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Sean P. Gunsten

Researcher at Washington University in St. Louis

Publications -  29
Citations -  870

Sean P. Gunsten is an academic researcher from Washington University in St. Louis. The author has contributed to research in topics: Cilium & Ciliogenesis. The author has an hindex of 13, co-authored 25 publications receiving 672 citations. Previous affiliations of Sean P. Gunsten include Case Western Reserve University.

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Temporal relationship between primary and motile ciliogenesis in airway epithelial cells.

TL;DR: The transient nature ofPrimary cilia, together with the temporal and spatial patterns of expression in the development and repair of airway epithelium, suggests a critical role of primary cilia in determining outcomes duringAirway epithelial cell differentiation.
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IL13 activates autophagy to regulate secretion in airway epithelial cells

TL;DR: It is indicated that autophagy is essential for airway mucus secretion in a type 2, IL13-dependent immune disease process and thereby provide a novel therapeutic strategy for attenuating airway obstruction in hypersecretory inflammatory diseases such as asthma, chronic obstructive pulmonary disease, and cystic fibrosis lung disease.
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Azithromycin attenuates airway inflammation in a mouse model of viral bronchiolitis.

TL;DR: These findings demonstrate anti-inflammatory effects of azithromycin that are not related to anti-viral activity and support the rationale for future prospective randomized clinical trials that will evaluate the effects of macrolides on acute viral bronchiolitis and their long-term consequences.
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Impact of hydrogel nanoparticle size and functionalization on in vivo behavior for lung imaging and therapeutics.

TL;DR: The results show that minor particle modifications may significantly impact in vivo behavior within the complex environments of the lung, underscoring the need for animal modeling.
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Azithromycin attenuates airway inflammation in a noninfectious mouse model of allergic asthma.

TL;DR: It is suggested that azithromycin may have beneficial effects in treating noninfectious airway inflammatory diseases, including asthma, after being demonstrated to attenuate the ovalbumin-dependent airway inflammation.