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The MHC I immunopeptidome conveys to the cell surface an integrative view of cellular regulation.

Caron E, Vincent K, Fortier MH, Laverdure JP, Bramoullé A, Hardy MP, Voisin G, Roux PP, Lemieux S, Thibault P, Perreault C.

Mol Syst Biol. 2011 Sep 27;7:533. doi: 10.1038/msb.2011.68.


Origin and plasticity of MHC I-associated self peptides.

de Verteuil D, Granados DP, Thibault P, Perreault C.

Autoimmun Rev. 2012 Jul;11(9):627-35. doi: 10.1016/j.autrev.2011.11.003. Epub 2011 Nov 12. Review.


The MHC class I peptide repertoire is molded by the transcriptome.

Fortier MH, Caron E, Hardy MP, Voisin G, Lemieux S, Perreault C, Thibault P.

J Exp Med. 2008 Mar 17;205(3):595-610. doi: 10.1084/jem.20071985. Epub 2008 Feb 25.


Immunogenicity and tolerogenicity of self-major histocompatibility complex peptides.

Benichou G, Takizawa PA, Ho PT, Killion CC, Olson CA, McMillan M, Sercarz EE.

J Exp Med. 1990 Nov 1;172(5):1341-6.


T cell responses to bluetongue virus are directed against multiple and identical CD4+ and CD8+ T cell epitopes from the VP7 core protein in mouse and sheep.

Rojas JM, Rodríguez-Calvo T, Peña L, Sevilla N.

Vaccine. 2011 Sep 16;29(40):6848-57. doi: 10.1016/j.vaccine.2011.07.061. Epub 2011 Jul 30.


The structure and location of SIMP/STT3B account for its prominent imprint on the MHC I immunopeptidome.

Caron E, Charbonneau R, Huppé G, Brochu S, Perreault C.

Int Immunol. 2005 Dec;17(12):1583-96. Epub 2005 Nov 1.


Deletion of immunoproteasome subunits imprints on the transcriptome and has a broad impact on peptides presented by major histocompatibility complex I molecules.

de Verteuil D, Muratore-Schroeder TL, Granados DP, Fortier MH, Hardy MP, Bramoullé A, Caron E, Vincent K, Mader S, Lemieux S, Thibault P, Perreault C.

Mol Cell Proteomics. 2010 Sep;9(9):2034-47. doi: 10.1074/mcp.M900566-MCP200. Epub 2010 May 19.


[MHC tetramers: tracking specific immunity].

Kosor E, Gagro A, Drazenović V, Kuzman I, Jeren T, Rakusić S, Rabatić S, Markotić A, Gotovac K, Sabioncello A, Cecuk E, Kerhin-Brkljacić V, Gjenero-Margan I, Kaić B, Mlinarić-Galinović G, Kastelan A, Dekaris D.

Acta Med Croatica. 2003;57(4):255-9. Review. Croatian.


The origin and role of MHC class I-associated self-peptides.

Perreault C.

Prog Mol Biol Transl Sci. 2010;92:41-60. doi: 10.1016/S1877-1173(10)92003-6.


How does the mammalian target of rapamycin (mTOR) influence CD8 T cell differentiation?

Salmond RJ, Zamoyska R.

Cell Cycle. 2010 Aug 1;9(15):2952-7. doi: 10.4161/cc.9.15.12358. Epub 2010 Aug 12.


Extensive major histocompatibility complex class I binding promiscuity for Mycobacterium tuberculosis TB10.4 peptides and immune dominance of human leucocyte antigen (HLA)-B*0702 and HLA-B*0801 alleles in TB10.4 CD8 T-cell responses.

Axelsson-Robertson R, Weichold F, Sizemore D, Wulf M, Skeiky YA, Sadoff J, Maeurer MJ.

Immunology. 2010 Apr;129(4):496-505. doi: 10.1111/j.1365-2567.2009.03201.x. Epub 2009 Nov 25.


Phosphorylated peptides are naturally processed and presented by major histocompatibility complex class I molecules in vivo.

Zarling AL, Ficarro SB, White FM, Shabanowitz J, Hunt DF, Engelhard VH.

J Exp Med. 2000 Dec 18;192(12):1755-62.


[Processing of MHC class I presented antigens].

van Endert P.

Med Sci (Paris). 2006 Aug-Sep;22(8-9):727-32. Review. French.

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