CFTR and Cystic Fibrosis
Author:
Publisher
Springer New York
Link
http://link.springer.com/content/pdf/10.1007/978-1-4939-3366-2_16
Reference144 articles.
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2. Aleksandrov L, Aleksandrov AA, Chang XB et al (2002) The first nucleotide binding domain of cystic fibrosis conductance regulator is a site of stable nucleotide interaction, whereas the second is a site of rapid turnover. J Biol Chem 277:15419–15425
3. Amaral MD (2005) Processing of CFTR: traversing the cellular maze–how much CFTR needs to go through to avoid cystic fibrosis? Pediatr Pulmonol 39(6):479–491
4. Amin ML (2013) P-glycoprotein inhibition for optimal drug delivery. Drug Target Insights 7:27–34
5. Andersen DH (1938) Cystic fibrosis of the pancreas and its relationship to celiac disease: a clinical and pathologic study. Am J Dis Child 56(2):344–399
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1. Coming Full Circle: Reflections and Inspirations from a Cystic Fibrosis Patient Scientist Panel;INQUIRY: The Journal of Health Care Organization, Provision, and Financing;2022-01
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3. Cystic fibrosis lung environment and Pseudomonas aeruginosa infection;BMC Pulmonary Medicine;2016-12
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