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The Journal of Experimental Medicine|October 1, 2008
Human PMS2 deficiency is associated with impaired immunoglobulin class switch recombinationSophie Péron, Ayse Metin, Pauline Gardès, et al.
The New England Journal of Medicine|May 5, 2006
Inherited and somatic CD3zeta mutations in a patient with T-cell deficiencyFrédéric Rieux-Laucat, Claire Hivroz, Annick Lim, et al.
Journal of Clinical Immunology|February 8, 2016
Genetic, Cellular and Clinical Features of ICF Syndrome: a French National SurveyDelphine Sterlin, Guillaume Velasco, Despina Moshous, et al.
Blood|February 12, 2016
Polygenic mutations in the cytotoxicity pathway increase susceptibility to develop HLH immunopathology in miceFernando E Sepulveda, Alexandrine Garrigue, Sophia Maschalidi, et al.
Pediatrics|October 27, 2010
Laronidase for cardiopulmonary disease in Hurler syndrome 12 years after bone marrow transplantationVassili Valayannopoulos, Jacques de Blic, Nizar Mahlaoui, et al.
Blood|December 11, 2012
Human iNKT and MAIT cells exhibit a PLZF-dependent proapoptotic propensity that is counterbalanced by XIAPStéphane Gérart, Sophie Sibéril, Emmanuel Martin, et al.
The Journal of Experimental Medicine|July 7, 2005
Regulation of natural cytotoxicity by the adaptor SAP and the Src-related kinase FynCoralie Bloch-Queyrat, Marie-Claude Fondanèche, Riyan Chen, et al.
Molecular and Cellular Biology|December 24, 2008
The C-terminal domain of Cernunnos/XLF is dispensable for DNA repair in vivoLaurent Malivert, Isabelle Callebaut, Paola Rivera-Munoz, et al.
The Journal of Allergy and Clinical Immunology. Global|December 4, 2025
Lymphedema in patients with X-linked severe combined immunodeficiencyFilippo Consonni, Suk See De Ravin, Stephane Vignes, et al.
European Journal of Pediatrics|December 6, 2005
Burkholderia pseudomallei infection in chronic granulomatous diseaseRaffaele Renella, Jean-Marie Perez, Sylvie Chollet-Martin, et al.
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