Showing the latest 487 publications
Publications 351-360 of 487
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Prevalence and clinical challenges among adults with primary immunodeficiency and recombination-activating gene deficiency
Lawless, D., Geier, C., Farmer, J., Lango Allen, H., Thwaites, D., Atschekzei, F., et al.
The Journal of Allergy and Clinical Immunology
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Abnormalities of age-related T cell senescence in Parkinson's disease
Williams-Gray, C., Wijeyekoon, R., Scott, K., Hayat, S., Barker, R., Jones, J.
Journal of Neuroinflammation
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A clinical and molecular characterisation of CRB1-associated maculopathy
Khan, K., Robson, A., Mahroo, O., Arno, G., Inglehearn, C., Armengol, M., et al.
European Journal of Human Genetics
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Better governance, better access: practising responsible data sharing in the METADAC governance infrastructure
Murtagh, M., Blell, M., Butters, O., Cowley, L., Dove, E., Goodman, A., et al.
Human Genomics
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Identification of rare sequence variation underlying heritable pulmonary arterial hypertension
Gräf, S., Haimel, M., Bleda, M., Hadinnapola, C., Southgate, L., Li, W., et al.
Nature Communications
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Shared genetic effects on chromatin and gene expression indicate a role for enhancer priming in immune response
Alasoo, K., Rodrigues, J., Mukhopadhyay, S., Knights, A., Mann, A., Kundu, K., et al.
Nature Genetics
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DETAILED RETINAL IMAGING IN CARRIERS OF OCULAR ALBINISM
Khan, K., Lord, E., Arno, G., Islam, F., Carss, K., Raymond, F., et al.
Retina (Philadelphia, Pa.)
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Multiple sclerosis risk variants alter expression of co-stimulatory genes in B cells
Smets, I., Fiddes, B., Garcia-Perez, J., He, D., Mallants, K., Liao, W., et al.
Brain: A Journal of Neurology
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NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease
Schwerd, T., Bryant, R., Pandey, S., Capitani, M., Meran, L., Cazier, J., et al.
Mucosal Immunology
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Nbeal2 interacts with Dock7, Sec16a, and Vac14
Mayer, L., Jasztal, M., Pardo, M., Aguera de Haro, S., Collins, J., Bariana, T., et al.
Blood