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Items: 31


Tomosyn functions as a PKCδ-regulated fusion clamp in mast cell degranulation.

Madera-Salcedo IK, Danelli L, Tiwari N, Dema B, Pacreau E, Vibhushan S, Birnbaum J, Agabriel C, Liabeuf V, Klingebiel C, Menasche G, Macias-Silva M, Benhamou M, Charles N, González-Espinosa C, Vitte J, Blank U.

Sci Signal. 2018 Jul 3;11(537). pii: eaan4350. doi: 10.1126/scisignal.aan4350.


Kinesin-1 Is a New Actor Involved in Platelet Secretion and Thrombus Stability.

Adam F, Kauskot A, Kurowska M, Goudin N, Munoz I, Bordet JC, Huang JD, Bryckaert M, Fischer A, Borgel D, de Saint Basile G, Christophe OD, Ménasché G.

Arterioscler Thromb Vasc Biol. 2018 May;38(5):1037-1051. doi: 10.1161/ATVBAHA.117.310373. Epub 2018 Mar 8.


A RAB27A duplication in several cases of Griscelli syndrome type 2: An explanation for cases lacking a genetic diagnosis.

Grandin V, Sepulveda FE, Lambert N, Al Zahrani M, Al Idrissi E, Al-Mousa H, Almanjomi F, Al-Ghonaium A, K Habazi M, A Alghamdi H, Picard C, Bole-Feysot C, Nitschke P, Ménasché G, de Saint Basile G.

Hum Mutat. 2017 Oct;38(10):1355-1359. doi: 10.1002/humu.23274. Epub 2017 Jun 19.


Kinesin-1 controls mast cell degranulation and anaphylaxis through PI3K-dependent recruitment to the granular Slp3/Rab27b complex.

Munoz I, Danelli L, Claver J, Goudin N, Kurowska M, Madera-Salcedo IK, Huang JD, Fischer A, González-Espinosa C, de Saint Basile G, Blank U, Ménasché G.

J Cell Biol. 2016 Oct 24;215(2):203-216.


HDAC6 regulates the dynamics of lytic granules in cytotoxic T lymphocytes.

Núñez-Andrade N, Iborra S, Trullo A, Moreno-Gonzalo O, Calvo E, Catalán E, Menasche G, Sancho D, Vázquez J, Yao TP, Martín-Cófreces NB, Sánchez-Madrid F.

J Cell Sci. 2016 Apr 1;129(7):1305-1311. doi: 10.1242/jcs.180885. Epub 2016 Feb 11.


Polygenic mutations in the cytotoxicity pathway increase susceptibility to develop HLH immunopathology in mice.

Sepulveda FE, Garrigue A, Maschalidi S, Garfa-Traore M, Ménasché G, Fischer A, de Saint Basile G.

Blood. 2016 Apr 28;127(17):2113-21. doi: 10.1182/blood-2015-12-688960. Epub 2016 Feb 10.


A novel immunoregulatory role for NK-cell cytotoxicity in protection from HLH-like immunopathology in mice.

Sepulveda FE, Maschalidi S, Vosshenrich CA, Garrigue A, Kurowska M, Ménasche G, Fischer A, Di Santo JP, de Saint Basile G.

Blood. 2015 Feb 26;125(9):1427-34. doi: 10.1182/blood-2014-09-602946. Epub 2014 Dec 18.


LYST controls the biogenesis of the endosomal compartment required for secretory lysosome function.

Sepulveda FE, Burgess A, Heiligenstein X, Goudin N, Ménager MM, Romao M, Côte M, Mahlaoui N, Fischer A, Raposo G, Ménasché G, de Saint Basile G.

Traffic. 2015 Feb;16(2):191-203. doi: 10.1111/tra.12244. Epub 2015 Jan 6.


Distinct severity of HLH in both human and murine mutants with complete loss of cytotoxic effector PRF1, RAB27A, and STX11.

Sepulveda FE, Debeurme F, Ménasché G, Kurowska M, Côte M, Pachlopnik Schmid J, Fischer A, de Saint Basile G.

Blood. 2013 Jan 24;121(4):595-603. doi: 10.1182/blood-2012-07-440339. Epub 2012 Nov 16.


Terminal transport of lytic granules to the immune synapse is mediated by the kinesin-1/Slp3/Rab27a complex.

Kurowska M, Goudin N, Nehme NT, Court M, Garin J, Fischer A, de Saint Basile G, Ménasché G.

Blood. 2012 Apr 26;119(17):3879-89. doi: 10.1182/blood-2011-09-382556. Epub 2012 Feb 3. Erratum in: Blood. 2014 Feb 27;123(9):1432.


Inherited defects causing hemophagocytic lymphohistiocytic syndrome.

de Saint Basile G, Ménasché G, Latour S.

Ann N Y Acad Sci. 2011 Dec;1246:64-76. doi: 10.1111/j.1749-6632.2011.06307.x.


Premature birth, respiratory distress, intracerebral hemorrhage, and silvery-gray hair: differential diagnosis of the 3 types of Griscelli syndrome.

Al-Idrissi E, ElGhazali G, Alzahrani M, Ménasché G, Pachlopnik Schmid J, Basile Gde S.

J Pediatr Hematol Oncol. 2010 Aug;32(6):494-6. doi: 10.1097/MPH.0b013e3181e34dc9. Erratum in: J Pediatr Hematol Oncol. 2011 May;33(4):319.


Molecular mechanisms of biogenesis and exocytosis of cytotoxic granules.

de Saint Basile G, Ménasché G, Fischer A.

Nat Rev Immunol. 2010 Aug;10(8):568-79. doi: 10.1038/nri2803. Epub 2010 Jul 16. Review.


Inherited defects in lymphocyte cytotoxic activity.

Pachlopnik Schmid J, Côte M, Ménager MM, Burgess A, Nehme N, Ménasché G, Fischer A, de Saint Basile G.

Immunol Rev. 2010 May;235(1):10-23. doi: 10.1111/j.0105-2896.2010.00890.x. Review. Erratum in: Immunol Rev. 2010 Jul;236(1):276. Schmid, Jana P (corrected to Pachlopnik Schmid, Jana]..


Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cells.

Côte M, Ménager MM, Burgess A, Mahlaoui N, Picard C, Schaffner C, Al-Manjomi F, Al-Harbi M, Alangari A, Le Deist F, Gennery AR, Prince N, Cariou A, Nitschke P, Blank U, El-Ghazali G, Ménasché G, Latour S, Fischer A, de Saint Basile G.

J Clin Invest. 2009 Dec;119(12):3765-73. doi: 10.1172/JCI40732. Epub 2009 Nov 2.


EBAG9 tempers lymphocyte killing activity.

Ménasché G, de Saint Basile G.

J Clin Invest. 2009 Aug;119(8):2136-40. doi: 10.1172/JCI40270. Epub 2009 Jul 20.


A newly identified isoform of Slp2a associates with Rab27a in cytotoxic T cells and participates to cytotoxic granule secretion.

Ménasché G, Ménager MM, Lefebvre JM, Deutsch E, Athman R, Lambert N, Mahlaoui N, Court M, Garin J, Fischer A, de Saint Basile G.

Blood. 2008 Dec 15;112(13):5052-62. doi: 10.1182/blood-2008-02-141069. Epub 2008 Sep 23.


Regulation of T-cell antigen receptor-mediated inside-out signaling by cytosolic adapter proteins and Rap1 effector molecules.

Ménasché G, Kliche S, Bezman N, Schraven B.

Immunol Rev. 2007 Aug;218:82-91. Review.


RIAM links the ADAP/SKAP-55 signaling module to Rap1, facilitating T-cell-receptor-mediated integrin activation.

Ménasché G, Kliche S, Chen EJ, Stradal TE, Schraven B, Koretzky G.

Mol Cell Biol. 2007 Jun;27(11):4070-81. Epub 2007 Apr 2.


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

Ménager MM, Ménasché G, Romao M, Knapnougel P, Ho CH, Garfa M, Raposo G, Feldmann J, Fischer A, de Saint Basile G.

Nat Immunol. 2007 Mar;8(3):257-67. Epub 2007 Jan 21.


The ADAP/SKAP55 signaling module regulates T-cell receptor-mediated integrin activation through plasma membrane targeting of Rap1.

Kliche S, Breitling D, Togni M, Pusch R, Heuer K, Wang X, Freund C, Kasirer-Friede A, Menasche G, Koretzky GA, Schraven B.

Mol Cell Biol. 2006 Oct;26(19):7130-44.


[Defect in lytic granule exocytosis: several causes, a same effect].

Ménasché G, Ménager M, Le Deist F, Fischer A, de Saint Basile G.

Med Sci (Paris). 2006 Aug-Sep;22(8-9):733-8. Review. French.


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

Ménasché G, Feldmann J, Fischer A, de Saint Basile G.

Immunol Rev. 2005 Feb;203:165-79. Review.


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

Feldmann J, Ménasché G, Callebaut I, Minard-Colin V, Bader-Meunier B, Le Clainche L, Fischer A, Le Deist F, Tardieu M, de Saint Basile G.

Blood. 2005 Apr 1;105(7):2658-63. Epub 2004 Dec 14.


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

Bizario JC, Feldmann J, Castro FA, Ménasché G, Jacob CM, Cristofani L, Casella EB, Voltarelli JC, de Saint-Basile G, Espreafico EM.

J Clin Immunol. 2004 Jul;24(4):397-410.


Rab27A and its effector MyRIP link secretory granules to F-actin and control their motion towards release sites.

Desnos C, Schonn JS, Huet S, Tran VS, El-Amraoui A, Raposo G, Fanget I, Chapuis C, Ménasché G, de Saint Basile G, Petit C, Cribier S, Henry JP, Darchen F.

J Cell Biol. 2003 Nov 10;163(3):559-70.


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

Ménasché G, Ho CH, Sanal O, Feldmann J, Tezcan I, Ersoy F, Houdusse A, Fischer A, de Saint Basile G.

J Clin Invest. 2003 Aug;112(3):450-6. Erratum in: J Clin Invest. 2005 Apr;115(4):1100.


Griscelli syndrome types 1 and 2.

Ménasché G, Fischer A, de Saint Basile G.

Am J Hum Genet. 2002 Nov;71(5):1237-8; author reply 1238. No abstract available.


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

Menasche G, Feldmann J, Houdusse A, Desaymard C, Fischer A, Goud B, de Saint Basile G.

Blood. 2003 Apr 1;101(7):2736-42. Epub 2002 Nov 21.


Griscelli disease: genotype-phenotype correlation in an array of clinical heterogeneity.

Sanal O, Ersoy F, Tezcan I, Metin A, Yel L, Ménasché G, Gürgey A, Berkel I, de Saint Basile G.

J Clin Immunol. 2002 Jul;22(4):237-43.


Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome.

Ménasché G, Pastural E, Feldmann J, Certain S, Ersoy F, Dupuis S, Wulffraat N, Bianchi D, Fischer A, Le Deist F, de Saint Basile G.

Nat Genet. 2000 Jun;25(2):173-6.


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