Parkinson Disease
|
0.100 |
Biomarker
|
disease |
BEFREE |
In the healthy brain, SYN and TPPP/p25 occur in neurons and oligodendrocytes, respectively; however, in PD and multiple system atrophy, they are co-enriched and co-localized in both cell types, thereby marking pathogenesis.
|
31148150 |
2019 |
Parkinson Disease
|
0.100 |
Biomarker
|
disease |
BEFREE |
α-SYN is the main component of round intracytoplasmic inclusions called Lewy bodies (LBs), which are the hallmark of PD and DLB.
|
29246765 |
2018 |
Parkinson Disease
|
0.100 |
Biomarker
|
disease |
BEFREE |
We then present preclinical and clinical data that introduce new concepts, such as the use of biased and partial agonists, as well as molecules recently introduced to the field of PD, such as eltoprazine, pimavanserin, nelotanserin, and SYN-120, to enhance therapeutic benefit while minimizing adverse events, notably on parkinsonian disability.
|
28460160 |
2017 |
Parkinson Disease
|
0.100 |
Biomarker
|
disease |
BEFREE |
The hallmarks of Parkinson's disease and other synucleinopathies, Tubulin Polymerization Promoting Protein (TPPP/p25) and α-synuclein (SYN) have two key features: they are disordered and co-enriched/co-localized in brain inclusions.
|
27671864 |
2017 |
Parkinson Disease
|
0.100 |
Biomarker
|
disease |
BEFREE |
Accumulation of α‑synuclein (α‑SYN) is a common pathology for Parkinson's disease (PD).
|
28990084 |
2017 |
Parkinson Disease
|
0.100 |
Biomarker
|
disease |
BEFREE |
Recent studies are now indicating that ɑ-SYN may act in a way similar to prions and that ɑ-SYN misfolded structural variants may behave as strains with distinct biochemical and functional properties inducing specific phenotypic traits, which might finally provide an explanation for the clinical heterogeneity observed between Parkinson's disease, MSA, and dementia with Lewy bodies patients.
|
26924014 |
2016 |
Parkinson Disease
|
0.100 |
Biomarker
|
disease |
BEFREE |
Alpha synuclein (SYN) is a central player in the pathogenesis of sporadic and familial Parkinson's disease (PD).
|
23223297 |
2012 |
Parkinson Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Familial PD with SYN gene mutations are rare because the majority of PD is sporadic and emerging evidence indicates that sporadic PD may result from genetic and environmental risk factors including neuroinflammation.
|
18650345 |
2008 |
Parkinson Disease
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
To examine the relationship between alpha-SYN, microglial activation, and adaptive immunity, we used a mouse model of Parkinson disease in which human alpha-SYN is overexpressed by a recombinant adeno-associated virus vector, serotype 2 (AAV2-SYN); this overexpression leads to slow degeneration of dopaminergic neurons.
|
19018246 |
2008 |
Parkinson Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
We have investigated the effect of UPS inhibition on the metabolism of alpha-synuclein (SYN) and parkin, two proteins genetically and histopathologically associated to PD.
|
14720204 |
2004 |
Parkinson Disease
|
0.100 |
Biomarker
|
disease |
BEFREE |
alpha-Synuclein (alpha-SYN) is deposited in intraneuronal cytoplasmic inclusions (Lewy bodies, LBs) characteristic for Parkinson's disease (PD) and LB dementias. alpha-SYN forms LB-like fibrils in vitro, in contrast to its homologue beta-SYN.
|
11733371 |
2001 |
Parkinson Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
The two Parkinson's disease-associated mutations accelerated the intrinsic aggregation property of alpha-SYN in vitro.
|
11193173 |
2000 |