Lista de obras -

2-(dialkylamino)-4H-1-benzopyran-4-one derivatives modify chloride conductance in CFTR expressing cells

artículo científico publicado en 2003

A minimal isoform of the TMEM16A protein associated with chloride channel activity.

artículo científico publicado en 2011

A novel missense mutation in ANO5/TMEM16E is causative for gnathodiaphyseal dyplasia in a large Italian pedigree.

artículo científico publicado en 2012

Anion-Transport Mechanism of a Triazole-Bearing Derivative of Prodigiosine: A Candidate for Cystic Fibrosis Therapy

artículo científico publicado en 2018

Antihypertensive 1,4-dihydropyridines as correctors of the cystic fibrosis transmembrane conductance regulator channel gating defect caused by cystic fibrosis mutations.

artículo científico publicado en 2005

Association of TMEM16A chloride channel overexpression with airway goblet cell metaplasia.

artículo científico publicado en 2012

Block of CFTR-dependent chloride currents by inhibitors of multidrug resistance-associated proteins.

artículo científico publicado en 2007

CD4(+)CD25(high)CD127(-) regulatory T-cells in COPD: smoke and drugs effect

artículo científico publicado en 2016

CFTR activation in human bronchial epithelial cells by novel benzoflavone and benzimidazolone compounds

artículo científico publicado en 2003

Click-tambjamines as efficient and tunable bioactive anion transporters

artículo científico publicado en 2020

Correction of G551D-CFTR transport defect in epithelial monolayers by genistein but not by CPX or MPB-07.

artículo científico publicado en 2002

Cytokines induce tight junction disassembly in airway cells via an EGFR-dependent MAPK/ERK1/2-pathway

artículo científico publicado en 2012

Dual activity of aminoarylthiazoles on the trafficking and gating defects of the cystic fibrosis transmembrane conductance regulator chloride channel caused by cystic fibrosis mutations.

artículo científico publicado en 2011

Effect of inflammatory stimuli on airway ion transport.

artículo científico publicado en 2004

Epithelial sodium channel inhibition in primary human bronchial epithelia by transfected siRNA.

artículo científico publicado en 2008

Epithelial sodium channel silencing as a strategy to correct the airway surface fluid deficit in cystic fibrosis

artículo científico publicado en 2013

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

artículo científico publicado en 2016

Evidence for direct CFTR inhibition by CFTR(inh)-172 based on Arg347 mutagenesis.

artículo científico publicado en 2008

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

artículo científico publicado en 2015

Functional human CFTR produced by a stable minichromosome

artículo científico publicado en 2002

Gelsolin Secretion in Interleukin-4–treated Bronchial Epithelia and in Asthmatic Airways

artículo científico publicado en 2005

Genetic Inhibition Of The Ubiquitin Ligase Rnf5 Attenuates Phenotypes Associated To F508del Cystic Fibrosis Mutation.

artículo científico publicado en 2015

Goblet Cell Hyperplasia Requires High Bicarbonate Transport To Support Mucin Release

artículo científico publicado en 2016

High-throughput screening identifies FAU protein as a regulator of mutant cystic fibrosis transmembrane conductance regulator channel.

artículo científico publicado en 2017

IL-12 can target human lung adenocarcinoma cells and normal bronchial epithelial cells surrounding tumor lesions

artículo científico publicado en 2009

IL-4 is a potent modulator of ion transport in the human bronchial epithelium in vitro

artículo científico publicado en 2002

Increased expression of ATP12A proton pump in cystic fibrosis airways

artículo científico publicado en 2018

Ion channel and lipid scramblase activity associated with expression of TMEM16F/ANO6 isoforms.

artículo científico publicado en 2015

Ionocytes and CFTR Chloride Channel Expression in Normal and Cystic Fibrosis Nasal and Bronchial Epithelial Cells

scientific article published on 13 September 2020

Methods for the Development and Analysis of Human Primary Airway Epithelia

article

Murine Rankl-/- Mesenchymal Stromal Cells Display an Osteogenic Differentiation Defect Improved by a RANKL-Expressing Lentiviral Vector

artículo científico publicado en 2017

Mutation-specific potency and efficacy of cystic fibrosis transmembrane conductance regulator chloride channel potentiators.

artículo científico publicado en 2009

Non-canonical translation start sites in the TMEM16A chloride channel

artículo científico publicado en 2013

Pharmacological Inhibition of the Ubiquitin Ligase RNF5 Rescues F508del-CFTR in Cystic Fibrosis Airway Epithelia

artículo científico publicado en 2018

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

artículo científico publicado en 2016

Rescue of the mutant CFTR chloride channel by pharmacological correctors and low temperature analyzed by gene expression profiling.

artículo científico publicado en 2011

SWATH label-free proteomics for cystic fibrosis research

scholarly article by Clarissa Braccia et al published 19 October 2018 in Journal of Cystic Fibrosis

Small Molecule Anion Carriers Correct Abnormal Airway Surface Liquid Properties in Cystic Fibrosis Airway Epithelia

artículo científico publicado en 2020

Small-molecule correctors of defective DeltaF508-CFTR cellular processing identified by high-throughput screening.

artículo científico publicado en 2005

TMEM16A, a membrane protein associated with calcium-dependent chloride channel activity

artículo científico publicado en 2008

TMEM16A-TMEM16B chimaeras to investigate the structure-function relationship of calcium-activated chloride channels.

artículo científico publicado en 2013

The Autophagy Inhibitor Spautin-1 Antagonizes Rescue of Mutant CFTR Through an Autophagy-Independent and USP13-Mediated Mechanism

The TMEM16A chloride channel as an alternative therapeutic target in cystic fibrosis.

artículo científico

Thiocyanate transport in resting and IL-4-stimulated human bronchial epithelial cells: role of pendrin and anion channels

artículo científico publicado en 2007

Thymosin α-1 does not correct F508del-CFTR in cystic fibrosis airway epithelia

artículo científico publicado en 2019

Thymosin α-1 does not correct F508del-CFTR in cystic fibrosis airway epithelia.

artículo científico publicado en 2018

Upregulation of TMEM16A Protein in Bronchial Epithelial Cells by Bacterial Pyocyanin

artículo científico publicado en 2015

Lista de obras de

2-(dialkylamino)-4H-1-benzopyran-4-one derivatives modify chloride conductance in CFTR expressing cells

A minimal isoform of the TMEM16A protein associated with chloride channel activity.

A novel missense mutation in ANO5/TMEM16E is causative for gnathodiaphyseal dyplasia in a large Italian pedigree.

Anion-Transport Mechanism of a Triazole-Bearing Derivative of Prodigiosine: A Candidate for Cystic Fibrosis Therapy

Antihypertensive 1,4-dihydropyridines as correctors of the cystic fibrosis transmembrane conductance regulator channel gating defect caused by cystic fibrosis mutations.

Association of TMEM16A chloride channel overexpression with airway goblet cell metaplasia.

Block of CFTR-dependent chloride currents by inhibitors of multidrug resistance-associated proteins.

CD4(+)CD25(high)CD127(-) regulatory T-cells in COPD: smoke and drugs effect

CFTR activation in human bronchial epithelial cells by novel benzoflavone and benzimidazolone compounds

Click-tambjamines as efficient and tunable bioactive anion transporters

Correction of G551D-CFTR transport defect in epithelial monolayers by genistein but not by CPX or MPB-07.

Cytokines induce tight junction disassembly in airway cells via an EGFR-dependent MAPK/ERK1/2-pathway

Dual activity of aminoarylthiazoles on the trafficking and gating defects of the cystic fibrosis transmembrane conductance regulator chloride channel caused by cystic fibrosis mutations.

Effect of inflammatory stimuli on airway ion transport.

Epithelial sodium channel inhibition in primary human bronchial epithelia by transfected siRNA.

Epithelial sodium channel silencing as a strategy to correct the airway surface fluid deficit in cystic fibrosis

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

Evidence for direct CFTR inhibition by CFTR(inh)-172 based on Arg347 mutagenesis.

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

Functional human CFTR produced by a stable minichromosome

Gelsolin Secretion in Interleukin-4–treated Bronchial Epithelia and in Asthmatic Airways

Genetic Inhibition Of The Ubiquitin Ligase Rnf5 Attenuates Phenotypes Associated To F508del Cystic Fibrosis Mutation.

Goblet Cell Hyperplasia Requires High Bicarbonate Transport To Support Mucin Release

High-throughput screening identifies FAU protein as a regulator of mutant cystic fibrosis transmembrane conductance regulator channel.

IL-12 can target human lung adenocarcinoma cells and normal bronchial epithelial cells surrounding tumor lesions

IL-4 is a potent modulator of ion transport in the human bronchial epithelium in vitro

Increased expression of ATP12A proton pump in cystic fibrosis airways

Ion channel and lipid scramblase activity associated with expression of TMEM16F/ANO6 isoforms.

Ionocytes and CFTR Chloride Channel Expression in Normal and Cystic Fibrosis Nasal and Bronchial Epithelial Cells

Methods for the Development and Analysis of Human Primary Airway Epithelia

Murine Rankl-/- Mesenchymal Stromal Cells Display an Osteogenic Differentiation Defect Improved by a RANKL-Expressing Lentiviral Vector

Mutation-specific potency and efficacy of cystic fibrosis transmembrane conductance regulator chloride channel potentiators.

Non-canonical translation start sites in the TMEM16A chloride channel

Pharmacological Inhibition of the Ubiquitin Ligase RNF5 Rescues F508del-CFTR in Cystic Fibrosis Airway Epithelia

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

Rescue of the mutant CFTR chloride channel by pharmacological correctors and low temperature analyzed by gene expression profiling.

SWATH label-free proteomics for cystic fibrosis research

Small Molecule Anion Carriers Correct Abnormal Airway Surface Liquid Properties in Cystic Fibrosis Airway Epithelia

Small-molecule correctors of defective DeltaF508-CFTR cellular processing identified by high-throughput screening.

TMEM16A, a membrane protein associated with calcium-dependent chloride channel activity

TMEM16A-TMEM16B chimaeras to investigate the structure-function relationship of calcium-activated chloride channels.

The Autophagy Inhibitor Spautin-1 Antagonizes Rescue of Mutant CFTR Through an Autophagy-Independent and USP13-Mediated Mechanism

The TMEM16A chloride channel as an alternative therapeutic target in cystic fibrosis.

Thiocyanate transport in resting and IL-4-stimulated human bronchial epithelial cells: role of pendrin and anion channels

Thymosin α-1 does not correct F508del-CFTR in cystic fibrosis airway epithelia

Thymosin α-1 does not correct F508del-CFTR in cystic fibrosis airway epithelia.

Upregulation of TMEM16A Protein in Bronchial Epithelial Cells by Bacterial Pyocyanin