Association of rare heterozygous PLA2G6 variants with the risk of Parkinson's disease
Author:
Funder
National Key Research and Development Program of China
Publisher
Elsevier BV
Subject
Geriatrics and Gerontology,Developmental Biology,Neurology (clinical),Aging,General Neuroscience
Reference24 articles.
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3. Cellular regulation and proposed biological functions of group VIA calcium-independent phospholipase A2 in activated cells;Balsinde;Cell Signal,2005
4. The genetic architecture of Parkinson's disease;Blauwendraat;Lancet Neurol.,2020
5. PARK14 (D331Y) PLA2G6 causes early-onset degeneration of substantia nigra dopaminergic neurons by inducing mitochondrial dysfunction, ER stress, mitophagy impairment and transcriptional dysregulation in a knockin mouse model;Chiu;Mol. Neurobiol.,2019
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1. Comprehensive variant analysis of phospholipase A2 superfamily genes in large Chinese Parkinson’ s disease cohorts;Mechanisms of Ageing and Development;2024-06
2. A novel variant of PLA2G6 gene related early-onset parkinsonism: a case report and literature review;Frontiers in Neurology;2024-04-18
3. PLA2: Implications in neurological disorders as a prospective therapeutic target;Phospholipases in Physiology and Pathology;2023
4. Mechanism of action of anti-Parkinson's drugs;How Synthetic Drugs Work;2023
5. Association of rare PPARGC1A variants with Parkinson’s disease risk;Journal of Human Genetics;2022-08-22
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