Michael J. Welsh, MD

Medicine and Physiology and Biophysics University of Iowa, Iowa City, IA 
Cystic fibrosis, Neuroscience
"Michael Welsh"
Mean distance: 15.32 (cluster 11)
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Ostedgaard LS, Price MP, Whitworth KM, et al. (2020) Lack of airway submucosal glands impairs respiratory host defenses. Elife. 9
Xie Y, Lu L, Tang XX, et al. (2020) Acidic Submucosal Gland pH and Elevated Protein Concentration Produce Abnormal Cystic Fibrosis Mucus. Developmental Cell
Rehman T, Thornell IM, Pezzulo AA, et al. (2020) TNFα and IL-17 Alkalinize Airway Surface Liquid through CFTR and Pendrin. American Journal of Physiology. Cell Physiology
Miller AC, Comellas AP, Hornick DB, et al. (2019) Cystic fibrosis carriers are at increased risk for a wide range of cystic fibrosis-related conditions. Proceedings of the National Academy of Sciences of the United States of America
Cai R, Zhang Y, Simmering JE, et al. (2019) Enhancing glycolysis attenuates Parkinson's disease progression in models and clinical databases. The Journal of Clinical Investigation
Muraglia KA, Chorghade RS, Kim BR, et al. (2019) Small-molecule ion channels increase host defences in cystic fibrosis airway epithelia. Nature
Fischer AJ, Pino-Argumedo MI, Hilkin BM, et al. (2019) Mucus strands from submucosal glands initiate mucociliary transport of large particles. Jci Insight. 4
Alaiwa MHA, Launspach JL, Grogan B, et al. (2018) Ivacaftor-induced sweat chloride reductions correlate with increases in airway surface liquid pH in cystic fibrosis. Jci Insight. 3
Reznikov LR, Meyerholz DK, Abou Alaiwa MH, et al. (2018) The vagal ganglia transcriptome identifies candidate therapeutics for airway hyperreactivity. American Journal of Physiology. Lung Cellular and Molecular Physiology
Benndorf R, Gilmont RR, Hirano S, et al. (2018) Small heat shock protein speciation: novel non-canonical 44 kDa HspB5-related protein species in rat and human tissues. Cell Stress & Chaperones
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