The DOI matches its Crossref record; 239 of the 240 references it cites were found in a registry or an index.
Extracellular matrix of the central nervous system: from neglect to challenge
Open accessAbstract
The basic concept, that specialized extracellular matrices rich in hyaluronan, chondroitin sulfate proteoglycans (aggrecan, versican, neurocan, brevican, phosphacan), link proteins and tenascins (Tn-R, Tn-C) can regulate cellular migration and axonal growth and thus, actively participate in the development and maturation of the nervous system, has in recent years gained rapidly expanding experimental support. The swift assembly and remodeling of these matrices have been associated with axonal guidance functions in the periphery and with the structural stabilization of myelinated fiber tracts and synaptic contacts in the maturating central nervous system. Particular interest has been focused on the putative role of chondroitin sulfate proteoglycans in suppressing central nervous system regeneration after lesions. The axon growth inhibitory properties of several of these chondroitin sulfate proteoglycans in vitro, and the partial recovery of structural plasticity in lesioned animals treated with chondroitin sulfate degrading enzymes in vivo have significantly contributed to the increased awareness of this long time neglected structure.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“During development, the ECM, and CSPGs in particular, regulate neuronal migration, axon outgrowth, synaptogenesis and synaptic maturation.23, 27, 28, 29, 30, 31”
From Aggrecan and chondroitin-6-sulfate abnormalities in schizophrenia and bipolar disorder: a postmortem study on the amygdala (2015) · cites this paper as [29]
Experimental — accuracy not yet measuredIn the citing paper
“The main components are hyaluronan (Figure 1), chondroitin sulfate proteoglycans (CSPGs) (i.e. aggrecan, brevican, neurocan, versican and phosphocan) (Figure 2), tenascins (Figure 3), and link proteins”
From Perineuronal nets and schizophrenia: The importance of neuronal coatings (2014) · cites this paper as Zimmermann and Dours-Zimmermann, 2008
In the citing paper
“the perinodal-matrix or peridonal net, a PNN-like structure (Dours-Zimmermann et al., 2009; Zimmermann and Dours-Zimmermann, 2008), is commonly associated with the node of Ranvier”
From Perineuronal nets and schizophrenia: The importance of neuronal coatings (2014) · cites this paper as Zimmermann and Dours-Zimmermann, 2008
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Genome-wide atlas of gene expression in the adult mouse brain
Lein, E. S., Hawrylycz, M. J., Ao, N., Ayres, M., Bensinger, A., Bernard, A., Boe, A. F., Boguski, M. S., Brockway, K. S., Byrnes, E. J., et al. (2007) · Nature · doi:10.1038/nature05453 · Cited by 5,572
Chondroitinase ABC promotes functional recovery after spinal cord injury
Bradbury, E. J., Moon, L. D. F., Popat, R. J., King, V. R., Bennett, G. S., Patel, P. N., Fawcett, J. W., & McMahon, S. B. (2002) · Nature · doi:10.1038/416636a · Cited by 2,357
Hyaluronan: from extracellular glue to pericellular cue
Toole, B. P. (2004) · Nature Reviews Cancer · doi:10.1038/nrc1391 · Cited by 2,125
PROTEOGLYCANS: STRUCTURES AND INTERACTIONS
Kjellén, L., & Lindahl, U. (1991) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.60.070191.002303 · Cited by 1,900
Thrombospondins are astrocyte-secreted proteins that promote CNS synaptogenesis
Christopherson, K. S., Ullian, E. M., Stokes, C. C. A., Mullowney, C. E., Hell, J. W., Agah, A., Lawler, J., Mosher, D. F., Bornstein, P., & Barres, B. A. (2005) · Cell · doi:10.1016/j.cell.2004.12.020 · Cited by 1,688
Reactivation of Ocular Dominance Plasticity in the Adult Visual Cortex
Pizzorusso, T., Medini, P., Berardi, N., Chierzi, S., Fawcett, J. W., & Maffei, L. (2002) · Science · doi:10.1126/science.1072699 · Cited by 1,679
Proteoglycans: Structures And Interactions
Kjellén, L. (1991) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.60.1.443 · Cited by 1,602
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
Camenisch, T. D., Spicer, A. P., Brehm-Gibson, T., Biesterfeldt, J., Augustine, M. L., Calabro, A., Kubalak, S., Klewer, S. E., & McDonald, J. A. (2000) · Journal of Clinical Investigation · doi:10.1172/jci10272 · Cited by 901
PORTER, S., CLARK, I. M., KEVORKIAN, L., & EDWARDS, D. R. (2005) · Biochemical Journal · doi:10.1042/bj20040424 · Cited by 779
Research works printed but not linked: 1
- Meyer-Puttlitz B, Junker E, Margolis RU, Margolis RK (1996) Chondroitin sulfate proteoglycans in the developing central nervous system. II. Immunocytochemical localization of neurocan and phosphacan. J Comp Neurol 366:44–54 · DOI
Cited by
Sorted by citations
Extracellular Matrix Degradation and Remodeling in Development and Disease
Lu, P., Takai, K., Weaver, V. M., & Werb, Z. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005058 · Cited by 2,265
Proteoglycan form and function: A comprehensive nomenclature of proteoglycans
Iozzo, R. V., & Schaefer, L. (2015) · Matrix Biology · doi:10.1016/j.matbio.2015.02.003 · Cited by 1,329
The extracellular matrix: tools and insights for the "omics" era
Naba, A., Clauser, K. R., Ding, H., Whittaker, C. A., Carr, S. A., & Hynes, R. O. (2016) · Matrix Biology · doi:10.1016/j.matbio.2015.06.003 · Cited by 1,037
A neurocentric perspective on glioma invasion
Cuddapah, V. A., Robel, S., Watkins, S., & Sontheimer, H. W. (2014) · Nature reviews. Neuroscience · doi:10.1038/nrn3765 · Cited by 877
The blood-brain barrier: an engineering perspective
Wong, A. D., Ye, M., Levy, A. F., Rothstein, J. D., Bergles, D. E., & Searson, P. C. (2013) · Frontiers in Neuroengineering · doi:10.3389/fneng.2013.00007 · Cited by 662
The roles of perineuronal nets and the perinodal extracellular matrix in neuronal function
Fawcett, J. W., Oohashi, T., & Pizzorusso, T. (2019) · Nature Reviews Neuroscience · doi:10.1038/s41583-019-0196-3 · Cited by 589
Engineered In Vitro Disease Models
Benam, K. H., Dauth, S., Hassell, B., Herland, A., Jain, A., Jang, K.-J., Karalis, K., Kim, H. J., MacQueen, L., Mahmoodian, R., et al. (2015) · Annual Review of Pathology: Mechanisms of Disease · doi:10.1146/annurev-pathol-012414-040418 · Cited by 554
Extracellular Matrix: Functions in the Nervous System
Barros, C. S., Franco, S. J., & Muller, U. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005108 · Cited by 506
Animals lacking link protein have attenuated perineuronal nets and persistent plasticity
Carulli, D., Pizzorusso, T., Kwok, J. C. F., Putignano, E., Poli, A., Forostyak, S., Andrews, M. R., Deepa, S. S., Glant, T. T., & Fawcett, J. W. (2010) · Brain · doi:10.1093/brain/awq145 · Cited by 495
Formation of the Ovarian Follicular Antrum and Follicular Fluid1
Rodgers, R. J., & Irving‐Rodgers, H. F. (2010) · Biology of Reproduction · doi:10.1095/biolreprod.109.082941 · Cited by 453
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
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 390
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
Interstitial guidance of cancer invasion
Gritsenko, P. G., Ilina, O., & Friedl, P. (2011) · The Journal of Pathology · doi:10.1002/path.3031 · Cited by 368
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 344
Regenerative Therapies for Central Nervous System Diseases: a Biomaterials Approach
Tam, R. Y., Führmann, T., Mitrousis, N., & Shoichet, M. S. (2013) · Neuropsychopharmacology · doi:10.1038/npp.2013.237 · Cited by 296
Current advances in electrospun gelatin-based scaffolds for tissue engineering applications
Aldana, A. A., & Abraham, G. A. (2016) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2016.09.044 · Cited by 286
How the extracellular matrix shapes neural development
Long, K. R., & Huttner, W. Β. (2019) · Open Biology · doi:10.1098/rsob.180216 · Cited by 276
Tumor Cell Invasion in Glioblastoma
Vollmann‐Zwerenz, A., Leidgens, V., Feliciello, G., Klein, C. A., & Hau, P. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21061932 · Cited by 270
Targeting the neural extracellular matrix in neurological disorders
Soleman, S., Filippov, M. A., Dityatev, A., & Fawcett, J. W. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.08.050 · Cited by 244
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 239
Drug and gene delivery across the blood–brain barrier with focused ultrasound
Timbie, K. F., Mead, B. P., & Price, R. J. (2015) · Journal of Controlled Release · doi:10.1016/j.jconrel.2015.08.059 · Cited by 237
Glioma infiltration and extracellular matrix: key players and modulators
Ferrer, V. P., Moura‐Neto, V., & Mentlein, R. (2018) · Glia · doi:10.1002/glia.23309 · Cited by 228
Provisional matrix: A role for versican and hyaluronan
Wight, T. N. (2016) · Matrix Biology · doi:10.1016/j.matbio.2016.12.001 · Cited by 223
Baiguera, S., Gaudio, C. D., Lucatelli, E., Kuevda, E. V., Boieri, M., Mazzanti, B., Bianco, A., & Macchiarini, P. (2013) · Biomaterials · doi:10.1016/j.biomaterials.2013.10.060 · Cited by 211
The brain interstitial system: Anatomy, modeling, in vivo measurement, and applications
Lei, Y., Han, H., Yuan, F., Javeed, A., & Zhao, Y. L. (2016) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2015.12.007 · Cited by 228
Perineuronal net formation and structure in aggrecan knockout mice
Giamanco, K. A., Morawski, M., & Matthews, R. T. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.08.032 · Cited by 207
Bioprinting for Neural Tissue Engineering
Knowlton, S. M., Anand, S., Shah, T., & Taşoğlu, S. (2017) · Trends in Neurosciences · doi:10.1016/j.tins.2017.11.001 · Cited by 208
Three mechanisms assemble central nervous system nodes of Ranvier
Susuki, K., Chang, K.-J., Zollinger, D. R., Liu, Y., Ogawa, Y., Eshed-Eisenbach, Y., Dours-Zimmermann, M. T., Oses-Prieto, J. A., Burlingame, A. L., Seidenbecher, C. I., et al. (2013) · Neuron · doi:10.1016/j.neuron.2013.03.005 · Cited by 186
“2008; Zimmermann and Dours-Zimmermann, 2008).”
Self-citationProteoglycans and their roles in brain cancer
Wade, A., Robinson, A. E., Engler, J. R., Petritsch, C. K., James, C. D., & Phillips, J. J. (2013) · FEBS Journal · doi:10.1111/febs.12109 · Cited by 197
The extracellular matrix as modifier of neuroinflammation and remyelination in multiple sclerosis
Ghorbani, S., & Yong, V. W. (2021) · Brain · doi:10.1093/brain/awab059 · Cited by 191
Nandadasa, S., Foulcer, S. J., & Apte, S. (2014) · Matrix Biology · doi:10.1016/j.matbio.2014.01.005 · Cited by 187
Extracellular matrix abnormalities in schizophrenia
Berretta, S. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.08.010 · Cited by 179
Hyaluronic Acid: Incorporating the Bio into the Material
Wolf, K. J., & Kumar, S. (2019) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.8b01268 · Cited by 178
Hemphill, M. A., Dauth, S., Yu, C. J., Dabiri, B. E., & Parker, K. K. (2015) · Neuron · doi:10.1016/j.neuron.2015.02.041 · Cited by 180
The performance of laminin-containing cryogel scaffolds in neural tissue regeneration
Jurga, M., Dainiak, M. B., Sarnowska, A., Jabłońska, A., Tripathi, A., Plieva, F. M., Savina, I. N., Strojek, L., Jungvid, H., Kumar, A., et al. (2011) · Biomaterials · doi:10.1016/j.biomaterials.2011.01.049 · Cited by 170
Miyata, S., & Kitagawa, H. (2017) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2017.06.010 · Cited by 171
Coleman, L. G., Liu, W., Oguz, I., Styner, M., & Crews, F. T. (2014) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2013.11.021 · Cited by 170
Human astrocytes develop physiological morphology and remain quiescent in a novel 3D matrix
Placone, A. L., McGuiggan, P. M., Bergles, D. E., Guerrero‐Cazares, H., Quiñones‐Hinojosa, A., & Searson, P. C. (2014) · Biomaterials · doi:10.1016/j.biomaterials.2014.11.046 · Cited by 162
Morawski, M., Brückner, G., Jäger, C., Seeger, G., & Arendt, T. (2010) · Neuroscience · doi:10.1016/j.neuroscience.2010.05.022 · Cited by 156
Dissecting and rebuilding the glioblastoma microenvironment with engineered materials
Wolf, K. J., Chen, J., Coombes, J. D., Aghi, M. K., & Kumar, S. (2019) · Nature Reviews Materials · doi:10.1038/s41578-019-0135-y · Cited by 164
The Brain’s Extracellular Matrix and Its Role in Synaptic Plasticity
Frischknecht, R., & Gundelfinger, E. D. (2012) · Advances in Experimental Medicine and Biology · doi:10.1007/978-3-7091-0932-8_7 · Cited by 156
Pantazopoulos, H., Markota, M., Jaquet, F., Ghosh, D., Wallin, A., Santos, A., Caterson, B., & Berretta, S. (2015) · Translational Psychiatry · doi:10.1038/tp.2014.128 · Cited by 153
Mechanical and Biological Interactions of Implants with the Brain and Their Impact on Implant Design
Prodanov, D., & Delbeke, J. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00011 · Cited by 152
Benchmarking in vitro tissue-engineered blood–brain barrier models
DeStefano, J. G., Jamieson, J. J., Linville, R. M., & Searson, P. C. (2018) · Fluids and Barriers of the CNS · doi:10.1186/s12987-018-0117-2 · Cited by 142
Fong, A. H., Romero-López, M., Heylman, C. M., Keating, M., Tran, D. D., Sobrino, A., Tran, A. Q., Pham, H. H., Fimbres, C., Gershon, P. D., et al. (2016) · Tissue Engineering Part A · doi:10.1089/ten.tea.2016.0027 · Cited by 145
Aggrecan: Beyond cartilage and into the brain
Morawski, M., Brückner, G., Arendt, T., & Matthews, R. T. (2012) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2012.01.010 · Cited by 136
Converting juvenile into adult plasticity: a role for the brain's extracellular matrix
Gundelfinger, E. D., Frischknecht, R., Choquet, D., & Heine, M. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07253.x · Cited by 136
Dzyubenko, E., Gottschling, C., & Faissner, A. (2016) · Neural Plasticity · doi:10.1155/2016/5214961 · Cited by 134
Extracellular matrix protein expression is brain region dependent
Dauth, S., Grevesse, T., Pantazopoulos, H., Campbell, P. H., Maoz, B. M., Berretta, S., & Parker, K. K. (2016) · The Journal of Comparative Neurology · doi:10.1002/cne.23965 · Cited by 137
Pyka, M., Wetzel, C., Aguado, A., Geissler, M., Hatt, H., & Faissner, A. (2011) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2011.07690.x · Cited by 131
Said, N. A., Sänchez‐Carbayo, M., Smith, S. C., & Theodorescu, D. (2012) · Journal of Clinical Investigation · doi:10.1172/jci61392 · Cited by 134
Oohashi, T., Edamatsu, M., Bekku, Y., & Carulli, D. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.09.010 · Cited by 131
3D brain angiogenesis model to reconstitute functional human blood–brain barrier in vitro
Lee, S., Chung, M., Lee, B., & Jeon, N. L. (2019) · Biotechnology and Bioengineering · doi:10.1002/bit.27224 · Cited by 131
Versican and the regulation of cell phenotype in disease
Wight, T. N., Kinsella, M. G., Evanko, S. P., Potter‐Perigo, S., & Merrilees, M. J. (2014) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2013.12.028 · Cited by 131
An Experimenter’s Guide to Glioblastoma Invasion Pathways
de Gooijer, M. C., Navarro, M. G., Bernards, R., Würdinger, T., & van Tellingen, O. (2018) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2018.07.003 · Cited by 129
Versican V2 Assembles the Extracellular Matrix Surrounding the Nodes of Ranvier in the CNS
Dours-Zimmermann, M. T., Maurer, K., Rauch, U., Stoffel, W., Fassler, R., & Zimmermann, D. R. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.4158-08.2009 · Cited by 123
Self-citationSood, D., Chwalek, K., Stuntz, E., Pouli, D., Du, C., Tang‐Schomer, M. D., Georgakoudi, I., Black, L. D., & Kaplan, D. L. (2015) · ACS Biomaterials Science & Engineering · doi:10.1021/acsbiomaterials.5b00446 · Cited by 123
Advancing models of neural development with biomaterials
Roth, J. G., Huang, M. S., Li, T. L., Feig, V. R., Jiang, Y., Cui, B., Greely, H. T., Bao, Z., Pașca, S. P., & Heilshorn, S. C. (2021) · Nature reviews. Neuroscience · doi:10.1038/s41583-021-00496-y · Cited by 122
Tunable hydrogel viscoelasticity modulates human neural maturation
Roth, J. G., Huang, M. S., Navarro, R. S., Akram, J., LeSavage, B. L., & Heilshorn, S. C. (2023) · Science Advances · doi:10.1126/sciadv.adh8313 · Cited by 122
Role of Microenvironment in Glioma Invasion: What We Learned from In Vitro Models
Manini, I., Caponnetto, F., Bartolini, A., Ius, T., Mariuzzi, L., Loreto, C. D., Beltrami, A. P., & Cesselli, D. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19010147 · Cited by 128
In Sickness and in Health: Perineuronal Nets and Synaptic Plasticity in Psychiatric Disorders
Pantazopoulos, H., & Berretta, S. (2015) · Neural Plasticity · doi:10.1155/2016/9847696 · Cited by 128
The extracellular matrix compartment of neural stem and glial progenitor cells
Faissner, A., & Reinhard, J. (2015) · Glia · doi:10.1002/glia.22839 · Cited by 116
Novel enzymatically cross-linked hyaluronan hydrogels support the formation of 3D neuronal networks
Broguière, N., Isenmann, L., & Zenobi‐Wong, M. (2016) · Biomaterials · doi:10.1016/j.biomaterials.2016.04.036 · Cited by 116
Chondroitin sulphate proteoglycans: Key modulators of spinal cord and brain plasticity
Bartus, K., James, N. D., Bosch, K. D., & Bradbury, E. J. (2011) · Experimental Neurology · doi:10.1016/j.expneurol.2011.08.008 · Cited by 121
Grifno, G. N., Farrell, A. M., Linville, R. M., Arevalo, D., Kim, J. H., Gu, L., & Searson, P. C. (2019) · Scientific Reports · doi:10.1038/s41598-019-50193-1 · Cited by 112
Role of the Microenvironment in Glioma Pathogenesis
Jayaram, M. A., & Phillips, J. J. (2023) · Annual Review of Pathology Mechanisms of Disease · doi:10.1146/annurev-pathmechdis-051122-110348 · Cited by 119
Gottschling, C., Wegrzyn, D., Denecke, B., & Faissner, A. (2019) · Scientific Reports · doi:10.1038/s41598-019-50404-9 · Cited by 111
Protective Properties of Neural Extracellular Matrix
Suttkus, A., Morawski, M., & Arendt, T. (2014) · Molecular Neurobiology · doi:10.1007/s12035-014-8990-4 · Cited by 110
Matrix Metalloproteinase 9 in Epilepsy: The Role of Neuroinflammation in Seizure Development
Bronisz, E., & Kurkowska‐Jastrzębska, I. (2016) · Mediators of Inflammation · doi:10.1155/2016/7369020 · Cited by 108
Li, H., Koenig, A. M., Sloan, P., & Leipzig, N. D. (2014) · Biomaterials · doi:10.1016/j.biomaterials.2014.07.038 · Cited by 105
Mechanosensation in traumatic brain injury
Keating, C. E., & Cullen, D. K. (2020) · Neurobiology of Disease · doi:10.1016/j.nbd.2020.105210 · Cited by 109
Katt, M. E., Linville, R. M., Mayo, L. N., Xu, Z. S., & Searson, P. C. (2018) · Fluids and Barriers of the CNS · doi:10.1186/s12987-018-0092-7 · Cited by 102
ADAMTS expression and function in central nervous system injury and disorders
Gottschall, P. E., & Howell, M. D. (2015) · Matrix Biology · doi:10.1016/j.matbio.2015.01.014 · Cited by 103
Hoffmann, C. J., Harms, U., Rex, A., Szulzewsky, F., Wolf, S. A., Grittner, U., Lättig-Tünnemann, G., Sendtner, M., Kettenmann, H., Dirnagl, U., et al. (2015) · Circulation · doi:10.1161/circulationaha.114.013003 · Cited by 98
Perineuronal nets and schizophrenia: The importance of neuronal coatings
Bitanihirwe, B. K. Y., & Woo, T.-U. W. (2014) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2014.03.018 · Cited by 95
Krishnaswamy, V. R., Benbenishty, A., Blinder, P., & Sagi, I. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03182-6 · Cited by 96
Hasanzadeh, E., Seifalian, A. M., Mellati, A., Saremi, J., Asadpour, S., Enderami, S. E., Nekounam, H., & Mahmoodi, N. (2023) · Materials Today Bio · doi:10.1016/j.mtbio.2023.100614 · Cited by 97
Astrocyte-secreted neurocan controls inhibitory synapse formation and function
Irala, D., Wang, S., Sakers, K., Nagendren, L., Severino, F. P. U., Bindu, D. S., Savage, J. T., & Eroğlu, Ç. (2024) · Neuron · doi:10.1016/j.neuron.2024.03.007 · Cited by 95
Seidlits, S. K., Liang, J., Bierman, R. D., Sohrabi, A., Karam, J., Holley, S. M., Cepeda, C., & Walthers, C. M. (2019) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.36603 · Cited by 87
(2012) · Europe PMC (PubMed Central) · Cited by 88
Delbeke, J., Hoffman, L., Mols, K., Braeken, D., & Prodanov, D. (2017) · Frontiers in Neuroscience · doi:10.3389/fnins.2017.00663 · Cited by 89
Nodes of Ranvier during development and repair in the CNS
Lubetzki, C., Sol‐Foulon, N., & Desmazières, A. (2020) · Nature Reviews Neurology · doi:10.1038/s41582-020-0375-x · Cited by 95
The crosstalk of hyaluronan-based extracellular matrix and synapses
Frischknecht, R., & Seidenbecher, C. I. (2008) · Neuron Glia Biology · doi:10.1017/s1740925x09990226 · Cited by 85
Lost in disruption: Role of proteases in glioma invasion and progression
Mentlein, R., Hattermann, K., & Held-Feindt, J. (2012) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2011.12.001 · Cited by 85
An advanced glioma cell invasion assay based on organotypic brain slice cultures
Eisemann, T., Costa, B., Strelau, J., Mittelbronn, M. G. A., Angel, P. E., & Peterziel, H. (2018) · BMC Cancer · doi:10.1186/s12885-018-4007-4 · Cited by 89
Inhibitors of myelination: ECM changes, CSPGs and PTPs
Harlow, D. E., & Macklin, W. B. (2013) · Experimental Neurology · doi:10.1016/j.expneurol.2013.10.017 · Cited by 79
Diverse functions of perineuronal nets
Karetko, M., & Skangiel-Kramska, J. (2009) · Acta Neurobiologiae Experimentalis · doi:10.55782/ane-2009-1766 · Cited by 76
Molecular Neuropathology of Astrocytes and Oligodendrocytes in Alcohol Use Disorders
Miguel-Hidalgo, J. J. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00078 · Cited by 78
Gritsenko, P. G., Leenders, W. P. J., & Friedl, P. (2017) · Histochemistry and Cell Biology · doi:10.1007/s00418-017-1604-2 · Cited by 85
Schneider, C. S., Perez, J. G., Cheng, E., Zhang, C., Mastorakos, P., Hanes, J. S., Winkles, J. A., Woodworth, G. F., & Kim, A. J. (2014) · Biomaterials · doi:10.1016/j.biomaterials.2014.11.054 · Cited by 78
Mentlein, R., Hattermann, K., Hemion, C., Jungbluth, A. A., & Held‐Feindt, J. (2010) · Biological Chemistry · doi:10.1515/bc.2010.119 · Cited by 78
Model systems for studying the blood-brain barrier: Applications and challenges
Jackson, S., Meeks, C., Vézina, A., Robey, R. W., Tanner, K., & Gottesman, M. M. (2019) · Biomaterials · doi:10.1016/j.biomaterials.2019.05.028 · Cited by 78
Extracellular matrix and biomimetic engineering microenvironment for neuronal differentiation
Yim, E. K. F., Jain, D., Mattiassi, S., & Goh, E. K. (2019) · Neural Regeneration Research · doi:10.4103/1673-5374.266907 · Cited by 76
Integration of neurogenesis and angiogenesis models for constructing a neurovascular tissue
Uwamori, H., Higuchi, T., Arai, K., & Sudo, R. (2017) · Scientific Reports · doi:10.1038/s41598-017-17411-0 · Cited by 75
Miyata, S., & Kitagawa, H. (2016) · Neural Plasticity · doi:10.1155/2016/1305801 · Cited by 70
Aggrecan in Cardiovascular Development and Disease
Koch, C. D., Lee, C. M., & Apte, S. (2020) · Journal of Histochemistry & Cytochemistry · doi:10.1369/0022155420952902 · Cited by 76
Nanotherapeutic treatment of the invasive glioblastoma tumor microenvironment
Pandey, N., Anastasiadis, P., Carney, C. P., Kanvinde, P. P., Woodworth, G. F., Winkles, J. A., & Kim, A. J. (2022) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2022.114415 · Cited by 74
Highly PEGylated DNA Nanoparticles Provide Uniform and Widespread Gene Transfer in the Brain
Mastorakos, P., Zhang, C., Berry, S., Oh, Y., Lee, S., Eberhart, C. G., Woodworth, G. F., Suk, J. S., & Hanes, J. (2015) · Advanced Healthcare Materials · doi:10.1002/adhm.201400800 · Cited by 80
Glioblastoma: To Target the Tumor Cell or the Microenvironment?
Vleeschouwer, S. D., & Bergers, G. (2017) · Codon Publications eBooks · doi:10.15586/codon.glioblastoma.2017.ch16 · Cited by 73
Metadata
- Authors
- Zimmermann, D. R., & Dours-Zimmermann, M. T.
- Affiliations
- University Hospital Zurich (CH)
- Corresponding author
- Zimmermann, Dieter R.
- Venue
- Histochemistry and Cell Biology
- Published
- 2008-08-12
- Volume
- 130
- Issue
- 4
- Pages
- 635-653
- ISSN
- 0948-6143 (ISSN-L)
- 1432-119X
- OpenAlex
- W2146369085
- Cited by
- 465
- References
- 240
- Citations by year
- 2026: 16 · 2025: 20 · 2024: 29 · 2023: 27 · 2022: 31 · 2021: 30 · 2020: 30 · 2019: 31 · 2018: 35 · 2017: 18 · 2016: 28 · 2015: 27 · 2014: 42 · 2013: 22 · 2012: 18
- FWCI
- 1.63
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Histochemistry and Cell Biology (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- Zurich Open Repository and Archive (University of Zurich) (acceptedVersion, other-oa)
- reroDoc Digital Library (submittedVersion)
- Zurich Open Repository and Archive (University of Zurich) (submittedVersion, other-oa)
- Zurich Open Repository and Archive (University of Zurich)
- Funders
- National Science Foundation
- Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
- Universität Zürich
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Proteoglycans and glycosaminoglycans research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Nerve injury and regeneration
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- extracellular matrix, central nervous system, hyaluronic acid, chondroitin sulfate proteoglycans, aggrecan, versican, neurocan, brevican, phosphacan, tenascin, axon guidance, axon growth, myelination, synapse maturation, central nervous system regeneration, lesion recovery, structural plasticity
- MeSH terms
- Animals, Axons, Central Nervous System, Extracellular Matrix, Humans, Chondroitin Sulfate Proteoglycans
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