The genetics of interstitial lung diseases due to surfactant dysfunction disorders in children
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[1] S. Guttentag,et al. Expression profiles of hydrophobic surfactant proteins in children with diffuse chronic lung disease , 2005, Respiratory research.
[2] C. Houdayer,et al. Mutation of SFTPC in infantile pulmonary alveolar proteinosis with or without fibrosing lung disease , 2004, American journal of medical genetics. Part A.
[3] J. Whitsett,et al. ABCA3 gene mutations in newborns with fatal surfactant deficiency. , 2004, The New England journal of medicine.
[4] L. Nogee. Alterations in SP-B and SP-C expression in neonatal lung disease. , 2004, Annual review of physiology.
[5] A. Hamvas,et al. Prolonged Survival in Hereditary Surfactant Protein B (SP-B) Deficiency Associated with a Novel Splicing Mutation , 2000, Pediatric Research.
[6] J. Whitsett,et al. Lamellar Body Formation in Normal and Surfactant Protein B-Deficient Fetal Mice , 2000, Laboratory Investigation.
[7] G. Holcomb. Lung transplantation for treatment of infants with surfactant protein B deficiency , 1998 .
[8] M. W. Thompson,et al. Transient surfactant protein B deficiency in a term infant with severe respiratory failure. , 1998, The Journal of pediatrics.
[9] C. Mendelson,et al. Molecular and cellular processing of lung surfactant 1 , 1994, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.
[10] H. Colten,et al. A mutation in the surfactant protein B gene responsible for fatal neonatal respiratory disease in multiple kindreds. , 1994, The Journal of clinical investigation.
[11] H. Colten,et al. Brief report: deficiency of pulmonary surfactant protein B in congenital alveolar proteinosis. , 1993, The New England journal of medicine.
[12] Michael F Beers,et al. Surfactant protein C biosynthesis and its emerging role in conformational lung disease. , 2005, Annual review of physiology.