[HTML][HTML] Microglia and astrocyte dysfunction in parkinson's disease
While glia are essential for regulating the homeostasis in the normal brain, their dysfunction
contributes to neurodegeneration in many brain diseases, including Parkinson's disease …
contributes to neurodegeneration in many brain diseases, including Parkinson's disease …
GBA Variants and Parkinson Disease: Mechanisms and Treatments
L Smith, AHV Schapira - Cells, 2022 - mdpi.com
The GBA gene encodes for the lysosomal enzyme glucocerebrosidase (GCase), which
maintains glycosphingolipid homeostasis. Approximately 5–15% of PD patients have …
maintains glycosphingolipid homeostasis. Approximately 5–15% of PD patients have …
Alpha-synuclein: Pathology, mitochondrial dysfunction and neuroinflammation in Parkinson's disease
Parkinson's disease (PD) is a complex, chronic and progressive neurodegenerative
disease. While the etiology of PD is likely multifactorial, the protein α-synuclein is a central …
disease. While the etiology of PD is likely multifactorial, the protein α-synuclein is a central …
α-Synuclein pathology in Parkinson's disease and related α-synucleinopathies
MX Henderson, JQ Trojanowski, VMY Lee - Neuroscience letters, 2019 - Elsevier
Over 20 years ago, the synaptic protein α-synuclein was identified as the primary component
of the Lewy bodies (LBs) that are a sine qua non of Parkinson's disease (PD). Since that …
of the Lewy bodies (LBs) that are a sine qua non of Parkinson's disease (PD). Since that …
Ambroxol for the treatment of patients with Parkinson disease with and without glucocerebrosidase gene mutations: a nonrandomized, noncontrolled trial
S Mullin, L Smith, K Lee, G D'Souza… - JAMA …, 2020 - jamanetwork.com
Importance Mutations of the glucocerebrosidase gene, GBA1 (OMIM606463), are the most
important risk factor for Parkinson disease (PD). In vitro and in vivo studies have reported …
important risk factor for Parkinson disease (PD). In vitro and in vivo studies have reported …
Neuropathology of incidental Lewy body & prodromal Parkinson's disease
T Koeglsperger, SL Rumpf, P Schließer… - Molecular …, 2023 - Springer
Background Parkinson's disease (PD) is a progressive neurodegenerative disorder
associated with a loss of dopaminergic (DA) neurons. Despite symptomatic therapies, there …
associated with a loss of dopaminergic (DA) neurons. Despite symptomatic therapies, there …
Glucocerebrosidase and its relevance to Parkinson disease
J Do, C McKinney, P Sharma, E Sidransky - Molecular neurodegeneration, 2019 - Springer
Mutations in GBA1, the gene encoding the lysosomal enzyme glucocerebrosidase, are
among the most common known genetic risk factors for the development of Parkinson …
among the most common known genetic risk factors for the development of Parkinson …
Activation of β-glucocerebrosidase reduces pathological α-synuclein and restores lysosomal function in Parkinson's patient midbrain neurons
Parkinson's disease (PD) is characterized by the accumulation of α-synuclein (α-syn) within
Lewy body inclusions in the nervous system. There are currently no disease-modifying …
Lewy body inclusions in the nervous system. There are currently no disease-modifying …
Glucosylsphingosine promotes α-synuclein pathology in mutant GBA-associated Parkinson's disease
YV Taguchi, J Liu, J Ruan, J Pacheco… - Journal of …, 2017 - Soc Neuroscience
Glucocerebrosidase 1 (GBA) mutations responsible for Gaucher disease (GD) are the most
common genetic risk factor for Parkinson's disease (PD). Although the genetic link between …
common genetic risk factor for Parkinson's disease (PD). Although the genetic link between …
The emerging role of the lysosome in Parkinson's disease
A Navarro-Romero, M Montpeyó, M Martinez-Vicente - Cells, 2020 - mdpi.com
Lysosomal function has a central role in maintaining neuronal homeostasis, and,
accordingly, lysosomal dysfunction has been linked to neurodegeneration and particularly to …
accordingly, lysosomal dysfunction has been linked to neurodegeneration and particularly to …