about
Glucose depletion in the airway surface liquid is essential for sterility of the airwaysNeonates with cystic fibrosis have a reduced nasal liquid pH; a small pilot study.Cystic fibrosis pigs develop lung disease and exhibit defective bacterial eradication at birth.Pigs and humans with cystic fibrosis have reduced insulin-like growth factor 1 (IGF1) levels at birth.Loss of cystic fibrosis transmembrane conductance regulator function produces abnormalities in tracheal development in neonatal pigs and young children.Expression of human paraoxonase 1 decreases superoxide levels and alters bacterial colonization in the gut of Drosophila melanogaster.The air-liquid interface and use of primary cell cultures are important to recapitulate the transcriptional profile of in vivo airway epithelia.The ΔF508 mutation causes CFTR misprocessing and cystic fibrosis-like disease in pigs.Glycaemic regulation and insulin secretion are abnormal in cystic fibrosis pigs despite sparing of islet cell mass.Inhaled hypertonic saline in adults hospitalised for exacerbation of cystic fibrosis lung disease: a retrospective study.Reduced airway surface pH impairs bacterial killing in the porcine cystic fibrosis lung.CFTR is required for maximal transepithelial liquid transport in pig alveolar epithelia.Sinus hypoplasia precedes sinus infection in a porcine model of cystic fibrosis.Idiopathic hyperammonemia after solid organ transplantation: Primarily a lung problem? A single-center experience and systematic review.Pancreatic and biliary secretion are both altered in cystic fibrosis pigs.Lentiviral vector gene transfer to porcine airways.Intestinal CFTR expression alleviates meconium ileus in cystic fibrosis pigs.Disruption of the CFTR gene produces a model of cystic fibrosis in newborn pigs.Protein composition of bronchoalveolar lavage fluid and airway surface liquid from newborn pigs.Effects of vitamin D supplementation on alveolar macrophage gene expression: preliminary results of a randomized, controlled trial.Do cell junction protein mutations cause an airway phenotype in mice or humans?Effect of vitamin D3 on the antimicrobial activity of human airway surface liquid: preliminary results of a randomised placebo-controlled double-blind trial.Newborn Cystic Fibrosis Pigs Have a Blunted Early Response to an Inflammatory Stimulus.Concentration of the antibacterial precursor thiocyanate in cystic fibrosis airway secretions.HSP90 inhibitor geldanamycin reverts IL-13- and IL-17-induced airway goblet cell metaplasiaUltrasound Diagnosis of Hemodynamic Compromise in a Patient with Hepatic HydrothoraxPolarized AAVR expression determines infectivity by AAV gene therapy vectorsHeterogeneous expression of the SARS-Coronavirus-2 receptor ACE2 in the human respiratory tract
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description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Alejandro A Pezzulo
@ast
Alejandro A Pezzulo
@en
Alejandro A Pezzulo
@es
Alejandro A Pezzulo
@nl
type
label
Alejandro A Pezzulo
@ast
Alejandro A Pezzulo
@en
Alejandro A Pezzulo
@es
Alejandro A Pezzulo
@nl
prefLabel
Alejandro A Pezzulo
@ast
Alejandro A Pezzulo
@en
Alejandro A Pezzulo
@es
Alejandro A Pezzulo
@nl
P106
P1153
9234179500
P21
P31
P496
0000-0001-7544-5109