scholarly article | Q13442814 |
P2093 | author name string | J Jacob | |
G Kelsoe | |||
R Kassir | |||
P2860 | cites work | Molecular cloning of the primary IgH repertoire: a quantitative analysis of VH gene usage in adult mice | Q33572492 |
Stochastic pairing of heavy-chain and kappa light-chain variable gene families occurs in polyclonally activated B cells | Q33652815 | ||
Preferential rearrangement of V kappa 4 gene segments in pre-B cell lines | Q33771048 | ||
Cell population kinetics of the germinal centres of lymph nodes of BALB/c mice | Q34039563 | ||
Early rearrangements of genes encoding murine immunoglobulin kappa chains, unlike genes encoding heavy chains, use variable gene segments dispersed throughout the locus | Q34301748 | ||
Induction of rheumatoid antibodies in the mouse. Regulated production of autoantibody in the secondary humoral response | Q36348899 | ||
Genotypic analysis of B cell colonies by in situ hybridization. Stoichiometric expression of three VH families in adult C57BL/6 and BALB/c mice | Q36353739 | ||
Lack of N regions in fetal and neonatal mouse immunoglobulin V-D-J junctional sequences | Q36353825 | ||
Inter- and intraclonal diversity in the antibody response to influenza hemagglutinin | Q36355399 | ||
Early onset of somatic mutation in immunoglobulin VH genes during the primary immune response | Q36356525 | ||
Growth of B-lymphocyte colonies in vitro | Q36358857 | ||
Heavy chain variable region contribution to the NPb family of antibodies: somatic mutation evident in a gamma 2a variable region | Q36630020 | ||
Direct intrafollicular differentiation of memory B cells into plasma cells | Q37922204 | ||
Inherited Immunoglobulin Idiotypes of the Mouse | Q39430367 | ||
Analysis of the repertoire of anti-NP antibodies in C57BL/6 mice by cell fusion. I. Characterization of antibody families in the primary and hyperimmune response | Q39606535 | ||
Evolution of antibody variable region structure during the immune response | Q39658887 | ||
Mutation drift and repertoire shift in the maturation of the immune response | Q39658890 | ||
Timing, genetic requirements and functional consequences of somatic hypermutation during B-cell development. | Q39658899 | ||
Functional anatomy of germinal centers | Q40186432 | ||
Analysis of the repertoire of anti-(4-hydroxy-3-nitro-phenyl)acetyl (NP) antibodies in C 57 BL/6 mice by cell fusion. II. Characterization of idiotopes by monoclonal anti-idiotope antibodies | Q41196929 | ||
Idiotypic analysis of the response of C57BL/6 mice to the (4-hydroxy-3-nitrophenyl)acetyl group | Q41314640 | ||
Murine V kappa gene expression does not follow the VH paradigm | Q41819022 | ||
Clonal recruitment and somatic mutation in the generation of immunological memory to the hapten NP | Q42573237 | ||
Antibody engineering for the analysis of affinity maturation of an anti-hapten response. | Q42735546 | ||
Mapping of antibody specificities to VH gene families | Q42800441 | ||
Strain-dependent expression of VH gene families | Q42800571 | ||
VH-gene expression in murine lipopolysaccharide blasts distributes over the nine known VH-gene groups and may be random | Q44171947 | ||
Synthesis of antibody and immunoglobulins without detectable antibody function in cells responding to horseradish peroxidase | Q44523695 | ||
Development of B cell lineages during a primary anti-hapten immune response | Q48248175 | ||
A limited number of B cell lineages generates the heterogeneity of a secondary immune response. | Q48333272 | ||
Somatic variants of murine immunoglobulin λ light chains | Q48403814 | ||
Two types of somatic recombination are necessary for the generation of complete immunoglobulin heavy-chain genes | Q48412817 | ||
Correlations between immunoglobulin- and antibody-synthesizing cells during primary and secondary immune responses of rats immunized with peroxidase | Q52242692 | ||
Peanut lectin binding properties of germinal centres of mouse lymphoid tissue. | Q52851284 | ||
Insertion of N regions into heavy-chain genes is correlated with expression of terminal deoxytransferase in B cells | Q53549666 | ||
Detection of antibody, idiotype, and anti-idiotype forming cells by in situ immunocytochemical staining | Q53803593 | ||
Strain differences in the fine specificity of mouse antihapten antibodies | Q54115136 | ||
Antigen-binding repertoire and Ig H chain gene usage among B cell hybridomas from normal and autoimmune mice | Q67273728 | ||
Cloning of mitogen- and antigen-reactive B lymphocytes on filter paper disks: phenotypic and genotypic analysis of B cell colonies | Q68836283 | ||
Monoclonal anti-allotype antibody towards BALB/c IgM. Analysis of specificity and site of a V-C crossover in recombinant strain BALB-Igh-Va/Igh-Cb | Q69021421 | ||
Comparison of V kappa gene family expression in adult and fetal B cells | Q69236908 | ||
Primary in situ immune response in popliteal lymph nodes and spleen of mice after subcutaneous immunization with thymus-dependent or thymus-independent (type 1 and 2) antigens | Q69595249 | ||
The de novo generation of germinal centers is an oligoclonal process | Q70266774 | ||
The anatomy of peripheral lymphoid organs with emphasis on accessory cells: light-microscopic immunocytochemical studies of mouse spleen, lymph node, and Peyer's patch | Q70606407 | ||
The development of specific antibody-containing cells in the spleen of rabbits during the secondary immune response against free or liposome-associated albumin antigen | Q71009730 | ||
Antibody with homogeneous antigen binding produced by splenic foci in organ culture | Q71220293 | ||
CELL PROLIFERATION IN GERMINAL CENTERS OF THE RAT SPLEEN | Q76721614 | ||
THE WHITE PULP OF THE SPLEEN. THE RELATIONSHIPS OF ARTERIAL VESSELS, RETICULUM AND FREE CELLS IN THE PERIARTERIAL LYMPHATIC SHEATH | Q76938409 | ||
P433 | issue | 5 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 1165-1175 | |
P577 | publication date | 1991-05-01 | |
P1433 | published in | Journal of Experimental Medicine | Q3186912 |
P1476 | title | In situ studies of the primary immune response to (4-hydroxy-3-nitrophenyl)acetyl. I. The architecture and dynamics of responding cell populations | |
P478 | volume | 173 |
Q31135078 | A Model of Somatic Hypermutation Targeting in Mice Based on High-Throughput Ig Sequencing Data |
Q41684239 | A Population Dynamics Model for Clonal Diversity in a Germinal Center |
Q37818921 | A case for regulatory B cells in controlling the severity of autoimmune-mediated inflammation in experimental autoimmune encephalomyelitis and multiple sclerosis |
Q36369352 | A coordinated change in chemokine responsiveness guides plasma cell movements |
Q35213561 | A dynamic T cell-limited checkpoint regulates affinity-dependent B cell entry into the germinal center |
Q35126729 | A form of immunologic tolerance through impairment of germinal center development |
Q36140212 | A forward genetic screen reveals roles for Nfkbid, Zeb1, and Ruvbl2 in humoral immunity |
Q36689920 | A genetic lesion that arrests plasma cell homing to the bone marrow |
Q36375322 | A member of the dendritic cell family that enters B cell follicles and stimulates primary antibody responses identified by a mannose receptor fusion protein |
Q41823343 | A multi-scale model for correlation in B cell VDJ usage of zebrafish |
Q33944575 | A novel ICOS-independent, but CD28- and SAP-dependent, pathway of T cell-dependent, polysaccharide-specific humoral immunity in response to intact Streptococcus pneumoniae versus pneumococcal conjugate vaccine |
Q34295816 | A role for secondary V(D)J recombination in oncogenic chromosomal translocations? |
Q73280962 | A spatial model of germinal center reactions: cellular adhesion based sorting of B cells results in efficient affinity maturation |
Q47153776 | ATP-degrading ENPP1 is required for survival (or persistence) of long-lived plasma cells |
Q28587099 | Abnormal development of secondary lymphoid tissues in lymphotoxin beta-deficient mice |
Q48056149 | Accumulation of somatic hypermutation and antigen-driven selection in rapidly cycling surface Ig+ germinal center (GC) B cells which occupy GC at a high frequency during the primary anti-hapten response in mice |
Q36366097 | Activation and negative selection of functionally distinct subsets of antibody-secreting cells by influenza hemagglutinin as a viral and a neo-self antigen. |
Q35119889 | Activation of Rheumatoid Factor (RF) B Cells and Somatic Hypermutation Outside of Germinal Centers in Autoimmune‐Prone MRL/lpr Mice |
Q37833726 | Activation-induced cytidine deaminase and aberrant germinal center selection in the development of humoral autoimmunities |
Q33569857 | Adjuvant-specific regulation of long-term antibody responses by ZBTB20 |
Q40801731 | Affinity maturation of lymphocyte receptors and positive selection of T cells in the thymus |
Q41708763 | Age-related changes in antibody repertoire: contribution from T cells |
Q42971089 | Aiolos is required for the generation of high affinity bone marrow plasma cells responsible for long-term immunity |
Q45007626 | Alistair Cunningham and the generation of antibody diversity after antigen |
Q52539460 | Alterations in splenic architecture and the localization of anti-double-stranded DNA B cells in aged mice. |
Q47933634 | Altered T-dependent antigen responses and development of autoimmune symptoms in mice lacking E2A in T lymphocytes |
Q41092267 | Among naive precursor cell subpopulations only progenitors of memory B cells originate germinal centers |
Q41615089 | An anti-B cell autoantibody from Wiskott-Aldrich syndrome which recognizes i blood group specificity on normal human B cells |
Q72119418 | Analysis of individual immunoglobulin lambda light chain genes amplified from single cells is inconsistent with variable region gene conversion in germinal-center B cell somatic mutation |
Q34328629 | Analysis of somatic mutation in five B cell subsets of human tonsil |
Q71800463 | Anatomy of autoantibody production: Dominant localization of antibody-producing cells to T cell zones in fas-deficient mice |
Q51679736 | Antibody response to influenza infection of mice: different patterns for glycoprotein and nucleocapsid antigens. |
Q52572832 | Antibody-independent B cell-intrinsic and -extrinsic roles for CD21/35. |
Q36228608 | Antigen recognition strength regulates the choice between extrafollicular plasma cell and germinal center B cell differentiation |
Q36361955 | Antigen-driven B cell differentiation in vivo |
Q36368499 | Antigen-specific B cell memory: expression and replenishment of a novel b220(-) memory b cell compartment |
Q34242650 | Antigen-specific immunity. Th cell-dependent B cell responses |
Q36607190 | Antioxidant treatment regulates the humoral immune response during acute viral infection. |
Q41493232 | Apoptosis and the B cell response to antigen |
Q47877284 | Arrest of B lymphocyte terminal differentiation by CD40 signaling: mechanism for lack of antibody-secreting cells in germinal centers |
Q35988832 | B Cell-Intrinsic IDO1 Regulates Humoral Immunity to T Cell-Independent Antigens |
Q40065439 | B cell activation state-governed formation of germinal centers following viral infection. |
Q42175508 | B cell diversification and differentiation in the periphery |
Q41975943 | B cell function in mice transgenic for mCTLA4-H gamma 1: lack of germinal centers correlated with poor affinity maturation and class switching despite normal priming of CD4+ T cells |
Q36091161 | B cell proliferation, somatic hypermutation, class switch recombination, and autoantibody production in ectopic lymphoid tissue in murine lupus |
Q35915979 | B cell signalling as therapeutic target |
Q43711793 | B cell-specific expression of inducible costimulator ligand is necessary for the induction of arthritis in mice. |
Q61853724 | B cells activated via CD40 and IL-4 undergo a division burst but require continued stimulation to maintain division, survival and differentiation |
Q40673455 | B lymphocyte ontogeny and immunoglobulin production. |
Q35725257 | B-Cell Response during Protozoan Parasite Infections |
Q41091833 | B-T lymphocyte interactions in the generation and survival of memory cells. |
Q33905208 | B-cell memory and the persistence of antibody responses |
Q74591320 | B-cell receptor regulation of peripheral B cells |
Q34300038 | B7h-expressing dendritic cells and plasma B cells mediate distinct outcomes of ICOS costimulation in T cell-dependent antibody responses |
Q52055673 | Bcl-2 increases memory B cell recruitment but does not perturb selection in germinal centers. |
Q52040363 | Bcl-2 obstructs negative selection of autoreactive, hypermutated antibody V regions during memory B cell development. |
Q52005022 | Blimp-1 Is Required for the Formation of Immunoglobulin Secreting Plasma Cells and Pre-Plasma Memory B Cells |
Q38204273 | Blood, sphingosine-1-phosphate and lymphocyte migration dynamics in the spleen. |
Q46745223 | CCR6 is transiently upregulated on B cells after activation and modulates the germinal center reaction in the mouse |
Q42124976 | CD11c expression identifies a population of extrafollicular antigen-specific splenic plasmablasts responsible for CD4 T-independent antibody responses during intracellular bacterial infection |
Q33639733 | CD21int CD23+ follicular B cells express antigen-specific secretory IgM mRNA as primary and memory responses. |
Q55035653 | CD23 defines two distinct subsets of immature B cells which differ in their responses to T cell help signals. |
Q28508535 | CD4 T cell cytokine differentiation: the B cell activation molecule, OX40 ligand, instructs CD4 T cells to express interleukin 4 and upregulates expression of the chemokine receptor, Blr-1 |
Q52007792 | CD4(+)CD3(-) accessory cells costimulate primed CD4 T cells through OX40 and CD30 at sites where T cells collaborate with B cells. |
Q61268446 | CD40 ligand-independent B cell activation revealed by CD40 ligand-deficient T cell clones: evidence for distinct activation requirements for antibody formation and B cell proliferation |
Q34082784 | CD40-mediated regulation of immune responses by TRAF-dependent and TRAF-independent signaling mechanisms. |
Q40900126 | CD5 is A potential selecting ligand for B-cell surface immunoglobulin: a possible role in maintenance and selective expansion of normal and malignant B cells |
Q38659933 | CD73 expression identifies a subset of IgM+ antigen-experienced cells with memory attributes that is T cell and CD40 signalling dependent. |
Q74660389 | CDK inhibitor p18(INK4c) is required for the generation of functional plasma cells |
Q74341297 | CM1, a possible novel activation molecule on human lymphocytes |
Q34797382 | Cannabinoid Receptor 2 (CB2) Plays a Role in the Generation of Germinal Center and Memory B Cells, but Not in the Production of Antigen-Specific IgG and IgM, in Response to T-dependent Antigens. |
Q42647823 | Canonical germinal center B cells may not dominate the memory response to antigenic challenge |
Q24805154 | Cell-cell interactions in synovitis. Interactions between T cells and B cells in rheumatoid arthritis |
Q36260505 | Cellular Dynamics of Memory B Cell Populations: IgM+ and IgG+ Memory B Cells Persist Indefinitely as Quiescent Cells |
Q37770981 | Cellular choreography in the germinal center: new visions from in vivo imaging |
Q36529012 | Checkpoints in memory B-cell evolution |
Q27312505 | Chemotaxis in densely populated tissue determines germinal center anatomy and cell motility: a new paradigm for the development of complex tissues |
Q46018300 | Chemotherapy induced transient B-cell depletion boosts antibody-forming cells expansion driven by an epidermal growth factor-based cancer vaccine. |
Q36371091 | Chronic lymphocytic leukemia B cells can undergo somatic hypermutation and intraclonal immunoglobulin V(H)DJ(H) gene diversification. |
Q35320898 | Coelomic and bone marrow-derived B cells. Developmental constraints versus antigen-specific selection |
Q37403161 | Colocalization of antigen-specific B and T cells within ectopic lymphoid tissue following immunization with exogenous antigen |
Q36369080 | Complement C4 inhibits systemic autoimmunity through a mechanism independent of complement receptors CR1 and CR2 |
Q42006087 | Compromised OX40 function in CD28-deficient mice is linked with failure to develop CXC chemokine receptor 5-positive CD4 cells and germinal centers. |
Q37681529 | Computational Model Reveals Limited Correlation between Germinal Center B-Cell Subclone Abundancy and Affinity: Implications for Repertoire Sequencing |
Q36371140 | Constitutive expression of the B7h ligand for inducible costimulator on naive B cells is extinguished after activation by distinct B cell receptor and interleukin 4 receptor-mediated pathways and can be rescued by CD40 signaling |
Q24317763 | Cross-linking of OX40 ligand, a member of the TNF/NGF cytokine family, induces proliferation and differentiation in murine splenic B cells |
Q39526308 | Crucial role of tumor necrosis factor receptor 1 expression on nonhematopoietic cells for B cell localization within the splenic white pulp |
Q42798925 | Cutting Edge: γδ T Cells Provide Help to B Cells with Altered Clonotypes and Are Capable of Inducing Ig Gene Hypermutation |
Q36824092 | Cutting edge: Macrophages are required for localization of antigen-activated B cells to the follicular perimeter and the subsequent germinal center response |
Q34484424 | Cyclin D3 Is Selectively Required for Proliferative Expansion of Germinal Center B Cells |
Q36828240 | DNA immunization: induction of higher avidity antibody and effect of route on T cell cytotoxicity. |
Q33689667 | Defective B-cell response to T-dependent immunization in lupus-prone mice |
Q33815470 | Dendritic cells, B cells and the regulation of antibody synthesis |
Q34921409 | Dendritic cells, BAFF, and APRIL: innate players in adaptive antibody responses. |
Q37644909 | Differences in the composition of the human antibody repertoire by B cell subsets in the blood |
Q99711521 | Differential Roles of IDO1 and IDO2 in T and B Cell Inflammatory Immune Responses |
Q41522446 | Differentiation and apoptosis of human germinal center B-lymphocytes |
Q40673767 | Differentiation of the secondary B-lymphocyte repertoire: the germinal center reaction |
Q36522053 | Disparate adjuvant properties among three formulations of "alum" |
Q28509600 | Disruption of the Bcl6 gene results in an impaired germinal center formation |
Q64078028 | Distinct Requirements of CHD4 during B Cell Development and Antibody Response |
Q42006236 | Distinct cell-specific control of autoimmunity and infection by FcgammaRIIb |
Q37331523 | Distinction of the memory B cell response to cognate antigen versus bystander inflammatory signals. |
Q46918689 | Diversity among memory B cells: origin, consequences, and utility. |
Q46172393 | Do Memory B Cells Form Secondary Germinal Centers? Impact of Antibody Class and Quality of Memory T-Cell Help at Recall. |
Q78298249 | Dominant, hierarchical induction of peripheral tolerance during foreign antigen-driven B cell development |
Q58546206 | Dynamics of Virus-Specific Memory B Cells and Plasmablasts following CNS Viral Infection |
Q36661580 | EAF2 mediates germinal centre B-cell apoptosis to suppress excessive immune responses and prevent autoimmunity. |
Q28251850 | EBI2 mediates B cell segregation between the outer and centre follicle |
Q47232451 | EZH2 Represses the B Cell Transcriptional Program and Regulates Antibody-Secreting Cell Metabolism and Antibody Production |
Q36214093 | Early and late B-cell development in the mouse |
Q37730206 | Enhanced antibody responses to an HIV-1 membrane-proximal external region antigen in mice reconstituted with cultured lymphocytes |
Q41091819 | Enumeration and characterization of memory cells in the TH compartment |
Q35901088 | Evaluation of Selected Immunomodulatory Glycoproteins as an Adjunct to Cancer Immunotherapy |
Q28595063 | Evidence from the generation of immunoglobulin G-secreting cells that stochastic mechanisms regulate lymphocyte differentiation |
Q41460441 | Experimental plasmacytomagenesis in mice |
Q84199195 | Expression of IgA class switching gene in tonsillar mononuclear cells in patients with IgA nephropathy |
Q42952003 | Extracellular signal-regulated protein kinase 2 is required for efficient generation of B cells bearing antigen-specific immunoglobulin G. |
Q34212117 | Extrafollicular antibody responses |
Q51990874 | Extrafollicular proliferation of B cells in the absence of follicular hyperplasia: a distinct reaction pattern in lymph nodes correlated with primary or recall type responses. |
Q90401160 | Factors Affecting Early Antibody Secreting Cell Maturation Into Long-Lived Plasma Cells |
Q36364652 | Facultative role of germinal centers and T cells in the somatic diversification of IgVH genes |
Q28294153 | Follicular dendritic cells and germinal centers |
Q42010309 | Follicular dendritic cells help resting B cells to become effective antigen-presenting cells: induction of B7/BB1 and upregulation of major histocompatibility complex class II molecules |
Q24600825 | Follicular helper T cells in immunity and systemic autoimmunity |
Q24647274 | Follicular helper T cells: lineage and location |
Q52070216 | Functional and molecular characterization of single, (4-hydroxy-3-nitrophenyl)acetyl (NP)-specific, IgG1+ B cells from antibody-secreting and memory B cell pathways in the C57BL/6 immune response to NP. |
Q71824259 | Gamma delta T cell help of B cells is induced by repeated parasitic infection, in the absence of other T cells |
Q34241427 | Gamma delta T cells recognize haptens and mount a hapten-specific response. |
Q33428789 | Genetic ablation or pharmacological blockade of dipeptidyl peptidase IV does not impact T cell-dependent immune responses |
Q38960786 | Germinal Center B Cell Dynamics |
Q36694162 | Germinal center B cells govern their own fate via antibody feedback |
Q42114332 | Germinal center founder cells display propensity for apoptosis before onset of somatic mutation |
Q36368941 | Germinal center initiation, variable gene region hypermutation, and mutant B cell selection without detectable immune complexes on follicular dendritic cells |
Q34268133 | Germinal center selection and the development of memory B and plasma cells |
Q42767398 | Germinal centers in human lymph nodes contain reactivated memory B cells |
Q36375933 | Germinal centers without T cells |
Q36774105 | Germinal centres in T-cell-dependent antibody responses |
Q36459345 | Germinal-center organization and cellular dynamics |
Q39455345 | Here, There, and Anywhere? Arguments for and against the Physical Plasma Cell Survival Niche |
Q38037738 | Heterogeneity in the differentiation and function of memory B cells |
Q36228042 | High affinity germinal center B cells are actively selected into the plasma cell compartment. |
Q34337263 | High frequency of virus-specific B lymphocytes in germinal centers of simian-human immunodeficiency virus-infected rhesus monkeys |
Q59126340 | High-affinity IgM memory B cells are defective in differentiation into IgM antibody-secreting cells by re-stimulation with a T cell-dependent antigen |
Q35170914 | Homing of antibody secreting cells |
Q52041305 | Host immunobiology and vaccine development. |
Q33355955 | How oligoclonal are germinal centers? A new method for estimating clonal diversity from immunohistological sections |
Q35170828 | Human tonsil B-cell lymphoma 6 (BCL6)-expressing CD4+ T-cell subset specialized for B-cell help outside germinal centers |
Q36933060 | Hyperproliferation of B cells specific for a weakly immunogenic PorA in a meningococcal vaccine model |
Q37326558 | ICOS, CD40, and lymphotoxin beta receptors signal sequentially and interdependently to initiate a germinal center reaction |
Q36979971 | ICOS-dependent extrafollicular helper T cells elicit IgG production via IL-21 in systemic autoimmunity |
Q34401702 | IDO2 is a critical mediator of autoantibody production and inflammatory pathogenesis in a mouse model of autoimmune arthritis |
Q37202839 | IL-6 produced by immune complex-activated follicular dendritic cells promotes germinal center reactions, IgG responses and somatic hypermutation |
Q36403611 | Identification of proteoglycans as the APRIL-specific binding partners. |
Q24631904 | IgM production by bone marrow plasmablasts contributes to long-term protection against intracellular bacterial infection |
Q28285566 | Immunoglobulin class switching |
Q35850383 | Immunoglobulin gene hyperconversion ongoing in chicken splenic germinal centers. |
Q48037871 | Immunoglobulin gene hypermutation in germinal centers is independent of the RAG-1 V(D)J recombinase |
Q31131763 | Immunoglobulin heavy chain gene expression in peripheral blood B lymphocytes |
Q36366690 | Immunoglobulin switch transcript production in vivo related to the site and time of antigen-specific B cell activation |
Q38690037 | Immunological processes underlying the slow acquisition of humoral immunity to malaria |
Q41339849 | Immunological tolerance in germinal centres |
Q41708767 | Immunosenescence and germinal center reaction |
Q38675682 | Impaired germinal center responses and suppression of local IgG production during intracellular bacterial infection |
Q30437109 | Imprinting the fate of antigen-reactive B cells through the affinity of the B cell receptor. |
Q36231790 | In situ studies of the primary immune response to (4-hydroxy-3-nitrophenyl)acetyl. II. A common clonal origin for periarteriolar lymphoid sheath-associated foci and germinal centers |
Q36362440 | In situ studies of the primary immune response to (4-hydroxy-3-nitrophenyl)acetyl. III. The kinetics of V region mutation and selection in germinal center B cells |
Q41888015 | In situ studies of the primary immune response to (4-hydroxy-3-nitrophenyl)acetyl. IV. Affinity-dependent, antigen-driven B cell apoptosis in germinal centers as a mechanism for maintaining self-tolerance |
Q41949877 | In situ studies of the primary immune response to (4-hydroxy-3-nitrophenyl)acetyl. V. Affinity maturation develops in two stages of clonal selection. |
Q36362569 | In vivo CD40-gp39 interactions are essential for thymus-dependent humoral immunity. I. In vivo expression of CD40 ligand, cytokines, and antibody production delineates sites of cognate T-B cell interactions |
Q34684380 | In vivo analysis of Aicda gene regulation: a critical balance between upstream enhancers and intronic silencers governs appropriate expression |
Q47370276 | In vivo expression of interleukin-8, and regulated on activation, normal, T-cell expressed, and secreted, by human germinal centre B lymphocytes |
Q73510662 | Increase in tonsillar germinal centre B-1 cell numbers in IgA nephropathy (IgAN) patients and reduced susceptibility to Fas-mediated apoptosis |
Q36916349 | Increased IL-12 inhibits B cells' differentiation to germinal center cells and promotes differentiation to short-lived plasmablasts |
Q36818340 | Independent Roles of Switching and Hypermutation in the Development and Persistence of B Lymphocyte Memory |
Q36366635 | Induction of long-lived germinal centers associated with persisting antigen after viral infection |
Q39639974 | Inhibition of Terminal Differentiation of B Cells Mediated by CD27 and CD40 Involves Signaling through JNK |
Q42064439 | Initial clonal expansion of germinal center B cells takes place at the perimeter of follicles |
Q41934489 | Integrating B cell lineage information into statistical tests for detecting selection in Ig sequences |
Q35832497 | Interactions between NK cells and B lymphocytes |
Q41839042 | Interleukin 6 influences germinal center development and antibody production via a contribution of C3 complement component |
Q38163422 | Interleukin-21 and T follicular helper cells in HIV infection: research focus and future perspectives |
Q41172275 | Intraclonal generation of antibody mutants in germinal centres |
Q36368882 | Intrinsic constraint on plasmablast growth and extrinsic limits of plasma cell survival |
Q36529022 | Intrinsic properties of human and murine memory B cells |
Q33897378 | Isolation of germinal centerlike events from human spleen RNA. Somatic hypermutation of a clonally related VH6DJH rearrangement expressed with IgM, IgG, and IgA |
Q42116914 | Isolation, maturational level, and functional capacity of human colon lamina propria plasma cells. |
Q48078189 | Kinetics of somatic mutation in lymph node germinal centres |
Q40983825 | Life and death in germinal centers (redux). |
Q34969945 | Life and death within germinal centres: a double-edged sword. |
Q34270556 | Long-lived bone marrow plasma cells are induced early in response to T cell-independent or T cell-dependent antigens |
Q37878485 | Long-term protection after immunization with protein-polysaccharide conjugate vaccines in infancy |
Q42944615 | Low-level hypermutation in T cell-independent germinal centers compared with high mutation rates associated with T cell-dependent germinal centers |
Q41853947 | Lymph node germinal centers form in the absence of follicular dendritic cell networks |
Q36368261 | MRL-lpr/lpr mice exhibit a defect in maintaining developmental arrest and follicular exclusion of anti-double-stranded DNA B cells |
Q42170932 | Manipulating the selection forces during affinity maturation to generate cross-reactive HIV antibodies |
Q50738767 | Manipulation of B-cell responses with histone deacetylase inhibitors. |
Q44296985 | Marginal zone and B1 B cells unite in the early response against T-independent blood-borne particulate antigens |
Q36171749 | Maturation and dispersal of B-cell clones during T cell-dependent antibody responses |
Q36363287 | Memory B cell development but not germinal center formation is impaired by in vivo blockade of CD40-CD40 ligand interaction |
Q38107252 | Memory B cells in mouse models |
Q37116099 | Mitochondrial Pyruvate Import Promotes Long-Term Survival of Antibody-Secreting Plasma Cells |
Q33958359 | Modeling and optimization of populations subject to time-dependent mutation |
Q40392133 | Molecular control of B Lymphocyte growth and differentiation |
Q37474929 | Molecular mechanism and function of CD40/CD40L engagement in the immune system. |
Q26829944 | Molecular programming of B cell memory |
Q42048360 | Morphological interactions of interdigitating dendritic cells with B and T cells in human mesenteric lymph nodes |
Q51978162 | Naive T-cell receptor transgenic T cells help memory B cells produce antibody. |
Q64084920 | Non-classical B Cell Memory of Allergic IgE Responses |
Q71169448 | Normal human IgD+IgM- germinal center B cells can express up to 80 mutations in the variable region of their IgD transcripts |
Q34707321 | Noxa mediates p18INK4c cell-cycle control of homeostasis in B cells and plasma cell precursors |
Q33889407 | OCA-B integrates B cell antigen receptor-, CD40L- and IL 4-mediated signals for the germinal center pathway of B cell development |
Q36263769 | Optimal Sequential Immunization Can Focus Antibody Responses against Diversity Loss and Distraction |
Q33598442 | Optimality of mutation and selection in germinal centers |
Q36380477 | Outer periarteriolar lymphoid sheath arrest and subsequent differentiation of both naive and tolerant immunoglobulin transgenic B cells is determined by B cell receptor occupancy |
Q41903686 | Paracrine regulation of germinal center B cell adhesion through the c-met-hepatocyte growth factor/scatter factor pathway |
Q36581971 | Phospholipids: "greasing the wheels" of humoral immunity |
Q37165615 | Plexin-D1 is a novel regulator of germinal centers and humoral immune responses |
Q44870111 | Predicted and inferred waiting times for key mutations in the germinal centre reaction: evidence for stochasticity in selection |
Q50471565 | Pro-B cells propagated in stromal cell-free cultures reconstitute functional B-cell compartments in immunodeficient mice. |
Q34059107 | Progression from IgD+ IgM+ to isotype-switched B cells is site specific during coronavirus-induced encephalomyelitis. |
Q28508346 | Rad51 expression and localization in B cells carrying out class switch recombination |
Q42691059 | Re-evaluating the recycling hypothesis in the germinal centre. |
Q34609455 | Recirculation of germinal center B cells: a multilevel selection strategy for antibody maturation |
Q41818598 | Reconstructing a B-cell clonal lineage. I. Statistical inference of unobserved ancestors |
Q64997349 | Recurrent group A Streptococcus tonsillitis is an immunosusceptibility disease involving antibody deficiency and aberrant TFH cells. |
Q28585862 | Reduced isotype switching in splenic B cells from mice deficient in mismatch repair enzymes |
Q73129004 | Regulation of VH gene repertoire and somatic mutation in germinal centre B cells by passively administered antibody |
Q36380737 | Regulation of anti-double-stranded DNA B cells in nonautoimmune mice: localization to the T-B interface of the splenic follicle |
Q50557277 | Regulation of bifurcating B cell trajectories by mutual antagonism between transcription factors IRF4 and IRF8. |
Q26766726 | Regulation of germinal center B-cell differentiation |
Q35748742 | Regulation of late B cell differentiation by intrinsic IKKalpha-dependent signals |
Q36058417 | Regulation of plasma-cell development |
Q40427517 | Regulatory T cells can migrate to follicles upon T cell activation and suppress GC-Th cells and GC-Th cell-driven B cell responses |
Q92824342 | Regulatory roles of IL-10-producing human follicular T cells |
Q36365981 | Relative contribution of T and B cells to hypermutation and selection of the antibody repertoire in germinal centers of aged mice |
Q42947038 | Relaxed negative selection in germinal centers and impaired affinity maturation in bcl-xL transgenic mice |
Q44432132 | Repertoire Shift in the Humoral Response to Phosphocholine-Keyhole Limpet Hemocyanin: VH Somatic Mutation in Germinal Center B Cells Impairs T15 Ig Function |
Q52020338 | Rewiring of CD40 is necessary for delivery of rescue signals to B cells in germinal centres and subsequent entry into the memory pool. |
Q47104417 | RhoB blockade selectively inhibits autoantibody production in autoimmune models of rheumatoid arthritis and lupus |
Q74139589 | Role of BCR affinity in T cell dependent antibody responses in vivo |
Q36670538 | Role of IL-21 and IL-21 receptor on B cells in HIV infection |
Q36478485 | SWAP-70 deficiency causes high-affinity plasma cell generation despite impaired germinal center formation |
Q54979506 | SYK Inhibition Induces Apoptosis in Germinal Center-Like B Cells by Modulating the Antiapoptotic Protein Myeloid Cell Leukemia-1, Affecting B-Cell Activation and Antibody Production. |
Q47876829 | Selective expression of the transcription elongation factor ELL3 in B cells prior to ELL2 drives proliferation and survival |
Q24536218 | Selective generation of functional somatically mutated IgM+CD27+, but not Ig isotype-switched, memory B cells in X-linked lymphoproliferative disease |
Q40373293 | Self-tolerance checkpoints in B lymphocyte development |
Q37156660 | Sequencing heavy- and light-chain variable genes of single B-hybridoma cells by total enzymatic amplification |
Q71420926 | Sequential antigen-specific growth of T cells in the T zones and follicles in response to pigeon cytochrome c |
Q28585021 | Severe attenuation of the B cell immune response in Msh2-deficient mice |
Q39737614 | Short-circuiting long-lived humoral immunity by the heightened engagement of CD40. |
Q41492235 | Signaling thresholds and interclonal competition in preimmune B-cell selection |
Q37132162 | Significance of glycosylphosphatidylinositol-anchored protein enrichment in lipid rafts for the control of autoimmunity |
Q33959225 | Silent development of memory progenitor B cells |
Q41602537 | Sites of B lymphocyte selection, activation, and tolerance in spleen |
Q43603650 | Sites of specific B cell activation in primary and secondary responses to T cell-dependent and T cell-independent antigens |
Q52053087 | Soluble antigen can cause enhanced apoptosis of germinal-centre B cells. |
Q41222940 | Somatic diversification of antibody responses |
Q47110972 | Spoiling for a Fight: B Lymphocytes As Initiator and Effector Populations within Tertiary Lymphoid Organs in Autoimmunity and Transplantation. |
Q36400509 | Spontaneous follicular exclusion of SHP1-deficient B cells is conditional on the presence of competitor wild-type B cells |
Q57897255 | Stochastic discrete event simulation of germinal center reactions |
Q34242639 | Studies of the humoral immune response |
Q35321772 | Surface markers, heavy chain sequences and B cell lineages |
Q38002491 | T cells that promote B-Cell maturation in systemic autoimmunity |
Q36400665 | T helper 1 (Th1) and Th2 characteristics start to develop during T cell priming and are associated with an immediate ability to induce immunoglobulin class switching |
Q36367277 | T helper cells in murine germinal centers are antigen-specific emigrants that downregulate Thy-1. |
Q40527478 | Targeting and regulation of immunoglobulin gene somatic hypermutation and isotype switch recombination |
Q41876688 | The B cell receptor itself can activate complement to provide the complement receptor 1/2 ligand required to enhance B cell immune responses in vivo |
Q35796008 | The Emu-bcl-2 transgene enhances antigen-induced germinal center formation in both BALB/c and SJL mice but causes age-dependent germinal center hyperplasia only in the lymphoma-prone SJL strain |
Q48011135 | The Fas antigen and Fas-mediated apoptosis in B-cell differentiation |
Q50349777 | The Rac Activator DOCK2 Mediates Plasma Cell Differentiation and IgG Antibody Production. |
Q36365985 | The T cell-B cell interaction via OX40-OX40L is necessary for the T cell-dependent humoral immune response |
Q37688958 | The anatomy of T-cell activation and tolerance |
Q41492213 | The changing preference of T and B cells for partners as T-dependent antibody responses develop |
Q36171758 | The development of B cells and the B-cell repertoire in the microenvironment of the germinal center |
Q35380833 | The dynamics of T cell-dependent B cell responses in vivo |
Q37784588 | The elusive identity of T follicular helper cells |
Q38070792 | The establishment of the plasma cell survival niche in the bone marrow |
Q33886727 | The extent of affinity maturation differs between the memory and antibody-forming cell compartments in the primary immune response |
Q41937356 | The extent of clonal structure in different lymphoid organs |
Q36366646 | The fate of self-reactive B cells depends primarily on the degree of antigen receptor engagement and availability of T cell help. |
Q79435564 | The germinal center response is impaired in the absence of T cell-expressed CXCR5 |
Q33922881 | The hepatocyte growth factor/Met pathway in development, tumorigenesis, and B-cell differentiation. |
Q56904544 | The impact of T helper and T regulatory cells on the regulation of anti-double-stranded DNA B cells |
Q35307418 | The miR-155-PU.1 axis acts on Pax5 to enable efficient terminal B cell differentiation |
Q52170468 | The origin of anti-nuclear antibodies in bcl-2 transgenic mice. |
Q36171744 | The path of memory B-cell development |
Q71047935 | The phenotype and fate of the antibody-forming cells of the splenic foci |
Q41492250 | The physiology of murine germinal center reactions |
Q36079896 | The regulation and activation of lupus-associated B cells |
Q34033732 | The road to the production of IgE is long and winding |
Q47933342 | The role of germinal centers for antiviral B cell responses |
Q52039310 | The roles of antibody variable region hypermutation and selection in the development of the memory B-cell compartment. |
Q35981133 | The specialized unfolded protein response of B lymphocytes: ATF6α-independent development of antibody-secreting B cells. |
Q34311595 | The tetraspanin CD37 orchestrates the α(4)β(1) integrin-Akt signaling axis and supports long-lived plasma cell survival |
Q41472333 | To 'B' or not to 'B' a germinal center? |
Q37374679 | Toll-like receptor 3 ligand and retinoic acid enhance germinal center formation and increase the tetanus toxoid vaccine response |
Q79818179 | Toll-like receptor engagement stimulates anti-snRNP autoreactive B cells for activation |
Q40874465 | Tracing B cell development in human germinal centres by molecular analysis of single cells picked from histological sections |
Q36366754 | Tracing the development of single memory-lineage B cells in a highly defined immune response |
Q50559773 | Trypanosoma cruzi infection induces a massive extrafollicular and follicular splenic B-cell response which is a high source of non-parasite-specific antibodies. |
Q33592023 | Tumor necrosis factor alpha p55 receptor is important for development of memory responses to blood-stage malaria infection |
Q48509911 | Twenty-five years of germinal centre physiology: implications for tolerance in the secondary B cell repertoire |
Q33979882 | Type I IFN enhances follicular B cell contribution to the T cell-independent antibody response |
Q41492243 | Unique site of IgG2a and rheumatoid factor production in MRL/lpr mice |
Q58591219 | Unresponsiveness following immunization with the T-cell-independent antigen dextran B512. Can it be abrogated? |
Q36370154 | Very low affinity B cells form germinal centers, become memory B cells, and participate in secondary immune responses when higher affinity competition is reduced |
Q36376518 | Viral superantigen drives extrafollicular and follicular B cell differentiation leading to virus-specific antibody production |
Q36404575 | Virus-induced maturation and activation of autoreactive memory B cells |
Q36370951 | Visualization of the genesis and fate of isotype-switched B cells during a primary immune response |
Q37078589 | Visualizing antibody affinity maturation in germinal centers |
Q29616233 | Visualizing dendritic cell networks in vivo |
Q37212132 | Vitamin A and retinoic acid in the regulation of B-cell development and antibody production |
Q41224472 | Within germinal centers, isotype switching of immunoglobulin genes occurs after the onset of somatic mutation |
Q37395797 | mTOR has distinct functions in generating versus sustaining humoral immunity. |
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