Downregulation of FOXP1 is required during germinal center B-cell function.
about
FOXP1 directly represses transcription of proapoptotic genes and cooperates with NF-κB to promote survival of human B cellsHomeobox NKX2-3 promotes marginal-zone lymphomagenesis by activating B-cell receptor signalling and shaping lymphocyte dynamics.miR-150 influences B-cell receptor signaling in chronic lymphocytic leukemia by regulating expression of GAB1 and FOXP1Biomarkers of HIV-associated Cancer.The significance of FOXP1 in diffuse large B-cell lymphoma.FOXP1 potentiates Wnt/β-catenin signaling in diffuse large B cell lymphoma.Uncovering MicroRNA Regulatory Hubs that Modulate Plasma Cell DifferentiationSubtype-specific addiction of the activated B-cell subset of diffuse large B-cell lymphoma to FOXP1.FOXP1 suppresses immune response signatures and MHC class II expression in activated B-cell-like diffuse large B-cell lymphomas.N-terminally truncated FOXP1 protein expression and alternate internal FOXP1 promoter usage in normal and malignant B cells.Non-IG aberrations of FOXP1 in B-cell malignancies lead to an aberrant expression of N-truncated isoforms of FOXP1.FOXP2-positive diffuse large B-cell lymphomas exhibit a poor response to R-CHOP therapy and distinct biological signatures.Primary mediastinal large B-cell lymphoma: transcriptional regulation by miR-92a through FOXP1 targeting.Systems biology of primary CNS lymphoma: from genetic aberrations to modeling in mice.Chronic lymphocytic leukaemia: could immunological tolerance mechanisms be the origin of lymphoid neoplasms?FOXP1 is a regulator of quiescence in healthy human CD4+ T cells and is constitutively repressed in T cells from patients with lymphoproliferative disorders.The forkhead transcription factor FOXP1 represses human plasma cell differentiationDeregulated FOX genes in Hodgkin lymphoma.Evolving DNA methylation and gene expression markers of B-cell chronic lymphocytic leukemia are present in pre-diagnostic blood samples more than 10 years prior to diagnosis.The transcription factor Foxo1 controls germinal center B cell proliferation in response to T cell helpReciprocal expression of the endocytic protein HIP1R and its repressor FOXP1 predicts outcome in R-CHOP-treated diffuse large B-cell lymphoma patients.Targeting the anion exchanger 2 with specific peptides as a new therapeutic approach in B lymphoid neoplasms.Foxp1 controls mature B cell survival and the development of follicular and B-1 B cells.The transcription factor Foxp1 preserves integrity of an active Foxp3 locus in extrathymic Treg cells
P2860
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P2860
Downregulation of FOXP1 is required during germinal center B-cell function.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
@zh
2013年论文
@zh-cn
name
Downregulation of FOXP1 is required during germinal center B-cell function.
@en
Downregulation of FOXP1 is required during germinal center B-cell function.
@nl
type
label
Downregulation of FOXP1 is required during germinal center B-cell function.
@en
Downregulation of FOXP1 is required during germinal center B-cell function.
@nl
prefLabel
Downregulation of FOXP1 is required during germinal center B-cell function.
@en
Downregulation of FOXP1 is required during germinal center B-cell function.
@nl
P2093
P2860
P50
P1433
P1476
Downregulation of FOXP1 is required during germinal center B-cell function
@en
P2093
Ainara Sagardoy
Ari Melnick
Eloy F Robles
Jose I Martinez-Ferrandis
Karen L Bunting
Linde De Smedt
María Angela Aznar
Olivier Elemento
Rita Shaknovich
Vicente Fresquet
P2860
P304
P356
10.1182/BLOOD-2012-10-462846
P407
P577
2013-04-11T00:00:00Z