Persistent and aggressive bacteria in the lungs of cystic fibrosis children
Author:
Publisher
Oxford University Press (OUP)
Subject
General Medicine
Link
http://academic.oup.com/bmb/article-pdf/61/1/81/25151948/81.pdf
Reference115 articles.
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2. Chace KV, Flux M, Sachdev GP. Comparison of physicochemical properties of purified mucus glycoproteins isolated from respiratory secretions of cystic fibrosis and asthmatic patients. Biochemistry1985; 24: 7334–41
3. Bals R, Weiner DJ, Wilson JM. The innate immune system in cystic fibrosis lung disease. J Clin Invest1999; 103: 303–7
4. Smith J, Travis S, Greenberg E, Welsh M. Cystic fibrosis airway epithelia fail to kill bacteria because of abnormal airway surface fluid. Cell1996; 85: 223–36
5. White SH, Wimley WC, Selsted ME. Structure function and membrane integration of defensins. Curr Opin Struct Biol1995; 5: 521–7
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