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Subject Areas on Research
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A cytosine-thymine (CT)-rich haplotype in intron 4 of SNCA confers risk for Lewy body pathology in Alzheimer's disease and affects SNCA expression.
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Abrogation of α-synuclein-mediated dopaminergic neurodegeneration in LRRK2-deficient rats.
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Alpha-synuclein lesions in normal aging, Parkinson disease, and Alzheimer disease: evidence from the Baltimore Longitudinal Study of Aging (BLSA).
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Alpha-synuclein: Pathology, mitochondrial dysfunction and neuroinflammation in Parkinson's disease.
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Analysis of Brain Protein Stability Changes in Mouse Models of Normal Aging and α-Synucleinopathy Reveals Age- and Disease-Related Differences.
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Breathing new life into an old target: pulmonary disease drugs for Parkinson's disease therapy.
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Convergence of Parkin, PINK1, and α-Synuclein on Stress-induced Mitochondrial Morphological Remodeling.
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Dopamine and α-synuclein dysfunction in Smad3 null mice.
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Downregulation of SNCA Expression by Targeted Editing of DNA Methylation: A Potential Strategy for Precision Therapy in PD.
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Effect of allelic variation at the NACP-Rep1 repeat upstream of the alpha-synuclein gene (SNCA) on transcription in a cell culture luciferase reporter system.
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Expansion of the Parkinson disease-associated SNCA-Rep1 allele upregulates human alpha-synuclein in transgenic mouse brain.
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Extensive uptake of α-synuclein oligomers in astrocytes results in sustained intracellular deposits and mitochondrial damage.
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Formation of α-synuclein Lewy neurite-like aggregates in axons impedes the transport of distinct endosomes.
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Functional analysis of intra-allelic variation at NACP-Rep1 in the alpha-synuclein gene.
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G2019S-LRRK2 Expression Augments α-Synuclein Sequestration into Inclusions in Neurons.
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Genetic analysis of α-synuclein 3' untranslated region and its corresponding microRNAs in relation to Parkinson's disease compared to dementia with Lewy bodies.
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Genetic and Environmental Factors in Parkinson's Disease Converge on Immune Function and Inflammation.
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Genetic regulation of alpha-synuclein mRNA expression in various human brain tissues.
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Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.
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Heterogeneity in α-synuclein fibril activity correlates to disease phenotypes in Lewy body dementia.
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Human and mouse alpha-synuclein genes: comparative genomic sequence analysis and identification of a novel gene regulatory element.
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Identification of Novel α-Synuclein Assemblies in Lewy Body Disease.
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Inhibition of LRRK2 kinase activity promotes anterograde axonal transport and presynaptic targeting of α-synuclein.
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LRRK2 activation in idiopathic Parkinson's disease.
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Leucine-rich Repeat Kinase 2 (LRRK2) Pharmacological Inhibition Abates α-Synuclein Gene-induced Neurodegeneration.
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Levels of alpha-synuclein mRNA in sporadic Parkinson disease patients.
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Lewy body pathology is a frequent co-pathology in familial Alzheimer's disease.
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Molecular Features Underlying Neurodegeneration Identified through In Vitro Modeling of Genetically Diverse Parkinson's Disease Patients.
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Multiplication of the SNCA locus exacerbates neuronal nuclear aging.
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Neuroinflammation and α-synuclein dysfunction potentiate each other, driving chronic progression of neurodegeneration in a mouse model of Parkinson's disease.
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Nitrated alpha-synuclein immunity accelerates degeneration of nigral dopaminergic neurons.
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PGC-1α, a potential therapeutic target for early intervention in Parkinson's disease.
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Parkinson's disease from the gut.
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Pathological α-synuclein recruits LRRK2 expressing pro-inflammatory monocytes to the brain.
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Phosphorylation of an alpha-synuclein peptide fragment enhances metal binding.
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Phosphorylation-dependent metal binding by alpha-synuclein peptide fragments.
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Regulation of alpha-synuclein expression by poly (ADP ribose) polymerase-1 (PARP-1) binding to the NACP-Rep1 polymorphic site upstream of the SNCA gene.
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Regulation of alpha-synuclein expression: implications for Parkinson's disease.
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Regulatory T cells attenuate Th17 cell-mediated nigrostriatal dopaminergic neurodegeneration in a model of Parkinson's disease.
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Revelations and revolutions in the understanding of Parkinson's disease.
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Sensitivity and specificity of phospho-Ser129 α-synuclein monoclonal antibodies.
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Structural variants in SNCA gene and the implication to synucleinopathies.
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Synergistic Interactions between Abeta, tau, and alpha-synuclein: acceleration of neuropathology and cognitive decline.
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Synthetic alpha-synuclein fibrils cause mitochondrial impairment and selective dopamine neurodegeneration in part via iNOS-mediated nitric oxide production.
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Tau induces formation of α-synuclein filaments with distinct molecular conformations.
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The alpha-synuclein gene is not a major risk factor in familial Parkinson disease.
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The effect of SNCA 3' region on the levels of SNCA-112 splicing variant.
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The genetic contributions of SNCA and LRRK2 genes to Lewy Body pathology in Alzheimer's disease.
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The interplay between monocytes, α-synuclein and LRRK2 in Parkinson's disease.
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The mechanistic role of alpha-synuclein in the nucleus: impaired nuclear function caused by familial Parkinson's disease SNCA mutations.
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The role of alpha-synuclein in Parkinson's disease: insights from animal models.
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The therapeutic potential of LRRK2 and alpha-synuclein in Parkinson's disease.
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The unlikely partnership between LRRK2 and α-synuclein in Parkinson's disease.
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Toward deciphering the mechanistic role of variations in the Rep1 repeat site in the transcription regulation of SNCA gene.
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Untwisted α-Synuclein Filaments Formed in the Presence of Lipid Vesicles.
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Up-regulation of SNCA gene expression: implications to synucleinopathies.
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Variation in the miRNA-433 binding site of FGF20 confers risk for Parkinson disease by overexpression of alpha-synuclein.
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alpha-Synuclein gene haplotypes are associated with Parkinson's disease.
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α-Synuclein fibril-induced inclusion spread in rats and mice correlates with dopaminergic Neurodegeneration.
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α-Synuclein fibrils recruit peripheral immune cells in the rat brain prior to neurodegeneration.
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α-synucleinopathy exerts sex-dimorphic effects on the multipurpose DNA repair/redox protein APE1 in mice and humans.