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1. CFTR‐dependent chloride efflux in cystic fibrosis mononuclear cells is increased by ivacaftor therapy. Issue 7 (26th April 2017)

2. Correction of defective CFTR/ENaC function and tightness of cystic fibrosis airway epithelium by amniotic mesenchymal stromal (stem) cells. Issue 8 (3rd June 2014)

3. Gap Junctions Are Involved in the Rescue of CFTR-Dependent Chloride Efflux by Amniotic Mesenchymal Stem Cells in Coculture with Cystic Fibrosis CFBE41o- Cells. (11th January 2018)

4. Hematopoietic and Mesenchymal Stem Cells for the Treatment of Chronic Respiratory Diseases: Role of Plasticity and Heterogeneity. (19th January 2014)

6. Impact of Lentiviral Vector-Mediated Transduction on the Tightness of a Polarized Model of Airway Epithelium and Effect of Cationic Polymer Polyethylenimine. (21st June 2010)

7. Nanocomplexes for gene therapy of respiratory diseases: Targeting and overcoming the mucus barrier. (October 2015)