Detection of CFTR function and modulation in primary human nasal cell spheroids-Reference-Cited by-同舟云学术

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

Published:2018-01 Issue:1 Volume:17 Page:26-33
ISSN:1569-1993
Container-title:Journal of Cystic Fibrosis
language:en
Short-container-title:Journal of Cystic Fibrosis

Author:

Brewington John J.,Filbrandt Erin T.,LaRosa F.J.,Ostmann Alicia J.,Strecker Lauren M.,Szczesniak Rhonda D.,Clancy John P.

Funder

Cystic Fibrosis Foundation Therapeutics

Cystic Fibrosis Foundation

Publisher

Elsevier BV

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health

Reference24 articles.

1. Cystic fibrosis;Rowe;N Engl J Med,2005

2. Role of CFTR in airway disease;Pilewski;Physiol Rev,1999

3. An apical-membrane chloride channel in human tracheal epithelium;Welsh;Science,1986

4. CFTR is a conductance regulator as well as a chloride channel;Schwiebert;Physiol Rev,1999

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1. Laboratory Tools to Predict CFTR Modulator Therapy Effectiveness and to Monitor Disease Severity in Cystic Fibrosis;Journal of Personalized Medicine;2024-01-13

2. Patient-derived cell models for personalized medicine approaches in cystic fibrosis;Journal of Cystic Fibrosis;2023-03

3. Phenotypic Alteration of an Established Human Airway Cell Line by Media Selection;International Journal of Molecular Sciences;2023-01-08

4. Gradual increase in sweat chloride concentration is associated with a higher risk of CRMS/CFSPID to CF reclassification;Pediatric Pulmonology;2023-01-06

5. Organoids;Nature Reviews Methods Primers;2022-12-01

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