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Peripheral B cell subsets

delete2008-04-01
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D
David Allman *
S
Shiv Pillai
DOI:10.1016/j.coi.2008.03.014delete
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Abstract

Abstract

En 中文
Our understanding of the origins and the biological functions of different peripheral B cell subsets continues to evolve. Some understanding has been obtained regarding the synergy between BCR-derived signals and other receptors and signaling pathways that drive the development of follicular, marginal zone, and B-1 B cells, but this remains a complex and poorly understood issue. More recent information regarding the origins of B-1 and B-2 B cells, the ability of follicular B cells to mature both in the bone marrow and the spleen, the existence of a definable precursor for MZ B cells, and the ability of follicular B cells to occupy two distinct niches are all highlighted in this review.
Keywords:
TOLL-LIKE RECEPTORS
MARGINAL-ZONE
BONE-MARROW
INDEPENDENT RESPONSES
POSITIVE SELECTION
SURVIVAL SIGNALS
DENDRITIC CELLS
T-CELLS
LYMPHOCYTES
SPLEEN
AI Summary

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Key information extracted from the uploaded paper, including a brief overview, abstract, background, key highlights, visual analysis, and future outlook.

Journal

Current Opinion in Immunology cover
Current Opinion in Immunology
IF:
5.8
Papers:
3.4K
Citations:
9.5K

Organization

H
Harvard University
Scholars:
26.5W
Papers: 22.0W
Citations: 28.7W
U
university of pennsylvania
Scholars:
9.2W
Papers: 7.8W
Citations: 153
Cited Papers

Cited Papers

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The recirculating B cell pool contains two functionally distinct, long-lived, posttransitional, follicular B cell Populations
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errKretschmer, K; Stopkowicz, J; Scheffer, S; Greten, TF; Weiss, S
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Notch2 is preferentially expressed in mature B cells and indispensable for marginal zone B lineage development
errIMMUNITY
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err2003-05-01
err548
errOAAI
errSaito, T; Chiba, S; Ichikawa, M; Kunisato, A; Asai, T; Shimizu, K; Yamaguchi, T; Yamamoto, G; Seo, S; Kumano, K; Nakagami-Yamaguchi, E; Hamada, Y; Aizawa, S; Hirai, H
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