CFTR Modulator Therapies in Cystic Fibrosis
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Publisher
Springer Basel
Link
http://link.springer.com/content/pdf/10.1007/978-3-0348-0977-1_6
Reference83 articles.
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2. Ambort D, Johansson ME, Gustafsson JK, Nilsson HE, Ermund A, Johansson BR, Koeck PJ, Hebert H, Hansson GC (2012) Calcium and pH-dependent packing and release of the gel-forming MUC2 mucin. Proc Natl Acad Sci USA 109(15):5645–5650. doi: 10.1073/pnas.1120269109
3. Anderson MP, Gregory RJ, Thompson S, Souza DW, Paul S, Mulligan RC, Smith AE, Welsh MJ (1991) Demonstration that CFTR is a chloride channel by alteration of its anion selectivity. Science 253(5016):202–205
4. Banner KH, De Jonge H, Elborn S, Growcott E, Gulbins E, Konstan M, Moss R, Poll C, Randell SH, Rossi AG, Thomas L, Waltz D (2009) Highlights of a workshop to discuss targeting inflammation in cystic fibrosis. J Cyst Fibros Off J Eur Cyst Fibros Soc 8(1):1–8
5. Bedwell DM, Kaenjak A, Benos DJ, Bebok Z, Bubien JK, Hong J, Tousson A, Clancy JP, Sorscher EJ (1997) Suppression of a CFTR premature stop mutation in a bronchial epithelial cell line. Nat Med 3(11):1280–1284
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