ABCA3‐mediated choline‐phospholipids uptake into intracellular vesicles in A549 cells
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Yoshihiro Matsumura | Hiromichi Sakai | Nobuya Inagaki | N. Inagaki | Y. Matsumura | Nobuhiro Ban | Hiromichi Sakai | Mayumi Sasaki | Mayumi Sasaki | N. Ban
[1] S. Yokoyama,et al. Human ABCA7 Supports Apolipoprotein-mediated Release of Cellular Cholesterol and Phospholipid to Generate High Density Lipoprotein* , 2004, Journal of Biological Chemistry.
[2] J. Whitsett,et al. Lamellar Body Formation in Normal and Surfactant Protein B-Deficient Fetal Mice , 2000, Laboratory Investigation.
[3] C. Higgins,et al. ABC transporters: from microorganisms to man. , 1992, Annual review of cell biology.
[4] S. Yokoyama,et al. Effects of Mutations of ABCA1 in the First Extracellular Domain on Subcellular Trafficking and ATP Binding/Hydrolysis* 210 , 2003, The Journal of Biological Chemistry.
[5] N. Cheong,et al. Functional and Trafficking Defects in ATP Binding Cassette A3 Mutants Associated with Respiratory Distress Syndrome* , 2006, Journal of Biological Chemistry.
[6] R. Xavier,et al. ABCA3 inactivation in mice causes respiratory failure, loss of pulmonary surfactant, and depletion of lung phosphatidylglycerols⃞ Published, JLR Papers in Press, December 1, 2006. , 2007, Journal of Lipid Research.
[7] H. Arai,et al. ABCA3 as a Lipid Transporter in Pulmonary Surfactant Biogenesis* , 2007, Journal of Biological Chemistry.
[8] I. Yoshida,et al. Expression of ABCA3, a causative gene for fatal surfactant deficiency, is up-regulated by glucocorticoids in lung alveolar type II cells. , 2004, Biochemical and biophysical research communications.
[9] M. Derrick,et al. Structure and properties of surfactant protein B. , 1998, Biochimica et biophysica acta.
[10] Kazumitsu Ueda,et al. ABCA7, a molecule with unknown function , 2006, FEBS letters.
[11] P. Sly,et al. Altered stability of pulmonary surfactant in SP-C-deficient mice , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[12] W. J. Dyer,et al. A rapid method of total lipid extraction and purification. , 1959, Canadian journal of biochemistry and physiology.
[13] O. Kawanami,et al. ABCA3 is a lamellar body membrane protein in human lung alveolar type II cells1 , 2001, FEBS letters.
[14] R. Veldhuizen,et al. The role of lipids in pulmonary surfactant. , 1998, Biochimica et biophysica acta.
[15] J. Whitsett,et al. ABCA3 gene mutations in newborns with fatal surfactant deficiency. , 2004, The New England journal of medicine.
[16] S. Yokoyama. Assembly of high density lipoprotein by the ABCA1/apolipoprotein pathway. , 2005, Current opinion in lipidology.
[17] J. Whitsett,et al. ABCA3 mutations associated with pediatric interstitial lung disease. , 2005, American journal of respiratory and critical care medicine.
[18] C. Dodia,et al. Isolation of lamellar bodies from rat granular pneumocytes in primary culture. , 1983, Biochimica et biophysica acta.
[19] A. Gilfillan,et al. Single plate separation of lung phospholipids including disaturated phosphatidylcholine. , 1983, Journal of lipid research.
[20] B. Stripp,et al. Targeted disruption of the surfactant protein B gene disrupts surfactant homeostasis, causing respiratory failure in newborn mice. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[21] K. Ueda,et al. Characterization and Classification of ATP-binding Cassette Transporter ABCA3 Mutants in Fatal Surfactant Deficiency* , 2006, Journal of Biological Chemistry.
[22] C. Dodia,et al. Localization, synthesis, and processing of surfactant protein SP-C in rat lung analyzed by epitope-specific antipeptide antibodies. , 1994, The Journal of biological chemistry.
[23] G. van Meer,et al. Natural Phosphatidylcholine Is Actively Translocated across the Plasma Membrane to the Surface of Mammalian Cells* , 2004, Journal of Biological Chemistry.
[24] H. Geuze,et al. Intracellular processing of pulmonary surfactant protein B in an endosomal/lysosomal compartment. , 1992, The American journal of physiology.
[25] G. van Meer,et al. Transport of sphingomyelin to the cell surface is inhibited by brefeldin A and in mitosis, where C6-NBD-sphingomyelin is translocated across the plasma membrane by a multidrug transporter activity. , 1997, Journal of cell science.
[26] S. Russo,et al. Biosynthesis of Surfactant Protein C (SP-C) , 2002, The Journal of Biological Chemistry.
[27] G. Chevalier,et al. In Vivo incorporation of choline‐3H, leucine‐3H and galactose‐3H in alveolar type II pneumocytes in relation to surfactant synthesis. A quantitative radioautographic study in mouse by electron microscopy , 1972 .
[28] M. Beers. Inhibition of Cellular Processing of Surfactant Protein C by Drugs Affecting Intracellular pH Gradients* , 1996, The Journal of Biological Chemistry.
[29] J. R. McMillan,et al. Mutations in lipid transporter ABCA12 in harlequin ichthyosis and functional recovery by corrective gene transfer. , 2005, The Journal of clinical investigation.
[30] J. Wenzel,et al. ABC A-subfamily transporters: structure, function and disease. , 2006, Biochimica et biophysica acta.