ExLibris header image
SFX Logo
Title: ATP13A2/PARK9 regulates endo-/lysosomal cargo sorting and proteostasis through a novel PI(3, 5)P2-mediated scaffolding function
Source:

Human Molecular Genetics [0964-6906] Demirsoy, S yr:2017


Collapse list of basic services Basic
Sorry, no full text available...
Please use the document delivery service (see below)  
Holding information
Holdings in library search engine ALBERT GO
Document delivery
Request document via Library/Bibliothek GO
Users interested in this article also expressed an interest in the following:
1. Schneider, Susanne A. "Mouse models of kufor-rakeb disease link Parkinson's disease closer to neuronal ceroid lipofuscinosis, suggesting lysosomal dysfunction as shared mechanism." Movement disorders 32.2 (2017): 209-209. Link to Full Text for this item Link to SFX for this item
2. Park, J. "The role of ATP13A2 in Parkinson's disease: Clinical phenotypes and molecular mechanisms." Movement disorders 30.6 (2015): 770-9. Link to Full Text for this item Link to SFX for this item
3. Estrada Cuzcano, A. "Loss-of-function mutations in the ATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78)." Brain 140.Pt 2 (2017): 287-305. Link to SFX for this item
4. "Synuclein impairs trafficking and signaling of BDNF in a mouse model of Parkinson's disease." Scientific reports. 7.1: 3868-. Link to SFX for this item
5. Kang, L. "Dihydrotestosterone treatment delays the conversion from mild cognitive impairment to Alzheimer's disease in SAMP8 mice." Hormones and behavior 65.5 (2014): 505-15. Link to SFX for this item
6. Jankovic, J. "The Future of Research in Parkinson Disease." JAMA neurology 71.11 (2014): 1351-1352. Link to SFX for this item
7. Bras, J. "Mutation of the Parkinsonism Gene ATP13A2 Causes Neuronal Ceroid-Lipofuscinosis." Human molecular genetics 21.12 (2012): 2646-2650. Link to SFX for this item
8. "-dopa response." Movement disorders 33.10: 1650-1656. Link to SFX for this item
9. Verbeek, Dineke S. "Unmet Needs in Dystonia: Genetics and Molecular Biology-How Many Dystonias?" Frontiers in neurology 7: 241-241. Link to SFX for this item
10. Wan, J. "Loss of function of SLC25A46 causes lethal congenital pontocerebellar hypoplasia." Brain (2016). Link to SFX for this item
11. Bajaj, A. "Parkinson's disease and cancer risk: a systematic review and meta-analysis." Cancer Causes & Control 21.5 (2010): 697-707. Link to Full Text for this item Link to SFX for this item
View More...
View Less...
Select All Clear All

Expand list of advanced services Advanced
A service provided by the Library of the Wissenschaftspark Albert Einstein, Potsdam, Germany.
© 2005 SFX by Ex Libris Inc.