Lista de obras - David Stoltz - Dominio Público Uruguay

A common mutation in paraoxonase-2 results in impaired lactonase activity.

scientific article published on December 2009

Abundant DNase I-Sensitive Bacterial DNA in Healthy Porcine Lungs and Its Implications for the Lung Microbiome ⬇️

artículo científico publicado el 19 de julio de 2013

Acid-Sensing Ion Channel 1a Contributes to Airway Hyperreactivity in Mice

artículo científico publicado en 2016

Acidic pH increases airway surface liquid viscosity in cystic fibrosis

artículo científico publicado en 2016

Acute ethanol intoxication inhibits neutrophil beta2-integrin expression in rats during endotoxemia

scientific article published on 01 February 1998

Adenoviral gene transfer corrects the ion transport defect in the sinus epithelia of a porcine CF model

artículo científico publicado en 2013

Adenoviral-Mediated Interferon-gamma Gene Therapy Augments Pulmonary Host Defense of Ethanol-Treated Rats ⬇️

artículo científico publicado el 1 de febrero de 1998

Air trapping and airflow obstruction in newborn cystic fibrosis piglets

scientific article published on December 2013

Airway acidification initiates host defense abnormalities in cystic fibrosis mice.

artículo científico publicado en 2016

Antibacterial properties of the CFTR potentiator ivacaftor

artículo científico publicado en 2014

Assessing mucociliary transport of single particles in vivo shows variable speed and preference for the ventral trachea in newborn pigs

artículo científico publicado en 2014

CFTR is required for maximal transepithelial liquid transport in pig alveolar epithelia

artículo científico publicado en 2012

Calcium and the effects of ultrasound on frog skin

artículo científico publicado en 1994

Computer-aided analysis of airway trees in micro-CT scans of ex vivo porcine lung tissue.

artículo científico publicado en 2012

Concentration of the antibacterial precursor thiocyanate in cystic fibrosis airway secretions

artículo científico publicado en 2011

Cystic Fibrosis Transmembrane Conductance Regulator Intracellular Processing, Trafficking, and Opportunities for Mutation-Specific Treatment ⬇️

artículo científico publicado el 1 de junio de 2011

Cystic Fibrosis Transmembrane Conductance Regulator Potentiation as a Therapeutic Strategy for Pulmonary Edema: A Proof-of-Concept Study in Pigs.

artículo científico publicado en 2017

Cystic Fibrosis Transmembrane Conductance Regulator in Sarcoplasmic Reticulum of Airway Smooth Muscle. Implications for Airway Contractility

artículo científico publicado en 2015

Cystic fibrosis pigs develop lung disease and exhibit defective bacterial eradication at birth

artículo científico publicado en 2010

Delayed neutrophil apoptosis enhances NET formation in cystic fibrosis

artículo científico publicado en 2017

Disruption of the CFTR gene produces a model of cystic fibrosis in newborn pigs

artículo científico publicado en 2008

Drosophila are protected from Pseudomonas aeruginosa lethality by transgenic expression of paraoxonase-1.

artículo científico publicado en 2008

Early airway structural changes in cystic fibrosis pigs as a determinant of particle distribution and deposition.

artículo científico publicado en 2013

Effect of free radical scavengers on changes in ion conductance during exposure to therapeutic ultrasound

artículo científico publicado en 1993

Electrolyte transport properties in distal small airways from cystic fibrosis pigs with implications for host defense

artículo científico publicado en 2016

Enhancement of peritoneal leukocyte function by granulocyte colony-stimulating factor in rats with abdominal sepsis

scientific article published on 01 February 1998

Expression of human paraoxonase 1 decreases superoxide levels and alters bacterial colonization in the gut of Drosophila melanogaster

artículo científico publicado en 2012

Gel-forming mucins form distinct morphologic structures in airways

artículo científico publicado en 2017

Genotype-specific alterations in vascular smooth muscle cell function in cystic fibrosis piglets ⬇️

artículo científico publicado en 2013

Glucose depletion in the airway surface liquid is essential for sterility of the airways

artículo científico publicado en 2011

Glycaemic regulation and insulin secretion are abnormal in cystic fibrosis pigs despite sparing of islet cell mass.

artículo científico publicado en 2015

Granulocyte colony-stimulating factor modulates the pulmonary host response to endotoxin in the absence and presence of acute ethanol intoxication

scientific article published on 01 June 1999

Histamine alters E-cadherin cell adhesion to increase human airway epithelial permeability.

artículo científico publicado en 2003

Immunohistochemical Detection of Markers for Translational Studies of Lung Disease in Pigs and Humans

artículo científico publicado en 2015

Impaired mucus detachment disrupts mucociliary transport in a piglet model of cystic fibrosis.

artículo científico publicado en 2014

Inhaled hypertonic saline in adults hospitalised for exacerbation of cystic fibrosis lung disease: a retrospective study.

artículo científico publicado en 2012

Intestinal CFTR expression alleviates meconium ileus in cystic fibrosis pigs

artículo científico publicado en 2013

Lack of cystic fibrosis transmembrane conductance regulator disrupts fetal airway development in pigs.

artículo científico publicado en 2018

Loss of cystic fibrosis transmembrane conductance regulator function produces abnormalities in tracheal development in neonatal pigs and young children

artículo científico publicado en 2010

Medical reversal of chronic sinusitis in a cystic fibrosis patient with ivacaftor

artículo científico publicado en 2014

Monocyte derived macrophages from CF pigs exhibit increased inflammatory responses at birth.

artículo científico publicado en 2017

Mounier-Kuhn syndrome: a case of tracheal smooth muscle remodeling.

artículo científico publicado en 2016

Mucociliary Transport in Healthy and Cystic Fibrosis Pig Airways

scientific article published on 01 November 2018

Neonates with cystic fibrosis have a reduced nasal liquid pH; a small pilot study

artículo científico publicado en 2014

Newborn Cystic Fibrosis Pigs Have a Blunted Early Response to an Inflammatory Stimulus

artículo científico publicado en 2016

Origins of cystic fibrosis lung disease

artículo científico publicado en 2015

Origins of cystic fibrosis lung disease

artículo científico publicado en 2015

Pancreatic and biliary secretion are both altered in cystic fibrosis pigs.

artículo científico publicado en 2012

Pancreatic damage in fetal and newborn cystic fibrosis pigs involves the activation of inflammatory and remodeling pathways

artículo científico publicado en 2012

Pigs and humans with cystic fibrosis have reduced insulin-like growth factor 1 (IGF1) levels at birth

artículo científico publicado en 2010

Postnatal airway growth in cystic fibrosis piglets

artículo científico publicado en 2017

Production of CFTR-null and CFTR-DeltaF508 heterozygous pigs by adeno-associated virus-mediated gene targeting and somatic cell nuclear transfer

artículo científico publicado en 2008

Reduced airway surface pH impairs bacterial killing in the porcine cystic fibrosis lung

artículo científico publicado en 2012

Restoring Cystic Fibrosis Transmembrane Conductance Regulator Function Reduces Airway Bacteria and Inflammation in People with Cystic Fibrosis and Chronic Lung Infections.

artículo científico publicado en 2017

Role of PON in anoxia-reoxygenation injury: a Drosophila melanogaster transgenic model

artículo científico publicado en 2014

Role of poliovirus receptors in the spread of the infection

artículo científico publicado en 1995

Sinus hypoplasia precedes sinus infection in a porcine model of cystic fibrosis

artículo científico publicado en 2012

Sonographic evidence of abnormal tracheal cartilage ring structure in cystic fibrosis.

artículo científico publicado en 2015

Suppression of the granulocyte colony-stimulating factor response to Escherichia coli challenge by alcohol intoxication

scientific journal article

The effect of chronic binge ethanol consumption on the primary stage of SIV infection in rhesus macaques.

artículo científico publicado en 2003

The porcine lung as a potential model for cystic fibrosis

artículo científico publicado en 2008

The ΔF508 mutation causes CFTR misprocessing and cystic fibrosis-like disease in pigs

artículo científico publicado en 2011

Tracheomalacia is associated with lower FEV1 and Pseudomonas acquisition in children with CF

artículo científico publicado en 2013

Use of granulocyte colony-stimulating factor in the treatment of acute infectious diseases ⬇️

artículo científico publicado el 1 de mayo de 1997

V-Type ATPase Mediates Airway Surface Liquid Acidification in Pig Small Airway Epithelial Cells

artículo científico publicado en 2021

pH modulates the activity and synergism of the airway surface liquid antimicrobials β-defensin-3 and LL-37

artículo científico publicado en 2014

Lista de obras de David Stoltz

A common mutation in paraoxonase-2 results in impaired lactonase activity.

Abundant DNase I-Sensitive Bacterial DNA in Healthy Porcine Lungs and Its Implications for the Lung Microbiome ⬇️

Acid-Sensing Ion Channel 1a Contributes to Airway Hyperreactivity in Mice

Acidic pH increases airway surface liquid viscosity in cystic fibrosis

Acute ethanol intoxication inhibits neutrophil beta2-integrin expression in rats during endotoxemia

Adenoviral gene transfer corrects the ion transport defect in the sinus epithelia of a porcine CF model

Adenoviral-Mediated Interferon-gamma Gene Therapy Augments Pulmonary Host Defense of Ethanol-Treated Rats ⬇️

Air trapping and airflow obstruction in newborn cystic fibrosis piglets

Airway acidification initiates host defense abnormalities in cystic fibrosis mice.

Antibacterial properties of the CFTR potentiator ivacaftor

Assessing mucociliary transport of single particles in vivo shows variable speed and preference for the ventral trachea in newborn pigs

CFTR is required for maximal transepithelial liquid transport in pig alveolar epithelia

Calcium and the effects of ultrasound on frog skin

Computer-aided analysis of airway trees in micro-CT scans of ex vivo porcine lung tissue.

Concentration of the antibacterial precursor thiocyanate in cystic fibrosis airway secretions

Cystic Fibrosis Transmembrane Conductance Regulator Intracellular Processing, Trafficking, and Opportunities for Mutation-Specific Treatment ⬇️

Cystic Fibrosis Transmembrane Conductance Regulator Potentiation as a Therapeutic Strategy for Pulmonary Edema: A Proof-of-Concept Study in Pigs.

Cystic Fibrosis Transmembrane Conductance Regulator in Sarcoplasmic Reticulum of Airway Smooth Muscle. Implications for Airway Contractility

Cystic fibrosis pigs develop lung disease and exhibit defective bacterial eradication at birth

Delayed neutrophil apoptosis enhances NET formation in cystic fibrosis

Disruption of the CFTR gene produces a model of cystic fibrosis in newborn pigs

Drosophila are protected from Pseudomonas aeruginosa lethality by transgenic expression of paraoxonase-1.

Early airway structural changes in cystic fibrosis pigs as a determinant of particle distribution and deposition.

Effect of free radical scavengers on changes in ion conductance during exposure to therapeutic ultrasound

Electrolyte transport properties in distal small airways from cystic fibrosis pigs with implications for host defense

Enhancement of peritoneal leukocyte function by granulocyte colony-stimulating factor in rats with abdominal sepsis

Expression of human paraoxonase 1 decreases superoxide levels and alters bacterial colonization in the gut of Drosophila melanogaster

Gel-forming mucins form distinct morphologic structures in airways

Genotype-specific alterations in vascular smooth muscle cell function in cystic fibrosis piglets ⬇️

Glucose depletion in the airway surface liquid is essential for sterility of the airways

Glycaemic regulation and insulin secretion are abnormal in cystic fibrosis pigs despite sparing of islet cell mass.

Granulocyte colony-stimulating factor modulates the pulmonary host response to endotoxin in the absence and presence of acute ethanol intoxication

Histamine alters E-cadherin cell adhesion to increase human airway epithelial permeability.

Immunohistochemical Detection of Markers for Translational Studies of Lung Disease in Pigs and Humans

Impaired mucus detachment disrupts mucociliary transport in a piglet model of cystic fibrosis.

Inhaled hypertonic saline in adults hospitalised for exacerbation of cystic fibrosis lung disease: a retrospective study.

Intestinal CFTR expression alleviates meconium ileus in cystic fibrosis pigs

Lack of cystic fibrosis transmembrane conductance regulator disrupts fetal airway development in pigs.

Loss of cystic fibrosis transmembrane conductance regulator function produces abnormalities in tracheal development in neonatal pigs and young children

Medical reversal of chronic sinusitis in a cystic fibrosis patient with ivacaftor

Monocyte derived macrophages from CF pigs exhibit increased inflammatory responses at birth.

Mounier-Kuhn syndrome: a case of tracheal smooth muscle remodeling.

Mucociliary Transport in Healthy and Cystic Fibrosis Pig Airways

Neonates with cystic fibrosis have a reduced nasal liquid pH; a small pilot study

Newborn Cystic Fibrosis Pigs Have a Blunted Early Response to an Inflammatory Stimulus

Origins of cystic fibrosis lung disease

Origins of cystic fibrosis lung disease

Pancreatic and biliary secretion are both altered in cystic fibrosis pigs.

Pancreatic damage in fetal and newborn cystic fibrosis pigs involves the activation of inflammatory and remodeling pathways

Pigs and humans with cystic fibrosis have reduced insulin-like growth factor 1 (IGF1) levels at birth

Postnatal airway growth in cystic fibrosis piglets

Production of CFTR-null and CFTR-DeltaF508 heterozygous pigs by adeno-associated virus-mediated gene targeting and somatic cell nuclear transfer

Reduced airway surface pH impairs bacterial killing in the porcine cystic fibrosis lung

Restoring Cystic Fibrosis Transmembrane Conductance Regulator Function Reduces Airway Bacteria and Inflammation in People with Cystic Fibrosis and Chronic Lung Infections.

Role of PON in anoxia-reoxygenation injury: a Drosophila melanogaster transgenic model

Role of poliovirus receptors in the spread of the infection

Sinus hypoplasia precedes sinus infection in a porcine model of cystic fibrosis

Sonographic evidence of abnormal tracheal cartilage ring structure in cystic fibrosis.

Suppression of the granulocyte colony-stimulating factor response to Escherichia coli challenge by alcohol intoxication

The effect of chronic binge ethanol consumption on the primary stage of SIV infection in rhesus macaques.

The porcine lung as a potential model for cystic fibrosis

The ΔF508 mutation causes CFTR misprocessing and cystic fibrosis-like disease in pigs

Tracheomalacia is associated with lower FEV1 and Pseudomonas acquisition in children with CF

Use of granulocyte colony-stimulating factor in the treatment of acute infectious diseases ⬇️

V-Type ATPase Mediates Airway Surface Liquid Acidification in Pig Small Airway Epithelial Cells

pH modulates the activity and synergism of the airway surface liquid antimicrobials β-defensin-3 and LL-37