Camille Ehré

University of North Carolina at Chapel Hill — United States

Medicine · Health Sciences

30h-index5.1kcitations104works1.22yr avg
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Research Topics

Cystic Fibrosis Research Advances(40), Neonatal Respiratory Health Research(28), Tracheal and airway disorders(24), Glycosylation and Glycoproteins Research(14), Respiratory viral infections research(14)

Publications104 total

353 Aberrant ileal mucus properties as a driver of DIOS in CF mice
Journal of Cystic Fibrosis·2025
Airway epithelial SARS-CoV-2 infectious and repair responses: relationships to age, sex, and post-COVID pulmonary syndromes
2025Open Access
STAT3-Dependent Regulation of CFTR and Ciliogenesis Is Essential for Mucociliary Clearance and Innate Airway Defense in Hyper-IgE Syndrome
American Journal of Respiratory and Critical Care Medicine·2025· 1 cited
Differential Mucociliary Clearance and Immune Response in House-Dust-Mite (HDM) Sensitized Mice Following SARS-CoV-2 and Sendai Virus Infections
American Journal of Respiratory and Critical Care Medicine·2025
Profiling endogenous airway proteases and antiproteases and modeling proteolytic activation of Influenza HA using in vitro and ex vivo human airway surface liquid samples
UNC Libraries·2025Open Access
Profiling endogenous airway proteases and antiproteases and modeling proteolytic activation of Influenza HA using in vitro and ex vivo human airway surface liquid samples
PLoS ONE·2024· 1 citedOpen Access
Asthma and COVID-19: Unveiling Outcome Disparities and Treatment Impact Based on Distinct Endotypes.
UNC Libraries·2024Open Access
Asthma and COVID-19: Unveiling Outcome Disparities and Treatment Impact Based on Distinct Endotypes
Annals of the American Thoracic Society·2024· 1 citedOpen Access
Editorial: Mechanisms of action of small molecules on CFTR mutants and the impact on cystic fibrosis pathogenesis
UNC Libraries·2024Open Access
Dysregulated Airway Host Defense in Hyper IgE Syndrome due to STAT3 Mutations
2024· 1 citedOpen Access
Biochemical and rheological analysis of human colonic culture mucus reveals similarity to gut mucus
UNC Libraries·2024Open Access
Editorial: Mechanisms of action of small molecules on CFTR mutants and the impact on cystic fibrosis pathogenesis
Frontiers in Molecular Biosciences·2024· 1 citedOpen Access
Mucus and mucus flake composition and abundance reflect inflammatory and infection status in cystic fibrosis
UNC Libraries·2024Open Access
Profiling endogenous airway proteases and antiproteases and measuring proteolytic activation of Influenza HA using <i>in vitro</i> and <i>ex vivo</i> human airway surface liquid samples
2024· 1 citedOpen Access
Reuse of cell culture inserts for in vitro human primary airway epithelial cell studies
UNC Libraries·2024· 1 citedOpen Access
Mucus concentration–dependent biophysical abnormalities unify submucosal gland and superficial airway dysfunction in cystic fibrosis
UNC Libraries·2024Open Access
Chronic airway epithelial hypoxia exacerbates injury in muco-obstructive lung disease through mucus hyperconcentration
UNC Libraries·2024Open Access
SARS-CoV-2 variant of concern fitness and adaptation in primary human airway epithelia
UNC Libraries·2024Open Access
SARS-CoV-2 variant of concern fitness and adaptation in primary human airway epithelia
Cell Reports·2024· 15 citedOpen Access
BPIFB1 loss alters airway mucus properties and diminishes mucociliary clearance
American Journal of Physiology-Lung Cellular and Molecular Physiology·2023· 8 citedOpen Access
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Frequent Co-authors

Richard C. Boucher(18), David B. Hill(14), Mehmet Kesımer(12), Matthew R. Markovetz(12), Cameron B. Morrison(11), Wanda K. O’Neal(8), Kenichi Okuda(7), Scott H. Randell(7), Brian Button(7), Scott H. Donaldson(7), C. William Davis(7), Takafumi Kato(7), Kendall M. Shaffer(7), Kenza C. Araba(7), Jason A. Wykoff(7), Ralph S. Baric(6), Kathryn Ramsey(6), Caitlin E. Edwards(5), Lubna H. Abdullah(5), Rodney C. Gilmore(5)