Drosophila as an In Vivo Model for Human Neurodegenerative Disease

L McGurk, A Berson, NM Bonini - Genetics, 2015 - academic.oup.com
With the increase in the ageing population, neurodegenerative disease is devastating to
families and poses a huge burden on society. The brain and spinal cord are extraordinarily …

Animal models of Parkinson's disease: a source of novel treatments and clues to the cause of the disease

S Duty, P Jenner - British journal of pharmacology, 2011 - Wiley Online Library
Animal models of Parkinson's disease (PD) have proved highly effective in the discovery of
novel treatments for motor symptoms of PD and in the search for clues to the underlying …

Mitochondrial ROS promotes susceptibility to infection via gasdermin D-mediated necroptosis

CG Weindel, EL Martinez, X Zhao, CJ Mabry, SL Bell… - Cell, 2022 - cell.com
Although mutations in mitochondrial-associated genes are linked to inflammation and
susceptibility to infection, their mechanistic contributions to immune outcomes remain ill …

Functional impairment in miro degradation and mitophagy is a shared feature in familial and sporadic Parkinson's disease

CH Hsieh, A Shaltouki, AE Gonzalez, AB da Cruz… - Cell stem cell, 2016 - cell.com
Mitochondrial movements are tightly controlled to maintain energy homeostasis and prevent
oxidative stress. Miro is an outer mitochondrial membrane protein that anchors mitochondria …

Mitochondrial dysfunction in Parkinson's disease: molecular mechanisms and pathophysiological consequences

N Exner, AK Lutz, C Haass, KF Winklhofer - The EMBO journal, 2012 - embopress.org
Neurons are critically dependent on mitochondrial integrity based on specific morphological,
biochemical, and physiological features. They are characterized by high rates of metabolic …

Genetic animal models of Parkinson's disease

TM Dawson, HS Ko, VL Dawson - Neuron, 2010 - cell.com
Parkinson's disease (PD) is a progressive neurodegenerative disorder that is characterized
by the degeneration of dopamine (DA) and non-DA neurons, the almost uniform presence of …

Mitochondrial diseases of the brain

RK Chaturvedi, MF Beal - Free Radical Biology and Medicine, 2013 - Elsevier
Neurodegenerative disorders are debilitating diseases of the brain, characterized by
behavioral, motor and cognitive impairments. Ample evidence underpins mitochondrial …

Increasing microtubule acetylation rescues axonal transport and locomotor deficits caused by LRRK2 Roc-COR domain mutations

VK Godena, N Brookes-Hocking, A Moller… - Nature …, 2014 - nature.com
Leucine-rich repeat kinase 2 (LRRK2) mutations are the most common genetic cause of
Parkinson's disease. LRRK2 is a multifunctional protein affecting many cellular processes …

The role of the LRRK2 gene in Parkinsonism

JQ Li, L Tan, JT Yu - Molecular neurodegeneration, 2014 - Springer
Abstract Parkinson's disease (PD), like many common age-related conditions, has been
recognized to have a substantial genetic component. Multiple lines of evidence suggest that …

Advancement in the modelling and therapeutics of Parkinson's disease

SN Rai, P Singh - Journal of chemical neuroanatomy, 2020 - Elsevier
Since the discovery of L-dopa in the middle of the 20th century (1960s), there is not any
neuroprotective therapy available although significant development has been made in the …