scholarly article | Q13442814 |
review article | Q7318358 |
P50 | author | Hazel L Roberts | Q59691682 |
P2093 | author name string | David R Brown | |
P2860 | cites work | Different species of alpha-synuclein oligomers induce calcium influx and seeding. | Q52581429 |
Mechanism of membrane interaction and disruption by α-synuclein. | Q52617078 | ||
alpha-Synuclein gene duplication is present in sporadic Parkinson disease. | Q53473267 | ||
Collaborative Analysis of α-Synuclein Gene Promoter Variability and Parkinson Disease | Q57977634 | ||
Islet amyloid polypeptide-induced membrane leakage involves uptake of lipids by forming amyloid fibers | Q61844539 | ||
In situ and in vitro study of colocalization and segregation of alpha-synuclein, ubiquitin, and lipids in Lewy bodies | Q64764806 | ||
Dityrosine cross-linking promotes formation of stable alpha -synuclein polymers. Implication of nitrative and oxidative stress in the pathogenesis of neurodegenerative synucleinopathies | Q73626218 | ||
Kinetic measurements give new insights into lipid membrane permeabilization by α-synuclein oligomers | Q82082237 | ||
Regional distribution of alpha-synuclein pathology in unimpaired aging and Alzheimer disease | Q42440540 | ||
ANS binding reveals common features of cytotoxic amyloid species | Q43021800 | ||
Detection of elevated levels of soluble alpha-synuclein oligomers in post-mortem brain extracts from patients with dementia with Lewy bodies. | Q44143951 | ||
Aggregated and monomeric alpha-synuclein bind to the S6' proteasomal protein and inhibit proteasomal function | Q44292891 | ||
Proteasomal inhibition by alpha-synuclein filaments and oligomers. | Q44719233 | ||
Permeabilization of lipid bilayers is a common conformation-dependent activity of soluble amyloid oligomers in protein misfolding diseases | Q45072759 | ||
The many faces of alpha-synuclein mutations | Q45387129 | ||
Human alpha-synuclein over-expression increases intracellular reactive oxygen species levels and susceptibility to dopamine. | Q45711545 | ||
Lipid bilayer disruption by oligomeric alpha-synuclein depends on bilayer charge and accessibility of the hydrophobic core. | Q45908123 | ||
Cell-produced alpha-synuclein oligomers are targeted to, and impair, the 26S proteasome | Q46351241 | ||
Aggregated alpha-synuclein activates microglia: a process leading to disease progression in Parkinson's disease | Q46404588 | ||
Dopamine promotes alpha-synuclein aggregation into SDS-resistant soluble oligomers via a distinct folding pathway | Q46537593 | ||
Single particle characterization of iron-induced pore-forming alpha-synuclein oligomers | Q46765690 | ||
Membrane interactions and fibrillization of α-synuclein play an essential role in membrane disruption | Q46807031 | ||
The role of stable α-synuclein oligomers in the molecular events underlying amyloid formation. | Q46931854 | ||
Pore-forming proteins share structural and functional homology with amyloid oligomers | Q46968526 | ||
The impact of the E46K mutation on the properties of alpha-synuclein in its monomeric and oligomeric states | Q48155270 | ||
Oligomeric alpha-synuclein inhibits tubulin polymerization | Q48234434 | ||
Toxic prefibrillar α-synuclein amyloid oligomers adopt a distinctive antiparallel β-sheet structure. | Q48668545 | ||
Pathogenic mutations shift the equilibria of alpha-synuclein single molecules towards structured conformers. | Q48806783 | ||
Lewy body-related alpha-synucleinopathy in the aged human brain. | Q50282783 | ||
Pre-fibrillar alpha-synuclein variants with impaired beta-structure increase neurotoxicity in Parkinson's disease models | Q24315670 | ||
The N-terminus of α-synuclein is essential for both monomeric and oligomeric interactions with membranes | Q24316619 | ||
α-Synuclein occurs physiologically as a helically folded tetramer that resists aggregation | Q24605589 | ||
Alpha-synuclein promotes SNARE-complex assembly in vivo and in vitro | Q24629968 | ||
α-Synuclein propagates from mouse brain to grafted dopaminergic neurons and seeds aggregation in cultured human cells | Q24633663 | ||
Inclusion formation and neuronal cell death through neuron-to-neuron transmission of alpha-synuclein | Q24655848 | ||
Alpha-synuclein blocks ER-Golgi traffic and Rab1 rescues neuron loss in Parkinson's models | Q24683059 | ||
Dopamine-modified alpha-synuclein blocks chaperone-mediated autophagy | Q24683089 | ||
α-Synuclein assembles into higher-order multimers upon membrane binding to promote SNARE complex formation | Q26269838 | ||
Membrane Permeabilization by Oligomeric α-Synuclein: In Search of the Mechanism | Q27315907 | ||
Parkinson's disease dementia: convergence of α-synuclein, tau and amyloid-β pathologies | Q27686837 | ||
Mutation in the alpha-synuclein gene identified in families with Parkinson's disease | Q27860459 | ||
Alpha-synuclein in Lewy bodies | Q27860680 | ||
The new mutation, E46K, of alpha-synuclein causes Parkinson and Lewy body dementia | Q29547174 | ||
Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease | Q29547175 | ||
Common structure of soluble amyloid oligomers implies common mechanism of pathogenesis | Q29547501 | ||
Impaired degradation of mutant alpha-synuclein by chaperone-mediated autophagy | Q29614178 | ||
Alpha-synuclein locus duplication as a cause of familial Parkinson's disease | Q29614762 | ||
Novel A18T and pA29S substitutions in α-synuclein may be associated with sporadic Parkinson's disease. | Q30352615 | ||
α-Synuclein mutations cluster around a putative protein loop | Q30430404 | ||
NADPH oxidase 1-mediated oxidative stress leads to dopamine neuron death in Parkinson's disease | Q30512262 | ||
α-Synuclein oligomers impair neuronal microtubule-kinesin interplay. | Q30541822 | ||
Glial innate immunity generated by non-aggregated alpha-synuclein in mouse: differences between wild-type and Parkinson's disease-linked mutants | Q30991616 | ||
Abberant alpha-synuclein confers toxicity to neurons in part through inhibition of chaperone-mediated autophagy | Q33444800 | ||
Compounds from an unbiased chemical screen reverse both ER-to-Golgi trafficking defects and mitochondrial dysfunction in Parkinson's disease models | Q33521022 | ||
Amyloid-beta-induced ion flux in artificial lipid bilayers and neuronal cells: resolving a controversy | Q33827991 | ||
EGCG remodels mature alpha-synuclein and amyloid-beta fibrils and reduces cellular toxicity. | Q33842865 | ||
Neuron-released oligomeric α-synuclein is an endogenous agonist of TLR2 for paracrine activation of microglia | Q33874305 | ||
Alpha-synuclein delays endoplasmic reticulum (ER)-to-Golgi transport in mammalian cells by antagonizing ER/Golgi SNAREs | Q33881676 | ||
Lewy bodies in Alzheimer's disease: a neuropathological review of 145 cases using alpha-synuclein immunohistochemistry. | Q33961445 | ||
Soluble, prefibrillar α-synuclein oligomers promote complex I-dependent, Ca2+-induced mitochondrial dysfunction. | Q33985326 | ||
Structure activity relationship of phenolic acid inhibitors of α-synuclein fibril formation and toxicity | Q34003885 | ||
Baicalein reduces E46K alpha-synuclein aggregation in vitro and protects cells against E46K alpha-synuclein toxicity in cell models of familiar Parkinsonism. | Q34020622 | ||
α-Synuclein in central nervous system and from erythrocytes, mammalian cells, and Escherichia coli exists predominantly as disordered monomer | Q34252869 | ||
Direct observation of the interconversion of normal and toxic forms of α-synuclein | Q34277399 | ||
The role of alpha-synuclein oligomerization and aggregation in cellular and animal models of Parkinson's disease | Q34305509 | ||
In vivo cross-linking reveals principally oligomeric forms of α-synuclein and β-synuclein in neurons and non-neural cells | Q34322594 | ||
Alpha-synuclein p.H50Q, a novel pathogenic mutation for Parkinson's disease. | Q34330786 | ||
G51D α-synuclein mutation causes a novel parkinsonian-pyramidal syndrome | Q34335126 | ||
Transglutaminase 2 exacerbates α-synuclein toxicity in mice and yeast | Q34365610 | ||
Single-channel electrophysiology reveals a distinct and uniform pore complex formed by α-synuclein oligomers in lipid membranes | Q34374310 | ||
Effect of familial Parkinson's disease point mutations A30P and A53T on the structural properties, aggregation, and fibrillation of human alpha-synuclein | Q34517780 | ||
Effects of curvature and composition on α-synuclein binding to lipid vesicles | Q34590790 | ||
Abeta42 neurotoxicity is mediated by ongoing nucleated polymerization process rather than by discrete Abeta42 species | Q34624507 | ||
In vivo demonstration that alpha-synuclein oligomers are toxic | Q34652122 | ||
Methylation regulates alpha-synuclein expression and is decreased in Parkinson's disease patients' brains. | Q34660005 | ||
Impairment of mitochondria in adult mouse brain overexpressing predominantly full-length, N-terminally acetylated human α-synuclein | Q34718257 | ||
Acceleration of oligomerization, not fibrillization, is a shared property of both alpha-synuclein mutations linked to early-onset Parkinson's disease: implications for pathogenesis and therapy | Q34964783 | ||
The many faces of α-synuclein: from structure and toxicity to therapeutic target | Q34972009 | ||
Direct membrane association drives mitochondrial fission by the Parkinson disease-associated protein alpha-synuclein | Q35063363 | ||
Toll-like receptor 4 promotes α-synuclein clearance and survival of nigral dopaminergic neurons | Q35167964 | ||
Exogenous α-synuclein fibrils induce Lewy body pathology leading to synaptic dysfunction and neuron death | Q35484581 | ||
Aggregation of αSynuclein promotes progressive in vivo neurotoxicity in adult rat dopaminergic neurons | Q35863939 | ||
Fibrillar α-synuclein and huntingtin exon 1 assemblies are toxic to the cells | Q36045483 | ||
Differential activation of the ER stress factor XBP1 by oligomeric assemblies | Q36070065 | ||
Soluble α-synuclein is a novel modulator of Alzheimer's disease pathophysiology | Q36182604 | ||
Endoplasmic reticulum stress is important for the manifestations of α-synucleinopathy in vivo | Q36289970 | ||
Soluble amyloid oligomers increase bilayer conductance by altering dielectric structure | Q36295920 | ||
Radiating amyloid fibril formation on the surface of lipid membranes through unit-assembly of oligomeric species of α-synuclein | Q36319183 | ||
Accumulation of toxic α-synuclein oligomer within endoplasmic reticulum occurs in α-synucleinopathy in vivo. | Q36543608 | ||
Microglial activation and antioxidant responses induced by the Parkinson's disease protein α-synuclein | Q36640417 | ||
Large α-synuclein oligomers inhibit neuronal SNARE-mediated vesicle docking | Q36673364 | ||
Mitochondrial import and accumulation of alpha-synuclein impair complex I in human dopaminergic neuronal cultures and Parkinson disease brain | Q36727241 | ||
Lewy body-like α-synuclein aggregates resist degradation and impair macroautophagy | Q36873680 | ||
In vitro study of α-synuclein protofibrils by cryo-EM suggests a Cu(2+)-dependent aggregation pathway | Q36939712 | ||
α-Synuclein and mitochondria: partners in crime? | Q36983221 | ||
Physiological and pathological role of alpha-synuclein in Parkinson's disease through iron mediated oxidative stress; the role of a putative iron-responsive element | Q37166339 | ||
The interplay between lipids and dopamine on α-synuclein oligomerization and membrane binding. | Q37246310 | ||
Cell-produced alpha-synuclein is secreted in a calcium-dependent manner by exosomes and impacts neuronal survival | Q37347595 | ||
α-Synuclein misfolding assessed with single molecule AFM force spectroscopy: effect of pathogenic mutations | Q37351690 | ||
Role of α-synuclein penetration into the membrane in the mechanisms of oligomer pore formation | Q37587111 | ||
Evidence of native α-synuclein conformers in the human brain | Q37635873 | ||
Amyloidogenic protein-membrane interactions: mechanistic insight from model systems | Q37771927 | ||
Α-synuclein misfolding and Parkinson's disease | Q37949158 | ||
Activation of the unfolded protein response is an early event in Alzheimer's and Parkinson's disease. | Q37981067 | ||
α-Synuclein and protein degradation systems: a reciprocal relationship | Q38039881 | ||
α-Synuclein oligomers: an amyloid pore? Insights into mechanisms of α-synuclein oligomer-lipid interactions | Q38041484 | ||
The function of α-synuclein | Q38139561 | ||
Biophysical groundwork as a hinge to unravel the biology of α-synuclein aggregation and toxicity | Q38180144 | ||
Effect of Ser-129 phosphorylation on interaction of α-synuclein with synaptic and cellular membranes. | Q38734429 | ||
Accumulation of oligomer-prone α-synuclein exacerbates synaptic and neuronal degeneration in vivo | Q38966914 | ||
The rescue of microtubule-dependent traffic recovers mitochondrial function in Parkinson's disease | Q39080090 | ||
A comparison of the biochemical modifications caused by toxic and non-toxic protein oligomers in cells | Q39545823 | ||
Amyloid-like aggregates sequester numerous metastable proteins with essential cellular functions | Q39610788 | ||
Alpha-synuclein, especially the Parkinson's disease-associated mutants, forms pore-like annular and tubular protofibrils | Q39632694 | ||
Copper binding regulates intracellular alpha-synuclein localisation, aggregation and toxicity | Q39742060 | ||
A causative link between the structure of aberrant protein oligomers and their toxicity. | Q39750915 | ||
Unique copper-induced oligomers mediate alpha-synuclein toxicity | Q39867665 | ||
Dynamics of alpha-synuclein aggregation and inhibition of pore-like oligomer development by beta-synuclein | Q40155070 | ||
Toll-like receptor 4 is required for α-synuclein dependent activation of microglia and astroglia. | Q41997706 | ||
α-Synuclein senses lipid packing defects and induces lateral expansion of lipids leading to membrane remodeling | Q42184977 | ||
Redox reactions of the α-synuclein-Cu(2+) complex and their effects on neuronal cell viability | Q42426545 | ||
P275 | copyright license | Creative Commons Attribution | Q6905323 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | toxicity | Q274160 |
neurodegeneration | Q1755122 | ||
nerve tissue protein | Q6996861 | ||
Parkinson disease associated proteins | Q77946709 | ||
Synuclein | Q24767155 | ||
P5008 | on focus list of Wikimedia project | ScienceSource | Q55439927 |
P304 | page(s) | 282-305 | |
P577 | publication date | 2015-03-25 | |
P1433 | published in | Biomolecules | Q23929963 |
P1476 | title | Seeking a mechanism for the toxicity of oligomeric α-synuclein | |
P478 | volume | 5 |
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