Detection of Cystic Fibrosis Serological Biomarkers Using a T7 Phage Display Library
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-017-18041-2.pdf
Reference50 articles.
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3. Carter, C. J. Pathogen and autoantigen homologous regions within the cystic fibrosis transmembrane conductance regulator (CFTR) protein suggest an autoimmune treatable component of cystic fibrosis. FEMS immunology and medical microbiology 62, 197–214, https://doi.org/10.1111/j.1574-695X.2011.00803.x (2011).
4. Budding, K., van de Graaf, E. A., Hoefnagel, T., Hack, C. E. & Otten, H. G. Anti-BPIFA1/SPLUNC1: a new autoantibody prevalent in patients with endstage cystic fibrosis. Journal of cystic fibrosis: official journal of the European Cystic Fibrosis Society 13, 281–288, https://doi.org/10.1016/j.jcf.2013.10.005 (2014).
5. Pedersen, S. K. et al. An immunoproteomic approach for identification of clinical biomarkers for monitoring disease: application to cystic fibrosis. Molecular & cellular proteomics: MCP 4, 1052–1060, https://doi.org/10.1074/mcp.M400175-MCP200 (2005).
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