Ménasché G - Search Results

1

Ménasché G, Fischer A, de Saint Basile G. Ménasché G, et al. Am J Hum Genet. 2002 Nov;71(5):1237-8; author reply 1238. doi: 10.1086/344140. Am J Hum Genet. 2002. PMID: 12452176 Free PMC article. No abstract available.

2

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. Ménasché G, et al. Nat Genet. 2000 Jun;25(2):173-6. doi: 10.1038/76024. Nat Genet. 2000. PMID: 10835631

3

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. Sanal O, et al. Among authors: menasche g. J Clin Immunol. 2002 Jul;22(4):237-43. doi: 10.1023/a:1016045026204. J Clin Immunol. 2002. PMID: 12148598

4

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. Menasche G, et al. Blood. 2003 Apr 1;101(7):2736-42. doi: 10.1182/blood-2002-09-2789. Epub 2002 Nov 21. Blood. 2003. PMID: 12446441 Free article.

5

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. Ménasché G, et al. J Clin Invest. 2003 Aug;112(3):450-6. doi: 10.1172/JCI18264. J Clin Invest. 2003. PMID: 12897212 Free PMC article.

6

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. Desnos C, et al. Among authors: menasche g. J Cell Biol. 2003 Nov 10;163(3):559-70. doi: 10.1083/jcb.200302157. J Cell Biol. 2003. PMID: 14610058 Free PMC article.

7

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. Bizario JC, et al. Among authors: menasche g. J Clin Immunol. 2004 Jul;24(4):397-410. doi: 10.1023/B:JOCI.0000029119.83799.cb. J Clin Immunol. 2004. PMID: 15163896

8

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. Feldmann J, et al. Among authors: menasche g. Blood. 2005 Apr 1;105(7):2658-63. doi: 10.1182/blood-2004-09-3590. Epub 2004 Dec 14. Blood. 2005. PMID: 15598808 Free article.

9

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

Ménasché G, Feldmann J, Fischer A, de Saint Basile G. Ménasché G, et al. Immunol Rev. 2005 Feb;203:165-79. doi: 10.1111/j.0105-2896.2005.00224.x. Immunol Rev. 2005. PMID: 15661029 Review.

10

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

Ménasché G, Ménager M, Le Deist F, Fischer A, de Saint Basile G. Ménasché G, et al. Med Sci (Paris). 2006 Aug-Sep;22(8-9):733-8. doi: 10.1051/medsci/20062289733. Med Sci (Paris). 2006. PMID: 16962048 Free article. Review. French.

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