Mitochondrial dysfunction in Parkinson's disease–a key disease hallmark with therapeutic potential
MT Henrich, WH Oertel, DJ Surmeier… - Molecular …, 2023 - Springer
Mitochondrial dysfunction is strongly implicated in the etiology of idiopathic and genetic
Parkinson's disease (PD). However, strategies aimed at ameliorating mitochondrial …
Parkinson's disease (PD). However, strategies aimed at ameliorating mitochondrial …
[HTML][HTML] New insights into the complex role of mitochondria in Parkinson's disease
New discoveries providing insights into mitochondrial bioenergetics, their dynamic
interactions as well as their role in cellular homeostasis have dramatically advanced our …
interactions as well as their role in cellular homeostasis have dramatically advanced our …
ROS and autophagy: interactions and molecular regulatory mechanisms
L Li, J Tan, Y Miao, P Lei, Q Zhang - Cellular and molecular neurobiology, 2015 - Springer
Reactive oxygen species (ROS) and antioxidant ingredients are a series of crucial signaling
molecules in oxidative stress response. Under some pathological conditions such as …
molecules in oxidative stress response. Under some pathological conditions such as …
Metabolomics of sebum reveals lipid dysregulation in Parkinson's disease
Parkinson's disease (PD) is a progressive neurodegenerative disorder, which is
characterised by degeneration of distinct neuronal populations, including dopaminergic …
characterised by degeneration of distinct neuronal populations, including dopaminergic …
The role of oxidative stress in Parkinson's disease
V Dias, E Junn, MM Mouradian - Journal of Parkinson's …, 2013 - content.iospress.com
Oxidative stress plays an important role in the degeneration of dopaminergic neurons in
Parkinson's disease (PD). Disruptions in the physiologic maintenance of the redox potential …
Parkinson's disease (PD). Disruptions in the physiologic maintenance of the redox potential …
[HTML][HTML] Loss of VPS13C function in autosomal-recessive parkinsonism causes mitochondrial dysfunction and increases PINK1/Parkin-dependent mitophagy
S Lesage, V Drouet, E Majounie, V Deramecourt… - The American Journal of …, 2016 - cell.com
Autosomal-recessive early-onset parkinsonism is clinically and genetically heterogeneous.
The genetic causes of approximately 50% of autosomal-recessive early-onset forms of …
The genetic causes of approximately 50% of autosomal-recessive early-onset forms of …
Autophagy, mitochondria and oxidative stress: cross-talk and redox signalling
Reactive oxygen and nitrogen species change cellular responses through diverse
mechanisms that are now being defined. At low levels, they are signalling molecules, and at …
mechanisms that are now being defined. At low levels, they are signalling molecules, and at …
Mitochondrial defects and oxidative stress in Alzheimer disease and Parkinson disease
Alzheimer disease (AD) and Parkinson disease (PD) are the two most common age-related
neurodegenerative diseases characterized by prominent neurodegeneration in selective …
neurodegenerative diseases characterized by prominent neurodegeneration in selective …
Mitochondrial transport in neurons: impact on synaptic homeostasis and neurodegeneration
ZH Sheng, Q Cai - Nature Reviews Neuroscience, 2012 - nature.com
Mitochondria have a number of essential roles in neuronal function. Their complex mobility
patterns within neurons are characterized by frequent changes in direction. Mobile …
patterns within neurons are characterized by frequent changes in direction. Mobile …
PINK1 is selectively stabilized on impaired mitochondria to activate Parkin
DP Narendra, SM Jin, A Tanaka, DF Suen… - PLoS …, 2010 - journals.plos.org
Loss-of-function mutations in PINK1 and Parkin cause parkinsonism in humans and
mitochondrial dysfunction in model organisms. Parkin is selectively recruited from the …
mitochondrial dysfunction in model organisms. Parkin is selectively recruited from the …