Molecular mechanisms of biogenesis and exocytosis of cytotoxic granules von de Saint Basile, Geneviève, Ménasché, Gaël, Fischer, Alain

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Immunotherapy of Familial Hemophagocytic Lymphohistiocytosis With Antithymocyte Globulins: A Single-Center Retrospective Report of 38 Patients von Mahlaoui, Nizar, Ouachee-Chardin, Marie, de Saint Basile, Genevieve, Neven, Benedicte, Picard, Capucine, Blanche, Stephane, Fischer, Alain

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TTC7A mutations disrupt intestinal epithelial apicobasal polarity von Bigorgne, Amélie E, Farin, Henner F, Lemoine, Roxane, Mahlaoui, Nizar, Lambert, Nathalie, Gil, Marine, Schulz, Ansgar, Philippet, Pierre, Schlesser, Patrick, Abrahamsen, Tore G, Oymar, Knut, Davies, E Graham, Ellingsen, Christian Lycke, Leteurtre, Emmanuelle, Moreau-Massart, Brigitte, Berrebi, Dominique, Bole-Feysot, Christine, Nischke, Patrick, Brousse, Nicole, Fischer, Alain, Clevers, Hans, de Saint Basile, Geneviève

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Gene Therapy of Human Severe Combined Immunodeficiency (SCID)-X1 Disease von Cavazzana-Calvo, Marina, Hacein-Bey, Salima, Geneviève de Saint Basile, Gross, Fabian, Yvon, Eric, Nusbaum, Patrick, Selz, Françoise, Hue, Christophe, Certain, Stéphanie, Casanova, Jean-Laurent, Bousso, Philippe, Le Deist, Françoise, Fischer, Alain

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Terminal transport of lytic granules to the immune synapse is mediated by the kinesin-1/Slp3/Rab27a complex von Kurowska, Mathieu, Goudin, Nicolas, Nehme, Nadine T., Court, Magali, Garin, Jérôme, Fischer, Alain, de Saint Basile, Geneviève, Ménasché, Gaël

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Kinesin-1 regulates antigen cross-presentation through the scission of tubulations from early endosomes in dendritic cells von Belabed, Meriem, Mauvais, François-Xavier, Maschalidi, Sophia, Kurowska, Mathieu, Goudin, Nicolas, Huang, Jian-Dong, Fischer, Alain, de Saint Basile, Geneviève, van Endert, Peter, Sepulveda, Fernando E., Ménasché, Gaël

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Hematopoietic Stem Cell Transplantation in Hemophagocytic Lymphohistiocytosis: A Single-Center Report of 48 Patients von Ouachee-Chardin, Marie, Elie, Caroline, de Saint Basile, Genevieve, Le Deist, Francoise, Mahlaoui, Nizar, Picard, Capucine, Neven, Benedicte, Casanova, Jean-Laurent, Tardieu, Marc, Cavazzana-Calvo, Marina, Blanche, Stephane, Fischer, Alain

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Perforin Gene Defects in Familial Hemophagocytic Lymphohistiocytosis von Stepp, Susan E., Dufourcq-Lagelouse, Rémi, Le Deist, Françoise, Bhawan, Sadhna, Certain, Stéphanie, Mathew, Porunelloor A., Henter, Jan-Inge, Bennett, Michael, Fischer, Alain, Geneviève de Saint Basile, Kumar, Vinay

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Inherited defects in lymphocyte cytotoxic activity von Schmid, Jana P, Côte, Marjorie, Ménager, Mickaël M, Burgess, Agathe, Nehme, Nadine, Ménasché, Gaël, Fischer, Alain, de Saint Basile, Geneviève

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Therapeutic effect of JAK1/2 blockade on the manifestations of hemophagocytic lymphohistiocytosis in mice von Maschalidi, Sophia, Sepulveda, Fernando E., Garrigue, Alexandrine, Fischer, Alain, de Saint Basile, Geneviève

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Chronic Infantile Neurological Cutaneous and Articular Syndrome Is Caused by Mutations in CIAS1, a Gene Highly Expressed in Polymorphonuclear Cells and Chondrocytes von Feldmann, Jérôme, Prieur, Anne-Marie, Quartier, Pierre, Berquin, Patrick, Certain, Stéphanie, Cortis, Elisabetta, Teillac-Hamel, Dominique, Fischer, Alain, Basile, Geneviève de Saint

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Secretory cytotoxic granule maturation and exocytosis require the effector protein hMunc13-4 von Ménager, Mickaël M, Ménasché, Gaël, Romao, Maryse, Knapnougel, Perrine, Ho, Chen-Hsuan, Garfa, Mériem, Raposo, Graça, Feldmann, Jérôme, Fischer, Alain, de Saint Basile, Geneviève

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Defective NKT cell development in mice and humans lacking the adapter SAP, the X-linked lymphoproliferative syndrome gene product von Pasquier, Benoit, Yin, Luo, Fondanèche, Marie-Claude, Relouzat, Francis, Bloch-Queyrat, Coralie, Lambert, Nathalie, Fischer, Alain, de Saint-Basile, Geneviève, Latour, Sylvain

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Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T cell lymphomas with hemophagocytic lymphohistiocytic syndrome von Gayden, Tenzin, Sepulveda, Fernando E., Khuong-Quang, Dong-Anh, Pratt, Jonathan, Valera, Elvis T., Garrigue, Alexandrine, Kelso, Susan, Sicheri, Frank, Mikael, Leonie G., Hamel, Nancy, Bajic, Andrea, Dali, Rola, Deshmukh, Shriya, Dervovic, Dzana, Schramek, Daniel, Guerin, Frédéric, Taipale, Mikko, Nikbakht, Hamid, Majewski, Jacek, Moshous, Despina, Charlebois, Janie, Abish, Sharon, Bole-Feysot, Christine, Nitschke, Patrick, Bader-Meunier, Brigitte, Mitchell, David, Thieblemont, Catherine, Battistella, Maxime, Gravel, Simon, Nguyen, Van-Hung, Conyers, Rachel, Diana, Jean-Sebastien, McCormack, Chris, Prince, H. Miles, Besnard, Marianne, Blanche, Stephane, Ekert, Paul G., Fraitag, Sylvie, Foulkes, William D., Fischer, Alain, Neven, Bénédicte, Michonneau, David, de Saint Basile, Geneviève, Jabado, Nada

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Autoimmunity in Wiskott-Aldrich Syndrome: Risk Factors, Clinical Features, and Outcome in a Single-Center Cohort of 55 Patients von Dupuis-Girod, Sophie, Medioni, Jacques, Haddad, Elie, Quartier, Pierre, Cavazzana-Calvo, Marina, Le Deist, Francoise, de Saint Basile, Genevieve, Delaunay, Jean, Schwarz, Klaus, Casanova, Jean-Laurent, Blanche, Stephane, Fischer, Alain

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Munc13-4 Regulates Granule Secretion in Human Neutrophils von Pivot-Pajot, Christophe, Varoqueaux, Frederique, de Saint Basile, Genevieve, Bourgoin, Sylvain G

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XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome von Rigaud, Stéphanie, Fondanèche, Marie-Claude, Lambert, Nathalie, Pasquier, Benoit, Mateo, Véronique, Soulas, Pauline, Galicier, Lionel, Le Deist, Françoise, Rieux-Laucat, Frédéric, Revy, Patrick, Fischer, Alain, de Saint Basile, Geneviève, Latour, Sylvain

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Small Molecule Inhibitors of Interferon‐Induced JAK‐STAT Signalling von Thoidingjam, Leishemba K., Blouin, Cédric M., Gaillet, Christine, Brion, Aurélien, Solier, Stéphanie, Niyomchon, Supaporn, El Marjou, Ahmed, Mouasni, Sara, Sepulveda, Fernando E., Saint Basile, Geneviève, Lamaze, Christophe, Rodriguez, Raphaël

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Progressive neurologic dysfunctions 20 years after allogeneic bone marrow transplantation for Chediak-Higashi syndrome von Tardieu, Marc, Lacroix, Catherine, Neven, Bénédicte, Bordigoni, Pierre, Basile, Geneviève de Saint, Blanche, Stéphane, Fischer, Alain

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Pediatric-onset Evans syndrome: Heterogeneous presentation and high frequency of monogenic disorders including LRBA and CTLA4 mutations von Besnard, Caroline, Levy, Eva, Aladjidi, Nathalie, Stolzenberg, Marie-Claude, Magerus-Chatinet, Aude, Alibeu, Olivier, Nitschke, Patrick, Blanche, Stéphane, Hermine, Olivier, Jeziorski, Eric, Landman-Parker, Judith, Leverger, Guy, Mahlaoui, Nizar, Michel, Gérard, Pellier, Isabelle, Suarez, Felipe, Thuret, Isabelle, de Saint-Basile, Geneviève, Picard, Capucine, Fischer, Alain, Neven, Bénédicte, Rieux-Laucat, Frédéric, Quartier, Pierre

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