Divergent motifs but overlapping binding repertoires of six HLA-DQ molecules frequently expressed in the worldwide human population.
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T-cell memory responses elicited by yellow fever vaccine are targeted to overlapping epitopes containing multiple HLA-I and -II binding motifsPeptide binding predictions for HLA DR, DP and DQ moleculesIdentification of conserved and HLA promiscuous DENV3 T-cell epitopes.Distinct evolutionary strategies of human leucocyte antigen loci in pathogen-rich environmentsSequence conservation analysis and in silico human leukocyte antigen-peptide binding predictions for the Mtb72F and M72 tuberculosis candidate vaccine antigens.Dissecting mechanisms of immunodominance to the common tuberculosis antigens ESAT-6, CFP10, Rv2031c (hspX), Rv2654c (TB7.7), and Rv1038c (EsxJ)A Quantitative Analysis of Complexity of Human Pathogen-Specific CD4 T Cell Responses in Healthy M. tuberculosis Infected South Africans.Analysis of T cell responses to the major allergens from German cockroach: epitope specificity and relationship to IgE productionT cell responses to known allergen proteins are differently polarized and account for a variable fraction of total response to allergen extracts.Citrullination only infrequently impacts peptide binding to HLA class II MHCThe identification of potentially pathogenic and therapeutic epitopes from common human allergens.Functional classification of class II human leukocyte antigen (HLA) molecules reveals seven different supertypes and a surprising degree of repertoire sharing across supertypesA strategy to determine HLA class II restriction broadly covering the DR, DP, and DQ allelic variants most commonly expressed in the general populationA deimmunised form of the ribotoxin, α-sarcin, lacking CD4+ T cell epitopes and its use as an immunotoxin warhead.Definition of CD4 Immunosignatures Associated with MTB.HLA-DM and HLA-DO, key regulators of MHC-II processing and presentation.Measurement of Peptide Binding to MHC Class II Molecules by Fluorescence Polarization.Associations of human leukocyte antigens with autoimmune diseases: challenges in identifying the mechanism.Peptidomic analysis of type 1 diabetes associated HLA-DQ molecules and the impact of HLA-DM on peptide repertoire editing.Measurement of MHC/peptide interactions by gel filtration or monoclonal antibody capture.T cells from patients with Parkinson's disease recognize α-synuclein peptides.CD4+ T cell autoimmunity to hypocretin/orexin and cross-reactivity to a 2009 H1N1 influenza A epitope in narcolepsy.T cells from hemophilia A subjects recognize the same HLA-restricted FVIII epitope with a narrow TCR repertoire.Global Assessment of Dengue Virus-Specific CD4+ T Cell Responses in Dengue-Endemic Areas.Development of a strategy and computational application to select candidate protein analogues with reduced HLA binding and immunogenicity.Characterizing the binding motifs of 11 common human HLA-DP and HLA-DQ molecules using NNAlign.Peptide Binding Prediction to Five Most Frequent HLA-DQ Proteins - a Proteochemometric Approach.HLA-DQ allele-restricted activation of nitroso sulfamethoxazole-specific CD4-positive T lymphocytes from patients with cystic fibrosis.The effect of acylation with fatty acids and other modifications on HLA class II:peptide binding and T cell stimulation for three model peptides.
P2860
Q28485408-D9CEAB9D-ABFA-4E70-B1A6-2D9258FF078DQ33751936-F4090374-048C-43AA-8E39-ACDB725BFBCDQ35018972-AF423F87-EA17-4DC9-91CB-3CE9FC005769Q35701120-85AD6121-12C0-4C6B-9A0A-F018048DA252Q35818040-5057D9B0-F1AF-472C-A35B-EB8896778144Q35936117-BD81CA5F-0B91-41B3-B942-BC950F1178B5Q36074922-131C41E3-E7CC-4F46-A3A5-992E239DEE30Q36083978-5D6D7AD0-D7D3-4566-9EFC-0AFCEC15BCECQ36140086-5C84C86C-F7B8-4232-B72A-43B5F3E34251Q36365784-BFB5580C-2FA4-4C67-BA59-BD4892E39030Q36541082-2FCC8C44-72FA-4164-9943-18E1E744AA49Q36766285-9216E5EF-2561-4E63-A68E-75EFFC582636Q36788055-8B27E543-4F8D-4CD6-90BC-69369D09FAD6Q37367958-4C828299-FC35-4F94-ABCB-1EA620EBF04EQ37672921-2BBD654B-4A55-4250-90E8-860AEC5E1459Q38181859-9F089644-B03B-4BFC-843B-A609D2554DECQ38235847-E1720D5B-67DA-4832-BAFC-0D62FD7929E9Q38569872-93A346DF-7B45-489C-B3D8-D15CBD9BDD0CQ39175672-F25B61AE-4360-45C7-ADB1-0E5AEA89920DQ39849181-36FA4A23-C3F4-4508-9A82-0520D93CA3A7Q40163812-E9BFA59A-CA4B-4F82-9615-85432B147F07Q42248160-BEFB3642-1425-44DC-9381-5BE571D6A46FQ42381250-0ACC36B7-20EC-4CD4-B574-D5301781BEF6Q43047038-60A7F985-3DBD-4A8A-B3A3-2AD7A051FDB0Q47716213-55677002-8C3F-4760-9FF6-35C1081A94F3Q51419330-724504B0-21D5-4BFF-BDB8-5A5AC9BD4FAFQ51595142-6BC7F964-ADDA-415A-8268-00547E3AA42DQ52837404-1F4C8323-8CC6-4948-A1F9-964549EEF713Q55097162-95CD189F-C20C-4D76-ABC3-F7C0F6A92A8A
P2860
Divergent motifs but overlapping binding repertoires of six HLA-DQ molecules frequently expressed in the worldwide human population.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
@zh-cn
name
Divergent motifs but overlappi ...... he worldwide human population.
@ast
Divergent motifs but overlappi ...... he worldwide human population.
@en
type
label
Divergent motifs but overlappi ...... he worldwide human population.
@ast
Divergent motifs but overlappi ...... he worldwide human population.
@en
prefLabel
Divergent motifs but overlappi ...... he worldwide human population.
@ast
Divergent motifs but overlappi ...... he worldwide human population.
@en
P2093
P2860
P356
P1476
Divergent motifs but overlappi ...... he worldwide human population.
@en
P2093
Amiyah Steen
Carrie Moore
John Sidney
Jolan Chung
P2860
P304
P356
10.4049/JIMMUNOL.1001006
P407
P577
2010-09-01T00:00:00Z