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Blood|December 25, 2012
Characteristics and outcome of early-onset, severe forms of Wiskott-Aldrich syndromeNizar Mahlaoui, Isabelle Pellier, Cécile Mignot, et al.
British Journal of Haematology|June 13, 2002
Functional consequences of perforin gene mutations in 22 patients with familial haemophagocytic lymphohistiocytosisJérôme Feldmann, Françoise Le Deist, Marie Ouachée-Chardin, et al.
Nature Immunology|September 6, 2003
Human uracil-DNA glycosylase deficiency associated with profoundly impaired immunoglobulin class-switch recombinationKohsuke Imai, Geir Slupphaug, Wen-I Lee, et al.
The New England Journal of Medicine|October 2, 2004
Autoimmune lymphoproliferative syndrome with somatic Fas mutationsEliska Holzelova, Cédric Vonarbourg, Marie-Claude Stolzenberg, et al.
Pediatrics|March 22, 2006
Hematopoietic stem cell transplantation in hemophagocytic lymphohistiocytosis: a single-center report of 48 patientsMarie Ouachée-Chardin, Caroline Elie, Geneviève de Saint Basile, et al.
The Journal of Allergy and Clinical Immunology|October 6, 2014
CD45RA depletion in HLA-mismatched allogeneic hematopoietic stem cell transplantation for primary combined immunodeficiency: A preliminary studyFabien Touzot, Bénédicte Neven, Liliane Dal-Cortivo, et al.
The Journal of Cell Biology|November 5, 2016
Kinesin-1 controls mast cell degranulation and anaphylaxis through PI3K-dependent recruitment to the granular Slp3/Rab27b complexIsabelle Munoz, Luca Danelli, Julien Claver, et al.
Hemasphere|April 3, 2023
CTP Synthase 1 Is a Novel Therapeutic Target in LymphomaHélène Asnagli, Norbert Minet, Christina Pfeiffer, et al.
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