Selective autophagy as a potential therapeutic target for neurodegenerative disorders
Cells rely on surveillance systems such as autophagy to handle protein alterations and
organelle damage. Dysfunctional autophagy, an evolutionarily conserved cellular …
organelle damage. Dysfunctional autophagy, an evolutionarily conserved cellular …
Parkinson disease from mendelian forms to genetic susceptibility: new molecular insights into the neurodegeneration process
Parkinson disease (PD) is known as a common progressive neurodegenerative disease
which is clinically diagnosed by the manifestation of numerous motor and nonmotor …
which is clinically diagnosed by the manifestation of numerous motor and nonmotor …
Alternative mitochondrial quality control mediated by extracellular release
Mitochondrial quality control, which is crucial for maintaining cellular homeostasis, has been
considered to be achieved exclusively through mitophagy. Here we report an alternative …
considered to be achieved exclusively through mitophagy. Here we report an alternative …
P arkin deficiency modulates NLRP 3 inflammasome activation by attenuating an A 20‐dependent negative feedback loop
F Mouton‐Liger, T Rosazza, J Sepulveda‐Diaz… - Glia, 2018 - Wiley Online Library
Neuroinflammation and mitochondrial dysfunction, key mechanisms in the pathogenesis of
Parkinson's disease (PD), are usually explored independently. Loss‐of‐function mutations …
Parkinson's disease (PD), are usually explored independently. Loss‐of‐function mutations …
PARIS induced defects in mitochondrial biogenesis drive dopamine neuron loss under conditions of parkin or PINK1 deficiency
SK Pirooznia, C Yuan, MR Khan… - Molecular …, 2020 - Springer
Background Mutations in PINK1 and parkin cause autosomal recessive Parkinson's disease
(PD). Evidence placing PINK1 and parkin in common pathways regulating multiple aspects …
(PD). Evidence placing PINK1 and parkin in common pathways regulating multiple aspects …
The endoplasmic reticulum-mitochondria interface is perturbed in PARK2 knockout mice and patients with PARK2 mutations
CA Gautier, Z Erpapazoglou… - Human molecular …, 2016 - academic.oup.com
Mutations in PARK2, encoding the E3 ubiquitin protein ligase Parkin, are a common cause
of autosomal recessive Parkinson's disease (PD). Loss of PARK2 function compromises …
of autosomal recessive Parkinson's disease (PD). Loss of PARK2 function compromises …
Defects in mitochondrial biogenesis drive mitochondrial alterations in PARKIN-deficient human dopamine neurons
Mutations and loss of activity in PARKIN, an E3 ubiquitin ligase, play a role in the
pathogenesis of Parkinson's disease (PD). PARKIN regulates many aspects of mitochondrial …
pathogenesis of Parkinson's disease (PD). PARKIN regulates many aspects of mitochondrial …
ER lipid defects in neuropeptidergic neurons impair sleep patterns in Parkinson's disease
Parkinson's disease patients report disturbed sleep patterns long before motor dysfunction.
Here, in parkin and pink1 models, we identify circadian rhythm and sleep pattern defects …
Here, in parkin and pink1 models, we identify circadian rhythm and sleep pattern defects …
Age-associated insolubility of parkin in human midbrain is linked to redox balance and sequestration of reactive dopamine metabolites
JM Tokarew, DN El-Kodsi, NA Lengacher, TK Fehr… - Acta …, 2021 - Springer
The mechanisms by which parkin protects the adult human brain from Parkinson disease
remain incompletely understood. We hypothesized that parkin cysteines participate in redox …
remain incompletely understood. We hypothesized that parkin cysteines participate in redox …
Autophagy, its mechanisms and regulation: implications in neurodegenerative diseases
Autophagy is a major regulatory cellular mechanism which gives the cell an ability to cope
with some of the destructive events that normally occur within a metabolically living cell. This …
with some of the destructive events that normally occur within a metabolically living cell. This …