CCDC88B is required for pathogenesis of inflammatory bowel disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry
Link
http://www.nature.com/articles/s41467-017-01381-y.pdf
Reference41 articles.
1. Jostins, L. et al. Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. Nature 491, 119-124 (2012).
2. Liu, J. Z. et al. Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. Nat. Genet. 47, 979–986 (2015).
3. Kaplan, G. G. The global burden of IBD: from 2015 to 2025. Nat Rev Gastroenterol. Hepatol. 12, 720–727 (2015).
4. Fodil, N., Langlais, D. & Gros, P. Primary Immunodeficiencies and Inflammatory Disease: A Growing Genetic Intersection. Trends Immunol. 37, 126–140 (2016).
5. Kennedy, J. M. et al. CCDC88B is a novel regulator of maturation and effector functions of T cells during pathological inflammation. J. Exp. Med. 211, 2519–2535 (2014).
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