Associated Papers
Lentiviral-mediated gene complementation rescues pathogenic ABCA3 variants.
Cooney AL et al.
Biorxiv : the Preprint Server for Biology, 2025
Evaluating the Use of iPSC-Derived Models in Understanding the Pathogenesis of Childhood Interstitial Lung Disease.
Jinson S et al.
Pediatric Pulmonology, 2025
Human pluripotent stem cell modeling of alveolar type 2 cell dysfunction caused by ABCA3 mutations.
Sun YL et al.
The Journal of Clinical Investigation, 2024
ABCA3 Deficiency-Variant-Specific Response to Hydroxychloroquine.
Yang X et al.
International Journal of Molecular Sciences, 2023
Cryo-EM structures of the human surfactant lipid transporter ABCA3.
Xie T et al.
Science Advances, 2022
35394827 (PubMed )
Supplement: sciadv.abn3727_sm.pdf
Candidate genes of idiopathic pulmonary fibrosis: current evidence and research.
Zhou W et al.
The Application of Clinical Genetics, 2016
A large kindred of pulmonary fibrosis associated with a novel ABCA3 gene variant.
Campo I et al.
Respiratory Research, 2014
Respiratory distress syndrome due to a novel homozygous ABCA3 mutation in a term neonate.
Parappil H et al.
Bmj Case Reports, 2011
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