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 · see citing works

Pathology of tumours

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

Selectins: Interpreters of Cell-Specific Carbohydrate Information During Inflammation

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

Selectin ligands.

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

Proteoglycans in Cell Regulation

Ruoslahti, E. I. (1989) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)80001-1 · Cited by 682 · see citing works

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 · see citing works

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 420 · see citing works

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 416 · see citing works

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 · see citing works

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 334 · see citing works

Cloning and primary structure of neurocan, a developmentally regulated, aggregating chondroitin sulfate proteoglycan of brain.

Rauch, U., Karthikeyan, L., Maurel, P., Margolis, R. U., & Margolis, R. K. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)41808-x · Cited by 333 · see citing works

Interactions of the chondroitin sulfate proteoglycan phosphacan, the extracellular domain of a receptor-type protein tyrosine phosphatase, with neurons, glia, and neural cell adhesion molecules.

Milev, P., Friedlander, D. R., Sakurai, T., Karthikeyan, L., Flad, M., Margolis, R. K., Grumet, M., & Margolis, R. U. (1994) · The Journal of Cell Biology · doi:10.1083/jcb.127.6.1703 · Cited by 328 · see citing works

Hyaluronate binding properties of versican.

LeBaron, R. G., Zimmermann, D., & Ruoslahti, E. I. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)50191-0 · Cited by 317 · see citing works

The extracellular matrix of the central and peripheral nervous systems: structure and function

Rutka, J. T., Apodaca, G., Stern, R., & Rosenblum, M. L. (1988) · Journal of neurosurgery · doi:10.3171/jns.1988.69.2.0155 · Cited by 307 · see citing works

Hyaluronan receptor-directed assembly of chondrocyte pericellular matrix.

Knudson, C. B. (1993) · The Journal of Cell Biology · doi:10.1083/jcb.120.3.825 · Cited by 280 · see citing works

Molecular forms, binding functions, and developmental expression patterns of cytotactin and cytotactin-binding proteoglycan, an interactive pair of extracellular matrix molecules

Hoffman, S., Crossin, K., & Edelman, G. M. (1988) · The Journal of Cell Biology · doi:10.1083/jcb.106.2.519 · Cited by 274 · see citing works

Peanut agglutinin and chondroitin-6-sulfate are molecular markers for tissues that act as barriers to axon advance in the avian embryo

Oakley, R. A., & Tosney, K. W. (1991) · Developmental Biology · doi:10.1016/s0012-1606(05)80017-x · Cited by 260 · see citing works

Interactions with tenascin and differential effects on cell adhesion of neurocan and phosphacan, two major chondroitin sulfate proteoglycans of nervous tissue.

Grumet, M., Milev, P., Sakurai, T., Karthikeyan, L., Bourdon, M. A., Margolis, R. K., & Margolis, R. U. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)32692-3 · Cited by 255 · see citing works

A novel glycosaminoglycan attachment domain identified in two alternative splice variants of human versican

Dours-Zimmermann, M. T., & Zimmermann, D. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(20)30089-2 · Cited by 249 · see citing works

A diverse set of developmentally regulated proteoglycans is expressed in the rat central nervous system

Herndon, M. E., & Lander, A. D. (1990) · Neuron · doi:10.1016/0896-6273(90)90148-9 · Cited by 245 · see citing works

A fibroblast chondroitin sulfate proteoglycan core protein contains lectin-like and growth factor-like sequences.

Krusius, T., Gehlsen, K. R., & Ruoslahti, E. I. (1987) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)45176-9 · Cited by 188 · see citing works

Molecular characterization and in situ mRNA localization of the neural recognition molecule J1-160/180: a modular structure similar to tenascin.

Fuss, B., Wintergerst, E. S., Bartsch, U., & Schachner, M. (1993) · The Journal of Cell Biology · doi:10.1083/jcb.120.5.1237 · Cited by 177 · see citing works

The chicken neural extracellular matrix molecule restrictin: Similarity with EGF-, fibronectin type III-, and fibrinogen-like motifs

Nörenberg, U., Ville, H., Wolff, J. M., Frank, R. W., & Rathjen, F. G. (1992) · Neuron · doi:10.1016/0896-6273(92)90199-n · Cited by 160 · see citing works

The versican C-type lectin domain recognizes the adhesion protein tenascin-R.

Aspberg, A., Binkert, C., & Ruoslahti, E. I. (1995) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.92.23.10590 · Cited by 142 · see citing works

Heparan sulfate proteoglycan in diffuse plaques of hippocampus but not of cerebellum in Alzheimer's disease brain.

Snow, A. D., Sekiguchi, R., Nochlin, D., Kalaria, R. N., & Kimata, K. (1994) · PubMed Central · Cited by 132 · see citing works

Chondroitin sulfate and chondroitin/keratan sulfate proteoglycans of nervous tissue: developmental changes of neurocan and phosphacan

Meyer‐Puttlitz, B., Milev, P., Junker, E., Zimmer, I., Margolis, R. U., & Margolis, R. K. (1995) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.1995.65052327.x · Cited by 124 · see citing works

Extracellular matrix of central nervous system white matter: Demonstration of an hyaluronate‐protein complex

Asher, R., Perides, G., Vanderhaeghen, J., & Bignami, A. (1991) · Journal of Neuroscience Research · doi:10.1002/jnr.490280314 · Cited by 120 · see citing works

A segment of the cartilage proteoglycan core protein has lectin-like activity.

Halberg, D. F., Proulx, G., Doege, K. J., Yamada, Y., & Drickamer, K. (1988) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)76567-3 · Cited by 116 · see citing works

Versican, a hyaluronate‐binding proteoglycan of embryonal precartilaginous mesenchyma, is mainly expressed postnatally in rat brain

Bignami, A., Perides, G., & Rahemtulla, F. G. (1993) · Journal of Neuroscience Research · doi:10.1002/jnr.490340110 · Cited by 109 · see citing works

Glioblastoma infiltration into central nervous system tissue in vitro: involvement of a metalloprotease.

Paganetti, P., Caroni, P., & Schwab, M. E. (1988) · The Journal of Cell Biology · doi:10.1083/jcb.107.6.2281 · Cited by 100 · see citing works

The tenascin gene family.

Chiquet‐Ehrismann, R., Hagios, C., & Matsumoto, K. (1994) · PubMed · Cited by 97 · see citing works

Isolation and characterization of an inhibitor of neovascularization from scapular chondrocytes.

Moses, M. A., Sudhalter, J., & Langer, R. (1992) · The Journal of Cell Biology · doi:10.1083/jcb.119.2.475 · Cited by 95 · see citing works

[6] Aggrecan-versican-neurocan family of proteoglycans

Margolis, R. U., & Margolis, R. K. (1994) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(94)45008-0 · Cited by 93 · see citing works

The high molecular weight Cat-301 chondroitin sulfate proteoglycan from brain is related to the large aggregating proteoglycan from cartilage, aggrecan.

Fryer, H. J., Kelly, G. M., Molinaro, L., & Hockfield, S. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)50175-2 · Cited by 92 · see citing works

Differential effects of glycosaminoglycans on neurite growth on laminin and L1 substrates

Dou, C., & Levine, J. (1995) · Journal of Neuroscience · doi:10.1523/jneurosci.15-12-08053.1995 · Cited by 85 · see citing works

Isolation of a large aggregating proteoglycan from human brain.

Perides, G., Rahemtulla, F. G., Lane, W. S., Asher, R. A., & Bignami, A. (1992) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)35919-2 · Cited by 73 · see citing works

A large chondroitin sulfate proteoglycan has the characteristics of a general extracellular matrix component of adult brain

Iwata, M., & Carlson, S. S. (1993) · Journal of Neuroscience · doi:10.1523/jneurosci.13-01-00195.1993 · Cited by 63 · see citing works

Expression and binding activity of the carboxyl-terminal portion of the core protein of PG-M, a large chondroitin sulfate proteoglycan.

Ujita, M., Shinomura, T., Ito, K., Kitagawa, Y., & Kimata, K. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)47027-5 · Cited by 52 · see citing works

Purification of a Meningeal Cell‐derived Chondroitin Sulphate Proteoglycan with Neurotrophic Activity for Brain Neurons and its Identification as Biglycan

Junghans, U., Koops, A., Westmeyer, A., Kappler, J., Meyer, H. E., & Müller, H. W. (1995) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.1995.tb00655.x · Cited by 51 · see citing works

Large chondroitin sulfate proteoglycans of developing chick CNS are expressed in cerebral hemisphere neuronal cultures

Hennig, A. K., Mangoura, D. A., & Schwartz, N. B. (1993) · Developmental Brain Research · doi:10.1016/0165-3806(93)90146-2 · Cited by 26 · see citing works

Extracellular Matrix Assembly: A Multiscale Deconstruction

Mouw, J. K., Ou, G., & Weaver, V. M. (2014) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3902 · Cited by 1,534 · see citing works

Diffusion in Brain Extracellular Space

Syková, E., & Nicholson, C. (2008) · Physiological Reviews · doi:10.1152/physrev.00027.2007 · Cited by 1,481 · see citing works

Extracellular space structure revealed by diffusion analysis

Nicholson, C., & Syková, E. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(98)01261-2 · Cited by 914 · see citing works

Lecticans: organizers of the brain extracellular matrix

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

Proteoglycans in the Developing Brain: New Conceptual Insights for Old Proteins

Bandtlow, C. E., & Zimmermann, D. R. (2000) · Physiological Reviews · doi:10.1152/physrev.2000.80.4.1267 · Cited by 632 · see citing works

Fluid transport in the brain

Rasmussen, M. K., Mestre, H., & Nedergaard, M. (2021) · Physiological Reviews · doi:10.1152/physrev.00031.2020 · Cited by 622 · see citing works

Extracellular matrix molecules and synaptic plasticity

Dityatev, A., & Schachner, M. (2003) · Nature Reviews Neuroscience · doi:10.1038/nrn1115 · Cited by 564 · see citing works

Diffusion and related transport mechanisms in brain tissue

Nicholson, C. (2001) · Reports on Progress in Physics · doi:10.1088/0034-4885/64/7/202 · Cited by 491 · see citing works

Extracellular matrix of the central nervous system: from neglect to challenge

Zimmermann, D. R., & Dours-Zimmermann, M. T. (2008) · Histochemistry and Cell Biology · doi:10.1007/s00418-008-0485-9 · Cited by 465 · see citing works

A stoichiometric complex of neurexins and dystroglycan in brain

Sugita, S., Saito, F., Tang, J., Satz, J., Campbell, K., & Südhof, T. (2001) · Journal of Cell Biology · doi:10.1083/jcb.200105003 · Cited by 453 · see citing works

Fibulins: a versatile family of extracellular matrix proteins

Timpl, R., Sasaki, T., Kostka, G., & Chu, M.-L. (2003) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1130 · Cited by 494 · see citing works

Extracellular matrix and perineuronal nets in CNS repair

Kwok, J. C. F., Dick, G., Wang, D., & Fawcett, J. W. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20974 · Cited by 395 · see citing works

The perineuronal net and the control of CNS plasticity

Wang, D., & Fawcett, J. (2012) · Cell and Tissue Research · doi:10.1007/s00441-012-1375-y · Cited by 373 · see citing works

Tissue mechanics promote IDH1-dependent HIF1α–tenascin C feedback to regulate glioblastoma aggression

Miroshnikova, Y. A., Mouw, J. K., Barnes, J. M., Pickup, M. W., Lakins, J. N., Kim, Y., Lobo, K. A., Persson, A. I., Reis, G. F., McKnight, T. R., et al. (2016) · Nature Cell Biology · doi:10.1038/ncb3429 · Cited by 380 · see citing works

Composition of Perineuronal Net Extracellular Matrix in Rat Brain

Deepa, S. S., Carulli, D., Galtrey, C., Rhodes, K., Fukuda, J., Mikami, T., Sugahara, K., & Fawcett, J. W. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m600544200 · Cited by 367 · see citing works

Cortical neurons immunoreactive for the potassium channel Kv3.1b subunit are predominantly surrounded by perineuronal nets presumed as a buffering system for cations

Härtig, W., Derouiche, A., Welt, K., Brauer, K., Grosche, J., Mäder, M., Reichenbach, A., & Brückner, G. (1999) · Brain Research · doi:10.1016/s0006-8993(99)01784-9 · Cited by 339 · see citing works

Molecular mechanisms of dendritic spine development and remodeling

Ethell, I. M., & Pasquale, E. B. (2005) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2005.02.003 · Cited by 349 · see citing works

Elucidating the mechanobiology of malignant brain tumors using a brain matrix-mimetic hyaluronic acid hydrogel platform

Ananthanarayanan, B., Kim, Y., & Kumar, S. (2011) · Biomaterials · doi:10.1016/j.biomaterials.2011.07.005 · Cited by 337 · see citing works

Tissue mechanics regulate brain development, homeostasis and disease

Barnes, J. M., Przybyla, L., & Weaver, V. M. (2017) · Journal of Cell Science · doi:10.1242/jcs.191742 · Cited by 313 · see citing works

Mechanics in Neuronal Development and Repair

Franze, K., Janmey, P. A., & Guck, J. R. (2013) · Annual Review of Biomedical Engineering · doi:10.1146/annurev-bioeng-071811-150045 · Cited by 315 · see citing works

Extracellular proteolysis in brain injury and inflammation: Role for plasminogen activators and matrix metalloproteinases

Lo, E. H., Wang, X., & Cuzner, M. L. (2002) · Journal of Neuroscience Research · doi:10.1002/jnr.10270 · Cited by 310 · see citing works

Hydrogels derived from central nervous system extracellular matrix

Medberry, C. J., Crapo, P. M., Siu, B. F., Carruthers, C. A., Wolf, M. T., Nagarkar, S. P., Agrawal, V., Jones, K. E., Kelly, J., Johnson, S. A., et al. (2012) · Biomaterials · doi:10.1016/j.biomaterials.2012.10.062 · Cited by 278 · see citing works

The C-type lectin domains of lecticans, a family of aggregating chondroitin sulfate proteoglycans, bind tenascin-R by protein– protein interactions independent of carbohydrate moiety

Aspberg, A., Miura, R., Bourdoulous, S., Shimonaka, M., Heinegård, D., Schachner, M., Ruoslahti, E., & Yamaguchi, Y. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.19.10116 · Cited by 275 · see citing works

Differential matrix metalloproteinase expression in cases of multiple sclerosis and stroke

Anthony, D. C., Ferguson, B., Matyzak, M. K., Miller, K., Esiri, M. M., & Perry, V. H. (1997) · Neuropathology and Applied Neurobiology · doi:10.1111/j.1365-2990.1997.tb01315.x · Cited by 268 · see citing works

The Medium of Haptic Perception: A Tensegrity Hypothesis

Turvey, M. T., & Fonseca, S. T. (2014) · Journal of Motor Behavior · doi:10.1080/00222895.2013.798252 · Cited by 235 · see citing works

Decellularized Porcine Brain Matrix for Cell Culture and Tissue Engineering Scaffolds

DeQuach, J. A., Yuan, S. H., Goldstein, L. S. B., & Christman, K. L. (2011) · Tissue Engineering Part A · doi:10.1089/ten.tea.2010.0724 · Cited by 234 · see citing works

A delicate balance: role of MMP-9 in brain development and pathophysiology of neurodevelopmental disorders.

Reinhard, S. M., Razak, K., & Ethell, I. M. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00280 · Cited by 219 · see citing works

3D in vitro modeling of the central nervous system

Hopkins, A. M., DeSimone, E. K., Chwalek, K., & Kaplan, D. L. (2014) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2014.11.003 · Cited by 230 · see citing works

CD44-Mediated Adhesion to Hyaluronic Acid Contributes to Mechanosensing and Invasive Motility

Kim, Y., & Kumar, S. (2014) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-13-0629 · Cited by 229 · see citing works

The Brain Chondroitin Sulfate Proteoglycan Brevican Associates with Astrocytes Ensheathing Cerebellar Glomeruli and Inhibits Neurite Outgrowth from Granule Neurons

Yamada, H., Fredette, B. J., Shitara, K., Hagihara, K., Miura, R., Ranscht, B., Stallcup, W. B., & Yamaguchi, Y. (1997) · Journal of Neuroscience · doi:10.1523/jneurosci.17-20-07784.1997 · Cited by 228 · see citing works

Immune determinants of the pre-metastatic niche

Pătraș, L., Shaashua, L., Matei, I. R., & Lyden, D. C. (2023) · Cancer Cell · doi:10.1016/j.ccell.2023.02.018 · Cited by 223 · see citing works

Versican Interacts with Fibrillin-1 and Links Extracellular Microfibrils to Other Connective Tissue Networks

Isogai, Z., Aspberg, A., Keene, D. R., Ono, R. N., Reinhardt, D. P., & Sakai, L. Y. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m110583200 · Cited by 222 · see citing works

Compression stiffening of brain and its effect on mechanosensing by glioma cells

Pogoda, K., Chin, L., Georges, P. C., Byfield, F. J., Bucki, R., Kim, R., Weaver, M. W., Wells, R. G., Marcinkiewicz, C., & Janmey, P. A. (2014) · New Journal of Physics · doi:10.1088/1367-2630/16/7/075002 · Cited by 216 · see citing works

Fibulin-1 Is a Ligand for the C-type Lectin Domains of Aggrecan and Versican

Aspberg, A., Adam, S., Kostka, G., Timpl, R., & Heinegård, D. K. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.29.20444 · Cited by 207 · see citing works

Defining and designing polymers and hydrogels for neural tissue engineering

Aurand, E. R., Lampe, K. J., & Bjugstad, K. B. (2011) · Neuroscience Research · doi:10.1016/j.neures.2011.12.005 · Cited by 207 · see citing works

The Proteoglycans Aggrecan and Versican Form Networks with Fibulin-2 through Their Lectin Domain Binding

Olin, A. I., Mörgelin, M., Sasaki, T., Timpl, R., Heinegård, D. K., & Aspberg, A. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m006783200 · Cited by 204 · see citing works

Cortical areas abundant in extracellular matrix chondroitin sulphate proteoglycans are less affected by cytoskeletal changes in Alzheimer's disease

Brückner, G., Hausen, D., Härtig, W., Drlicek, M., Arendt, T., & Brauer, K. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00071-8 · Cited by 196 · see citing works

Brain derived versican V2 is a potent inhibitor of axonal growth

Schmalfeldt, M., Bandtlow, C. E., Dours-Zimmermann, M. T., Winterhalter, K. H., & Zimmermann, D. R. (2000) · Journal of Cell Science · doi:10.1242/jcs.113.5.807 · Cited by 197 · see citing works

Extracellular matrix components associated with remodeling processes in brain

Rauch, U. (2004) · Cellular and Molecular Life Sciences (CMLS) · doi:10.1007/s00018-004-4043-x · Cited by 205 · see citing works

Synaptic plasticity and cell cycle activation in neurons are alternative effector pathways: the 'Dr. Jekyll and Mr. Hyde concept' of Alzheimer's disease or the yin and yang of neuroplasticity

Arendt, T. (2003) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2003.09.007 · Cited by 188 · see citing works

Developmental Regulation of the Sulfation Profile of Chondroitin Sulfate Chains in the Chicken Embryo Brain

Kitagawa, H., Tsutsumi, K., Tone, Y., & Sugahara, K. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.50.31377 · Cited by 187 · see citing works

Extracellular matrix abnormalities in schizophrenia

Berretta, S. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.08.010 · Cited by 179 · see citing works

Biology of Fibrocartilage Cells

BENJAMIN, M., & Ralphs, J. R. (2004) · International review of cytology · doi:10.1016/s0074-7696(04)33001-9 · Cited by 184 · see citing works

A peptide for targeted, systemic delivery of imaging and therapeutic compounds into acute brain injuries

Mann, A. P., Scodeller, P., Hussain, S., Joo, J., Kwon, E. J., Braun, G. B., Mölder, T., She, Z. G., Kotamraju, V. R., Ranscht, B., et al. (2016) · Nature Communications · doi:10.1038/ncomms11980 · Cited by 181 · see citing works

Matrix metalloproteinase expression in an experimentally-induced DTH model of multiple sclerosis in the rat CNS

Anthony, D. C., Miller, K., Fearn, S., Townsend, M. J., Opdenakker, G., Wells, G., Clements, J. M., Chandler, S., Gearing, A. J. H., & Perry, V. H. (1998) · Journal of Neuroimmunology · doi:10.1016/s0165-5728(98)00046-0 · Cited by 180 · see citing works

Formation and remodeling of the brain extracellular matrix in neural plasticity: Roles of chondroitin sulfate and hyaluronan

Miyata, S., & Kitagawa, H. (2017) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2017.06.010 · Cited by 171 · see citing works

Brevican Is Degraded by Matrix Metalloproteinases and Aggrecanase-1 (ADAMTS4) at Different Sites

Nakamura, H., Fujii, Y., Inoki, I., Sugimoto, K., Tanzawa, K., Matsuki, H., Miura, R., Yamaguchi, Y., & Okada, Y. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m003875200 · Cited by 168 · see citing works

Scaffolds for 3D in vitro culture of neural lineage cells

Murphy, A. R., Laslett, A. L., O’Brien, C., & Cameron, N. R. (2017) · Acta Biomaterialia · doi:10.1016/j.actbio.2017.02.046 · Cited by 157 · see citing works

The mode and dynamics of glioblastoma cell invasion into a decellularized tissue-derived extracellular matrix-based three-dimensional tumor model

Koh, I., Cha, J., Park, J., Choi, J., Kang, S., & Kim, P. (2018) · Scientific Reports · doi:10.1038/s41598-018-22681-3 · Cited by 157 · see citing works

PTEN suppresses hyaluronic acid induced matrix metalloproteinase-9 expression in U87MG glioblastoma cells through focal adhesion kinase dephosphorylation

Park, M., Kim, M., Park, I., Kang, H., Yoo, H., Park, S. H., Rhee, C. H., Hong, S., & Lee, S. (2002) · European Journal of Cancer · doi:10.1016/s0959-8049(02)80906-6 · Cited by 155 · see citing works

In Vitro Microfluidic Models for Neurodegenerative Disorders

Osaki, T., Shin, Y., Sivathanu, V., Campisi, M., & Kamm, R. (2018) · Advanced Healthcare Materials · doi:10.1002/adhm.201700489 · Cited by 127 · see citing works

Collagen–Alginate Composite Hydrogel: Application in Tissue Engineering and Biomedical Sciences

Hu, T., & Lo, A. C. Y. (2021) · Polymers · doi:10.3390/polym13111852 · Cited by 155 · see citing works

The perineuronal net component of the extracellular matrix in plasticity and epilepsy

McRae, P. A., & Porter, B. E. (2012) · Neurochemistry International · doi:10.1016/j.neuint.2012.08.007 · Cited by 143 · see citing works

Blended alginate/collagen hydrogels promote neurogenesis and neuronal maturation

Moxon, S. R., Corbett, N. J., Fisher, K., Potjewyd, G., Domingos, M. A. N., & Hooper, N. M. (2019) · Materials Science and Engineering C · doi:10.1016/j.msec.2019.109904 · Cited by 143 · see citing works

Novel immunogenic antigen homologous to hyaluronidase in meningioma

Heckel, D., Comtesse, N., Brass, N., Blin, N., Zang, K. D., & Meese, E. (1998) · Human Molecular Genetics · doi:10.1093/hmg/7.12.1859 · Cited by 140 · see citing works

Molecular Cloning and Expression of Two Distinct Human Chondroitin 4-O-Sulfotransferases That Belong to the HNK-1 Sulfotransferase Gene Family

Hiraoka, N., Nakagawa, H., Ong, E., Akama, T. O., Fukuda, M. N., & Fukuda, M. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m002443200 · Cited by 139 · see citing works

Mechanobiology of the brain in ageing and Alzheimer's disease

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Biology and Models of the Blood–Brain Barrier

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