Titlebook: Immunobiology of Proteins and Peptides IV; T-Cell Recognition a M. Zouhair Atassi Book 1987 The Editor(s) (if applicable) and The Author(s)

LH941

书目名称Immunobiology of Proteins and Peptides IV影响因子(影响力)




书目名称Immunobiology of Proteins and Peptides IV影响因子(影响力)学科排名




书目名称Immunobiology of Proteins and Peptides IV网络公开度




书目名称Immunobiology of Proteins and Peptides IV网络公开度学科排名




书目名称Immunobiology of Proteins and Peptides IV被引频次




书目名称Immunobiology of Proteins and Peptides IV被引频次学科排名




书目名称Immunobiology of Proteins and Peptides IV年度引用




书目名称Immunobiology of Proteins and Peptides IV年度引用学科排名




书目名称Immunobiology of Proteins and Peptides IV读者反馈




书目名称Immunobiology of Proteins and Peptides IV读者反馈学科排名

诗集

Murine Ia Genes: Organization, Polymorphism and Heterogeneity,s evolved millions of years ago, and that they are part of a super-gene family. Studies in man and mouse have clearly identified at least four classes of MHC genes, class I, class II, class III and class IV. The class I genes code for the classical ‘transplantation antigens’ which consist of a 45,00

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Trinitrophenyl Reactive T-Cell Clones in Functional and Molecular Analysis of the HLA-D Region,ong the seminal studies demonstrating this phenomenon . those of Shearer and associates demonstrating that recognition of mouse target cells by trinitrophenyl (TNP)-specific cytolytic T cells required genetic homologies between the killer and target cells at H-2 class I loci (rev., Shearer et al., 1

craving

T-Cells Recognize IA Conformation in the Interaction with Antigen Presenting Cells,minant (Shevach and Rosenthal, 1973). Although the T cell antigen receptor has been identified and sequenced (Hedrick et al., 1984; Fink et al., 1986), the nature of the ligand that triggers the T cells remains unclear. The early experiments of Lin et al. (1981) and Michaelides et al. (1983) using t

Spinal-Fusion

T-Cell Recognition and Antigen Presentaion of Myoglobin,ncide with the antigenic sites while one site was recognized exclusively by T cells and not by any detectable levels of antibody. Recognition of the synthetic T sites by protein-primed T cell lines or clones indicated that T cells display an unusual peptide size requirement beyond the essential cont

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T-Cell Recognition and Antigen Presentation of Lysozyme,re involved in B- and T-cell recognition. The strategy depends on the synthesis of consecutive overlapping peptides that together account for the entire protein chain. Using this approach, the full submolecular profile of continuous regions on hen egg lysozyme recognized by T cells (T sites) were lo

清澈

,The Regions of T-cell Recognition on the Extracellular Part of the α Chain of ,, Acetylcholine ReceChR). Eighteen synthetic consecutive overlapping peptides, of uniform size and overlaps, that spanned the entire extracellular part (residues 1–210) of the a chain were examined for their . stimulation of lymph node cells from AChR-primed C57BL/6 (H-2.), C3H/He (H-2.), SWR(H-2.) and SJL (H-2.) mice.

深渊

Structural Considerations of T-Cell Cognizance of Antigen,R are I-A. and I-A. respectively. Using various antigens to stimulate, ., primed T lymphocytes, studies on the responsiveness of these two strains to immunization with TMVP and with its tryptic peptide number 8 representing residues 93–112 of the protein are described. These studies revealed that in

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