Alveolar injury and regeneration following deletion of ABCA3
Author:
Funder
National Institutes of Health
Publisher
American Society for Clinical Investigation
Subject
General Medicine
Link
https://insight.jci.org/articles/view/97381/files/pdf
Reference57 articles.
1. Diseases of Pulmonary Surfactant Homeostasis
2. Genotype–Phenotype Correlations for Infants and Children with ABCA3 Deficiency
3. ABCA3 is a lamellar body membrane protein in human lung alveolar type II cells1
4. Primary structure of a novel ABC transporter with a chromosomal localization on the band encoding the multidrug resistance-associated protein
5. ABCA3 Is Critical for Lamellar Body Biogenesis in Vivo
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