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Titlebook: Drebrin; From Structure and F Tomoaki Shirao,Yuko Sekino Book 2017 The Editor(s) (if applicable) and The Author(s), under exclusive license

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樓主: introspective
41#
發(fā)表于 2025-3-28 16:20:19 | 只看該作者
42#
發(fā)表于 2025-3-28 20:15:13 | 只看該作者
Molecular Cloning of Drebrin: Progress and Perspectives Drebrin protein, which is well conserved in various vertebrate species, although mammalian drebrin has only two isoforms, namely, drebrin E and drebrin A, is different from chicken drebrin that has three isoforms. Drebrin belongs to an actin-depolymerizing factor homology (ADF-H) domain protein fam
43#
發(fā)表于 2025-3-29 00:09:15 | 只看該作者
44#
發(fā)表于 2025-3-29 05:20:57 | 只看該作者
Localization of Drebrin: Light Microscopy Study regulated by a drebrin A-specific mechanism, is likely to affect the localization of drebrin E. In the adult brain, drebrin is mainly localized in dendritic spines, but in some nuclei, drebrin can be detected in neuronal somata as well as dendritic spines. The fact that the developmental changes in
45#
發(fā)表于 2025-3-29 10:28:36 | 只看該作者
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發(fā)表于 2025-3-29 13:58:52 | 只看該作者
47#
發(fā)表于 2025-3-29 15:41:59 | 只看該作者
48#
發(fā)表于 2025-3-29 22:02:54 | 只看該作者
Drebrin in Alzheimer’s Diseasepresynaptic change in AD brains. In addition, dysregulation of glutamate receptor trafficking and the p21-activated kinase/LIM kinase pathway has been observed in AD brains. It is now believed that soluble Aβ oligomers, namely, Aβ-derived diffusible ligands (ADDLs), but not insoluble Aβ aggregation
49#
發(fā)表于 2025-3-30 00:39:40 | 只看該作者
Drebrins and Connexins: A Biomedical Perspectivethology involved in neurodegeneration, Alzheimer’s disease (AD), other cognitive disorders, and aging..Bidirectional connexin channels are permeable to Ca. ions, IP3, ATP, and cAMP. Connexin hemichannels are important for paracrine regulation and can release and exchange energy with other cells usin
50#
發(fā)表于 2025-3-30 05:25:41 | 只看該作者
Homer, Spikar, and Other Drebrin-Binding Proteins in the Brain morphogenesis by cooperating with shank and activated Cdc42 small GTPase, suggesting a novel signaling pathway comprising Homer, drebrin, shank, and Cdc42 for spine morphogenesis. Drebrin sequesters spikar in the cytoplasm and stabilizes it in dendritic spines, leading to spine formation. Finally,
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