Functional Characterization of ATP-Binding Cassette Transporter A3 Mutations from Infants with Respiratory Distress Syndrome-Reference-Cited by-同舟云学术

Functional Characterization of ATP-Binding Cassette Transporter A3 Mutations from Infants with Respiratory Distress Syndrome

Published:2016-11 Issue:5 Volume:55 Page:716-721
ISSN:1044-1549
Container-title:American Journal of Respiratory Cell and Molecular Biology
language:en
Short-container-title:Am J Respir Cell Mol Biol

Author:

Wambach Jennifer A.,Yang Ping,Wegner Daniel J.,Heins Hillary B.,Kaliberova Lyudmila N.,Kaliberov Sergey A.,Curiel David T.,White Frances V.,Hamvas Aaron,Hackett Brian P.,Cole F. Sessions

Publisher

American Thoracic Society

Subject

Cell Biology,Clinical Biochemistry,Pulmonary and Respiratory Medicine,Molecular Biology

Reference29 articles.

1. ABCA3 inactivation in mice causes respiratory failure, loss of pulmonary surfactant, and depletion of lung phosphatidylglycerol

2. Identification of LBM180, a Lamellar Body Limiting Membrane Protein of Alveolar Type II Cells, as the ABC Transporter Protein ABCA3

3. ABCA3 as a Lipid Transporter in Pulmonary Surfactant Biogenesis

4. ABCA3 Is Critical for Lamellar Body Biogenesis in Vivo

5. Genotype–Phenotype Correlations for Infants and Children with ABCA3 Deficiency

Cited by 49 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Innovations in Childhood Interstitial and Diffuse Lung Disease;Clinics in Chest Medicine;2024-09

2. Cyclosporine A in children with ABCA3 deficiency;Pediatric Pulmonology;2024-07-23

3. Interstitial lung disease in the newborn;Journal of Perinatology;2024-07-02

4. ABCA3 mutation-induced congenital pulmonary surfactant deficiency: A case report;Medicine;2024-03-29

5. Human pluripotent stem cell modeling of alveolar type 2 cell dysfunction caused by ABCA3 mutations;Journal of Clinical Investigation;2024-01-16