Abstract is: Charles Alderson Janeway, Jr. (1943–2003) was a noted immunologist who helped create the modern field of innate immunity. A member of the National Academy of Sciences, he held a faculty position at Yale University's Medical School and was an HHMI Investigator.
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| P271 | NACSIS-CAT author ID | DA09118167 |
| P5380 | National Academy of Sciences member ID | 3009515 |
| P5034 | National Library of Korea ID | KAC201886104 |
| P7293 | National Library of Poland MMS ID | 9810584307105606 |
| P1006 | Nationale Thesaurus voor Auteursnamen ID | 069699208 |
| P349 | NDL Authority ID | 00514091 |
| P691 | NL CR AUT ID | xx0073225 |
| P12458 | Parsifal cluster ID | 344481 |
| P3368 | Prabook ID | 2494522 |
| P396 | SBN author ID | MILV156363 |
| P906 | SELIBR ID | 268197 |
| P3987 | SHARE Catalogue author ID | 101323 |
| P3430 | SNAC ARK ID | w61c2t4d |
| P11686 | University of Barcelona authority ID | 981058519678406706 |
| P214 | VIAF cluster ID | 100308245 |
| P10832 | WorldCat Entities ID | E39PBJq74TkKvbyQWrDdVQcQMP |
| P166 | award received | German Immunology Prize | Q790636 |
| William B. Coley Award | Q918979 | ||
| American Association of Immunologists Lifetime Achievement Award | Q56667085 | ||
| P27 | country of citizenship | United States | Q30 |
| P1343 | described by source | Medvik | Q99413897 |
| P69 | educated at | Harvard Medical School | Q49121 |
| Phillips Exeter Academy | Q1426464 | ||
| P108 | employer | Yale University | Q49112 |
| P734 | family name | Janeway | Q37450939 |
| P22 | father | Charles Alderson Janeway | Q5075026 |
| P101 | field of work | immunology | Q101929 |
| P8017 | generational suffix | L252247-F2 | |
| P735 | given name | Charles | Q2958359 |
| Charles | Q2958359 | ||
| P1412 | languages spoken, written or signed | English | Q1860 |
| P463 | member of | National Academy of Sciences | Q270794 |
| P106 | occupation | university teacher | Q1622272 |
| researcher | Q1650915 | ||
| immunologist | Q12119633 | ||
| P21 | sex or gender | male | Q6581097 |
| Q35080761 | A B-cell receptor-specific selection step governs immature to mature B cell differentiation |
| Q74279758 | A NK1.1+ thymocyte-derived TCR beta-chain transgene promotes positive selection of thymic NK1.1+ alpha beta T cells |
| Q74545036 | A Tale of Two T Cells |
| Q72841442 | A cloned, antigen-specific, Ia-restricted Lyt-1+,2- T cell with suppressive activity |
| Q72906752 | A column method for deoxygenating human hemoglobin |
| Q28131769 | A human homologue of the Drosophila Toll protein signals activation of adaptive immunity |
| Q52184759 | A molecular map of T cell development. |
| Q41256327 | A novel MHC class II epitope expressed in thymic medulla but not cortex |
| Q77552459 | A novel method for concurrent visualization of immunostain under light and electron microscopy in pancreatic islets |
| Q44355383 | A pool of central memory-like CD4 T cells contains effector memory precursors |
| Q59057981 | A primitive immune system |
| Q73630433 | A role for accessibility to self-peptide-self-MHC complexes in intrathymic negative selection |
| Q41734424 | A simple method for the radioactive iodination of CD4 molecules |
| Q48735173 | A trip through my life with an immunological theme |
| Q70039557 | Ability of fixed B-lymphoma cells to present foreign protein antigen fragments and allogenic MHC molecules to a cloned helper-T-cell line |
| Q72607766 | Absence of an antigen-specific helper T cell required for the expression of the Tn 15 idiotype in mice treated with anti-μ antibody |
| Q58991614 | Accessories or coreceptors? |
| Q46592828 | Activity of migration inhibitory factor in the absence of antigen |
| Q71159158 | Advances in paediatrics |
| Q58869466 | Affinity-purified antigen-specific products produced by T cells share epitopes recognized by heterologous antisera raised against several different antigen-specific products from T cells |
| Q73002892 | Alpha(1,3)-fucosyltransferase VII and alpha(2,3)-sialyltransferase IV are up-regulated in activated CD4 T cells and maintained after their differentiation into Th1 and migration into inflammatory sites |
| Q36368633 | Alteration at a single amino acid residue in the T cell receptor alpha chain complementarity determining region 2 changes the differentiation of naive CD4 T cells in response to antigen from T helper cell type 1 (Th1) to Th2. |
| Q34982958 | Altered positive selection due to corecognition of floppy peptide/MHC II conformers supports an integrative model of thymic selection |
| Q67490020 | An MHC interaction site maps to the amino-terminal half of the T cell receptor α chain variable domain |
| Q66878910 | An analysis of the defective response of CBA/N mice to T-dependent antigens |
| Q41729786 | An ancient system of host defense |
| Q59081580 | An explanation for the protective effect of the MHC class II I–E molecule in murine diabetes |
| Q67244072 | An external stimulus that mimics Mls locus responses |
| Q40890469 | An islet-specific CD8+ T cell hybridoma generated from non-obese diabetic mice recognizes insulin as an autoantigen |
| Q34025467 | Analysis of structure and function relationships of an autoantigenic peptide of insulin bound to H-2K(d) that stimulates CD8 T cells in insulin-dependent diabetes mellitus |
| Q72056665 | Anti-CD45 augments response of a Th2 clone to TCR cross-linking |
| Q57135580 | Antibody-activated immunoregulatory T cells are defective in B cell deprived mice |
| Q58990592 | Antigen presentation by B cells |
| Q70237087 | Antigen-dependent selection of B lymphoma cells varying in Ia density by cloned antigen-specific L3T4a+ T cells: a possible in vitro model for B cell adaptive differentiation |
| Q28274344 | Approaching the asymptote? Evolution and revolution in immunology |
| Q72243537 | Are All Baby Foods Special Dietary Foods? |
| Q40903645 | Are there cellular superantigens? |
| Q43990281 | Asymmetry in the recognition of antigen: self class II MHC and non-self class II MHC molecules by the same T-cell receptor |
| Q35595889 | Autocrine growth inhibition of a cloned line of helper T cells |
| Q57137913 | B cell-deprived mice lack functional expression of certain T suppressor cell subsets |
| Q41746420 | Bacterial proteins that mediate the association of a defined subset of T cell receptor:CD4 complexes with class II MHC. |
| Q72114819 | Beneficial autoimmunity? |
| Q79880097 | Blood and Blood Derivatives-A New Public Health Field |
| Q36348048 | Both a monoclonal antibody and antisera specific for determinants unique to individual cloned helper T cell lines can substitute for antigen and antigen-presenting cells in the activation of T cells |
| Q41440548 | Both high and low avidity antibodies to the T cell receptor can have agonist or antagonist activity |
| Q67854327 | Breaking T cell tolerance with foreign and self co-immunogens. A study of autoimmune B and T cell epitopes of cytochrome c |
| Q38186373 | CD4+ T cells: specificity and function. |
| Q73719540 | CD62L is required on effector cells for local interactions in the CNS to cause myelin damage in experimental allergic encephalomyelitis |
| Q36366075 | CD8 T cell clones from young nonobese diabetic (NOD) islets can transfer rapid onset of diabetes in NOD mice in the absence of CD4 cells. |
| Q35159175 | CHEMICAL, CLINICAL, AND IMMUNOLOGICAL STUDIES ON THE PRODUCTS OF HUMAN PLASMA FRACTIONATION. VII. CONCENTRATED HUMAN SERUM ALBUMIN. |
| Q40974770 | CHEMICAL, CLINICAL, AND IMMUNOLOGICAL STUDIES ON THE PRODUCTS OF HUMAN PLASMA FRACTIONATION. XII. THE USE OF CONCENTRATED NORMAL HUMAN SERUM GAMMA GLOBULIN (HUMAN IMMUNE SERUM GLOBULIN) IN THE PREVENTION AND ATTENUATION OF MEASLES. |
| Q35388074 | CHEMICAL, CLINICAL, AND IMMUNOLOGICAL STUDIES ON THE PRODUCTS OF HUMAN PLASMA FRACTIONATION. XXXVI. INACTIVATION OF THE VIRUS OF HOMOLOGOUS SERUM HEPATITIS IN SOLUTIONS OF NORMAL HUMAN SERUM ALBUMIN BY MEANS OF HEAT. |
| Q33366765 | CIITA activates the expression of MHC class II genes in mouse T cells |
| Q52229971 | Cell cooperation during in vivo anti-hapten antibody responses. V. Two synergistic Ly-1+23- helper T cells with distinctive specificities |
| Q52229993 | Cell cooperation during in vivo anti-hapten antibody responses. VI. Evidence for an allogeneic effect replacing one of two helper T cells |
| Q70011292 | Cell interactions in the immune system: the role of self recognition in the targeting of nonspecific effector molecules by helper T cells |
| Q70377367 | Cell surface expression and alloantigenic function of a human class I MHC heavy chain gene (HLA-B7) in transgenic mice |
| Q37599148 | Cells that present both specific ligand and costimulatory activity are the most efficient inducers of clonal expansion of normal CD4 T cells. |
| Q66875588 | Cellular cooperation during in vivo anti-hapten antibody responses. I. The effect of cell number on the response |
| Q66875591 | Cellular cooperation during in vivo anti-hapten antibody responses. II. The effect of in vivo and in vitro x-irradiation on T and B cells |
| Q66875594 | Cellular cooperation during in vivo anti-hapten antibody responses. III. The helper cell activity of activated thymocytes, of spleen cells treated with anti-theta serum, and of spleen cells from anti-thymocyte serum-treated or adult thymectomized do |
| Q71785417 | Characterization of H4: a mouse T lymphocyte activation molecule functionally associated with the CD3/T cell receptor |
| Q31406838 | Characterization of a novel human surface molecule selectively expressed by mature thymocytes, activated T cells and subsets of T cell lymphomas |
| Q36263328 | Chronic treatment with rabbit anti-mouse mu-chain antibody alters the characteristic immunoglobulin heavy-chain restriction of murine suppressor T-cell factors |
| Q54217791 | Cloned helper T cells can kill B lymphoma cells in the presence of specific antigen: Ia restriction and cognatevs. noncognate interactions in cytolysis |
| Q36365469 | Cloning and expression of a Leishmania donovani gene instructed by a peptide isolated from major histocompatibility complex class II molecules of infected macrophages |
| Q80505309 | Co-receptor selection: chance or necessity? |
| Q28587141 | Co-stimulation of murine CD4 T cell growth: cooperation between B7 and heat-stable antigen |
| Q34340219 | Coclustering of CD4 (L3T4) molecule with the T-cell receptor is induced by specific direct interaction of helper T cells and antigen-presenting cells |
| Q60962704 | Continuity and Change |
| Q44493498 | Control of T cell responses to staphylococcal enterotoxins by stimulator cell MHC class II polymorphism. |
| Q59067228 | Cooperative interaction of B lymphocytes with antigen-specific helper T lymphocytes is MHC restricted |
| Q73065666 | Cross-antagonism of a T cell clone expressing two distinct T cell receptors |
| Q38787617 | Cross-linking and conformational change in T-cell receptors: role in activation and in repertoire selection |
| Q34396895 | Danger - pathogen on the premises! Immunological tolerance |
| Q72672701 | Deciphering the mysteries of RNA-containing lupus antigens |
| Q29618448 | Decoding the patterns of self and nonself by the innate immune system |
| Q70387554 | Defective antigen presentation in chronically protein-deprived mice |
| Q77879066 | Designing and maintaining the mature TCR repertoire: the continuum of self-peptide:self-MHC complex recognition |
| Q42008648 | Development of CD8alpha/alpha and CD8alpha/beta T cells in major histocompatibility complex class I-deficient mice |
| Q54446860 | Diagnosis and treatment of antibody deficiency syndromes |
| Q71829171 | Differences in the avidity of TCR interactions with a superantigenic ligand affect negative selection but do not allow positive selection |
| Q42812488 | Different phenotypic variants of the mouse B cell tumor A20/2J are selected by antigen- and mitogen-triggered cytotoxicity of L3T4-positive, I-A-restricted T cell clones |
| Q36366515 | Different superantigens interact with distinct sites in the Vbeta domain of a single T cell receptor |
| Q73822011 | Differential adhesion molecule requirements for immune surveillance and inflammatory recruitment |
| Q41384220 | Differential effects of antibodies to Lyt-2 and L3T4 on cytolysis by cloned, Ia-restricted T cells expressing both proteins. |
| Q71629738 | Differential expression of Ia glycoprotein complexes in F1 hybrid mice detected with alloreactive cloned T cell lines |
| Q30966114 | Differential sensitivity to mutations in a single peptide by two TCRs having identical beta-chains and closely related alpha-chains |
| Q36351526 | Direct interactions between B and T lymphocytes bearing complementary receptors |
| Q71702645 | Direct physical interaction involving CD40 ligand on T cells and CD40 on B cells is required to propagate MMTV |
| Q70072984 | Direct receptor:receptor interactions between T and B lymphocytes: idiotypic restriction in the antibody response to a cloned helper T cell receptor |
| Q38521828 | Distinctive immunological properties of cultured murine thymic epithelial cells |
| Q34291745 | Diversity in T-cell receptor gamma gene usage in intestinal epithelium |
| Q37113954 | Diversity, Development, Ligands, and Probable Functions of γδ T Cells |
| Q38263019 | Diversity, development, ligands, and probable functions of gamma delta T cells. |
| Q72219989 | Do B cells drive the diversification of immune responses? |
| Q70058118 | Do suppressor T cells exist? A reply |
| Q34111446 | Dual receptor T cells extend the immune repertoire for foreign antigens. |
| Q22010492 | ECSIT is an evolutionarily conserved intermediate in the Toll/IL-1 signal transduction pathway |
| Q72798024 | Efficiency of antigen presentation differs in mice differing at the Mls locus |
| Q40771367 | Elevated temperature regulates tumor necrosis factor-mediated immune killing |
| Q48194701 | Epicutaneous immunization with autoantigenic peptides induces T suppressor cells that prevent experimental allergic encephalomyelitis. |
| Q59046883 | Epithelial homing of γδ T cells? |
| Q59049347 | Erratum: An explanation for the protective effect of the MHC class II I–E molecule in murine diabetes |
| Q40951076 | Evidence for Fas-dependent and Fas-independent mechanisms in the pathogenesis of experimental autoimmune encephalomyelitis |
| Q58974599 | Evidence for a physical association of CD4 and the CD3: α : β T-cell receptor |
| Q35058262 | Evidence for an immunoglobulin-dependent antigen-specific helper T cell |
| Q67898914 | Exclusive Expression of MHC Class II Proteins on CD45+ Cells in Pancreatic Islets of NOD Mice |
| Q36400766 | Exogenously Provided Peptides of a Self-antigen Can Be Processed into Forms that Are Recognized by Self–T Cells |
| Q34411828 | Experimental autoimmune encephalomyelitis induction in genetically B cell-deficient mice |
| Q41120203 | Experimental malaria in the CBA/N mouse |
| Q36343940 | Expression of an idiotype (Id-460) during in vivo anti-dinitrophenyl antibody responses. I. Mapping of genes for Id-460 expression to the variable region of immunoglobulin heavy-chain locus and to the variable region of immunoglobulin kappa-light-ch |
| Q36345891 | Expression of an idiotype (Id-460) during in vivo anti-dinitrophenyl antibody responses. II. Transient idiotypic dominance |
| Q36345896 | Expression of an idiotype (Id-460) during in vivo anti-dinitrophenyl antibody responses. III. Detection of Id-460 in normal serum that does not bind dinitrophenyl |
| Q71679204 | Expression of the co-stimulator molecule B7-1 in pancreatic beta-cells accelerates diabetes in the NOD mouse |
| Q73703190 | Expression of the novel T cell activation molecule hpH4 in HIV-infected patients: correlation with disease status |
| Q44169854 | Expression of transgene encoded TGF-beta in islets prevents autoimmune diabetes in NOD mice by a local mechanism. |
| Q41603286 | Extensive CD4 cross-linking inhibits T cell activation by anti-receptor antibody but not by antigen |
| Q53723181 | Family Medicine — Fad or for Real? |
| Q59061027 | Frontiers of the immune system |
| Q72095821 | Functional activities of antibodies against brain-associated T cell antigens. I. Induction of T cell proliferation |
| Q73709090 | Functional and phenotypic evidence for presentation of E alpha 52-68 structurally related self-peptide(s) in I-E alpha-deficient mice |
| Q39729177 | Functional heterogeneity among the T-derived lymphocytes of the mouse. IV. Nature of spontaneously induced suppressor cells |
| Q44187779 | Further observations on the Swiss type of agammaglobulinemia (alymphocytosis). The effect of syngeneic bone-marrow cells |
| Q68443450 | Gamma delta T cells: research on the frontlines of defence |
| Q63363246 | Gamma delta T-cell lines isolated from intestinal epithelium respond to a B-cell lymphoma |
| Q44917921 | Generation, propagation, and variation in cloned, antigen-specific, Ia-restricted cytolytic T-cell lines |
| Q69813051 | Goals and constraints in the education of physicians |
| Q72820239 | Growth of a cloned helper T cell line induced by a monoclonal antibody specific for the antigen receptor: interleukin 1 is required for the expression of receptors for interleukin 2 |
| Q36260793 | HISTOLOGICAL AND SEROLOGICAL SEQUENCES IN EXPERIMENTAL HYPERSENSITIVITY. |
| Q47941090 | Hapten-specific augmentation of the anti-idiotype antibody response to hapten-myeloma protein conjugates in mice |
| Q28508401 | Heat-stable antigen is a costimulatory molecule for CD4 T cell growth |
| Q67241059 | Helper T Cells Specific for Protein Antigens: Role of Self Major Histocompatibility Complex and Immunoglobulin Gene Products |
| Q40711763 | Helper T cell interactions. |
| Q71687834 | High density insulin receptor-positive T lymphocytes from nonobese diabetic mice transfer insulitis and diabetes |
| Q80506072 | High fives or hand clasps? |
| Q67885876 | High levels of IL-2 alter signal transduction in cloned IL-4-producing CD4 T cells |
| Q40102550 | How T lymphocytes recognize antigen |
| Q74054495 | How does the immune system distinguish self from nonself? |
| Q34439868 | How the immune system protects the host from infection |
| Q40766883 | How the immune system recognizes invaders. |
| Q34272671 | How the immune system works to protect the host from infection: a personal view |
| Q58999702 | Human T-cell receptor expression |
| Q24302640 | IRAK-M is a negative regulator of Toll-like receptor signaling |
| Q30763625 | Identification of an MHC class I-restricted autoantigen in type 1 diabetes by screening an organ-specific cDNA library. |
| Q40097641 | Idiotypes, T-Cell Receptors, and T-B Cooperation |
| Q48294358 | IgG anti-DNA autoantibodies within an individual autoimmune mouse are the products of clonal selection |
| Q63363260 | Immune recognition and effector function in subsets of CD4 T cells |
| Q36346112 | Immune response gene function correlates with the expression of an Ia antigen. I. Preferential association of certain Ae and E alpha chains results in a quantitative deficiency in expression of an Ae:E alpha complex |
| Q36346118 | Immune response gene function correlates with the expression of an Ia antigen. II. A quantitative deficiency in A(e):E(a), complex expression causes a corresponding defect in antigen-presenting cell function |
| Q39448586 | Immune responses of BALB/c mice to the idiotype of T15 and of other myeloma proteins of BALB/c origin: implications for an immune network and antibody multispecificity |
| Q54421792 | Immune serum from mice contact-sensitized with picryl chloride contains an antigen-specific T cell factor that transfers immediate cutaneous reactivity |
| Q36466805 | Immunochemical identification of cytophilic antibody in human lymphocytes |
| Q55059065 | Immunogenicity signals 1,2,3 ... and 0. |
| Q93703899 | Immunoglobulin determinants on the lymphocytes of normal rabbits. 3. As4 and As6 determinants on individual lymphocytes and the concept of allelic exclusion |
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| Q57136187 | Immunoregulatory role of Ig isotypes. II. Activation of cells that block induction of contact sensitivity responses by antibodies of IgG2a and IgG2b isotypes |
| Q59047650 | Immunotherapy by peptides? |
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| Q27860721 | Innate immune recognition |
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| Q28138782 | Innate immune recognition: mechanisms and pathways |
| Q74520742 | Innate immunity |
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| Q33814945 | Insulin-dependent diabetes mellitus and its animal models. |
| Q36354156 | Interferon gamma plays a critical role in induced cell death of effector T cell: a possible third mechanism of self-tolerance |
| Q59065280 | Intestinal intraepithelial lymphocytes are a distinct set of γδ T cells |
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| Q47967599 | Introduction: T-cell:B-cell interaction. |
| Q95440614 | Introduction: The role of innate immunity in the adaptive immune response |
| Q40888700 | Invasive Haemophilus influenzae type b infections in vaccinated and unvaccinated children in Canada, 2001-2003. |
| Q70363593 | Inverse Ir gene control of the antibody and T cell proliferative responses to human basement membrane collagen |
| Q52078248 | Isoform-specific associations of CD45 with accessory molecules in human T lymphocytes |
| Q39407717 | Isolation of antigen-binding cells from unprimed mice. II. Evidence for monospecificity of antigen-binding cells |
| Q80506162 | It is easier for a camel to pass the needle's eye |
| Q41010582 | John Howland Award Acceptance Address: From the American Pediatric Society, April 26,1978, New York, New York |
| Q68442292 | Ligand thresholds at different stages of T cell development |
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| Q39548662 | Lipid-modified antigens. I. Specificity of guinea pig T lymphocyte responses and I-region restriction |
| Q73294953 | Lipoproteins take their toll on the host |
| Q36367622 | Local expression of transgene encoded TNF alpha in islets prevents autoimmune diabetes in nonobese diabetic (NOD) mice by preventing the development of auto-reactive islet-specific T cells |
| Q44975100 | Low doses of interleukin 2 induce bystander cell lysis by antigen-specific CD4+ inflammatory T cell clones in short-term assay |
| Q72870993 | Lymphocyte activation and effector functions. Editorial overview. The role of cell surface molecules |
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| Q52099252 | Microbial induction of co-stimulatory activity for CD4 T-cell growth |
| Q67295598 | Modes of cell:cell communication in the immune system |
| Q52105374 | Molecular associations on the T cell surface correlate with immunological memory |
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| Q36351229 | Molecular characterization of antibodies bearing Id-460. II. Molecular basis for Id-460 expression |
| Q44662131 | Monoclonal Antibodies Against T Cell Receptor/CD3 Complex Induce Cell Death of Th1 Clones in the Absence of Accessory Cells |
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| Q69070994 | Monoclonal antibodies to murine CD3 epsilon define distinct epitopes, one of which may interact with CD4 during T cell activation |
| Q29616423 | Monoclonal antibodies to nucleic acid-containing cellular constituents: probes for molecular biology and autoimmune disease |
| Q36344030 | Monoclonal antibody against an Ir gene product? |
| Q67896783 | Monoclonal antibody detection of a major self peptide. MHC class II complex |
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| Q44063328 | Nathalie Masse, 1919-1975 |
| Q34067924 | Negative selection of thymocytes expressing the D10 TCR |
| Q36348440 | Non-dinitrophenyl-binding immunoglobulin that bears a dominant idiotype (Id460) associated with antidinitrophenyl antibody is specific for an antigen on Pasteurella pneumotropica |
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| Q38460224 | On the semantics of immune recognition |
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| Q40429223 | PVF2, a PDGF/VEGF-like growth factor, induces hemocyte proliferation in Drosophila larvae |
| Q33930556 | Paradoxical intrathymic positive selection in mice with only a covalently presented agonist peptide |
| Q70108359 | Passive immunization against chicken pox |
| Q72881461 | Pediatric education in the United States |
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| Q73287492 | Peptide antagonists inhibit proliferation and the production of IL-4 and/or IFN-gamma in T helper 1, T helper 2, and T helper 0 clones bearing the same TCR |
| Q59028086 | Peptides bound to MHC |
| Q28144345 | Phylogenetic perspectives in innate immunity |
| Q33854139 | Physical association of CD4 and the T-cell receptor can be induced by anti-T-cell receptor antibodies |
| Q41640150 | Physical association of CD4 with the T cell receptor |
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| Q47861987 | Polymorphism of the mouse T-cell receptor AV20S1 gene |
| Q48423537 | Presentation of the Howland Award to Louis K. Diamond |
| Q48176320 | Presentation of the self antigen myelin basic protein by dendritic cells leads to experimental autoimmune encephalomyelitis. |
| Q34749528 | Presidential Address to The American Association of Immunologists. The road less traveled by: the role of innate immunity in the adaptive immune response |
| Q71739896 | Prevention of Posttransfusion Hepatitis |
| Q41758960 | Prevention of diabetes in NOD mice by injection of autoreactive T-lymphocytes |
| Q39877080 | Progress in immunology. Syndromes of diminished resistance to infection |
| Q36368555 | Qa-2-dependent selection of CD8alpha/alpha T cell receptor alpha/beta(+) cells in murine intestinal intraepithelial lymphocytes |
| Q38257795 | Quantitative variation in la antigen expression plays a central role in immune regulation |
| Q24292468 | RICK/Rip2/CARDIAK mediates signalling for receptors of the innate and adaptive immune systems |
| Q44044768 | Receptor-directed focusing of lymphokine release by helper T cells |
| Q34294731 | Recognition of a self major histocompatibility complex TL region product by gamma delta T-cell receptors. |
| Q44122425 | Recognition of core and flanking amino acids of MHC class II-bound peptides by the T cell receptor |
| Q35082019 | Recognition of immunoglobulin idiotypes by thymus-derived lymphocytes |
| Q40938432 | Recurrent infections, episodic lymphopenia and impaired cellular immunity |
| Q70490926 | Regulation of the immune response through idiotypic interactions |
| Q57134954 | Regulatory responses in contact sensitivity: Afferent suppressor T cells inhibit the activation of efferent suppressor T cells |
| Q52539853 | Relapsing and remitting experimental autoimmune encephalomyelitis in B cell deficient mice |
| Q52457524 | Reminiscences of late Professor S.T. Achar |
| Q48913563 | Requirement for CD40 ligand in costimulation induction, T cell activation, and experimental allergic encephalomyelitis |
| Q41207462 | Responses of T cells to ligands for the T-cell receptor |
| Q40808115 | Rules for peptide presentation by MHC class II molecules |
| Q40982703 | STAT5 interaction with the T cell receptor complex and stimulation of T cell proliferation. |
| Q40972958 | STUDIES ON INFECTIOUS MONONUCLEOSIS. II. THE RELATIONSHIP OF THE ORGANISMS OF THE GENUS LISTERELLA TO THE DISEASE, AS STUDIED BY THE AGGLUTINATION REACTION. |
| Q35157374 | STUDIES ON THE PLASMA PROTEINS. V. THE EFFECT OF CONCENTRATED SOLUTIONS OF HUMAN AND BOVINE SERUM ALBUMIN ON BLOOD VOLUME AFTER ACUTE BLOOD LOSS IN MAN. |
| Q71767844 | Screening for inherited diseases |
| Q42261752 | Selected populations of alloreactive T cells contain helper T cells but lack ThId, an antigen-specific helper T cell required for dominant production of the T15 idiotype |
| Q37113963 | Selective Elements for the Vß Region of the T Cell Receptor: MIs and the Bacterial Toxic Mitogens |
| Q69377330 | Selective induction of growth factor production and growth factor receptor expression by different signals to a single T cell |
| Q72813834 | Self la-recognizing T cells undergo an ordered series of interactions with ia-bearing substrate cells of defined function during their development: A model |
| Q72303912 | Self peptides isolated from MHC glycoproteins of non-obese diabetic mice |
| Q37976429 | Self superantigens? |
| Q36046613 | Self-defense: The fruit fly style |
| Q52943711 | Self-recognition and the biased mature repertoire in TCR beta transgenic mice: the exception that supports the rule. |
| Q28303686 | Sequence analysis of peptides bound to MHC class II molecules |
| Q41282431 | Signaling by a new anti-Thy 1 monoclonal antibody inhibits T cell proliferation and interferes with T-cell-mediated induction of costimulatory molecule B7-2. |
| Q40620206 | Signals and signs for lymphocyte responses |
| Q72279459 | Some shortcomings of medical education in a free society |
| Q66887226 | Specific and Nonspecific Cooperation Between M-Locus-Incompatible T and B Cells During Adoptive Anti-Hapten Antibody Responses in Mice |
| Q39802093 | Specific loss of stimulator activity following mixed lymphocyte reactions is due to cytotoxic cells |
| Q44385574 | Specificity and function of T cells bearing gamma delta receptors |
| Q41492321 | Stimulator cell type influences the response of T cells to staphylococcal enterotoxins |
| Q40789973 | Studies on naturally processed peptides associated with MHC class II molecules. |
| Q54662921 | Studies with intravenous gamma globulin |
| Q36285397 | Subtle conformational changes induced in major histocompatibility complex class II molecules by binding peptides |
| Q72332839 | Superantigen-like properties of an antibody bispecific for MHC class II molecules and the V beta domain of the T cell antigen receptor |
| Q39499469 | Suppressor T cells and immunoregulation: an overview |
| Q36361169 | Surface expression of alpha 4 integrin by CD4 T cells is required for their entry into brain parenchyma |
| Q72027965 | Synthetic antigens composed exclusively of L- or D- amino acids. II. Effect of optical configuration on the metabolism and fate of synthetic polypeptide antigens in mice |
| Q71240187 | Synthetic antigens composed exclusively of L- or D-amino acids. 3. Anamnestic response to a synthetic polypeptide composed exclusively of D-amino acids |
| Q72226911 | Synthetic antigens composed exclusively of L- or D-amino acids. I. Effect of optical configuration on the immunogenicity of synthetic polypeptides in mice |
| Q67540230 | T and B cell receptors discriminate major histocompatibility complex class II conformations influenced by the invariant chain |
| Q48819718 | T cell adhesion to endothelial cells and extracellular matrix is modulated upon transendothelial cell migration |
| Q47989582 | T cell-mediated immunity in malaria. I. The Ly phenotype of T cells mediating resistance to Plasmodium yoelii. |
| Q33864874 | T cells from epicutaneously immunized mice are prone to T cell receptor revision |
| Q40676778 | T cells specific for hapten-modified self are precommitted for self major histocompatibility complex antigens before encounter with the hapten |
| Q34756338 | T cells with two functional antigen-specific receptors |
| Q39816014 | T lymphocyte responses to Mls locus antigens involve recognition of H-2 I region gene products |
| Q47743587 | T lymphocytes responding to Mls-locus antigens are Lyt-1+, 2− andI-A restricted |
| Q72082792 | T-Cell receptor idiotypes |
| Q33632307 | T-cell development: a role for self-peptides in positive selection |
| Q66875670 | T-cell populations with different functions |
| Q41441623 | T-cell receptors: is the repertoire inherently MHC-specific? |
| Q85701076 | T-cell regulation of IgA responses |
| Q38249158 | T-cell responses to Mls and to bacterial proteins that mimic its behavior |
| Q72873502 | TAP1-dependent peptide translocation in vitro is ATP dependent and peptide selective |
| Q41537404 | TCR-CD4 and TCR-TCR interactions as distinctive mechanisms for the induction of increased intracellular calcium in T-cell signalling |
| Q45228667 | The B cell is the initiating antigen-presenting cell in peripheral lymph nodes. |
| Q71155887 | The Child With Recurrent Infections |
| Q36348755 | The Fab fragment of a directly activating monoclonal antibody that precipitates a disulfide-linked heterodimer from a helper T cell clone blocks activation by either allogeneic Ia or antigen and self-Ia |
| Q36060959 | The Immunological System of the Child: Part I: Development of Immunity in the Child |
| Q36060950 | The Immunological System of the Child: Part II: Immunological Deficiency States |
| Q73838326 | The Imprint of Intrathymic Self-Peptides on the Mature T Cell Receptor Repertoire |
| Q43837212 | The L3T4 molecule is part of the helper T-cell antigen/Ia recognition complex |
| Q67256810 | The Mls locus: new clues to a lingering mystery |
| Q41287605 | The Mls locus: past, present and future |
| Q34170758 | The PTK-STAT signaling pathway has essential roles in T-cell activation in response to antigen stimulation |
| Q72595917 | The Structure and Function of T Cell Receptor Complexes |
| Q35876939 | The T cell receptor as a multicomponent signalling machine: CD4/CD8 coreceptors and CD45 in T cell activation |
| Q47234164 | The alpha- and beta-subunits of a murine T cell antigen/Ia receptor have a molecular weight of 31,000 in the absence of N-linked glycosylation |
| Q41251975 | The biologic activity of anti-T cell receptor V region monoclonal antibodies is determined by the epitope recognized. |
| Q80505725 | The case of the missing CD4s |
| Q72368991 | The child with frequent infections: diagnostic considerations |
| Q36680146 | The co-receptor function of CD4. |
| Q38680368 | The co-receptor function of murine CD4. |
| Q50255246 | The discovery of T cell help for B cell antibody formation: a perspective from the 30th anniversary of this discovery |
| Q72742910 | The expression of I-Ed molecules in F1 hybrid mice detected with antigen-specific, I-Ed-restricted cloned T-cell lines |
| Q72435840 | The fate of a D-amino acid polypeptide [p(D-Tyr, D-Glu, D-Ala), 247] in newborn and adult mice: relationship to the induction of tolerance |
| Q40038188 | The gamma globulins. 3. The antibody deficiency syndromes |
| Q71191861 | The gamma globulins. 3. The antibody deficiency syndromes |
| Q39876099 | The gamma globulins. II. Hypergammaglobulinemia |
| Q70067775 | The gamma globulins. II. Hypergammaglobulinemia |
| Q39876085 | The gamma globulins. IV. Therapeutic uses of gamma globulin |
| Q85699855 | The immune destruction of pancreatic β cells |
| Q36774100 | The immune system evolved to discriminate infectious nonself from noninfectious self |
| Q41279371 | The immunobiology of T cell responses to Mls-locus-disparate stimulator cells. II. Effects of Mls-locus-disparate stimulator cells on cloned, protein antigen-specific, Ia-restricted T cell lines. |
| Q69980480 | The immunobiology of T cell responses to Mls-locus-disparate stimulator cells. III. Helper and cytolytic functions of cloned, Mls-reactive T cell lines |
| Q70060738 | The immunobiology of the T cell response to Mls locus disparate stimulator cells |
| Q65001745 | The immunobiology of the T cell response to Mls-locus-disparate stimulator cells. I. Unidirectionality, new strain combinations, and the role of Ia antigens. |
| Q44187650 | The immunosuppressive agent 15-deoxyspergualin functions by inhibiting cell cycle progression and cytokine production following naive T cell activation |
| Q41356845 | The influence of valence on the functional activities of monoclonal anti-L3T4 antibodies. Discrimination of signaling from other effects |
| Q47975958 | The mechanism of a hapten-specific helper effect in mice |
| Q36362806 | The mouse mammary tumor virus envelope gene product is required for superantigen presentation to T cells |
| Q41085131 | The orientation of a T cell receptor to its MHC class II:peptide ligands |
| Q34140758 | The pathogenesis of adoptive murine autoimmune diabetes requires an interaction between alpha 4-integrins and vascular cell adhesion molecule-1. |
| Q35999275 | The priming of helper T cells. |
| Q43546974 | The response in vitro of human lymphocytes to phytohemagglutinin and to antigens after fractionation on discontinuous density gradients of albumin |
| Q41628525 | The role of CD4 and CD8 T cells in type I diabetes in the NOD mouse. |
| Q38706502 | The role of CD4 in T-cell activation: accessory molecule or co-receptor? |
| Q33767934 | The role of CD4 vs. CD8 T cells in IDDM. |
| Q73205341 | The role of Fas in autoimmune diabetes |
| Q68856856 | The role of L3T4 in T cell activation: L3T4 may be both an Ia-binding protein and a receptor that transduces a negative signal |
| Q57137515 | The role of immunoglobulin and B cells in T cell ontogeny and repertoire formation--a commentary |
| Q36401103 | The role of lymphocyte subsets in accelerated diabetes in nonobese diabetic-rat insulin promoter-B7-1 (NOD-RIP-B7-1) mice |
| Q33735987 | The role of self-recognition in receptor repertoire development. Members of the Janeway Laboratory |
| Q41359310 | The role of the murine L3T4 molecule in T cell activation: differential effects of anti-L3T4 on activation by monoclonal anti-receptor antibodies |
| Q41066379 | The role of thymus-derived lymphocytes in an antibody-mediated hapten-specific helper effect |
| Q85699573 | The selection of self-MHC recognizing T lymphocytes: a role for idiotypes? |
| Q74321445 | The source of early IFN-gamma that plays a role in Th1 priming |
| Q37395408 | The specific direct interaction of helper T cells and antigen-presenting B cells |
| Q28592120 | The specificity and orientation of a TCR to its peptide-MHC class II ligands |
| Q28317910 | The specificity of T lymphocyte responses to chemically defined antigens |
| Q36360089 | The specificity of cellular immune responses II. The structure of antigenic determinants leading to T-lymphocyte stimulation |
| Q36360200 | The specificity of cellular immune responses in guinea pigs. I. T cells specific for 2,4-dinitrophenyl-o-tyrosyl residues |
| Q36360077 | The specificity of cellular immune responses in guinea pigs. III. The precision of antigen recognition by T lymphocytes |
| Q68813751 | The targeting of effector molecules in the immune system |
| Q67702854 | The use of the polymerase chain reaction to map CD4+ T cell epitopes |
| Q85702147 | Through a glass, darkly … |
| Q40612322 | Thymic selection: two pathways to life and two to death |
| Q33656002 | Tissue-specific and cell surface expression of human major histocompatibility complex class I heavy (HLA-B7) and light (beta 2-microglobulin) chain genes in transgenic mice |
| Q80506335 | To thine own self be true... |
| Q33713298 | Transgenes and knockout mutations in animal models of type 1 diabetes and multiple sclerosis |
| Q36350890 | Transgenic mice demonstrate that epithelial homing of gamma/delta T cells is determined by cell lineages independent of T cell receptor specificity. |
| Q41063958 | Treatment of l(2)mbn Drosophila tumorous blood cells with the steroid hormone ecdysone amplifies the inducibility of antimicrobial peptide gene expression |
| Q41599064 | Truncation variants of peptides isolated from MHC class II molecules suggest sequence motifs |
| Q39414474 | Two Different VH Gene Products Make Up the T-Cell Receptors |
| Q36343852 | Two distinct antigen-specific suppressor factors induced by the oral administration of antigen |
| Q40770827 | Type 1 diabetes mellitus: an imbalance between effector and regulatory T cells? |
| Q40015489 | Unnecessary and preventable hospitalizations: report on an internal audit |
| Q42080455 | Use of Concentrated Human Serum gamma-Globulin in the Prevention and Attenuation of Measles |
| Q37605603 | Use of anti-idiotype immunosorbents to isolate circulating antigen-specific T cell-derived molecules from hyperimmune sera |
| Q41695997 | V beta selective elements: self and non-self |
| Q58662373 | Variability of invariant mouse CD3ε chains detected by anti-CD3 antibodies |
| Q70072978 | Varieties of idiotype-specific helper T cells--a commentary |
| Q44176131 | graal: a Drosophila gene coding for several mosaic serine proteases |
| Q48687110 | A goodbye to Charlie Janeway: Charles A. Janeway Jr (1943-2003). |
| Q60962705 | Charles A Janeway Jr |
| Q50426900 | Charles Janeway, Jr. |
| Q48675649 | In memoriam. Charles A. Janeway, Jr. February 5, 1943-April 12, 2003. |
| Q30336203 | Obituary. Charles A. Janeway, Jr. (1943-2003). |
| Q30332847 | Obituary: Charles A. Janeway Jr (1943-2003). |
| Q45778904 | Recollections of Charlie: Dr. Charles Alderson Janeway, Jr. (1943-2003). |
| Q24611211 | Toward a modern synthesis of immunity: Charles A. Janeway Jr. and the immunologist's dirty little secret |
| Q5075026 | Charles Alderson Janeway | child | P40 |
| Arabic (ar / Q13955) | تشارلز جانواي | wikipedia |
| Egyptian Arabic (arz / Q29919) | تشارلز جانواى | wikipedia |
| Charles Janeway | wikipedia | |
| Charles Janeway | wikipedia | |
| Charles Janeway | wikipedia | |
| Charles Janeway | wikipedia | |
| 찰스 제인웨이 | wikipedia | |
| Charles Janeway | wikipedia | |
| Джейнуэй, Чарлз | wikipedia |
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