Novel one-step immunoassays to quantify α-synuclein: applications for biomarker development and high-throughput screening.
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Detection and Quantification of the Fragile X Mental Retardation Protein 1 (FMRP)Value of cerebrospinal fluid α-synuclein species as biomarker in Parkinson's diagnosis and prognosisModelling idiopathic Parkinson disease as a complex illness can inform incidence rate in healthy adults: the PREDIGT scoreTowards translational therapies for multiple system atrophyEbolavirus nucleoprotein C-termini potently attract single domain antibodies enabling monoclonal affinity reagent sandwich assay (MARSA) formulation.Cerebellar soluble mutant ataxin-3 level decreases during disease progression in Spinocerebellar Ataxia Type 3 miceA generic method for design of oligomer-specific antibodies.A novel multiplex assay for simultaneous quantification of total and S129 phosphorylated human alpha-synuclein.Alpha-synuclein post-translational modifications as potential biomarkers for Parkinson disease and other synucleinopathies.Toxic species in amyloid disorders: Oligomers or mature fibrils.The utility of α-synuclein as biofluid marker in neurodegenerative diseases: a systematic review of the literature.Biological confounders for the values of cerebrospinal fluid proteins in Parkinson's disease and related disorders.Validation of electrochemiluminescence assays for highly sensitive and reproducible quantification of α-synuclein in cerebrospinal fluid.Discovery, validation and optimization of cerebrospinal fluid biomarkers for use in Parkinson's disease.A quantitative homogeneous assay for fragile X mental retardation 1 protein.AlphaLISA detection of alpha-synuclein in the cerebrospinal fluid and its potential application in Parkinson's disease diagnosis.Non-motor parkinsonian pathology in aging A53T α-synuclein mice is associated with progressive synucleinopathy and altered enzymatic function.An alpha-synuclein MRM assay with diagnostic potential for Parkinson's disease and monitoring disease progression.Extracellular α-synuclein alters synaptic transmission in brain neurons by perforating the neuronal plasma membrane.Are We Ready for Detecting α-Synuclein Prone to Aggregation in Patients? The Case of "Protein-Misfolding Cyclic Amplification" and "Real-Time Quaking-Induced Conversion" as Diagnostic Tools.
P2860
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P2860
Novel one-step immunoassays to quantify α-synuclein: applications for biomarker development and high-throughput screening.
description
2012 nî lūn-bûn
@nan
2012 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Novel one-step immunoassays to ...... and high-throughput screening.
@ast
Novel one-step immunoassays to ...... and high-throughput screening.
@en
Novel one-step immunoassays to ...... and high-throughput screening.
@nl
type
label
Novel one-step immunoassays to ...... and high-throughput screening.
@ast
Novel one-step immunoassays to ...... and high-throughput screening.
@en
Novel one-step immunoassays to ...... and high-throughput screening.
@nl
prefLabel
Novel one-step immunoassays to ...... and high-throughput screening.
@ast
Novel one-step immunoassays to ...... and high-throughput screening.
@en
Novel one-step immunoassays to ...... and high-throughput screening.
@nl
P2093
P2860
P356
P1476
Novel one-step immunoassays to ...... and high-throughput screening.
@en
P2093
Andreas Weiss
David Marcellin
Derya R Shimshek
Gregor P Lotz
Michael Bidinosti
Michael G Schlossmacher
Tatjana Schweizer
P2860
P304
33691-33705
P356
10.1074/JBC.M112.379792
P407
P577
2012-07-27T00:00:00Z