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The Inhibitory Receptor NKG2A Sustains Virus-Specific CD8⁺ T Cells in Response to a Lethal Poxvirus Infection.
Rapaport AS, Schriewer J, Gilfillan S, Hembrador E, Crump R, Plougastel BF, Wang Y, Le Friec G, Gao J, Cella M, Pircher H, Yokoyama WM, Buller RM, Colonna M.
Immunity. 2015 Dec 15;43(6):1112-24. doi: 10.1016/j.immuni.2015.11.005. Epub 2015 Dec 8.
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Isolation of murine natural killer cells.
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Curr Protoc Immunol. 2014 Apr 2;105:3.22.1-3.22.9. doi: 10.1002/0471142735.im0322s105. Review.
Ly49h is necessary for genetic resistance to murine cytomegalovirus.
Cheng TP, French AR, Plougastel BF, Pingel JT, Orihuela MM, Buller ML, Yokoyama WM.
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Extending missing-self? Functional interactions between lectin-like NKrp1 receptors on NK cells with lectin-like ligands.
Plougastel BF, Yokoyama WM.
Curr Top Microbiol Immunol. 2006;298:77-89. Review.
Genetically linked C-type lectin-related ligands for the NKRP1 family of natural killer cell receptors.
Iizuka K, Naidenko OV, Plougastel BF, Fremont DH, Yokoyama WM.
Nat Immunol. 2003 Aug;4(8):801-7. Epub 2003 Jul 13.
Immune functions encoded by the natural killer gene complex.
Yokoyama WM, Plougastel BF.
Nat Rev Immunol. 2003 Apr;3(4):304-16. Review.
Costimulation of multiple NK cell activation receptors by NKG2D.
Ho EL, Carayannopoulos LN, Poursine-Laurent J, Kinder J, Plougastel B, Smith HR, Yokoyama WM.
J Immunol. 2002 Oct 1;169(7):3667-75.
Analysis of a 1-Mb BAC contig overlapping the mouse Nkrp1 cluster of genes: cloning of three new Nkrp1 members, Nkrp1d, Nkrp1e, and Nkrp1f.
Plougastel B, Matsumoto K, Dubbelde C, Yokoyama WM.
Immunogenetics. 2001 Sep;53(7):592-8.
Cloning of Clr, a new family of lectin-like genes localized between mouse Nkrp1a and Cd69.
Plougastel B, Dubbelde C, Yokoyama WM.
Immunogenetics. 2001 Apr;53(3):209-14.
Sequence analysis of a 62-kb region overlapping the human KLRC cluster of genes.
Plougastel B, Trowsdale J.
Genomics. 1998 Apr 15;49(2):193-9.
Cloning of NKG2-F, a new member of the NKG2 family of human natural killer cell receptor genes.
Eur J Immunol. 1997 Nov;27(11):2835-9.
Dynamics of proteasome distribution in living cells.
Reits EA, Benham AM, Plougastel B, Neefjes J, Trowsdale J.
EMBO J. 1997 Oct 15;16(20):6087-94.
Genomic structure, chromosome location, and alternative splicing of the human NKG2A gene.
Plougastel B, Jones T, Trowsdale J.
Immunogenetics. 1996;44(4):286-91.
Cloning and chromosome localization of the mouse Ews gene.
Plougastel B, Mattei MG, Thomas G, Delattre O.
Genomics. 1994 Sep 1;23(1):278-81.
Genetic alterations in the chromosome 22q12 region associated with development of neuroectodermal tumors.
Thomas G, Delattre O, Zucman J, Merel P, Desmaze C, Melot T, Sanson M, Hoang-Xuan K, Plougastel B, Dejong P, et al.
Cold Spring Harb Symp Quant Biol. 1994;59:555-64. No abstract available.
Genomic structure of the EWS gene and its relationship to EWSR1, a site of tumor-associated chromosome translocation.
Plougastel B, Zucman J, Peter M, Thomas G, Delattre O.
Genomics. 1993 Dec;18(3):609-15.
Physical mapping by FISH of the DiGeorge critical region (DGCR): involvement of the region in familial cases.
Desmaze C, Prieur M, Amblard F, Aikem M, LeDeist F, Demczuk S, Zucman J, Plougastel B, Delattre O, Croquette MF, et al.
Am J Hum Genet. 1993 Dec;53(6):1239-49.
Combinatorial generation of variable fusion proteins in the Ewing family of tumours.
Zucman J, Melot T, Desmaze C, Ghysdael J, Plougastel B, Peter M, Zucker JM, Triche TJ, Sheer D, Turc-Carel C, et al.
EMBO J. 1993 Dec;12(12):4481-7.
Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2.
Rouleau GA, Merel P, Lutchman M, Sanson M, Zucman J, Marineau C, Hoang-Xuan K, Demczuk S, Desmaze C, Plougastel B, et al.
Nature. 1993 Jun 10;363(6429):515-21.
Cloning and characterization of the Ewing's sarcoma and peripheral neuroepithelioma t(11;22) translocation breakpoints.
Zucman J, Delattre O, Desmaze C, Plougastel B, Joubert I, Melot T, Peter M, De Jong P, Rouleau G, Aurias A, et al.
Genes Chromosomes Cancer. 1992 Nov;5(4):271-7.
Mapping around the Xq13.1 breakpoints of two X/A translocations in hypohidrotic ectodermal dysplasia (EDA) female patients.
Plougastel B, Couillin P, Blanquet V, Le Guern E, Bakker E, Turleau C, De Grouchy J, Créau-Goldberg N.
Genomics. 1992 Oct;14(2):523-5.
Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumours.
Delattre O, Zucman J, Plougastel B, Desmaze C, Melot T, Peter M, Kovar H, Joubert I, de Jong P, Rouleau G, et al.
Nature. 1992 Sep 10;359(6391):162-5.
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