Lista de obras - Elvira Sondo - Dominio Público Uruguay

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

artículo científico publicado en 2011

Alternative splicing at a NAGNAG acceptor site as a novel phenotype modifier

artículo científico publicado en 2010

Alternative splicing of in-frame exon associated with premature termination codons: implications for readthrough therapies.

artículo científico publicado en 2012

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

Chemically modified hCFTR mRNAs recuperate lung function in a mouse model of cystic fibrosis

scientific article published in Scientific Reports

Discovery of a picomolar potency pharmacological corrector of the mutant CFTR chloride channel

scientific article published on 21 February 2020

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

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

artículo científico publicado en 2013

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

artículo científico publicado en 2015

High-Content Screening Identifies Vanilloids as a Novel Class of Inhibitors of NET Formation

scientific article published on 30 April 2019

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

artículo científico publicado en 2017

Influence of cell background on pharmacological rescue of mutant CFTR.

artículo científico publicado en 2010

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

artículo científico publicado en 2015

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

RNF5, DAB2 and Friends: Novel Drug Targets for Cystic Fibrosis

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

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

The anoctamin family: TMEM16A and TMEM16B as calcium-activated chloride channels

artículo científico publicado en 2012

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 2018

Upregulation of TMEM16A Protein in Bronchial Epithelial Cells by Bacterial Pyocyanin

artículo científico publicado en 2015

Lista de obras de Elvira Sondo

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

Alternative splicing at a NAGNAG acceptor site as a novel phenotype modifier

Alternative splicing of in-frame exon associated with premature termination codons: implications for readthrough therapies.

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

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

Chemically modified hCFTR mRNAs recuperate lung function in a mouse model of cystic fibrosis

Discovery of a picomolar potency pharmacological corrector of the mutant CFTR chloride channel

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

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

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

High-Content Screening Identifies Vanilloids as a Novel Class of Inhibitors of NET Formation

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

Influence of cell background on pharmacological rescue of mutant CFTR.

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

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

RNF5, DAB2 and Friends: Novel Drug Targets for Cystic Fibrosis

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

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.

The anoctamin family: TMEM16A and TMEM16B as calcium-activated chloride channels

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.

Upregulation of TMEM16A Protein in Bronchial Epithelial Cells by Bacterial Pyocyanin