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The Journal of Biological Chemistry|October 22, 2005
The cystic fibrosis transmembrane conductance regulator is regulated by a direct interaction with the protein phosphatase 2AWilliam R Thelin, Mehmet Kesimer, Robert Tarran, et al.The Journal of Clinical Investigation|January 20, 2007
Direct interaction with filamins modulates the stability and plasma membrane expression of CFTRWilliam R Thelin, Yun Chen, Martina Gentzsch, et al.Journal of Proteome Research|June 15, 2005
Improved protein identification through the use of unstained gelsDavid R Loiselle, William R Thelin, Carol E Parker, et al.The Journal of Pharmacology and Experimental Therapeutics|January 26, 2008
Pharmacological properties of N-(3,5-diamino-6-chloropyrazine-2-carbonyl)-N'-4-[4-(2,3-dihydroxypropoxy)phenyl]butyl-guanidine methanesulfonate (552-02), a novel epithelial sodium channel blocker with potential clinical efficacy for cystic fibrosis lung diseaseAndrew J Hirsh, Jim Zhang, Andra Zamurs, et al.American Journal of Respiratory and Critical Care Medicine|September 14, 2018
An Improved Inhaled Mucolytic to Treat Airway Muco-obstructive DiseasesCamille Ehre, Zachary L Rushton, Boya Wang, et al.Alternatives to Laboratory Animals : ATLA|January 8, 2025
The Use of MPS in Three Rs and Regulatory Applications: Perspectives From Developers on Stakeholder ResponsibilitiesMegan R LaFollette, Szczepan W Baran, J Lowry Curley, et al.Nature Communications|December 19, 2018
Muc5b overexpression causes mucociliary dysfunction and enhances lung fibrosis in miceLaura A Hancock, Corinne E Hennessy, George M Solomon, et al.Science Translational Medicine|April 5, 2019
Mucus accumulation in the lungs precedes structural changes and infection in children with cystic fibrosisCharles R Esther, Marianne S Muhlebach, Camille Ehre, et al.Nature Communications|January 12, 2021
Disulfide disruption reverses mucus dysfunction in allergic airway diseaseLeslie E Morgan, Ana M Jaramillo, Siddharth K Shenoy, et al.Pageof 2