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A single-round of antigen receptor signaling programs naÃ¯ve B cells to receive T cell help

ChEBI2010-06-08 更新2026-07-21 收录

B细胞激活

T细胞辅助信号

数据链接：

https://www.ebi.ac.uk/biostudies/ArrayExpress/studies/E-GEOD-20477 数据链接链接失效反馈

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资源简介：

A single-round of antigen receptor signaling programs naÃ¯ve B cells to receive T cell help

应用场景：

创建时间：

2010-06-08

B细胞激活

计算模型

We proposed a spatially extended model of early events of B cell receptors (BCR) activation, which is based on mutual kinase-receptor interactions that are characteristic for the immune receptors and

NIAID Data Ecosystem80

Whole genome transcription profile showing early changes in gene expression in antigen receptor activated B cells. Mus musculus

B细胞激活

转录组学

To search for rapid changes in gene expression following BCR activation, we performed DNA microarray analysis of activated splenic B cells with and without anti-IgM treatment for 1 and 2 hour. Overall

NIAID Data Ecosystem60

microRNA expression profile of activated versus non activated primary B cells. Mus musculus

B细胞激活

microRNA表达谱

microRNA expression profile in 5 indepent sets of paired samples of LPS+IL-4 activated versus non activated primary mouse spleen B cells Keywords: cell type comparison Overall design: Activated B cell

NIAID Data Ecosystem50

Combinatorial Signaling through TLR-2 and CD86 Augments Activation and Differentiation of Resting B Cells

B细胞激活

体液免疫调控

B cells are an integral component in mounting humoral immune responses and they are also crucial in programming T cell mediated immunity. Usually, B cell activation is initiated by recognition of anti

NIAID Data Ecosystem60

Gene expression in Ramos human B cell line induced by treatment with anti-FCRL1 antibody treatment

B细胞激活

抗体治疗基因表达

B cell receptor CD40 and FCRL1 are highly expressed in Ramos B cell line. Therefore, these receptors are considered to cooperate in B cell activation. In this study, we compared gene expression profil

NIAID Data Ecosystem60

A single-round of antigen receptor signaling programs naÃ¯ve B cells to receive T cell help

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