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Astrocytic laminin regulates pericyte differentiation and maintains blood brain barrier integrity

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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/(sici)1097-4547(19980915)53:6<637::aid-jnr1>3.0.co;2-6openalex-snapshot

Role of the CNS microvascular pericyte in the blood-brain barrier

inferredcites →https://doi.org/10.1002/ana.21549openalex-snapshot

Lacunar stroke is associated with diffuse blood–brain barrier dysfunction

inferredcites →https://doi.org/10.1002/glia.10216openalex-snapshot

Severe alterations of endothelial and glial cells in the blood‐brain barrier of dystrophic mdx mice

inferredcites →https://doi.org/10.1002/glia.20876openalex-snapshot

Conditional deletion of beta1-integrin in astroglia causes partial reactive gliosis.

inferredcites →https://doi.org/10.1002/jnr.21877openalex-snapshot

Ultrastructural and temporal changes of the microvascular basement membrane and astrocyte interface following focal cerebral ischemia

inferredcites →https://doi.org/10.1006/dbio.1997.8668openalex-snapshot

Developmental Regulation of the Laminin α5 Chain Suggests a Role in Epithelial and Endothelial Cell Maturation

inferredcites →https://doi.org/10.1007/978-1-60761-938-3_2openalex-snapshot

Morphology and Properties of Pericytes

inferredcites →https://doi.org/10.1007/bf00306112openalex-snapshot

Fibronectin and the basement membrane components laminin and collagen type IV influence the phenotypic properties of subcultured rat aortic smooth muscle cells differently

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/s11481-006-9025-3openalex-snapshot

Blood–brain Barrier: Structural Components and Function Under Physiologic and Pathologic Conditions

inferredcites →https://doi.org/10.1016/0306-4522(95)00496-3openalex-snapshot

Laminin α2 is a component of brain capillary basement membrane: Reduced expression in dystrophic dy mice

inferredcites →https://doi.org/10.1016/j.biocel.2011.05.002openalex-snapshot

The impact of pericytes on the blood–brain barrier integrity depends critically on the pericyte differentiation stage

inferredcites →https://doi.org/10.1016/j.brainresrev.2010.05.003openalex-snapshot

Looking at the blood–brain barrier: Molecular anatomy and possible investigation approaches

inferredcites →https://doi.org/10.1016/j.conb.2010.06.005openalex-snapshot

Astrocyte heterogeneity: an underappreciated topic in neurobiology

inferredcites →https://doi.org/10.1016/j.devcel.2011.07.001openalex-snapshot

Pericytes: Developmental, Physiological, and Pathological Perspectives, Problems, and Promises

inferredcites →https://doi.org/10.1016/j.gde.2004.08.003openalex-snapshot

Control of smooth muscle development by the myocardin family of transcriptional coactivators

inferredcites →https://doi.org/10.1016/j.mvr.2009.06.009openalex-snapshot

Reproductive age-related changes in the blood brain barrier: Expression of IgG and tight junction proteins

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.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.neuroscience.2004.02.008openalex-snapshot

Altered blood–brain barrier development in dystrophic MDX mice

inferredcites →https://doi.org/10.1016/j.pneurobio.2007.07.006openalex-snapshot

Critical role of microvasculature basal lamina in ischemic brain injury

inferredcites →https://doi.org/10.1016/j.resp.2010.06.009openalex-snapshot

ATP, glia and central respiratory control

inferredcites →https://doi.org/10.1016/j.ydbio.2008.12.006openalex-snapshot

Cortical deficiency of laminin γ1 impairs the AKT/GSK-3β signaling pathway and leads to defects in neurite outgrowth and neuronal migration

inferredcites →https://doi.org/10.1016/s0021-9258(18)53058-1openalex-snapshot

Differential expression of Na,K-ATPase alpha and beta subunit isoforms at the blood-brain barrier and the choroid plexus.

inferredcites →https://doi.org/10.1016/s0026-2862(03)00055-4openalex-snapshot

TGF-β1 signaling controls retinal pericyte contractile protein expression

inferredcites →https://doi.org/10.1016/s0166-2236(00)02004-xopenalex-snapshot

Molecular physiology and pathophysiology of tight junctions in the blood–brain barrier

inferredcites →https://doi.org/10.1016/s0167-4889(98)00125-6openalex-snapshot

Tight junction proteins1This review is dedicated to the memory of Thomas Kreis.1

inferredcites →https://doi.org/10.1016/s0304-3940(03)00348-3openalex-snapshot

Changes in cytoskeletal and tight junctional proteins correlate with decreased permeability induced by dexamethasone in cultured rat brain endothelial cells

inferredcites →https://doi.org/10.1016/s0896-6273(01)00374-9openalex-snapshot

β1-Class Integrins Regulate the Development of Laminae and Folia in the Cerebral and Cerebellar Cortex

inferredcites →https://doi.org/10.1016/s1537-1891(02)00200-8openalex-snapshot

Tight junctions of the blood-brain barrier: development, composition and regulation.

inferredcites →https://doi.org/10.1038/icb.1963.17openalex-snapshot

AN ELECTRON MICROSCOPIC STUDY OF LEUCOCYTIC EMIGRATION AND VASCULAR PERMEABILITY IN RAT SKIN

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/nature11087openalex-snapshot

Apolipoprotein E controls cerebrovascular integrity via cyclophilin A

inferredcites →https://doi.org/10.1038/nm.2022openalex-snapshot

Pericyte contraction induced by oxidative-nitrative stress impairs capillary reflow despite successful opening of an occluded cerebral artery

inferredcites →https://doi.org/10.1038/nrm2889openalex-snapshot

Breaching multiple barriers: leukocyte motility through venular walls and the interstitium

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/sj.jcbfm.9600272openalex-snapshot

CNS Microvascular Pericytes Exhibit Multipotential Stem Cell Activity

inferredcites →https://doi.org/10.1073/pnas.0608251104openalex-snapshot

Serum response factor and myocardin mediate arterial hypercontractility and cerebral blood flow dysregulation in Alzheimer's phenotype

inferredcites →https://doi.org/10.1073/pnas.1011321108openalex-snapshot

Pericytes in capillaries are contractile in vivo, but arterioles mediate functional hyperemia in the mouse brain

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.201212032openalex-snapshot

Ablation of astrocytic laminin impairs vascular smooth muscle cell function and leads to hemorrhagic stroke

inferredcites →https://doi.org/10.1089/ars.2007.1713openalex-snapshot

Physiologic Angiodynamics in the Brain

inferredcites →https://doi.org/10.1093/brain/awl318openalex-snapshot

Blood-brain barrier leakage may lead to progression of temporal lobe epilepsy

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

Pericyte physiology

inferredcites →https://doi.org/10.1097/mol.0b013e3282ef77e9openalex-snapshot

Role of the extracellular matrix and its receptors in smooth muscle cell function: implications in vascular development and disease

inferredcites →https://doi.org/10.1111/j.1471-4159.2009.06288.xopenalex-snapshot

Determinants of regional and local diversity within the astroglial lineage of the normal central nervous system

inferredcites →https://doi.org/10.1126/science.1203165openalex-snapshot

A Pericyte Origin of Spinal Cord Scar Tissue

inferredcites →https://doi.org/10.1161/01.res.12.4.375openalex-snapshot

Dimensions of Blood Vessels from Distributing Artery to Collecting Vein

inferredcites →https://doi.org/10.1161/circresaha.110.223800openalex-snapshot

Vascular Smooth Muscle Progenitor Cells

inferredcites →https://doi.org/10.1161/strokeaha.108.533117openalex-snapshot

Pericyte Signaling in the Neurovascular Unit

inferredcites →https://doi.org/10.1182/blood-2009-05-222364openalex-snapshot

Pericyte recruitment during vasculogenic tube assembly stimulates endothelial basement membrane matrix formation

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/10.1189/jlb.0303114openalex-snapshot

Microglia, macrophages, perivascular macrophages, and pericytes: a review of function and identification

inferredcites →https://doi.org/10.1242/dev.02486openalex-snapshot

Basement membrane attachment is dispensable for radial glial cell fate and for proliferation, but affects positioning of neuronal subtypes

inferredcites →https://doi.org/10.1371/journal.pbio.1000176openalex-snapshot

β1 Integrin Maintains Integrity of the Embryonic Neocortical Stem Cell Niche

inferredcites →https://doi.org/10.14670/hh-24.909openalex-snapshot

Pericytes. Morphofunction, interactions and pathology in a quiescent and activated mesenchymal cell niche.

inferredcites →https://doi.org/10.1523/jneurosci.5032-04.2005openalex-snapshot

Schwann Cell-Specific Ablation of Laminin γ1 Causes Apoptosis and Prevents Proliferation

inferredcites →https://doi.org/10.2174/138161208784705469openalex-snapshot

Pericytes: Pluripotent Cells of the Blood Brain Barrier

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

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inferred← citeshttps://doi.org/10.1016/j.drudis.2016.05.020openalex-snapshot

In vitro blood–brain barrier models for drug research: state-of-the-art and new perspectives on reconstituting these models on artificial basement membrane platforms

inferred← citeshttps://doi.org/10.1016/j.expneurol.2020.113257openalex-snapshot

Brain injury-induced dysfunction of the blood brain barrier as a risk for dementia

inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2025.01.046openalex-snapshot

Laminin-dystroglycan mediated ferroptosis in hemorrhagic shock and reperfusion induced-cognitive impairment through AMPK/Nrf2

inferred← citeshttps://doi.org/10.1016/j.ijdevneu.2015.05.005openalex-snapshot

Astrocytic β1‐integrin affects cellular composition of murine blood brain barrier in the cerebral cortex

inferred← citeshttps://doi.org/10.1016/j.immuni.2021.01.013openalex-snapshot

Astrocyte-immune cell interactions in physiology and pathology

inferred← citeshttps://doi.org/10.1016/j.jchemneu.2018.06.001openalex-snapshot

Markers for human brain pericytes and smooth muscle cells

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.jneumeth.2019.108349openalex-snapshot

Quantifying blood-brain-barrier leakage using a combination of evans blue and high molecular weight FITC-Dextran

inferred← citeshttps://doi.org/10.1016/j.labinv.2024.102190openalex-snapshot

D30 Alleviates β2-Microglobulin–Facilitated Neurotoxic Microglial Responses in Isoflurane/Surgery-Induced Cognitive Dysfunction in Aged Mice

inferred← citeshttps://doi.org/10.1016/j.lfs.2025.123413openalex-snapshot

Cell–cell communications in the brain of hepatic encephalopathy: The neurovascular unit

inferred← citeshttps://doi.org/10.1016/j.lmot.2024.102083openalex-snapshot

Emerging role of aquaporin in neurodegenerative diseases: A novel target for drug development

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.matbio.2017.11.009openalex-snapshot

Laminin-deficient muscular dystrophy: Molecular pathogenesis and structural repair strategies

inferred← citeshttps://doi.org/10.1016/j.matbio.2018.05.009openalex-snapshot

Tissue linkage through adjoining basement membranes: The long and the short term of it

inferred← citeshttps://doi.org/10.1016/j.matbio.2025.02.005openalex-snapshot

Laminins and the blood-brain barrier

inferred← citeshttps://doi.org/10.1016/j.matbio.2025.08.006openalex-snapshot

Laminin γ1 chain is essential for the cardiorespiratory and muscular systems

inferred← citeshttps://doi.org/10.1016/j.matbio.2026.102015openalex-snapshot

Glycocalyx and basal lamina in neurological disorders

inferred← citeshttps://doi.org/10.1016/j.matbio.2026.102030openalex-snapshot

Oligodendrocyte integrin-β1 regulates blood-brain barrier and remyelination in hemorrhagic brain

inferred← citeshttps://doi.org/10.1016/j.mattod.2020.02.001openalex-snapshot

Overcoming blood–brain barrier transport: Advances in nanoparticle-based drug delivery strategies

inferred← citeshttps://doi.org/10.1016/j.mod.2015.07.007openalex-snapshot

Formation and maintenance of the BBB

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.mvr.2019.103930openalex-snapshot

Advances on fluid shear stress regulating blood-brain barrier

inferred← citeshttps://doi.org/10.1016/j.nbd.2017.02.008openalex-snapshot

Metabolite transport across the mammalian and insect brain diffusion barriers

inferred← citeshttps://doi.org/10.1016/j.nbd.2025.107166openalex-snapshot

Exercise and the blood–brain barrier: Mechanistic insights and therapeutic implications

inferred← citeshttps://doi.org/10.1016/j.neuint.2019.03.002openalex-snapshot

Defective vascular signaling & prospective therapeutic targets in brain arteriovenous malformations

inferred← citeshttps://doi.org/10.1016/j.neulet.2018.06.027openalex-snapshot

Low-dose cisplatin causes growth inhibition and loss of autophagy of rat astrocytes in vitro

inferred← citeshttps://doi.org/10.1016/j.neulet.2019.134681openalex-snapshot

Rapid differentiation of astrocytes from human embryonic stem cells

inferred← citeshttps://doi.org/10.1016/j.neuroscience.2024.12.050openalex-snapshot

Neurovascular unit impairment in iron deficiency anemia

inferred← citeshttps://doi.org/10.1016/j.pharmr.2026.100143openalex-snapshot

Friend or foe? Glial–vascular interactions in health and neurodegenerative disease

inferred← citeshttps://doi.org/10.1016/j.pharmthera.2018.03.002openalex-snapshot

The role of TAM family receptors and ligands in the nervous system: From development to pathobiology

inferred← citeshttps://doi.org/10.1016/j.pneurobio.2017.09.001openalex-snapshot

The role of non-endothelial cells on the penetration of nanoparticles through the blood brain barrier

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

Neurovascular dysfunction in glaucoma

inferred← citeshttps://doi.org/10.1016/j.preteyeres.2025.101375openalex-snapshot

Pericytes in the optic nerve head

inferred← citeshttps://doi.org/10.1016/j.psychres.2025.116558openalex-snapshot

The role of astrocytes in attention-deficit hyperactivity disorder: An update

inferred← citeshttps://doi.org/10.1016/j.resp.2018.11.004openalex-snapshot

Prophylactic effect and mechanism of p-coumaric acid against hypoxic cerebral edema in mice

inferred← citeshttps://doi.org/10.1016/j.stem.2017.10.002openalex-snapshot

Targeting Glioma Stem Cell-Derived Pericytes Disrupts the Blood-Tumor Barrier and Improves Chemotherapeutic Efficacy

inferred← citeshttps://doi.org/10.1016/j.stemcr.2019.10.004openalex-snapshot

Patient-Specific iPSC Model of a Genetic Vascular Dementia Syndrome Reveals Failure of Mural Cells to Stabilize Capillary Structures

inferred← citeshttps://doi.org/10.1016/j.thromres.2024.109154openalex-snapshot

The hemostatic system in chronic brain diseases: A new challenging frontier?

inferred← citeshttps://doi.org/10.1016/j.toxicon.2020.06.019openalex-snapshot

VEGF/VEGFR-2 system exerts neuroprotection against Phoneutria nigriventer spider envenomation through PI3K-AKT-dependent pathway

inferred← citeshttps://doi.org/10.1016/j.ydbio.2026.07.017openalex-snapshot

Fibulin-1 is required for microvascular integrity in the developing brain and retina

inferred← citeshttps://doi.org/10.1016/j.yexcr.2017.04.007openalex-snapshot

Involvement of PUMA in pericyte migration induced by methamphetamine

inferred← citeshttps://doi.org/10.1016/j.yfrne.2020.100857openalex-snapshot

Blood-brain barrier integrity in the pathogenesis of Alzheimer’s disease

inferred← citeshttps://doi.org/10.1016/s1474-4422(21)00031-4openalex-snapshot

Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies

inferred← citeshttps://doi.org/10.1016/s1875-5364(26)61099-0openalex-snapshot

Battle of the wall for aromatic “orifice-opening” agents: defending and breaching the blood-brain barrier

inferred← citeshttps://doi.org/10.1017/s143192762200006xopenalex-snapshot

Development of the Blood–Brain Barrier in Ducks

inferred← citeshttps://doi.org/10.1021/acs.bioconjchem.5c00379openalex-snapshot

Antibody Engineering for Receptor-Mediated Transcytosis Across the Blood–Brain Barrier

inferred← citeshttps://doi.org/10.1021/acsbiomaterials.1c00406openalex-snapshot

Engineering 3D Cortical Spheroids for an In Vitro Ischemic Stroke Model

inferred← citeshttps://doi.org/10.1038/jcbfm.2015.62openalex-snapshot

Perturbations of the cerebrovascular matrisome: A convergent mechanism in small vessel disease of the brain?

inferred← citeshttps://doi.org/10.1038/ncomms11415openalex-snapshot

Laminin regulates PDGFRβ+ cell stemness and muscle development

inferred← citeshttps://doi.org/10.1038/s41380-022-01511-zopenalex-snapshot

The blood-brain barrier in aging and neurodegeneration

inferred← citeshttps://doi.org/10.1038/s41398-025-03458-5openalex-snapshot

Complement C1q is associated with neuroinflammation and mediates the association between amyloid-β and tau pathology in Alzheimer’s disease

inferred← citeshttps://doi.org/10.1038/s41413-022-00203-2openalex-snapshot

Versatile subtypes of pericytes and their roles in spinal cord injury repair, bone development and repair

inferred← citeshttps://doi.org/10.1038/s41467-020-19042-yopenalex-snapshot

Transplantation of hPSC-derived pericyte-like cells promotes functional recovery in ischemic stroke mice

inferred← citeshttps://doi.org/10.1038/s41467-022-29475-2openalex-snapshot

Astrocyte plasticity in mice ensures continued endfoot coverage of cerebral blood vessels following injury and declines with age

inferred← citeshttps://doi.org/10.1038/s41467-023-41326-2openalex-snapshot

Human blood vessel organoids reveal a critical role for CTGF in maintaining microvascular integrity

inferred← citeshttps://doi.org/10.1038/s41531-021-00175-wopenalex-snapshot

Astrocytic atrophy as a pathological feature of Parkinson’s disease with LRRK2 mutation

inferred← citeshttps://doi.org/10.1038/s41571-021-00529-6openalex-snapshot

The blood–tumour barrier in cancer biology and therapy

inferred← citeshttps://doi.org/10.1038/s41583-020-0322-2openalex-snapshot

Neuronal regulation of the blood–brain barrier and neurovascular coupling

inferred← citeshttps://doi.org/10.1038/s41583-025-00976-5openalex-snapshot

Dynamic modulation of the blood–brain barrier in the healthy brain

inferred← citeshttps://doi.org/10.1038/s41591-023-02268-wopenalex-snapshot

Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease

inferred← citeshttps://doi.org/10.1038/s41593-018-0234-xopenalex-snapshot

The role of brain vasculature in neurodegenerative disorders

inferred← citeshttps://doi.org/10.1038/s41598-019-55844-xopenalex-snapshot

The Adult Murine Intestine is Dependent on Constitutive Laminin-γ1 Synthesis

inferred← citeshttps://doi.org/10.1038/s41598-023-45570-wopenalex-snapshot

Proteomic characterization of aging-driven changes in the mouse brain by co-expression network analysis

inferred← citeshttps://doi.org/10.1038/s43018-021-00297-3openalex-snapshot

Astrocytic laminin-211 drives disseminated breast tumor cell dormancy in brain

inferred← citeshttps://doi.org/10.1038/s43018-021-00321-6openalex-snapshot

Keeping brain metastases dormant

inferred← citeshttps://doi.org/10.1038/srep35642openalex-snapshot

Silencing microRNA-143 protects the integrity of the blood-brain barrier: implications for methamphetamine abuse

inferred← citeshttps://doi.org/10.1038/srep36450openalex-snapshot

The role of pericytic laminin in blood brain barrier integrity maintenance

inferred← citeshttps://doi.org/10.1042/cs20160720openalex-snapshot

Neurovascular dysfunction in dementia – human cellular models and molecular mechanisms

inferred← citeshttps://doi.org/10.1042/cs20230148openalex-snapshot

Astrocytes at the intersection of ageing, obesity, and neurodegeneration

inferred← citeshttps://doi.org/10.1055/s-0045-1804893openalex-snapshot

Alterations in the Blood–Brain Barrier in Mood Disorders and Neurodegenerative Diseases

inferred← citeshttps://doi.org/10.1063/5.0043338openalex-snapshot

Progress in mimicking brain microenvironments to understand and treat neurological disorders

inferred← citeshttps://doi.org/10.1080/02699052.2018.1531311openalex-snapshot

The roles of astrocyte in the brain pathologies following ischemic stroke

inferred← citeshttps://doi.org/10.1080/07853890.2024.2445194openalex-snapshot

Deciphering the role of APOE in cerebral amyloid angiopathy: from genetic insights to therapeutic horizons

inferred← citeshttps://doi.org/10.1080/10408398.2026.2659866openalex-snapshot

Nutritional modulation of the glymphatic system: mechanistic insights and clinical implications

inferred← citeshttps://doi.org/10.1080/1040841x.2022.2163613openalex-snapshot

Porphyromonas gingivalis and the pathogenesis of Alzheimer’s disease

inferred← citeshttps://doi.org/10.1080/15384047.2026.2725357openalex-snapshot

Elevated miR-103b in exosomes derived from brain-metastatic triple-negative breast cancer cells remodels the brain pre-metastatic niche (PMN)

inferred← citeshttps://doi.org/10.1080/19336950.2020.1870088openalex-snapshot

TRPM2 in ischemic stroke: Structure, molecular mechanisms, and drug intervention

inferred← citeshttps://doi.org/10.1083/jcb.201807178openalex-snapshot

Perlecan regulates pericyte dynamics in the maintenance and repair of the blood–brain barrier

inferred← citeshttps://doi.org/10.1083/jcb.202103098openalex-snapshot

Endothelial depletion of Atg7 triggers astrocyte–microvascular disassociation at blood–brain barrier

inferred← citeshttps://doi.org/10.1088/1758-5090/abf741openalex-snapshot

An engineered neurovascular unit for modeling neuroinflammation

inferred← citeshttps://doi.org/10.1089/ars.2016.6873openalex-snapshot

Nitration of TRPM2 as a Molecular Switch Induces Autophagy During Brain Pericyte Injury

inferred← citeshttps://doi.org/10.1089/ars.2021.0120openalex-snapshot

Extracellular Matrix and Oxidative Stress Following Traumatic Spinal Cord Injury: Physiological and Pathophysiological Roles and Opportunities for Therapeutic Intervention

inferred← citeshttps://doi.org/10.1101/2021.05.08.443259openalex-snapshot

Astrocyte plasticity ensures continued endfoot coverage of cerebral blood vessels and integrity of the blood brain barrier, with plasticity declining with normal aging

inferred← citeshttps://doi.org/10.1101/2022.02.18.481046openalex-snapshot

Mural norrin/β-catenin signaling regulates Lama2 expression to promote neurovascular unit assembly

inferred← citeshttps://doi.org/10.1101/2023.01.04.522758openalex-snapshot

Human Brain Endothelial Cell Seeded on Inner Surface of Alginate Hollow Microfibers

inferred← citeshttps://doi.org/10.1101/2024.08.02.606279openalex-snapshot

Cleavage of the vascular matrix attracts glioblastoma cells to infiltrate the brain parenchyma

inferred← citeshttps://doi.org/10.1101/cshperspect.a027847openalex-snapshot

Directional Fluid Transport across Organ–Blood Barriers: Physiology and Cell Biology

inferred← citeshttps://doi.org/10.1101/cshperspect.a041422openalex-snapshot

The Blood–Brain Barrier: Composition, Properties, and Roles in Brain Health

inferred← citeshttps://doi.org/10.1111/acel.12370openalex-snapshot

Enhanced microglial pro‐inflammatory response to lipopolysaccharide correlates with brain infiltration and blood–brain barrier dysregulation in a mouse model of telomere shortening

inferred← citeshttps://doi.org/10.1111/acel.70712openalex-snapshot

IGF ‐1/ SLC25A33 Maintains Blood‐Labyrinth Barrier Integrity by Suppressing TGF ‐β/Smad2‐Mediated Pericyte Activation in Age‐Related Hearing Loss

inferred← citeshttps://doi.org/10.1111/brv.12454openalex-snapshot

Laminins and their receptors in the CNS

inferred← citeshttps://doi.org/10.1111/cen3.12359openalex-snapshot

Immunohistochemical analysis of laminin components in the blood–nerve barrier and blood–brain barrier

inferred← citeshttps://doi.org/10.1111/febs.13412openalex-snapshot

The dynamic blood–brain barrier

inferred← citeshttps://doi.org/10.1111/imr.13120openalex-snapshot

The emergence of the calvarial hematopoietic niche in health and disease

inferred← citeshttps://doi.org/10.1111/imr.13121openalex-snapshot

Targetability of the neurovascular unit in inflammatory diseases of the central nervous system

inferred← citeshttps://doi.org/10.1111/imr.13126openalex-snapshot

Neuroimmune signaling at the brain borders

inferred← citeshttps://doi.org/10.1111/jnc.14271openalex-snapshot

White matter degeneration in vascular and other ageing‐related dementias

inferred← citeshttps://doi.org/10.1111/jnc.70196openalex-snapshot

Common miRNAs , Genes, and Regulatory Pathways in Alzheimer's Disease and Type 2 Diabetes Mellitus: An Integrative Analysis of Systematic Reviews, Bioinformatics and Data Mining

inferred← citeshttps://doi.org/10.1111/micc.12554openalex-snapshot

The pericyte microenvironment during vascular development

inferred← citeshttps://doi.org/10.1111/neup.12374openalex-snapshot

Extracellular matrix in the CNS induced by neuropathogenic viral infection

inferred← citeshttps://doi.org/10.1124/jpet.121.000831openalex-snapshot

Glutamate Buffering Capacity and Blood-Brain Barrier Protection of Opioid Receptor Agonists Biphalin and Nociceptin

inferred← citeshttps://doi.org/10.1126/sciadv.abq2423openalex-snapshot

Astrocytic NDRG2-PPM1A interaction exacerbates blood-brain barrier disruption after subarachnoid hemorrhage

inferred← citeshttps://doi.org/10.1136/bmjdrc-2019-001120openalex-snapshot

En face slab optical coherence tomography imaging successfully monitors progressive degenerative changes in the innermost layer of the diabetic retina

inferred← citeshttps://doi.org/10.1136/svn-2018-000198openalex-snapshot

Basement membrane and blood–brain barrier

inferred← citeshttps://doi.org/10.1146/annurev-cellbio-100617-062608openalex-snapshot

Development and Cell Biology of the Blood-Brain Barrier

inferred← citeshttps://doi.org/10.1152/ajpcell.00151.2018openalex-snapshot

Roles of blood-brain barrier integrins and extracellular matrix in stroke

inferred← citeshttps://doi.org/10.1152/physrev.00050.2017openalex-snapshot

Blood-Brain Barrier: From Physiology to Disease and Back

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