Abstract
B lymphopoiesis is regulated by multiple signals from stromal cell contact, soluble cytokines, antigen, and T helper cells. In vitro and biochemical experiments have implicated tyrosine kinases as key components of many of these signaling pathways. Genetic analysis of the role of these tyrosine kinases has been facilitated by recent advances in transgenic and gene targeting technology as well as by the identification of the genetic basis of several human and murine immune deficiencies. This review discusses the effect of gain and loss of function mutations of selected tyrosine kinases and their regulators and substrates on B cell development and function.
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Dates
Type | When |
---|---|
Created | 23 years, 1 month ago (July 27, 2002, 7:43 a.m.) |
Deposited | 2 years, 4 months ago (April 23, 2023, 2:44 p.m.) |
Indexed | 5 months ago (March 30, 2025, 2:02 p.m.) |
Issued | 29 years, 4 months ago (April 1, 1996) |
Published | 29 years, 4 months ago (April 1, 1996) |
Published Print | 29 years, 4 months ago (April 1, 1996) |
@article{Satterthwaite_1996, title={Genetic Analysis of Tyrosine Kinase Function in B Cell Development}, volume={14}, ISSN={1545-3278}, url={http://dx.doi.org/10.1146/annurev.immunol.14.1.131}, DOI={10.1146/annurev.immunol.14.1.131}, number={1}, journal={Annual Review of Immunology}, publisher={Annual Reviews}, author={Satterthwaite, Anne and Witte, Owen}, year={1996}, month=apr, pages={131–154} }