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Nasal Epithelial Cell-Based Models for Individualized Study in Cystic Fibrosis

International journal of molecular sciences, 2021-04, Vol.22 (9), p.4448

2021

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When CFSPID becomes CF

Journal of cystic fibrosis, 2022-01, Vol.21 (1), p.e23-e27

2022

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Novel Applications of Biomarkers and Personalized Medicine in Cystic Fibrosis

Clinics in chest medicine, 2022-12, Vol.43 (4), p.617-630

2022

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Direct Lung Sampling Indicates That Established Pathogens Dominate Early Infections in Children with Cystic Fibrosis

Cell reports (Cambridge), 2019-04, Vol.27 (4), p.1190-1204.e3

2019

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Gradual increase in sweat chloride concentration is associated with a higher risk of CRMS/CFSPID to CF reclassification

Pediatric pulmonology, 2023-04, Vol.58 (4), p.1074-1084

2023

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Phenotypic Alteration of an Established Human Airway Cell Line by Media Selection

International journal of molecular sciences, 2023-01, Vol.24 (2), p.1246

2023

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Neutrophil extracellular traps activate IL-8 and IL-1 expression in human bronchial epithelia

American journal of physiology. Lung cellular and molecular physiology, 2020-07, Vol.319 (1), p.L137-L147

2020

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Personalised CFTR pharmacotherapeutic response testing and therapy of cystic fibrosis

The European respiratory journal, 2018-06, Vol.51 (6), p.1702457-1702457

2018

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CRISPRi links COVID-19 GWAS loci to LZTFL1 and RAVER1

EBioMedicine, 2022-01, Vol.75, p.103806-103806, Article 103806

2022

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Patient personalized translational tools in Cystic fibrosis to transform data from bench to bed-side and back

American journal of physiology: Gastrointestinal and liver physiology, 2021-06, Vol.320 (6), p.G1123-G1130

2021

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Flexible Bronchoscopic Thrombus Cryoextraction in a Neonate on Extracorporeal Membrane Oxygenation

American journal of respiratory and critical care medicine, 2021-03, Vol.203 (5), p.633-635

2021

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Detection of CFTR function and modulation in primary human nasal cell spheroids

Journal of cystic fibrosis, 2018-01, Vol.17 (1), p.26-33

2018

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Quantifying abnormal alveolar microstructure in cystic fibrosis lung disease via hyperpolarized 129Xe diffusion MRI

Journal of cystic fibrosis, 2024-09, Vol.23 (5), p.926-935

2024

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Lyme disease risk in southern California: abiotic and environmental drivers of Ixodes pacificus (Acari: Ixodidae) density and infection prevalence with Borrelia burgdorferi

Parasites & vectors, 2017-01, Vol.10 (1), p.7-7, Article 7

2017

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Brushed nasal epithelial cells are a surrogate for bronchial epithelial CFTR studies

JCI insight, 2018-07, Vol.3 (13)

2018

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Diagnostic Testing in Cystic Fibrosis

Clinics in chest medicine, 2016-03, Vol.37 (1), p.31-46

2016

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Rapid cystic fibrosis lung-function decline and in-vitro CFTR modulation

Journal of cystic fibrosis, 2021-09, Vol.20 (5), p.e69-e71

2021

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Lumacaftor alone and combined with ivacaftor: preclinical and clinical trial experience of F508del CFTR correction

Expert review of respiratory medicine, 2016-01, Vol.10 (1), p.5-17

2016

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Generation of Human Nasal Epithelial Cell Spheroids for Individualized Cystic Fibrosis Transmembrane Conductance Regulator Study

Journal of visualized experiments, 2018-04 (134)

2018

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Update in Pediatric Lung Disease 2014

American journal of respiratory and critical care medicine, 2015-10, Vol.192 (8), p.918-923

2015

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CRISPRi-mediated functional analysis of lung disease-associated loci at non-coding regions

NAR genomics and bioinformatics, 2020-06, Vol.2 (2)

2020

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Chronic β2AR stimulation limits CFTR activation in human airway epithelia

JCI insight, 2018-02, Vol.3 (4)

2018

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HYPER-LOCALIZATION AND PREDICTIVE MODELING OF RAPID CYSTIC FIBROSIS DISEASE PROGRESSION

Annals of epidemiology, 2024-09, Vol.97, p.76-76

2024

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Sweat Chloride Testing

JAMA : the journal of the American Medical Association, 2019-02, Vol.321 (7), p.701

2019

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Clinically-approved CFTR modulators rescue Nrf2 dysfunction in cystic fibrosis airway epithelia

The Journal of clinical investigation, 2019-08, Vol.129 (8), p.3448-3463

2019

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Nasal Epithelial Cell-Based Models for Individualized Study in Cystic Fibrosis

When CFSPID becomes CF

Novel Applications of Biomarkers and Personalized Medicine in Cystic Fibrosis

Direct Lung Sampling Indicates That Established Pathogens Dominate Early Infections in Children with Cystic Fibrosis

Gradual increase in sweat chloride concentration is associated with a higher risk of CRMS/CFSPID to CF reclassification

Phenotypic Alteration of an Established Human Airway Cell Line by Media Selection

Neutrophil extracellular traps activate IL-8 and IL-1 expression in human bronchial epithelia

Personalised CFTR pharmacotherapeutic response testing and therapy of cystic fibrosis

CRISPRi links COVID-19 GWAS loci to LZTFL1 and RAVER1

Patient personalized translational tools in Cystic fibrosis to transform data from bench to bed-side and back

Flexible Bronchoscopic Thrombus Cryoextraction in a Neonate on Extracorporeal Membrane Oxygenation

Detection of CFTR function and modulation in primary human nasal cell spheroids

Quantifying abnormal alveolar microstructure in cystic fibrosis lung disease via hyperpolarized 129Xe diffusion MRI

Lyme disease risk in southern California: abiotic and environmental drivers of Ixodes pacificus (Acari: Ixodidae) density and infection prevalence with Borrelia burgdorferi

Brushed nasal epithelial cells are a surrogate for bronchial epithelial CFTR studies

Diagnostic Testing in Cystic Fibrosis

Rapid cystic fibrosis lung-function decline and in-vitro CFTR modulation

Lumacaftor alone and combined with ivacaftor: preclinical and clinical trial experience of F508del CFTR correction

Generation of Human Nasal Epithelial Cell Spheroids for Individualized Cystic Fibrosis Transmembrane Conductance Regulator Study

Update in Pediatric Lung Disease 2014

CRISPRi-mediated functional analysis of lung disease-associated loci at non-coding regions

Chronic β2AR stimulation limits CFTR activation in human airway epithelia

HYPER-LOCALIZATION AND PREDICTIVE MODELING OF RAPID CYSTIC FIBROSIS DISEASE PROGRESSION

Sweat Chloride Testing

Clinically-approved CFTR modulators rescue Nrf2 dysfunction in cystic fibrosis airway epithelia

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