Brain extracellular matrix

Proteoglycans as modulators of growth factor activities

Ruoslahti, E. I., & Yamaguchi, Y. (1991) · Cell · doi:10.1016/0092-8674(91)90308-l · Cited by 1,342

Pathology of tumours

Willis, R. A. (1948) · Butterworths eBooks · Cited by 1,254

Selectins: Interpreters of Cell-Specific Carbohydrate Information During Inflammation

Lasky, L. A. (1992) · Science · doi:10.1126/science.1439808 · Cited by 1,236

Selectin ligands.

Varki, A. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.16.7390 · Cited by 946

Proteoglycans in Cell Regulation

Ruoslahti, E. I. (1989) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)80001-1 · Cited by 679

Multiple domains of the large fibroblast proteoglycan, versican.

Zimmermann, D., & Ruoslahti, E. I. (1989) · The EMBO Journal · doi:10.1002/j.1460-2075.1989.tb08447.x · Cited by 652

Glioblastoma expression of vitronectin and the alpha v beta 3 integrin. Adhesion mechanism for transformed glial cells.

Gladson, C. L., & Cheresh, D. A. (1991) · Journal of Clinical Investigation · doi:10.1172/jci115516 · Cited by 415

Chondroitin Sulfate as a Regulator of Neuronal Patterning in the Retina

Brittis, P. A., Canning, D. R., & Silver, J. (1992) · Science · doi:10.1126/science.1738848 · Cited by 415

Isolation of a neural chondroitin sulfate proteoglycan with neurite outgrowth promoting properties.

Faissner, A., Clement, A. M., Lochter, A., Streit, A., Mandl, C., & Schachner, M. (1994) · The Journal of Cell Biology · doi:10.1083/jcb.126.3.783 · Cited by 354

Effects of platelet-derived growth factor and transforming growth factor-beta 1 on the synthesis of a large versican-like chondroitin sulfate proteoglycan by arterial smooth muscle cells.

Schönherr, E., Järveläinen, H., Sandell, L. J., & Wight, T. N. (1991) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)47419-x · Cited by 335

Central Nervous System Extracellular Matrix as a Therapeutic Bioscaffold for Central Nervous System Injury

Medberry, C. J. (2014) · D-Scholarship@Pitt (University of Pittsburgh) · Cited by 2

Matrix Metalloproteinases in Fragile X Syndrome

Ethell, D. W., & Sidhu, H. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-804461-2.00015-9 · Cited by 2

Anglemetry of neural axis cell differentiation genes by structural pressurotopy of DNA loop strand segment tropy in reference to tissue macro-compliance

Sarin, H. (2019) · Translational Medicine Communications · doi:10.1186/s41231-019-0045-4 · Cited by 2

Mechano-Biological Features in a Patient-Specific Computational Model of Glioblastoma

Acerbi, F., Agosti, A., Falco, J., Marchesi, S., Vetrano, I. G., DiMeco, F., Bizzi, A., Ferroli, P., Scita, G., & Ciarletta, P. (2020) · Neuromethods · doi:10.1007/978-1-0716-0856-2_12 · Cited by 3

Unveiling the biological role of serglycin proteoglycans

Carlos, T. B. M. C. (2008) · Epsilon Open Archive (Sveriges lantbruksuniversitet biblioteket (Swedish University of Agricultural Sciences)) · Cited by 2

ECM‐Inspired Chemical Cues: Biomimetic Molecules and Techniques of Immobilization

Tam, R. Y., Owen, S. C., & Shoichet, M. S. (2014) · Wiley eBooks · doi:10.1002/9781118843499.ch1 · Cited by 2

Plasticity of Astrocytes in Culture

Vernadakis, A., & Kentroti, S. (1995) · Humana Press eBooks · doi:10.1007/978-1-59259-468-9_17 · Cited by 2

The role of integrin α v and CD44 in GBM migration in human brainPreprint

Binder, Z. A., Kim, S. H. J., Wu, P.-H., Giri, A., Gallia, G. L., Pardo, C. A., & Wirtz, D. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/841726 · Cited by 2

Etude de la structure nanométrique et de la viscosité locale de l’espace extracellulaire du cerveau par microscopie de fluorescence de nanotubes de carbone uniques

Danné, N. (2018) · theses.fr (ABES) · doi:10.70675/d6f3cff4zdc76z4d72zb88ezf02ea84ee162 · Cited by 2

Distribution of a brain-specific extracellular matrix protein in developing and adult zebrafish

Kanai, T., Imai, K., & Nakayasu, H. (2006) · Brain Research · doi:10.1016/j.brainres.2006.09.037 · Cited by 1

Brain extracellular matrix: Novel decellularization protocols for thin rat and human brain tissue slices

de Jong, J. M., Werkman, I. L., Kats, K., Bosma, J., Kooistra, S. M., Eggen, B. J. L., & Baron, W. (2026) · Heliyon · doi:10.1016/j.heliyon.2026.e44653 · Cited by 1

The Role of Extracellular Matrix Proteins on Epithelial to Mesenchymal Transition in Glioblastoma Multiforme

Orey, S. C. (2013) · Language arts journal of Michigan · Cited by 1

The Role of the Brain Extracellular Matrix in Synaptic Plasticity After Brain Injuries (Review)

Dembitskaya, Y., Tyurikova, O., & Semyanov, A. V. (2016) · Современные технологии в медицине · doi:10.17691/stm2016.8.4.31 · Cited by 1

Biomaterials Application in Stem Cell Therapies for Stroke

Moshayedi, P., & Carmichael, S. T. (2015) · Springer eBooks · doi:10.1007/978-3-319-15063-5_13 · Cited by 1

Understanding the Role of the Solid Tumour Microenvironment in Brain Tumour Progression

Richards, R. (2017) · University of Liverpool · doi:10.17638/03005579 · Cited by 1

Dynamic Interactions Between Stem Cells and Biomaterials

Virdi, J. K., & Pethe, P. S. (2021) · Springer eBooks · doi:10.1007/978-981-16-4420-7_15 · Cited by 1

Prostate Apoptosis Response-4: a Therapeutic Target for Malignant Gliomas

Ghosalkar, J., Sonawane, V. R., Khan, M., Joshi, K. S., & Shastry, P. (2021) · Springer eBooks · doi:10.1007/978-3-030-80558-6_6 · Cited by 1

Novel schizophrenia risk genesand gene expression

Knight, D. A. (2012) · ORCA Online Research @Cardiff (Cardiff University) · Cited by 1

Enzymatic synthesis of known and novel oligosaccharides

Natunen, J. (1999) · Työväentutkimus Vuosikirja · Cited by 1

Glycosyltransferases promote development and prevent promiscuous cell aggregation in the choanoflagellate S. rosettaPreprint

Wetzel, L. A., Levin, T. C., Hulett, R. E., Chan, D., King, G. A., Aldayafleh, R., Booth, D. S., Sigg, M. A., & King, N. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/384453 · Cited by 1

Recycling as a mechanism for extracellular matrix remodeling at the synapse

Dankovich, T. M. (2021) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-8998 · Cited by 1

Modeling an extracellular environment for axonal pathfinding and fasciculation in the central nervous system

Rauch, U. (1997) · Springer eBooks · doi:10.1007/978-3-642-60905-3_21 · Cited by 1

Gen-Expressionsanalyse aus autoptischen Formalin-fixierten und Paraffin- eingebetteten Gewebeproben von Multiple Sklerose Patienten

Eisele, S. C. (2013) · Electronic Theses of LMU Munich (Ludwig-Maximilians-Universität München) · doi:10.5282/edoc.15639

Isolamento, expressão, e caracterização de três variantes de splicing do gene supressor de tumor RECK em modelo de astrocitoma humano

Trombetta-Lima, M. (2014) · doi:10.11606/t.46.2014.tde-01102014-111030

Inibição da migração mediada pelo gene RECK em modelo de glioma humano através de alterações no citoesqueleto e adesão focal

Haga, R. B. (2012) · doi:10.11606/d.9.2012.tde-11092012-134839

Regeneration in the Mammalian CNS

Filogamo, G., & Vercelli, A. (1995) · Humana Press eBooks · doi:10.1007/978-1-59259-468-9_9

A Role for Focal Adhesions and Extracellular Matrix in Traumatic Axonal Injury

Hemphill, M. A. (2014) · Digital Access to Scholarship at Harvard (DASH) (Harvard University)

Investigating the oncogenic function of FUBP1 in glioblastoma cell lines

Kolluru, V. (2015) · Technischen Universität Darmstadt · doi:10.26083/tuprints-00004492

Extracellular Matrix Molecules in Neuromuscular Junctions and Central Nervous System Synapses

Bogdanik, L. P., & Burgess, R. W. (2009) · Springer eBooks · doi:10.1007/978-0-387-92708-4_20

Hyaluronic Acid and Its Receptors in the Mechanobiology of Gliomblastoma Multiforme

Kim, Y. (2015) · eScholarship (California Digital Library)

Recent Developments in the Molecular Biology of Human Brain Tumors

Rutka, J. T., Tsugu, A., Jung, S., Dirks, P. B., & Kurimoto, M. (1998) · Springer eBooks · doi:10.1007/978-1-4613-9350-4_17

Amyloid fibrils in neurodegenerative diseases: villains or heroes? "The lesson being taught to us is that nothing is only black or white, and that, especially for the particular case of amyloid-b and Alzheimer's disease, we are not yet in possession of the final answer."

Fernàndez, X. (2013)

Role of Biomaterials in Neural Stem Cell Fate

K.S., P. C. S. (2015) · Global Journal of Human Social Science

Characterization and Analysis of Extracellular Matrix in Malignant Brain Tumors and Their Cellular Derivatives

Sinyuk, M., Lathia, J. D., & Viapiano, M. S. (2014) · Neuromethods · doi:10.1007/978-1-4939-2083-9_11

Deciphering the role of SerpinB2 in cancer invasion and metastasis

Harris, N. L. E. (2017) · Research Online (University of Wollongong)

Extracellular Electric Signals Regulate Neuroblast Behaviours in Adult Brain

Cao, L., McCaig, C., & Pu, J. (2015)

Three-dimensional Immobilization of Proteins within Agarose Hydrogels using Two-photon Chemistry

Wylie, R. G. (2012) · TSpace (University of Toronto)

On the role of macrophages, microglia and the extracellular matrix in remyelination

Wang, P. (2018) · University of Groningen research database (University of Groningen / Centre for Information Technology)

Impacts des rythmes du sommeil sur la connectivité fonctionnelle et effets des changements ioniques sur la synchronisation neuronale et la connectivité fonctionnelle

Seigneur, J. (2013) · Corpus Université Laval (Université Laval)

Physical and Molecular Characterizations of Galvanotaxis and Its Implication in Glioblastoma

Huang, Y.-J. (2015)

Local Delivery of Therapeutic Nanoparticles for Treatment of Malignant Glioma

Zhang, C. (2015)

Papel de Caveolina-1 en la biogénesis de exosomas: implicación en la organización de la matriz extracelular y la progresión tumoral

Albacete-Albacete, L. (2018) · doi:10.4321/repisalud.6735

Acute effects of LGI1 on network excitability

Lugarà, E. (2019) · UCL Discovery (University College London)

Attributes of Astrocyte Response to Mechano-Stimulation by High-Rate Overpressure

Hlavac, N. (2018) · VTechWorks (Virginia Tech)

Engineered Biomaterials for Human Neural Stem Cell Applications

Ma, W. (2019) · TUScholarShare (Temple University)

Heparan Sulfate in Normal and Cancer Stem Cells of the Brain

Xiong, A., Roy, A., Spyrou, A., & Forsberg‐Nilsson, K. (2021) · Biology of extracellular matrix · doi:10.1007/978-3-030-73453-4_9

Análise do perfil de expressão metaloproteinases (MMPs) e seus inibidores, Timp e Reck, em modelo animal de Doença de Parkinson

Spindola, A. (2019) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/d.87.2019.tde-15052020-152022

Business Considerations

Minnick, C. (2017) · Wiley eBooks · doi:10.1002/9781394406418.part4

Brain Edema

Moritani, T., Daou, B. J., Palmateer, G., & Pandey, A. S. (2021) · Springer eBooks · doi:10.1007/978-3-030-62120-9_8

Versican

Zimmermann, D. R., & Dours-Zimmermann, M. T. (2002) · Wiley Encyclopedia of Molecular Medicine · doi:10.1002/0471203076.emm0885

The Molecular Basis of Memory: Remembering and Forgetting

Marx, G. S., & Gilon, C. (2022) · International Journal of Psychiatry Research · doi:10.33425/2641-4317.1140

Transcriptome-guided optimization of in vitro culture conditions to study microglia in health and disease

Timmerman, R. (2022) · Utrecht University Repository (Utrecht University) · doi:10.33540/1603

Characterization and Classification of Fibrillar Collagen Networks using Gray-Level Texture Analysis

Poole, J. J. A. (2022) · Carleton University's Institutional Repository (MacOdrum Library, Carleton University) · doi:10.22215/etd/2022-15210

Emerging Insights into the Interstitial Distribution of Neuraxial Therapeutics via the Cerebrospinal Fluid Compartment

Jansson, D., & Iliff, J. J. (2023) · Springer eBooks · doi:10.1007/978-3-031-39558-1_8

Activity-dependent turnover of the Perineural Extracellular Matrix

Petersen, G. C. (2024) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-10429

Recent Advances in Blood Brain Barrier on Chip ModelsPreprint

Vetter, J., Palagi, I., Waisman, A., & Blaeser, A. (2024) · SSRN Electronic Journal · doi:10.2139/ssrn.5047806

Viral-mediated fluorescent labeling of hyaluronan reveals extracellular matrix dynamics in the mouse brain in vivoPreprint

Fernandez-Ballester, M., Ardaya, M., Dutheil, N., Largitte, L.-A., Martín, A., & Soria, F. N. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.01.31.635882

Hyaluronan-Based Glioblastoma Tumor Constructs Maintain Patient Tumor Drug Responses and Genomic Parity

Sivakumar, H., Forsythe, S. D., Laxton, A. W., Tatter, S. B., Miller, L. D., Strowd, R. E., III, & Skardal, A. (2026) · Micromachines · doi:10.3390/mi17030276 · Cited by 1

Etude des mécanismes d'adressage et de positionnement de l'ankyrine G et de la protéine kinase CK2 au segment initial de l'axone

Hien, Y. E. (2014) · theses.fr (ABES) · doi:10.70675/d9139da1zea65z43f3za59cz427338ccecff

Nouveaux outils de RMN pondérée en diffusion pour la caractérisation des différents compartiments tissulaires dans le cerveau de rongeur in vivo

Vincent, M. (2021) · theses.fr (ABES) · doi:10.70675/e0d5400ez6ba7z4f05zb521zf41e85497eb4

Epigenetic Regulation of Hyaluronan-Associated Genes in the Brain: Identifying Key Regulatory Sites

Acevedo, R. E., Walton, E., & Mifsud, K. R. (2026) · Epigenomes · doi:10.3390/epigenomes10020028

Extracellular Matrix–Tumor Crosstalk and Its Influence on Tumor Dormancy

Gawarguru, R., Shinde, S., & Dey, T. (2026) · Biology of extracellular matrix · doi:10.1007/978-3-032-22618-1_1

Mechanobiology of hippocampal neurogenesis: directing neural stem cell fate through physical cues

Akyel, I., Moeendarbary, E., & Sheridan, G. K. (2026) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2026.1868741 · Cited by 1

Decoupling the Role of Nanoparticle Rigidity and Chemistry in Particle Transport through the Brain Parenchyma

Wiegand, K. R., Sun, K., Balistreri, G. N., Ramanan, S., Butler, B., Deptula, A., Nance, E. A., Espinosa-Marzal, R. M., & Guironnet, D. (2026) · Biomacromolecules · doi:10.1021/acs.biomac.6c00925

Lysosomal Glycosaminoglycan Catabolism Regulates Microglial Cell State in the Developing CNSPreprint

Hope, K. T., Zhang, Y., Basu, A., Luo, B., Chassie, K., Weiss, R. J., & Yellajoshyula, D. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.10.11.758365

Histopathological growth patterns represent a dynamic biological and clinically-relevant terminus of the metastatic cascade

Dankner, M., Tabariès, S., Girondel, C., Sillis, Y., Vermeulen, P. B., & Siegel, P. M. (2026) · Cancer and Metastasis Reviews · doi:10.1007/s10555-026-10389-0

Progenitor Cell Tissue Engineering

Aroom, K., & Gill, B. S. (2010) · Humana Press eBooks · doi:10.1007/978-1-60761-965-9_2

Untitled work

Hagihara (1999) · doi:10.1002/(sici)1096-9861(19990726)410:2

Lecticans: organizers of the brain extracellular matrix

Yamaguchi, Y. (2000) · Cellular and Molecular Life Sciences · doi:10.1007/pl00000690 · Cited by 642

Brain sweet brain: importance of sugars for the cerebral microenvironment and tumor development

Quírico‐Santos, T., da Fonseca, C. O., & Lagrota-Cândido, J. (2010) · Arquivos de Neuro-Psiquiatria · doi:10.1590/s0004-282x2010000500024 · Cited by 35

Brevican: a major proteoglycan in adult brain.

Yamaguchi, Y. (1996) · PubMed · Cited by 84

Hyaluronic acid and hyaluronic acid-binding proteins in brain extracellular matrix

Bignami, A., Hosley, M., & Dahl, D. R. (1993) · Anatomy and Embryology · doi:10.1007/bf00190136 · Cited by 224

When the Matrix Warns: Unraveling Brain Extracellular Matrix Components as Danger Signals in Glioma Progression

Grechukhina, A. A., Mishchenko, T. A., Gudkov, S. V., & Vedunova, M. V. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27198757