Olga Moran-Zegarra

Genoa, Italy

Last Updated: 09/26/2026

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Found 18 publications

Lack of Kcnn4 improves mucociliary clearance in muco-obstructive lung disease.

Lack of Kcnn4 improves mucociliary clearance in muco-obstructive lung disease.

Journal: JCI insight

Published: May 08, 2020

Small molecule anionophores promote transmembrane anion permeation matching CFTR activity.

Small molecule anionophores promote transmembrane anion permeation matching CFTR activity.

Journal: Scientific reports

Published: November 09, 2017

In vitro recapitulation of the site-specific editing (to wild-type) of mutant IDS mRNA transcripts, and the characterization of IDS protein translated from the edited mRNAs.

In vitro recapitulation of the site-specific editing (to wild-type) of mutant IDS mRNA transcripts, and the characterization of IDS protein translated from the edited mRNAs.

Journal: Human mutation

Published: November 08, 2016

CFTR pharmacology.

CFTR pharmacology.

Journal: Cellular and molecular life sciences : CMLS

Published: September 27, 2016

Rheological Properties of Cystic Fibrosis Bronchial Secretion and in Vitro Drug Permeation Study: The Effect of Sodium Bicarbonate.

Rheological Properties of Cystic Fibrosis Bronchial Secretion and in Vitro Drug Permeation Study: The Effect of Sodium Bicarbonate.

Journal: Journal of aerosol medicine and pulmonary drug delivery

Published: January 08, 2016

Pharmacological analysis of epithelial chloride secretion mechanisms in adult murine airways.

Pharmacological analysis of epithelial chloride secretion mechanisms in adult murine airways.

Journal: European journal of pharmacology

Published: November 06, 2015

Structure of wild type and mutant F508del CFTR: A small-angle X-ray scattering study of the protein-detergent complexes.

Structure of wild type and mutant F508del CFTR: A small-angle X-ray scattering study of the protein-detergent complexes.

Journal: Journal of structural biology

Published: October 12, 2015

Pharmacological rescue of mutant CFTR protein improves the viscoelastic properties of CF mucus.

Pharmacological rescue of mutant CFTR protein improves the viscoelastic properties of CF mucus.

Journal: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society

Published: September 25, 2015

Evaluation of a systems biology approach to identify pharmacological correctors of the mutant CFTR chloride channel.

Evaluation of a systems biology approach to identify pharmacological correctors of the mutant CFTR chloride channel.

Journal: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society

Published: July 14, 2015

Synthesis and structure-activity relationship of aminoarylthiazole derivatives as correctors of the chloride transport defect in cystic fibrosis.

Synthesis and structure-activity relationship of aminoarylthiazole derivatives as correctors of the chloride transport defect in cystic fibrosis.

Journal: European journal of medicinal chemistry

Published: January 15, 2015

Functional analysis of acid-activated Cl⁻ channels: properties and mechanisms of regulation.

Functional analysis of acid-activated Cl⁻ channels: properties and mechanisms of regulation.

Journal: Biochimica et biophysica acta

Published: July 08, 2014

Functional and pharmacological induced structural changes of the cystic fibrosis transmembrane conductance regulator in the membrane solved using SAXS.

Functional and pharmacological induced structural changes of the cystic fibrosis transmembrane conductance regulator in the membrane solved using SAXS.

Journal: Cellular and molecular life sciences : CMLS

Published: May 07, 2014

Showing 1-12 of 18

Last Updated: 09/26/2026