The DOI matches its Crossref record; 101 of the 101 references it cites were found in a registry or an index.
A ‘GAG’ reflex prevents repair of the damaged CNS
Abstract
The extracellular matrix of the central nervous system (CNS) serves as both a supporting structure for cells and a rich source of signaling molecules that can influence cell proliferation, survival, migration and differentiation. A large proportion of this matrix is composed of proteoglycans--proteins with long chains of polysaccharides, called glycosaminoglycans (GAGs), covalently attached. Although many of the activities of proteoglycans depend on their core proteins, GAGs themselves can influence cell signaling. Here we review accumulating evidence that two GAGs, chondroitin sulfate and hyaluronan, play essential roles during nervous system development but also accumulate in chronic CNS lesions and inhibit axonal regeneration and remyelination, making them significant hindrances to CNS repair. We propose that the balance between the synthesis and degradation of these molecules dictates, in part, how regeneration and recovery from CNS damage occurs.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
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?
In the citing paper
“These chondroitin sulfate side chains are a type of GAG polysaccharide consisting of disaccharide blocks of N-acetylgalactosamine and glucuronic acid (Sherman and Back, 2007).”
From The Perineuronal ‘Safety’ Net? Perineuronal Net Abnormalities in Neurological Disorders (2018) · cites this paper as Sherman and Back, 2007
Citations
Cites
Regeneration beyond the glial scar
Silver, J., & Miller, J. H. (2004) · Nature reviews. Neuroscience · doi:10.1038/nrn1326 · Cited by 3,151
CD44: From adhesion molecules to signalling regulators
Ponta, H., Sherman, L. S., & Herrlich, P. A. (2003) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1004 · Cited by 2,458
Self-citationReactivation 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
Astrocyte activation and reactive gliosis
Pekny, M., & Nilsson, M. (2005) · Glia · doi:10.1002/glia.20207 · Cited by 1,611
LYVE-1, a New Homologue of the CD44 Glycoprotein, Is a Lymph-specific Receptor for Hyaluronan
Banerji, S., Ni, J., Wang, S.-X., Clasper, S., Su, J. Y., Tammi, R., Jones, M., & Jackson, D. G. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.144.4.789 · Cited by 1,586
Regulation of lung injury and repair by Toll-like receptors and hyaluronan
Jiang, D., Liang, J., Fan, J., Yu, S., Chen, S., Luo, Y., Prestwich, G. D., Mascarenhas, M. M., Garg, H. G., Quinn, D. A., et al. (2005) · Nature Medicine · doi:10.1038/nm1315 · Cited by 1,401
Oligosaccharides of Hyaluronan Activate Dendritic Cells via Toll-like Receptor 4
Termeer, C., Benedix, F., Sleeman, J., Fieber, C., Voith, U., Ahrens, T., Miyake, K., Freudenberg, M., Galanos, C., & Simon, J. C. (2002) · The Journal of Experimental Medicine · doi:10.1084/jem.20001858 · Cited by 1,378
McKeon, R., Schreiber, R., Rudge, J., & Silver, J. (1991) · The Journal of Neuroscience · doi:10.1523/jneurosci.11-11-03398.1991 · Cited by 1,188
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
Hyaluronan in Tissue Injury and Repair
Jiang, D., Liang, J., & Noble, P. W. (2007) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.23.090506.123337 · Cited by 835
Cited by
Sorted by citations
The Pathobiology of Vascular Dementia
Iadecola, C. (2013) · Neuron · doi:10.1016/j.neuron.2013.10.008 · Cited by 1,857
“HA is a component of the matrix and is involved in neurodevelopment promoting neuronal migration (Sherman and Back, 2008).”
Pathophysiology of the brain extracellular matrix: a new target for remyelination
Lau, L. W., Cua, R., Keough, M. B., Haylock-Jacobs, S., & Yong, V. W. (2013) · Nature reviews. Neuroscience · doi:10.1038/nrn3550 · Cited by 549
Arrested preoligodendrocyte maturation contributes to myelination failure in premature infants
Buser, J. R., Maire, J. J., Riddle, A., Gong, X., Nguyen, T. D., Nelson, K., Luo, N. L., Ren, J., Struve, J. N., Sherman, L. S., et al. (2011) · Annals of Neurology · doi:10.1002/ana.22627 · Cited by 447
Self-citationBrain injury in premature neonates: A primary cerebral dysmaturation disorder?
Back, S. A., & Miller, S. P. (2014) · Annals of Neurology · doi:10.1002/ana.24132 · Cited by 360
Self-citationArrested oligodendrocyte lineage maturation in chronic perinatal white matter injury
Segovia, K. N., McClure, M., Moravec, M., Luo, N. L., Wan, Y., Gong, X., Riddle, A., Craig, A., Struve, J., Sherman, L. S., et al. (2008) · Annals of Neurology · doi:10.1002/ana.21359 · Cited by 340
Self-citationFisher, D., Xing, B., Dill, J., Li, H., Hoang, H. H., Zhao, Z., Yang, X.-L., Bachoo, R., Cannon, S., Longo, F. M., et al. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.1737-11.2011 · Cited by 312
Chondroitin sulfate proteoglycans in demyelinated lesions impair remyelination
Lau, L. W., Keough, M. B., Haylock‐Jacobs, S., Cua, R., Döring, A., Sloka, S., Stirling, D. P., Rivest, S., & Yong, V. W. (2012) · Annals of Neurology · doi:10.1002/ana.23599 · Cited by 255
Cortical remyelination: A new target for repair therapies in multiple sclerosis
Chang, A., Staugaitis, S. M., Dutta, R., Batt, C. E., Easley, K. E., Chomyk, A. M., Yong, V. W., Fox, R. J., Kidd, G. J., & Trapp, B. D. (2012) · Annals of Neurology · doi:10.1002/ana.23693 · Cited by 216
Pathophysiology of glia in perinatal white matter injury
Back, S. A., & Rosenberg, P. A. (2014) · Glia · doi:10.1002/glia.22658 · Cited by 202
Self-citationHer, G. J., Wu, H., Chen, M., Chen, M., Chang, S.-C., & Wang, T. (2012) · Acta Biomaterialia · doi:10.1016/j.actbio.2012.10.012 · Cited by 189
Dyck, S. M., & Karimi‐Abdolrezaee, S. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.04.006 · Cited by 194
Scar-mediated inhibition and CSPG receptors in the CNS
Sharma, K., Selzer, M. E., & Li, S. (2012) · Experimental Neurology · doi:10.1016/j.expneurol.2012.07.009 · Cited by 192
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
The Perineuronal ‘Safety’ Net? Perineuronal Net Abnormalities in Neurological Disorders
Wen, T. H., Binder, D. K., Ethell, I. M., & Razak, K. A. (2018) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2018.00270 · Cited by 170
Perineuronal Nets in the Adult Sensory Cortex Are Necessary for Fear Learning
Banerjee, S. B., Gutzeit, V. A., Baman, J., Aoued, H. S., Doshi, N. K., Liu, R. C., & Ressler, K. J. (2017) · Neuron · doi:10.1016/j.neuron.2017.06.007 · Cited by 163
Mohan, H., Krumbholz, M., Sharma, R. D., Eisele, S. C., Junker, A., Sixt, M., Newcombe, J., Wekerle, H., Hohlfeld, R., Lassmann, H., et al. (2010) · Brain Pathology · doi:10.1111/j.1750-3639.2010.00399.x · Cited by 164
Neural stem cell niches: Roles for the hyaluronan-based extracellular matrix
Preston, M. (2011) · Frontiers in Bioscience-Scholar · doi:10.2741/218 · Cited by 160
Riddle, A., Dean, J. M., Buser, J. R., Gong, X., Maire, J. J., Chen, K., Ahmad, T., Cai, V., Nguyen, T. D., Kroenke, C. D., et al. (2011) · Annals of Neurology · doi:10.1002/ana.22501 · Cited by 139
Self-citationKohama, S. G., Rosene, D. L., & Sherman, L. S. (2011) · AGE · doi:10.1007/s11357-011-9357-7 · Cited by 142
Self-citationChondroitin sulfate proteoglycans inhibit oligodendrocyte myelination through PTPσ
Pendleton, J. C., Shamblott, M. J., Gary, D. S., Belegu, V., Hurtado, A., Malone, M. L., & McDonald, J. W. (2013) · Experimental Neurology · doi:10.1016/j.expneurol.2013.04.003 · Cited by 143
From demyelination to remyelination: The road toward therapies for spinal cord injury
Papastefanaki, F., & Matsas, R. (2015) · Glia · doi:10.1002/glia.22809 · Cited by 115
Digestion products of the PH20 hyaluronidase inhibit remyelination
Preston, M., Gong, X., Su, W., Matsumoto, S. G., Banine, F., Winkler, C., Foster, S., Xing, R., Struve, J., Dean, J., et al. (2013) · Annals of Neurology · doi:10.1002/ana.23788 · Cited by 107
Self-citationVanishing white matter: a leukodystrophy due to astrocytic dysfunction
Bugiani, M., Vuong, C., Breur, M., & van der Knaap, M. S. (2018) · Brain Pathology · doi:10.1111/bpa.12606 · Cited by 106
Glial scar and immune cell involvement in tissue remodeling and repair following acute CNS injuries
Rapôso, C., & Schwartz, M. (2014) · Glia · doi:10.1002/glia.22676 · Cited by 112
Brain Injury in the Preterm Infant: New Horizons for Pathogenesis and Prevention
Back, S. A. (2015) · Pediatric Neurology · doi:10.1016/j.pediatrneurol.2015.04.006 · Cited by 109
Self-citationBugiani, M., Postma, N. L., Polder, E., Dieleman, N., Scheffer, P. G., Sim, F. J., van der Knaap, M. S., & Boor, I. (2013) · Brain · doi:10.1093/brain/aws320 · Cited by 105
Using extracellular matrix for regenerative medicine in the spinal cord
Volpato, F. Z., Führmann, T., Migliaresi, C., Hutmacher, D. W., & Dalton, P. D. (2013) · Biomaterials · doi:10.1016/j.biomaterials.2013.03.057 · Cited by 103
Molecular mechanisms of scar-sourced axon growth inhibitors
Ohtake, Y., & Li, S. (2014) · Brain Research · doi:10.1016/j.brainres.2014.08.064 · Cited by 105
Systemic inflammation, oligodendroglial maturation, and the encephalopathy of prematurity
Volpe, J. J. (2011) · Annals of Neurology · doi:10.1002/ana.22533 · Cited by 98
Cerebral White and Gray Matter Injury in Newborns
Back, S. A. (2014) · Clinics in Perinatology · doi:10.1016/j.clp.2013.11.001 · Cited by 97
Self-citationKrishnaswamy, V. R., Benbenishty, A., Blinder, P., & Sagi, I. (2019) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-019-03182-6 · Cited by 96
Zebrafish as a model to investigate CNS myelination
Preston, M., & Macklin, W. B. (2014) · Glia · doi:10.1002/glia.22755 · Cited by 90
Hyaluronan Synthesis, Catabolism, and Signaling in Neurodegenerative Diseases
Sherman, L. S., Matsumoto, S. G., Su, W., Srivastava, T., & Back, S. A. (2015) · International Journal of Cell Biology · doi:10.1155/2015/368584 · Cited by 84
Self-citationRecent insights on astrocyte mechanisms in CNS homeostasis, pathology, and repair
Hart, C. G., & Karimi‐Abdolrezaee, S. (2021) · Journal of Neuroscience Research · doi:10.1002/jnr.24922 · Cited by 88
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
Susarla, B. T. S., Laing, E. D., Yu, P., Katagiri, Y., Geller, H. M., & Symes, A. J. (2011) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2011.07470.x · Cited by 81
Advances in the Signaling Pathways Downstream of Glial-Scar Axon Growth Inhibitors
Sami, A., Selzer, M. E., & Li, S. (2020) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2020.00174 · Cited by 77
Dubois-Dalcq, M. E., Williams, A., Stadelmann, C., Stankoff, B., Zalc, B., & Lubetzki, C. (2008) · Brain · doi:10.1093/brain/awn076 · Cited by 74
Role of CSPG receptor LAR phosphatase in restricting axon regeneration after CNS injury
Xu, B., Park, D., Ohtake, Y., Li, H., Hayat, U., Liu, J., Selzer, M. E., Longo, F. M., & Li, S. (2014) · Neurobiology of Disease · doi:10.1016/j.nbd.2014.08.030 · Cited by 76
Gallart‐Palau, X., Lee, B. S. T., Adav, S. S., Qian, J., Serra, A., Park, J. E., Lai, M. K. P., Chen, C., Kalaria, R. N., & Sze, S. K. (2016) · Molecular Brain · doi:10.1186/s13041-016-0205-7 · Cited by 72
Biomarkers for Severity of Spinal Cord Injury in the Cerebrospinal Fluid of Rats
Lubieniecka, J. M., Streijger, F., Lee, J. H. T., Stoynov, N., Liu, J., Mottus, R., Pfeifer, T. A., Kwon, B. K., Coorssen, J. R., Foster, L. J., et al. (2011) · PLoS ONE · doi:10.1371/journal.pone.0019247 · Cited by 74
Gardner, R. T., & Habecker, B. A. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.5866-12.2013 · Cited by 66
A mouse model for testing remyelinating therapies
Bai, C. B., Sun, H. S., Roholt, A., Benson, E. K., Edberg, D. D., Medicetty, S., Dutta, R., Kidd, G. J., Macklin, W. B., & Trapp, B. D. (2016) · Experimental Neurology · doi:10.1016/j.expneurol.2016.06.033 · Cited by 67
Hyaluronic acid and neural stem cells: implications for biomaterial design
Khaing, Z. Z., & Seidlits, S. K. (2015) · Journal of Materials Chemistry B · doi:10.1039/c5tb00974j · Cited by 63
Two PTP receptors mediate CSPG inhibition by convergent and divergent signaling pathways in neurons
Ohtake, Y., Wong, D., Abdul-Muneer, P. M., Selzer, M. E., & Li, S. (2016) · Scientific Reports · doi:10.1038/srep37152 · Cited by 59
Haylock‐Jacobs, S., Keough, M. B., Lau, L. W., & Yong, V. W. (2011) · Autoimmunity Reviews · doi:10.1016/j.autrev.2011.05.019 · Cited by 60
Extracellular matrix in the CNS
Benarroch, E. E. (2015) · Neurology · doi:10.1212/wnl.0000000000002044 · Cited by 59
The axon–glia unit in white matter stroke: Mechanisms of damage and recovery
Rosenzweig, S., & Carmichael, S. T. (2015) · Brain Research · doi:10.1016/j.brainres.2015.02.019 · Cited by 58
Lindwall, C., Lindvall, M. O., Osman, A. M., Kuhn, H. G., & Curtis, M. A. (2013) · Brain Research · doi:10.1016/j.brainres.2013.01.045 · Cited by 57
Elkin, B. S., Shaik, M. A., & Morrison, B. (2010) · Philosophical Transactions of the Royal Society A Mathematical Physical and Engineering Sciences · doi:10.1098/rsta.2009.0223 · Cited by 52
Contribution of Chondroitin Sulfate A to the Binding of Complement Proteins to Activated Platelets
Hamad, O. A., Nilsson, P. H., Lasaosa, M., Ricklin, D., Lambris, J. D., Nilsson, B., & Ekdahl, K. N. (2010) · PLoS ONE · doi:10.1371/journal.pone.0012889 · Cited by 45
Evaluation of Long-Term Cryostorage of Brain Tissue Sections for Quantitative Histochemistry
Estrada, L. I., Robinson, A. A., Amaral, A. C. S., Giannaris, E. L., Heyworth, N. C., Mortazavi, F., Ngwenya, L. B., Roberts, D. E., Cabral, H., Killiany, R., et al. (2017) · Journal of Histochemistry & Cytochemistry · doi:10.1369/0022155416686934 · Cited by 43
Role of Recurrent Hypoxia-Ischemia in Preterm White Matter Injury Severity
Hagen, M. W., Riddle, A., McClendon, E., Gong, X., Shaver, D. C., Srivastava, T., Dean, J. M., Bai, J., Fowke, T. M., Gunn, A. J., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0112800 · Cited by 40
Self-citationChondroitin Sulfates Act as Extracellular Gating Modifiers on Voltage-Dependent Ion Channels
Vigetti, D., Andrini, O., Clerici, M., Negrini, D., Passi, A., & Moriondo, A. (2008) · Cellular Physiology and Biochemistry · doi:10.1159/000149791 · Cited by 38
Ferrari, L. F., Araldi, D., Bogen, O., & Levine, J. D. (2016) · Neuroscience · doi:10.1016/j.neuroscience.2016.03.032 · Cited by 38
Diverse functions of protein tyrosine phosphatase σ in the nervous and immune systems
Ohtake, Y., Saito, A., & Li, S. (2018) · Experimental Neurology · doi:10.1016/j.expneurol.2018.01.014 · Cited by 39
Dean, J. M., Riddle, A., Maire, J. J., Hansen, K., Preston, M., Barnes, A. P., Sherman, L. S., & Back, S. A. (2011) · Molecular Neurodegeneration · doi:10.1186/1750-1326-6-46 · Cited by 36
Self-citationSaraswat, D., Shayya, H. J., Polanco, J. J., Tripathi, A. K., Welliver, R. R., Pol, S. U., Seidman, R. A., Broome, J. E., O’Bara, M. A., Kuppevelt, T. H. V., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-22263-4 · Cited by 32
Deng, Y.-P., Sun, Y., Hu, L., Li, Z., Xu, Q., Pei, Y.-L., Huang, Z., Yang, Z., & Chen, C. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.03.026 · Cited by 30
Hyaluronan oligosaccharides promote functional recovery after spinal cord injury in rats
Wakao, N., Imagama, S., Zhang, H., Tauchi, R., Muramoto, A., Natori, T., Takeshita, S., Ishiguro, N., Matsuyama, Y., & Kadomatsu, K. (2010) · Neuroscience Letters · doi:10.1016/j.neulet.2010.11.051 · Cited by 31
Flangea, C., Schiopu, C., Şişu, E., Serb, A. F., Przybylski, M., Seidler, D. G., & Zamfir, A. D. (2009) · Analytical and Bioanalytical Chemistry · doi:10.1007/s00216-009-3167-0 · Cited by 28
Post-Stroke Timing of ECM Hydrogel Implantation Affects Biodegradation and Tissue Restoration
Damian, C., Ghuman, H., Mauney, C., Azar, R. M., Reinartz, J., Badylak, S. F., & Modo, M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222111372 · Cited by 25
Rezaei, S., Dabirmanesh, B., Zare, L., Golestani, A., Javan, M., & Khajeh, K. (2019) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2019.12.258 · Cited by 28
Plug, B. C., Revers, I. M., Breur, M., González, G. M., Timmerman, J. A., Meijns, N. R. C., Hamberg, D., Wagendorp, J., Nutma, E., Wolf, N. I., et al. (2024) · Acta Neuropathologica Communications · doi:10.1186/s40478-024-01784-1 · Cited by 25
Detection of Glycan Shedding in the Blood: New Class of Multiple Sclerosis Biomarkers?
DellaValle, B., Manresa-Arraut, A., Hasseldam, H., Stensballe, A., Rungby, J., Larsen, A., & Hempel, C. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01254 · Cited by 23
Dysregulation of Hyaluronan Homeostasis During White Matter Injury
Srivastava, T., Sherman, L. S., & Back, S. A. (2019) · Neurochemical Research · doi:10.1007/s11064-019-02879-1 · Cited by 26
Self-citationGlycosaminoglycans of the Porcine Central Nervous System
Liu, Z., Masuko, S., Solakyildirim, K., Pu, D., Linhardt, R. J., & Zhang, F. (2010) · Biochemistry · doi:10.1021/bi101305b · Cited by 24
A novel myelin protein zero transgenic zebrafish designed for rapid readout of in vivo myelination
Preston, M., Finseth, L. T., Bourne, J. N., & Macklin, W. B. (2019) · Glia · doi:10.1002/glia.23559 · Cited by 23
Danielson, B. T., Knudson, C. B., & Knudson, W. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.643171 · Cited by 23
Traumatology of the optic nerve and contribution of crystallins to axonal regeneration
Thanos, S., Böhm, M. R. R., Schallenberg, M., & Oellers, P. R. (2012) · Cell and Tissue Research · doi:10.1007/s00441-012-1442-4 · Cited by 21
Pinzón, N. E., Brevé, J. J. P., Bol, J. G. J. M., Drukarch, B., Baron, W., & van Dam, A. (2017) · Journal of Neuroinflammation · doi:10.1186/s12974-017-1031-2 · Cited by 22
Beneficial Effects of Hyaluronan-Based Hydrogel Implantation after Cortical Traumatic Injury
Lainé, A., Brot, S., & Gaillard, A. (2022) · Cells · doi:10.3390/cells11233831 · Cited by 20
Xiong, M., Chen, L.-X., Ma, S., Yang, Y., & Zhou, W. (2013) · Developmental Neuroscience · doi:10.1159/000346324 · Cited by 19
Flangea, C., Serb, A. F., Schiopu, C., Tudor, S., Şişu, E., Seidler, D. G., & Zamfir, A. D. (2009) · Open Chemistry · doi:10.2478/s11532-009-0070-7 · Cited by 19
Small Molecules Targeting PTPσ–Trk Interactions Promote Sympathetic Nerve Regeneration
Blake, M. R., Gardner, R. T., Jin, H., Staffenson, M. A., Rueb, N. J., Barrios, A. M., Dudley, G. B., Cohen, M. S., & Habecker, B. A. (2022) · ACS Chemical Neuroscience · doi:10.1021/acschemneuro.1c00854 · Cited by 17
Milton, A. J., Kwok, J. C. F., McClellan, J., Randall, S., Lathia, J. D., Warren, P. M., Silver, D. J., & Silver, J. (2023) · Journal of Neurotrauma · doi:10.1089/neu.2023.0117 · Cited by 19
McNeal, D. W., Brandner, D. D., Gong, X., Postupna, N. O., Montine, T. J., Keene, C. D., & Back, S. A. (2016) · Journal of Neuropathology & Experimental Neurology · doi:10.1093/jnen/nlw032 · Cited by 17
Self-citationSexual dimorphism in the nociceptive effects of hyaluronan
Bonet, I. J. M., Green, P. G., & Levine, J. D. (2020) · Pain · doi:10.1097/j.pain.0000000000002116 · Cited by 15
Sutiwisesak, R., Burns, T. C., Rodriguez, M., & Warrington, A. E. (2021) · Expert Opinion on Investigational Drugs · doi:10.1080/13543784.2021.1942840 · Cited by 14
Chondroitinase ABC Reduces Brain Tissue Swelling In Vitro
Elkin, B. S., Shaik, M. A., & Morrison, B. (2011) · Journal of Neurotrauma · doi:10.1089/neu.2010.1603 · Cited by 13
Astrogliosis and Axonal Regeneration
Sharma, K., Zhang, G., & Li, S. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-801732-6.00011-2 · Cited by 14
Jiang, B., Xu, F., Li, L., Chen, W., Hong, S., & Chen, R. (2018) · Journal of Molecular Histology · doi:10.1007/s10735-018-9803-2 · Cited by 11
Klüppel, M. (2011) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-010-0705-1 · Cited by 11
Wu, X., Zhang, T., Jia, J., Chen, Y., Zhang, Y., Fang, Z., Zhang, C., Bai, Y., Li, Z., & Li, Y. (2024) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2024.116309 · Cited by 11
Jorge, M. S., & Bugiani, M. (2019) · Advances in experimental medicine and biology · doi:10.1007/978-981-13-9913-8_9 · Cited by 11
Martín-Rojas, T., Sastre-Oliva, T., de Ruz, A. E., Gil-Dones, F., Mouriño-Álvarez, L., Corbacho-Alonso, N., Moreno‐Luna, R., Hernández-Fernández, G., López, J. A., Oliviero, A., et al. (2020) · Journal of Personalized Medicine · doi:10.3390/jpm10040183 · Cited by 9
The Role of Extracellular Matrix in Myelination and Oligodendrogenesis of the Central Nervous System
Khaksar, Z., Morovvati, H., Moradi, H. R., & Negah, S. S. (2019) · The Neuroscience Journal of Shefaye Khatam · doi:10.29252/shefa.7.2.66 · Cited by 6
Seehusen, F., Al-Azreg, S., Raddatz, B., Haist, V., Puff, C., Spitzbarth, I., Ulrich, R., & Baumgärtner, W. (2016) · PLoS ONE · doi:10.1371/journal.pone.0159752 · Cited by 7
Inflammatory Oriented Nanospheres-Reconstructed Extracellular Matrix in Ischemic Stroke
Gao, Z., Wang, X., Zhang, W., Wang, J., & Liu, C. (2025) · ACS Nano · doi:10.1021/acsnano.5c02105 · Cited by 6
Wang, J., Wang, X., Rong, W., Lv, J., Wei, F., & Liu, Z. (2014) · Neurochemical Research · doi:10.1007/s11064-014-1442-8 · Cited by 5
Chondroitin 6-sulfate-binding peptides improve recovery in spinal cord-injured mice
Li, C., Sahu, S. S., Kou, G., Jagadeesan, N., Joseph, T. P., Lin, S. L., & Schachner, M. (2021) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2021.174421 · Cited by 5
Brito, R. M. D. M., Meurer, Y. D. S. R., Santos, L. D. S., Marcelino, B. M. D. M., & de Andrade‐Neto, V. F. (2020) · Parasitology Research · doi:10.1007/s00436-020-06674-8 · Cited by 5
Cspg4 sculpts oligodendrocyte precursor cell morphology
Bromley‐Coolidge, S., Iruegas, D., & Appel, B. (2024) · Differentiation · doi:10.1016/j.diff.2024.100819 · Cited by 4
Pathophysiology of Neonatal White Matter Injury
Miller, S. P., & Back, S. A. (2016) · Elsevier eBooks · doi:10.1016/b978-0-323-35214-7.00169-4 · Cited by 3
Self-citationKiran, S., Xue, Y., Sarker, D. B., & Sang, Q. A. (2025) · Cancers · doi:10.3390/cancers17060997 · Cited by 2
Park, H., Pham, N. C., Chun, H., & Ryu, S. E. (2013) · Bulletin of the Korean Chemical Society · doi:10.5012/bkcs.2013.34.7.2006 · Cited by 2
Wu, W., Lan, Q., Lu, H., Xu, J., Zhu, A., Fang, W., Jiang, Y., & Hui, G. (2010) · Cited by 2
Zhao, L., Zhang, X., & Zhang, C. (2020) · Mediators of Inflammation · doi:10.1155/2020/4027470 · Cited by 2
Development of a multi-functional biopolymer scaffold for neural tissue engineering
Francis, N. L., & Wheatley, M. A. (2012) · doi:10.17918/etd-3976 · Cited by 1
CD44 Expression in Microglia of the Retina and Cerebellum of Developing and Adult Chicken
Kim, J. Y., Sohn, H. J., Seo, J. H., & Lee, E. Y. (2017) · Korean Journal of Physical Anthropology · doi:10.11637/kjpa.2017.30.1.29
Metadata
- Authors
- Sherman, L. S., & Back, S. A.
- Affiliations
- Oregon National Primate Research Center (US)
- Oregon Health & Science University (US)
- Venue
- Trends in Neurosciences
- Publisher
- Elsevier BV
- Published
- 2008-01
- Volume
- 31
- Issue
- 1
- Pages
- 44-52
- ISSN
- 0166-2236 (ISSN-L)
- OpenAlex
- W2027830942
- Cited by
- 116
- References
- 101
- Citations by year
- 2026: 1 · 2025: 2 · 2024: 11 · 2023: 1 · 2022: 3 · 2021: 6 · 2020: 6 · 2019: 6 · 2018: 5 · 2017: 5 · 2016: 7 · 2015: 11 · 2014: 10 · 2013: 10 · 2012: 7
- FWCI
- 0.29
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Trends in Neurosciences (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Neurological Disorders and Stroke (R01NS056234, NS056234, R01NS054044, NS054044)
- 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
- Health Sciences › Medicine › Clinical Neurology › Spinal Cord Injury Research
- Keywords
- glycosaminoglycans, chondroitin sulfate, hyaluronic acid, proteoglycans, extracellular matrix, central nervous system repair, axon regeneration, remyelination, central nervous system injury, brain development
- MeSH terms
- Animals, Central Nervous System, Chondroitin, Extracellular Matrix, Glycosaminoglycans, Humans, Hyaluronic Acid, Neurons
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