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Titlebook: Leucine-Rich Repeat Kinase 2 (LRRK2); Hardy J. Rideout Book 2017 Springer International Publishing AG 2017 GTPase.Parkinson‘s Disease.kina

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發(fā)表于 2025-3-21 18:49:49 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱Leucine-Rich Repeat Kinase 2 (LRRK2)
編輯Hardy J. Rideout
視頻videohttp://file.papertrans.cn/586/585293/585293.mp4
概述Thorough overview of the current state of knowledge on LRRK2.Discussed the links between LRRK2 mutations and Parkinson‘s Disease.Explores what we know about the normal function of LRRK2.Includes suppl
叢書名稱Advances in Neurobiology
圖書封面Titlebook: Leucine-Rich Repeat Kinase 2 (LRRK2);  Hardy J. Rideout Book 2017 Springer International Publishing AG 2017 GTPase.Parkinson‘s Disease.kina
描述This is the first book to assemble the leading researchers in the field of LRRK2 biology and neurology and provide a snapshot of the current state of knowledge, encompassing all major aspects of its function and dysfunction. The?contributors are experts in cell biology and physiology, neurobiology, and medicinal chemistry, bringing a multidisciplinary perspective on the gene and its role in disease. The book?covers the identification of?LRRK2?as a major contributor to the pathogenesis of Parkinson‘s Disease. It also discusses the current state of the field after a decade of research, putative normal physiological roles of LRRK2, and the various pathways that have been identified in the search for the mechanism(s) of its induction of neurodegeneration.
出版日期Book 2017
關(guān)鍵詞GTPase; Parkinson‘s Disease; kinase; neurodegeneration; signaling
版次1
doihttps://doi.org/10.1007/978-3-319-49969-7
isbn_softcover978-3-319-84287-5
isbn_ebook978-3-319-49969-7Series ISSN 2190-5215 Series E-ISSN 2190-5223
issn_series 2190-5215
copyrightSpringer International Publishing AG 2017
The information of publication is updating

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沙發(fā)
發(fā)表于 2025-3-21 21:23:13 | 只看該作者
978-3-319-84287-5Springer International Publishing AG 2017
板凳
發(fā)表于 2025-3-22 02:38:09 | 只看該作者
Leucine-Rich Repeat Kinase 2 (LRRK2)978-3-319-49969-7Series ISSN 2190-5215 Series E-ISSN 2190-5223
地板
發(fā)表于 2025-3-22 05:37:06 | 只看該作者
Hardy J. RideoutThorough overview of the current state of knowledge on LRRK2.Discussed the links between LRRK2 mutations and Parkinson‘s Disease.Explores what we know about the normal function of LRRK2.Includes suppl
5#
發(fā)表于 2025-3-22 12:39:50 | 只看該作者
Advances in Neurobiologyhttp://image.papertrans.cn/l/image/585293.jpg
6#
發(fā)表于 2025-3-22 16:13:48 | 只看該作者
7#
發(fā)表于 2025-3-22 19:55:31 | 只看該作者
Clinical Features of , Carriers with Parkinson’s Diseaseciated with PD, the most common of which is the Gly2019Ser mutation. In the following review, we summarize the demographics and motor and non-motor symptoms of . carriers with PD, as well as symptoms in non-manifesting carriers. The clinical features of .-associated PD are often indistinguishable fr
8#
發(fā)表于 2025-3-22 23:07:26 | 只看該作者
LRRK2 Phosphorylationnson’s disease. LRRK2 is a large multi-domain protein with a functional GTPase and kinase domain. The signal transduction pathways in which LRRK2 is dysfunctional in the disease state are only now being resolved, but we do know that LRRK2 is, itself, a substrate of multiple kinases and phosphatases
9#
發(fā)表于 2025-3-23 03:10:31 | 只看該作者
Understanding the GTPase Activity of LRRK2: Regulation, Function, and Neurotoxicityto the ROCO superfamily of proteins, characterized by a Ras-of-complex (Roc) GTPase domain in tandem with a C-terminal-of-Roc (COR) domain. LRRK2 also contains a protein kinase domain adjacent to the Roc-COR tandem domain in addition to multiple repeat domains. Disease-causing familial mutations clu
10#
發(fā)表于 2025-3-23 08:54:52 | 只看該作者
LRRK2 and Autophagyd as autophagy. In this chapter, the evidence linking LRRK2 to autophagy will be examined, along with how regulation of autophagy and lysosomal pathways may provide a nexus between the physiological function of this protein and the different diseases with which it has been associated. Data from cell
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