Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Michael J Welsh

Showing results (151-160 of 198) with videos related to

Pageof 20
Sort By:
Cell|December 1, 2009
The amygdala is a chemosensor that detects carbon dioxide and acidosis to elicit fear behaviorAdam E Ziemann, Jason E Allen, Nader S Dahdaleh, et al.
The Journal of Clinical Investigation|August 15, 2023
CFTR-rich ionocytes mediate chloride absorption across airway epitheliaLei Lei, Soumba Traore, Guillermo S Romano Ibarra, et al.
Neuron|January 13, 2010
The ion channel ASIC2 is required for baroreceptor and autonomic control of the circulationYongjun Lu, Xiuying Ma, Rasna Sabharwal, 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.
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.
Biorxiv : the Preprint Server for Biology|September 5, 2025
Molecular prosthetics for CFTR designed for anion selectivity outperform amphotericin B in cultured cystic fibrosis airway epitheliaJonnathan P Marin-Toledo, Daniel Greenan, Nohemy Celis, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology|September 1, 2012
Pancreatic and biliary secretion are both altered in cystic fibrosis pigsAliye Uc, Radhamma Giriyappa, David K Meyerholz, et al.
American Journal of Respiratory Cell and Molecular Biology|May 8, 2013
Post-transcriptional regulation of cystic fibrosis transmembrane conductance regulator expression and function by microRNAsShyam Ramachandran, Philip H Karp, Samantha R Osterhaus, 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.
Pageof 20

Showing results (151-160 of 198) with videos related to

Sort By:
Pageof 20
Cell|December 1, 2009
The amygdala is a chemosensor that detects carbon dioxide and acidosis to elicit fear behaviorAdam E Ziemann, Jason E Allen, Nader S Dahdaleh, et al.
The Journal of Clinical Investigation|August 15, 2023
CFTR-rich ionocytes mediate chloride absorption across airway epitheliaLei Lei, Soumba Traore, Guillermo S Romano Ibarra, et al.
Neuron|January 13, 2010
The ion channel ASIC2 is required for baroreceptor and autonomic control of the circulationYongjun Lu, Xiuying Ma, Rasna Sabharwal, 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.
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.
Biorxiv : the Preprint Server for Biology|September 5, 2025
Molecular prosthetics for CFTR designed for anion selectivity outperform amphotericin B in cultured cystic fibrosis airway epitheliaJonnathan P Marin-Toledo, Daniel Greenan, Nohemy Celis, et al.
American Journal of Physiology. Gastrointestinal and Liver Physiology|September 1, 2012
Pancreatic and biliary secretion are both altered in cystic fibrosis pigsAliye Uc, Radhamma Giriyappa, David K Meyerholz, et al.
American Journal of Respiratory Cell and Molecular Biology|May 8, 2013
Post-transcriptional regulation of cystic fibrosis transmembrane conductance regulator expression and function by microRNAsShyam Ramachandran, Philip H Karp, Samantha R Osterhaus, 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.
Pageof 20