Autophagy in Parkinson's disease
Impaired protein homeostasis and accumulation of damaged or abnormally modified protein
are common disease mechanisms in many neurodegenerative disorders, including …
are common disease mechanisms in many neurodegenerative disorders, including …
Genetics in Parkinson disease: Mendelian versus non‐Mendelian inheritance
DG Hernandez, X Reed… - Journal of …, 2016 - Wiley Online Library
Parkinson's disease is a common, progressive neurodegenerative disorder, affecting 3% of
those older than 75 years of age. Clinically, Parkinson's disease (PD) is associated with …
those older than 75 years of age. Clinically, Parkinson's disease (PD) is associated with …
Synaptic, mitochondrial, and lysosomal dysfunction in Parkinson's disease
The discovery of genetic forms of Parkinson's disease (PD) has highlighted the importance
of the autophagy/lysosomal and mitochondrial/oxidative stress pathways in disease …
of the autophagy/lysosomal and mitochondrial/oxidative stress pathways in disease …
Mutation in VPS35 associated with Parkinson's disease impairs WASH complex association and inhibits autophagy
E Zavodszky, MNJ Seaman, K Moreau… - Nature …, 2014 - nature.com
Endosomal protein sorting controls the localization of many physiologically important
proteins and is linked to several neurodegenerative diseases. VPS35 is a component of the …
proteins and is linked to several neurodegenerative diseases. VPS35 is a component of the …
Parkinson's disease–associated mutant VPS35 causes mitochondrial dysfunction by recycling DLP1 complexes
Mitochondrial dysfunction represents a critical step during the pathogenesis of Parkinson's
disease (PD), and increasing evidence suggests abnormal mitochondrial dynamics and …
disease (PD), and increasing evidence suggests abnormal mitochondrial dynamics and …
A molecular mechanism to regulate lysosome motility for lysosome positioning and tubulation
To mediate the degradation of biomacromolecules, lysosomes must traffic towards cargo-
carrying vesicles for subsequent membrane fusion or fission. Mutations of the lysosomal …
carrying vesicles for subsequent membrane fusion or fission. Mutations of the lysosomal …
GPCR signaling and trafficking: the long and short of it
NJ Pavlos, PA Friedman - Trends in Endocrinology & Metabolism, 2017 - cell.com
Emerging findings disclose unexpected components of G protein-coupled receptor (GPCR)
signaling and cell biology. Select GPCRs exhibit classical signaling, that is restricted to cell …
signaling and cell biology. Select GPCRs exhibit classical signaling, that is restricted to cell …
Progress in unraveling the genetic etiology of Parkinson disease in a genomic era
A Verstraeten, J Theuns, C Van Broeckhoven - Trends in Genetics, 2015 - cell.com
Parkinson disease (PD) and Parkinson-plus syndromes are genetically heterogeneous
neurological diseases. Initial studies into the genetic causes of PD relied on classical …
neurological diseases. Initial studies into the genetic causes of PD relied on classical …
VPS35 in dopamine neurons is required for endosome-to-Golgi retrieval of Lamp2a, a receptor of chaperone-mediated autophagy that is critical for α-synuclein …
Vacuolar protein sorting-35 (VPS35) is essential for endosome-to-Golgi retrieval of
membrane proteins. Mutations in the VPS35 gene have been identified in patients with …
membrane proteins. Mutations in the VPS35 gene have been identified in patients with …
Cellular functions of WASP family proteins at a glance
O Alekhina, E Burstein… - Journal of cell …, 2017 - journals.biologists.com
ABSTRACT Proteins of the Wiskott–Aldrich syndrome protein (WASP) family function as
nucleation-promoting factors for the ubiquitously expressed Arp2/3 complex, which drives …
nucleation-promoting factors for the ubiquitously expressed Arp2/3 complex, which drives …