous cell metaplasia, offering a therapeutic target for airway diseases.

bioRxiv · Jun 2, 2020 · PreprintCell Biology