Novel insights into Parkin-mediated mitochondrial dysfunction and neuroinflammation in Parkinson's disease
Author:
Publisher
Elsevier BV
Subject
General Neuroscience
Reference88 articles.
1. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism;Kitada;Nature,1998
2. Genotype-phenotype relations for the Parkinson's disease genes parkin, PINK1, DJ1: MDSGene systematic review;Kasten;Mov Disord,2018
3. Parkin-linked Parkinson's disease: from clinical insights to pathogenic mechanisms and novel therapeutic approaches;Wasner;Neurosci Res,2020
4. Next-generation phenotyping using the parkin example: time to catch up with genetics;Grunewald;JAMA Neurol,2013
5. Structure and function of Parkin E3 ubiquitin ligase reveals aspects of RING and HECT ligases;Riley;Nat Commun,2013
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1. Parkin R274W mutation affects muscle and mitochondrial physiology;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;2024-10
2. Targeting protein interaction networks in mitochondrial dynamics for neurodegenerative diseases;Journal of Proteins and Proteomics;2024-07-05
3. Novel Insights into Parkin–Mediated Mitochondrial Dysfunction and “Mito-Inflammation” in α-Synuclein Toxicity. The Role of the cGAS–STING Signalling Pathway;Journal of Inflammation Research;2024-07
4. Glycolic acid and D-lactate—putative products of DJ-1—restore neurodegeneration in FUS - and SOD1-ALS;Life Science Alliance;2024-05-17
5. Pterostilbene attenuates oxidative stress induced by hydrogen peroxide in MAC-T cells through activating PINK1/Parkin-mediated mitophagy;Italian Journal of Animal Science;2024-05-17
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