Showing the latest 464 publications
Publications 401-410 of 464
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C13orf31 (FAMIN) is a central regulator of immunometabolic function
Cader, M., Boroviak, K., Zhang, Q., Assadi, G., Kempster, S., Sewell, G., et al.
Nature Immunology
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Increased THEMIS First Exon Usage in CD4+ T-Cells Is Associated with a Genotype that Is Protective against Multiple Sclerosis
Davies, J., Thompson, S., Kaur-Sandhu, H., Sawcer, S., Coles, A., Ban, M., et al.
PloS One
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Information recovery from low coverage whole-genome bisulfite sequencing
Libertini, E., Heath, S., Hamoudi, R., Gut, M., Ziller, M., Czyz, A., et al.
Nature Communications
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Carrots and sticks fail to change behavior in cocaine addiction
Ersche, K., Gillan, C., Jones, P., Williams, G., Ward, L., Luijten, M., et al.
Science (New York, N.Y.)
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Inherited platelet disorders: toward DNA-based diagnosis
Lentaigne, C., Freson, K., Laffan, M., Turro, E., Ouwehand, W.
Blood
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A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders
Simeoni, I., Stephens, J., Hu, F., Deevi, S., Megy, K., Bariana, T., et al.
Blood
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A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing loss
Stritt, S., Nurden, P., Turro, E., Greene, D., Jansen, S., Westbury, S., et al.
Blood
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Peripheral Immune Cell Populations Associated with Cognitive Deficits and Negative Symptoms of Treatment-Resistant Schizophrenia
Fernandez-Egea, E., Vértes, P., Flint, S., Turner, L., Mustafa, S., Hatton, A., et al.
PloS One
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De Novo Mutations in PDE10A Cause Childhood-Onset Chorea with Bilateral Striatal Lesions
Mencacci, N., Kamsteeg, E., Nakashima, K., R'Bibo, L., Lynch, D., Balint, B., et al.
American Journal of Human Genetics
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The cellular composition of the human immune system is shaped by age and cohabitation
Carr, E., Dooley, J., Garcia-Perez, J., Lagou, V., Lee, J., Wouters, C., et al.
Nature Immunology