Curcumin can improve Parkinson's disease via activating BDNF/PI3k/Akt signaling pathways

T Jin, Y Zhang, BOA Botchway, J Zhang, R Fan… - Food and Chemical …, 2022 - Elsevier
Parkinson's disease is a common progressive neurodegenerative disease, and presently
has no curative agent. Curcumin, as one of the natural polyphenols, has great potential in …

Mitochondrial function and Parkinson's disease: from the perspective of the electron transport chain

JL Li, TY Lin, PL Chen, TN Guo, SY Huang… - Frontiers in molecular …, 2021 - frontiersin.org
Parkinson's disease (PD) is known as a mitochondrial disease. Some even regarded it
specifically as a disorder of the complex I of the electron transport chain (ETC). The ETC is …

Global trends in the incidence, prevalence, and years lived with disability of Parkinson's disease in 204 countries/territories from 1990 to 2019

Z Ou, J Pan, S Tang, D Duan, D Yu, H Nong… - Frontiers in public …, 2021 - frontiersin.org
Background: Parkinson's disease (PD) is an increasing challenge to public health. Tracking
the temporal trends of PD burden would inform health strategies. Methods: Data of PD …

Deficiency in endocannabinoid synthase DAGLB contributes to early onset Parkinsonism and murine nigral dopaminergic neuron dysfunction

Z Liu, N Yang, J Dong, W Tian, L Chang, J Ma… - Nature …, 2022 - nature.com
Abstract Endocannabinoid (eCB), 2-arachidonoyl-glycerol (2-AG), the most abundant eCB in
the brain, regulates diverse neural functions. Here we linked multiple homozygous loss-of …

Genome-wide association study using whole-genome sequencing identifies risk loci for Parkinson's disease in Chinese population

H Pan, Z Liu, J Ma, Y Li, Y Zhao, X Zhou… - npj Parkinson's …, 2023 - nature.com
Genome-wide association studies (GWASs) have identified numerous susceptibility loci for
Parkinson's disease (PD), but its genetic architecture remains underexplored in populations …

Long‐Read Sequencing Resolves a Complex Structural Variant in PRKN Parkinson's Disease

K Daida, M Funayama, KJ Billingsley… - Movement …, 2023 - Wiley Online Library
Abstract Background Parkin RBR E3 ubiquitin‐protein ligase (PRKN) mutations are the most
common cause of young onset and autosomal recessive Parkinson's disease (PD). PRKN is …

Nomenclature of genetic movement disorders: recommendations of the International Parkinson and Movement Disorder Society task force–an update

LM Lange, P Gonzalez‐Latapi… - Movement …, 2022 - Wiley Online Library
Abstract In 2016, the Movement Disorder Society Task Force for the Nomenclature of
Genetic Movement Disorders presented a new system for naming genetically determined …

GP2: the global Parkinson's genetics program

Global Parkinson's Genetics Program - Movement Disorders, 2021 - Wiley Online Library
Fundamentally, the identification of causes and contributors of disease represents the first
step in an etiology-based understanding of disease. This, in turn, is a required step in the …

Genetic heterogeneity on sleep disorders in Parkinson's disease: a systematic review and meta-analysis

J Huang, Y Cheng, C Li, H Shang - Translational Neurodegeneration, 2022 - Springer
A growing amount of evidence has indicated contributions of variants in causative genes of
Parkinson's disease (PD) to the development of sleep disturbance in PD and prodromal PD …

Mutational spectrum and clinical features of GBA1 variants in a Chinese cohort with Parkinson's disease

Y Zhou, Y Wang, J Wan, Y Zhao, H Pan, Q Zeng… - npj Parkinson's …, 2023 - nature.com
GBA1 variants are important risk factors for Parkinson's disease (PD). Most studies
assessing GBA1-related PD risk have been performed in European-derived populations …