On the public citation graph

Blood-Brain Barrier Dysfunction and the Pathogenesis of Alzheimer’s Disease

https://doi.org/10.3390/ijms18091965

0 signed · 608 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

1 of the 173 references listed on this page is in the Retraction Watch database as retracted (export 2026-10-21): 10.1038/ncomms3932 (notice 2024-04-03).

Dataset join, best-effort; this page does not check the publisher record. Retraction Watch data via Crossref Labs, used with credit; OpenCitations Index (CC0) and Meta (CC BY 4.0); dataset doi:10.7910/DVN/WT8VOA (CC BY 4.0).

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

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

inferredcites →https://doi.org/10.1001/jamaneurol.2016.4370openalex-snapshot

Association of Perivascular Localization of Aquaporin-4 With Cognition and Alzheimer Disease in Aging Brains

inferredcites →https://doi.org/10.1002/ana.23648openalex-snapshot

The blood–brain barrier in health and disease

inferredcites →https://doi.org/10.1002/dneu.20954openalex-snapshot

Extracellular matrix and matrix receptors in blood–brain barrier formation and stroke

inferredcites →https://doi.org/10.1007/bf00193951openalex-snapshot

Immunolabelling of hippocampal microvessel glucose transporter protein is reduced in Alzheimer's disease

inferredcites →https://doi.org/10.1007/bf00693782openalex-snapshot

Blood-brain barrier in Alzheimer dementia and in non-demented elderly

inferredcites →https://doi.org/10.1007/s00401-003-0688-zopenalex-snapshot

Localization of claudin-3 in tight junctions of the blood-brain barrier is selectively lost during experimental autoimmune encephalomyelitis and human glioblastoma multiforme

inferredcites →https://doi.org/10.1007/s00401-011-0834-yopenalex-snapshot

Vascular β-amyloid and early astrocyte alterations impair cerebrovascular function and cerebral metabolism in transgenic arcAβ mice

inferredcites →https://doi.org/10.1007/s00401-016-1555-zopenalex-snapshot

Vascular basement membranes as pathways for the passage of fluid into and out of the brain

inferredcites →https://doi.org/10.1007/s00401-016-1580-yopenalex-snapshot

Impact of sex and APOE4 on cerebral amyloid angiopathy in Alzheimer’s disease

inferredcites →https://doi.org/10.1007/s004010000180openalex-snapshot

Claudin-1 and claudin-5 expression and tight junction morphology are altered in blood vessels of human glioblastoma multiforme

inferredcites →https://doi.org/10.1007/s00441-005-1101-0openalex-snapshot

Contribution of claudin-5 to barrier properties in tight junctions of epithelial cells

inferredcites →https://doi.org/10.1007/s40263-016-0361-4openalex-snapshot

Apolipoprotein E as a Therapeutic Target in Alzheimer’s Disease: A Review of Basic Research and Clinical Evidence

inferredcites →https://doi.org/10.1016/0006-3223(90)90410-4openalex-snapshot

Rapid dynamic CT scanning in primary degenerative dementia and age-matched controls

inferredcites →https://doi.org/10.1016/0006-8993(95)01250-8openalex-snapshot

Increased collagen content of cerebral microvessels in Alzheimer's disease

inferredcites →https://doi.org/10.1016/0022-510x(83)90157-0openalex-snapshot

Albumin and immunoglobulin in plasma and cerebrospinal fluid, and blood-cerebrospinal fluid barrier function in patients with dementia of alzheimer type and multi-infarct dementia

inferredcites →https://doi.org/10.1016/0022-510x(85)90189-3openalex-snapshot

CSF in Alzheimer's disease

inferredcites →https://doi.org/10.1016/0026-2862(85)90042-1openalex-snapshot

Morphometric analysis of CNS microvascular endothelium

inferredcites →https://doi.org/10.1016/j.bbadis.2015.12.023openalex-snapshot

Vascular contributions to cognitive impairment, clinical Alzheimer's disease, and dementia in older persons

inferredcites →https://doi.org/10.1016/j.braindev.2009.02.008openalex-snapshot

The expanding phenotype of GLUT1-deficiency syndrome

inferredcites →https://doi.org/10.1016/j.brainres.2007.08.063openalex-snapshot

Amyloid beta deposition is related to decreased glucose transporter-1 levels and hippocampal atrophy in brains of aged APP/PS1 mice

inferredcites →https://doi.org/10.1016/j.brainres.2008.06.124openalex-snapshot

Hippocampal RAGE immunoreactivity in early and advanced Alzheimer's disease

inferredcites →https://doi.org/10.1016/j.brainres.2014.10.047openalex-snapshot

In vitro discrimination of the role of LRP1 at the BBB cellular level: Focus on brain capillary endothelial cells and brain pericytes

inferredcites →https://doi.org/10.1016/j.dadm.2017.01.005openalex-snapshot

Pathophysiologic relationship between Alzheimer's disease, cerebrovascular disease, and cardiovascular risk: A review and synthesis

inferredcites →https://doi.org/10.1016/j.jalz.2016.03.001openalex-snapshot

2016 Alzheimer's disease facts and figures

inferredcites →https://doi.org/10.1016/j.jns.2009.02.089openalex-snapshot

Blood brain barrier: ageing and microvascular disease-systematic review and meta-analysis

inferredcites →https://doi.org/10.1016/j.nbd.2007.12.005openalex-snapshot

LRP promotes endocytosis and degradation, but not transcytosis, of the amyloid-β peptide in a blood–brain barrier in vitro model

inferredcites →https://doi.org/10.1016/j.nbd.2016.07.007openalex-snapshot

The blood-brain barrier in Alzheimer's disease

inferredcites →https://doi.org/10.1016/j.neulet.2006.03.047openalex-snapshot

Amyloid β-peptide1–42 alters tight junction protein distribution and expression in brain microvessel endothelial cells

inferredcites →https://doi.org/10.1016/j.neurobiolaging.2006.05.016openalex-snapshot

Microvascular injury and blood–brain barrier leakage in Alzheimer's disease

inferredcites →https://doi.org/10.1016/j.neurobiolaging.2007.07.015openalex-snapshot

Blood–brain barrier: Ageing and microvascular disease – systematic review and meta-analysis

inferredcites →https://doi.org/10.1016/j.neurobiolaging.2008.08.024openalex-snapshot

Is it appropriate to use albumin CSF/plasma ratio to assess blood brain barrier permeability?

inferredcites →https://doi.org/10.1016/j.neurobiolaging.2010.05.025openalex-snapshot

LRP1 mediates bidirectional transcytosis of amyloid-β across the blood-brain barrier

inferredcites →https://doi.org/10.1016/j.neuron.2004.07.017openalex-snapshot

LRP/Amyloid β-Peptide Interaction Mediates Differential Brain Efflux of Aβ Isoforms

inferredcites →https://doi.org/10.1016/j.neuron.2008.01.003openalex-snapshot

The Blood-Brain Barrier in Health and Chronic Neurodegenerative Disorders

inferredcites →https://doi.org/10.1016/j.neuron.2010.09.043openalex-snapshot

Pericytes Control Key Neurovascular Functions and Neuronal Phenotype in the Adult Brain and during Brain Aging

inferredcites →https://doi.org/10.1016/j.neuron.2013.04.005openalex-snapshot

Innate Immunity in the CNS: Redefining the Relationship between the CNS and Its Environment

inferredcites →https://doi.org/10.1016/j.neuron.2014.05.004openalex-snapshot

The Intersection of Amyloid Beta and Tau at Synapses in Alzheimer’s Disease

inferredcites →https://doi.org/10.1016/j.neuron.2014.12.032openalex-snapshot

Blood-Brain Barrier Breakdown in the Aging Human Hippocampus

inferredcites →https://doi.org/10.1016/j.neuroscience.2009.01.023openalex-snapshot

Vascular amyloid alters astrocytic water and potassium channels in mouse models and humans with Alzheimer's disease

inferredcites →https://doi.org/10.1016/j.pscychresns.2008.04.003openalex-snapshot

Blood–brain barrier permeability in Alzheimer's disease: a case–control MRI study

inferredcites →https://doi.org/10.1016/j.seizure.2013.07.003openalex-snapshot

GLUT1 deficiency syndrome 2013: Current state of the art

inferredcites →https://doi.org/10.1016/j.tins.2005.02.001openalex-snapshot

Neurovascular mechanisms of Alzheimer's neurodegeneration

inferredcites →https://doi.org/10.1016/j.tins.2015.08.003openalex-snapshot

The Molecular Constituents of the Blood–Brain Barrier

inferredcites →https://doi.org/10.1016/s0169-409x(98)00085-4openalex-snapshot

P-Glycoprotein, a gatekeeper in the blood–brain barrier

inferredcites →https://doi.org/10.1016/s0197-4580(88)80085-xopenalex-snapshot

Lack of evidence for dysfunction of the blood-brain barrier in Alzhiemer's disease: An immunohistochemical study

inferredcites →https://doi.org/10.1016/s0197-4580(97)00111-5openalex-snapshot

GLUT-1 Expression in the Cerebra of Patients with Alzheimer’s Disease

inferredcites →https://doi.org/10.1016/s0301-0082(00)00068-xopenalex-snapshot

Cerebral microvascular pathology in aging and Alzheimer's disease

inferredcites →https://doi.org/10.1016/s0962-8924(99)01578-0openalex-snapshot

Occludin and claudins in tight-junction strands: leading or supporting players?

inferredcites →https://doi.org/10.1016/s1474-4422(15)70016-5openalex-snapshot

Neuroinflammation in Alzheimer's disease

inferredcites →https://doi.org/10.1038/325253a0openalex-snapshot

Astrocytes induce blood–brain barrier properties in endothelial cells

inferredcites →https://doi.org/10.1038/cddis.2014.258openalex-snapshot

Aβ1–42 reduces P-glycoprotein in the blood–brain barrier through RAGE–NF-κB signaling

inferredcites →https://doi.org/10.1038/jcbfm.1987.1openalex-snapshot

Examination of Blood — Brain Barrier Permeability in Dementia of the Alzheimer Type with [ 68 Ga]EDTA and Positron Emission Tomography

inferredcites →https://doi.org/10.1038/jcbfm.2012.153openalex-snapshot

Immunologic Privilege in the Central Nervous System and the Blood–Brain Barrier

inferredcites →https://doi.org/10.1038/jcbfm.2013.135openalex-snapshot

Blood–Brain Barrier Dysfunction as a Cause and Consequence of Alzheimer's Disease

inferredcites →https://doi.org/10.1038/jcbfm.2014.102openalex-snapshot

Ablation of MMP9 Gene Ameliorates Paracellular Permeability and Fibrinogen–Amyloid Beta Complex Formation during Hyperhomocysteinemia

inferredcites →https://doi.org/10.1038/nature05193openalex-snapshot

Bidirectional control of CNS capillary diameter by pericytes

inferredcites →https://doi.org/10.1038/nature09513openalex-snapshot

Pericytes are required for blood–brain barrier integrity during embryogenesis

inferredcites →https://doi.org/10.1038/nature09522openalex-snapshot

Pericytes regulate the blood–brain barrier

inferredcites →https://doi.org/10.1038/nature09613openalex-snapshot

Glial and neuronal control of brain blood flow

inferredcites →https://doi.org/10.1038/ncomms3932openalex-snapshot

RETRACTED ARTICLE: Pericyte loss influences Alzheimer-like neurodegeneration in mice

inferredcites →https://doi.org/10.1038/nm.3913openalex-snapshot

Neutrophils promote Alzheimer's disease–like pathology and cognitive decline via LFA-1 integrin

inferredcites →https://doi.org/10.1038/nm889openalex-snapshot

SSeCKS regulates angiogenesis and tight junction formation in blood-brain barrier

inferredcites →https://doi.org/10.1038/nm890openalex-snapshot

RAGE mediates amyloid-β peptide transport across the blood-brain barrier and accumulation in brain

inferredcites →https://doi.org/10.1038/nn.2946openalex-snapshot

Central nervous system pericytes in health and disease

inferredcites →https://doi.org/10.1038/nn.3966openalex-snapshot

GLUT1 reductions exacerbate Alzheimer's disease vasculo-neuronal dysfunction and degeneration

inferredcites →https://doi.org/10.1038/nn.4288openalex-snapshot

Pericytes of the neurovascular unit: key functions and signaling pathways

inferredcites →https://doi.org/10.1038/nn.4475openalex-snapshot

The role of peripheral immune cells in the CNS in steady state and disease

inferredcites →https://doi.org/10.1038/nri2852openalex-snapshot

The impact of the extracellular matrix on inflammation

inferredcites →https://doi.org/10.1038/nri3265openalex-snapshot

The anatomical and cellular basis of immune surveillance in the central nervous system

inferredcites →https://doi.org/10.1038/nrn1824openalex-snapshot

Astrocyte–endothelial interactions at the blood–brain barrier

inferredcites →https://doi.org/10.1038/nrneurol.2012.263openalex-snapshot

Apolipoprotein E and Alzheimer disease: risk, mechanisms and therapy

inferredcites →https://doi.org/10.1038/sj.jcbfm.9600249openalex-snapshot

The Rat Blood—Brain Barrier Transcriptome

inferredcites →https://doi.org/10.1046/j.1471-4159.1998.71031151.xopenalex-snapshot

Basement Membrane Proteins Influence Brain Capillary Endothelial Barrier Function In Vitro

inferredcites →https://doi.org/10.1056/nejm199109053251006openalex-snapshot

Defective Glucose Transport across the Blood-Brain Barrier as a Cause of Persistent Hypoglycorrhachia, Seizures, and Developmental Delay

inferredcites →https://doi.org/10.1073/pnas.0805165106openalex-snapshot

Wnt/β-catenin signaling is required for CNS, but not non-CNS, angiogenesis

inferredcites →https://doi.org/10.1074/jbc.273.45.29745openalex-snapshot

The Tight Junction Protein ZO-1 Establishes a Link between the Transmembrane Protein Occludin and the Actin Cytoskeleton

inferredcites →https://doi.org/10.1074/jbc.m110.102277openalex-snapshot

Reduction of Brain β-Amyloid (Aβ) by Fluvastatin, a Hydroxymethylglutaryl-CoA Reductase Inhibitor, through Increase in Degradation of Amyloid Precursor Protein C-terminal Fragments (APP-CTFs) and Aβ Clearance

inferredcites →https://doi.org/10.1074/jbc.m608853200openalex-snapshot

Study of Claudin Function by RNA Interference

inferredcites →https://doi.org/10.1074/jbc.m801487200openalex-snapshot

The Low Density Lipoprotein Receptor-related Protein 1 Mediates Uptake of Amyloid β Peptides in an in Vitro Model of the Blood-Brain Barrier Cells

inferredcites →https://doi.org/10.1083/jcb.123.6.1777openalex-snapshot

Occludin: a novel integral membrane protein localizing at tight junctions.

inferredcites →https://doi.org/10.1083/jcb.136.2.399openalex-snapshot

A Synthetic Peptide Corresponding to the Extracellular Domain of Occludin Perturbs the Tight Junction Permeability Barrier

inferredcites →https://doi.org/10.1083/jcb.143.2.391openalex-snapshot

A Single Gene Product, Claudin-1 or -2, Reconstitutes Tight Junction Strands and Recruits Occludin in Fibroblasts

inferredcites →https://doi.org/10.1083/jcb.147.1.185openalex-snapshot

Endothelial Claudin

inferredcites →https://doi.org/10.1083/jcb.147.6.1351openalex-snapshot

Direct Binding of Three Tight Junction-Associated Maguks, Zo-1, Zo-2, and Zo-3, with the Cooh Termini of Claudins

inferredcites →https://doi.org/10.1083/jcb.153.2.263openalex-snapshot

Conversion of Zonulae Occludentes from Tight to Leaky Strand Type by Introducing Claudin-2 into Madin-Darby Canine Kidney I Cells

inferredcites →https://doi.org/10.1083/jcb.153.5.933openalex-snapshot

Endothelial Cell Laminin Isoforms, Laminins 8 and 10, Play Decisive Roles in T Cell Recruitment across the Blood–Brain Barrier in Experimental Autoimmune Encephalomyelitis

inferredcites →https://doi.org/10.1083/jcb.200302070openalex-snapshot

Size-selective loosening of the blood-brain barrier in claudin-5–deficient mice

inferredcites →https://doi.org/10.1083/jcb.201404140openalex-snapshot

ZO-1 controls endothelial adherens junctions, cell–cell tension, angiogenesis, and barrier formation

inferredcites →https://doi.org/10.1089/ars.2011.3895openalex-snapshot

Amyloid Beta Induces Oxidative Stress-Mediated Blood–Brain Barrier Changes in Capillary Amyloid Angiopathy

inferredcites →https://doi.org/10.1091/mbc.11.12.4131openalex-snapshot

Complex Phenotype of Mice Lacking Occludin, a Component of Tight Junction Strands

inferredcites →https://doi.org/10.1093/brain/awr298openalex-snapshot

Blood–brain barrier P-glycoprotein function in Alzheimer's disease

inferredcites →https://doi.org/10.1093/brain/aws271openalex-snapshot

Cerebrovascular atherosclerosis correlates with Alzheimer pathology in neurodegenerative dementias

inferredcites →https://doi.org/10.1096/fasebj.7.11.8370472openalex-snapshot

Pericyte physiology

inferredcites →https://doi.org/10.1097/00001756-200004070-00035openalex-snapshot

Neurons and ECM regulate occludin localization in brain endothelial cells

inferredcites →https://doi.org/10.1097/00002093-199912001-00015openalex-snapshot

Cerebrospinal Fluid Markers of Pathogenetic Processes in Vascular Dementia, with Special Reference to the Subcortical Subtype

inferredcites →https://doi.org/10.1097/00008571-200210000-00005openalex-snapshot

Deposition of Alzheimer's ??-amyloid is inversely correlated with P-glycoprotein expression in the brains of elderly non-demented humans

inferredcites →https://doi.org/10.1097/01.jnen.0000173894.09553.13openalex-snapshot

Basement Membrane Proteins in Multiple Sclerosis-Associated Inflammatory Cuffs: Potential Role in Influx and Transport of Leukocytes

inferredcites →https://doi.org/10.1097/nen.0b013e31818f9ca8openalex-snapshot

Perivascular Spaces and the Two Steps to Neuroinflammation

inferredcites →https://doi.org/10.1097/nen.0b013e3181fd252copenalex-snapshot

Aquaporin Expression in the Brains of Patients With or Without Cerebral Amyloid Angiopathy

inferredcites →https://doi.org/10.1097/nen.0b013e3182632566openalex-snapshot

Characteristics of Aquaporin Expression Surrounding Senile Plaques and Cerebral Amyloid Angiopathy in Alzheimer Disease

inferredcites →https://doi.org/10.1101/cshperspect.a006189openalex-snapshot

Neuropathological Alterations in Alzheimer Disease

inferredcites →https://doi.org/10.1101/cshperspect.a006379openalex-snapshot

Proteolytic Degradation of Amyloid -Protein

inferredcites →https://doi.org/10.1101/cshperspect.a020412openalex-snapshot

The Blood–Brain Barrier

inferredcites →https://doi.org/10.1111/acel.12045openalex-snapshot

Regional differences in the morphological and functional effects of aging on cerebral basement membranes and perivascular drainage of amyloid‐β from the mouse brain

inferredcites →https://doi.org/10.1111/bpa.12004openalex-snapshot

Deficiency in Mural Vascular Cells Coincides with Blood–Brain Barrier Disruption in A lzheimer's Disease

inferredcites →https://doi.org/10.1111/cns.12503openalex-snapshot

Hyperglycemia Increases the Production of Amyloid Beta‐Peptide Leading to Decreased Endothelial Tight Junction

inferredcites →https://doi.org/10.1111/j.1365-2990.2006.00732.xopenalex-snapshot

Relationships in Alzheimer's disease between the extent of Aβ deposition in cerebral blood vessel walls, as cerebral amyloid angiopathy, and the amount of cerebrovascular smooth muscle cells and collagen

inferredcites →https://doi.org/10.1111/j.1471-4159.2010.06708.xopenalex-snapshot

Lack of brain‐to‐blood efflux transport activity of low‐density lipoprotein receptor‐related protein‐1 (LRP‐1) for amyloid‐β peptide(1–40) in mouse: involvement of an LRP‐1‐independent pathway

inferredcites →https://doi.org/10.1111/j.1582-4934.2009.00717.xopenalex-snapshot

Amyloid-β-induced occludin down-regulation and increased permeability in human brain endothelial cells is mediated by MAPK activation

inferredcites →https://doi.org/10.1111/j.1600-0404.1990.tb01563.xopenalex-snapshot

Blood-brain barrier disturbance in patients with Alzheimer's disease is related to vascular factors

inferredcites →https://doi.org/10.1111/j.1600-0404.1991.tb04675.xopenalex-snapshot

White-matter lesions on CT in Alzheimer patients: relation to clinical symptomatology and vascular factors

inferredcites →https://doi.org/10.1111/j.1600-0404.2007.00823.xopenalex-snapshot

The integrity of the blood?brain barrier in Alzheimer?s disease

inferredcites →https://doi.org/10.1111/j.1749-6632.1982.tb26848.xopenalex-snapshot

Evidence for Blood‐Brain Barrier Changes in Senile Dementia of the Alzheimer Type (SDAT)

inferredcites →https://doi.org/10.1111/j.1749-6632.1997.tb48468.xopenalex-snapshot

Amyloid Angiopathy and Blood–Brain Barrier Changes in Alzheimer's Disease a, b

inferredcites →https://doi.org/10.1111/jnc.13122openalex-snapshot

Aβ1–42oligomer‐induced leakage in anin vitroblood–brain barrier model is associated with up‐regulation of RAGE and metalloproteinases, and down‐regulation of tight junction scaffold proteins

inferredcites →https://doi.org/10.1111/nan.12295openalex-snapshot

Early changes in extracellular matrix in Alzheimer's disease

inferredcites →https://doi.org/10.1113/expphysiol.2010.053132openalex-snapshot

Bidirectional control of arteriole diameter by astrocytes

inferredcites →https://doi.org/10.1124/mol.109.061754openalex-snapshot

Restoring Blood-Brain Barrier P-Glycoprotein Reduces Brain Amyloid-β in a Mouse Model of Alzheimer’s Disease

inferredcites →https://doi.org/10.1126/science.6101511openalex-snapshot

γ-Glutamyl Transpeptidase in Isolated Brain Endothelial Cells: Induction by Glial Cells in Vitro

inferredcites →https://doi.org/10.1126/scitranslmed.3003748openalex-snapshot

A Paravascular Pathway Facilitates CSF Flow Through the Brain Parenchyma and the Clearance of Interstitial Solutes, Including Amyloid β

inferredcites →https://doi.org/10.1139/y92-252openalex-snapshot

Changes in the glucose transporter of brain capillaries

inferredcites →https://doi.org/10.1152/physrev.00001.2003openalex-snapshot

Transcytosis: Crossing Cellular Barriers

inferredcites →https://doi.org/10.1152/physrev.00019.2012openalex-snapshot

Claudins and the Modulation of Tight Junction Permeability

inferredcites →https://doi.org/10.1152/physrev.00049.2005openalex-snapshot

Astrocyte Control of Synaptic Transmission and Neurovascular Coupling

inferredcites →https://doi.org/10.1158/1078-0432.ccr-06-2854openalex-snapshot

The Blood-Brain Barrier and Cancer: Transporters, Treatment, and Trojan Horses

inferredcites →https://doi.org/10.1159/000334916openalex-snapshot

Neuroinflammation and Blood-Brain Barrier Changes in Capillary Amyloid Angiopathy

inferredcites →https://doi.org/10.1159/000444053openalex-snapshot

Dietary Advanced Glycation End Products and Their Potential Role in Cardiometabolic Disease in Children

inferredcites →https://doi.org/10.1161/01.res.0000182903.16652.d7openalex-snapshot

Endothelial/Pericyte Interactions

inferredcites →https://doi.org/10.1161/01.res.0000255690.03436.aeopenalex-snapshot

Phenotypic Heterogeneity of the Endothelium

inferredcites →https://doi.org/10.1161/01.str.0000143318.70292.47openalex-snapshot

Risk Factors for Vascular Dementia and Alzheimer Disease

inferredcites →https://doi.org/10.1161/01.str.27.11.2069openalex-snapshot

Alterations of the Blood-Brain Barrier and Glial Cells in White-Matter Lesions in Cerebrovascular and Alzheimer's Disease Patients

inferredcites →https://doi.org/10.1161/atvbaha.107.158014openalex-snapshot

VE-Cadherin

inferredcites →https://doi.org/10.1161/circresaha.109.212217openalex-snapshot

The RAGE Axis

inferredcites →https://doi.org/10.1172/jci10498openalex-snapshot

Clearance of Alzheimer’s amyloid-β1-40 peptide from brain by LDL receptor–related protein-1 at the blood-brain barrier

inferredcites →https://doi.org/10.1172/jci12464openalex-snapshot

Regulated expression of claudin-4 decreases paracellular conductance through a selective decrease in sodium permeability

inferredcites →https://doi.org/10.1172/jci25247openalex-snapshot

P-glycoprotein deficiency at the blood-brain barrier increases amyloid- deposition in an Alzheimer disease mouse model

inferredcites →https://doi.org/10.1172/jci58642openalex-snapshot

A multimodal RAGE-specific inhibitor reduces amyloid β–mediated brain disorder in a mouse model of Alzheimer disease

inferredcites →https://doi.org/10.1172/jci81108openalex-snapshot

Endothelial LRP1 transports amyloid-β1–42 across the blood-brain barrier

inferredcites →https://doi.org/10.1176/jnp.10.1.78openalex-snapshot

Blood–Brain Barrier Integrity in Alzheimer's Disease Patients and Elderly Control Subjects

inferredcites →https://doi.org/10.1177/0192623310385254openalex-snapshot

Role of Astrocytes in Brain Function and Disease

inferredcites →https://doi.org/10.1182/blood.v91.10.3527openalex-snapshot

Endothelial cells in physiology and in the pathophysiology of vascular disorders.

inferredcites →https://doi.org/10.1186/1471-2121-11-68openalex-snapshot

Effect of cAMP derivates on assembly and maintenance of tight junctions in human umbilical vein endothelial cells

inferredcites →https://doi.org/10.1186/1742-2094-8-26openalex-snapshot

Neurovascular dysfunction, inflammation and endothelial activation: Implications for the pathogenesis of Alzheimer's disease

inferredcites →https://doi.org/10.1186/2045-8118-8-8openalex-snapshot

The CNS microvascular pericyte: pericyte-astrocyte crosstalk in the regulation of tissue survival

inferredcites →https://doi.org/10.1186/s12916-014-0130-5openalex-snapshot

Cardiovascular risk factors and future risk of Alzheimer’s disease

inferredcites →https://doi.org/10.1189/jlb.0710432openalex-snapshot

Vascular inflammation in central nervous system diseases: adhesion receptors controlling leukocyte–endothelial interactions

inferredcites →https://doi.org/10.1189/jlb.1012519openalex-snapshot

RAGE regulation and signaling in inflammation and beyond

inferredcites →https://doi.org/10.1212/wnl.0b013e31828726f5openalex-snapshot

Alzheimer disease in the United States (2010–2050) estimated using the 2010 census

inferredcites →https://doi.org/10.1212/wnl.46.6.1592openalex-snapshot

Cerebral amyloid angiopathy in the brains of patients with Alzheimer's disease

inferredcites →https://doi.org/10.1212/wnl.50.4.966openalex-snapshot

A population study on blood-brain barrier function in 85-year-olds

inferredcites →https://doi.org/10.1212/wnl.57.10.1763openalex-snapshot

The cerebrospinal fluid production rate is reduced in dementia of the Alzheimer’s type

inferredcites →https://doi.org/10.1242/jcs.017897openalex-snapshot

The role of adherens junctions and VE-cadherin in the control of vascular permeability

inferredcites →https://doi.org/10.1242/jcs.109.9.2287openalex-snapshot

Occludin is a functional component of the tight junction

inferredcites →https://doi.org/10.1371/journal.pone.0013741openalex-snapshot

The Mouse Blood-Brain Barrier Transcriptome: A New Resource for Understanding the Development and Function of Brain Endothelial Cells

inferredcites →https://doi.org/10.1371/journal.pone.0041636openalex-snapshot

Disruption of Arterial Perivascular Drainage of Amyloid-β from the Brains of Mice Expressing the Human APOE ε4 Allele

inferredcites →https://doi.org/10.1385/1-59259-419-0:193openalex-snapshot

A Review of Blood–Brain Barrier Transport Techniques

inferredcites →https://doi.org/10.1523/jneurosci.0350-15.2016openalex-snapshot

Aβ40 Reduces P-Glycoprotein at the Blood–Brain Barrier through the Ubiquitin–Proteasome Pathway

inferredcites →https://doi.org/10.1523/jneurosci.14-04-02225.1994openalex-snapshot

Increased levels of hemoglobin-derived and other peptides in Alzheimer's disease cerebellum

inferredcites →https://doi.org/10.1523/jneurosci.4707-08.2009openalex-snapshot

Uniquely Hominid Features of Adult Human Astrocytes

inferredcites →https://doi.org/10.1523/jneurosci.5103-08.2009openalex-snapshot

ABCG2 Is Upregulated in Alzheimer's Brain with Cerebral Amyloid Angiopathy and May Act as a Gatekeeper at the Blood–Brain Barrier for Aβ 1–40 Peptides

inferredcites →https://doi.org/10.1523/jneurosci.6102-11.2012openalex-snapshot

A 1-42-RAGE Interaction Disrupts Tight Junctions of the Blood-Brain Barrier Via Ca2+-Calcineurin Signaling

inferredcites →https://doi.org/10.1530/jme-11-0035openalex-snapshot

Endocrine cells and blood vessels work in tandem to generate hormone pulses

inferredcites →https://doi.org/10.2174/156720508785132334openalex-snapshot

Structural Changes in Alzheimers Disease Brain Microvessels

inferredcites →https://doi.org/10.3233/jad-2011-110725openalex-snapshot

Loss of Astrocyte Polarization in the Tg-ArcSwe Mouse Model of Alzheimer's Disease

inferredcites →https://doi.org/10.3233/jad-2012-112189openalex-snapshot

ABCG2- and ABCG4-Mediated Efflux of Amyloid-β Peptide 1-40 at the Mouse Blood-Brain Barrier

inferredcites →https://doi.org/10.3389/fnagi.2014.00093openalex-snapshot

The low-density lipoprotein receptor-related protein 1 and amyloid-β clearance in Alzheimer’s disease

inferredcites →https://doi.org/10.3389/fnagi.2014.00251openalex-snapshot

The Cerebrovascular Basement Membrane: Role in the Clearance of β-amyloid and Cerebral Amyloid Angiopathy

inferredcites →https://doi.org/10.3389/fnene.2010.00005openalex-snapshot

Pericyte-mediated regulation of capillary diameter: a component of neurovascular coupling in health and disease

inferredcites →https://doi.org/10.3389/fneng.2013.00007openalex-snapshot

The blood-brain barrier: an engineering perspective

inferredcites →https://doi.org/10.4049/jimmunol.158.4.1825openalex-snapshot

Cytokine-induced VCAM-1 and ICAM-1 expression in different organs of the mouse

inferredcites →https://doi.org/10.4161/cam.22680openalex-snapshot

Laminin isoforms in endothelial and perivascular basement membranes

inferredcites →https://doi.org/10.4199/c00029ed1v01y201103isp017openalex-snapshot

Regulation of Tissue Oxygenation

inferredcites →https://doi.org/10.55782/ane-2006-1623openalex-snapshot

The role of astrocytes in the physiology and pathology of the central nervous system

What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.4661733openalex-extracted

Taking Advantages of Blood–Brain Barrier to Optimize Delivery of Drugs in Central Neurological Conditions

inferred← citeshttps://doi.org/10.1002/adfm.201909529openalex-snapshot

Amyloid‐β Oligomer‐Targeted Gadolinium‐Based NIR/MR Dual‐Modal Theranostic Nanoprobe for Alzheimer's Disease

inferred← citeshttps://doi.org/10.1002/advs.202403892openalex-snapshot

Challenges and Future Perspectives in Modeling Neurodegenerative Diseases Using Organ‐on‐a‐Chip Technology

inferred← citeshttps://doi.org/10.1002/advs.76761openalex-snapshot

Aberrant GRP78 Phase Transition Sustains Endothelial IRE1α Signaling and Drives Blood–Brain Barrier Failure in Cerebral Amyloid Angiopathy

inferred← citeshttps://doi.org/10.1002/alz.12104openalex-snapshot

Tau and apolipoprotein E modulate cerebrovascular tight junction integrity independent of cerebral amyloid angiopathy in Alzheimer's disease

inferred← citeshttps://doi.org/10.1002/alz.13086openalex-snapshot

Retinal arterial Aβ40 deposition is linked with tight junction loss and cerebral amyloid angiopathy in MCI and AD patients

inferred← citeshttps://doi.org/10.1002/alz.13457openalex-snapshot

sPDGFRβ and neuroinflammation are associated with AD biomarkers and differ by race: The ASCEND Study

inferred← citeshttps://doi.org/10.1002/alz.70103openalex-snapshot

Structural changes in cerebral microvasculature induced by ferroptosis contribute to blood–brain barrier disruption in Alzheimer's disease: an autopsy study

inferred← citeshttps://doi.org/10.1002/alz.70814openalex-snapshot

Reviewing the possible connection between cerebral amyloid angiopathy and blood–brain barrier integrity in Down syndrome

inferred← citeshttps://doi.org/10.1002/ana.26134openalex-snapshot

Blood–Brain Barrier Breakdown in Relationship to Alzheimer and Vascular Disease

inferred← citeshttps://doi.org/10.1002/brb3.1601openalex-snapshot

Association between atherosclerosis and Alzheimer's disease: A systematic review and meta‐analysis

inferred← citeshttps://doi.org/10.1002/cne.25299openalex-snapshot

Anti‐LINGO‐1 antibody treatment alleviates cognitive deficits and promotes maturation of oligodendrocytes in the hippocampus of APP/PS1 mice

inferred← citeshttps://doi.org/10.1002/cpt.2638openalex-snapshot

Transporters and Toxicity: Insights From the International Transporter Consortium Workshop 4

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/10.1002/dad2.70316openalex-snapshot

Copper isotope shifts in biofluids track Alzheimer's pathology

inferred← citeshttps://doi.org/10.1002/elsc.70039openalex-snapshot

Menthol and Its Derivatives: Exploring the Medical Application Potential

inferred← citeshttps://doi.org/10.1002/glia.23878openalex-snapshot

Priming of microglia with IFN ‐γ impairs adult hippocampal neurogenesis and leads to depression‐like behaviors and cognitive defects

inferred← citeshttps://doi.org/10.1002/jcla.70217openalex-snapshot

Evaluation of Soluble Triggering Receptor Expressed on Myeloid Cells 2 ( sTREM2 ) in Cerebrospinal Fluid, Serum, and Plasma Using the Fully Automated Lumipulse Platform

inferred← citeshttps://doi.org/10.1002/jcp.31287openalex-snapshot

Does the liver facilitate aging‐related cognitive impairment: Conversation between liver and brain during exercise?

inferred← citeshttps://doi.org/10.1002/jmri.28729openalex-snapshot

The Consistence of Dynamic Contrast‐Enhanced MRI and Filter‐Exchange Imaging in Measuring Water Exchange Across the Blood–Brain Barrier in High‐Grade Glioma

inferred← citeshttps://doi.org/10.1002/jnr.24718openalex-snapshot

Locus Coeruleus and neurovascular unit: From its role in physiology to its potential role in Alzheimer’s disease pathogenesis

inferred← citeshttps://doi.org/10.1002/med.21719openalex-snapshot

A multitude of signaling pathways associated with Alzheimer's disease and their roles in AD pathogenesis and therapy

inferred← citeshttps://doi.org/10.1002/mrm.70049openalex-snapshot

The contributions of aquaporin‐4 to water exchange across the blood–brain barrier measured by filter‐exchange imaging

inferred← citeshttps://doi.org/10.1002/nep3.60openalex-snapshot

Recent advances in therapeutic strategies for Alzheimer's and Parkinson's disease using protein/peptide co‐modified polymer nanoparticles

inferred← citeshttps://doi.org/10.1002/wnan.1818openalex-snapshot

Brain‐targeting drug delivery systems

inferred← citeshttps://doi.org/10.1007/978-3-030-62129-2_4openalex-snapshot

Effects of Cytomegalovirus on Pericytes

inferred← citeshttps://doi.org/10.1007/978-3-031-69188-1_4openalex-snapshot

Adeno-associated Virus-Mediated Gene Delivery Across the Blood-Brain Barrier

inferred← citeshttps://doi.org/10.1007/978-981-16-6867-8_11openalex-snapshot

Homocysteine Determinants as Risk Markers for Neurological Diseases

inferred← citeshttps://doi.org/10.1007/978-981-95-0125-0_11openalex-snapshot

Neurovascular Coupling Dysfunction: Natural Products as a Remedy to Manage Neurodegenerative Disorders

inferred← citeshttps://doi.org/10.1007/s00259-021-05421-0openalex-snapshot

Preclinical and clinical study on [18F]DRKXH1: a novel β-amyloid PET tracer for Alzheimer’s disease

inferred← citeshttps://doi.org/10.1007/s00401-019-01967-4openalex-snapshot

Beta-amyloid pathology in human brain microvessel extracts from the parietal cortex: relation with cerebral amyloid angiopathy and Alzheimer’s disease

inferred← citeshttps://doi.org/10.1007/s00401-022-02431-6openalex-snapshot

FMNL2 regulates gliovascular interactions and is associated with vascular risk factors and cerebrovascular pathology in Alzheimer’s disease

inferred← citeshttps://doi.org/10.1007/s00428-023-03581-yopenalex-snapshot

Bringing pathology to nanomedicine: a comparison of in vivo toxicity of polymeric nanoparticle carriers with and without chitosan coating

inferred← citeshttps://doi.org/10.1007/s10456-022-09834-9openalex-snapshot

In vivo dissection of Rhoa function in vascular development using zebrafish

inferred← citeshttps://doi.org/10.1007/s10571-022-01191-xopenalex-snapshot

The Role of ERK1/2 Pathway in the Pathophysiology of Alzheimer’s Disease: An Overview and Update on New Developments

inferred← citeshttps://doi.org/10.1007/s10571-026-01738-2openalex-snapshot

Association Between Blood-Brain Barrier Disruption and Gut Microbiota Dysbiosis in Parkinson’s Disease

inferred← citeshttps://doi.org/10.1007/s11011-018-0239-xopenalex-snapshot

Impaired tissue barriers as potential therapeutic targets for Parkinson’s disease and amyotrophic lateral sclerosis

inferred← citeshttps://doi.org/10.1007/s11011-025-01617-7openalex-snapshot

Butyrate: a key mediator of gut-brain communication in Alzheimer’s disease

inferred← citeshttps://doi.org/10.1007/s11011-025-01623-9openalex-snapshot

A second act for spironolactone: cognitive benefits in renal dysfunction – a critical review

inferred← citeshttps://doi.org/10.1007/s11033-023-08968-3openalex-snapshot

Current non-invasive strategies for brain drug delivery: overcoming blood–brain barrier transport

inferred← citeshttps://doi.org/10.1007/s11064-021-03448-1openalex-snapshot

Research Progress on Mechanism of Neuroprotective Roles of Apelin-13 in Prevention and Treatment of Alzheimer’s Disease

inferred← citeshttps://doi.org/10.1007/s11154-019-09486-zopenalex-snapshot

Associations between atherosclerosis and neurological diseases, beyond ischemia-induced cerebral damage

inferred← citeshttps://doi.org/10.1007/s12031-022-02052-4openalex-snapshot

The Role of Blood–Brain Barrier Dysfunction in Mild Cognitive Impairment: a Scientometric and Visualization Analysis from 2000 to 2021

inferred← citeshttps://doi.org/10.1007/s12035-019-1615-1openalex-snapshot

Panoramic Visualization of Circulating MicroRNAs Across Neurodegenerative Diseases in Humans

inferred← citeshttps://doi.org/10.1007/s12035-020-02013-1openalex-snapshot

Extracellular Vesicles of Alzheimer’s Disease Patients as a Biomarker for Disease Progression

inferred← citeshttps://doi.org/10.1007/s12035-021-02311-2openalex-snapshot

Roles and Mechanisms of Axon-Guidance Molecules in Alzheimer’s Disease

inferred← citeshttps://doi.org/10.1007/s12035-025-05417-zopenalex-snapshot

Targeted Nanoparticles for Drug Delivery Across the Blood–Brain Barrier in Early and Late Stages of Alzheimer's Disease: A Review

inferred← citeshttps://doi.org/10.1007/s12265-021-10171-3openalex-snapshot

Physical Exercise Protects Against Endothelial Dysfunction in Cardiovascular and Metabolic Diseases

inferred← citeshttps://doi.org/10.1007/s12272-019-01128-xopenalex-snapshot

In vivo imaging for neurovascular disease research

inferred← citeshttps://doi.org/10.1007/s12272-019-01168-3openalex-snapshot

Preventive approach for overcoming dementia

inferred← citeshttps://doi.org/10.1007/s12640-022-00561-zopenalex-snapshot

Calpain Inhibitor Calpeptin Improves Alzheimer’s Disease–Like Cognitive Impairments and Pathologies in a Diabetes Mellitus Rat Model

inferred← citeshttps://doi.org/10.1007/s13205-024-04159-4openalex-snapshot

Unveiling biomarker detection in Alzheimer’s disease: a computational approach to microarray analysis

inferred← citeshttps://doi.org/10.1007/s13346-025-01814-yopenalex-snapshot

Low-intensity pulsed ultrasound enhances delivery of 30 nm Q10 for improving mental and memory disorder in APP/PS1 mice

inferred← citeshttps://doi.org/10.1007/s13770-021-00356-xopenalex-snapshot

Research Models of the Nanoparticle-Mediated Drug Delivery across the Blood–Brain Barrier

inferred← citeshttps://doi.org/10.1007/s40572-018-0186-zopenalex-snapshot

Environmental Exposures and Neuropsychiatric Disorders: What Role Does the Gut–Immune–Brain Axis Play?

inferred← citeshttps://doi.org/10.1007/s43152-020-00014-9openalex-snapshot

Pericytes in Vascular Development

inferred← citeshttps://doi.org/10.1016/b978-0-12-815854-8.00038-0openalex-snapshot

Linking astrocytes' exosomes to Alzheimer pathogenesis and therapy

inferred← citeshttps://doi.org/10.1016/b978-0-12-815868-5.00026-8openalex-snapshot

Brain susceptibility to hypoxia/hypoxemia and metabolic dysfunction in Alzheimer's disease

inferred← citeshttps://doi.org/10.1016/b978-0-12-819528-4.00055-9openalex-snapshot

Neuroprotective effects of oleocanthal in neurological disorders

inferred← citeshttps://doi.org/10.1016/b978-0-12-819641-0.00128-6openalex-snapshot

Vascular Dementia

inferred← citeshttps://doi.org/10.1016/b978-0-323-89835-5.00032-6openalex-snapshot

Magnesium and Alzheimer's disease

inferred← citeshttps://doi.org/10.1016/b978-0-443-13979-6.00006-6openalex-snapshot

New frontiers of lymphangiogenesis

inferred← citeshttps://doi.org/10.1016/b978-0-443-24064-5.00001-9openalex-snapshot

Quantum dots for the treatment of neurodegenerative disorders

inferred← citeshttps://doi.org/10.1016/bs.ircmb.2021.01.001openalex-snapshot

Ca2+ homeostasis in brain microvascular endothelial cells

inferred← citeshttps://doi.org/10.1016/bs.pbr.2019.03.009openalex-snapshot

REMOVED: Nanowired delivery of cerebrolysin with neprilysin and p-Tau antibodies induces superior neuroprotection in Alzheimer's disease

inferred← citeshttps://doi.org/10.1016/bs.pbr.2025.04.004openalex-snapshot

Emotional stress and cardiovascular health: Impacts on neurodegenerative disease progression

inferred← citeshttps://doi.org/10.1016/bs.pmbts.2019.06.003openalex-snapshot

Blood-brain barrier and innate immunity in the pathogenesis of Alzheimer's disease

inferred← citeshttps://doi.org/10.1016/j.addr.2023.114777openalex-snapshot

From cells to organoids: The evolution of blood-brain barrier technology for modelling drug delivery in brain cancer

inferred← citeshttps://doi.org/10.1016/j.apsb.2020.11.023openalex-snapshot

Evolution of blood–brain barrier in brain diseases and related systemic nanoscale brain-targeting drug delivery strategies

inferred← citeshttps://doi.org/10.1016/j.arr.2021.101397openalex-snapshot

Western diet as a trigger of Alzheimer’s disease: From metabolic syndrome and systemic inflammation to neuroinflammation and neurodegeneration

inferred← citeshttps://doi.org/10.1016/j.arr.2024.102224openalex-snapshot

Unveiling the impact of aging on BBB and Alzheimer's disease: Factors and therapeutic implications

inferred← citeshttps://doi.org/10.1016/j.arr.2024.102309openalex-snapshot

Mechanistic insights and emerging therapeutic stratagems for Alzheimer’s disease

inferred← citeshttps://doi.org/10.1016/j.bbadis.2023.166967openalex-snapshot

Blood-brain barrier transporters: An overview of function, dysfunction in Alzheimer's disease and strategies for treatment

inferred← citeshttps://doi.org/10.1016/j.bbrc.2022.07.063openalex-snapshot

Construction of brain-like spheroids containing endothelial tubular networks by an adhesive culture system

inferred← citeshttps://doi.org/10.1016/j.bbrc.2024.150418openalex-snapshot

Role of astrocytes in Alzheimer's disease pathogenesis and the impact of exercise-induced remodeling

inferred← citeshttps://doi.org/10.1016/j.bcp.2022.114945openalex-snapshot

Metformin in Alzheimer’s disease: An overview of potential mechanisms, preclinical and clinical findings

inferred← citeshttps://doi.org/10.1016/j.bcp.2026.118107openalex-snapshot

From capillaries to cognition: decoding neurovascular unit dysfunction and cerebrovascular contributions in Alzheimer’s disease

inferred← citeshttps://doi.org/10.1016/j.bioorg.2025.109248openalex-snapshot

Recent advances in bioisosteric modifications for targeting Alzheimer's disease pathways

inferred← citeshttps://doi.org/10.1016/j.bmc.2020.115609openalex-snapshot

Modulation of TRPV4 and BKCa for treatment of brain diseases

inferred← citeshttps://doi.org/10.1016/j.bprint.2026.e00497openalex-snapshot

Advancing neurovascular engineering models with integrated 3D bioprinting and microfluidic chips for study of neurovascular and neurodegenerative disease pathophysiology

inferred← citeshttps://doi.org/10.1016/j.brainres.2022.147937openalex-snapshot

Factors influencing the blood-brain barrier permeability

inferred← citeshttps://doi.org/10.1016/j.brainres.2024.149262openalex-snapshot

A multifactorial lens on risk factors promoting the progression of Alzheimer’s disease

inferred← citeshttps://doi.org/10.1016/j.brainresbull.2023.110820openalex-snapshot

The relationship between TGF-β1 and cognitive function in the brain

inferred← citeshttps://doi.org/10.1016/j.cccb.2025.100378openalex-snapshot

Endothelial progenitor cells and cerebral small vessel disease in APOE4 carriers

inferred← citeshttps://doi.org/10.1016/j.cellimm.2023.104743openalex-snapshot

Crosstalk between peripheral immunity and central nervous system in Alzheimer’s disease

inferred← citeshttps://doi.org/10.1016/j.dscb.2024.100162openalex-snapshot

Recent developments in selective therapeutic targeting of functionalized nanomaterials to neurovascular units in overcoming the gaps in neurovascular therapy

inferred← citeshttps://doi.org/10.1016/j.envpol.2019.113429openalex-snapshot

Perfluorooctane sulfonate disrupts the blood brain barrier through the crosstalk between endothelial cells and astrocytes in mice

inferred← citeshttps://doi.org/10.1016/j.expneurol.2019.113094openalex-snapshot

MicroRNAs in central nervous system diseases: A prospective role in regulating blood-brain barrier integrity

inferred← citeshttps://doi.org/10.1016/j.expneurol.2019.113112openalex-snapshot

Neural stem cell therapy for neurovascular injury in Alzheimer's disease

inferred← citeshttps://doi.org/10.1016/j.gene.2021.146164openalex-snapshot

PART1 destabilized by NOVA2 regulates blood–brain barrier permeability in endothelial cells via STAU1-mediated mRNA degradation

inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.138747openalex-snapshot

Modulating the blood-brain barrier in CNS disorders: A review of the therapeutic implications of secreted protein acidic and rich in cysteine (SPARC)

inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2026.151872openalex-snapshot

Design of albumin-based nanotherapeutics for glioblastoma management: Biological barriers, targeting strategies, and translational perspectives

inferred← citeshttps://doi.org/10.1016/j.intimp.2023.109791openalex-snapshot

An insight into the TAM system in Alzheimer’s disease

inferred← citeshttps://doi.org/10.1016/j.isci.2021.102936openalex-snapshot

Alzheimer's Aβ assembly binds sodium pump and blocks endothelial NOS activity via ROS-PKC pathway in brain vascular endothelial cells

inferred← citeshttps://doi.org/10.1016/j.jcis.2025.138083openalex-snapshot

Near-infrared light-triggered methylene blue/berberine co-loaded polydopamine nanoparticles modified with sialic acid for Alzheimer’s disease therapy

inferred← citeshttps://doi.org/10.1016/j.jconrel.2019.03.010openalex-snapshot

Dual-drug loaded nanoparticles of Epigallocatechin-3-gallate (EGCG)/Ascorbic acid enhance therapeutic efficacy of EGCG in a APPswe/PS1dE9 Alzheimer's disease mice model

inferred← citeshttps://doi.org/10.1016/j.jddst.2023.104174openalex-snapshot

Blood brain barrier-on-a-chip to model neurological diseases

inferred← citeshttps://doi.org/10.1016/j.jece.2025.117701openalex-snapshot

Co-exposure of microcystin-LR and polystyrene microplastics induced testosterone synthesis inhibition by disrupting the hypothalamic-pituitary-testicular axis via PP2A/JNK and PKC signaling pathway in mice

inferred← citeshttps://doi.org/10.1016/j.jfluidstructs.2019.04.008openalex-snapshot

Fluid–structure interaction for highly complex, statistically defined, biological media: Homogenisation and a 3D multi-compartmental poroelastic model for brain biomechanics

inferred← citeshttps://doi.org/10.1016/j.jlr.2025.100944openalex-snapshot

The role of fatty acids in neurodegenerative diseases: mechanistic insights and therapeutic strategies

inferred← citeshttps://doi.org/10.1016/j.lfs.2021.119790openalex-snapshot

An update on Alzheimer's disease: Immunotherapeutic agents, stem cell therapy and gene editing

inferred← citeshttps://doi.org/10.1016/j.mad.2021.111560openalex-snapshot

Microbiota-gut-brain axis and Alzheimer’s disease: Implications of the blood-brain barrier as an intervention target

inferred← citeshttps://doi.org/10.1016/j.mser.2019.100522openalex-snapshot

Materials for blood brain barrier modeling in vitro

inferred← citeshttps://doi.org/10.1016/j.nbd.2023.106316openalex-snapshot

Time- and region-dependent blood-brain barrier impairment in a rat model of organophosphate-induced status epilepticus

inferred← citeshttps://doi.org/10.1016/j.ncrna.2021.06.003openalex-snapshot

Involvement of noncoding RNA in blood-brain barrier integrity in central nervous system disease

inferred← citeshttps://doi.org/10.1016/j.neuint.2019.03.014openalex-snapshot

Can magnesium reduce central neurodegeneration in Alzheimer's disease? Basic evidences and research needs

inferred← citeshttps://doi.org/10.1016/j.neuint.2022.105278openalex-snapshot

NMDA mediates disruption of blood-brain barrier permeability via Rho/ROCK signaling pathway

inferred← citeshttps://doi.org/10.1016/j.neuint.2026.106115openalex-snapshot

Redox-sensitive high mobility group box 1 (HMGB1) protein is a multipotent regulator in the pathogenesis of Alzheimer's disease

inferred← citeshttps://doi.org/10.1016/j.neuint.2026.106258openalex-snapshot

Neuroinflammation and vascular pathology in Alzheimer's Disease: The NRF2/HO-1 axis as a modulator of microglial phenotypes

inferred← citeshttps://doi.org/10.1016/j.neulet.2021.136221openalex-snapshot

Molecular mechanisms of sex hormones in the development and progression of Alzheimer's disease

inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2019.09.017openalex-snapshot

White matter hyperintensities mediate the association between blood-brain barrier leakage and information processing speed

inferred← citeshttps://doi.org/10.1016/j.neuroimage.2018.09.044openalex-snapshot

Exploring Alzheimer's disease mouse brain through X-ray phase contrast tomography: From the cell to the organ

inferred← citeshttps://doi.org/10.1016/j.neuroimage.2020.116944openalex-snapshot

White matter hyperintensities are associated with subthreshold amyloid accumulation

inferred← citeshttps://doi.org/10.1016/j.neuron.2019.06.002openalex-snapshot

Cerebral Microvascular Injury: A Potentially Treatable Endophenotype of Traumatic Brain Injury-Induced Neurodegeneration

inferred← citeshttps://doi.org/10.1016/j.neuron.2020.02.034openalex-snapshot

Alzheimer’s Risk Factors Age, APOE Genotype, and Sex Drive Distinct Molecular Pathways

inferred← citeshttps://doi.org/10.1016/j.neuroscience.2020.11.015openalex-snapshot

A Multilevel View of the Development of Alzheimer’s Disease

inferred← citeshttps://doi.org/10.1016/j.neurot.2023.10.009openalex-snapshot

Alzheimer's disease brain endothelial-like cells reveal differential drug transporter expression and modulation by potentially therapeutic focused ultrasound

inferred← citeshttps://doi.org/10.1016/j.npep.2026.102652openalex-snapshot

Perioperative orexin-A protects brain microvascular endothelial integrity in experimental sepsis-associated encephalopathy

inferred← citeshttps://doi.org/10.1016/j.nxnano.2026.100495openalex-snapshot

Nanomedicine approaches for Alzheimer’s disease: Advances in drug delivery and theranostic applications

inferred← citeshttps://doi.org/10.1016/j.patol.2024.100800openalex-snapshot

Histopathological changes of nervous tissue in women over 60 years of age with Alzheimer's disease and their relationship with menopause

inferred← citeshttps://doi.org/10.1016/j.phrs.2024.107101openalex-snapshot

The VEGFs/VEGFRs system in Alzheimer’s and Parkinson’s diseases: Pathophysiological roles and therapeutic implications

inferred← citeshttps://doi.org/10.1016/j.phymed.2026.157813openalex-snapshot

Unraveling the Anti-Alzheimer's mechanisms of optimal constituent from Arisaema heterophyllum Blume through multi-model and phytochemical analysis

inferred← citeshttps://doi.org/10.1016/j.preteyeres.2023.101217openalex-snapshot

Neurovascular dysfunction in glaucoma

inferred← citeshttps://doi.org/10.1016/j.prp.2025.156109openalex-snapshot

Unravelling the Alzheimer's pathogenesis: Molecular and cellular pathways to neurodegeneration and therapeutic targets

inferred← citeshttps://doi.org/10.1016/j.semcdb.2019.12.014openalex-snapshot

Cerebrospinal fluid and central nervous system development

inferred← citeshttps://doi.org/10.1016/j.trsl.2022.12.003openalex-snapshot

Vascular contributions to Alzheimer's disease

inferred← citeshttps://doi.org/10.1016/j.yexcr.2018.05.025openalex-snapshot

Aβ1–42 oligomer induces alteration of tight junction scaffold proteins via RAGE-mediated autophagy in bEnd.3 cells

inferred← citeshttps://doi.org/10.1016/j.yjmcc.2021.11.005openalex-snapshot

Computational model of brain endothelial cell signaling pathways predicts therapeutic targets for cerebral pathologies

inferred← citeshttps://doi.org/10.1017/9781009086974.017openalex-snapshot

Supplemental Tables and Figures

inferred← citeshttps://doi.org/10.1017/s0033291720000586openalex-snapshot

Migration and dementia: a meta-analysis of epidemiological studies in Europe

inferred← citeshttps://doi.org/10.1021/acsami.1c18465openalex-snapshot

Generation of Interconnected Neural Clusters in Multiscale Scaffolds from Human-Induced Pluripotent Stem Cells

inferred← citeshttps://doi.org/10.1021/acsami.8b03962openalex-snapshot

Establishment of a Human iPSC- and Nanofiber-Based Microphysiological Blood–Brain Barrier System

inferred← citeshttps://doi.org/10.1021/acschemneuro.4c00326openalex-snapshot

The Usnic Acid Analogue 4-FPBUA Enhances the Blood–Brain Barrier Function and Induces Autophagy in Alzheimer’s Disease Mouse Models

inferred← citeshttps://doi.org/10.1038/s41371-020-0352-2openalex-snapshot

Blood–brain barrier dysfunction: the undervalued frontier of hypertension

inferred← citeshttps://doi.org/10.1038/s41392-025-02426-1openalex-snapshot

Rapid amyloid-β clearance and cognitive recovery through multivalent modulation of blood–brain barrier transport

inferred← citeshttps://doi.org/10.1038/s41398-020-01102-yopenalex-snapshot

Correction: Correlation between cognition and plasma noradrenaline level in Alzheimer’s disease: a potential new blood marker of disease evolution

inferred← citeshttps://doi.org/10.1038/s41398-020-0841-7openalex-snapshot

Correlation between cognition and plasma noradrenaline level in Alzheimer’s disease: a potential new blood marker of disease evolution

inferred← citeshttps://doi.org/10.1038/s41419-024-06804-5openalex-snapshot

Mitophagy-related regulated cell death: molecular mechanisms and disease implications

inferred← citeshttps://doi.org/10.1038/s41467-026-71379-yopenalex-snapshot

Intraocular pressure induced blood retinal barrier compromise in mouse models and human glaucoma

inferred← citeshttps://doi.org/10.1038/s41536-023-00311-5openalex-snapshot

Nerve growth factor receptor (Ngfr) induces neurogenic plasticity by suppressing reactive astroglial Lcn2/Slc22a17 signaling in Alzheimer’s disease

inferred← citeshttps://doi.org/10.1038/s41598-019-42439-9openalex-snapshot

Assembly of Human Stem Cell-Derived Cortical Spheroids and Vascular Spheroids to Model 3-D Brain-like Tissues

inferred← citeshttps://doi.org/10.1038/s41598-021-84730-8openalex-snapshot

Blast-induced temporal alterations in blood–brain barrier properties in a rodent model

inferred← citeshttps://doi.org/10.1038/s41598-025-95183-8openalex-snapshot

Exome sequencing of a Portuguese cohort of early-onset Alzheimer’s disease implicates the X-linked lysosomal gene GLA

inferred← citeshttps://doi.org/10.1038/s41598-025-99364-3openalex-snapshot

Optimized enrichment of murine blood–brain barrier vessels with a critical focus on network hierarchy in post-collection analysis

inferred← citeshttps://doi.org/10.1038/s42003-024-06591-xopenalex-snapshot

Exploring cross-tissue DNA methylation patterns: blood–brain CpGs as potential neurodegenerative disease biomarkers

inferred← citeshttps://doi.org/10.1038/s43587-026-01204-0openalex-snapshot

Fibronectin mediates APOE4-driven blood–brain barrier dysfunction in Alzheimer’s disease

inferred← citeshttps://doi.org/10.1039/d1fo01755aopenalex-snapshot

Safflower leaf ameliorates cognitive impairment through moderating excessive astrocyte activation in APP/PS1 mice

inferred← citeshttps://doi.org/10.1039/d2lc00305hopenalex-snapshot

Blood–brain barrier (BBB)-on-a-chip: a promising breakthrough in brain disease research

inferred← citeshttps://doi.org/10.1042/bsr20193629openalex-snapshot

Peripheral inflammation promotes brain tau transmission via disrupting blood–brain barrier

inferred← citeshttps://doi.org/10.1073/pnas.1811172115openalex-snapshot

Blood-derived plasminogen drives brain inflammation and plaque deposition in a mouse model of Alzheimer’s disease

inferred← citeshttps://doi.org/10.1080/10717544.2020.1762262openalex-snapshot

Brain delivery of quercetin-loaded exosomes improved cognitive function in AD mice by inhibiting phosphorylated tau-mediated neurofibrillary tangles

inferred← citeshttps://doi.org/10.1080/10717544.2022.2094501openalex-snapshot

Nanoparticles-based anti-aging treatment of Alzheimer’s disease

inferred← citeshttps://doi.org/10.1080/14737175.2025.2500752openalex-snapshot

Uncertainties in anti-amyloid monoclonal antibody therapy for Alzheimer’s disease: the challenges ahead

inferred← citeshttps://doi.org/10.1080/14787210.2021.1925540openalex-snapshot

Possible effects of Porphyromonas gingivalis on the blood–brain barrier in Alzheimer’s disease

inferred← citeshttps://doi.org/10.1080/17425247.2019.1583205openalex-snapshot

Blood-brain barrier receptors and transporters: an insight on their function and how to exploit them through nanotechnology

inferred← citeshttps://doi.org/10.1080/26895293.2025.2543709openalex-snapshot

Research progress in mechanisms of neurotoxicity induced by micro(nano)plastic exposure

inferred← citeshttps://doi.org/10.1089/ars.2022.0107openalex-snapshot

Advances in Antioxidant Nanomedicines for Imaging and Therapy of Alzheimer's Disease

inferred← citeshttps://doi.org/10.1089/ten.teb.2020.0091openalex-snapshot

Engineering Brain-Specific Pericytes from Human Pluripotent Stem Cells

inferred← citeshttps://doi.org/10.1093/abbs/gmaa002openalex-snapshot

Inhibition of glycogen synthase kinase 3β improves cognitive function in aged mice by upregulating claudin presences in cerebral endothelial cells

inferred← citeshttps://doi.org/10.1093/brain/awaa325openalex-snapshot

Pathophysiological subtypes of Alzheimer’s disease based on cerebrospinal fluid proteomics

inferred← citeshttps://doi.org/10.1093/brain/awac236openalex-snapshot

Activation of Wnt/β-catenin pathway mitigates blood–brain barrier dysfunction in Alzheimer’s disease

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/brain/awz011openalex-snapshot

Selective loss of cortical endothelial tight junction proteins during Alzheimer’s disease progression

inferred← citeshttps://doi.org/10.1093/braincomms/fcac288openalex-snapshot

Ependymal cells and neurodegenerative disease: outcomes of compromised ependymal barrier function

inferred← citeshttps://doi.org/10.1093/jnen/nlaa019openalex-snapshot

Elevated Cerebrospinal Fluid and Plasma N-Cadherin in Alzheimer Disease

inferred← citeshttps://doi.org/10.1097/wad.0000000000000420openalex-snapshot

β-Amyloid Orchestrates Factor XII and Platelet Activation Leading to Endothelial Dysfunction and Abnormal Fibrinolysis in Alzheimer Disease

inferred← citeshttps://doi.org/10.1098/rsob.200286openalex-snapshot

Alzheimer's disease-like perturbations in HIV-mediated neuronal dysfunctions: understanding mechanisms and developing therapeutic strategies

inferred← citeshttps://doi.org/10.1101/2020.03.25.20043158openalex-snapshot

Pathophysiological subtypes of Alzheimer’s disease based on cerebrospinal fluid proteomics

inferred← citeshttps://doi.org/10.1101/2021.03.27.437282openalex-snapshot

In vivo dissection of Rhoa function in vascular development using zebrafish

inferred← citeshttps://doi.org/10.1101/2024.06.11.24308689openalex-snapshot

Aquaporin-4 as an early cerebrospinal fluid biomarker of Alzheimer’s disease

inferred← citeshttps://doi.org/10.1101/2025.01.24.634732openalex-snapshot

APOE- ε4-induced Fibronectin at the blood-brain barrier is a conserved pathological mediator of disrupted astrocyte-endothelia interaction in Alzheimer’s disease

inferred← citeshttps://doi.org/10.1101/2025.09.02.673886openalex-snapshot

Predicting emergent phenotypes from single cell populations using CELLECTION

inferred← citeshttps://doi.org/10.1101/768267openalex-snapshot

Claudin-12 deficiency causes nerve barrier breakdown, mechanical hypersensitivity and painfulness in polyneuropathy

inferred← citeshttps://doi.org/10.1109/iccasit55263.2022.9986646openalex-snapshot

Study on blood vessel segmentation of laser scattering microscopic image

inferred← citeshttps://doi.org/10.1111/acel.70719openalex-snapshot

Rethinking Senescence Hallmarks in the Brain: Lessons From Peripheral Tissues and Challenges in Defining Neuronal Senescence

inferred← citeshttps://doi.org/10.1111/apha.13642openalex-snapshot

Cognitive impairment in myocardial infarction and heart failure

inferred← citeshttps://doi.org/10.1111/bpa.12895openalex-snapshot

Distinct changes in all major components of the neurovascular unit across different neuropathological stages of Alzheimer's disease

inferred← citeshttps://doi.org/10.1111/bpa.13061openalex-snapshot

Pathological changes within the cerebral vasculature in Alzheimer’s disease: New perspectives

inferred← citeshttps://doi.org/10.1111/bpa.13097openalex-snapshot

Evidence of beta amyloid independent small vessel disease in familial Alzheimer's disease

inferred← citeshttps://doi.org/10.1111/bpa.13270openalex-snapshot

Decreased microvascular claudin‐5 levels in cerebral amyloid angiopathy associated with intracerebral haemorrhage

inferred← citeshttps://doi.org/10.1111/bph.16243openalex-snapshot

Adipose tissue as a therapeutic target for vascular damage in Alzheimer's disease

inferred← citeshttps://doi.org/10.1111/jnc.15819openalex-snapshot

Brain iron acquisition: An overview of homeostatic regulation and disease dysregulation

inferred← citeshttps://doi.org/10.1111/micc.70079openalex-snapshot

Beyond Viral Control: Tenofovir's Hidden Impact on Blood–Brain Barrier Endothelial Cells

inferred← citeshttps://doi.org/10.1111/neup.13021openalex-snapshot

Blood–brain barrier dysfunction in multiple system atrophy: A human postmortem study

inferred← citeshttps://doi.org/10.1111/nyas.13998openalex-snapshot

Emerging insights from the genetics of cerebral small‐vessel disease

inferred← citeshttps://doi.org/10.1117/12.2524427openalex-snapshot

Optical monitoring of the meningeal lymphatic clearance after opening of blood-brain barrier

inferred← citeshttps://doi.org/10.1124/jpet.124.002280openalex-snapshot

Molecular Mechanisms Underlying Amyloid Beta Peptide Mediated Upregulation of Vascular Cell Adhesion Molecule-1 in Alzheimer Disease

inferred← citeshttps://doi.org/10.1134/s1990750821030057openalex-snapshot

Features of the In Vitro Expression Profile of Hippocampal Neurogenic Niche Cells during Optogenetic Stimulation

inferred← citeshttps://doi.org/10.1136/bmj.n1954openalex-snapshot

Residential exposure to transportation noise in Denmark and incidence of dementia: national cohort study

inferred← citeshttps://doi.org/10.1152/physrev.00040.2024openalex-snapshot

Neuropathological links between T2DM and LOAD: systematic review and meta-analysis

inferred← citeshttps://doi.org/10.1155/2017/7905486openalex-snapshot

P‐glycoprotein (ABCB1) and Oxidative Stress: Focus on Alzheimer’s Disease

inferred← citeshttps://doi.org/10.1155/2021/1995766openalex-snapshot

Identification of Chemical Components of Qi-Fu-Yin and Its Prototype Components and Metabolites in Rat Plasma and Cerebrospinal Fluid via UPLC-Q-TOF-MS

inferred← citeshttps://doi.org/10.1155/2021/6521146openalex-snapshot

DL0410 Alleviates Memory Impairment in D‐Galactose‐Induced Aging Rats by Suppressing Neuroinflammation via the TLR4/MyD88/NF‐κB Pathway

inferred← citeshttps://doi.org/10.1161/circresaha.122.319951openalex-snapshot

Post-Stroke Cognitive Impairment and Dementia

inferred← citeshttps://doi.org/10.1161/circulationaha.125.077356openalex-snapshot

Apolipoprotein D, a Novel Ligand for CD36, Is Essential for Blood–Brain Barrier Integrity

inferred← citeshttps://doi.org/10.1161/strokeaha.120.031611openalex-snapshot

Cognitive Impairment and Dementia After Stroke: Design and Rationale for the DISCOVERY Study

inferred← citeshttps://doi.org/10.1172/jci.insight.163822openalex-snapshot

LRP1 in vascular mural cells modulates cerebrovascular integrity and function in the presence of APOE4

inferred← citeshttps://doi.org/10.1177/0004867418796955openalex-snapshot

Leaky brain in neurological and psychiatric disorders: Drivers and consequences

inferred← citeshttps://doi.org/10.1177/0271678x231180035openalex-snapshot

Blood-brain barrier breakdown is linked to tau pathology and neuronal injury in a differential manner according to amyloid deposition

inferred← citeshttps://doi.org/10.1177/03601293261470424openalex-snapshot

Acupuncture at Jing-Well Points in Neurological Disorders: Clinical Efficacy, Mechanisms, and Future Directions

showing the first 200 of 435

Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.