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Tau hyperphosphorylation on T217 in cerebrospinal fluid is specifically associated to amyloid-β pathology
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1001/archgenpsychiatry.2011.155openalex-snapshot
Cerebrospinal Fluid Levels ofβ-Amyloid 1-42, but Not of Tau, Are Fully Changed Already 5 to 10 Years Before the Onset of Alzheimer Dementia
inferredcites →https://doi.org/10.1001/archneur.58.11.1803openalex-snapshot
Clinical and Pathological Diagnosis of Frontotemporal Dementia
inferredcites →https://doi.org/10.1001/archneur.64.3.431openalex-snapshot
Molecular Imaging With Pittsburgh Compound B Confirmed at Autopsy
inferredcites →https://doi.org/10.1001/archneur.64.3.noc60123openalex-snapshot
Cerebrospinal Fluid tau/β-Amyloid42 Ratio as a Prediction of Cognitive Decline in Nondemented Older Adults
inferredcites →https://doi.org/10.1002/ana.21559openalex-snapshot
Decreased cerebrospinal fluid Aβ 42 correlates with brain atrophy in cognitively normal elderly
inferredcites →https://doi.org/10.1002/ana.24454openalex-snapshot
Age and amyloid effects on human central nervous system amyloid‐beta kinetics
inferredcites →https://doi.org/10.1002/j.1460-2075.1992.tb05204.xopenalex-snapshot
The switch of tau protein to an Alzheimer‐like state includes the phosphorylation of two serine‐proline motifs upstream of the microtubule binding region.
inferredcites →https://doi.org/10.1007/s00401-012-0943-2openalex-snapshot
Early AD pathology in a [C-11]PiB-negative case: a PiB-amyloid imaging, biochemical, and immunohistochemical study
inferredcites →https://doi.org/10.1007/s00415-013-7160-3openalex-snapshot
Impact of cerebro-spinal fluid biomarkers of Alzheimer’s disease in clinical practice: a multicentric study
inferredcites →https://doi.org/10.1016/0304-3940(95)11484-eopenalex-snapshot
Monoclonal antibody AT8 recognises tau protein phosphorylated at both serine 202 and threonine 205
inferredcites →https://doi.org/10.1016/j.bbrc.2007.04.187openalex-snapshot
Epitope mapping of mAbs AT8 and Tau5 directed against hyperphosphorylated regions of the human tau protein
inferredcites →https://doi.org/10.1016/j.brainres.2010.08.022openalex-snapshot
Correlations between soluble α/β forms of amyloid precursor protein and Aβ38, 40, and 42 in human cerebrospinal fluid
inferredcites →https://doi.org/10.1016/j.expneurol.2009.09.011openalex-snapshot
GSK3: A possible link between beta amyloid peptide and tau protein
inferredcites →https://doi.org/10.1016/j.jalz.2011.03.005openalex-snapshot
The diagnosis of dementia due to Alzheimer's disease: Recommendations from the National Institute on Aging‐Alzheimer's Association workgroups on diagnostic guidelines for Alzheimer's disease
inferredcites →https://doi.org/10.1016/j.jalz.2014.04.517openalex-snapshot
The influence of cerebrospinal fluid (CSF) biomarkers on clinical dementia evaluations
inferredcites →https://doi.org/10.1016/j.jalz.2014.05.1753openalex-snapshot
Diagnostic impact of CSF biomarkers for Alzheimer's disease in a tertiary memory clinic
inferredcites →https://doi.org/10.1016/j.jalz.2014.12.006openalex-snapshot
CSF biomarkers for the differential diagnosis of Alzheimer's disease: A large‐scale international multicenter study
inferredcites →https://doi.org/10.1016/s1474-4422(13)70194-7openalex-snapshot
Preclinical Alzheimer's disease and its outcome: a longitudinal cohort study
inferredcites →https://doi.org/10.1021/acs.jproteome.5b01001openalex-snapshot
Tau Protein Quantification in Human Cerebrospinal Fluid by Targeted Mass Spectrometry at High Sequence Coverage Provides Insights into Its Primary Structure Heterogeneity
inferredcites →https://doi.org/10.1038/nm.3810openalex-snapshot
Understanding Biomarkers of Neurodegeneration: Ultrasensitive detection techniques pave the way for mechanistic understanding
inferredcites →https://doi.org/10.1046/j.1471-4159.1997.69041548.xopenalex-snapshot
Tau Released from Paired Helical Filaments with Formic Acid or Guanidine Is Susceptible to Calpain‐Mediated Proteolysis
inferredcites →https://doi.org/10.1056/nejmoa1202753openalex-snapshot
Clinical and Biomarker Changes in Dominantly Inherited Alzheimer's Disease
inferredcites →https://doi.org/10.1073/pnas.1017033108openalex-snapshot
Soluble amyloid β-protein dimers isolated from Alzheimer cortex directly induce Tau hyperphosphorylation and neuritic degeneration
inferredcites →https://doi.org/10.1074/jbc.m703269200openalex-snapshot
Novel Phosphorylation Sites in Tau from Alzheimer Brain Support a Role for Casein Kinase 1 in Disease Pathogenesis
inferredcites →https://doi.org/10.1074/mcp.m900254-mcp200openalex-snapshot
An Automated and Multiplexed Method for High Throughput Peptide Immunoaffinity Enrichment and Multiple Reaction Monitoring Mass Spectrometry-based Quantification of Protein Biomarkers
inferredcites →https://doi.org/10.1093/ageing/30.1.53openalex-snapshot
Health and ill-health in the older population in England and Wales
inferredcites →https://doi.org/10.1093/jnen/61.6.557openalex-snapshot
Colocalization and Fluorescence Resonance Energy Transfer between cdk5 and AT8 Suggests a Close Association in Pre-Neurofibrillary Tangles and Neurofibrillary Tangles
inferredcites →https://doi.org/10.1111/j.1471-4159.1993.tb09823.xopenalex-snapshot
Detection of Proteins in Normal and Alzheimer's Disease Cerebrospinal Fluid with a Sensitive Sandwich Enzyme‐Linked Immunosorbent Assay
inferredcites →https://doi.org/10.1212/wnl.0b013e31823ed0f0openalex-snapshot
Cerebrospinal fluid markers for differential dementia diagnosis in a large memory clinic cohort
inferredcites →https://doi.org/10.1212/wnl.44.5.964openalex-snapshot
The Mattis Dementia Rating Scale
inferredcites →https://doi.org/10.1212/wnl.47.5.1113openalex-snapshot
Consensus guidelines for the clinical and pathologic diagnosis of dementia with Lewy bodies (DLB)
inferredcites →https://doi.org/10.1212/wnl.53.4.795openalex-snapshot
Pathologic heterogeneity in clinically diagnosed corticobasal degeneration
inferredcites →https://doi.org/10.1212/wnl.54.4.827openalex-snapshot
Memory impairment on free and cued selective reminding predicts dementia
inferredcites →https://doi.org/10.1385/1-59259-874-9:175openalex-snapshot
Intrinsic Fluorescent Detection of Tau Conformation and Aggregation
inferredcites →https://doi.org/10.1515/cclm.2011.086openalex-snapshot
Tau and p-tau as CSF biomarkers in dementia: a meta-analysis
inferredcites →https://doi.org/10.1586/14789450.5.2.207openalex-snapshot
Biochemistry of Tau in Alzheimer’s disease and related neurological disorders
inferredcites →https://doi.org/10.3233/jad-121549openalex-snapshot
Impact of the 2008–2012 French Alzheimer Plan on the Use of Cerebrospinal Fluid Biomarkers in Research Memory Center: The PLM Study
inferredcites →https://doi.org/10.3233/jad-150962openalex-snapshot
Differential Mass Spectrometry Profiles of Tau Protein in the Cerebrospinal Fluid of Patients with Alzheimer’s Disease, Progressive Supranuclear Palsy, and Dementia with Lewy Bodies
inferredcites →https://doi.org/10.3233/jad-2006-9s347openalex-snapshot
Consensus guidelines for the clinical and pathologic diagnosis of dementia with Lewy bodies (DLB): Report of the Consortium on DLB International Workshop
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/advs.202514783openalex-snapshot
Autophagy Activators Normalize Aberrant Tau Proteostasis and Rescue Synapses in Human Familial Alzheimer's Disease iPSC‐Derived Cortical Organoids
inferred← citeshttps://doi.org/10.1002/alz.12749openalex-snapshot
Phosphorylated tau sites that are elevated in Alzheimer's disease fluid biomarkers are visualized in early neurofibrillary tangle maturity levels in the post mortem brain
inferred← citeshttps://doi.org/10.1002/dad2.12204openalex-snapshot
Development and validation of a high‐sensitivity assay for measuring p217+tau in plasma
inferred← citeshttps://doi.org/10.1007/978-3-031-80849-4_1openalex-snapshot
Fluid and Imaging Markers of Amyloid Pathology
inferred← citeshttps://doi.org/10.1016/j.chroma.2021.462299openalex-snapshot
Development of immunoprecipitation – two-dimensional liquid chromatography – mass spectrometry methodology as biomarker read-out to quantify phosphorylated tau in cerebrospinal fluid from Alzheimer disease patients
inferred← citeshttps://doi.org/10.1016/j.neuron.2018.02.015openalex-snapshot
Tau Kinetics in Neurons and the Human Central Nervous System
inferred← citeshttps://doi.org/10.1021/acschemneuro.5c00301openalex-snapshot
Development of New Blood Immunoassay and Biomarkers for Tau in the Diagnosis of Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1038/s41467-020-15436-0openalex-snapshot
Cerebrospinal fluid p-tau217 performs better than p-tau181 as a biomarker of Alzheimer’s disease
inferred← citeshttps://doi.org/10.1038/s41591-020-0755-1openalex-snapshot
Plasma P-tau181 in Alzheimer’s disease: relationship to other biomarkers, differential diagnosis, neuropathology and longitudinal progression to Alzheimer’s dementia
inferred← citeshttps://doi.org/10.1084/jem.20200861openalex-snapshot
Blood plasma phosphorylated-tau isoforms track CNS change in Alzheimer’s disease
inferred← citeshttps://doi.org/10.1101/2025.06.17.660179openalex-snapshot
Tau-seed interactome analysis reveals distinct functional signatures in Alzheimer’s disease across model systems
inferred← citeshttps://doi.org/10.1212/wnl.0000000000010814openalex-snapshot
Evaluation of a novel immunoassay to detect p-tau Thr217 in the CSF to distinguish Alzheimer disease from other dementias
inferred← citeshttps://doi.org/10.1212/wnl.0000000000012727openalex-snapshot
Comparing the Clinical Utility and Diagnostic Performance of CSF P-Tau181, P-Tau217, and P-Tau231 Assays
inferred← citeshttps://doi.org/10.3233/jad-210677openalex-snapshot
Site-Specific Cerebrospinal Fluid Tau Hyperphosphorylation in Response to Alzheimer’s Disease Brain Pathology: Not All Tau Phospho-Sites are Hyperphosphorylated
inferred← citeshttps://doi.org/10.3390/cells11081279openalex-snapshot
Mass Spectrometry for Neurobiomarker Discovery: The Relevance of Post-Translational Modifications
inferred← citeshttps://doi.org/10.3410/f.732876856.793545483openalex-snapshot
Faculty Opinions recommendation of Tau kinetics in neurons and the human central nervous system.
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