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Genetic Epidemiology|March 20, 2001
Genome-wide linkage analyses of total serum IgE using variance components analysis in asthmatic familiesR A Mathias, L R Freidhoff, M N Blumenthal, et al.Proceedings of the National Academy of Sciences of the United States of America|September 4, 2024
Inherited human RelB deficiency impairs innate and adaptive immunity to infectionTom Le Voyer, Majistor Raj Luxman Maglorius Renkilaraj, Kunihiko Moriya, et al.The Journal of Experimental Medicine|June 13, 2024
Gain-of-function human UNC93B1 variants cause systemic lupus erythematosus and chilblain lupusClémence David, Carlos A Arango-Franco, Mihaly Badonyi, et al.The Journal of Experimental Medicine|July 16, 2026
Familial pulmonary alveolar proteinosis and type I interferonopathy by mutation of STAT2 (TIMS2)Conor Gruber, Meredith Ramba, Bineeta Debnath, et al.Science Immunology|February 10, 2023
Human IL-23 is essential for IFN-γ-dependent immunity to mycobacteriaQuentin Philippot, Masato Ogishi, Jonathan Bohlen, et al.Cell|October 24, 2023
Human MCTS1-dependent translation of JAK2 is essential for IFN-γ immunity to mycobacteriaJonathan Bohlen, Qinhua Zhou, Quentin Philippot, et al.Journal of Human Immunity|May 25, 2026
Chronic granulomatous disease: Clinical, microbial, and genetic findings in 39 Colombian patientsJulian Rojas, Carlos A Arango-Franco, Marcela Moncada-Velez, et al.The Journal of Clinical Investigation|October 15, 2024
Autoinflammation in patients with leukocytic CBL loss of heterozygosity is caused by constitutive ERK-mediated monocyte activationJonathan Bohlen, Ivan Bagarić, Taja Vatovec, et al.The Journal of Clinical Investigation|July 4, 2018
Inherited p40phox deficiency differs from classic chronic granulomatous diseaseAnnemarie van de Geer, Alejandro Nieto-Patlán, Douglas B Kuhns, et al.Cell|December 29, 2023
Human inherited CCR2 deficiency underlies progressive polycystic lung diseaseAnna-Lena Neehus, Brenna Carey, Marija Landekic, et al.Pageof 30