Author

John F. LaDisa

Marquette UniversityORCID 0000-0002-2339-743XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Assay:proteomics· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Organism:human· 1 Organism:mouse· 1

Frequent Co-Authors

Abdel A. AlliiD· 2 shared Alexander Armstrong· 1 shared Dylan Schock· 1 shared Leah Kessler· 1 shared Ling YuiD· 1 shared Niharika BalaiD· 1 shared Van-Anh L. Nguyen· 1 shared

Activity by Year

2025-2025 · peak 2/yr

Co-Author Collaboration Network

7 top collaborators · 13 mutual co-author links

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2 shared papersPhysiology

Abdel A. AlliORCID

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2 papers

Recent·Most cited

PhysiologybioRxivPreprintMay 23, 2025

A benchtop bioreactor to impart coarctation-induced deformation and assess mechanisms of endothelial dysfunction

Dylan Schock, Alexander Armstrong, Abdel A. Alli, John F. LaDisa

The paper develops an in vitro system to mimic CoA-induced mechanical strain on endothelial cells and study NPRC dysfunction mechanisms.

DOI 10.1101/2025.05.23.655865

humanproteomics

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PhysiologyAmerican Journal of Physiology-Cell PhysiologyPeer-reviewedFeb 21, 2025

Activity and function of the endothelial sodium channel is regulated by the effector domain of MARCKS like protein 1 in mouse aortic endothelial cells

Ling Yu, Niharika Bala, Van-Anh L. Nguyen…·Abdel A. Alli

This study shows that MLP1's effector domain and PIP2 regulate EnNaC activity in mouse aortic endothelial cells by affecting membrane association and fluidity.

2 citations

mouseproteomics

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