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Cerebral Microvascular Accumulation of Tau Oligomers in Alzheimer’s Disease and Related Tauopathies

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1 of the 45 references listed on this page is in the Retraction Watch database as retracted (export 2026-10-28): 10.1038/nature04533 (notice 2024-06-24).

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/ana.20493openalex-snapshot
Cerebral hypoperfusion and clinical onset of dementia: The Rotterdam study
inferredcites →https://doi.org/10.1002/ana.23845openalex-snapshot
Pathogenesis of cerebral microbleeds: In vivo imaging of amyloid and subcortical ischemic small vessel disease in 226 individuals with cognitive impairment
inferredcites →https://doi.org/10.1007/s10571-016-0334-7openalex-snapshot
The Science of Vascular Contributions to Cognitive Impairment and Dementia (VCID): A Framework for Advancing Research Priorities in the Cerebrovascular Biology of Cognitive Decline
inferredcites →https://doi.org/10.1016/j.biopsych.2014.12.019openalex-snapshot
Pathological Interface Between Oligomeric Alpha-Synuclein and Tau in Synucleinopathies
inferredcites →https://doi.org/10.1016/j.jalz.2014.10.008openalex-snapshot
Vascular contributions to cognitive impairment and dementia including Alzheimer's disease
inferredcites →https://doi.org/10.1016/j.nbd.2014.08.008openalex-snapshot
Amyloid-β oligomers as a template for secondary amyloidosis in Alzheimer's disease
inferredcites →https://doi.org/10.1016/j.neurobiolaging.2015.07.016openalex-snapshot
Matrix metalloproteinase 9–mediated intracerebral hemorrhage induced by cerebral amyloid angiopathy
inferredcites →https://doi.org/10.1016/j.neuroimage.2011.06.070openalex-snapshot
Impaired cerebral vasoreactivity to CO2 in Alzheimer's disease using BOLD fMRI
inferredcites →https://doi.org/10.1016/s0969-9961(03)00079-2openalex-snapshot
Dendritic spine loss in the hippocampus of young PDAPP and Tg2576 mice and its prevention by the ApoE2 genotype
inferredcites →https://doi.org/10.1021/bi061359oopenalex-snapshot
Granular Tau Oligomers as Intermediates of Tau Filaments
inferredcites →https://doi.org/10.1021/bi1016233openalex-snapshot
Preparation and Characterization of Neurotoxic Tau Oligomers
inferredcites →https://doi.org/10.1021/cn500143nopenalex-snapshot
Advances in Therapeutics for Neurodegenerative Tauopathies: Moving toward the Specific Targeting of the Most Toxic Tau Species
inferredcites →https://doi.org/10.1038/jcbfm.2013.82openalex-snapshot
Chronic Rapamycin Restores Brain Vascular Integrity and Function Through NO Synthase Activation and Improves Memory in Symptomatic Mice Modeling Alzheimer’s Disease
inferredcites →https://doi.org/10.1038/nature04533openalex-snapshot
RETRACTED ARTICLE: A specific amyloid-β protein assembly in the brain impairs memory
inferredcites →https://doi.org/10.1038/ncomms11934openalex-snapshot
Early role of vascular dysregulation on late-onset Alzheimer’s disease based on multifactorial data-driven analysis
inferredcites →https://doi.org/10.1038/nn.4328openalex-snapshot
Neuronal activity enhances tau propagation and tau pathology in vivo
inferredcites →https://doi.org/10.1038/nrn1387openalex-snapshot
Neurovascular regulation in the normal brain and in Alzheimer's disease
inferredcites →https://doi.org/10.1038/nrn3114openalex-snapshot
Neurovascular pathways to neurodegeneration in Alzheimer's disease and other disorders
inferredcites →https://doi.org/10.1038/srep00700openalex-snapshot
Alzheimer brain-derived tau oligomers propagate pathology from endogenous tau
inferredcites →https://doi.org/10.1073/pnas.092136199openalex-snapshot
Tau is essential to β-amyloid-induced neurotoxicity
inferredcites →https://doi.org/10.1073/pnas.83.13.4913openalex-snapshot
Abnormal phosphorylation of the microtubule-associated protein tau (tau) in Alzheimer cytoskeletal pathology.
inferredcites →https://doi.org/10.1074/jbc.m112.396176openalex-snapshot
Tau Oligomers Impair Artificial Membrane Integrity and Cellular Viability
inferredcites →https://doi.org/10.1093/brain/awv107openalex-snapshot
The role of tau in the pathological process and clinical expression of Huntington’s disease
inferredcites →https://doi.org/10.1096/fj.09-139584openalex-snapshot
Differential activation of mitochondrial apoptotic pathways by vasculotropic amyloid‐β variants in cells composing the cerebral vessel walls
inferredcites →https://doi.org/10.1096/fj.11-199851openalex-snapshot
Identification of oligomers at early stages of tau aggregation in Alzheimer's disease
inferredcites →https://doi.org/10.1097/00005072-199709000-00002openalex-snapshot
APPSW Transgenic Mice Develop Age-related Aβ Deposits and Neuropil Abnormalities, but no Neuronal Loss in CA1
inferredcites →https://doi.org/10.1111/ejn.12507openalex-snapshot
Tau phosphorylation and tau mislocalization mediate soluble Aβ oligomer‐induced AMPA glutamate receptor signaling deficits
inferredcites →https://doi.org/10.1111/j.1365-2990.2005.00663.xopenalex-snapshot
Relationship of neurofibrillary pathology to cerebral amyloid angiopathy in Alzheimer's disease
inferredcites →https://doi.org/10.1111/j.1365-2990.2010.01137.xopenalex-snapshot
Review: Sporadic cerebral amyloid angiopathy
inferredcites →https://doi.org/10.1126/science.1141736openalex-snapshot
Reducing Endogenous Tau Ameliorates Amyloid ß-Induced Deficits in an Alzheimer's Disease Mouse Model
inferredcites →https://doi.org/10.1126/science.274.5284.99openalex-snapshot
Correlative Memory Deficits, Aβ Elevation, and Amyloid Plaques in Transgenic Mice
inferredcites →https://doi.org/10.1155/2013/260787openalex-snapshot
Trimeric Tau Is Toxic to Human Neuronal Cells at Low Nanomolar Concentrations
inferredcites →https://doi.org/10.1159/000332821openalex-snapshot
Insights into Caspase-Mediated Apoptotic Pathways Induced by Amyloid-β in Cerebral Microvascular Endothelial Cells
inferredcites →https://doi.org/10.1159/000337230openalex-snapshot
Amyloid Oligomers Exacerbate Tau Pathology in a Mouse Model of Tauopathy
inferredcites →https://doi.org/10.1161/str.0b013e3182299496openalex-snapshot
Vascular Contributions to Cognitive Impairment and Dementia
inferredcites →https://doi.org/10.1186/1750-1326-6-39openalex-snapshot
Tau oligomers impair memory and induce synaptic and mitochondrial dysfunction in wild-type mice
inferredcites →https://doi.org/10.1186/2051-5960-2-73openalex-snapshot
Characterization of tau oligomeric seeds in progressive supranuclear palsy
inferredcites →https://doi.org/10.1186/s40478-015-0186-2openalex-snapshot
Tau depletion prevents progressive blood-brain barrier damage in a mouse model of tauopathy
inferredcites →https://doi.org/10.1215/s1152851705000232openalex-snapshot
The role of pericytes in blood-vessel formation and maintenance
inferredcites →https://doi.org/10.1523/jneurosci.3192-13.2014openalex-snapshot
Passive Immunization with Tau Oligomer Monoclonal Antibody Reverses Tauopathy Phenotypes without Affecting Hyperphosphorylated Neurofibrillary Tangles
inferredcites →https://doi.org/10.2174/156720511796717177openalex-snapshot
Tau Oligomers as Potential Targets for Immunotherapy for Alzheimers Disease and Tauopathies
inferredcites →https://doi.org/10.3233/jad-132477openalex-snapshot
Specific Targeting of Tau Oligomers in Htau Mice Prevents Cognitive Impairment and Tau Toxicity Following Injection with Brain-Derived Tau Oligomeric Seeds
inferredcites →https://doi.org/10.3233/jad-151130openalex-snapshot
Cerebral Microbleeds and Cerebrovascular Reactivity in the General Population: The EDAN Study
inferredcites →https://doi.org/10.3389/fnagi.2014.00290openalex-snapshot
New Therapeutic Approaches for Alzheimer’s Disease and Cerebral Amyloid Angiopathy
inferredcites →https://doi.org/10.3389/fneur.2013.00093openalex-snapshot
Formation and Propagation of Tau Oligomeric Seeds

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Nanotherapy for Early Dementia: Targeting Senile Endothelium
inferred← citeshttps://doi.org/10.2139/ssrn.3041744openalex-extracted
Nanotherapy for Alzheimer's Disease and Vascular Dementia: Targeting Senile Endothelium
inferred← citeshttps://doi.org/10.1002/alz.13490openalex-snapshot
Senescence, brain inflammation, and oligomeric tau drive cognitive decline in Alzheimer's disease: Evidence from clinical and preclinical studies
inferred← citeshttps://doi.org/10.1002/alz.13896openalex-snapshot
Entorhinal vessel density correlates with phosphorylated tau and TDP‐43 pathology
inferred← citeshttps://doi.org/10.1002/alz.14618openalex-snapshot
The interaction between dysfunction of vasculature and tauopathy in Alzheimer's disease and related dementias
inferred← citeshttps://doi.org/10.1002/alz.70077openalex-snapshot
Fibrillar tau alters cerebral endothelial cell metabolism, vascular inflammatory activation, and barrier function in vitro and in vivo
inferred← citeshttps://doi.org/10.1002/alz.70957openalex-snapshot
CSF markers of vascular injury correlate with tau and cognitive decline in early Alzheimer's disease
inferred← citeshttps://doi.org/10.1002/dad2.12070openalex-snapshot
Peri‐arterial pathways for clearance of α‐Synuclein and tau from the brain: Implications for the pathogenesis of dementias and for immunotherapy
inferred← citeshttps://doi.org/10.1002/ibra.12154openalex-snapshot
Endothelial cellular senescence and tau accumulation: An interplay full of opportunities?
inferred← citeshttps://doi.org/10.1002/iub.2324openalex-snapshot
Multifarious roles of mTOR signaling in cognitive aging and cerebrovascular dysfunction of Alzheimer's disease
inferred← citeshttps://doi.org/10.1007/978-1-0716-2597-2_14openalex-snapshot
A Validated Method to Prepare Stable Tau Oligomers
inferred← citeshttps://doi.org/10.1007/978-1-0716-3629-9_9openalex-snapshot
Tau Oligomers as Pathogenic Seeds: Preparation, Characterization, and Propagation In Vitro and In Vivo
inferred← citeshttps://doi.org/10.1007/978-3-031-72156-4_6openalex-snapshot
Imaging Alzheimer’s Retinopathy
inferred← citeshttps://doi.org/10.1007/s00401-024-02696-zopenalex-snapshot
The contribution of β-amyloid, Tau and α-synuclein to blood–brain barrier damage in neurodegenerative disorders
inferred← citeshttps://doi.org/10.1007/s11357-017-9991-9openalex-snapshot
Hypertension impairs neurovascular coupling and promotes microvascular injury: role in exacerbation of Alzheimer’s disease
inferred← citeshttps://doi.org/10.1007/s11357-018-0044-9openalex-snapshot
Repeated Valsalva maneuvers promote symptomatic manifestations of cerebral microhemorrhages: implications for the pathogenesis of vascular cognitive impairment in older adults
inferred← citeshttps://doi.org/10.1007/s11357-020-00177-1openalex-snapshot
Single-cell RNA sequencing identifies senescent cerebromicrovascular endothelial cells in the aged mouse brain
inferred← citeshttps://doi.org/10.1007/s11357-023-00913-3openalex-snapshot
Exposome and unhealthy aging: environmental drivers from air pollution to occupational exposures
inferred← citeshttps://doi.org/10.1007/s11357-025-01654-1openalex-snapshot
Clonal hematopoiesis of indeterminate potential (CHIP) in cerebromicrovascular aging: implications for vascular contributions to cognitive impairment and dementia (VCID)
inferred← citeshttps://doi.org/10.1007/s11357-025-01694-7openalex-snapshot
Amyloid neuropathy, tauopathy, decreased cholinergic and dopaminergic neurons, long-term memory and motor deficits, and sleep disturbance in motopsin deficient mice
inferred← citeshttps://doi.org/10.1007/s12035-020-01913-6openalex-snapshot
Polymorphic α-Synuclein Strains Modified by Dopamine and Docosahexaenoic Acid Interact Differentially with Tau Protein
inferred← citeshttps://doi.org/10.1007/s12035-020-02061-7openalex-snapshot
Tau Pathology Triggered by Spinal Cord Injury Can Play a Critical Role in the Neurotrauma Development
inferred← citeshttps://doi.org/10.1007/s12035-024-04138-zopenalex-snapshot
Oligomeric Amyloid-β and Tau Alter Cell Adhesion Properties and Induce Inflammatory Responses in Cerebral Endothelial Cells Through the RhoA/ROCK Pathway
inferred← citeshttps://doi.org/10.1007/s12975-017-0570-2openalex-snapshot
Cerebral Hypoperfusion and Other Shared Brain Pathologies in Ischemic Stroke and Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1016/j.bpj.2026.07.003openalex-snapshot
Tau protein differentially affects Piezo1 and Kir2.1 channels in brain capillary endothelial cells
inferred← citeshttps://doi.org/10.1016/j.brainresbull.2026.111872openalex-snapshot
Characterisation of a patient-derived iPSC-based model for studying the blood-brain barrier in Alzheimer’s disease
inferred← citeshttps://doi.org/10.1016/j.cis.2017.12.002openalex-snapshot
Nanotherapy for Alzheimer's disease and vascular dementia: Targeting senile endothelium
inferred← citeshttps://doi.org/10.1016/j.ebiom.2025.105694openalex-snapshot
Dissection of blood–brain barrier dysfunction through CSF PDGFRβ and amyloid, tau, neuroinflammation, and synaptic CSF biomarkers in neurodegenerative disorders
inferred← citeshttps://doi.org/10.1016/j.exer.2021.108879openalex-snapshot
Age dependence of retinal vascular plexus attenuation in the triple transgenic mouse model of Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2024.05.044openalex-snapshot
Oligomeric Tau-induced oxidative damage and functional alterations in cerebral endothelial cells: Role of RhoA/ROCK signaling pathway
inferred← citeshttps://doi.org/10.1016/j.jare.2021.07.001openalex-snapshot
CRISPR/Cas9 gene editing: New hope for Alzheimer's disease therapeutics
inferred← citeshttps://doi.org/10.1016/j.jconrel.2022.07.026openalex-snapshot
Ultrasound-mediated delivery of novel tau-specific monoclonal antibody enhances brain uptake but not therapeutic efficacy
inferred← citeshttps://doi.org/10.1016/j.jff.2021.104463openalex-snapshot
Dietary intervention with edible medicinal plants and derived products for prevention of Alzheimer's disease: A compendium of time-tested strategy
inferred← citeshttps://doi.org/10.1016/j.lfs.2023.122257openalex-snapshot
Mitochondrial dysfunction and neurological disorders: A narrative review and treatment overview
inferred← citeshttps://doi.org/10.1016/j.lfs.2025.123756openalex-snapshot
A targeted approach: Gene and RNA editing for neurodegenerative disease treatment
inferred← citeshttps://doi.org/10.1016/j.nbas.2024.100110openalex-snapshot
Targeted brain-specific tauopathy compromises peripheral skeletal muscle integrity and function
inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2018.07.022openalex-snapshot
Beta-sheet assembly of Tau and neurodegeneration in Drosophila melanogaster
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2024.05.042openalex-snapshot
Influence of Tau on Neurotoxicity and Cerebral Vasculature Impairment Associated with Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2022.108119openalex-snapshot
Blood-brain barrier leakage in Alzheimer’s disease: From discovery to clinical relevance
inferred← citeshttps://doi.org/10.1016/j.preteyeres.2024.101273openalex-snapshot
Alzheimer's disease pathophysiology in the Retina
inferred← citeshttps://doi.org/10.1021/acs.molpharmaceut.8b00870openalex-snapshot
Transferrin Receptor-Mediated Uptake at the Blood–Brain Barrier Is Not Impaired by Alzheimer’s Disease Neuropathology
inferred← citeshttps://doi.org/10.1021/acschemneuro.5c00122openalex-snapshot
Tau Oligomers in Alzheimer’s Disease: Modulation Effect of Osmolytes on Amplified Brain-Derived Tau Oligomers
inferred← citeshttps://doi.org/10.1038/s41467-023-37840-yopenalex-snapshot
Soluble pathogenic tau enters brain vascular endothelial cells and drives cellular senescence and brain microvascular dysfunction in a mouse model of tauopathy
inferred← citeshttps://doi.org/10.1038/s41598-019-50870-1openalex-snapshot
Three-Dimensional Microscopy by Milling with Ultraviolet Excitation
inferred← citeshttps://doi.org/10.1039/c8cs00034dopenalex-snapshot
Effects of in vivo conditions on amyloid aggregation
inferred← citeshttps://doi.org/10.1073/pnas.1710329115openalex-snapshot
Tau induces blood vessel abnormalities and angiogenesis-related gene expression in P301L transgenic mice and human Alzheimer’s disease
inferred← citeshttps://doi.org/10.1074/jbc.ra120.014630openalex-snapshot
Modulating disease-relevant tau oligomeric strains by small molecules
inferred← citeshttps://doi.org/10.1080/00325481.2019.1657776openalex-snapshot
Alzheimer’s dementia: pathogenesis and impact of cardiovascular risk factors on cognitive decline
inferred← citeshttps://doi.org/10.1080/10641963.2020.1764014openalex-snapshot
CBF regulation in hypertension and Alzheimer’s disease
inferred← citeshttps://doi.org/10.1080/17435889.2026.2629031openalex-snapshot
The application of CRISPR-Cas9 system in brain diseases
inferred← citeshttps://doi.org/10.1093/brain/awae156openalex-snapshot
The vascular contribution of apolipoprotein E to Alzheimer’s disease
inferred← citeshttps://doi.org/10.1093/oso/9780190634230.003.0014openalex-snapshot
Hemodynamics in Alzheimer’s Disease and Vascular Cognitive Impairment and Dementia
inferred← citeshttps://doi.org/10.1096/fj.202000051rrropenalex-snapshot
Virulent Pseudomonas aeruginosa infection converts antimicrobial amyloids into cytotoxic prions
inferred← citeshttps://doi.org/10.1101/2023.08.17.553682openalex-snapshot
Central and peripheral tau retention modulated by an anti-tau antibody
inferred← citeshttps://doi.org/10.1101/2023.10.24.563706openalex-snapshot
Increased tau expression in the APOE4 blood-brain barrier model is associated with reduced anti-tau therapeutic antibody delivery in vitro
inferred← citeshttps://doi.org/10.1111/jnc.15909openalex-snapshot
Function and regulation of cis P‐tau in the pathogenesis and treatment of conventional and nonconventional tauopathies
inferred← citeshttps://doi.org/10.1152/ajpheart.00514.2017openalex-snapshot
Age-related impairment of metabovascular coupling during cortical spreading depolarizations
inferred← citeshttps://doi.org/10.1159/000485381openalex-snapshot
A Perfect sTORm: The Role of the Mammalian Target of Rapamycin (mTOR) in Cerebrovascular Dysfunction of Alzheimer's Disease: A Mini-Review
inferred← citeshttps://doi.org/10.1177/0271678x211062274openalex-snapshot
Arterial spin labeling demonstrates preserved regional cerebral blood flow in the P301L mouse model of tauopathy
inferred← citeshttps://doi.org/10.1177/26331055251323292openalex-snapshot
Traumatic Brain Injury and Alzheimer’s Disease: A Shared Neurovascular Hypothesis
inferred← citeshttps://doi.org/10.1186/s12987-024-00581-1openalex-snapshot
Data-independent acquisition proteomic analysis of the brain microvasculature in Alzheimer’s disease identifies major pathways of dysfunction and upregulation of cytoprotective responses
inferred← citeshttps://doi.org/10.1186/s12987-024-00599-5openalex-snapshot
Role of the transcription factor NRF2 in maintaining the integrity of the Blood-Brain Barrier
inferred← citeshttps://doi.org/10.1186/s12987-025-00708-yopenalex-snapshot
Modeling neurovascular dysfunction in Alzheimer’s disease using an isogenic brain-chip model
inferred← citeshttps://doi.org/10.1186/s13024-025-00799-zopenalex-snapshot
Molecular and cellular characteristics of cerebrovascular cell types and their contribution to neurodegenerative diseases
inferred← citeshttps://doi.org/10.1186/s13041-025-01208-8openalex-snapshot
Divergent disruptive effects of soluble recombinant tau assemblies on synaptic plasticity in vivo
inferred← citeshttps://doi.org/10.1186/s13195-021-00935-zopenalex-snapshot
Intermittent hypoxia treatment alleviates memory impairment in the 6-month-old APPswe/PS1dE9 mice and reduces amyloid beta accumulation and inflammation in the brain
inferred← citeshttps://doi.org/10.1186/s13195-024-01392-0openalex-snapshot
A nonhuman primate model with Alzheimer’s disease-like pathology induced by hippocampal overexpression of human tau
inferred← citeshttps://doi.org/10.1186/s40478-019-0680-zopenalex-snapshot
Tau as a mediator of neurotoxicity associated to cerebral amyloid angiopathy
inferred← citeshttps://doi.org/10.1186/s40478-019-0754-yopenalex-snapshot
Intersection of pathological tau and microglia at the synapse
inferred← citeshttps://doi.org/10.1186/s40478-020-01014-4openalex-snapshot
Tau reduction in aged mice does not impact Microangiopathy
inferred← citeshttps://doi.org/10.1186/s40478-020-01076-4openalex-snapshot
Retinal capillary degeneration and blood-retinal barrier disruption in murine models of Alzheimer’s disease
inferred← citeshttps://doi.org/10.1364/boe.11.000099openalex-snapshot
Multiplex protein-specific microscopy with ultraviolet surface excitation
inferred← citeshttps://doi.org/10.1371/journal.pone.0266405openalex-snapshot
Analysis of modular gene co-expression networks reveals molecular pathways underlying Alzheimer’s disease and progressive supranuclear palsy
inferred← citeshttps://doi.org/10.1371/journal.pone.0328470openalex-snapshot
Peripheral administration of blood from tau transgenic animals exacerbates brain tau-associated pathology
inferred← citeshttps://doi.org/10.14336/ad.2019.0225openalex-snapshot
AmpliSeq Transcriptome of Laser Captured Neurons from Alzheimer Brain: Comparison of Single Cell Versus Neuron Pools
inferred← citeshttps://doi.org/10.1523/jneurosci.1230-20.2020openalex-snapshot
Associations between Vascular Function and Tau PET Are Associated with Global Cognition and Amyloid
inferred← citeshttps://doi.org/10.15761/gmc.1000111openalex-snapshot
Treating early dementia: Drug targeting and circumventing the blood-brain barrier
inferred← citeshttps://doi.org/10.21037/atm.2018.10.22openalex-snapshot
Cerebrovascular contribution to dementia development after traumatic brain injury: promises and problems
inferred← citeshttps://doi.org/10.21203/rs.3.rs-40746/v1openalex-snapshot
Mitochondrial perturbation drives tau oligomers pathology in Alzheimer’s disease
inferred← citeshttps://doi.org/10.2147/cia.s400527openalex-snapshot
Pathophysiological Association of Alzheimer’s Disease and Hypertension: A Clinical Concern for Elderly Population
inferred← citeshttps://doi.org/10.31219/osf.io/3vysuopenalex-snapshot
Nanotherapy for Early Dementia: Targeting Senile Dementia
inferred← citeshttps://doi.org/10.31219/osf.io/9afh2openalex-snapshot
Nanotherapy for Alzheimer's disease and vascular dementia: Targeting senile endothelium
inferred← citeshttps://doi.org/10.3233/jad-180451openalex-snapshot
Heme Oxygenase 1 Induces Tau Oligomer Formation and Synapse Aberrations in Hippocampal Neurons
inferred← citeshttps://doi.org/10.3233/jad-190764openalex-snapshot
Vascular Risk Factors and Alzheimer’s Disease: Blood-Brain Barrier Disruption, Metabolic Syndromes, and Molecular Links
inferred← citeshttps://doi.org/10.3233/jad-215323openalex-snapshot
Systematic Review on the Role of Lobar Cerebral Microbleeds in Cognition
inferred← citeshttps://doi.org/10.3233/jad-220838openalex-snapshot
Cerebrospinal Fluid Biomarkers and Amyloid-β Elimination from the Brain in Cerebral Amyloid Angiopathy-Related Inflammation
inferred← citeshttps://doi.org/10.3233/jad-230603openalex-snapshot
Immunotherapy in Alzheimer’s Disease: Current Status and Future Directions
inferred← citeshttps://doi.org/10.3389/fcell.2024.1343962openalex-snapshot
The role of the Pin1-cis P-tau axis in the development and treatment of vascular contribution to cognitive impairment and dementia and preeclampsia
inferred← citeshttps://doi.org/10.3389/fendo.2023.1087053openalex-snapshot
Cell non-autonomous regulation of cerebrovascular aging processes by the somatotropic axis
inferred← citeshttps://doi.org/10.3389/fimmu.2022.782434openalex-snapshot
Rapamycin Attenuated Zinc-Induced Tau Phosphorylation and Oxidative Stress in Rats: Involvement of Dual mTOR/p70S6K and Nrf2/HO-1 Pathways
inferred← citeshttps://doi.org/10.3389/fnagi.2018.00205openalex-snapshot
It’s Never Too Early or Too Late—End the Epidemic of Alzheimer’s by Preventing or Reversing Causation From Pre-birth to Death
inferred← citeshttps://doi.org/10.3389/fnagi.2021.772278openalex-snapshot
Carbonic Anhydrases as Potential Targets Against Neurovascular Unit Dysfunction in Alzheimer’s Disease and Stroke
inferred← citeshttps://doi.org/10.3389/fnagi.2025.1608631openalex-snapshot
Increased tau-induced inflammatory responses are associated with a greater degree of atherosclerosis in progressive supranuclear palsy
inferred← citeshttps://doi.org/10.3389/fnagi.2025.1632365openalex-snapshot
Exercise-mediated cerebrovascular repair in Alzheimer's disease: from pathophysiology to therapeutic precision
inferred← citeshttps://doi.org/10.3389/fnagi.2025.1671986openalex-snapshot
Cytosolic phospholipase A2 links tau pathology to insulin signaling impairment in Alzheimer’s disease
inferred← citeshttps://doi.org/10.3389/fnbeh.2018.00320openalex-snapshot
Vitamin B12 Levels in Methamphetamine Addicts
inferred← citeshttps://doi.org/10.3389/fncel.2019.00073openalex-snapshot
The Potential Role of the NLRP3 Inflammasome Activation as a Link Between Mitochondria ROS Generation and Neuroinflammation in Postoperative Cognitive Dysfunction
inferred← citeshttps://doi.org/10.3389/fneur.2020.573324openalex-snapshot
Impact of Tau on Neurovascular Pathology in Alzheimer's Disease
inferred← citeshttps://doi.org/10.3389/fneur.2020.575953openalex-snapshot
Cerebrovascular Senescence Is Associated With Tau Pathology in Alzheimer's Disease
inferred← citeshttps://doi.org/10.3389/fneur.2021.637176openalex-snapshot
Clinical Features Observed in General Practice Associated With the Subsequent Diagnosis of Progressive Supranuclear Palsy
inferred← citeshttps://doi.org/10.3389/fneur.2021.772836openalex-snapshot
Secondary Prevention of Dementia: Combining Risk Factors and Scalable Screening Technology
inferred← citeshttps://doi.org/10.3389/fneur.2024.1413023openalex-snapshot
Unveiling the hidden connection: the blood-brain barrier’s role in epilepsy
inferred← citeshttps://doi.org/10.3389/fnins.2021.731614openalex-snapshot
Retinal Vasculopathy in Alzheimer’s Disease
inferred← citeshttps://doi.org/10.3390/biom13050830openalex-snapshot
Microvascular Contributions to Alzheimer Disease Pathogenesis: Is Alzheimer Disease Primarily an Endotheliopathy?
inferred← citeshttps://doi.org/10.3390/biom14010003openalex-snapshot
Beta-Amyloid Enhances Vessel Formation in Organotypic Brain Slices Connected to Microcontact Prints
inferred← citeshttps://doi.org/10.3390/biomedicines10040742openalex-snapshot
Addressing Blood–Brain Barrier Impairment in Alzheimer’s Disease
inferred← citeshttps://doi.org/10.3390/biomedicines13010029openalex-snapshot
Novel Role of Pin1-Cis P-Tau-ApoE Axis in the Pathogenesis of Preeclampsia and Its Connection with Dementia
inferred← citeshttps://doi.org/10.3390/biomimetics3010004openalex-snapshot
Targeting Early Dementia: Using Lipid Cubic Phase Nanocarriers to Cross the Blood–Brain Barrier
inferred← citeshttps://doi.org/10.3390/biophysica2040039openalex-snapshot
Heterogeneous Tau Oligomers as Molecular Targets for Alzheimer’s Disease and Related Tauopathies
inferred← citeshttps://doi.org/10.3390/cancers14215386openalex-snapshot
Tau Protein as Therapeutic Target for Cancer? Focus on Glioblastoma
inferred← citeshttps://doi.org/10.3390/ijms20246319openalex-snapshot
The Amyloid-Tau-Neuroinflammation Axis in the Context of Cerebral Amyloid Angiopathy
inferred← citeshttps://doi.org/10.3390/ijms22147710openalex-snapshot
Blood–Brain Barrier and Neurodegenerative Diseases—Modeling with iPSC-Derived Brain Cells
inferred← citeshttps://doi.org/10.3390/jcm8050651openalex-snapshot
Vascular Dysfunction in Alzheimer’s Disease: A Prelude to the Pathological Process or a Consequence of It?
inferred← citeshttps://doi.org/10.3390/pharmaceutics12090801openalex-snapshot
CRISPR/Cas9 Delivery Potentials in Alzheimer’s Disease Management: A Mini Review
inferred← citeshttps://doi.org/10.3929/ethz-b-000520246openalex-snapshot
Arterial spin labeling demonstrates preserved regional cerebral blood flow in the P301L mouse model of tauopathy
inferred← citeshttps://doi.org/10.4172/2161-0460.1000443openalex-snapshot
Targeting Prion-like Cis Phosphorylated Tau Pathology in Neurodegenerative Diseases
inferred← citeshttps://doi.org/10.6084/m9.figshare.12825330openalex-snapshot
Additional file 1 of Tau reduction in aged mice does not impact Microangiopathy
inferred← citeshttps://doi.org/10.6084/m9.figshare.13279800openalex-snapshot
Additional file 3 of Retinal capillary degeneration and blood-retinal barrier disruption in murine models of Alzheimer’s disease
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