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The Lancet. Neurology|November 5, 2013
Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control studyGillian I Rice, Gabriella M A Forte, Marcin Szynkiewicz, et al.The New England Journal of Medicine|October 23, 2009
Multicenter analysis of glucocerebrosidase mutations in Parkinson's diseaseE Sidransky, M A Nalls, J O Aasly, et al.The Journal of Experimental Medicine|September 12, 2022
Impaired IL-23-dependent induction of IFN-γ underlies mycobacterial disease in patients with inherited TYK2 deficiencyMasato Ogishi, Andrés Augusto Arias, Rui Yang, et al.Scientific Reports|July 3, 2026
Risk factors for acquisition of SARS-CoV-2 Omicron variant among a prospective cohort of French Healthcare Workers: impact of hybrid immunityDavid Lebeaux, Estelle Lu, Béatrice Parfait, et al.Scientific Data|March 2, 2022
Worldwide diversity of endophytic fungi and insects associated with dormant tree twigsIva Franić, Simone Prospero, Kalev Adamson, et al.Scientific Reports|July 18, 2023
Climate, host and geography shape insect and fungal communities of treesIva Franić, Eric Allan, Simone Prospero, et al.Cell|February 3, 2023
Human IRF1 governs macrophagic IFN-γ immunity to mycobacteriaJérémie Rosain, Anna-Lena Neehus, Jérémy Manry, et al.The Journal of Experimental Medicine|October 1, 2024
Incontinentia pigmenti underlies thymic dysplasia, autoantibodies to type I IFNs, and viral diseasesJérémie Rosain, Tom Le Voyer, Xian Liu, et al.Science (New York, N.Y.)|December 20, 2022
Inborn errors of OAS-RNase L in SARS-CoV-2-related multisystem inflammatory syndrome in childrenDanyel Lee, Jérémie Le Pen, Ahmad Yatim, et al.Science (New York, N.Y.)|February 29, 2024
The immunopathological landscape of human pre-TCRα deficiency: From rare to common variantsMarie Materna, Ottavia M Delmonte, Marita Bosticardo, et al.Pageof 166