| scholarly article | Q13442814 |
| P356 | DOI | 10.1038/292497A0 |
| P953 | full work available at URL | http://www.nature.com/articles/292497a0 |
| http://www.nature.com/articles/292497a0.pdf | ||
| P698 | PubMed publication ID | 6166871 |
| P50 | author | Polly Matzinger | Q3395388 |
| P2860 | cites work | Genes and antibodies | Q28185156 |
| Immunological surveillance against altered self components by sensitised T lymphocytes in lymphocytes choriomeningitis | Q34699212 | ||
| Role of major histocompatibility complex gene products in delayed-type hypersensitivity | Q35012164 | ||
| Determinants of antigenic molecules responsible for genetically controlled regulation of immune responses | Q35018149 | ||
| Killer cells reactive to altered-self antigens can also be alloreactive | Q35027922 | ||
| Nature of the antigenic complex recognized by T lymphocytes: specific sensitization by antigens associated with allogeneic macrophages | Q35028017 | ||
| Complementation of H-2-linked Ir genes in the mouse | Q35089563 | ||
| The somatic generation of immune recognition | Q35673404 | ||
| Biological significance of alloreactivity: T cells stimulated by Sendai virus-coated syngeneic cells specifically lyse allogeneic target cells | Q35996507 | ||
| The frequency of antigen-sensitive cells in tissue transplantation. A commentary on clonal selection | Q36269558 | ||
| Cell interactions between histoincompatible T and B lymphocytes. II. Failure of physiologic cooperative interactions between T and B lymphocytes from allogeneic donor strains in humoral response to hapten-protein conjugates | Q36272251 | ||
| Genetic control of immune responses in vitro. V. Stimulation of suppressor T cells in nonresponder mice by the terpolymer L-glutamic acid 60-L-alanine 30-L-tyrosine 10 (GAT). | Q36273247 | ||
| Spleen cell proliferation in response to homologous antigens studied in congenic resistant strains of mice | Q36334593 | ||
| Histocompatibility antigen-activated cytotoxic T lymphocytes. II. Estimates of the frequency and specificity of precursors | Q36335542 | ||
| Coupled complementation of immune response genes controlling responsiveness to the H-2.2 alloantigen | Q36335798 | ||
| The lymphoreticular system in triggering virus plus self-specific cytotoxic T cells: evidence for T help | Q36339973 | ||
| On the thymus in the differentiation of "H-2 self-recognition" by T cells: evidence for dual recognition? | Q36340069 | ||
| The role of H-2 linked genes in helper T-cell function. II. Isolation on antigen-pulsed macrophages of two separate populations of F1 helper T cells each specific for antigen and one set of parental H-2 products | Q36340749 | ||
| Structural studies on the murine Ia alloantigens. V. Evidence that the structural gene for the I-E/C beta polypeptide is encoded within the I-A subregion | Q36341363 | ||
| H-2 antigens of the thymus determinelymphocyte specificity | Q36341908 | ||
| The biologic significance of alloreactivity. The ontogeny of T-cell sets specific for alloantigens or modified self antigens | Q36342063 | ||
| Major histocompatibility complex-restricted antibody reactivity mainly, but not exclusively, directed against cells from male donors | Q36343030 | ||
| Suppression of T cells specific for the nonthymic parental H-2 haplotype in thymus-grafted chimeras | Q36343268 | ||
| Gene complementation. Neither Ir-GLphi gene need be present in the proliferative T cell to generate an immune response to Poly(Glu55Lys36Phe9)n | Q36343676 | ||
| Antigen-inducible, H-2-restricted, interleukin-2-producing T cell hybridomas. Lack of independent antigen and H-2 recognition | Q36344766 | ||
| Relationship between Fc receptors, antigen-binding sites on T and B cells, and H-2 complex-associated determinants | Q36357724 | ||
| Collaboration of allogeneic T and B lymphocytes in the primary antibody response to sheep erythrocytes in vitro | Q36358453 | ||
| Dissection of the B10.D2 anti-H-2Kb cytolytic T lymphocyte receptor repertoire | Q42935133 | ||
| Specific suppression of antigen-reactive cells in neonatal transplantation tolerance | Q44348354 | ||
| Specific control of responsiveness by two complementing Ir loci in the H-2 complex | Q44594923 | ||
| Cell-mediated cytotoxicity to trinitrophenyl-modified syngeneic lymphocytes | Q48533870 | ||
| Blocking of syngeneic effector T cells by soluble tumour antigens | Q53692270 | ||
| A Theory of Self-Nonself Discrimination: Paralysis and induction involve the recognition of one and two determinants on an antigen, respectively | Q55888521 | ||
| Quantitative Studies on Tissue Transplantation Immunity. III. Actively Acquired Tolerance | Q55967936 | ||
| T-cell specificity for H–2 and Ir gene phenotype correlates with the phenotype of thymic antigen-presenting cells | Q59061484 | ||
| Transplantation tolerance | Q66705187 | ||
| Cytolytic thymus-derived lymphocytes specific for allogeneic stimulator cells crossreact with chemically modified syngeneic cells | Q66875943 | ||
| T cells mediate transplantation tolerance | Q66903310 | ||
| Can tolerant allogeneic cells restore nude mice? | Q67353188 | ||
| Lymphocyte-mediated cytolysis of allogeneic tumor cells in vitro. I. Search for target antigens in subcellular fractions | Q67509615 | ||
| Genetic control of the immune response to the radom linear terpolymer of L-glutamic acid, L-lysine and L-leucine (GLleu) by complementing Ir genes | Q67833202 | ||
| Cell transfer studies in a genetically controlled immune response | Q69415024 | ||
| An examination of MHC restriction in the context of a minimal clonal abortion model for self tolerance | Q70539966 | ||
| A Certain Symmetry : Histocompatibility Antigens compared with Immunocyte Receptors | Q71547967 | ||
| Three-receptor, clonal expansion model for selection of self-recognition in the thymus | Q72073261 | ||
| Genetic Control of the Antibody Response: Relationship between Immune Response and Histocompatibility (H-2) Type | Q72339461 | ||
| Formation of SV40 specific and H–2 restricted target cell antigen by somatic cell fusion | Q72842180 | ||
| Strong and weak histocompatibility gene differences in mice and their role in the rejection of homografts of tumors and skin | Q74203665 | ||
| IMMUNOGENETIC CONSEQUENCES OF VASCULAR ANASTOMOSES BETWEEN BOVINE TWINS | Q80949985 | ||
| The Clonal Selection Hypothesis Evaluated by Grafted Cells Reacting Against their Hosts | Q113816133 | ||
| The major histocompatibility complex determines susceptibility to cytotoxic T cells directed against minor histocompatibility antigens | Q36358831 | ||
| Genetic control of specific immune suppression. III. Mapping of H-2 complex complementing genes controlling immune suppression by the random copolymer L-glutamic acid50-L-tyrosine50 (GT) | Q36359694 | ||
| Regulation by the H-2 gene complex of macrophage-lymphoid cell interactions in secondary antibody responses in vitro | Q36359776 | ||
| The effect of allogeneic presensitization on H-Y graft survival and in vitro cell-mediated responses to H-y antigen | Q36359795 | ||
| Functional interactions of viral and histocompatibility antigens at tumor cell surfaces | Q37466036 | ||
| Participation of histocompatibility antigens in capping of molecularly independent cell surface components by their specific antibodies | Q37586801 | ||
| Major histocompatibility complex-linked immune-responsiveness is acquired by lymphocytes of low-responder mice differentiating in thymus of high-responder mice | Q37586973 | ||
| The influence of thymus on the development of MHC restrictions exhibited by T-helper cells | Q38595843 | ||
| Lymphocyte-mediated cytolysis of allogenic tumor cell in vitro. II. Binding of cytotoxic lymphocytes to formaldehyde-fixed target cells | Q39359826 | ||
| H-2 antigen-specific cytotoxic T cells induced by concanavalin A: estimation of their relative frequency | Q39407711 | ||
| Two Different VH Gene Products Make Up the T-Cell Receptors | Q39414474 | ||
| Genetic Control of Specific Immune Responses and Immune Suppressions by I-region Genes | Q39448552 | ||
| Responsiveness to HY Antigen Ir Gene Complementation and Target Cell Specificity | Q39449141 | ||
| The immune response genes of the major histocompatibility complex | Q39475236 | ||
| A clonal deletion model for Ir gene control of the immune response | Q39482093 | ||
| Major histocompatibility complex restricted cell-mediated immunity | Q39482748 | ||
| A dual recognition model for cytotoxic T cells based on thymic selection of precursors with low affinity for Self H-2 antigens | Q39489681 | ||
| Studies on the nature of the cell surface antigen reacting with cytolytic T lymphocytes in murine oncornavirus-induced tumors | Q39497014 | ||
| Association of Mouse Major Histocompatibility and Rauscher Murine Leukaemia Virus Envelope Glycoprotein Antigens on Leukaemia Cells and their Recognition by Syngeneic Virus-Immune-Cytotoxic T-Lymphocytes | Q39526384 | ||
| Role of H-2 Gene Products in the Function of T Helper Cells from Normal and Chimeric Mice in Vivo1 | Q39526566 | ||
| Amputation of a suppressor determinant on lysozyme reveals underlying T-cell reactivity to other determinants | Q39551665 | ||
| Fine specificity of a continuously growing killer cell clone specific for H-Y antigen | Q39572567 | ||
| The role of H-2 linked genes in helper T-cell function. IV. Importance of T-cell genotype and host environment in I-region and Ir gene expression | Q39634636 | ||
| Influence of Thymus Genotype on Acquisition of Responsiveness in Delayed-type Hypersensitivity | Q39646886 | ||
| Patterns of virus-immune T-cell responsiveness. Comparison of (H-2(k) x H-2(b)) {arrow} H-2(b) Radiation Chimeras and negatively selected H-2(b) lymphocytes | Q39694872 | ||
| Why do so many cells take part in mixed lymphocyte reactions? | Q39750147 | ||
| H-2 Mutations: Their Genetics and Effect on Immune Functions | Q39773316 | ||
| Histocompatibility-linked immune response genes | Q39866999 | ||
| Cell-mediated immunity and the major histocompatibility complex | Q39877107 | ||
| Genetic Control of Specific Immune Responses | Q39988595 | ||
| Lymphocytotoxic antibodies produced by H—2 allo-immunisation distinguish between MuLV-positive and -negative substrains of the same H-2 haplotype | Q40276704 | ||
| Early cellular events in a systemic graft-vs.-host reaction. II. Autoradiographic estimates of the frequency of donor lymphocytes which respond to each Ag-B-determined antigenic complex | Q40309613 | ||
| Hypothesis: why do so many lymphocytes respond to major histocompatibility antigens? | Q40643054 | ||
| A Simple, Conservative Explanation of the H-2 Restriction of Interactions Between Lymphocytes | Q40644138 | ||
| Neonatally tolerant mice fail to react against virus-infected tolerated cells | Q40648298 | ||
| The generation of killer cells to trinitrophenyl-modified allogeneic targets by lymphocyte populations negatively selected to strong alloantigens | Q40649920 | ||
| In a radiation chimaera, host H–2 antigens determine immune responsiveness of donor cytotoxic cells | Q40658124 | ||
| Clones of alloreactive T cells | Q40674926 | ||
| Influence of the major histocompatibility complex on lymphocyte interactions in antibody formation | Q40680962 | ||
| Restricted helper function of F1 leads to parent bone marrow chimeras controlled by K-end of H-2 complex | Q40685944 | ||
| T-cell inhibition of humoral responsiveness. II. Theory on the role of restrictive recognition in immune regulation | Q40690063 | ||
| Vaccinia-specific cytotoxic T-cell responses in the context of H-2 antigens not encountered in thymus may reflect aberrant recognition of a virus-H-2 complex | Q40701083 | ||
| The involvement of a suppressor mechanism in neonatally induced allograft tolerance in mice | Q40765918 | ||
| Helper function of T cells depleted of alloantigen-reactive lymphocytes by filtration through irradiated F1 hybrid recipients. I. Failure to collaborate with allogeneic B cells in a secondary response to sheep erythrocytes measured in vivo | Q42118420 | ||
| P433 | issue | 5823 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | surface antigens | Q66660287 |
| P304 | page(s) | 497-501 | |
| P577 | publication date | 1981-08-01 | |
| 1981-08-06 | |||
| P1433 | published in | Nature | Q180445 |
| P1476 | title | A one-receptor view of T-cell behaviour | |
| P478 | volume | 292 |
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| Q36347707 | Antigen-presenting cells from nonresponder strain 2 guinea pigs are fully competent to present bovine insulin B chain to responder strain 13 T cells. Evidence against a determinant selection model and in favor of a clonal deletion model of immune re |
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| Q42182694 | Clonal heterogeneity in the functional requirement for Lyt-2/3 molecules on cytolytic T lymphocytes: analysis by antibody blocking and selective trypsinization |
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| Q36348326 | Cross-reactivity of self-HLA-restricted Epstein-Barr virus-specific cytotoxic T lymphocytes for allo-HLA determinants |
| Q68796882 | Cytotoxic T cell lysis of H-2-negative murine sarcoma cells |
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| Q41934641 | Development of T cell clones reactive to two defined restriction elements in conjunction with two defined epitopes of antigen |
| Q36350310 | Distinct recognition phenotypes exist for T cell clones specific for small peptide regions of proteins. Implications for the mechanisms underlying major histocompatibility complex-restricted antigen recognition and clonal deletion models of immune r |
| Q58976498 | Does the T-cell receptor bind to the MHC? |
| Q93519758 | Elimination of self-tolerogen turns nonresponder mice into responders |
| Q72813262 | Evidence from in vitro studies that tolerance to self antigens is MHC-restricted |
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| Q68940183 | Fine specificity analysis of lactate dehydrogenase B-specific proliferating T cell clones: implications for the mechanism of alloreactivity |
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