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Titlebook: B Cell Receptor Signaling; Tomohiro Kurosaki,Jürgen Wienands Book 2016 Springer International Publishing Switzerland 2016 B cell developme

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41#
發(fā)表于 2025-3-28 16:01:16 | 只看該作者
Robert J. McGovern,Wade H. Elmeranding the molecular mechanism of receptor-mediated activation of the IKK complex, focusing on the roles of the ubiquitin system. In the last section, we describe oncogenic mutations that induce NF-κB activation in B-cell lymphoma.
42#
發(fā)表于 2025-3-28 19:19:54 | 只看該作者
43#
發(fā)表于 2025-3-29 00:44:22 | 只看該作者
Assembly and Function of the Precursor B-Cell Receptor,ation. Nonetheless, the pre-BCR downstream signaling cascade is largely similar to that of the BCR suggesting that the characteristic LC of the pre-BCR mediates important receptor interactions thereby providing distinctive, germ line-encoded features to the pre-BCR. In fact, the SLC enables the pre-
44#
發(fā)表于 2025-3-29 05:56:27 | 只看該作者
The Memory Function of the B Cell Antigen Receptor,al principles of B cell memory were enigmatic for decades. Only recently, we have begun to understand the underlying mechanisms. This review summarizes our current understanding of how different subpopulations of MBCs are generated during primary immune responses and how their functional heterogenei
45#
發(fā)表于 2025-3-29 10:48:51 | 只看該作者
PI3K Signaling in Normal B Cells and Chronic Lymphocytic Leukemia (CLL),toire, but also support the growth and survival of neoplastic B cells, focusing on chronic lymphocytic leukemia (CLL) B cells. Perhaps because of the central role played by PI3K in BCR signaling, B cell leukemia and lymphomas are the first diseases for which a PI3K inhibitor has been approved for cl
46#
發(fā)表于 2025-3-29 14:16:48 | 只看該作者
47#
發(fā)表于 2025-3-29 15:40:41 | 只看該作者
48#
發(fā)表于 2025-3-29 23:21:44 | 只看該作者
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