| P2093 | author name string | J Sprent | |
| | R Korngold | |
| | K Molnar-Kimber | |
| P2860 | cites work | Functional Activity of T Cells which Differentiate from Nude Mouse Precursors in a Congenic or Allogeneic Thymus Graft | Q33707583 |
| | Cross-priming for a secondary cytotoxic response to minor H antigens with H-2 congenic cells which do not cross-react in the cytotoxic assay | Q33903838 |
| | Interaction Between Antigen-Presenting Cells and Primed T Lymphocytes. An Assessment of Ir Gene Expression in the Antigen-Presenting Cell | Q34154332 |
| | The Role of I Region Gene Products in Macrophage - T Lymphocyte Interaction | Q34154351 |
| | Influence of the Major Histocompatibility Complex on T-Cell Activation | Q34205764 |
| | In a fully H-2 incompatible chimera, T cells of donor origin can respond to minor histocompatibility antigens in association with either donor or host H-2 type | Q34321361 |
| | Role of major histocompatibility complex gene products in delayed-type hypersensitivity | Q35012164 |
| | Nature of the antigenic complex recognized by T lymphocytes: specific sensitization by antigens associated with allogeneic macrophages | Q35028017 |
| | The somatic generation of immune recognition | Q35673404 |
| | Histocompatibility-linked immune response gene function in guinea pigs. Specific inhibition of antigen-induced lymphocyte proliferation by alloantisera | Q36272091 |
| | 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 |
| | Function of macrophages in antigen recognition by guinea pig T lymphocytes. I. Requirement for histocompatible macrophages and lymphocytes | Q36272607 |
| | Function of macrophages in antigen recognition by guinea pig T lymphocytes. II. Role of the macrophage in the regulation of genetic control of the immune response | Q36272651 |
| | Effect of recent antigen priming on adoptive immune responses. II. Specific unresponsiveness of circulating lymphocytes from mice primed with heterologous erythrocytes | Q36272849 |
| | Independent populations of primed F1 guinea pig T lymphocytes respond to antigen-pulsed parental peritoneal exudate cells | Q36335481 |
| | Antigen presentation in the murine T-lymphocyte proliferative response. I. Requirement for genetic identity at the major histocompatibility complex | Q36335803 |
| | H-2 effects on cell-cell interactions in the response to single non-H-2 alloantigens. II. H-2 D region control of H-7.1-specific stimulator function in mixed lymphocyte culture and susceptibility to lysis by H-7.1- specific cytotoxic cells | Q36336155 |
| | H-2 effects on cell-cell interactions in the response to single non-H-2 alloantigens. I. Donor H-2D region control of H-7.1-immunogenicity and lack of restriction in vivo | Q36336226 |
| | MHC-Restricted Cytotoxic T Cells: Studies on the Biological Role of Polymorphic Major Transplantation Antigens Determining T-Cell Restriction-Specificity, Function, and Responsiveness | Q39576364 |
| | 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 |
| | The role of H-2-linked genes in helper T-cell function. VI. Expression of Ir genes by helper T cells | Q39655894 |
| | Association of immunity and tolerance to host H-2 determinants in irradiated F1 hybrid mice reconstituted with bone marrow cells from one parental strain | Q39736459 |
| | Techniques for Separation and Selection of Antigen Specific Lymphocytes | Q39785486 |
| | T cell proliferation in the mixed lymphocyte culture does not necessarily result in the generation of cytotoxic T effector cells | Q39788638 |
| | T Lymphocyte Stimulation by Hapten-Conjugated Macrophages. A Model System for the Study of Immunocompetent Cell Interactions | Q39802469 |
| | T lymphocyte responses to Mls locus antigens involve recognition of H-2 I region gene products | Q39816014 |
| | Nature of the antigenic complex recognized by T lymphocytes. V. Genetic predisposition of independent F1 T cell subpopulations responsive to antigen-pulsed parental macrophages | Q39841534 |
| | Functions of macrophages in antibody responses in vitro | Q39869384 |
| | Immunogenetic and biological aspects of in vitro lymphocyte allotransformation (MLR) in the mouse | Q39869822 |
| | Allotype-specific analysis of anti-(TYR,GLU)-ALA-LYS antibodies produced by Ir-1A high and low responder chimeric mice | Q36337172 |
| | 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 |
| | Cytotoxic T cells recognize male antigen and H-2 as distinct entities | Q36340116 |
| | Cellular and genetic control of antibody responses in vitro. III. Immune response gene regulation of accessory cell function | Q36340360 |
| | The immune response of allophenic mice to 2,4-dinitrophenyl (DNP)-bovine gamma globulin. I. Allotype analysis of anti-DNP antibody | Q36340433 |
| | 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 |
| | Gene complementation in the T-lymphocyte proliferative response to poly (Glu55Lys36Phe9)n. A demonstration that both immune response gene products must be expressed in the same antigen-presenting cell | Q36341092 |
| | Nature of T-cell macrophage interaction in helper-cell induction in vitro. II. Two stages of T-helper-cell differentiation analyzed in irradiation and allophenic chimeras | Q36341283 |
| | Cellular and genetic control of antibody responses. V. Helper T-cell recognition of H-2 determinants on accessory cells but not B cells | Q36341427 |
| | The in vitro generation and sustained culture of nude mouse cytolytic T-lymphocytes | Q36341555 |
| | Adaptive differentiation of murine lymphocytes. II. The thymic microenvironment does not restrict the cooperative partner cell preference of helper T cells differentiating in F1 leads to F1 thymic chimeras | Q36341593 |
| | T-cell populations specifically depleted of alloreactive potential cannot be induced to lyse H-2-different virus-infected target cells | Q36341706 |
| | H-2 antigens of the thymus determinelymphocyte specificity | Q36341908 |
| | The histocompatibility restrictions on macrophage T-helper cell interaction determine the histocompatibility restrictions on T-helper cell B-cell interaction | Q36342042 |
| | The biologic significance of alloreactivity. The ontogeny of T-cell sets specific for alloantigens or modified self antigens | Q36342063 |
| | Lethal graft-versus-host disease after bone marrow transplantation across minor histocompatibility barriers in mice. Prevention by removing mature T cells from marrow | Q36342244 |
| | T cells recognize minor histocompatibility antigens on H-2 allogeneic cells | Q36342916 |
| | Delayed-type hypersensitivity to allogeneic cells in mice. III. Sensitivity to cell-surface antigens coded by the major histocompatibility complex and by other genes | Q36342929 |
| | The specific binding of Listeria monocytogenes-immune T lymphocytes to macrophages. I. Quantitation and role of H-2 gene products | Q36343002 |
| | Distinct Ir genes for helper and killer cells in the cytotoxic response to H-Y antigen | Q36343026 |
| | Functional analysis of T cells expressing Ia antigens. I. Demonstration of helper T-cell heterogeneity | Q36343076 |
| | Mice whose B cells cannot produce the T15 idiotype also lack an antigen-specific helper T cell required for T15 expression | Q36343082 |
| | Suppression of T cells specific for the nonthymic parental H-2 haplotype in thymus-grafted chimeras | Q36343268 |
| | Absence of H-2 restriction in primary and secondary mixed-lymphocyte reactions to strong M1s determinants | Q36343343 |
| | Cell-mediated lympholysis of trinitrophenyl-modified autologous lymphocytes. Effector cell specificity to modified cell surface components controlled by H-2K and H-2D serological regions of the murine major histocompatibility complex | Q36358161 |
| | Collaboration of allogeneic T and B lymphocytes in the primary antibody response to sheep erythrocytes in vitro | Q36358453 |
| | The allogeneic bisection of carrier-specific enhancement of monoclonal B-cell responses | Q36358547 |
| | In vitro cell-mediated immune responses to the male specific(H-Y) antigen in mice | Q36358603 |
| | The major histocompatibility complex determines susceptibility to cytotoxic T cells directed against minor histocompatibility antigens | Q36358831 |
| | Effect of recent antigen priming on adoptive immune responses. III. Antigen-induced selective recruitment of subsets of recirculating lymphocytes reactive to H-2 determinants | Q36359104 |
| | T-lymphocyte-enriched murine peritoneal exudate cells. II. Genetic control of antigen-induced T-lymphocyte proliferation | Q36359167 |
| | T-cell regulation of antibody responses: demonstration of allotype-specific helper T cells and their specific removal by suppressor T cells | Q36359717 |
| | Cell-mediated immunity and the major histocompatibility complex | Q39877107 |
| | Cross-reactivity exists between Mlsa and Mlsd lymphocyte-activating determinants as demonstrated by the negative clonal selection of responder cells in a mixed lymphocyte reaction | Q39891545 |
| | Genetics and immunology of sex-linked antigens | Q39907579 |
| | Thymus and antigen-reactive cells | Q40005247 |
| | Immunologic complementation between thymus and marrow cells--a model for the two-cell theory of immunocompetence. | Q40005259 |
| | H–2 restriction and non-restriction of T-cell-mediated cytotoxicity against mouse mammary tumour targets | Q40205661 |
| | 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 |
| | The role of Langerhans cells in allergic contact hypersensitivity. A review of findings in man and guinea pigs | Q40525519 |
| | Lymphocytes as Models for the Study of Mammalian Cellular Differentiation | Q40643388 |
| | In vitro induction of tumor-specific immunity. III. Lack of requirement for H-2 compatibility in lysis of tumor targets by T cells activated in vitro to oncofetal and plasmacytoma antigens | Q40643617 |
| | 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 |
| | Generation of T helper cells in vitro. IV. F1 T helper cells primed with antigen-pulsed parental macrophages are genetically restricted in their antigen-specific helper activity | Q40666442 |
| | T cells specific for hapten-modified self are precommitted for self major histocompatibility complex antigens before encounter with the hapten | Q40676778 |
| | Restricted helper function of F1 hybrid T cells positively selected to heterologous erythrocytes in irradiated parental strain mice. I. Failure to collaborate with B cells of the opposite parental strain not associated with active suppression | Q40676798 |
| | Restricted helper function of F1 hybrid T cells positively selected to heterologous erythrocytes in irradiated parental strain mice. II. Evidence for restrictions affecting helper cell induction and T-B collaboration, both mapping to the K-end of th | Q40676806 |
| | Restricted helper function of F1 leads to parent bone marrow chimeras controlled by K-end of H-2 complex | Q40685944 |
| | Idiotype-specific T helper cells are required to induce idiotype-positive B memory cells to secrete antibody | Q40690288 |
| | Role of the H-2 complex in induction of T helper cells in vivo. I. Antigen-specific selection of donor T cells to sheep erythrocytes in irradiated mice dependent upon sharing of H-2 determinants between donor and host | Q40690826 |
| | Two subgroups of T helper cells in F1 hybrid mice revealed by negative selection to heterologous erythrocytes in vivo | Q40693510 |
| | Nature of T cell-macrophage interaction in helper cell inductionin vitro I. Evidence for genetic restriction of T cell-macrophage interactions prior to T cell priming | Q40695350 |
| | 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 |
| | T-helper function of parent leads to F1 chimeras. Presence of a separate T-cell subgroup able to stimulate allogeneic B cells but not syngeneic B cells | Q40701106 |
| | Studies on the generation and expression of H-2-controlled T helper function in chimeric mice: Evidence for two levels of H-2 restriction | Q40728646 |
| | Ia antigen expression on human epidermal Langerhans cells | Q40792234 |
| | Two distinct types of helper T cells involved in the secondary antibody response: independent and synergistic effects of Ia- and Ia+ helper T cells | Q41367783 |
| | Selection of cytotoxic T-cell precursors specific for minor histocompatibility determinants. I. Negative selection across H-2 barriers induced with disrupted cells but not with glutaraldehyde-treated cells: evidence for antigen processing | Q41789078 |
| | On the role of the H-2 histocompatibility complex in determining the specificity of cytotoxic effector cells sensitized against syngeneic trinitrophenyl-modified targets | Q41816941 |
| | The role of macrophages in the generation of T-helper cells. II. The genetic control of the macrophage-T-cell interaction for helper cell induction with soluble antigens | Q41833807 |
| | Antibody response of C3H in equilibrium (CKB X CWB)F1 tetraparental mice to poly-L(Tyr,Glu)-poly-D,L-Ala-poly-L-Lys immunization | Q41879326 |
| | Minor H antigens introduced on H-2 different stimulating cells cross-react at the cytotoxic T cell level during in vivo priming | Q41895196 |
| | The specific selection of recirculating lymphocytes by antigen in normal and preimmunized rats | Q41898561 |
| | 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 |
| | Effect of recent antigen priming on adoptive immune responses. IV. Antigen-induced selective recruitment of recirculating lymphocytes to the spleen demonstrable with a microculture system | Q42137715 |
| | In vivo requirement for a radiation-resistant cells in the immune response to sheep erythrocytes | Q42206069 |
| | Negative selection of T cells causing lethal graft-versus-host disease across minor histocompatibility barriers. Role of the H-2 complex | Q42259756 |
| | Allogeneic carrier-specific enhancement of hapten-specific secondary B-cell responses | Q42941082 |
| | Antigen-induced selective recruitment of circulating lymphocytes | Q44125070 |
| | Antigen-specific and nonspecific mediators of T cell/B cell cooperation. I. Evidence for their production by different T cells | Q44354770 |
| | Helper T cells recognise antigen and macrophage surface components simultaneously. | Q52241720 |
| | H-2 dependence of co-operation between T and B cells in vivo. | Q53765275 |
| | Cell interactions in the immune response in vitro. I. Metabolic activities of T cells in a collaborative antibody response. | Q54586871 |
| | The cross-linking of proteins with glutaraldehyde and its use for the preparation of immunoadsorbents. | Q54645824 |
| | The function and interrelationships of T-cell receptors, Ir genes and other histocompatibility gene products | Q66875394 |
| | Adaptive differentiation of murine lymphocytes. I. Both T and B lymphocytes differentiating in F1 transplanted to parental chimeras manifest preferential cooperative activity for partner lymphocytes derived from the same parental type corresponding | Q66877735 |
| | Cytotoxic T lymphocytes recognise allogeneic tolerated TNP-conjugated cells | Q66884284 |
| | Five types of lymphocytes (lg− θ−, lg− θ+ weak, lg− θ+strong, lg+ θ− and lg+ θ+) characterized by double immunofluorescence and electrophoretic mobility Organ distribution in normal and nude mice | Q66888042 |
| | Macrophage Ia antigens. I. macrophage populations differ in their expression of Ia antigens | Q67253568 |
| | Can tolerant allogeneic cells restore nude mice? | Q67353188 |
| | Specific unresponsiveness of recirculating lymphocytes ater exposure to histocompatibility antigen in F 1 hybrid rats | Q68760146 |
| | The H-2D and H-2K regions of the major histocompatibility system and the M locus of the mouse investigated by parabiosis | Q70007455 |
| | 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 |
| | Nature of the antigenic complex recognized by T lymphocytes. I. Analysis with an in vitro primary response to soluble protein antigens | Q36359978 |
| | T-cell-dependent B-cell stimulation is H-2 restricted and antigen dependent only at the resting B-cell level | Q36360899 |
| | H-2 gene complex restricts transfer of delayed-type hypersensitivity in mice | Q37466327 |
| | Inhibition of dual Ir gene-controlled T-lymphocyte proliferative response to poly (Glu56Lys35Phe9)n with anti-Ia antisera directed against products of either I-A or I-C subregion | Q37586710 |
| | 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 |
| | Induction of H-2-restricted cytotoxic T cells: in vivo induction has the appearance of being unrestricted | Q39164207 |
| | Tolerance to histocompatibility determinants in tetraparental bone marrow chimeras | Q39314527 |
| | Two genes in the major histocompatibility complex control immune response | Q39338895 |
| | The role of macrophages in the generation of T-helper cells. I. The requirement for macrophages in helper cell induction and characteristics of the macrophage-T cell interaction | Q39353253 |
| | Role of the Murine Major Histocompatibility Complex in the Specificity of in vitro T-Cell-Mediated Lympholysis Against Chemically-Modified Autologous Lymphocytes | Q39383683 |
| | T cell function in bone marrow chimeras: absence of host-reactive T cells and cooperation of helper T cells across allogeneic barriers | Q39383698 |
| | Specificity of Virus-Immune Effector T Cells for H-2K or H-2D Compatible Interactions: Implications for H-Antigen Diversity | Q39383715 |
| | Two Different VH Gene Products Make Up the T-Cell Receptors | Q39414474 |
| | On the Possibility of Multiple T-cell Receptors | Q39448568 |
| | Responsiveness to HY Antigen Ir Gene Complementation and Target Cell Specificity | Q39449141 |
| | The role of Ia antigens in T cell activation | Q39449149 |
| | Genetic control of the immune response to Thy-1 antigens | Q39475222 |
| | The immune response genes of the major histocompatibility complex | Q39475236 |
| | A dual recognition model for cytotoxic T cells based on thymic selection of precursors with low affinity for Self H-2 antigens | Q39489681 |
| | A hypothesis to relate the specificity of T lymphocytes and the activity of I region-specific Ir genes in macrophages and B lymphocytes | Q39491805 |
| | Apparent lack of H-2 restriction of allograft rejection | Q39506429 |
| | Expression and Function of Idiotypes on Lymphocytes | Q39509367 |
| | A subpopulation of adherent accessory cells bearing both I-A and I-E or C subregion antigens is required for antigen-specific murine T lymphocyte proliferation | Q39515162 |
| | Role of H-2 Gene Products in the Function of T Helper Cells from Normal and Chimeric Mice in Vivo1 | Q39526566 |
| | Alloreactivity, the Development of the T Cell Repertoire and the Understanding of T Cell Function | Q39526572 |
| | The Influence of the Major Histocompatibility Complex on the Function of T-Helper Cells in Antibody Formation | Q39526580 |
| | Thymus and Lymphohemopoietic Cells: Their Role in T Cell Maturation in Selection of T Cells' H-2-Restriction-Specificity and in H-2 Linked Ir Gene Control | Q39526586 |
| | The Influence of Thymus H-2 Antigens on the Specificity of Maturing Killer and Helper Cells | Q39526592 |
| | Cell types required for H-2-restricted cytotoxic responses generated by trinitrobenzene sulfonate-modified syngeneic cells or trinitrophenyl-conjugated proteins | Q39548557 |
| | Determinant Selection and Macrophage Function in Genetic Control of the Immune Response | Q39558237 |
| | In vitro evidence from anti-hapten antibody responses for T helper and suppressor cells directed against major histocompatibility antigens in the mouse. Participation of I region determinants in the induction of T helper cells | Q39572550 |
| P433 | issue | 2 | |
| P304 | page(s) | 213-245 | |
| P577 | publication date | 1980-08-01 | |
| P1433 | published in | Seminars in Immunopathology | Q15724576 |
| P1476 | title | T cell recognition of antigen in vivo: role of the H-2 complex | |
| P478 | volume | 3 | |