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Cell Reports. Medicine|January 27, 2023
Severe hematopoietic stem cell inflammation compromises chronic granulomatous disease gene therapySteicy Sobrino, Alessandra Magnani, Michaela Semeraro, et al.
Blood|September 3, 2011
A survey of 90 patients with autoimmune lymphoproliferative syndrome related to TNFRSF6 mutationBénédicte Neven, Aude Magerus-Chatinet, Benoit Florkin, et al.
The Journal of Allergy and Clinical Immunology|September 2, 2014
Immune deficiency-related enteropathy-lymphocytopenia-alopecia syndrome results from tetratricopeptide repeat domain 7A deficiencyRoxane Lemoine, Jana Pachlopnik-Schmid, Henner F Farin, et al.
Science Immunology|March 25, 2022
Gain-of-function IKZF1 variants in humans cause immune dysregulation associated with abnormal T/B cell late differentiationAkihiro Hoshino, David Boutboul, Yuan Zhang, et al.
Science Advances|October 17, 2025
Kinesin-1 coordinates cross-talk between microtubule and actin cytoskeletons during dendritic cell migrationPierre Duquesne, Céline Aoun, Mathieu Kurowska, et al.
The Journal of Clinical Investigation|November 4, 2009
Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cellsMarjorie Côte, Mickaël M Ménager, Agathe Burgess, et al.
Plos One|April 22, 2009
Chronic granulomatous disease: the European experienceJ Merlijn van den Berg, Elsbeth van Koppen, Anders Ahlin, et al.
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