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Molecular mechanisms in B cell antigen receptor signaling
Abstract
Recent gene-targeting experiments have highlighted the importance of the intracellular protein tyrosine kinases Lyn, Syk, and Btk in BCR signal transduction and B cell development. In addition, the interactions of these kinases and their regulatory mechanisms have been reported. Activation loop phosphorylation of these kinases is critical for their participation in signal propagation. Several substrates have been identified for these kinases and this has led to elucidation of the mechanisms by which these kinases mediate the downstream signaling events that lead to cellular responses of B cells.
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“BCR engagement rapidly induces an array of signal cascades, particularly the activity of three nonreceptor protein-tyrosine kinase families including members of Src (Lyn, Fyn, and Blk), ZAP-70 (Syk), and Tec (Btk) (6-9”
From AKT Induces Transcriptional Activity of PU.1 through Phosphorylation-mediated Modifications within Its Transactivation Domain (2001) · cites this paper as [7]
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Metadata
- Authors
- Kurosaki, T.
- Venue
- Current Opinion in Immunology
- Publisher
- Elsevier BV
- Published
- 1997-06
- Volume
- 9
- Issue
- 3
- Pages
- 309-318
- ISSN
- 0952-7915
- Cited by
- 150
- References
- 0
- Language
- en
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