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Gaël Ménasché

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Fernando E Sepulveda; Marjorie Côte; Franck Debeurme; Alain Fischer; Mathieu Kurowska; Gaël Ménasché; Jana Pachlopnik Schmid; Geneviève de Saint Basile
Distinct severity of HLH in both human and murine mutants with complete loss of cytotoxic effector PRF1, RAB27A, and STX11.
Mathieu Kurowska; Nadine T Nehme; Magali Court; Geneviève de Saint Basile; Alain Fischer; Jérôme Garin; Nicolas Goudin; Gaël Ménasché
Terminal transport of lytic granules to the immune synapse is mediated by the kinesin-1/Slp3/Rab27a complex.
Eman Al-Idrissi; Geyhad ElGhazali; Mofarah Alzahrani; Gaël Ménasché; Jana Pachlopnik Schmid; Geneviève de Saint Basile
Premature birth, respiratory distress, intracerebral hemorrhage, and silvery-gray hair: differential diagnosis of the 3 types of Griscelli syndrome.

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All Publications

2013: Fernando E Sepulveda; Marjorie Côte; Franck Debeurme; Alain Fischer; Mathieu Kurowska; Gaël Ménasché; Jana Pachlopnik Schmid; Geneviève de Saint Basile
Distinct severity of HLH in both human and murine mutants with complete loss of cytotoxic effector PRF1, RAB27A, and STX11.
Blood 2013;121(4):595-603.
2012: Mathieu Kurowska; Nadine T Nehme; Magali Court; Geneviève de Saint Basile; Alain Fischer; Jérôme Garin; Nicolas Goudin; Gaël Ménasché
Terminal transport of lytic granules to the immune synapse is mediated by the kinesin-1/Slp3/Rab27a complex.
Blood 2012;119(17):3879-89.
2010: Eman Al-Idrissi; Geyhad ElGhazali; Mofarah Alzahrani; Gaël Ménasché; Jana Pachlopnik Schmid; Geneviève de Saint Basile
Premature birth, respiratory distress, intracerebral hemorrhage, and silvery-gray hair: differential diagnosis of the 3 types of Griscelli syndrome.
Journal of pediatric hematology/oncology 2010;32(6):494-6.
2010: Geneviève de Saint Basile; Gaël Ménasché; Alain Fischer
Molecular mechanisms of biogenesis and exocytosis of cytotoxic granules.
Nature reviews. Immunology 2010;10(8):568-79.
2010: Jana Pachlopnik Schmid; Jana P Schmid; Marjorie Côte; Mickaël Ménager; Agathe Burgess; Nadine Nehme; Gaël Ménasché; Alain Fischer; Geneviève de Saint Basile
Inherited defects in lymphocyte cytotoxic activity.
Immunological reviews 2010;235(1):10-23.
2009: Marjorie Côte; Mickaël M Ménager; Agathe Burgess; Nizar Mahlaoui; Capucine Picard; Catherine Schaffner; Fahad Al-Manjomi; Musa Al-Harbi; Abdullah Alangari; Françoise Le Deist; Andrew R Gennery; Nathalie Prince; Astrid Cariou; Patrick Nitschke; Ulrich Blank; Gehad El-Ghazali; Gaël Ménasché; Sylvain Latour; Alain Fischer; Geneviève de Saint Basile
Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cells.
The Journal of clinical investigation 2009;119(12):3765-73.
2009: Gaël Ménasché; Geneviève de Saint Basile
EBAG9 tempers lymphocyte killing activity.
The Journal of clinical investigation 2009;119(8):2136-40.
2008: Gaël Ménasché; Mickaël M Ménager; Juliette M Lefebvre; Einat Deutsch; Rafika Athman; Nathalie Lambert; Nizar Mahlaoui; Magali Court; Jérôme Garin; Alain Fischer; Geneviève de Saint Basile
A newly identified isoform of Slp2a associates with Rab27a in cytotoxic T cells and participates to cytotoxic granule secretion.
Blood 2008;112(13):5052-62.
2007: Gaël Ménasché; Stefanie Kliche; Natalie A. Bezman; Burkhart Schraven
Regulation of T-cell antigen receptor-mediated inside-out signaling by cytosolic adapter proteins and Rap1 effector molecules.
Immunological reviews 2007;218():82-91.
2007: Gaël Ménasché; Stefanie Kliche; Emily J H Chen; Theresia E B Stradal; Burkhart Schraven; Gary A Koretzky
RIAM links the ADAP/SKAP-55 signaling module to Rap1, facilitating T-cell-receptor-mediated integrin activation.
Molecular and cellular biology 2007;27(11):4070-81.
2007: Mickaël Ménager; Gaël Ménasché; Maryse Romao; Perrine Knapnougel; Chen-Hsuan Ho; Mériem Garfa; Graça Raposo; Jérôme Feldmann; Alain Fischer; Geneviève de Saint Basile
Secretory cytotoxic granule maturation and exocytosis require the effector protein hMunc13-4.
Nature immunology 2007;8(3):257-67.
2006: Gaël Ménasché; Mickaël Ménager; Françoise Le Deist; Alain Fischer; Geneviève de Saint Basile
[Defect in lytic granule exocytosis: several causes, a same effect].
Médecine sciences : M/S 2006;22(8-9):733-8.
2005: Jérôme Feldmann; Gaël Ménasché; Isabelle Callebaut; Véronique Minard-Colin; Brigitte Bader-Meunier; Laurence Le Clainche; Alain Fischer; Françoise Le Deist; Marc Tardieu; Geneviève de Saint Basile
Severe and progressive encephalitis as a presenting manifestation of a novel missense perforin mutation and impaired cytolytic activity.
Blood 2005;105(7):2658-63.
2005: Gaël Ménasché; Jérôme Feldmann; Alain Fischer; Geneviève de Saint Basile
Primary hemophagocytic syndromes point to a direct link between lymphocyte cytotoxicity and homeostasis.
Immunological reviews 2005;203():165-79.
2004: João Bizario; Jérôme Feldmann; Fabíola A Castro; Gaël Ménasché; Cristina M A Jacob; L Cristofani; Erasmo Barbante Casella; Julio C Voltarelli; Geneviève de Saint Basile; Enilza M Espreafico
Griscelli syndrome: characterization of a new mutation and rescue of T-cytotoxic activity by retroviral transfer of RAB27A gene.
Journal of clinical immunology 2004;24(4):397-410.
2003: Claire Desnos; Jean-Sébastien SCHONN; Sébastien Huet; Viet Samuel Tran; Aziz El-Amraoui; Graça Raposo; Isabelle Fanget; Catherine Chapuis; Gaël Ménasché; Geneviève de Saint Basile; Christine Petit; Sophie Cribier; Jean-Pierre Henry; François Darchen
Rab27A and its effector MyRIP link secretory granules to F-actin and control their motion towards release sites.
The Journal of cell biology 2003;163(3):559-70.
2003: Gaël Ménasché; Chen Hsuan Ho; Ozden Sanal; Jérôme Feldmann; Ilhan Tezcan; Fügen Ersoy; Anne Houdusse; Alain Fischer; Geneviève de Saint Basile
Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1).
The Journal of clinical investigation 2003;112(3):450-6.
2002: Gaël Ménasché; Alain Fischer; Geneviève de Saint Basile
Griscelli syndrome types 1 and 2.
American journal of human genetics 2002;71(5):1237-8; author reply 1238.
2002: Ozden Sanal; Fügen Ersoy; Ilhan Tezcan; Ayse Metin; Leman Yel; Gaël Ménasché; Aytemiz Gürgey; Izzet Berkel; Geneviève de Saint Basile
Griscelli disease: genotype-phenotype correlation in an array of clinical heterogeneity.
Journal of clinical immunology 2002;22(4):237-43.
2000: Gaël Ménasché; E Pastural; Jérôme Feldmann; Stéphanie Certain; Fügen Ersoy; Stéphanie Dupuis; Nico M Wulffraat; D Bianchi; Alain Fischer; Françoise Le Deist; Geneviève de Saint Basile
Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome.
Nature genetics 2000;25(2):173-6.