Abstract
By the early 1990’s it had become abundantly clear that protein tyrosine kinases (PTK) were critical elements in growth and regulation of virtually all cell types. Impressed by the emerging importance of PTK in lymphocyte activation, it seemed likely that there might be a panoply of lymphoid-specific PTK that presumably would have critical functions in regulating immune responses. We thought it would be a good idea to try to get our hands on some of our own lymphoid-expressed kinases to study. Andrew Wilks’ PCR-based strategy for identifying novel PTK’s looked like an outstanding approach; Wilks, of course, had identified Jak1 and Jak2 using this method (1–4). At this point however, this was not what made an impression on us — who knew what these Jaks were anyway. The importance to us was that this was a rapid way of getting some kinases in hand.
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Candotti, F., Notarangelo, L., Johnston, J.A., McVicar, D., O’Shea, J.J. (2003). Jak3 and the Pathogenesis of Severe Combined Immunodeficiency. In: Sehgal, P.B., Levy, D.E., Hirano, T. (eds) Signal Transducers and Activators of Transcription (STATs). Springer, Dordrecht. https://doi.org/10.1007/978-94-017-3000-6_39
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