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Michael J Welsh

Showing results (161-170 of 198) with videos related to

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Nature|March 15, 2019
Small-molecule ion channels increase host defences in cystic fibrosis airway epitheliaKatrina A Muraglia, Rajeev S Chorghade, Bo Ram Kim, et al.
American Journal of Respiratory Cell and Molecular Biology|March 2, 2022
A Single-Cell Atlas of Large and Small Airways at Birth in a Porcine Model of Cystic FibrosisAndrew L Thurman, Xiaopeng Li, Raul Villacreses, et al.
Parkinsonism & Related Disorders|December 11, 2021
A pilot to assess target engagement of terazosin in Parkinson's diseaseJordan L Schultz, Alivia N Brinker, Jia Xu, et al.
American Journal of Respiratory and Critical Care Medicine|July 13, 2010
Loss of cystic fibrosis transmembrane conductance regulator function produces abnormalities in tracheal development in neonatal pigs and young childrenDavid K Meyerholz, David A Stoltz, Eman Namati, et al.
JCI Insight|September 23, 2016
Lentiviral-mediated phenotypic correction of cystic fibrosis pigsAshley L Cooney, Mahmoud H Abou Alaiwa, Viral S Shah, et al.
The Journal of Clinical Investigation|June 24, 2021
Inflammatory cytokines TNF-α and IL-17 enhance the efficacy of cystic fibrosis transmembrane conductance regulator modulatorsTayyab Rehman, Philip H Karp, Ping Tan, et al.
International Journal of Pharmaceutics|December 11, 2023
Injectable long-acting ivacaftor-loaded poly (lactide-co-glycolide) microparticle formulations for the treatment of cystic fibrosis: In vitro characterization and in vivo pharmacokinetics in miceDavid S Nakhla, Aml I Mekkawy, Youssef W Naguib, et al.
International Forum of Allergy & Rhinology|November 4, 2014
Medical reversal of chronic sinusitis in a cystic fibrosis patient with ivacaftorEugene H Chang, Xiao Xiao Tang, Viral S Shah, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 3, 2012
A microRNA network regulates expression and biosynthesis of wild-type and DeltaF508 mutant cystic fibrosis transmembrane conductance regulatorShyam Ramachandran, Philip H Karp, Peng Jiang, 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 20

Showing results (161-170 of 198) with videos related to

Sort By:
Pageof 20
Nature|March 15, 2019
Small-molecule ion channels increase host defences in cystic fibrosis airway epitheliaKatrina A Muraglia, Rajeev S Chorghade, Bo Ram Kim, et al.
American Journal of Respiratory Cell and Molecular Biology|March 2, 2022
A Single-Cell Atlas of Large and Small Airways at Birth in a Porcine Model of Cystic FibrosisAndrew L Thurman, Xiaopeng Li, Raul Villacreses, et al.
Parkinsonism & Related Disorders|December 11, 2021
A pilot to assess target engagement of terazosin in Parkinson's diseaseJordan L Schultz, Alivia N Brinker, Jia Xu, et al.
American Journal of Respiratory and Critical Care Medicine|July 13, 2010
Loss of cystic fibrosis transmembrane conductance regulator function produces abnormalities in tracheal development in neonatal pigs and young childrenDavid K Meyerholz, David A Stoltz, Eman Namati, et al.
JCI Insight|September 23, 2016
Lentiviral-mediated phenotypic correction of cystic fibrosis pigsAshley L Cooney, Mahmoud H Abou Alaiwa, Viral S Shah, et al.
The Journal of Clinical Investigation|June 24, 2021
Inflammatory cytokines TNF-α and IL-17 enhance the efficacy of cystic fibrosis transmembrane conductance regulator modulatorsTayyab Rehman, Philip H Karp, Ping Tan, et al.
International Journal of Pharmaceutics|December 11, 2023
Injectable long-acting ivacaftor-loaded poly (lactide-co-glycolide) microparticle formulations for the treatment of cystic fibrosis: In vitro characterization and in vivo pharmacokinetics in miceDavid S Nakhla, Aml I Mekkawy, Youssef W Naguib, et al.
International Forum of Allergy & Rhinology|November 4, 2014
Medical reversal of chronic sinusitis in a cystic fibrosis patient with ivacaftorEugene H Chang, Xiao Xiao Tang, Viral S Shah, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 3, 2012
A microRNA network regulates expression and biosynthesis of wild-type and DeltaF508 mutant cystic fibrosis transmembrane conductance regulatorShyam Ramachandran, Philip H Karp, Peng Jiang, 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 20