Lysosomal dysfunction in Parkinson disease: ATP13A2 gets into the groove
about
Deconvoluting the complexity of autophagy and Parkinson's disease for potential therapeutic purposeCellular function and pathological role of ATP13A2 and related P-type transport ATPases in Parkinson's disease and other neurological disordersA lipid switch unlocks Parkinson's disease-associated ATP13A2ATP13A2 (PARK9) protein levels are reduced in brain tissue of cases with Lewy bodiesAcceleration of α-synuclein aggregation by exosomes.Identification of Cerebral Metal Ion Imbalance in the Brain of Aging Octodon degus.Efficient GSH delivery using PAMAM-GSH into MPP-induced PC12 cellular model for Parkinson's disease.Lysosomal impairment in Parkinson's disease.Excess iron harms the brain: the syndromes of neurodegeneration with brain iron accumulation (NBIA).The hallmarks of Parkinson's disease.Aberrant autophagy and parkinsonism: does correction rescue from disease progression?Defective autophagy in Parkinson's disease: lessons from genetics.Peripheral neuropathy and parkinsonism: a large clinical and pathogenic spectrum.Impaired endo-lysosomal membrane integrity accelerates the seeding progression of α-synuclein aggregates.Thioredoxin-interacting protein induced α-synuclein accumulation via inhibition of autophagic flux: Implications for Parkinson's disease.Endocytic membrane trafficking and neurodegenerative disease.Disorders of lysosomal acidification-The emerging role of v-ATPase in aging and neurodegenerative disease.The roles of non-coding RNAs in Parkinson's disease.Systematic Genetic Analysis of the SMPD1 Gene in Chinese Patients with Parkinson's Disease.Selective imaging of internalized proteopathic α-synuclein seeds in primary neurons reveals mechanistic insight into transmission of synucleinopathies.Lysosomal Proteolysis Is Associated With Exercise-Induced Improvement of Mitochondrial Quality Control in Aged Hippocampus.-NMDA R/+VDR pharmacological phenotype as a novel therapeutic target in relieving motor-cognitive impairments in Parkinsonism.Epigenome-wide association study for Parkinson's disease.
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P2860
Lysosomal dysfunction in Parkinson disease: ATP13A2 gets into the groove
description
2012 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2012
@ast
im September 2012 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2012/09/01)
@sk
vědecký článek publikovaný v roce 2012
@cs
wetenschappelijk artikel (gepubliceerd op 2012/09/01)
@nl
наукова стаття, опублікована у вересні 2012
@uk
مقالة علمية (نشرت في سبتمبر 2012)
@ar
name
Lysosomal dysfunction in Parkinson disease: ATP13A2 gets into the groove
@ast
Lysosomal dysfunction in Parkinson disease: ATP13A2 gets into the groove
@en
Lysosomal dysfunction in Parkinson disease: ATP13A2 gets into the groove
@nl
type
label
Lysosomal dysfunction in Parkinson disease: ATP13A2 gets into the groove
@ast
Lysosomal dysfunction in Parkinson disease: ATP13A2 gets into the groove
@en
Lysosomal dysfunction in Parkinson disease: ATP13A2 gets into the groove
@nl
prefLabel
Lysosomal dysfunction in Parkinson disease: ATP13A2 gets into the groove
@ast
Lysosomal dysfunction in Parkinson disease: ATP13A2 gets into the groove
@en
Lysosomal dysfunction in Parkinson disease: ATP13A2 gets into the groove
@nl
P50
P921
P3181
P356
P1433
P1476
Lysosomal dysfunction in Parkinson disease: ATP13A2 gets into the groove
@en
P2093
Benjamin Dehay
Celine Perier
P304
P3181
P356
10.4161/AUTO.21011
P577
2012-09-01T00:00:00Z