Showing the latest 487 publications
Publications 381-390 of 487
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HGVA: the Human Genome Variation Archive
Lopez, J., Coll, J., Haimel, M., Kandasamy, S., Tarraga, J., Furio-Tari, P., et al.
Nucleic Acids Research
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CMV immune evasion and manipulation of the immune system with aging
Jackson, S., Redeker, A., Arens, R., van Baarle, D., van den Berg, S., Benedict, C., et al.
GeroScience
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Common genetic variation drives molecular heterogeneity in human iPSCs
Kilpinen, H., Goncalves, A., Leha, A., Afzal, V., Alasoo, K., Ashford, S., et al.
Nature
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Factors Affecting Mortality and Length of Stay Following Clostridium Difficile Associated Diarrhoea: Validating A Consistent Scoring System
W, W., D, C., G, M., E, G., V, U.
Archives of Clinical Microbiology
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Latent Cytomegalovirus (CMV) Infection Does Not Detrimentally Alter T Cell Responses in the Healthy Old, But Increased Latent CMV Carriage Is Related to Expanded CMV-Specific T Cells
Jackson, S., Sedikides, G., Okecha, G., Poole, E., Sinclair, J., Wills, M.
Frontiers in Immunology
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Human IL-6RhiTIGIT- CD4+CD127lowCD25+ T cells display potent in vitro suppressive capacity and a distinct Th17 profile
Ferreira, R., Rainbow, D., Rubio García, A., Pekalski, M., Porter, L., Oliveira, J., et al.
Clinical Immunology (Orlando, Fla.)
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Specific Alleles of CLN7/MFSD8, a Protein That Localizes to Photoreceptor Synaptic Terminals, Cause a Spectrum of Nonsyndromic Retinal Dystrophy
Khan, K., El-Asrag, M., Ku, C., Holder, G., McKibbin, M., Arno, G., et al.
Investigative Ophthalmology & Visual Science
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In-depth immunophenotyping data of IL-6R on the human peripheral regulatory T cell (Treg) compartment
Ferreira, R., Rainbow, D., Rubio García, A., Pekalski, M., Porter, L., Oliveira, J., et al.
Data in Brief
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Atomoxetine effects on attentional bias to drug-related cues in cocaine dependent individuals
Passamonti, L., Luijten, M., Ziauddeen, H., Coyle-Gilchrist, I., Rittman, T., Brain, S., et al.
Psychopharmacology
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PIGO deficiency: palmoplantar keratoderma and novel mutations
Morren, M., Jaeken, J., Visser, G., Salles, I., Van Geet, C., et al.
Orphanet Journal of Rare Diseases