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Functional dissection of BCR signaling pathways
Abstract
Signal transduction by the BCR is critical for progression through developmental checkpoints as well as for immune responses. Recent results obtained in mice deficient either in an adaptor molecule, BLNK (alternatively named SLP-65 or BASH), or in phosphatidylinositol 3-kinase have revealed similar - though not identical - phenotypes to those of Btk(-/-) mice, suggesting a functional link between BLNK, Btk and phosphatidylinositol 3-kinase.
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BCR engagement rapidly induces signal cascades, particularly activity of Src, ZAP-70, and Tec families.
“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 [6]
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Kurosaki, T., & Tsukada, S. (2000) · Immunity · doi:10.1016/s1074-7613(00)80153-3 · Cited by 223
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Metadata
- Authors
- Kurosaki, T.
- Venue
- Current Opinion in Immunology
- Publisher
- Elsevier BV
- Published
- 2000-06
- Volume
- 12
- Issue
- 3
- Pages
- 276-281
- ISSN
- 0952-7915
- Cited by
- 103
- References
- 1
- Language
- en
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