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V Rector

Showing results (1-10 of 10) with videos related to

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Developmental Cell|September 15, 2022
Pulmonary neuroendocrine cells sense succinate to stimulate myoepithelial cell contractionWenjie Yu, Thomas O Moninger, Michael V Rector, et al.
Plos One|September 7, 2012
Expression of human paraoxonase 1 decreases superoxide levels and alters bacterial colonization in the gut of Drosophila melanogasterAlejandro A Pezzulo, Emma E Hornick, Michael V Rector, 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.
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.
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.
American Journal of Respiratory and Critical Care Medicine|October 22, 2015
Cystic Fibrosis Transmembrane Conductance Regulator in Sarcoplasmic Reticulum of Airway Smooth Muscle. Implications for Airway ContractilityDaniel P Cook, Michael V Rector, Drake C Bouzek, et al.
Clinical Science (London, England : 1979)|August 22, 2014
Glycaemic regulation and insulin secretion are abnormal in cystic fibrosis pigs despite sparing of islet cell massAliye Uc, Alicia K Olivier, Michelle A Griffin, et al.
Nucleic Acids Research|September 24, 2024
Amphiphilic shuttle peptide delivers base editor ribonucleoprotein to correct the CFTR R553X mutation in well-differentiated airway epithelial cellsKatarina Kulhankova, Anna X Cheng, Soumba Traore, et al.
Science Translational Medicine|March 18, 2011
The ΔF508 mutation causes CFTR misprocessing and cystic fibrosis-like disease in pigsLynda S Ostedgaard, David K Meyerholz, Jeng-Haur Chen, et al.
The Journal of Clinical Investigation|May 17, 2013
Intestinal CFTR expression alleviates meconium ileus in cystic fibrosis pigsDavid A Stoltz, Tatiana Rokhlina, Sarah E Ernst, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Developmental Cell|September 15, 2022
Pulmonary neuroendocrine cells sense succinate to stimulate myoepithelial cell contractionWenjie Yu, Thomas O Moninger, Michael V Rector, et al.
Plos One|September 7, 2012
Expression of human paraoxonase 1 decreases superoxide levels and alters bacterial colonization in the gut of Drosophila melanogasterAlejandro A Pezzulo, Emma E Hornick, Michael V Rector, 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.
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.
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.
American Journal of Respiratory and Critical Care Medicine|October 22, 2015
Cystic Fibrosis Transmembrane Conductance Regulator in Sarcoplasmic Reticulum of Airway Smooth Muscle. Implications for Airway ContractilityDaniel P Cook, Michael V Rector, Drake C Bouzek, et al.
Clinical Science (London, England : 1979)|August 22, 2014
Glycaemic regulation and insulin secretion are abnormal in cystic fibrosis pigs despite sparing of islet cell massAliye Uc, Alicia K Olivier, Michelle A Griffin, et al.
Nucleic Acids Research|September 24, 2024
Amphiphilic shuttle peptide delivers base editor ribonucleoprotein to correct the CFTR R553X mutation in well-differentiated airway epithelial cellsKatarina Kulhankova, Anna X Cheng, Soumba Traore, et al.
Science Translational Medicine|March 18, 2011
The ΔF508 mutation causes CFTR misprocessing and cystic fibrosis-like disease in pigsLynda S Ostedgaard, David K Meyerholz, Jeng-Haur Chen, et al.
The Journal of Clinical Investigation|May 17, 2013
Intestinal CFTR expression alleviates meconium ileus in cystic fibrosis pigsDavid A Stoltz, Tatiana Rokhlina, Sarah E Ernst, et al.
Pageof 1