about
Hematopoietic and mesenchymal stem cells for the treatment of chronic respiratory diseases: role of plasticity and heterogeneityS-CMC-Lys protective effects on human respiratory cells during oxidative stress.Na+/H+ exchanger regulatory factor 1 overexpression-dependent increase of cytoskeleton organization is fundamental in the rescue of F508del cystic fibrosis transmembrane conductance regulator in human airway CFBE41o- cellsEngraftment of bone marrow-derived stem cells to the lung in a model of acute respiratory infection by Pseudomonas aeruginosa.A ligand-free, soluble urokinase receptor is present in the ascitic fluid from patients with ovarian cancer.Evaluation of genome-wide expression profiles of blood and sputum neutrophils in cystic fibrosis patients before and after antibiotic therapy.Nonmucoid Pseudomonas aeruginosa expresses alginate in the lungs of patients with cystic fibrosis and in a mouse model.Correction of defective CFTR/ENaC function and tightness of cystic fibrosis airway epithelium by amniotic mesenchymal stromal (stem) cells.Non-viral approach toward gene therapy of cystic fibrosis lung disease.Gene therapy progress and prospects: episomally maintained self-replicating systems.Lentivirus-mediated gene transfer to the respiratory epithelium: a promising approach to gene therapy of cystic fibrosis.Neutrophil recruitment and airway epithelial cell involvement in chronic cystic fibrosis lung disease.Stem cells and cystic fibrosis.Genomic context vectors and artificial chromosomes for cystic fibrosis gene therapy.Human amnion-derived cells: prospects for the treatment of lung diseases.Paracrine effects and heterogeneity of marrow-derived stem/progenitor cells: relevance for the treatment of respiratory diseases.Nanocarriers for respiratory diseases treatment: recent advances and current challenges.Human airway epithelial cells investigated by atomic force microscopy: A hint to cystic fibrosis epithelial pathology.NHERF1 and CFTR restore tight junction organisation and function in cystic fibrosis airway epithelial cells: role of ezrin and the RhoA/ROCK pathway.Pilot Randomized Controlled Trial Evaluating the Effect of Hypertonic Saline With and Without Hyaluronic Acid in Reducing Inflammation in Cystic Fibrosis.Late generation lentiviral vectors: evaluation of inflammatory potential in human airway epithelial cells.Burkholderia cenocepacia strains isolated from cystic fibrosis patients are apparently more invasive and more virulent than rhizosphere strains.The novel complex allele [A238V;F508del] of the CFTR gene: clinical phenotype and possible implications for cystic fibrosis etiological therapies.Metabolic correction in oligodendrocytes derived from metachromatic leukodystrophy mouse model by using encapsulated recombinant myoblasts.Gene transfer by means of lipo- and polyplexes: role of clathrin and caveolae-mediated endocytosis.S-CMC-Lys-dependent stimulation of electrogenic glutathione secretion by human respiratory epithelium.Na+/H+ exchanger regulatory factor isoform 1 overexpression modulates cystic fibrosis transmembrane conductance regulator (CFTR) expression and activity in human airway 16HBE14o- cells and rescues DeltaF508 CFTR functional expression in cystic fibroSerum albumin enhances polyethylenimine-mediated gene delivery to human respiratory epithelial cells.The urokinase/urokinase-receptor system and cancer invasion.Role of clathrin- and caveolae-mediated endocytosis in gene transfer mediated by lipo- and polyplexes.Urokinase/urokinase receptor system: internalization/degradation of urokinase-serpin complexes: mechanism and regulation.Inhibition of nonviral cationic liposome-mediated gene transfer into primary human respiratory cells by interferon-gamma.Amniotic mesenchymal stem cells: a new source for hepatocyte-like cells and induction of CFTR expression by coculture with cystic fibrosis airway epithelial cellsComparison between cationic polymers and lipids in mediating systemic gene delivery to the lungs.Hematopoietic stem/progenitor cells express functional mitochondrial energy-dependent cystic fibrosis transmembrane conductance regulator.Removal of domain D2 or D3 of the human urokinase receptor does not affect ligand affinity.PMA-induced down-regulation of the receptor for alpha 2-macroglobulin in human U937 cells.Protease nexin-1-urokinase complexes are internalized and degraded through a mechanism that requires both urokinase receptor and alpha 2-macroglobulin receptor.Polyethylenimine-mediated gene delivery to the lung and therapeutic applications.Procoagulant activity of mononuclear phagocytes from different anatomical sites in patients with gynecological malignancies.
P50
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P50
description
hulumtues
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onderzoeker
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researcher
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հետազոտող
@hy
name
Massimo Conese
@ast
Massimo Conese
@en
Massimo Conese
@es
Massimo Conese
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type
label
Massimo Conese
@ast
Massimo Conese
@en
Massimo Conese
@es
Massimo Conese
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prefLabel
Massimo Conese
@ast
Massimo Conese
@en
Massimo Conese
@es
Massimo Conese
@sl
P106
P21
P31
P496
0000-0003-3465-6641