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Titlebook: Endocytosis and Signaling; Christophe Lamaze,Ian Prior Book 2018 Springer International Publishing AG, part of Springer Nature 2018 cell s

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發(fā)表于 2025-3-25 06:09:40 | 只看該作者
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發(fā)表于 2025-3-25 11:32:49 | 只看該作者
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發(fā)表于 2025-3-25 13:46:27 | 只看該作者
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發(fā)表于 2025-3-25 18:32:02 | 只看該作者
Fusion: Helium-3 Power Economics,s at the plasma membrane and the nuclear envelop. In this chapter, we briefly discuss membrane protein ubiquitination, endocytosis, and summarize current knowledge on the ESCRT machinery in the MVB pathway.
25#
發(fā)表于 2025-3-25 22:36:49 | 只看該作者
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發(fā)表于 2025-3-26 00:32:54 | 只看該作者
https://doi.org/10.1007/978-1-349-10538-0 compartment can provide a mechanism to both specify, and yet also diversify, GPCR signal transduction. These new evolving models could aid mechanistic understanding of complex disease and provide novel therapeutic avenues.
27#
發(fā)表于 2025-3-26 04:53:07 | 只看該作者
Returning to Primordially Creative Thinking and specification which play a central role in development and physiology. In this chapter, we cover a number of significant works on endosomal trafficking evincing the importance of endocytosis in Notch-mediated cell fate specification during development.
28#
發(fā)表于 2025-3-26 09:39:27 | 只看該作者
ESCRT and Membrane Protein Ubiquitination,s at the plasma membrane and the nuclear envelop. In this chapter, we briefly discuss membrane protein ubiquitination, endocytosis, and summarize current knowledge on the ESCRT machinery in the MVB pathway.
29#
發(fā)表于 2025-3-26 14:25:15 | 只看該作者
EGFR Trafficking in Physiology and Cancer,regions of the cell surface. We also highlight how communication between organelles controls EGFR activity along the endocytic route. Finally, we illustrate how abnormal trafficking of EGFR oncogenic mutants, as well as alterations of the endocytic machinery, contributes to aberrant EGFR signaling in cancer.
30#
發(fā)表于 2025-3-26 19:31:09 | 只看該作者
Evolving View of Membrane Trafficking and Signaling Systems for G Protein-Coupled Receptors, compartment can provide a mechanism to both specify, and yet also diversify, GPCR signal transduction. These new evolving models could aid mechanistic understanding of complex disease and provide novel therapeutic avenues.
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