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Macromolecular Rapid Communications|August 21, 2021
Polyglycerol-Based Mucus-Inspired HydrogelsAntara Sharma, Boonya Thongrom, Sumati Bhatia, et al.
European Journal of Pediatrics|January 26, 2012
Homozygous CFTR mutation M348K in a boy with respiratory symptoms and failure to thrive. Disease-causing mutation or benign alteration?Julia Hentschel, Gabriele Riesener, Heike Nelle, et al.
Der Radiologe|June 8, 2019
Ten years of chest MRI for patients with cystic fibrosis : Translation from the bench to clinical routinePatricia Leutz-Schmidt, Monika Eichinger, Mirjam Stahl, et al.
Respirology (Carlton, Vic.)|February 25, 2025
Functional Lung Imaging Identifies Peripheral Ventilation Changes in ꞵ-ENaC MiceNicole Reyne, Ronan Smith, Patricia Cmielewski, et al.
Frontiers in Physiology|August 22, 2022
An optimized protocol for assessment of sputum macrorheology in health and muco-obstructive lung diseaseMirjam Völler, Annalisa Addante, Hanna Rulff, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 11, 2011
The ENaC-overexpressing mouse as a model of cystic fibrosis lung diseaseZhe Zhou, Julia Duerr, Bjarki Johannesson, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|June 14, 2014
Lung arginase expression and activity is increased in cystic fibrosis mouse modelsThomas Jaecklin, Julia Duerr, Hailu Huang, et al.
Immunopharmacology and Immunotoxicology|May 1, 1994
Acrylamide induced immunosuppression in rats and its modulation by 6-MFA, an interferon inducerS I Zaidi, S Raisuddin, K P Singh, et al.
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