[HTML][HTML] Prevalence of ten LRRK2 variants in Parkinson's disease: A comprehensive review

C Simpson, L Vinikoor-Imler, FL Nassan… - Parkinsonism & Related …, 2022 - Elsevier
Introduction Variants in the leucine-rich repeat kinase 2 gene (LRRK2) are risk factors for
Parkinson's disease (PD), but their prevalence varies geographically, reflecting the locations …

Molecular and metabolic bases of tetrahydrobiopterin (BH4) deficiencies

N Himmelreich, N Blau, B Thöny - Molecular genetics and metabolism, 2021 - Elsevier
Tetrahydrobiopterin (BH 4) deficiency is caused by genetic variants in the three genes
involved in de novo cofactor biosynthesis, GTP cyclohydrolase I (GTPCH/GCH1), 6-pyruvoyl …

Quantitative and causal analysis for inflammatory genes and the risk of Parkinson's disease

M Yi, J Li, S Jian, B Li, Z Huang, L Shu… - Frontiers in …, 2023 - frontiersin.org
Background The dysfunction of immune system and inflammation contribute to the
Parkinson's disease (PD) pathogenesis. Cytokines, oxidative stress, neurotoxin and …

Review of the epidemiology and variability of LRRK2 non-p. Gly2019Ser pathogenic mutations in Parkinson's disease

P Turski, I Chaberska, P Szukało, P Pyska… - Frontiers in …, 2022 - frontiersin.org
Parkinson's disease (PD) is a heterogenous neurodegenerative disorder. Genetic factors
play a significant role, especially in early onset and familial cases. Mutations are usually …

Sepiapterin reductase: Characteristics and role in diseases

Y Wu, P Chen, L Sun, S Yuan, Z Cheng… - Journal of Cellular …, 2020 - Wiley Online Library
Sepiapterin reductase, a homodimer composed of two subunits, plays an important role in
the biosynthesis of tetrahydrobiopterin. Furthermore, sepiapterin reductase exhibits a wide …

Differences in MTHFR and LRRK2 variant's association with sporadic Parkinson's disease in Mexican Mestizos correlated to Native American ancestry

E Romero-Gutiérrez, P Vázquez-Cárdenas… - npj Parkinson's …, 2021 - nature.com
Abstract Parkinson's disease (PD), a common neurodegenerative disorder, has a complex
etiology where environmental and genetic factors intervene. While a number of genes and …

MTHFR C677T and A1298C polymorphisms may contribute to the risk of Parkinson's disease: A meta-analysis of 19 studies

L Liu, L Zhang, L Guo, Q Yu, H Li, J Teng, A **e - Neuroscience Letters, 2018 - Elsevier
Abstract The 5, 10-methylenetetrahydrofolate reductase (MTHFR) gene has been reported
to be a candidate gene for susceptibility to Parkinson's disease (PD), but results of different …

A278C mutation of dihydropteridine reductase decreases autophagy via mTOR signaling

Q Si, S Sun, Y Gu - Acta Biochimica et Biophysica Sinica, 2017 - academic.oup.com
Dihydropteridine reductase (QDPR) plays an important role in the recycling of BH4 and is
closely related to oxidative stress. We have previously reported that the overexpression of …

Association between ZNF184 and symptoms of Parkinson's disease in southern Chinese

B Zhang, C Cui, H Yu, G Li - Neurological Sciences, 2020 - Springer
Study objectives The aim was to investigate the association between ZNF184 and symptoms
of Parkinson's disease (PD) in southern Chinese. Methods A total of 241 PD patients were …

Association between MTHFR genetic polymorphism and Parkinson's disease susceptibility: a meta-analysis

HM Diao, ZF Song, HD Xu - Open Medicine, 2019 - degruyter.com
Folate metabolism plays quite a critical role in Parkinson's disease (PD). Previous published
research works have studied the link existing between the folate metabolism genetic …