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Michael J Welsh

Showing results (81-90 of 198) with videos related to

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Cells, Tissues, Organs|April 29, 2011
Enamel pathology resulting from loss of function in the cystic fibrosis transmembrane conductance regulator in a porcine animal modelEugene H Chang, Rodrigo S Lacruz, Timothy G Bromage, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 28, 2024
Mitochondrial uncoupling proteins protect human airway epithelial ciliated cells from oxidative damageAkansha Jain, Bo Ram Kim, Wenjie Yu, et al.
Developmental Cell|July 31, 2020
Acidic Submucosal Gland pH and Elevated Protein Concentration Produce Abnormal Cystic Fibrosis MucusYuliang Xie, Lin Lu, Xiao Xiao Tang, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 3, 2011
Cystic fibrosis transmembrane conductance regulator with a shortened R domain rescues the intestinal phenotype of CFTR-/- miceLynda S Ostedgaard, David K Meyerholz, Daniel W Vermeer, et al.
American Journal of Respiratory Cell and Molecular Biology|October 19, 2013
Chemosensory functions for pulmonary neuroendocrine cellsXiaoling Gu, Philip H Karp, Steven L Brody, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 13, 2003
cAMP-dependent protein kinase phosphorylation of the acid-sensing ion channel-1 regulates its binding to the protein interacting with C-kinase-1A Soren Leonard, Olena Yermolaieva, Alesia Hruska-Hageman, et al.
Neuron|July 10, 2003
Contribution of Drosophila DEG/ENaC genes to salt tasteLei Liu, A Soren Leonard, David G Motto, et al.
Nature Medicine|November 13, 2007
Acid-sensing ion channel-1 contributes to axonal degeneration in autoimmune inflammation of the central nervous systemManuel A Friese, Matthew J Craner, Ruth Etzensperger, et al.
Methods in Molecular Biology (Clifton, N.J.)|May 4, 2002
An in vitro model of differentiated human airway epithelia. Methods for establishing primary culturesPhilip H Karp, Thomas O Moninger, S Pary Weber, et al.
ACS Chemical Biology|October 20, 2025
Molecular Prosthetics and CFTR Modulators Additively Increase Secretory HCO<sub>3</sub><sup>-</sup> Flux in Cystic Fibrosis Airway EpitheliaNohemy Celis, Danforth P Miller, Thomas E Tarara, et al.
Pageof 20

Showing results (81-90 of 198) with videos related to

Sort By:
Pageof 20
Cells, Tissues, Organs|April 29, 2011
Enamel pathology resulting from loss of function in the cystic fibrosis transmembrane conductance regulator in a porcine animal modelEugene H Chang, Rodrigo S Lacruz, Timothy G Bromage, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 28, 2024
Mitochondrial uncoupling proteins protect human airway epithelial ciliated cells from oxidative damageAkansha Jain, Bo Ram Kim, Wenjie Yu, et al.
Developmental Cell|July 31, 2020
Acidic Submucosal Gland pH and Elevated Protein Concentration Produce Abnormal Cystic Fibrosis MucusYuliang Xie, Lin Lu, Xiao Xiao Tang, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 3, 2011
Cystic fibrosis transmembrane conductance regulator with a shortened R domain rescues the intestinal phenotype of CFTR-/- miceLynda S Ostedgaard, David K Meyerholz, Daniel W Vermeer, et al.
American Journal of Respiratory Cell and Molecular Biology|October 19, 2013
Chemosensory functions for pulmonary neuroendocrine cellsXiaoling Gu, Philip H Karp, Steven L Brody, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 13, 2003
cAMP-dependent protein kinase phosphorylation of the acid-sensing ion channel-1 regulates its binding to the protein interacting with C-kinase-1A Soren Leonard, Olena Yermolaieva, Alesia Hruska-Hageman, et al.
Neuron|July 10, 2003
Contribution of Drosophila DEG/ENaC genes to salt tasteLei Liu, A Soren Leonard, David G Motto, et al.
Nature Medicine|November 13, 2007
Acid-sensing ion channel-1 contributes to axonal degeneration in autoimmune inflammation of the central nervous systemManuel A Friese, Matthew J Craner, Ruth Etzensperger, et al.
Methods in Molecular Biology (Clifton, N.J.)|May 4, 2002
An in vitro model of differentiated human airway epithelia. Methods for establishing primary culturesPhilip H Karp, Thomas O Moninger, S Pary Weber, et al.
ACS Chemical Biology|October 20, 2025
Molecular Prosthetics and CFTR Modulators Additively Increase Secretory HCO<sub>3</sub><sup>-</sup> Flux in Cystic Fibrosis Airway EpitheliaNohemy Celis, Danforth P Miller, Thomas E Tarara, et al.
Pageof 20