scholarly article | Q13442814 |
P2093 | author name string | T. Yoshida | |
S. Okabe | |||
K. Ishibashi | |||
T. Miki | |||
H. Koseki | |||
M. Taniguchi | |||
N. Miyasaka | |||
S. Hirosawa | |||
S. Okada | |||
T. Fukuda | |||
T. Tokuhisa | |||
M. Hatano | |||
P2860 | cites work | BCL-6 protein is expressed in germinal-center B cells | Q24324053 |
The BTB domain, found primarily in zinc finger proteins, defines an evolutionarily conserved family that includes several developmentally regulated genes in Drosophila | Q24562764 | ||
The POZ domain: a conserved protein-protein interaction motif | Q28115868 | ||
LAZ3, a novel zinc-finger encoding gene, is disrupted by recurring chromosome 3q27 translocations in human lymphomas | Q28255448 | ||
Alterations of a zinc finger-encoding gene, BCL-6, in diffuse large-cell lymphoma | Q28256118 | ||
A putative chemokine receptor, BLR1, directs B cell migration to defined lymphoid organs and specific anatomic compartments of the spleen | Q28300225 | ||
The immune responses in CD40-deficient mice: impaired immunoglobulin class switching and germinal center formation | Q28586300 | ||
RAG-1-deficient mice have no mature B and T lymphocytes | Q28592133 | ||
Immune and inflammatory responses in TNF alpha-deficient mice: a critical requirement for TNF alpha in the formation of primary B cell follicles, follicular dendritic cell networks and germinal centers, and in the maturation of the humoral immune re | Q28594116 | ||
Germinal centers | Q29616234 | ||
Reexpression of RAG-1 and RAG-2 genes in activated mature mouse B cells | Q71854871 | ||
Rearrangements of the BCL6 gene in diffuse large cell non-Hodgkin's lymphoma | Q72327581 | ||
Mice deficient for the CD40 ligand | Q72610555 | ||
Distinct pathways of B cell differentiation. I. Residual T cells in athymic mice support the development of splenic germinal centers and B cell memory without an induction of antibody | Q72670275 | ||
AN AUTORADIOGRAPHIC STUDY OF THE GERMINAL CENTER IN SPLEEN WHITE PULP DURING EARLY INTERVALS OF THE IMMUNE RESPONSE | Q76846938 | ||
Analysis of somatic mutation in five B cell subsets of human tonsil | Q34328629 | ||
The LAZ3/BCL6 oncogene encodes a sequence-specific transcriptional inhibitor: a novel function for the BTB/POZ domain as an autonomous repressing domain. | Q34415305 | ||
In situ studies of the primary immune response to (4-hydroxy-3-nitrophenyl)acetyl. I. The architecture and dynamics of responding cell populations | Q34885732 | ||
CD40-deficient mice generated by recombination-activating gene-2-deficient blastocyst complementation. | Q35962812 | ||
The path of memory B-cell development | Q36171744 | ||
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 | Q36231790 | ||
The repertoire of somatic antibody mutants accumulating in the memory compartment after primary immunization is restricted through affinity maturation and mirrors that expressed in the secondary response | Q36354168 | ||
Antibody response to a T-dependent antigen requires B cell expression of complement receptors | Q36366376 | ||
Mutant mice without B lymphocyte follicles | Q36367422 | ||
The murine BCL6 gene is induced in activated lymphocytes as an immediate early gene. | Q36669935 | ||
Gene involved in the 3q27 translocation associated with B-cell lymphoma, BCL5, encodes a Krüppel-like zinc-finger protein | Q36759209 | ||
BCL-6, a POZ/zinc-finger protein, is a sequence-specific transcriptional repressor | Q37477121 | ||
Chromosomal translocations cause deregulated BCL6 expression by promoter substitution in B cell lymphoma. | Q37626496 | ||
BCL6 encodes a sequence‐specific DNA‐binding Protein | Q38293781 | ||
Recognition DNA sequence of a novel putative transcription factor, BCL6. | Q38303448 | ||
Transcriptional repression by the proto-oncogene BCL-6. | Q38356856 | ||
Mechanism and regulation of immunoglobulin isotype switching. | Q40850235 | ||
In situ studies of the germinal center reaction | Q40973828 | ||
Sequential triggering of apoptosis, somatic mutation and isotype switch during germinal center development. | Q41062386 | ||
Among naive precursor cell subpopulations only progenitors of memory B cells originate germinal centers | Q41092267 | ||
Intraclonal generation of antibody mutants in germinal centres | Q41172275 | ||
Molecular cloning of the breakpoint for 3q27 translocation in B-cell lymphomas and leukemias. | Q41497101 | ||
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 | Q41888015 | ||
The BCL6 gene is predominantly expressed in keratinocytes at their terminal differentiation stage | Q42526807 | ||
CD40 and B cell antigen receptor dual triggering of resting B lymphocytes turns on a partial germinal center phenotype | Q42706157 | ||
Establishment of mouse cell lines which constitutively secrete large quantities of interleukin 2, 3, 4 or 5, using modified cDNA expression vectors | Q42805800 | ||
Germinal centers develop oligoclonally | Q43487651 | ||
Sites of specific B cell activation in primary and secondary responses to T cell-dependent and T cell-independent antigens | Q43603650 | ||
IgG response is impaired in H2-c-fos transgenic mice | Q45343424 | ||
Primary antibody-forming cells and secondary B cells are generated from separate precursor cell subpopulations. | Q45980652 | ||
Antigen-induced B-cell death and elimination during germinal-centre immune responses | Q46147419 | ||
BCL-6 expression during B-cell activation | Q48063185 | ||
Locus-specific somatic hypermutation in germinal centre T cells | Q48077130 | ||
Maturation of the immune response in germinal centers | Q48194763 | ||
CD28 is required for germinal center formation. | Q52047631 | ||
Soluble antigen can cause enhanced apoptosis of germinal-centre B cells. | Q52053087 | ||
Generation of memory B cells and plasma cells in vitro. | Q52053106 | ||
Is rapid proliferation in B centroblasts linked to somatic mutation in memory B cell clones? | Q52122457 | ||
LAZ3 rearrangements in non-Hodgkin's lymphoma: correlation with histology, immunophenotype, karyotype, and clinical outcome in 217 patients. | Q52514761 | ||
Disruption of the Cr2 locus results in a reduction in B-1a cells and in an impaired B cell response to T-dependent antigen. | Q52519424 | ||
Cellular interaction in germinal centers. Roles of CD40 ligand and B7-2 in established germinal centers. | Q54167674 | ||
BCL-6 gene product, a 92- to 98-kD nuclear phosphoprotein, is highly expressed in germinal center B cells and their neoplastic counterparts. | Q55065145 | ||
CD40 ligand-transduced co-stimulation of T cells in the development of helper function | Q58882277 | ||
Alternative pathways for the selection of antigen-specific peripheral T cells | Q60089786 | ||
Role of lymphotoxin and the type I TNF receptor in the formation of germinal centers | Q71095987 | ||
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | B cell leukemia/lymphoma 6 | Q21428928 |
P304 | page(s) | 439–448 | |
P577 | publication date | 1997-08-04 | |
P1433 | published in | Journal of Experimental Medicine | Q3186912 |
P1476 | title | Disruption of the Bcl6 gene results in an impaired germinal center formation | |
P478 | volume | 186 |
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Q42824972 | A new functional domain of Bcl6 family that recruits histone deacetylases |
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Q28279743 | Aggressive lymphomas |
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Q38334286 | Alternate pathways for Bcl6-mediated regulation of B cell to plasma cell differentiation |
Q35055621 | Ambivalent role of BCL6 in cell survival and transformation |
Q35088890 | An incoherent regulatory network architecture that orchestrates B cell diversification in response to antigen signaling. |
Q35887152 | Antigen-specific antibody responses in B-1a and their relationship to natural immunity |
Q35209481 | Are follicular dendritic cells really good for nothing? |
Q35102310 | B cell priming for extrafollicular antibody responses requires Bcl-6 expression by T cells |
Q61449528 | B-Cell Lymphoma 6 (BCL6) Is a Host Restriction Factor That Can Suppress HBV Gene Expression and Modulate Immune Responses |
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Q24522565 | BAZF, a novel Bcl6 homolog, functions as a transcriptional repressor |
Q33917162 | BCL-6 in the pathogenesis of non-Hodgkin's lymphoma |
Q40639572 | BCL-6 is expressed in breast cancer and prevents mammary epithelial differentiation |
Q36322298 | BCL-6 mutations in normal germinal center B cells: evidence of somatic hypermutation acting outside Ig loci |
Q74268408 | BCL-6 regulates chemokine gene transcription in macrophages |
Q55034216 | BCL-6 represses genes that function in lymphocyte differentiation, inflammation, and cell cycle control. |
Q91689214 | BCL6 Evolved to Enable Stress Tolerance in Vertebrates and Is Broadly Required by Cancer Cells to Adapt to Stress |
Q47269833 | BCL6 as a therapeutic target for lymphoma |
Q37352854 | BCL6 cooperates with CD40 stimulation and loss of p53 function to rapidly transform primary B cells |
Q54774359 | BCL6 gene translocation in follicular lymphoma: a harbinger of eventual transformation to diffuse aggressive lymphoma |
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Q38196695 | BTB-ZF transcription factors, a growing family of regulators of early and late B-cell development |
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Q28592364 | Bcl6 controls granzyme B expression in effector CD8+ T cells |
Q28216493 | Blimp-1 orchestrates plasma cell differentiation by extinguishing the mature B cell gene expression program |
Q39153232 | Circulating CXCR5+CD4+ T cells assist in the survival and growth of primary diffuse large B cell lymphoma cells through interleukin 10 pathway |
Q36943399 | Common mechanisms for the regulation of B cell differentiation and transformation by the transcriptional repressor protein BCL-6. |
Q37003485 | Constitutive CD40L expression on B cells prematurely terminates germinal center response and leads to augmented plasma cell production in T cell areas |
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Q37338162 | Critical roles of mTOR Complex 1 and 2 for T follicular helper cell differentiation and germinal center responses. |
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Q90522892 | Cutting Edge: T Cell-Dependent Plasmablasts Form in the Absence of Single Differentiated CD4+ T Cell Subsets |
Q38781630 | Cytogenetic alterations affecting BCL6 are predominantly found in follicular lymphomas grade 3B with a diffuse large B-cell component |
Q47933757 | Cytokine regulation of secondary lymphoid organ development. |
Q37589643 | Cytokine-Mediated Regulation of Plasma Cell Generation: IL-21 Takes Center Stage. |
Q33706071 | Deficiency of the transcriptional repressor B cell lymphoma 6 (Bcl6) is accompanied by dysregulated lipid metabolism |
Q52861941 | Determining the Origin of Human Germinal Center B Cell-Derived Malignancies. |
Q37831694 | Development of PLZF-expressing innate T cells |
Q41889503 | Development of chronic allergic responses by dampening Bcl6-mediated suppressor activity in memory T helper 2 cells |
Q28585295 | Differential gene expression between sensory neocortical areas: potential roles for Ten_m3 and Bcl6 in patterning visual and somatosensory pathways |
Q37117559 | Distinct regulation of effector and memory T-cell differentiation. |
Q27860529 | Distinct types of diffuse large B-cell lymphoma identified by gene expression profiling |
Q46918689 | Diversity among memory B cells: origin, consequences, and utility. |
Q36949937 | Dynamic changes in Id3 and E-protein activity orchestrate germinal center and plasma cell development. |
Q35198527 | Dynamic expression of BCL6 in murine conventional dendritic cells during in vivo development and activation |
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Q36646675 | Enhanced susceptibility to Citrobacter rodentium infection in microRNA-155-deficient mice |
Q33741881 | Epitope Density Influences CD8+ Memory T Cell Differentiation |
Q41827741 | Evolution of two prototypic T cell lineages. |
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Q47933820 | Germinal centers: form and function. |
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