Perspective on the current state of the LRRK2 field

JM Taymans, M Fell, T Greenamyre, WD Hirst… - npj Parkinson's …, 2023 - nature.com
Almost 2 decades after linking LRRK2 to Parkinson's disease, a vibrant research field has
developed around the study of this gene and its protein product. Recent studies have begun …

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 …

Mitochondrial dysfunction in Parkinson's disease: from mechanistic insights to therapy

XY Gao, T Yang, Y Gu, XH Sun - Frontiers in aging neuroscience, 2022 - frontiersin.org
Parkinson's disease (PD) is one of the most common neurodegenerative movement
disorders worldwide. There are currently no cures or preventative treatments for PD …

Clinical progression in Parkinson disease and the neurobiology of axons

HC Cheng, CM Ulane, RE Burke - Annals of neurology, 2010 - Wiley Online Library
Despite tremendous growth in recent years in our knowledge of the molecular basis of
Parkinson disease (PD) and the molecular pathways of cell injury and death, we remain …

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 …

Axon degeneration in Parkinson's disease

RE Burke, K O'Malley - Experimental neurology, 2013 - Elsevier
Parkinson's disease (PD) is the most common neurodegenerative disease of the basal
ganglia. Like other adult-onset neurodegenerative disorders, it is without a treatment that …

LRRK2 inhibition attenuates microglial inflammatory responses

MS Moehle, PJ Webber, T Tse, N Sukar… - Journal of …, 2012 - Soc Neuroscience
Missense mutations in leucine-rich repeat kinase 2 (LRRK2) cause late-onset Parkinson's
disease (PD), and common genetic variation in LRRK2 modifies susceptibility to Crohn's …

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 …

Neuroinflammation and oxidative stress: co-conspirators in the pathology of Parkinson's disease

JM Taylor, BS Main, PJ Crack - Neurochemistry international, 2013 - Elsevier
Parkinson's disease (PD) is a complex disease, with genetics and environment contributing
to the disease onset. Recent studies of causative PD genes have confirmed the involvement …