| scholarly article | Q13442814 |
| P2093 | author name string | Werblin TP | |
| Kim YT | |||
| Siskind GW | |||
| Quagliata F | |||
| P2860 | cites work | The generation of antihapten antibodies with electrophoretically homogeneous L chains | Q33563095 |
| A study of the distribution of 2,4-dinitrobenzene sensitizers between isolated lymph node cells and extracellular medium in relation to induction of contact skin sensitivity | Q36264285 | ||
| Studies on the regulation of avidity at the level of the single antibody-forming cell. The effect of antigen dose and time after immunization | Q36270069 | ||
| Receptors on immunocompetent cells. IV. Direct measurement of avidity of cell receptors and cooperative binding of multivalent ligands | Q36271422 | ||
| Receptors on immunocompetent cells. V. Cellular correlates of the "maturation" of the immune response | Q36271460 | ||
| Cell Selection by Antigen in the Immune Response | Q39985236 | ||
| Separation of antibodies into fractions with different binding properties | Q45093021 | ||
| The effect of antigen dose and time after immunization on the amount and affinity of anti-hapten antibody | Q47816295 | ||
| Learning and memory in the immune response. | Q52276531 | ||
| Heterogeneity and average combining constants of antibodies from individual rabbits. | Q54005001 | ||
| Determination of antibody-hapten equilibrium constants by an ammonium sulfate precipitation technique | Q72521153 | ||
| VARIATIONS IN AFFINITIES OF ANTIBODIES DURING THE IMMUNE RESPONSE | Q76969494 | ||
| A quantitative immunochemical measure of the primary interaction between I BSA and antibody | Q78479672 | ||
| Distribution of antibody affinities: technique of measurement | Q93730066 | ||
| P433 | issue | 3 | |
| P921 | main subject | heterogeneity | Q928498 |
| P304 | page(s) | 477-492 | |
| P577 | publication date | 1973-03-01 | |
| P1433 | published in | Immunology | Q15754984 |
| P1476 | title | Studies on the control of antibody synthesis. 3. Changes in heterogeneity of antibody affinity during the course of the immune response | |
| P478 | volume | 24 |
| Q66879950 | A proposition on the distribution of antibody affinities, with implications for the mechanism of B-cell activation |
| Q38616902 | A study of the specificities of sequential antisera to variola and monkeypox viruses by radioimmunoassay |
| Q69569963 | Affinity maturation in the arsonate system: lack of dominance of high-affinity antibody subpopulations |
| Q40187963 | Application of low-avidity immunoglobulin G studies to diagnosis of Epstein-Barr virus infectious mononucleosis |
| Q39405995 | Avidity of Aspergillus umbrosus IgG antibodies in farmer's lung disease |
| Q36980926 | Characterization of the immunodeficiency of RIIIS/J mice: immune response to polysaccharide antigens |
| Q33565902 | Complement activating properties of monoreactive and polyreactive IgM rheumatoid factors |
| Q35085686 | Congenital toxoplasmosis and prenatal care state programs |
| Q52242692 | Correlations between immunoglobulin- and antibody-synthesizing cells during primary and secondary immune responses of rats immunized with peroxidase |
| Q57339622 | Development of immunoglobulin and antibody-synthesizing cells after immunization with different doses of antigen |
| Q39432506 | Differences in the mechanism of tolerance to dinitrophenylated bovine gamma globulin when induced in normal adult mice or in reconstituted irradiated mice: dependence of the mechanism of tolerance on the structural organization of the lymphoid system |
| Q36545092 | Differentiation of primary from nonprimary genital herpes infections by a herpes simplex virus-specific immunoglobulin G avidity assay. |
| Q40867302 | Effect of carrier priming on antibody avidity in the in vivo and in vitro immune response |
| Q36359879 | Immunological studies of aging. II. Loss of IgG and high avidity plaque-forming cells and increased suppressor cell activity in aging mice |
| Q36341969 | Immunological studies of aging. IV. The contribution of thymic involution to the immune deficiencies of aging mice and reversal with thymopoietin32-36 |
| Q33553845 | Old mice recover the ability to produce IgG and high-avidity antibody following irradiation with partial bone marrow shielding |
| Q36273625 | Ontogeny of B-lymphocyte function. I. Restricted heterogeneity of the antibody response of B lymphocytes from neonatal and fetal mice |
| Q36359412 | Ontogeny of B-lymphocyte function. II. Ability of endotoxin to increase the heterogeneity of affinity of the immune response of B lymphocytes from fetal mice |
| Q36335453 | Ontogeny of B-lymphocyte function. III. In vivo and in vitro studies on the ease of tolerance induction in B lymphocytes from fetal, neonatal, and adult mice |
| Q41034287 | Ontogeny of B-lymphocyte function. IX. Difference in the time of maturation of the capacity of B lymphocytes from foetal and neonatal mice to produce a heterogeneous antibody response to thymic-dependent and thymic-independent antigens |
| Q36339884 | Ontogeny of B-lymphocyte function. V. Thymus cell involvement in the functional maturation of B-lymphocytes from fetal mice transferred into adult irradiated hosts |
| Q52838573 | Optimal strategies in immunology. I. B-cell differentiation and proliferation |
| Q36342648 | Production of auto-anti-idiotypic antibody during the normal immune response to TNP-ficoll. I. Occurrence in AKR/J and BALB/c mice of hapten-augmentable, anti-TNP plaque-forming cells and their accelerated appearance in recipients of immune spleen c |
| Q40712678 | Production of auto-anti-idiotypic antibody during the normal immune response to TNP-ficoll. II. Hapten-reversible inhibition of anti-TNP plaque-forming cells by immune serum as an assay for auto-anti-idiotypic antibody |
| Q36342876 | Production of auto-anti-idiotypic antibody during the normal immune response to TNP-ficoll. III. Absence in nu/nu mice: evidence for T-cell dependence of the anti-idiotypic-antibody response |
| Q36416413 | Production of auto-anti-idiotypic antibody during the normal immune response: changes in the auto-anti-idiotypic antibody response and the idiotype repertoire associated with aging |
| Q36347758 | Production of auto-antiidiotypic antibody during the normal immune response. VII. Analysis of the cellular basis for the increased auto-antiidiotype antibody production by aged mice |
| Q45832685 | Recent rubella virus infection indicated by a low avidity of specific IgG. |
| Q52224569 | Role of T cells in the development of memory B cells. Quantitative and qualitative analysis. |
| Q26829346 | Serological diagnosis of Epstein-Barr virus infection: Problems and solutions |
| Q52124805 | Stochastic humoral expression of human growth hormone epitopes. |
| Q47836644 | Studies on antigenic competition. 3. Effect on antigenic competition on antibody affinity. |
| Q68919295 | Studies on the control of antibody synthesis. VI. Effect of antigen dose and time after immunization on antibody affinity and heterogeneity in the mouse |
| Q39350662 | Studies on the control of antibody synthesis. VII. Change in affinity of direct and indirect plaque-forming cells with time after immunization in the mouse: loss of high affinity plaques late after immunization |
| Q44688019 | Studies on the control of antibody synthesis. XII. Genetic influences on antibody affinity |
| Q41132222 | Studies on the control of antibody synthesis. XIII. Preferential depeletion of precursors of high affinity antibody-secreting cells by specific immunoadsorbents |
| Q52229589 | Studies on the control of antibody synthesis. XVII. Effect of specific suppressor cells on the affinity of the antibody response by naive or primed lymphocytes. |
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