A novel panel of α-synuclein antibodies reveal distinctive staining profiles in synucleinopathies.

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A novel panel of α-synuclein antibodies reveal distinctive staining profiles in synucleinopathies. is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1371/JOURNAL.PONE.0184731
P932PMC publication ID5599040
P698PubMed publication ID28910367

P50authorBenoit I GiassonQ88244471
P2093author name stringYong Ran
Todd E Golde
Paramita Chakrabarty
Brenda D Moore
Jess-Karan S Dhillon
Cara Riffe
P2860cites workA hydrophobic stretch of 12 amino acid residues in the middle of alpha-synuclein is essential for filament assembly.Q54031652
A panel of epitope-specific antibodies detects protein domains distributed throughout human alpha-synuclein in Lewy bodies of Parkinson's diseaseQ64796863
The synucleinsQ24551013
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Mice lacking alpha-synuclein display functional deficits in the nigrostriatal dopamine systemQ28594502
Passive immunization reduces behavioral and neuropathological deficits in an alpha-synuclein transgenic model of Lewy body diseaseQ28740551
Next-generation active immunization approach for synucleinopathies: implications for Parkinson's disease clinical trialsQ30578913
Intramuscular injection of α-synuclein induces CNS α-synuclein pathology and a rapid-onset motor phenotype in transgenic mice.Q30585365
Comparison of ethanol versus formalin fixation on preservation of histology and RNA in laser capture microdissected brain tissuesQ33203703
Aggregation promoting C-terminal truncation of alpha-synuclein is a normal cellular process and is enhanced by the familial Parkinson's disease-linked mutationsQ33836384
Reducing C-terminal-truncated alpha-synuclein by immunotherapy attenuates neurodegeneration and propagation in Parkinson's disease-like modelsQ33865366
The alpha-synucleinopathies: Parkinson's disease, dementia with Lewy bodies, and multiple system atrophy.Q34148223
The biochemistry of Parkinson's diseaseQ34426026
Amyloid-ß-directed immunotherapy for Alzheimer's diseaseQ34548700
Anti-human α-synuclein N-terminal peptide antibody protects against dopaminergic cell death and ameliorates behavioral deficits in an AAV-α-synuclein rat model of Parkinson's diseaseQ35058359
E46K human alpha-synuclein transgenic mice develop Lewy-like and tau pathology associated with age-dependent, detrimental motor impairmentQ35266392
Α-synuclein immunotherapy blocks uptake and templated propagation of misfolded α-synuclein and neurodegenerationQ35542169
Active immunization against alpha-synuclein ameliorates the degenerative pathology and prevents demyelination in a model of multiple system atrophyQ35544737
Fiber diffraction of synthetic alpha-synuclein filaments shows amyloid-like cross-beta conformationQ35700288
Studies of lipopolysaccharide effects on the induction of α-synuclein pathology by exogenous fibrils in transgenic miceQ35903351
Intracerebral inoculation of pathological α-synuclein initiates a rapidly progressive neurodegenerative α-synucleinopathy in miceQ35946149
Insights into prion strains and neurotoxicityQ36856446
Antibody-aided clearance of extracellular α-synuclein prevents cell-to-cell aggregate transmissionQ37117527
Divergent α-synuclein solubility and aggregation properties in G2019S LRRK2 Parkinson's disease brains with Lewy Body pathology compared to idiopathic casesQ37119983
Characterization of antibodies that selectively detect alpha-synuclein in pathological inclusionsQ37148311
Structural and functional characterization of two alpha-synuclein strainsQ37305236
Molecular mechanisms of alpha-synuclein neurodegenerationQ37309838
Transmission of multiple system atrophy prions to transgenic miceQ37353012
Robust Central Nervous System Pathology in Transgenic Mice following Peripheral Injection of α-Synuclein FibrilsQ37560714
Anti-α-synuclein immunotherapy reduces α-synuclein propagation in the axon and degeneration in a combined viral vector and transgenic model of synucleinopathyQ37586721
First-in-human assessment of PRX002, an anti-α-synuclein monoclonal antibody, in healthy volunteersQ37664213
The propagation of prion-like protein inclusions in neurodegenerative diseasesQ37759499
Vaccination for Parkinson's diseaseQ37968018
The amyloid state of proteins in human diseasesQ37994283
Immunotherapy for neurodegenerative diseases: focus on α-synucleinopathiesQ38079317
Cell-to-cell transmission of pathogenic proteins in neurodegenerative diseasesQ38185934
Active immunization therapies for Parkinson's disease and multiple system atrophyQ38564102
Cellular Uptake of α-Synuclein Oligomer-Selective Antibodies is Enhanced by the Extracellular Presence of α-Synuclein and Mediated via Fcγ ReceptorsQ38787483
Cellular response of human neuroblastoma cells to α-synuclein fibrils, the main constituent of Lewy bodiesQ38827784
Like prions: the propagation of aggregated tau and α-synuclein in neurodegeneration.Q38961743
α-Synuclein vaccination prevents the accumulation of parkinson disease-like pathologic inclusions in striatum in association with regulatory T cell recruitment in a rat modelQ39138968
Immunotherapy targeting α-synuclein protofibrils reduced pathology in (Thy-1)-h[A30P] α-synuclein miceQ39188281
Anti-amyloid beta protein antibody passage across the blood-brain barrier in the SAMP8 mouse model of Alzheimer's disease: an age-related selective uptake with reversal of learning impairmentQ40117145
T cells from patients with Parkinson's disease recognize α-synuclein peptidesQ40163812
A precipitating role for truncated alpha-synuclein and the proteasome in alpha-synuclein aggregation: implications for pathogenesis of Parkinson diseaseQ40433173
MHCII is required for α-synuclein-induced activation of microglia, CD4 T cell proliferation, and dopaminergic neurodegenerationQ41894807
Immunohistochemical and biochemical studies demonstrate a distinct profile of alpha-synuclein permutations in multiple system atrophyQ42493792
Effects of alpha-synuclein immunization in a mouse model of Parkinson's diseaseQ44769508
Differential effects of immunotherapy with antibodies targeting α-synuclein oligomers and fibrils in a transgenic model of synucleinopathyQ46124320
Phosphorylation of Ser-129 is the dominant pathological modification of alpha-synuclein in familial and sporadic Lewy body diseaseQ46593989
Role of alpha-synuclein carboxy-terminus on fibril formation in vitroQ47762431
100 years of Lewy pathologyQ48278741
Novel antibodies to synuclein show abundant striatal pathology in Lewy body diseases.Q48494226
Accumulation of tubular structures in oligodendroglial and neuronal cells as the basic alteration in multiple system atrophyQ48544275
Neuronal alpha-synucleinopathy with severe movement disorder in mice expressing A53T human alpha-synuclein.Q48581887
Proteolysis of α-synuclein fibrils in the lysosomal pathway limits induction of inclusion pathology.Q48619578
P275copyright licenseCreative Commons Attribution 4.0 InternationalQ20007257
P6216copyright statuscopyrightedQ50423863
P433issue9
P407language of work or nameEnglishQ1860
P921main subjectSynucleinQ24767155
P304page(s)e0184731
P577publication date2017-09-14
P1433published inPLOS OneQ564954
P1476titleA novel panel of α-synuclein antibodies reveal distinctive staining profiles in synucleinopathies
P478volume12

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cites work (P2860)
Q64266885Comparative analyses of the in vivo induction and transmission of α-synuclein pathology in transgenic mice by MSA brain lysate and recombinant α-synuclein fibrils
Q55003043Differential induction of mutant SOD1 misfolding and aggregation by tau and α-synuclein pathology.
Q91429961Dissecting α-synuclein inclusion pathology diversity in multiple system atrophy: implications for the prion-like transmission hypothesis
Q57458019Physiological carboxy-truncation of α-synuclein potentiates the prion-like formation of pathological inclusions
Q90275269Prominent amyloid plaque pathology and cerebral amyloid angiopathy in APP V717I (London) carrier - phenotypic variability in autosomal dominant Alzheimer's disease
Q58700515Skin α-synuclein deposits differ in clinical variants of synucleinopathy: an in vivo study
Q93060745Unique α-synuclein pathology within the amygdala in Lewy body dementia: implications for disease initiation and progression

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