scholarly article | Q13442814 |
P50 | author | Michel C. Nussenzweig | Q24804686 |
Anna Gazumyan | Q65089949 | ||
Alexander D Gitlin | Q99708568 | ||
Lotta von Boehmer | Q114408569 | ||
Thiago Yukio Kikuchi Oliveira | Q56490386 | ||
P2093 | author name string | Ziv Shulman | |
P2860 | cites work | Cre reporter strains produced by targeted insertion of EYFP and ECFP into the ROSA26 locus | Q24797230 |
The role of Fc-FcγR interactions in IgG-mediated microbial neutralization | Q26797466 | ||
S1PR2 links germinal center confinement and growth regulation | Q26829249 | ||
Molecular programming of B cell memory | Q26829944 | ||
VARIATIONS IN AFFINITIES OF ANTIBODIES DURING THE IMMUNE RESPONSE | Q76969494 | ||
A chemokine-driven positive feedback loop organizes lymphoid follicles | Q28142202 | ||
A putative chemokine receptor, BLR1, directs B cell migration to defined lymphoid organs and specific anatomic compartments of the spleen | Q28300225 | ||
Class switch recombination and hypermutation require activation-induced cytidine deaminase (AID), a potential RNA editing enzyme | Q29547201 | ||
Predominant autoantibody production by early human B cell precursors | Q29619656 | ||
Neutralizing antibodies derived from the B cells of 1918 influenza pandemic survivors. | Q30371529 | ||
Intrinsic properties of immunoglobulin IgG1 isotype-switched B cell receptors promote microclustering and the initiation of signaling | Q30495504 | ||
Germinal center dynamics revealed by multiphoton microscopy with a photoactivatable fluorescent reporter | Q30498133 | ||
The sphingosine 1-phosphate receptor S1P₂ maintains the homeostasis of germinal center B cells and promotes niche confinement | Q30503547 | ||
Premature replacement of mu with alpha immunoglobulin chains impairs lymphopoiesis and mucosal homing but promotes plasma cell maturation. | Q33733998 | ||
53BP1 regulates DNA resection and the choice between classical and alternative end joining during class switch recombination | Q33794964 | ||
The extent of affinity maturation differs between the memory and antibody-forming cell compartments in the primary immune response | Q33886727 | ||
Germinal centers | Q34245271 | ||
Antigen receptors on B lymphocytes | Q34420640 | ||
The generation of antibody-secreting plasma cells. | Q34463732 | ||
Mature B cells class switched to IgD are autoreactive in healthy individuals | Q34629514 | ||
The immunoglobulin tail tyrosine motif upgrades memory-type BCRs by incorporating a Grb2-Btk signalling module. | Q34677828 | ||
Liver-expressed Igkappa superantigen induces tolerance of polyclonal B cells by clonal deletion not kappa to lambda receptor editing. | Q34681437 | ||
Mechanism and regulation of class switch recombination | Q34764888 | ||
In situ studies of the primary immune response to (4-hydroxy-3-nitrophenyl)acetyl. I. The architecture and dynamics of responding cell populations | Q34885732 | ||
Homing of antibody secreting cells | Q35170914 | ||
Memory B cells, but not long-lived plasma cells, possess antigen specificities for viral escape mutants | Q35627714 | ||
Autoreactivity in human IgG+ memory B cells | Q35729131 | ||
c-Myb is required for plasma cell migration to bone marrow after immunization or infection | Q35824200 | ||
A germinal center-independent pathway generates unswitched memory B cells early in the primary response | Q35825984 | ||
Surrogate light chain expressing human peripheral B cells produce self-reactive antibodies | Q35834694 | ||
Bone marrow is a major site of long-term antibody production after acute viral infection | Q35835410 | ||
The scaffolding protein synapse-associated protein 97 is required for enhanced signaling through isotype-switched IgG memory B cell receptors | Q36145652 | ||
Immunization for HIV-1 Broadly Neutralizing Antibodies in Human Ig Knockin Mice | Q36159067 | ||
Endogenous antigen tunes the responsiveness of naive B cells but not T cells | Q36223587 | ||
High affinity germinal center B cells are actively selected into the plasma cell compartment. | Q36228042 | ||
Plasma cell S1P1 expression determines secondary lymphoid organ retention versus bone marrow tropism | Q36228105 | ||
Enhancement and suppression of signaling by the conserved tail of IgG memory-type B cell antigen receptors | Q36229232 | ||
IgG1 B cell receptor signaling is inhibited by CD22 and promotes the development of B cells whose survival is less dependent on Ig alpha/beta | Q36229267 | ||
Rabbit lymphoid cells differentiated with respect to alpha-, gamma-, and mu- heavy polypeptide chains and to allotypic markers Aa1 and Aa2 | Q36268033 | ||
lambda 5, but not mu, is required for B cell maturation in a unique gamma 2b transgenic mouse line | Q36364512 | ||
Gene dose-dependent maturation and receptor editing of B cells expressing immunoglobulin (Ig)G1 or IgM/IgG1 tail antigen receptors | Q36368371 | ||
A coordinated change in chemokine responsiveness guides plasma cell movements | Q36369352 | ||
Germinal-center organization and cellular dynamics | Q36459345 | ||
Rapid elimination of mature autoreactive B cells demonstrated by Cre-induced change in B cell antigen receptor specificity in vivo | Q36642612 | ||
Autoreactive IgG memory antibodies in patients with systemic lupus erythematosus arise from nonreactive and polyreactive precursors | Q36775342 | ||
Polyreactivity increases the apparent affinity of anti-HIV antibodies by heteroligation | Q36977531 | ||
AID is required for the chromosomal breaks in c-myc that lead to c-myc/IgH translocations | Q37269390 | ||
The distinctive germinal center phase of IgE+ B lymphocytes limits their contribution to the classical memory response | Q37322165 | ||
Different B cell populations mediate early and late memory during an endogenous immune response | Q37712769 | ||
Heterogeneity in the differentiation and function of memory B cells | Q38037738 | ||
Elimination of germinal-center-derived self-reactive B cells is governed by the location and concentration of self-antigen. | Q39246618 | ||
HUMORAL IMMUNITY. T cell help controls the speed of the cell cycle in germinal center B cells. | Q39553791 | ||
Recruitment of the cytoplasmic adaptor Grb2 to surface IgG and IgE provides antigen receptor-intrinsic costimulation to class-switched B cells | Q39814347 | ||
Humoral immunity. Apoptosis and antigen affinity limit effector cell differentiation of a single naïve B cell | Q40019887 | ||
C-terminal deletion of AID uncouples class switch recombination from somatic hypermutation and gene conversion. | Q40627624 | ||
Clonal selection and learning in the antibody system | Q41002744 | ||
Mice carrying a knock-in mutation of Aicda resulting in a defect in somatic hypermutation have impaired gut homeostasis and compromised mucosal defense | Q41430473 | ||
Immunoglobulin gamma 2b transgenes inhibit heavy chain gene rearrangement, but cannot promote B cell development | Q41964652 | ||
Cutting edge: An in vivo reporter reveals active B cell receptor signaling in the germinal center. | Q41976378 | ||
Clonal selection in the germinal centre by regulated proliferation and hypermutation | Q42185336 | ||
Dynamic signaling by T follicular helper cells during germinal center B cell selection. | Q42406102 | ||
AID mutant analyses indicate requirement for class-switch-specific cofactors | Q42798287 | ||
Separate domains of AID are required for somatic hypermutation and class-switch recombination | Q42828095 | ||
Cellular localization of immunoglobulins with different allotypic specificities in rabbit lymphoid tissues | Q42830658 | ||
Multiple layers of B cell memory with different effector functions | Q43255281 | ||
Sites of specific B cell activation in primary and secondary responses to T cell-dependent and T cell-independent antigens | Q43603650 | ||
Repression of the transcription factor Bach2 contributes to predisposition of IgG1 memory B cells toward plasma cell differentiation. | Q43744129 | ||
A distinct signaling pathway used by the IgG-containing B cell antigen receptor | Q44257389 | ||
Fluorescent in vivo detection reveals that IgE(+) B cells are restrained by an intrinsic cell fate predisposition. | Q45671838 | ||
Duration of humoral immunity to common viral and vaccine antigens | Q45872621 | ||
Antigen-induced B-cell death and elimination during germinal-centre immune responses | Q46147419 | ||
Imaging of germinal center selection events during affinity maturation | Q46722429 | ||
Diversity among memory B cells: origin, consequences, and utility. | Q46918689 | ||
Cutting Edge: Long-Term B Cell Memory in Humans after Smallpox Vaccination | Q47395264 | ||
Tracking human antigen-specific memory B cells: a sensitive and generalized ELISPOT system | Q47756393 | ||
Memory B-cell persistence is independent of persisting immunizing antigen. | Q47821945 | ||
Memory B cell survival and function in the absence of secreted antibody and immune complexes on follicular dendritic cells. | Q51983578 | ||
Burst-enhancing role of the IgG membrane tail as a molecular determinant of memory. | Q52014781 | ||
Kinetics of establishing the memory B cell population as revealed by CD38 expression. | Q52039439 | ||
The roles of gamma 1 heavy chain membrane expression and cytoplasmic tail in IgG1 responses. | Q52043164 | ||
Effect of transmembrane and cytoplasmic domains of IgE on the IgE response. | Q52043166 | ||
Soluble antigen can cause enhanced apoptosis of germinal-centre B cells. | Q52053087 | ||
Persistence of memory B cells in mice deprived of T cell help. | Q52111523 | ||
P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 769-781 | |
P577 | publication date | 2016-02-29 | |
P1433 | published in | Immunity | Q6005457 |
P1476 | title | Independent Roles of Switching and Hypermutation in the Development and Persistence of B Lymphocyte Memory | |
P478 | volume | 44 |
Q53053529 | A Brake for B Cell Proliferation: Appropriate responses to metabolic stress are crucial to maintain B cell viability and prevent malignant outgrowth. |
Q96174215 | A Combination of Human Broadly Neutralizing Antibodies against Hepatitis B Virus HBsAg with Distinct Epitopes Suppresses Escape Mutations |
Q100755368 | A broadly neutralizing macaque monoclonal antibody against the HIV-1 V3-Glycan patch |
Q54216843 | An Unmutated IgM Response to the Vi Polysaccharide of Salmonella Typhi Contributes to Protective Immunity in a Murine Model of Typhoid. |
Q99608150 | An apoptosis-dependent checkpoint for autoimmunity in memory B and plasma cells |
Q46253139 | B Cell Intrinsic Mechanisms Constraining IgE Memory. |
Q59349637 | Basics of memory B-cell responses: lessons from and for the real world |
Q38742784 | Deconstructing the germinal center, one cell at a time. |
Q52716066 | Diversity of Immunoglobulin (Ig) Isotypes and the Role of Activation-Induced Cytidine Deaminase (AID) in Fish. |
Q46172393 | Do Memory B Cells Form Secondary Germinal Centers? Impact of Antibody Class and Quality of Memory T-Cell Help at Recall. |
Q33757966 | Early derivation of IgM memory cells and bone marrow plasmablasts. |
Q64117250 | Efficacy and association analysis of high-dose methotrexate in the treatment of children with acute lymphoblastic leukemia |
Q38960786 | Germinal Center B Cell Dynamics |
Q49852352 | Heterogeneity of memory B cells |
Q64107709 | Higher levels of B-cell mutation in the early germinal centres of an inefficient secondary antibody response to a variant influenza haemagglutinin |
Q50995525 | Host- and pathogen-derived adjuvant coatings on protein nanoparticle vaccines. |
Q38921183 | Human memory B cells |
Q47661716 | IgH isotype-specific B cell receptor expression influences B cell fate |
Q48022399 | Memory B cell heterogeneity: Remembrance of things past. |
Q58722256 | Memory B cells are reactivated in subcapsular proliferative foci of lymph nodes |
Q39313226 | Metabolic Regulation of the Immune Humoral Response |
Q89046278 | Naive B Cells with High-Avidity Germline-Encoded Antigen Receptors Produce Persistent IgM+ and Transient IgG+ Memory B Cells |
Q57155622 | New insights into the development of B cell responses: Implications for solid organ transplantation |
Q56967366 | Pathogenic citrulline-multispecific B cell receptor clades in rheumatoid arthritis |
Q92383022 | Plasma cells: You are what you eat |
Q92203848 | Programming Isotype-Specific Plasma Cell Function |
Q39077274 | RNA Exosome and Non-coding RNA-Coupled Mechanisms in AID-Mediated Genomic Alterations |
Q92650550 | Remembrance of Things Past: Long-Term B Cell Memory After Infection and Vaccination |
Q39206970 | Role of germinal centers for the induction of broadly-reactive memory B cells |
Q39369098 | Scarcity of autoreactive human blood IgA+ memory B cells |
Q50623862 | Sequencing and cloning of antigen-specific antibodies from mouse memory B cells. |
Q64094866 | Sex Differences in Older Adults' Immune Responses to Seasonal Influenza Vaccination |
Q37427351 | Somatically Hypermutated Plasmodium-Specific IgM(+) Memory B Cells Are Rapid, Plastic, Early Responders upon Malaria Rechallenge |
Q47110972 | Spoiling for a Fight: B Lymphocytes As Initiator and Effector Populations within Tertiary Lymphoid Organs in Autoimmunity and Transplantation. |
Q90468446 | T-Bet+ IgM Memory Cells Generate Multi-lineage Effector B Cells |
Q37549732 | The aryl hydrocarbon receptor controls cell-fate decisions in B cells. |
Q48312712 | The microanatomic segregation of selection by apoptosis in the germinal center |
Q41986026 | ZBTB32 Restricts the Duration of Memory B Cell Recall Responses. |
Search more.