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8. Investigation of peptide involvement in T cell allorecognition using recombinant HLA class I multimers. Whitelegg AM; Oosten LE; Jordan S; Kester M; van Halteren AG; Madrigal JA; Goulmy E; Barber LD J Immunol; 2005 Aug; 175(3):1706-14. PubMed ID: 16034111 [TBL] [Abstract][Full Text] [Related]
9. Definition of specific peptide motifs for four major HLA-A alleles. Kubo RT; Sette A; Grey HM; Appella E; Sakaguchi K; Zhu NZ; Arnott D; Sherman N; Shabanowitz J; Michel H J Immunol; 1994 Apr; 152(8):3913-24. PubMed ID: 8144960 [TBL] [Abstract][Full Text] [Related]
10. Identification and characterisation of peptide binding motifs of six autoimmune disease-associated human leukocyte antigen-class I molecules including HLA-B*39:06. Eichmann M; de Ru A; van Veelen PA; Peakman M; Kronenberg-Versteeg D Tissue Antigens; 2014 Oct; 84(4):378-88. PubMed ID: 25154780 [TBL] [Abstract][Full Text] [Related]
11. Naturally processed HLA class I bound peptides from c-myc-transfected cells reveal allele-specific motifs. Harris PE; Colovai A; Liu Z; Dalla Favera R; Suciu-Foca N J Immunol; 1993 Dec; 151(11):5966-74. PubMed ID: 8245441 [TBL] [Abstract][Full Text] [Related]
12. Naturally processed HLA class II peptides reveal highly conserved immunogenic flanking region sequence preferences that reflect antigen processing rather than peptide-MHC interactions. Godkin AJ; Smith KJ; Willis A; Tejada-Simon MV; Zhang J; Elliott T; Hill AV J Immunol; 2001 Jun; 166(11):6720-7. PubMed ID: 11359828 [TBL] [Abstract][Full Text] [Related]
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14. Identification of five different Patr class I molecules that bind HLA supertype peptides and definition of their peptide binding motifs. McKinney DM; Erickson AL; Walker CM; Thimme R; Chisari FV; Sidney J; Sette A J Immunol; 2000 Oct; 165(8):4414-22. PubMed ID: 11035079 [TBL] [Abstract][Full Text] [Related]
15. Purification and characterization of endogenous peptides extracted from HLA-DR isolated from the spleen of a patient with rheumatoid arthritis. Gordon RD; Young JA; Rayner S; Luke RW; Crowther ML; Wordsworth P; Bell J; Hassall G; Evans J; Hinchliffe SA Eur J Immunol; 1995 May; 25(5):1473-6. PubMed ID: 7539763 [TBL] [Abstract][Full Text] [Related]
16. Naturally processed peptides from two disease-resistance-associated HLA-DR13 alleles show related sequence motifs and the effects of the dimorphism at position 86 of the HLA-DR beta chain. Davenport MP; Quinn CL; Chicz RM; Green BN; Willis AC; Lane WS; Bell JI; Hill AV Proc Natl Acad Sci U S A; 1995 Jul; 92(14):6567-71. PubMed ID: 7604034 [TBL] [Abstract][Full Text] [Related]
17. T cell reactivity to MHC class II-bound self peptides in systemic lupus erythematosus-prone MRL/lpr mice. Suh CH; Freed JH; Cohen PL J Immunol; 2003 Feb; 170(4):2229-35. PubMed ID: 12574397 [TBL] [Abstract][Full Text] [Related]
18. Structure of celiac disease-associated HLA-DQ8 and non-associated HLA-DQ9 alleles in complex with two disease-specific epitopes. Moustakas AK; van de Wal Y; Routsias J; Kooy YM; van Veelen P; Drijfhout JW; Koning F; Papadopoulos GK Int Immunol; 2000 Aug; 12(8):1157-66. PubMed ID: 10917890 [TBL] [Abstract][Full Text] [Related]
19. Endogenous peptides with distinct amino acid anchor residue motifs bind to HLA-A1 and HLA-B8. DiBrino M; Parker KC; Shiloach J; Turner RV; Tsuchida T; Garfield M; Biddison WE; Coligan JE J Immunol; 1994 Jan; 152(2):620-31. PubMed ID: 7506728 [TBL] [Abstract][Full Text] [Related]
20. HLA-B15 peptide ligands are preferentially anchored at their C termini. Prilliman KR; Jackson KW; Lindsey M; Wang J; Crawford D; Hildebrand WH J Immunol; 1999 Jun; 162(12):7277-84. PubMed ID: 10358176 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]