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Eric White

As seen in: Nature, Wiley Online Library, MarketWatch, Chicago Sun-Times, Patch, Barron's, HCP Live, The Gospel Coalition, Lexology, Federal News Network and
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Articles

PFAS from a Discrete-Event Terrestrial Source Migrates with Groundwater to Intertidal Seepages

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By Martin Briggs, Eric White, Patrick T. Scordato
| Wiley Online Library Verified
Introduction The ecosystems of coastal salt marshes are often hydrologically connected to terrestrial groundwater flow systems (Guimond et al. 2025), rendering the marshes susceptible to complex legacies of contamination (Hort et al. 2024). Springs and seeps along shoreline areas create ecological niches where animals tend to concentrate and are often targeted for harvesting (Moosdorf and Oehler 2017).
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AI CT Tool for Early Pulmonary Fibrosis Detection Enters Phase 3, With Eric White, MD

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By Eric White
| consultantlive.com
Early identification remains one of the most persistent challenges in interstitial lung disease and pulmonary fibrosis, where patients are often diagnosed after irreversible lung damage has already occurred. By that point, prognosis is poor, with survival frequently measured in just a few years.
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Durotaxis is a driver and potential therapeutic target in lung fibrosis and metastatic pancreatic cancer - Nature Cell Biology

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By Maria-Anna Chrysovergi, Fei Liu, Zebin Xiao, Mark Anthony Leon-Duque, Delphine Sicard, Tejaswini S. Reddi, Edward Chaum, Kaveh Daneshvar, Allan C. Mullen, David Ting, Eric White, Raghu Kalluri, Christina M. Woo, Ellen Puré, Wolfgang H. Goldmann, Adam Engler
| Nature Verified
Abstract Durotaxis, cell migration along stiffness gradients, is linked to embryonic development, tissue repair and disease. Despite solid in vitro evidence, its role in vivo remains largely speculative. Here we demonstrate that durotaxis actively drives disease progression in vivo in mouse models of lung fibrosis and metastatic pancreatic cancer. In lung fibrosis, durotaxis directs fibroblast recruitment to sites of injury, where they undergo mechano-activation into scar-forming myofibroblasts.
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