Cited by 444Barrier Structure and Function StudiesCerebrospinal fluid and hydrocephalusIon Transport and Channel Regulation

The DOI matches its Crossref record; 25 of the 25 references it cites were found in a registry or an index.

Junctions in the meninges and marginal glia.

Nabeshima, Sachio, Reese, T. S., Landis, Dennis M. D., Brightman, M. W.·1975·Journal of Comparative Neurology

DOI 10.1002/cne.901640202

Open this paper in CoChat — free account

Abstract

The meninges of various mammals were prepared for examination with the electronmicroscope by thin sectioning or freeze-fracturing. Particular attention was given to the distribution of tight junctions in order to determine the basis for the meningeal barrier between the blood circulating in dural vessels and the cerebrospinal fluid in the subarachnoid space. While some dural blood vessels are fenestrated, those in the subarachnoid space are not and their component endothelial cells are joined by an extensive system of tight junctions. An extensive and continuous system of tight junctions was also found in a layer of specialized cells at the border of the arachnoid with the dura. This arachnoid barrier layer is apparently the only basis of the meningeal barrier because often cellular layers in the dura and arachnoid lack tight junctions although they are linked by gap junctions and desmosomes. In particular, tight junctions are lacking at the border of the "subdural space" which is actually a fascial plane within the dura. Tight junctions are also lacking between astrocytes at the surface of the brain but these cells are linked by gap junctions and a new type of intercellular junction. The distribution of these junctions, as well as assemblies of intramembranous particles at the astrocytic border, raises the question whether this layer might have a role in the exchange of certain substances between the brain and cerebrospinal fluid.

Integrity signals

Registry

Crossref · 10.1002/cne.901640202

Cites

25 of 25 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

JUNCTIONAL COMPLEXES IN VARIOUS EPITHELIA
Farquhar, M. G., & Palade, G. E. (1963) · The Journal of Cell Biology · doi:10.1083/jcb.17.2.375 · Cited by 3,637
FINE STRUCTURAL LOCALIZATION OF A BLOOD-BRAIN BARRIER TO EXOGENOUS PEROXIDASE
Reese, T. S., & Karnovsky, M. J. (1967) · The Journal of Cell Biology · doi:10.1083/jcb.34.1.207 · Cited by 2,629
JUNCTIONS BETWEEN INTIMATELY APPOSED CELL MEMBRANES IN THE VERTEBRATE BRAIN
Brightman, M., & Reese, T. S. (1969) · The Journal of Cell Biology · doi:10.1083/jcb.40.3.648 · Cited by 2,457
A Textbook of Histology
Bloom, W., & Fawcett, D. W. (1962) · Cited by 2,210
FRACTURE FACES OF ZONULAE OCCLUDENTES FROM "TIGHT" AND "LEAKY" EPITHELIA
Claude, P., & Goodenough, D. A. (1973) · The Journal of Cell Biology · doi:10.1083/jcb.58.2.390 · Cited by 1,094
Further observations on the fine structure of freeze-cleaved tight junctions
Staehelin, L. A. (1973) · Journal of Cell Science · doi:10.1242/jcs.13.3.763 · Cited by 512
The effect on the isolated rabbit heart of vagal stimulation and its modification by cocaine, hexamethonium and ouabain
McEwen, L. M. (1956) · The Journal of Physiology · doi:10.1113/jphysiol.1956.sp005493 · Cited by 395
ARRAYS OF PARTICLES IN FREEZE-FRACTURED ASTROCYTIC MEMBRANES
Landis, D. M. D., & Reese, T. S. (1974) · The Journal of Cell Biology · doi:10.1083/jcb.60.1.316 · Cited by 257
Untitled work
(1962) · PubMed · Cited by 173
ULTRASTRUCTURAL STUDIES ON THE PERMEABILITY OF THE MESOTHELIUM TO HORSERADISH PEROXIDASE
Cotran, R. S., & Karnovsky, M. J. (1968) · The Journal of Cell Biology · doi:10.1083/jcb.37.1.123 · Cited by 161

Flagged first, then by citations

Show all 25 references

Research works printed but not linked: 6

Brightman M. W., 1975, Brain‐Endocrine Interaction II. The Ventricular System, 134
Broman T., 1949, The Permeability of the Cerebrospinal Vessels in Normal and Pathological Conditions
Key G., 1876, Anatomie des Nervensystems und des Bindesgewebe
Landis D. M. D., 1974, Membrane structure in rapidly frozen, freeze‐fractured cerebellar cortex, J. Cell Biol., 63, 184a
Matter A., 1969, A study on the permeability barriers between Disse's space and the bile canaliculus, J. Ultrastruct. Res., 11, 5
Nabeshima S., 1972, Barrier to proteins within the spinal meninges, J. Neuropath. Exp. Neurol., 31, 176

Sorted by citations

Items 301–400 of 444

Freeze-fracture studies of the macromolecular organization of glial membranes
Cullen, M. J., & Gulley, R. L. (1980) · Trends in Neurosciences · doi:10.1016/0166-2236(80)90043-0 · Cited by 8
Formation and Function of the Meninges Arachnoid Barrier Around the Developing BrainPreprint
Derk, J., Como, C. N., Jones, H. E., Joyce, L. R., Bonney, S. K., O’Rourke, R., Pawlikowski, B. T., Doran, K. S., & Siegenthaler, J. A. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.06.10.495709 · Cited by 8
Tau-aggregation inhibition: promising role of nanoencapsulated dietary molecules in the management of Alzheimer’s disease
Nagaraju, P. G., Ashwini, S., & G., P. P. C. (2022) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2022.2092446 · Cited by 7
Torcular Dural Sinus Malformation: Fetal and Postnatal Imaging Findings and Their Associations With Clinical Outcomes
Goldman-Yassen, A. E., Shifrin, A., Mirsky, D. M., Vossough, A., Licht, D. J., & Feygin, T. (2022) · Pediatric Neurology · doi:10.1016/j.pediatrneurol.2022.07.004 · Cited by 7
Brain Maturation as a Fundamental Factor in Immune-Neurovascular Interactions in Stroke
Martino, E. D., Rayasam, A., & Vexler, Z. S. (2023) · Translational Stroke Research · doi:10.1007/s12975-022-01111-7 · Cited by 7
Dural microvessels: molecular properties of their luminal anionic sites
Lawrenson, J. G., Reid, A. R., Ghabriel, M. N., & Allt, G. (1996) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(96)00048-2 · Cited by 7
Arachnoidea and subarachnoid spaces of the vault of the skull in man
Rascol, M. M., & Izard, J. Y. (1978) · Acta Neuropathologica · doi:10.1007/bf00689555 · Cited by 7
Muscarinic Binding of Pial Vessels and Arachnoid Membrane
Lasbennes, F., VERRECCHIA, C., Philipson, V., & Seylaz, J. (1992) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.1992.tb10968.x · Cited by 7
Freeze-fracture analysis of plasma membranes of isolated astrocytes from rat brain
Andres, J. J., Blessing, P. M., & Brightman, M. (1983) · Brain Research · doi:10.1016/0006-8993(83)90226-3 · Cited by 7
Newly discovered base barrier cells provide compartmentalization of choroid plexus, brain and CSFPreprint
Verhaege, D., Nolf, C. D., Castelein, J., Claeys, W., Wonterghem, E. V., Imschoot, G. V., Dujardin, P., Spiegelaere, W. D., Hoste, E., Boone, F., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.07.08.601696 · Cited by 7
In vivo imaging of the barrier properties of the glia limitans during health and neuroinflammation
Hélie, P., Kloster, F., Pareja, J. R., Vladymyrov, M., Mapunda, J. A., Bouillet, E., Oetiker, Y., Spera, I., Barcos, S., Brenna, A., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-63945-7 · Cited by 7
Response to Commentary on “Structural characterization of SLYM – a 4th meningeal membrane” by Julie Siegenthaler and Christer Betsholtz
Plá, V., Bitsika, S., Giannetto, M. J., Ladrón-de-Guevara, A., Gahn‐Martinez, D., Mori, Y., Nedergaard, M., & Møllgård, K. (2024) · Fluids and Barriers of the CNS · doi:10.1186/s12987-024-00567-z · Cited by 6
Blood-Arachnoid Barrier as a Dynamic Physiological and Pharmacological Interface Between Cerebrospinal Fluid and Blood
Uchida, Y., Goto, R., Usui, T., Tachikawa, M., & Terasaki, T. (2022) · AAPS advances in the pharmaceutical sciences series · doi:10.1007/978-3-030-88773-5_4 · Cited by 6
Development of the Cerebrospinal Fluid Pathways During Embryonic and Fetal Life in Humans
Catala, M. (2005) · Springer eBooks · doi:10.1007/978-88-470-2121-1_2 · Cited by 6
The ultrastructure of the rhombencephalic posterior tela and adjacent tissues in an amphibian, Rana pipiens.
Jones, H. C. (1982) · Europe PMC (PubMed Central) · Cited by 6
History and Basic Concepts
Davson, H., Zloković, B. V., Rakić, L., & Segal, M. B. (1993) · doi:10.1007/978-1-349-11882-3_1 · Cited by 6
Chapter 57: Aspects of normal cerebrospinal fluid circulation and circumventricular organs
Hashimoto, P. H. (1992) · Progress in brain research · doi:10.1016/s0079-6123(08)62364-x · Cited by 6
Geschwülste des zentralen und peripheren Nervensystems
Mennel, H. D. (1988) · Spezielle pathologische Anatomie · doi:10.1007/978-3-642-73410-6_2 · Cited by 6
The meninges as a neuroimmune interface: structure, barriers and roles in CNS disease
Joost, S., Kaddatz, H., Vankriekelsvenne, E., & Brandenburg, L. (2026) · Fluids and Barriers of the CNS · doi:10.1186/s12987-026-00795-5 · Cited by 7
Use of Intraventricular Medications in Critically Ill Patients
Erdman, M. J., Marrese, A. R., Haller, J. T., Barthol, C. A., & Small, C. E. (2020) · Critical Care Nursing Quarterly · doi:10.1097/cnq.0000000000000300 · Cited by 5
Torcular pseudomass in newborns and its association with delivery: follow up or leave it alone?
Ceylan, A. H., Nascene, D. R., Huang, H., Luedemann, C., Rubin, N., & Özütemiz, C. (2022) · Neuroradiology · doi:10.1007/s00234-022-02981-2 · Cited by 5
The Cerebellum and Its Wrapping Meninge: Developmental Interplay between Two Major Structures
Catala, M. (2017) · Neuropediatrics · doi:10.1055/s-0037-1601322 · Cited by 5
Origin and Pathological Significance of Smooth Muscle Cells and Myofibroblasts in the Subdural Neomembrane
Kawano, N., Endo, M., SAITO, M., NAKAYAMA, K., & Beppu, T. (1986) · Neurologia medico-chirurgica · doi:10.2176/nmc.26.361 · Cited by 5
Ultrastructure of complex carbohydrates of rodent and monkey ependymal glycocalyx and meninges
Rhodes, R. H. (1987) · American Journal of Anatomy · doi:10.1002/aja.1001790407 · Cited by 5
Cerebrospinal Fluid Physiology
McComb, J. G., & Yamada, S. (2011) · Elsevier eBooks · doi:10.1016/b978-1-4160-5316-3.00191-x · Cited by 5
The perineurial vessel: A possible candidate for the structural basis of the meridian (Jing-Luo) in Chinese medicine*
Hashimoto, P. H. (2005) · Anatomical Science International · doi:10.1111/j.1447-073x.2005.00118.x · Cited by 5
Transcytosis of Macromolecules through the Blood—Brain Fluid Barriers in Vivo
Broadwell, R. D. (1993) · Pharmaceutical biotechnology · doi:10.1007/978-1-4615-2898-2_11 · Cited by 5
DRUG TRANSPORT IN THE BRAIN
Sangha, V., Williams, E. I., Ronaldson, P. T., & Bendayan, R. (2022) · Wiley eBooks · doi:10.1002/9781119739883.ch14 · Cited by 5
Heterogeneity in cranial dura mater at the microscale: An In-situ and ex-vivo structural and mechanical investigation of sulcus and gyrus Dura
Tabatabaei, M., & Williams, L. N. (2025) · Acta Biomaterialia · doi:10.1016/j.actbio.2025.02.053 · Cited by 4
In-vitro and In-silico Examinations on Baicalein-loaded Solid Lipid Nanoparticles for Neurodegeneration
Varshney, M., Kumar, B., Varshney, P., Lal, D. K., & Sethiya, N. K. (2024) · Drug Delivery Letters · doi:10.2174/0122103031263883231230085819 · Cited by 4
Regulation of folate transport at the mouse arachnoid barrier
Sangha, V., Aboulhassane, S., & Bendayan, R. (2024) · Fluids and Barriers of the CNS · doi:10.1186/s12987-024-00566-0 · Cited by 4
Introduction to and Applications of Injury Biomechanics
King, A. I. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1732-7_1 · Cited by 4
Venous drainage through the internal auditory meatus of the guinea pig cochlea
Tono, T., & Morimitsu, T. (1992) · European Archives of Oto-Rhino-Laryngology · doi:10.1007/bf00175667 · Cited by 4
Physical Injury to the Nervous System
Leestma, J. E., & Thibault, K. L. (2014) · CRC Press eBooks · doi:10.1201/b16882-13 · Cited by 4
Fine structure of the lateral areas of the rhombencephalic tela of the bullfrog, Rana catesbeiana
Michaels, J. E., & Tornheim, P. (1980) · Cell and Tissue Research · doi:10.1007/bf00234399 · Cited by 4
Initial process of diffusion of small molecules from blood vessels to the meninges in the young rat
Lefauconnier, J.-M., Bouchaud, C., & Bernard, G. (1991) · Neuroscience Letters · doi:10.1016/0304-3940(91)90636-8 · Cited by 4
An immunocytochemical and ultrastructural study of a specialized glial region of the medulla oblongata of the adult and juvenile grey mullet
Díaz‐Regueira, S. M., Álvarez‐Otero, R., & Anadón, R. (1993) · Tissue and Cell · doi:10.1016/0040-8166(93)90048-p · Cited by 4
Glial Linings of the Brain
Bigio, M. R. D. (2002) · Humana Press eBooks · doi:10.1007/978-1-59259-108-4_13 · Cited by 4
Meningeal Inflammation and Arachnoid Barrier Breakdown in a Mouse Model of Neonatal Bacterial MeningitisPreprint
Kim, S., Joyce, L. R., Brady, A., Spencer, B. L., Pawlikowski, B. T., Derk, J., Doran, K. S., & Siegenthaler, J. A. (2026) · SSRN Electronic Journal · doi:10.64898/2026.03.04.709573 · Cited by 4
Skull–meninges–brain connectivity and extra-axial brain tumours
Islim, A. I., Vyziotis, A., Pathmanaban, O. N., Coope, D. J., King, A. T., Brough, D., Jardine, L., Couper, K. N., & Greenhalgh, A. D. (2025) · Brain Communications · doi:10.1093/braincomms/fcaf311 · Cited by 4
The dura mater: A hub for immune surveillance at the central nervous system borders
Neish, K., Wang, Q., Richoz, N., & Clatworthy, M. R. (2026) · The Journal of Immunology · doi:10.1093/jimmun/vkaf344 · Cited by 3
Chronic Subdural Hematoma Is Not Subdural: Anatomical, Biological, and Therapeutic Implications of a Misleading Definition
Simone, M. D., Ciaglia, E., Santurro, A., Choucha, A., Messuti, B., Fasolino, S., Feo, R. D., Romano, D. G., Guerra, G., Luca, A. D., et al. (2026) · Brain Sciences · doi:10.3390/brainsci16060623 · Cited by 3
Postnatal meningeal CSF transport is primarily mediated by the arachnoid and pia maters and is not altered after intraventricular hemorrhage-posthemorrhagic hydrocephalus
Pan, S., Koleske, J. P., Koller, G. M., Halupnik, G. L., Alli, A.-H. O., Koneru, S., DeFreitas, D., Ramagiri, S., & Strahle, J. M. (2024) · Fluids and Barriers of the CNS · doi:10.1186/s12987-023-00503-7 · Cited by 3
The Legacy of John Caffey: Shaken Baby or Pyloric Stenosis?
Talbert, D. G. (2014) · Journal of Trauma & Treatment · doi:10.4172/2167-1222.1000192 · Cited by 3
The Subdural Myth: Space or Place?
Talbert, D. G. (2016) · Anatomy & Physiology · doi:10.4172/2161-0940.1000242 · Cited by 3
The posterior cranial fossa’s dura mater innervation and its clinical implication in headache: a comprehensive review
Hage, D., Mathkour, M., Iwanaga, J., Dumont, A. S., & Tubbs, R. S. (2021) · Folia Morphologica · doi:10.5603/fm.a2021.0114 · Cited by 3
Anatomy and Physiology of the Blood-Brain Barriers*
Abbott, N. J. (2022) · AAPS advances in the pharmaceutical sciences series · doi:10.1007/978-3-030-88773-5_1 · Cited by 4
Biomimetic and Nonbiomimetic Approaches in Dura Substitutes: The Influence of Mechanical Properties
Muniz, N. O., & Baudequin, T. (2024) · Tissue Engineering Part B Reviews · doi:10.1089/ten.teb.2024.0079 · Cited by 3
Trans-meningeal drug delivery to optic nerve ganglion cell axons using a nanoparticle drug delivery system
Grove, K., Dobish, J. N., Harth, E. M., Ingram, M.-C. E., Galloway, R. L., & Mawn, L. A. (2013) · Experimental Eye Research · doi:10.1016/j.exer.2013.10.016 · Cited by 3
Barrier Properties of the Spinal Meninges Are Markedly Decreased by Freezing Meningeal Tissues
Thompson, S., & Bernards, C. M. (1998) · Anesthesiology · doi:10.1097/00000542-199811000-00036 · Cited by 3
Histomorfometria das meninges encefálicas de ratos Wistar em diferentes faixas etárias
Pereira, K. F., Lima, V. M., Conegero, C. I., & Chopard, R. P. (2010) · Pesquisa Veterinária Brasileira · doi:10.1590/s0100-736x2010001100015 · Cited by 3
The Human Cerebral Cortex Microvascular System: Development and Composition of the Meningeal and Intracerebral Extrinsic and Intrinsic (Blood-Brain Barrier) Compartments
Marín‐Padilla, M. (2015) · CRC Press eBooks · doi:10.1201/b18606-3 · Cited by 3
Blood Supply, Meninges and Cerebrospinal Fluid Circulation
(2007) · Springer eBooks · doi:10.1007/978-3-540-34686-9_4 · Cited by 3
Die Neuroglia: Historischer Überblick
Niessing, V. K., Scharrer, E., Scharrer, B., & Oksche, A. (1980) · Handbuch der mikroskopischen Anatomie des Menschen · doi:10.1007/978-3-642-81358-0_1 · Cited by 3
Biology of the Blood–Brain and “Blood–Brain Tumor” Barriers
Engelhard, H. H., & Vályi-Nagy, T. (2006) · Elsevier eBooks · doi:10.1016/b978-012088410-0/50054-8 · Cited by 3
Meningeal Immunity: Anatomy, Function, and Neonatal Unique Features
Lorga, I., & Andrade, E. B. (2025) · European Journal of Immunology · doi:10.1002/eji.202451618 · Cited by 3
Current evidence on the cell of origin of meningiomas disputes the arachnoid cap cell dogma
Pamir, M. N., Erşen-Danyeli, A., & Özduman, K. (2026) · Acta Neurochirurgica · doi:10.1007/s00701-026-06908-1 · Cited by 2
Torcular pseudomass in a 14-month-old child: illustrative case
Villeneuve, L. M., Nagarajan, M., Cornwell, B. O., Propester, L., Zhao, X., Valenzuela, J., Gernsback, J. E., Desai, V. R., & Jea, A. H. (2022) · Journal of Neurosurgery Case Lessons · doi:10.3171/case22377 · Cited by 2
Torcular pseudomass is frequently detected on fetal magnetic resonance imaging and reduces with gestational age
Miranda, A. M., Bem, P., Araújo, A., Brito, C., Nunes, J., & Geraldo, A. F. (2022) · Pediatric Radiology · doi:10.1007/s00247-022-05549-7 · Cited by 2
Imaging and Clinical Outcomes Six Months After Middle Meningeal Artery Embolization with Squid for Chronic Subdural Hematoma: A Prospective Study
Schmolling, Á. H., Pérez-García, C., Bermúdez-Escobar, I. C., López‐Frías, A., Fandiño, E., Gallego, C. T., Rosati, S., Padrón, D., Guardado, L., Méndez, J. C., et al. (2025) · Diagnostics · doi:10.3390/diagnostics15111424 · Cited by 2
The Macroglia Of Teleosts: Characterization, Distribution and Development
Díaz‐Regueira, S. M., & Anadón, R. (1998) · Springer eBooks · doi:10.1007/978-1-4615-5737-1_2 · Cited by 2
A comprehensive review of its history, anatomy, imaging, and pathology
Adeeb, N., Deep, A., Griessenauer, C. J., Mortazavi, M. M., Watanabe, K., Loukas, M., Tubbs, R. S., & Cohen‐Gadol, A. (2013) · Cited by 2
Postmeningeal puncture headache and spontaneous intracranial hypotension
Hurley, R. W., Jerman, J. D., & Benzon, H. T. (2011) · Elsevier eBooks · doi:10.1016/b978-1-4377-2242-0.00049-3 · Cited by 2
Physical Injury to the Nervous System
Leestma, J. E., & Thibault, K. L. (2014) · CRC Press eBooks · doi:10.1201/b16882-7 · Cited by 2
Cerebral Microvessels
Marín‐Padilla, M. (2015) · Springer eBooks · doi:10.1007/978-1-4614-6434-1_137-1 · Cited by 2
Cranial Meninges
Galper, M. W., Naidich, T. P., Kleinman, G. M., Stein, E. G., & Lento, P. A. (2013) · Elsevier eBooks · doi:10.1016/b978-1-4160-5009-4.50016-9 · Cited by 2
Cerebrospinal Fluid: Physiology and Pharmacology
Artru, A. A. (1993) · Developments in critical care medicine and anestesiology · doi:10.1007/978-94-011-1610-7_3 · Cited by 2
Human Cerebral Cortex Intrinsic Microvascular System: Development and Cytoarchitecture
Marín‐Padilla, M. (2010) · Springer eBooks · doi:10.1007/978-3-642-14724-1_7 · Cited by 2
Ultrastructure of Arachnoid Cysts
Rabiei, K. K., & Johansson, B. R. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-809932-2.00005-3 · Cited by 2
Gap junctions in freeze-fractured membranes of the arachnoid mater
Omlin, F. X., & Bischoff, A. (1977) · Die Naturwissenschaften · doi:10.1007/bf00450658 · Cited by 2
The ultrastructure of the supporting system in the guinea pig semicircular canal
Arimal, T., Shibata, Y., & Uemural, T. (1990) · European Archives of Oto-Rhino-Laryngology · doi:10.1007/bf00178998 · Cited by 2
Morphological changes in the junctional complex of cells in the arachnoid layer of the rat after cold injury
Anders, J., & Goss, G. (1989) · Cell and Tissue Research · doi:10.1007/bf00218887 · Cited by 2
The interdural hematoma: A subtype of convexity subdural/dural hematoma with specific radioanatomical characteristics
Kiss-Bodolay, D., Papadimitriou, K., Hedjoudje, A., Duc, C., Vargas, M. I., Kiss, J. Z., Schaller, K., & Fournier, J. (2023) · Surgical Neurology International · doi:10.25259/sni_564_2023 · Cited by 1
Layered neuroimmune interfaces at CNS borders: Stress reshapes CNS immunity
Matsubara, K., Prinz, M., & Masuda, T. (2026) · Neuroscience Research · doi:10.1016/j.neures.2026.105063 · Cited by 1
Brain barriers at the crossroads of glioma immune surveillance and immunotherapy response
Engelhardt, B., & Platten, M. (2026) · Nature reviews. Cancer · doi:10.1038/s41568-026-00960-w · Cited by 2
Intestinal infections establish antigen-specific, long-lived memory CD4+ T cells in the brain and meninges
Fleming, A., Neish, K., Barros, R. D. M., Posner, D. A., Lee, C. Y. C., Stewart, A. P., Tuong, Z. K., Bremridge, M., Peñalver, A., Cabantous, M., et al. (2026) · Nature Neuroscience · doi:10.1038/s41593-026-02428-4 · Cited by 1
Membrane specializations and their relation to HRP transport in the medial habenular nucleus of the rat
Cup�do, R. N. J., Weerd, H., & van Dijk, F. (1985) · Anatomy and Embryology · doi:10.1007/bf00319051 · Cited by 1
Physiological & Cellular Mechanisms of Ammonia Tolerance in the Goldfi sh (Carassius auratus)
Sidhu, S. (2012) · Scholars Commons (Wilfrid Laurier University) · Cited by 1
Postdural Puncture Headache and Spontaneous Intracranial Hypotension
MOORE, J. (2005) · Elsevier eBooks · doi:10.1016/b978-0-443-06651-1.50041-1 · Cited by 1
The basal subarachnoid cisterns
Couldwell, M. W., & Tubbs, R. S. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-819509-3.00004-3 · Cited by 1
Cerebral Microvessels
Marín‐Padilla, M. (2022) · Springer eBooks · doi:10.1007/978-3-030-88832-9_137 · Cited by 1
Embracing digital innovation in neuroscience: 2023 in review at NEUROCCINO
Chacón, E. G., Ovando‐Tellez, M., de Schotten, M. T., & Forkel, S. J. (2024) · Brain Structure and Function · doi:10.1007/s00429-024-02768-6 · Cited by 1
Structure of the subarachnoid lymphatic-like membrane as a meningeal selective barrier and immunological regulator
Nikolenko, V. N., Oganesyan, M. V., Urazmetova, K., Rizaeva, N. A., Sankova, M. V., Moiseeva, A. V., Moiseenko, A., Belichenko, A. A., Nikitina, A. T., & Александрович, Г. Л. (2025) · Neurology neuropsychiatry Psychosomatics · doi:10.14412/2074-27112025-3-112-119 · Cited by 1
VIII. The Neuroglia of the CNS
Pannese, E. (2014) · Springer eBooks · doi:10.1007/978-3-319-06856-5_8 · Cited by 1
A Comparative Study of the Capsular Vessels of Acute Subdural Hematoma in the Chronic Healing Stage and Those of Chronic Subdural Hematoma
Yamashima, T., Yamamoto, S., & Friede, R. L. (1983) · Neurologia medico-chirurgica · doi:10.2176/nmc.23.428 · Cited by 1
Challenges of Brain Drug Delivery and G-Technology as One of Solution
Garg, S., Dwivedi, A., Saini, P., Pareek, A. K., & Trivedi, S. (2013) · Research and reviews : journal of pharmacy and pharmaceutical sciences · Cited by 1
General Introduction to Barrier Mechanisms in the Central Nervous System
Saunders, N. R., Dzięgielewska, K. M., Møllgård, K., & Habgood, M. D. (2017) · Springer eBooks · doi:10.1007/978-3-319-45514-3_1 · Cited by 1
Meninges and Vasculature
Siegenthaler, J. A., & Pleasure, S. J. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-397265-1.00087-3 · Cited by 1
Development of the Cerebrospinal Fluid Pathways during Embryonic and Fetal Life in Humans
Catala, M. (2018) · Springer eBooks · doi:10.1007/978-3-319-31889-9_2-2 · Cited by 1
Development of the Cerebrospinal Fluid Pathways during Embryonic and Fetal Life in Humans
Catala, M. (2018) · Springer eBooks · doi:10.1007/978-3-319-31889-9_2-1 · Cited by 1
Cytogenesis and Developmental Anatomy of the Pia-Arachnoid and Pacchionian Granules
Rigobello, L. (1993) · Principles of pediatric neurosurgery · doi:10.1007/978-1-4615-7281-7_2 · Cited by 1
The permeability to exogenous protein of the wall of the superior sagittal sinus of the cat
Leslie, R. A., MacDonald, L., & Love, J. A. (1983) · Brain Research Bulletin · doi:10.1016/0361-9230(83)90127-2 · Cited by 1
Organization of the cerebellar cortex viewed by scanning electron microscopy
Reese, B. F., Landis, D. M. D., & Reese, T. S. (1985) · Neuroscience · doi:10.1016/0306-4522(85)90169-1 · Cited by 1
Endothelial cells of the meningeal capillaries in the rainbow trout: A freeze‐fracture study
Caruncho, H. J., & Anadón, R. (1990) · Journal of Morphology · doi:10.1002/jmor.1052060309 · Cited by 1
Previously unreported "hemidesmosomal junctions" between folliculo-stellate cells and pituitary adenoma cells.
Tachibana, O., & Yamashima, T. (1988) · PubMed · Cited by 1
Letter to the Editor Regarding “Surgical Treatment of Chronic Subdural Hematoma: Predicting Recurrence and Cure”
Brown, N. J., & Lien, B. V. (2020) · World Neurosurgery · doi:10.1016/j.wneu.2020.03.012 · Cited by 1
Introduction
Segal, M. B., & Zloković, B. V. (1990) · Springer eBooks · doi:10.1007/978-94-009-2229-7_1 · Cited by 1
Distinct Ca2+ signatures of leptomeningeal fibroblast subgroups in awake mouse brains in health and inflammationPreprint
Cai, C., He, C., Grubb, S., Tao, L., Kılıç, K., Zhang, X., Sheikh, N., & Devor, A. (2025) · Research Square · doi:10.21203/rs.3.rs-6649539/v1 · Cited by 1
Development of novel therapeutics for stroke : preclinical investigations of osteopontin and 3-iodothyronamine.
Doyle, K. P. (2007) · doi:10.6083/m4cf9n3b
Oxytalan fibres in meningiomas and meningeal neomembranes
Karyofilis, K., & Friede, R. L. (1991) · Acta Neuropathologica · doi:10.1007/bf00293388

Authors: Nabeshima, S., Reese, T. S., Landis, D. M. D., & Brightman, M. W.
Affiliations: National Institutes of Health (US)
ORCID: Nabeshima, Sachio
Reese, T. S.
Venue: Journal of Comparative Neurology
Publisher: Wiley
Published: 1975-11-15
Volume: 164
Issue: 2
Pages: 127-169
ISSN: 0021-9967 (ISSN-L)
1096-9861
DOI: 10.1002/cne.901640202
OpenAlex: W1975635783
Cited by: 444
References: 25
Citations by year: 2026: 15 · 2025: 16 · 2024: 25 · 2023: 14 · 2022: 27 · 2021: 12 · 2020: 11 · 2019: 12 · 2018: 12 · 2017: 20 · 2016: 9 · 2015: 7 · 2014: 8 · 2013: 13 · 2012: 7
FWCI: 7.65
Type: journal article
Language: en
Open access: closed
Licence: onlinelibrary.wiley.com/termsAndConditions#vor (vor, 10556 d)
Locations: The Journal of Comparative Neurology (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Neuroscience › Neurology › Barrier Structure and Function Studies
Health Sciences › Medicine › Clinical Neurology › Cerebrospinal fluid and hydrocephalus
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion Transport and Channel Regulation
Keywords: tight junctions, subarachnoid space, cerebrospinal fluid, gap junctions, desmosomes, astrocytes, subdural space, intercellular junctions, meninges
MeSH terms: Animals, Haplorhini, Arachnoid, Astrocytes, Cats, Chinchilla, Desmosomes, Dura Mater, Freeze Fracturing, Intercellular Junctions, Macaca, Meninges, Microscopy, Electron, Neuroglia, Pia Mater, Rabbits, Species Specificity, Mice, Rats

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Junctions in the meninges and marginal glia.

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks