Search Results - "FELDMANN, Jérome" :: K.UTB vyhledávací portál | TBU Library Retrieval Portal

Chronic Infantile Neurological Cutaneous and Articular Syndrome Is Caused by Mutations in CIAS1, a Gene Highly Expressed in Polymorphonuclear Cells and Chondrocytes

Chronic Infantile Neurological Cutaneous and Articular Syndrome Is Caused by Mutations in CIAS1, a Gene Highly Expressed in Polymorphonuclear Cells and Chondrocytes

by Feldmann, Jérôme, Prieur, Anne-Marie, Quartier, Pierre, Berquin, Patrick, Certain, Stéphanie, Cortis, Elisabetta, Teillac-Hamel, Dominique, Fischer, Alain, Basile, Geneviève de Saint
Published in American journal of human genetics (01.07.2002)

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Primary hemophagocytic syndromes point to a direct link between lymphocyte cytotoxicity and homeostasis

Primary hemophagocytic syndromes point to a direct link between lymphocyte cytotoxicity and homeostasis

by Ménasché, Gael, Feldmann, Jérôme, Fischer, Alain, De Saint Basile, Geneviève
Published in Immunological reviews (01.02.2005)

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Molecular basis of the spectral expression of CIAS1 mutations associated with phagocytic cell-mediated autoinflammatory disorders CINCA/NOMID, MWS, and FCU

Molecular basis of the spectral expression of CIAS1 mutations associated with phagocytic cell-mediated autoinflammatory disorders CINCA/NOMID, MWS, and FCU

by 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
Published in Blood (01.04.2004)

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Simultaneous Cell-to-Cell Transmission of Human Immunodeficiency Virus to Multiple Targets through Polysynapses

Simultaneous Cell-to-Cell Transmission of Human Immunodeficiency Virus to Multiple Targets through Polysynapses

by RUDNICKA, Dominika, FELDMANN, Jérôme, PORROT, Françoise, WIETGREFE, Steve, GUADAGNINI, Stéphanie, PREVOST, Marie-Christine, ESTAQUIER, Jérôme, HAASE, Ashley T, SOL-FOULON, Nathalie, SCHWARTZ, Olivier
Published in Journal of Virology (15.06.2009)

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Functional consequences of perforin gene mutations in 22 patients with familial haemophagocytic lymphohistiocytosis

Functional consequences of perforin gene mutations in 22 patients with familial haemophagocytic lymphohistiocytosis

by 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
Published in British journal of haematology (01.06.2002)

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Severe and progressive encephalitis as a presenting manifestation of a novel missense perforin mutation and impaired cytolytic activity

Severe and progressive encephalitis as a presenting manifestation of a novel missense perforin mutation and impaired cytolytic activity

by 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
Published in Blood (01.04.2005)

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Secretory cytotoxic granule maturation and exocytosis require the effector protein hMunc13-4

Secretory cytotoxic granule maturation and exocytosis require the effector protein hMunc13-4

by Romao, Maryse, de Saint Basile, Geneviève, Ménager, Mickaël M, Knapnougel, Perrine, Garfa, Mériem, Feldmann, Jérôme, Fischer, Alain, Ménasché, Gaël, Ho, Chen-Hsuan, Raposo, Graça
Published in Nature Immunology (01.03.2007)

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Tetherin restricts productive HIV-1 cell-to-cell transmission

Tetherin restricts productive HIV-1 cell-to-cell transmission

by Casartelli, Nicoletta, Sourisseau, Marion, Feldmann, Jerome, Guivel-Benhassine, Florence, Mallet, Adeline, Marcelin, Anne-Geneviève, Guatelli, John, Schwartz, Olivier
Published in PLoS pathogens (01.06.2010)

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Journal Article

Defective CTLA-4 Cycling Pathway in Chediak-Higashi Syndrome: A Possible Mechanism for Deregulation of T Lymphocyte Activation

Defective CTLA-4 Cycling Pathway in Chediak-Higashi Syndrome: A Possible Mechanism for Deregulation of T Lymphocyte Activation

by Barrat, Franck J., Le Deist, Françoise, Benkerrou, Malika, Bousso, Philippe, Feldmann, Jérome, Fischer, Alain, Geneviève de Saint Basile
Published in Proceedings of the National Academy of Sciences - PNAS (20.07.1999)

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Journal Article

HIV-1 Virological Synapse: Live Imaging of Transmission

HIV-1 Virological Synapse: Live Imaging of Transmission

by Feldmann, Jerome, Schwartz, Olivier
Published in Viruses (01.08.2010)

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Journal Article Book Review

Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1)

Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1)

by Ménasché, Gaël, Ho, Chen Hsuan, Sanal, Ozden, Feldmann, Jérôme, Tezcan, Ilhan, Ersoy, Fügen, Houdusse, Anne, Fischer, Alain, Basile, Geneviève de Saint
Published in The Journal of clinical investigation (01.08.2003)

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Journal Article

Direct Relationship between Virus Load and Systemic Immune Activation in HIV-2 Infection

Direct Relationship between Virus Load and Systemic Immune Activation in HIV-2 Infection

by Leligdowicz, Aleksandra, Feldmann, Jérôme, Jaye, Assan, Cotten, Matthew, Dong, Tao, McMichael, Andrew, Whittle, Hilton, Rowland-Jones, Sarah
Published in The Journal of infectious diseases (01.01.2010)

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Journal Article

Downregulation of the T-Cell Receptor by Human Immunodeficiency Virus Type 2 Nef Does Not Protect against Disease Progression

Downregulation of the T-Cell Receptor by Human Immunodeficiency Virus Type 2 Nef Does Not Protect against Disease Progression

by FELDMANN, Jérôme, LELIGDOWICZ, Aleksandra, JAYE, Assan, TAO DONG, WHITTLE, Hilton, ROWLAND-JONES, Sarah L
Published in Journal of Virology (15.12.2009)

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Journal Article

Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome

Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome

by Certain, Stéphanie, Le Deist, Françoise, Feldmann, Jérôme, Fischer, Alain, de Saint Basile, Geneviève, Ménasché, Gaël, Pastural, Elodie, Wulffraat, Nico, Dupuis, Sophie, Ersoy, Fügen, Bianchi, Diana
Published in Nature genetics (01.06.2000)

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Journal Article

Biochemical and functional characterization of Rab27a mutations occurring in Griscelli syndrome patients

Biochemical and functional characterization of Rab27a mutations occurring in Griscelli syndrome patients

by Ménasché, Gaël, Feldmann, Jérôme, Houdusse, Anne, Desaymard, Catherine, Fischer, Alain, Goud, Bruno, Basile, Geneviève de Saint
Published in Blood (01.04.2003)

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Journal Article

Griscelli syndrome: characterization of a new mutation and rescue of T-cytotoxic activity by retroviral transfer of RAB27A gene

Griscelli syndrome: characterization of a new mutation and rescue of T-cytotoxic activity by retroviral transfer of RAB27A gene

by 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
Published in Journal of clinical immunology (01.07.2004)

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Journal Article

Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1)

Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1)

by Ménasché, Gaël, Ho, Chen Hsuan, Sanal, Ozden, Feldmann, Jérôme, Tezcan, Ilhan, Ersoy, Fügen, Houdusse, Anne, Fischer, Alain, de Saint Basile, Geneviève
Published in The Journal of clinical investigation (01.08.2003)

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Journal Article

Biochemical and functional characterization of Rab27a mutations occurring in Griscelli syndrome patients

Biochemical and functional characterization of Rab27a mutations occurring in Griscelli syndrome patients

by Ménasché, Gaël, Feldmann, Jerome, Houdusse, Anne, Desaymard, Catherine, Fischer, Alain, Goud, Bruno, de Saint Basile, Geneviève, Ménasché, Gaël, Feldmann, Jérôme, Basile, Geneviève de Saint
Published in Blood (01.04.2003)

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Journal Article

Munc13-4 Is Essential for Cytolytic Granules Fusion and Is Mutated in a Form of Familial Hemophagocytic Lymphohistiocytosis (FHL3)

Munc13-4 Is Essential for Cytolytic Granules Fusion and Is Mutated in a Form of Familial Hemophagocytic Lymphohistiocytosis (FHL3)

by 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
Published in Cell (14.11.2003)

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Journal Article

Tetherin Restricts Productive HIV-1 Cell-to-Cell Transmission: e1000955

Tetherin Restricts Productive HIV-1 Cell-to-Cell Transmission: e1000955

by Casartelli, Nicoletta, Sourisseau, Marion, Feldmann, Jerome, Guivel-Benhassine, Florence, Mallet, Adeline, Marcelin, Anne-Geneviève, Guatelli, John, Schwartz, Olivier
Published in PLoS pathogens (01.06.2010)

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Journal Article