Brushed nasal epithelial cells are a surrogate for bronchial epithelial CFTR studies (Q89574920)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29997283 AND SRC:MED&resulttype=core&format=json

6 April 2020

title

Brushed nasal epithelial cells are a surrogate for bronchial epithelial CFTR studies (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29997283 AND SRC:MED&resulttype=core&format=json

6 April 2020

main subject

nasal epithelial cell

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John J Brewington

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29997283 AND SRC:MED&resulttype=core&format=json

6 April 2020

Erin T Filbrandt

2

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6 April 2020

F J LaRosa

3

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6 April 2020

Jessica D Moncivaiz

4

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6 April 2020

Alicia J Ostmann

5

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6 April 2020

Lauren M Strecker

6

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6 April 2020

John P Clancy

7

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6 April 2020

publication date

12 July 2018

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6 April 2020

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29997283 AND SRC:MED&resulttype=core&format=json

6 April 2020

volume

3

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6 April 2020

issue

13

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Human nasal and bronchial epithelial cells in culture: an overview of their characteristics and function.

6 April 2020

cites work

1 reference

12 December 2020

Culture and comparison of human bronchial and nasal epithelial cells in vitro

1 reference

12 December 2020

An apical-membrane chloride channel in human tracheal epithelium

1 reference

12 December 2020

Measurements of nasal transepithelial electric potential differences in normal human subjects in vivo

1 reference

12 December 2020

Ion transport in epithelial spheroids derived from human airway cells

1 reference

12 December 2020

Electrolyte abnormalities of the sweat in fibrocystic disease of the pancreas

1 reference

12 December 2020

A test for concentration of electrolytes in sweat in cystic fibrosis of the pancreas utilizing pilocarpine by iontophoresis

1 reference

12 December 2020

Polarized cultures of human airway epithelium from nasal scrapings and bronchial brushings

1 reference

12 December 2020

Intestinal current measurements to diagnose cystic fibrosis

1 reference

12 December 2020

1 reference

12 December 2020

The cystic fibrosis transmembrane conductance regulator gene and ion channel function in patients with idiopathic pancreatitis

1 reference

12 December 2020

Ex vivo biochemical analysis of CFTR in human rectal biopsies

1 reference

12 December 2020

Evidence for airway surface dehydration as the initiating event in CF airway disease

1 reference

12 December 2020

Feasibility of nasal epithelial brushing for the study of airway epithelial functions in CF infants.

1 reference

12 December 2020

Effect of VX-770 in persons with cystic fibrosis and the G551D-CFTR mutation

1 reference

12 December 2020

Methods for ASL Measurements and Mucus Transport Rates in Cell Cultures

1 reference

12 December 2020

Primary Epithelial Cell Models for Cystic Fibrosis Research

1 reference

12 December 2020

Use of Primary Cultures of Human Bronchial Epithelial Cells Isolated from Cystic Fibrosis Patients for the Pre-clinical Testing of CFTR Modulators

1 reference

12 December 2020

Differential global gene expression in cystic fibrosis nasal and bronchial epithelium

1 reference

12 December 2020

Correction of the F508del-CFTR protein processing defect in vitro by the investigational drug VX-809

1 reference

12 December 2020

CFTR: folding, misfolding and correcting the ΔF508 conformational defect.

1 reference

12 December 2020

ROCK inhibitor and feeder cells induce the conditional reprogramming of epithelial cells

1 reference

12 December 2020

Efficacy and safety of ivacaftor in patients aged 6 to 11 years with cystic fibrosis with a G551D mutation

1 reference

12 December 2020

A functional CFTR assay using primary cystic fibrosis intestinal organoids

1 reference

12 December 2020

Effect of ivacaftor on CFTR forms with missense mutations associated with defects in protein processing or function

1 reference

12 December 2020

In vivo readout of CFTR function: ratiometric measurement of CFTR-dependent secretion by individual, identifiable human sweat glands

1 reference

12 December 2020

Nasal epithelial cells can act as a physiological surrogate for paediatric asthma studies

1 reference

12 December 2020

Efficacy and safety of ivacaftor in patients with cystic fibrosis and a non-G551D gating mutation

1 reference

12 December 2020

Cystic fibrosis genetics: from molecular understanding to clinical application

1 reference

12 December 2020

A bioassay using intestinal organoids to measure CFTR modulators in human plasma

1 reference

12 December 2020

Lumacaftor-Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del CFTR.

1 reference

12 December 2020

Efficacy and safety of ivacaftor in patients with cystic fibrosis who have an Arg117His-CFTR mutation: a double-blind, randomised controlled trial

1 reference

12 December 2020

Understanding Bland Altman analysis

1 reference

12 December 2020

Personalized medicine for cystic fibrosis: establishing human model systems

1 reference

12 December 2020

Comparison of innate immune responses towards rhinovirus infection of primary nasal and bronchial epithelial cells

1 reference

12 December 2020

From CFTR biology toward combinatorial pharmacotherapy: expanded classification of cystic fibrosis mutations

1 reference

12 December 2020

Airway Progenitor Clone Formation Is Enhanced by Y-27632-Dependent Changes in the Transcriptome

1 reference

12 December 2020

Pharmacological Rescue of Conditionally Reprogrammed Cystic Fibrosis Bronchial Epithelial Cells

1 reference

12 December 2020

Efficacy and safety of lumacaftor and ivacaftor in patients aged 6-11 years with cystic fibrosis homozygous for F508del-CFTR: a randomised, placebo-controlled phase 3 trial

1 reference

12 December 2020

Phenotypic profiling of CFTR modulators in patient-derived respiratory epithelia

1 reference

12 December 2020

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

1 reference

12 December 2020

Correction of CFTR function in nasal epithelial cells from cystic fibrosis patients predicts improvement of respiratory function by CFTR modulators

1 reference

12 December 2020

Tezacaftor-Ivacaftor in Residual-Function Heterozygotes with Cystic Fibrosis

1 reference

12 December 2020

Tezacaftor-Ivacaftor in Patients with Cystic Fibrosis Homozygous for Phe508del

1 reference

12 December 2020

Nasospheroids permit measurements of CFTR-dependent fluid transport

1 reference

12 December 2020

Characterization of pediatric cystic fibrosis airway epithelial cell cultures at the air-liquid interface obtained by non-invasive nasal cytology brush sampling.

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12 December 2020

10.1172/JCI.INSIGHT.99385

Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29997283 AND SRC:MED&resulttype=core&format=json

6 April 2020

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29997283 AND SRC:MED&resulttype=core&format=json

6 April 2020

PubMed publication ID

29997283

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