Lista de obras -

A high‐resolution 3D atlas of the spectrum of tuberculous and COVID ‐19 lung lesions

artículo científico publicado en 2022

Acquired Cystic Fibrosis Transmembrane Conductance Regulator Dysfunction and Radiographic Bronchiectasis in Current and Former Smokers: A Cross-Sectional Study

artículo científico publicado en 2019

Ataluren/ivacaftor combination therapy: Two N-of-1 trials in cystic fibrosis patients with nonsense mutations

artículo científico publicado en 2020

CFTR targeted therapies: recent advances in cystic fibrosis and possibilities in other diseases of the airways

scientific article published on 16 June 2020

Changes in Airway Microbiome and Inflammation with Ivacaftor Treatment in Patients with Cystic Fibrosis and the G551D Mutation

artículo científico publicado en 2020

Clinical development of triple-combination CFTR modulators for cystic fibrosis patients with one or two F508del alleles

artículo científico publicado en 2019

Development of an airway mucus defect in the cystic fibrosis rat.

artículo científico publicado en 2018

Discovery of Clinically Approved Agents That Promote Suppression of Cystic Fibrosis Transmembrane Conductance Regulator Nonsense Mutations.

artículo científico publicado en 2016

Evaluation of 1,2,3-Triazoles as Amide Bioisosteres In Cystic Fibrosis Transmembrane Conductance Regulator Modulators VX-770 and VX-809

scientific article published on 11 February 2019

Excess mucus viscosity and airway dehydration impact COPD airway clearance

scientific article published on 30 January 2020

Functional Anatomic Imaging of the Airway Surface

scientific article published on 01 November 2018

Heme scavenging reduces pulmonary endoplasmic reticulum stress, fibrosis, and emphysema

artículo científico publicado en 2018

Human distal airways contain a multipotent secretory cell that can regenerate alveoli

Influenza-mediated reduction of lung epithelial ion channel activity leads to dysregulated pulmonary fluid homeostasis

artículo científico publicado en 2018

Intranasal micro-optical coherence tomography imaging for cystic fibrosis studies

scientific article published on 01 August 2019

Lumacaftor/Ivacaftor Treatment of Patients with Cystic Fibrosis Heterozygous for F508del-CFTR.

artículo científico publicado en 2016

Mutation of Growth Arrest Specific 8 Reveals a Role in Motile Cilia Function and Human Disease

artículo científico publicado en 2016

Not simply the lesser of two evils.

artículo científico publicado en 2017

Recovery of Acquired Cystic Fibrosis Transmembrane Conductance Regulator Dysfunction after Smoking Cessation.

artículo científico publicado en 2015

Revealing the molecular signaling pathways of mucus stasis in cystic fibrosis

artículo científico publicado en 2019

Roflumilast reverses CFTR-mediated ion transport dysfunction in cigarette smoke-exposed mice

artículo científico publicado en 2017

Sensitivity of ivacaftor to drug-drug interactions with rifampin, a cytochrome P450 3A4 inducer.

artículo científico publicado en 2018

Toward inclusive therapy with CFTR modulators: Progress and challenges.

artículo científico publicado en 2017

Use of ferrets for electrophysiologic monitoring of ion transport

artículo científico publicado en 2017

Vaporized E-Cigarette Liquids Induce Ion Transport Dysfunction in Airway Epithelia

artículo científico publicado en 2019

Lista de obras de

A high‐resolution 3D atlas of the spectrum of tuberculous and COVID ‐19 lung lesions

Acquired Cystic Fibrosis Transmembrane Conductance Regulator Dysfunction and Radiographic Bronchiectasis in Current and Former Smokers: A Cross-Sectional Study

Ataluren/ivacaftor combination therapy: Two N-of-1 trials in cystic fibrosis patients with nonsense mutations

CFTR targeted therapies: recent advances in cystic fibrosis and possibilities in other diseases of the airways

Changes in Airway Microbiome and Inflammation with Ivacaftor Treatment in Patients with Cystic Fibrosis and the G551D Mutation

Clinical development of triple-combination CFTR modulators for cystic fibrosis patients with one or two F508del alleles

Development of an airway mucus defect in the cystic fibrosis rat.

Discovery of Clinically Approved Agents That Promote Suppression of Cystic Fibrosis Transmembrane Conductance Regulator Nonsense Mutations.

Evaluation of 1,2,3-Triazoles as Amide Bioisosteres In Cystic Fibrosis Transmembrane Conductance Regulator Modulators VX-770 and VX-809

Excess mucus viscosity and airway dehydration impact COPD airway clearance

Functional Anatomic Imaging of the Airway Surface

Heme scavenging reduces pulmonary endoplasmic reticulum stress, fibrosis, and emphysema

Human distal airways contain a multipotent secretory cell that can regenerate alveoli

Influenza-mediated reduction of lung epithelial ion channel activity leads to dysregulated pulmonary fluid homeostasis

Intranasal micro-optical coherence tomography imaging for cystic fibrosis studies

Lumacaftor/Ivacaftor Treatment of Patients with Cystic Fibrosis Heterozygous for F508del-CFTR.

Mutation of Growth Arrest Specific 8 Reveals a Role in Motile Cilia Function and Human Disease

Not simply the lesser of two evils.

Recovery of Acquired Cystic Fibrosis Transmembrane Conductance Regulator Dysfunction after Smoking Cessation.

Revealing the molecular signaling pathways of mucus stasis in cystic fibrosis

Roflumilast reverses CFTR-mediated ion transport dysfunction in cigarette smoke-exposed mice

Sensitivity of ivacaftor to drug-drug interactions with rifampin, a cytochrome P450 3A4 inducer.

Toward inclusive therapy with CFTR modulators: Progress and challenges.

Use of ferrets for electrophysiologic monitoring of ion transport

Vaporized E-Cigarette Liquids Induce Ion Transport Dysfunction in Airway Epithelia