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Simon Y Graeber

Showing results (31-40 of 54) with videos related to

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Computational and Structural Biotechnology Journal|November 10, 2025
Automated scoring of airway abnormalities and mucus plugging in chest magnetic resonance imaging of cystic fibrosis using artificial intelligenceFriedemann G Ringwald, Lena Wucherpfennig, Anna Martynova, et al.
Cell Systems|April 3, 2026
Systemic effects of cystic fibrosis transmembrane conductance regulator modulators on the plasma and serum proteomeKerstin Fentker, Marieluise Kirchner, Matthias Ziehm, et al.
American Journal of Respiratory and Critical Care Medicine|January 13, 2018
Effects of Lumacaftor-Ivacaftor Therapy on Cystic Fibrosis Transmembrane Conductance Regulator Function in Phe508del Homozygous Patients with Cystic FibrosisSimon Y Graeber, Christian Dopfer, Lutz Naehrlich, et al.
Nature Communications|March 24, 2024
Ion mobility-tandem mass spectrometry of mucin-type O-glycansLeïla Bechtella, Jin Chunsheng, Kerstin Fentker, et al.
American Journal of Respiratory and Critical Care Medicine|January 23, 2024
Pharmacological Improvement of Cystic Fibrosis Transmembrane Conductance Regulator Function Rescues Airway Epithelial Homeostasis and Host Defense in Children with Cystic FibrosisJennifer Loske, Mirjam Völler, Sören Lukassen, et al.
Annals of the American Thoracic Society|December 22, 2022
Longitudinal Magnetic Resonance Imaging Detects Onset and Progression of Chronic Rhinosinusitis from Infancy to School Age in Cystic FibrosisLena Wucherpfennig, Felix Wuennemann, Monika Eichinger, et al.
The European Respiratory Journal|April 20, 2023
A novel thiol-saccharide mucolytic for the treatment of muco-obstructive lung diseasesAnnalisa Addante, Wilfred Raymond, Irina Gitlin, et al.
Frontiers in Pharmacology|April 27, 2023
Long-term effects of lumacaftor/ivacaftor on paranasal sinus abnormalities in children with cystic fibrosis detected with magnetic resonance imagingLena Wucherpfennig, Felix Wuennemann, Monika Eichinger, et al.
American Journal of Respiratory and Critical Care Medicine|November 10, 2018
Preventive Inhalation of Hypertonic Saline in Infants with Cystic Fibrosis (PRESIS). A Randomized, Double-Blind, Controlled StudyMirjam Stahl, Mark O Wielpütz, Isabell Ricklefs, et al.
The Lancet. Respiratory Medicine|July 13, 2026
The role of sweat chloride in determining CFTR protein restoration in people with cystic fibrosisEdith T Zemanick, Simon Y Graeber, Carlo Castellani, et al.
Pageof 6

Showing results (31-40 of 54) with videos related to

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Pageof 6
Computational and Structural Biotechnology Journal|November 10, 2025
Automated scoring of airway abnormalities and mucus plugging in chest magnetic resonance imaging of cystic fibrosis using artificial intelligenceFriedemann G Ringwald, Lena Wucherpfennig, Anna Martynova, et al.
Cell Systems|April 3, 2026
Systemic effects of cystic fibrosis transmembrane conductance regulator modulators on the plasma and serum proteomeKerstin Fentker, Marieluise Kirchner, Matthias Ziehm, et al.
American Journal of Respiratory and Critical Care Medicine|January 13, 2018
Effects of Lumacaftor-Ivacaftor Therapy on Cystic Fibrosis Transmembrane Conductance Regulator Function in Phe508del Homozygous Patients with Cystic FibrosisSimon Y Graeber, Christian Dopfer, Lutz Naehrlich, et al.
Nature Communications|March 24, 2024
Ion mobility-tandem mass spectrometry of mucin-type O-glycansLeïla Bechtella, Jin Chunsheng, Kerstin Fentker, et al.
American Journal of Respiratory and Critical Care Medicine|January 23, 2024
Pharmacological Improvement of Cystic Fibrosis Transmembrane Conductance Regulator Function Rescues Airway Epithelial Homeostasis and Host Defense in Children with Cystic FibrosisJennifer Loske, Mirjam Völler, Sören Lukassen, et al.
Annals of the American Thoracic Society|December 22, 2022
Longitudinal Magnetic Resonance Imaging Detects Onset and Progression of Chronic Rhinosinusitis from Infancy to School Age in Cystic FibrosisLena Wucherpfennig, Felix Wuennemann, Monika Eichinger, et al.
The European Respiratory Journal|April 20, 2023
A novel thiol-saccharide mucolytic for the treatment of muco-obstructive lung diseasesAnnalisa Addante, Wilfred Raymond, Irina Gitlin, et al.
Frontiers in Pharmacology|April 27, 2023
Long-term effects of lumacaftor/ivacaftor on paranasal sinus abnormalities in children with cystic fibrosis detected with magnetic resonance imagingLena Wucherpfennig, Felix Wuennemann, Monika Eichinger, et al.
American Journal of Respiratory and Critical Care Medicine|November 10, 2018
Preventive Inhalation of Hypertonic Saline in Infants with Cystic Fibrosis (PRESIS). A Randomized, Double-Blind, Controlled StudyMirjam Stahl, Mark O Wielpütz, Isabell Ricklefs, et al.
The Lancet. Respiratory Medicine|July 13, 2026
The role of sweat chloride in determining CFTR protein restoration in people with cystic fibrosisEdith T Zemanick, Simon Y Graeber, Carlo Castellani, et al.
Pageof 6