Deficient Hydrophilic Lung Surfactant Proteins A and D with Normal Surfactant Phospholipid Molecular Species in Cystic Fibrosis-Reference-Cited by-同舟云学术

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Deficient Hydrophilic Lung Surfactant Proteins A and D with Normal Surfactant Phospholipid Molecular Species in Cystic Fibrosis

Published:1999-01 Issue:1 Volume:20 Page:90-98
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:

Postle Anthony D.,Mander Ann,Reid Kenneth B. M.,Wang Jiu-Yao,Wright Sarah M.,Moustaki Maria,Warner John O.

Publisher

American Thoracic Society

Subject

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

Reference31 articles.

1. Cystic Fibrosis Airway Epithelia Fail to Kill Bacteria Because of Abnormal Airway Surface Fluid

2. Disruption of pulmonary surfactant's ability to maintain openness of a narrow tube

3. Immunoregulatory properties of pulmonary surfactant: effect of lung lining fluid on proliferation of human blood lymphocytes.

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3. Lung surfactant as a biophysical assay for inhalation toxicology;Current Research in Toxicology;2023

4. Genetic Association With Pseudomonas aeruginosa Acquisition in Cystic Fibrosis: Influence of Surfactant Protein D and Mannose-Binding Lectin;Frontiers in Immunology;2021-02-19

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