Simultaneous Cell-to-Cell Transmission of Human Immunodeficiency Virus to Multiple Targets through Polysynapses von RUDNICKA, Dominika, FELDMANN, Jérôme, PORROT, Françoise, WIETGREFE, Steve, GUADAGNINI, Stéphanie, PREVOST, Marie-Christine, ESTAQUIER, Jérôme, HAASE, Ashley T, SOL-FOULON, Nathalie, SCHWARTZ, Olivier

Volltext

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

Volltext

Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1) von Ménasché, Gaël, Ho, Chen Hsuan, Sanal, Ozden, Feldmann, Jérôme, Tezcan, Ilhan, Ersoy, Fügen, Houdusse, Anne, Fischer, Alain, Basile, Geneviève de Saint

Volltext

Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome von Ménasché, Gaël, Pastural, Elodie, Feldmann, Jérôme, Certain, Stéphanie, Ersoy, Fügen, Dupuis, Sophie, Wulffraat, Nico, Bianchi, Diana, Fischer, Alain, Le Deist, Françoise, de Saint Basile, Geneviève

Volltext

Downregulation of the T-Cell Receptor by Human Immunodeficiency Virus Type 2 Nef Does Not Protect against Disease Progression von FELDMANN, Jérôme, LELIGDOWICZ, Aleksandra, JAYE, Assan, TAO DONG, WHITTLE, Hilton, ROWLAND-JONES, Sarah L

Volltext

Biochemical and functional characterization of Rab27a mutations occurring in Griscelli syndrome patients von Ménasché, Gaël, Feldmann, Jérôme, Houdusse, Anne, Desaymard, Catherine, Fischer, Alain, Goud, Bruno, Basile, Geneviève de Saint

Volltext

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

Volltext

Primary hemophagocytic syndromes point to a direct link between lymphocyte cytotoxicity and homeostasis von Ménasché, Gael, Feldmann, Jérôme, Fischer, Alain, De Saint Basile, Geneviève

Volltext

HIV-1 Virological Synapse: Live Imaging of Transmission von Feldmann, Jerome, Schwartz, Olivier

Volltext

Tetherin restricts productive HIV-1 cell-to-cell transmission von Casartelli, Nicoletta, Sourisseau, Marion, Feldmann, Jerome, Guivel-Benhassine, Florence, Mallet, Adeline, Marcelin, Anne-Geneviève, Guatelli, John, Schwartz, Olivier

Volltext

Molecular basis of the spectral expression of CIAS1 mutations associated with phagocytic cell-mediated autoinflammatory disorders CINCA/NOMID, MWS, and FCU von NEVEN, Bénédicte, CALLEBAUT, Isabelle, OERTLE, Stefan, ALLEN, Roger, MORGAN, Gareth, BORKHARDT, Arndt, HILL, Clare, GARDNER-MEDWIN, Janet, FISCHER, Alain, DE SAINT BASILE, Geneviève, PRIEUR, Anne-Marie, FELDMANN, Jérome, BODEMER, Christine, LEPORE, Loredana, DERFALVI, Beata, BENJAPONPITAK, Suata, VESELY, Richard, SAUVAIN, Marie Jose

Volltext

Direct Relationship between Virus Load and Systemic Immune Activation in HIV-2 Infection von Leligdowicz, Aleksandra, Feldmann, Jérôme, Jaye, Assan, Cotten, Matthew, Dong, Tao, McMichael, Andrew, Whittle, Hilton, Rowland-Jones, Sarah

Volltext

Munc13-4 Is Essential for Cytolytic Granules Fusion and Is Mutated in a Form of Familial Hemophagocytic Lymphohistiocytosis (FHL3) von Feldmann, Jérôme, Callebaut, Isabelle, Raposo, Graça, Certain, Stéphanie, Bacq, Delphine, Dumont, Cécile, Lambert, Nathalie, Ouachée-Chardin, Marie, Chedeville, Gaëlle, Tamary, Hannah, Minard-Colin, Véronique, Vilmer, Etienne, Blanche, Stéphane, Le Deist, Françoise, Fischer, Alain, de Saint Basile, Geneviève

Volltext

Griscelli syndrome: characterization of a new mutation and rescue of T-cytotoxic activity by retroviral transfer of RAB27A gene von Bizario, João C S, Feldmann, Jérôme, Castro, Fabíola A, Ménasché, Gaël, Jacob, Cristina M A, Cristofani, L, Casella, Erasmo B, Voltarelli, Júlio C, de Saint-Basile, Geneviève, Espreafico, Enilza M

Volltext

Functional consequences of perforin gene mutations in 22 patients with familial haemophagocytic lymphohistiocytosis von Feldmann, Jérôme, Le Deist, Françoise, Ouachée‐Chardin, Marie, Certain, Stéphanie, Alexander, Sarah, Quartier, Pierre, Haddad, Elie, Wulffraat, Nico, Casanova, Jean Laurent, Blanche, Stéphane, Fischer, Alain, De Saint Basile, Geneviève

Volltext

Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1) von Ménasché, Gaël, Ho, Chen Hsuan, Sanal, Ozden, Feldmann, Jérôme, Tezcan, Ilhan, Ersoy, Fügen, Houdusse, Anne, Fischer, Alain, de Saint Basile, Geneviève

Volltext

Severe and progressive encephalitis as a presenting manifestation of a novel missense perforin mutation and impaired cytolytic activity von Feldmann, Jérôme, Ménasché, Gaël, Callebaut, Isabelle, Minard-Colin, Véronique, Bader-Meunier, Brigitte, Le Clainche, Laurence, Fischer, Alain, Le Deist, Françoise, Tardieu, Marc, de Saint Basile, Geneviève

Volltext

Defective CTLA-4 Cycling Pathway in Chediak-Higashi Syndrome: A Possible Mechanism for Deregulation of T Lymphocyte Activation von Barrat, Franck J., Le Deist, Françoise, Benkerrou, Malika, Bousso, Philippe, Feldmann, Jérome, Fischer, Alain, Geneviève de Saint Basile

Volltext

Biochemical and functional characterization of Rab27a mutations occurring in Griscelli syndrome patients von Ménasché, Gaël, Feldmann, Jerome, Houdusse, Anne, Desaymard, Catherine, Fischer, Alain, Goud, Bruno, de Saint Basile, Geneviève, Ménasché, Gaël, Feldmann, Jérôme, Basile, Geneviève de Saint

Volltext

Selective Inhibition of Dipeptidyl Peptidase I, Not Caspases, Prevents the Partial Processing of Procaspase-3 in CD3-activated Human CD8+ T Lymphocytes von Nicolas Bidère, Marie Briet, Antoine Dürrbach, Céline Dumont, Jérôme Feldmann, Bernard Charpentier, Geneviève de Saint-Basile, Anna Senik

Volltext