Showing the latest 475 publications
Publications 441-450 of 475
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Transcriptional diversity during lineage commitment of human blood progenitors
Chen, L., Kostadima, M., Martens, J., Canu, G., Garcia, S., Turro, E., et al.
Science (New York, N.Y.)
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Multi-parametric flow cytometric and genetic investigation of the peripheral B cell compartment in human type 1 diabetes
Thompson, W., Pekalski, M., Simons, H., Smyth, D., Castro-Dopico, X., Guo, H., et al.
Clinical and Experimental Immunology
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Role of dopamine D2 receptors in human reinforcement learning
Eisenegger, C., Naef, M., Linssen, A., Clark, L., Gandamaneni, P., Müller, U., et al.
Neuropsychopharmacology: Official Publication of the American College of Neuropsychopharmacology
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Investigation of soluble and transmembrane CTLA-4 isoforms in serum and microvesicles
Esposito, L., Hunter, K., Clark, J., Rainbow, D., Stevens, H., Denesha, J., et al.
Journal of Immunology (Baltimore, Md.: 1950)
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A type I interferon transcriptional signature precedes autoimmunity in children genetically at risk for type 1 diabetes
Ferreira, R., Guo, H., Coulson, R., Smyth, D., Pekalski, M., Burren, O., et al.
Diabetes
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Plasma concentrations of soluble IL-2 receptor α (CD25) are increased in type 1 diabetes and associated with reduced C-peptide levels in young patients
Downes, K., Marcovecchio, M., Clarke, P., Cooper, J., Ferreira, R., Howson, J., et al.
Diabetologia
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The IL23R A/Gln381 allele promotes IL-23 unresponsiveness in human memory T-helper 17 cells and impairs Th17 responses in psoriasis patients
Di Meglio, P., Villanova, F., Napolitano, L., Tosi, I., Terranova Barberio, M., Mak, R., et al.
The Journal of Investigative Dermatology
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FOXO in the hole: leveraging GWAS for outcome and function
Gregersen, P., Manjarrez-Orduño, N.
Cell
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Human SNP links differential outcomes in inflammatory and infectious disease to a FOXO3-regulated pathway
Lee, J., Espéli, M., Anderson, C., Linterman, M., Pocock, J., Williams, N., et al.
Cell
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Negligible impact of rare autoimmune-locus coding-region variants on missing heritability
Hunt, K., Mistry, V., Bockett, N., Ahmad, T., Ban, M., Barker, J., et al.
Nature