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David B Hill

Showing results (51-60 of 66) with videos related to

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ACS Biomaterials Science & Engineering|March 30, 2022
Development of an Intranasal Gel for the Delivery of a Broadly Acting Subunit Influenza VaccineDevika M Varma, Cole J Batty, Rebeca T Stiepel, et al.
American Journal of Respiratory and Critical Care Medicine|January 13, 2022
Hereditary Mucin Deficiency Caused by Biallelic Loss of Function of <i>MUC5B</i>Gregory Costain, Zhen Liu, Vito Mennella, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|October 17, 2023
BPIFB1 loss alters airway mucus properties and diminishes mucociliary clearanceLauren J Donoghue, Matthew R Markovetz, Cameron B Morrison, et al.
The European Respiratory Journal|June 26, 2021
Treatment of cystic fibrosis airway cells with CFTR modulators reverses aberrant mucus properties <i>via</i> hydrationCameron B Morrison, Kendall M Shaffer, Kenza C Araba, et al.
American Journal of Respiratory and Critical Care Medicine|September 14, 2018
An Improved Inhaled Mucolytic to Treat Airway Muco-obstructive DiseasesCamille Ehre, Zachary L Rushton, Boya Wang, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|April 19, 2022
Mucus and mucus flake composition and abundance reflect inflammatory and infection status in cystic fibrosisMatthew R Markovetz, Ian C Garbarine, Cameron B Morrison, et al.
Allergy|July 3, 2026
Detergent-Containing Toothpaste Decreases Esophageal Mucosal Impedance and Alters Salivary Properties in HumansBenjamin L Wright, Michael D Crowell, Huijun Luo, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|August 8, 2019
Endotracheal tube mucus as a source of airway mucus for rheological studyMatthew R Markovetz, Durai B Subramani, William J Kissner, et al.
Nature Communications|December 19, 2018
Muc5b overexpression causes mucociliary dysfunction and enhances lung fibrosis in miceLaura A Hancock, Corinne E Hennessy, George M Solomon, et al.
Science Translational Medicine|April 5, 2019
Mucus accumulation in the lungs precedes structural changes and infection in children with cystic fibrosisCharles R Esther, Marianne S Muhlebach, Camille Ehre, et al.
Pageof 7

Showing results (51-60 of 66) with videos related to

Sort By:
Pageof 7
ACS Biomaterials Science & Engineering|March 30, 2022
Development of an Intranasal Gel for the Delivery of a Broadly Acting Subunit Influenza VaccineDevika M Varma, Cole J Batty, Rebeca T Stiepel, et al.
American Journal of Respiratory and Critical Care Medicine|January 13, 2022
Hereditary Mucin Deficiency Caused by Biallelic Loss of Function of <i>MUC5B</i>Gregory Costain, Zhen Liu, Vito Mennella, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|October 17, 2023
BPIFB1 loss alters airway mucus properties and diminishes mucociliary clearanceLauren J Donoghue, Matthew R Markovetz, Cameron B Morrison, et al.
The European Respiratory Journal|June 26, 2021
Treatment of cystic fibrosis airway cells with CFTR modulators reverses aberrant mucus properties <i>via</i> hydrationCameron B Morrison, Kendall M Shaffer, Kenza C Araba, et al.
American Journal of Respiratory and Critical Care Medicine|September 14, 2018
An Improved Inhaled Mucolytic to Treat Airway Muco-obstructive DiseasesCamille Ehre, Zachary L Rushton, Boya Wang, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|April 19, 2022
Mucus and mucus flake composition and abundance reflect inflammatory and infection status in cystic fibrosisMatthew R Markovetz, Ian C Garbarine, Cameron B Morrison, et al.
Allergy|July 3, 2026
Detergent-Containing Toothpaste Decreases Esophageal Mucosal Impedance and Alters Salivary Properties in HumansBenjamin L Wright, Michael D Crowell, Huijun Luo, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|August 8, 2019
Endotracheal tube mucus as a source of airway mucus for rheological studyMatthew R Markovetz, Durai B Subramani, William J Kissner, et al.
Nature Communications|December 19, 2018
Muc5b overexpression causes mucociliary dysfunction and enhances lung fibrosis in miceLaura A Hancock, Corinne E Hennessy, George M Solomon, et al.
Science Translational Medicine|April 5, 2019
Mucus accumulation in the lungs precedes structural changes and infection in children with cystic fibrosisCharles R Esther, Marianne S Muhlebach, Camille Ehre, et al.
Pageof 7