| scholarly article | Q13442814 |
| P2093 | author name string | M Daniels | |
| D M Kranz | |||
| S C Jameson | |||
| H R Churchill | |||
| P U Lee | |||
| P2860 | cites work | Selection of functional T cell receptor mutants from a yeast surface-display library | Q24679820 |
| Structure, specificity and CDR mobility of a class II restricted single-chain T-cell receptor | Q27618536 | ||
| Four A6-TCR/peptide/HLA-A2 structures that generate very different T cell signals are nearly identical | Q27619289 | ||
| An alphabeta T cell receptor structure at 2.5 A and its orientation in the TCR-MHC complex | Q27733448 | ||
| Structure of the complex between human T-cell receptor, viral peptide and HLA-A2 | Q27733853 | ||
| Structural insights into the evolution of an antibody combining site | Q27738883 | ||
| Structural basis of plasticity in T cell receptor recognition of a self peptide-MHC antigen | Q27748865 | ||
| Two human T cell receptors bind in a similar diagonal mode to the HLA-A2/Tax peptide complex using different TCR amino acids | Q27757472 | ||
| Structural basis of 2C TCR allorecognition of H-2Ld peptide complexes | Q27758459 | ||
| Phenotypic analysis of antigen-specific T lymphocytes | Q28290058 | ||
| Control of MHC restriction by TCR Valpha CDR1 and CDR2 | Q28589517 | ||
| A basis for alloreactivity: MHC helical residues broaden peptide recognition by the TCR. | Q32061562 | ||
| Binding energetics of T-cell receptors: correlation with immunological consequences | Q33720544 | ||
| The MHC reactivity of the T cell repertoire prior to positive and negative selection. | Q34418401 | ||
| Thermodynamics of T cell receptor binding to peptide-MHC: evidence for a general mechanism of molecular scanning | Q35651348 | ||
| Conformational isomerism and the diversity of antibodies | Q35851135 | ||
| High-affinity reactions between antigen-specific T-cell receptors and peptides associated with allogeneic and syngeneic major histocompatibility complex class I proteins | Q35918289 | ||
| Immunoprecipitation of cell surface structures of cloned cytotoxic T lymphocytes by clone-specific antisera | Q36247967 | ||
| The cytoplasmic domain of CD4 promotes the development of CD4 lineage T cells | Q36365908 | ||
| A single T cell receptor recognizes structurally distinct MHC/peptide complexes with high specificity | Q36367304 | ||
| Effects of complementarity determining region mutations on the affinity of an alpha/beta T cell receptor: measuring the energy associated with CD4/CD8 repertoire skewing | Q36367702 | ||
| The final maturation of at least some single-positive CD4(hi) thymocytes does not require T cell receptor-major histocompatibility complex contact | Q36375309 | ||
| Analysis of the expression of peptide-major histocompatibility complexes using high affinity soluble divalent T cell receptors | Q36398857 | ||
| A soluble divalent class I major histocompatibility complex molecule inhibits alloreactive T cells at nanomolar concentrations | Q36424948 | ||
| Self-MHC-restricted peptides recognized by an alloreactive T lymphocyte clone | Q36813012 | ||
| Attachment of an anti-receptor antibody to non-target cells renders them susceptible to lysis by a clone of cytotoxic T lymphocytes | Q37580704 | ||
| The mode of ligand recognition by two peptide:MHC class I-specific monoclonal antibodies | Q40930624 | ||
| Altered peptide ligand-induced partial T cell activation: molecular mechanisms and role in T cell biology | Q41039639 | ||
| The role of the T cell receptor in positive and negative selection of developing T cells | Q41174331 | ||
| T-cell-receptor affinity and thymocyte positive selection | Q41192128 | ||
| Antigen-specific T-cell receptors and their reactions with complexes formed by peptides with major histocompatibility complex proteins | Q41202687 | ||
| Evidence that the antigen receptors of cytotoxic T lymphocytes interact with a common recognition pattern on the H-2Kb molecule | Q41278555 | ||
| In thymic selection, peptide diversity gives and takes away | Q41585792 | ||
| Qualitative and quantitative differences in T cell receptor binding of agonist and antagonist ligands. | Q41612272 | ||
| Ligand recognition by alpha beta T cell receptors | Q46222293 | ||
| Preferential expression of TCR V alpha regions in CD4/CD8 subsets: class discrimination or co-receptor recognition? | Q47927783 | ||
| MHC class II-specific T cells can develop in the CD8 lineage when CD4 is absent. | Q51115513 | ||
| Binding properties and solubility of single-chain T cell receptors expressed in E. coli. | Q54587478 | ||
| Yeast polypeptide fusion surface display levels predict thermal stability and soluble secretion efficiency | Q56902099 | ||
| T Cells Can Be Activated by Peptides That Are Unrelated in Sequence to Their Selecting Peptide | Q56922149 | ||
| 18 Systematic mutational analyses of protein-protein interfaces | Q67709743 | ||
| Characterization of a murine monoclonal antibody specific for an allotypic determinant on T cell antigen receptor | Q69382735 | ||
| Marked differences in the efficiency of expression of distinct alpha beta T cell receptor heterodimers | Q69787694 | ||
| A residue in the center of peptide QL9 affects binding to both Ld and the T cell receptor | Q71755899 | ||
| Identification of a common docking topology with substantial variation among different TCR-peptide-MHC complexes | Q74450340 | ||
| Alanine scanning mutagenesis of an alphabeta T cell receptor: mapping the energy of antigen recognition | Q74545050 | ||
| A very high level of crossreactivity is an essential feature of the T-cell receptor | Q77324273 | ||
| TCR binding to peptide-MHC stabilizes a flexible recognition interface | Q77328526 | ||
| Alloreactive and syngeneic CTL are comparably dependent on interaction with MHC class I alpha-helical residues | Q78224783 | ||
| P433 | issue | 8 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 1355-1364 | |
| P577 | publication date | 2000-04-01 | |
| P1433 | published in | Journal of Experimental Medicine | Q3186912 |
| P1476 | title | Role of 2CT cell receptor residues in the binding of self- and allo-major histocompatibility complexes | |
| P478 | volume | 191 |
| Q36537962 | A minimal binding footprint on CD1d-glycolipid is a basis for selection of the unique human NKT TCR. |
| Q38050479 | A structural voyage toward an understanding of the MHC-I-restricted immune response: lessons learned and much to be learned |
| Q40763160 | Activation of a T cell hybridoma by an alloligand results in differential effects on IL-2 secretion and activation-induced cell death |
| Q57363751 | Allogeneic and syngeneic class I MHC complexes drive the association of CD8 and TCR on 2C T cells |
| Q45012658 | Antibody specific for the peptide.major histocompatibility complex. Is it T cell receptor-like? |
| Q27640417 | CDR3 loop flexibility contributes to the degeneracy of TCR recognition |
| Q27627292 | Crystal structure of a T cell receptor bound to an allogeneic MHC molecule |
| Q34439729 | Design of T-cell receptor libraries with diverse binding properties to examine adoptive T-cell responses |
| Q34099738 | Differences in antigen recognition and cytolytic activity of CD8(+) and CD8(-) T cells that express the same antigen-specific receptor |
| Q37432048 | Different strategies adopted by K(b) and L(d) to generate T cell specificity directed against their respective bound peptides |
| Q34984478 | Direct stimulation of T cells by membrane vesicles from antigen-presenting cells |
| Q27652612 | Distinct CDR3 conformations in TCRs determine the level of cross-reactivity for diverse antigens, but not the docking orientation |
| Q47782025 | Emerging Concepts in TCR Specificity: Rationalizing and (Maybe) Predicting Outcomes |
| Q37096091 | Evolutionarily conserved amino acids that control TCR-MHC interaction |
| Q35632925 | Evolutionarily conserved features contribute to αβ T cell receptor specificity |
| Q28237177 | Germline-encoded amino acids in the alphabeta T-cell receptor control thymic selection |
| Q56917232 | Germline-encoded recognition of diverse glycolipids by natural killer T cells |
| Q36369186 | Identification of a crucial energetic footprint on the alpha1 helix of human histocompatibility leukocyte antigen (HLA)-A2 that provides functional interactions for recognition by tax peptide/HLA-A2-specific T cell receptors |
| Q73035390 | Incompatible differences: view of an allogeneic pMHC-TCR complex |
| Q35228107 | Mutagenesis of beryllium-specific TCRs suggests an unusual binding topology for antigen recognition |
| Q34953926 | Plasticity in the contribution of T cell receptor variable region residues to binding of peptide-HLA-A2 complexes |
| Q37002818 | Specificity of T-cell alloreactivity |
| Q34602699 | Structural basis of T cell recognition of peptides bound to MHC molecules |
| Q27647150 | Structural evidence for a germline-encoded T cell receptor-major histocompatibility complex interaction 'codon' |
| Q27666863 | Structure of a TCR with high affinity for self-antigen reveals basis for escape from negative selection |
| Q81301466 | T cell receptor CDRs: starring versus supporting roles |
| Q37711339 | TCR scanning of peptide/MHC through complementary matching of receptor and ligand molecular flexibility |
| Q34360502 | TCR usage in naive and committed alloreactive cells: implications for the understanding of TCR biases in transplantation |
| Q30873107 | TCRs with high affinity for foreign pMHC show self-reactivity |
| Q56917578 | The CDR3 regions of an immunodominant T cell receptor dictate the 'energetic landscape' of peptide-MHC recognition |
| Q41447071 | The contribution of major histocompatibility complex contacts to the affinity and kinetics of T cell receptor binding |
| Q33737674 | The impact of TCR-binding properties and antigen presentation format on T cell responsiveness |
| Q34167226 | Two mechanisms that account for major histocompatibility complex restriction of T cells |
| Q42050788 | Two-step binding mechanism for T-cell receptor recognition of peptide MHC. |
| Q35196417 | What do TCR-pMHC crystal structures teach us about MHC restriction and alloreactivity? |
| Q24673986 | Structure of a complex of the human alpha/beta T cell receptor (TCR) HA1.7, influenza hemagglutinin peptide, and major histocompatibility complex class II molecule, HLA-DR4 (DRA*0101 and DRB1*0401): insight into TCR cross-restriction and alloreactiv |
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