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Thomas O Moninger

Showing results (21-30 of 37) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|January 20, 2022
Cellular and molecular architecture of submucosal glands in wild-type and cystic fibrosis pigsWenjie Yu, Thomas O Moninger, Andrew L Thurman, et al.
The Journal of Clinical Investigation|January 26, 2016
Acidic pH increases airway surface liquid viscosity in cystic fibrosisXiao Xiao Tang, Lynda S Ostedgaard, Mark J Hoegger, et al.
Plos One|December 19, 2013
Integrin α6β4 identifies human distal lung epithelial progenitor cells with potential as a cell-based therapy for cystic fibrosis lung diseaseXiaopeng Li, Nathan Rossen, Patrick L Sinn, et al.
The Journal of Clinical Investigation|December 18, 2012
Transepithelial migration of neutrophils into the lung requires TREM-1Julia Klesney-Tait, Kathy Keck, Xiaopeng Li, et al.
Biorxiv : the Preprint Server for Biology|February 27, 2026
Defining Functional Correction Thresholds in Primary Ciliary Dyskinesia for Effective Gene TherapiesBeck E Fitzpatrick, Brett J Wineinger, Jason E Babcock, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 6, 2013
CFTR-deficient pigs display peripheral nervous system defects at birthLeah R Reznikov, Qian Dong, Jeng-Haur Chen, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 27, 2008
Loss of Bardet-Biedl syndrome proteins alters the morphology and function of motile cilia in airway epitheliaAlok S Shah, Sara L Farmen, Thomas O Moninger, et al.
Cell|December 15, 2010
Loss of anion transport without increased sodium absorption characterizes newborn porcine cystic fibrosis airway epitheliaJeng-Haur Chen, David A Stoltz, Philip H Karp, et al.
Science (New York, N.Y.)|August 16, 2014
Impaired mucus detachment disrupts mucociliary transport in a piglet model of cystic fibrosisMark J Hoegger, Anthony J Fischer, James D McMenimen, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|May 29, 2012
CFTR is required for maximal transepithelial liquid transport in pig alveolar epitheliaXiaopeng Li, Alejandro P Comellas, Philip H Karp, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
Proceedings of the National Academy of Sciences of the United States of America|January 20, 2022
Cellular and molecular architecture of submucosal glands in wild-type and cystic fibrosis pigsWenjie Yu, Thomas O Moninger, Andrew L Thurman, et al.
The Journal of Clinical Investigation|January 26, 2016
Acidic pH increases airway surface liquid viscosity in cystic fibrosisXiao Xiao Tang, Lynda S Ostedgaard, Mark J Hoegger, et al.
Plos One|December 19, 2013
Integrin α6β4 identifies human distal lung epithelial progenitor cells with potential as a cell-based therapy for cystic fibrosis lung diseaseXiaopeng Li, Nathan Rossen, Patrick L Sinn, et al.
The Journal of Clinical Investigation|December 18, 2012
Transepithelial migration of neutrophils into the lung requires TREM-1Julia Klesney-Tait, Kathy Keck, Xiaopeng Li, et al.
Biorxiv : the Preprint Server for Biology|February 27, 2026
Defining Functional Correction Thresholds in Primary Ciliary Dyskinesia for Effective Gene TherapiesBeck E Fitzpatrick, Brett J Wineinger, Jason E Babcock, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 6, 2013
CFTR-deficient pigs display peripheral nervous system defects at birthLeah R Reznikov, Qian Dong, Jeng-Haur Chen, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 27, 2008
Loss of Bardet-Biedl syndrome proteins alters the morphology and function of motile cilia in airway epitheliaAlok S Shah, Sara L Farmen, Thomas O Moninger, et al.
Cell|December 15, 2010
Loss of anion transport without increased sodium absorption characterizes newborn porcine cystic fibrosis airway epitheliaJeng-Haur Chen, David A Stoltz, Philip H Karp, et al.
Science (New York, N.Y.)|August 16, 2014
Impaired mucus detachment disrupts mucociliary transport in a piglet model of cystic fibrosisMark J Hoegger, Anthony J Fischer, James D McMenimen, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|May 29, 2012
CFTR is required for maximal transepithelial liquid transport in pig alveolar epitheliaXiaopeng Li, Alejandro P Comellas, Philip H Karp, et al.
Pageof 4