The DOI matches its Crossref record; 76 of the 77 references it cites were found in a registry or an index.
Perineuronal net formation and structure in aggrecan knockout mice
Open accessAbstract
Perineuronal nets (PNNs) are specialized substructures of the neural extracellular matrix (ECM) which envelop the cell soma and proximal neurites of particular sets of neurons with apertures at sites of synaptic contact. Previous studies have shown that PNNs are enriched with chondroitin sulfate proteoglycans (CSPGs) and hyaluronan, however, a complete understanding of their precise molecular composition has been elusive. In addition, identifying which specific PNN components are critical to the formation of this structure has not been demonstrated. Previous work in our laboratory has demonstrated that the CSPG, aggrecan, is a key activity-dependent component of PNNs in vivo. In order to assess the contribution of aggrecan to PNN formation, we utilized cartilage matrix deficiency (cmd) mice, which lack aggrecan. Herein, we utilized an in vitro model, dissociated cortical culture, and an ex vivo model, organotypic slice culture, to specifically investigate the role aggrecan plays in PNN formation. Our work demonstrates that staining with the lectin, Wisteria floribunda agglutinin (WFA), considered a broad PNN marker, is eliminated in the absence of aggrecan, suggesting the loss of PNNs. However, in contrast, we found that the expression patterns of other PNN markers, including hyaluronan and proteoglycan link protein 1 (HAPLN1), tenascin-R, brevican, and hyaluronan are unaffected by the absence of aggrecan. Lastly, we determined that while all PNN components are bound to the surface in a hyaluronan-dependent manner, only HAPLN1 remains attached to the cell surface when neurons are treated with chondroitinase. These results suggest a different model for the molecular association of PNNs to the cell surface. Together our work has served to assess the contribution of aggrecan to PNN formation while providing key evidence concerning the molecular composition of PNNs in addition to determining how these components ultimately form PNNs.
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
“ChABC degrades chondroitin sulfate proteoglycans, which are a major component of the PNNs (32).”
From Perineuronal nets protect fast-spiking interneurons against oxidative stress (2013) · cites this paper as [32]
In the citing paper
“cortical primary neurons derived from aggrecan--deficient mice are abnormal in that they are not stained by the lectin Wisteria floribunda agglutinin (WFA), a broad PNN marker, indicating an essential role of aggrecan in PNN formation (Giamanco et al., 2010).”
From Casting a Wide Net: Role of Perineuronal Nets in Neural Plasticity (2016) · cites this paper as Giamanco et al., 2010
In the citing paper
“heterozygote aggrecan-deficient (ACAN+/−) mice”
From Aggrecan, link protein and tenascin-R are essential components of the perineuronal net to protect neurons against iron-induced oxidative stress (2014) · cites this paper as [36]
In the citing paper
“Aggrecan is a major component of the brain ECM and of at least a subgroup of PNNs, and contains numerous CS chains with a predominant CS-6 representation.45, 46”
From Aggrecan and chondroitin-6-sulfate abnormalities in schizophrenia and bipolar disorder: a postmortem study on the amygdala (2015) · cites this paper as [45]
In the citing paper
“Reports that aggrecan knockout results in loss of WFA-positive PNNs45, 46 support this possibility.”
From Aggrecan and chondroitin-6-sulfate abnormalities in schizophrenia and bipolar disorder: a postmortem study on the amygdala (2015) · cites this paper as [45]
In the citing paper
“Together, these findings indicate that WFA may not detect CS-6 sulfation patterns, at least not those recognized by 3B3 and CS56, and may label only some forms of aggrecan (see below).45”
From Aggrecan and chondroitin-6-sulfate abnormalities in schizophrenia and bipolar disorder: a postmortem study on the amygdala (2015) · cites this paper as [45]
In the citing paper
“Notably, aggrecan is necessary for PNN formation, as shown in the HEK cell model (Kwok et al., 2010) and in organotypic cultures derived from aggrecan knockout mice (Giamanco et al., 2010).”
From The hyaluronan and proteoglycan link proteins: Organizers of the brain extracellular matrix and key molecules for neuronal function and plasticity (2015) · cites this paper as Giamanco et al., 2010
Citations
Cites
Hyaluronan: from extracellular glue to pericellular cue
Toole, B. P. (2004) · Nature Reviews Cancer · doi:10.1038/nrc1391 · Cited by 2,125
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
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
Organotypic slice cultures: a technique has come of age
Gähwiler, B. H. (1997) · Trends in Neurosciences · doi:10.1016/s0166-2236(97)01122-3 · Cited by 884
Lecticans: organizers of the brain extracellular matrix
Yamaguchi, Y. (2000) · Cellular and Molecular Life Sciences · doi:10.1007/pl00000690 · Cited by 642
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
Numbers and proportions of GABA-immunoreactive neurons in different areas of monkey cerebral cortex
Hendry, S., Schwark, H. D., Jones, E. G., & Yan, J. (1987) · Journal of Neuroscience · doi:10.1523/jneurosci.07-05-01503.1987 · Cited by 601
Perineuronal nets: past and present
Celio, M. R., Spreafico, R., De Biasi, S., & Vitellaro-Zuccarello, L. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(98)01298-3 · Cited by 497
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
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
Perineuronal nets — a specialized form of extracellular matrix in the adult nervous system
Celio, M. R., & Blümcke, I. (1994) · Brain Research Reviews · doi:10.1016/0165-0173(94)90006-x · Cited by 386
Structural and functional recovery from early monocular deprivation in adult rats
Pizzorusso, T., Medini, P., Landi, S., Baldini, S., Berardi, N., & Maffei, L. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0602657103 · Cited by 367
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
Dityatev, A., Brückner, G., Dityateva, G., Grosche, J., Kleene, R., & Schachner, M. (2007) · Developmental Neurobiology · doi:10.1002/dneu.20361 · Cited by 365
Brückner, G., Brauer, K., Härtig, W., Wolff, J. R., Rickmann, M. J., Derouiche, A., Delpech, B., Girard, N., Oertel, W. H., & Reichenbach, A. (1993) · Glia · doi:10.1002/glia.440080306 · Cited by 358
Aggrecan Glycoforms Contribute to the Molecular Heterogeneity of Perineuronal Nets
Matthews, R. T., Kelly, G. M., Zerillo, C. A., Gray, G., Tiemeyer, M., & Hockfield, S. (2002) · The Journal of Neuroscience · doi:10.1523/jneurosci.22-17-07536.2002 · Cited by 341
Self-citationCarulli, D., Rhodes, K. E., Brown, D. J., Bonnert, T. P., Pollack, S. J., Oliver, K., Strata, P., & Fawcett, J. W. (2006) · Journal of Comparative Neurology · doi:10.1002/cne.20822 · Cited by 341
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
Mjaatvedt, C. H., Yamamura, H., Capehart, A. A., Turner, D., & Markwald, R. R. (1998) · Developmental Biology · doi:10.1006/dbio.1998.9001 · Cited by 321
Maurel, P., Rauch, U., Flad, M., Margolis, R. K., & Margolis, R. U. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.7.2512 · Cited by 305
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
Sensory Deprivation Alters Aggrecan and Perineuronal Net Expression in the Mouse Barrel Cortex
McRae, P. A., Rocco, M. M., Kelly, G., Brumberg, J. C., & Matthews, R. T. (2007) · The Journal of Neuroscience · doi:10.1523/jneurosci.5425-06.2007 · Cited by 272
Self-citationHockfield, S., Kalb, R. G., Zaremba, S., & Fryer, H. (1990) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.1990.055.01.049 · Cited by 271
Brakebusch, C., Seidenbecher, C. I., Asztely, F., Rauch, U., Matthies, H., Meyer, H., Krug, M., Böckers, T. M., Zhou, X., Kreutz, M. R., et al. (2002) · Molecular and Cellular Biology · doi:10.1128/mcb.22.21.7417-7427.2002 · Cited by 264
Mouse cartilage matrix deficiency (cmd) caused by a 7 bp deletion in the aggrecan gene
Watanabe, H., Kimata, K., Line, S. R. P., Strong, D., Gao, L., Kozak, C. A., & Yamada, Y. (1994) · Nature Genetics · doi:10.1038/ng0694-154 · Cited by 245
Neurocan Is Dispensable for Brain Development
Zhou, X.-H., Brakebusch, C., Matthies, H., Oohashi, T., Hirsch, E., Moser, M., Krug, M., Seidenbecher, C. I., Boeckers, T. M., Rauch, U., et al. (2001) · Molecular and Cellular Biology · doi:10.1128/mcb.21.17.5970-5978.2001 · Cited by 206
Galtrey, C. M., Kwok, J. C. F., Carulli, D., Rhodes, K. E., & Fawcett, J. W. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06108.x · Cited by 203
Matthews, R. T., Gary, S. C., Zerillo, C. A., Pratta, M. A., Solomon, K. A., Arner, E. C., & Hockfield, S. J. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m909764199 · Cited by 197
Self-citationGABA immunoreactive neurons in rat visual cortex
Meinecke, D. L., & Peters, A. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902610305 · Cited by 196
Lander, C., Kind, P., Maleski, M., & Hockfield, S. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-06-01928.1997 · Cited by 195
Mice lacking link protein develop dwarfism and craniofacial abnormalities
Watanabe, H., & Yamada, Y. (1999) · Nature Genetics · doi:10.1038/6016 · Cited by 187
Zaremba, S., Guimaraes, A., Kalb, R. G., & Hockfield, S. J. (1989) · Neuron · doi:10.1016/0896-6273(89)90305-x · Cited by 183
A surface antigen expressed by a subset of neurons in the vertebrate central nervous system.
Hockfield, S. J., & McKay, R. D. G. (1983) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.80.18.5758 · Cited by 175
Kwok, J. C. F., Carulli, D., & Fawcett, J. W. (2010) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2010.06878.x · Cited by 170
Brückner, G., Bringmann, A., Härtig, W., Köppe, G., Delpech, B., & Brauer, K. (1998) · Experimental Brain Research · doi:10.1007/s002210050463 · Cited by 162
Carulli, D., Rhodes, K. E., & Fawcett, J. W. (2007) · Journal of Comparative Neurology · doi:10.1002/cne.21231 · Cited by 158
Sur, M., Frost, D., & Hockfield, S. J. (1988) · Journal of Neuroscience · doi:10.1523/jneurosci.08-03-00874.1988 · Cited by 156
Dwarfism and age-associated spinal degeneration of heterozygote cmd mice defective in aggrecan
Watanabe, H., Nakata, K., Kimata, K., Nakanishi, I., & Yamada, Y. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.13.6943 · Cited by 156
Ha¨rtig, W., Brauer, K., Bigl, V., & Bru¨ckner, G. (1994) · Brain Research · doi:10.1016/0006-8993(94)91452-4 · Cited by 147
Maeda, N., Hamanaka, H., Oohira, A., & Noda, M. (1995) · Neuroscience · doi:10.1016/0306-4522(94)00069-h · Cited by 134
Köppe, G., Brückner, G., Brauer, K., Härtig, W., & Bigl, V. (1997) · Cell and Tissue Research · doi:10.1007/s004410050790 · Cited by 129
Guimaraes, A., Zaremba, S., & Hockfield, S. (1990) · The Journal of Neuroscience · doi:10.1523/jneurosci.10-09-03014.1990 · Cited by 128
Organization of neurons in the visual cortex, area 17, of the rat.
Parnavelas, J. G., Lieberman, A. R., & Webster, K. E. (1977) · PubMed · Cited by 127
John, N., Krügel, H., Frischknecht, R., Smalla, K.-H., Schultz, C., Kreutz, M. R., Gundelfinger, E. D., & Seidenbecher, C. I. (2006) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2006.01.011 · Cited by 122
Kimata, K., Barrach, H.-J., Brown, K. S., & Pennypacker, J. P. (1981) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)69084-8 · Cited by 118
Bekku, Y., Su, W.-D., Hirakawa, S., Fässler, R., Ohtsuka, A., Kang, J. S., Sanders, J., Murakami, T., Ninomiya, Y., & Oohashi, T. (2003) · Molecular and Cellular Neuroscience · doi:10.1016/s1044-7431(03)00133-7 · Cited by 114
Neurons Produce a Neuronal Cell Surface-Associated Chondroitin Sulfate Proteoglycan
Lander, C., Zhang, H., & Hockfield, S. (1998) · The Journal of Neuroscience · doi:10.1523/jneurosci.18-01-00174.1998 · Cited by 107
Perineuronal nets protect against amyloid β-protein neurotoxicity in cultured cortical neurons
Miyata, S., Nishimura, Y., & Nakashima, T. (2007) · Brain Research · doi:10.1016/j.brainres.2007.02.066 · Cited by 101
Köppe, G., Brückner, G., Härtig, W., Delpech, B., & Bigl, V. (1997) · The Histochemical Journal · doi:10.1023/a:1026408716522 · Cited by 100
Jaworski, D. M., Kelly, G. M., & Hockfield, S. J. (1994) · The Journal of Cell Biology · doi:10.1083/jcb.125.2.495 · Cited by 98
Morris, N. P., & Henderson, Z. (2000) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.2000.00970.x · Cited by 98
Extracellular matrix alterations in brains lacking four of its components
Rauch, U., Zhou, X.-H., & Roos, G. (2005) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2005.01.026 · Cited by 88
Cartilage matrix deficiency (cmd) : a new autosomal recessive lethal mutation in the mouse
Rittenhouse, E. W., Dunn, L. C., Cookingham, J., Calo, C., Spiegelman, M., Dooher, G. B., & Bennett, D. (1978) · Development · doi:10.1242/dev.43.1.71 · Cited by 84
Kosaka, T., Isogai, K., Barnstable, C. J., & Heizmann, C. W. (1990) · Experimental Brain Research · doi:10.1007/bf00228797 · Cited by 79
Diño, M. R., Harroch, S., Hockfield, S. J., & Matthews, R. T. (2006) · Neuroscience · doi:10.1016/j.neuroscience.2006.07.054 · Cited by 76
Self-citationBrauer, K., Ha¨rtig, W., Bigl, V., & Bru¨ckner, G. (1993) · Brain Research · doi:10.1016/0006-8993(93)91205-7 · Cited by 75
Construction of perineuronal net-like structure by cortical neurons in culture
Miyata, S., Nishimura, Y., Hayashi, N., & Oohira, A. (2005) · Neuroscience · doi:10.1016/j.neuroscience.2005.07.031 · Cited by 75
‘Perineuronal nets’ around cortical interneurons expressing parvalbumin are rich in tenascin
Celio, M. R., & Chiquet‐Ehrismann, R. (1993) · Neuroscience Letters · doi:10.1016/0304-3940(93)90579-a · Cited by 71
Hirakawa, S., Oohashi, T., Su, W.-D., Yoshioka, H., MURAKAMI, T., Arata, J., & Ninomiya, Y. (2000) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2000.3583 · Cited by 70
Morphology of perineuronal nets in tenascin-R and parvalbumin single and double knockout mice
Haunsø, A., Ibrahim, M., Bartsch, U., Letiembre, M., Celio, M. R., & Menoud, P.-A. (2000) · Brain Research · doi:10.1016/s0006-8993(00)02173-9 · Cited by 61
Grosche, J., & Br�ckner, G. (2001) · Experimental Brain Research · doi:10.1007/s002210000617 · Cited by 55
Haunsø, A., Celio, M. R., Margolis, R. K., & Menoud, P.-A. (1999) · Brain Research · doi:10.1016/s0006-8993(99)01596-6 · Cited by 52
Schüppel, K., Brauer, K., Härtig, W., Grosche, J., Earley, B., Leonard, B. E., & Brückner, G. (2002) · Brain Research · doi:10.1016/s0006-8993(02)03569-2 · Cited by 47
Wintergerst, E. S., Faissner, A., & Celio, M. R. (1996) · International Journal of Developmental Neuroscience · doi:10.1016/0736-5748(96)00011-1 · Cited by 46
Wintergerst, E. S., Weisenhorn, D. M. V., Rathjen, F. G., Riederer, B. M., Lambert, S., & Celio, M. R. (1996) · Neuroscience Letters · doi:10.1016/0304-3940(96)12643-4 · Cited by 44
Reimers, S., Hartlage‐Rübsamen, M., Brückner, G., & Roßner, S. (2007) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2007.05514.x · Cited by 40
Brückner, G., Kacza, J., & Grosche, J. (2004) · Journal of Molecular Histology · doi:10.1023/b:hijo.0000023374.22298.50 · Cited by 33
Kind, P. C., Beaver, C. J., & Mitchell, D. E. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903590402 · Cited by 32
Jojović, M., Delpech, B., Prehm, P., & Schumacher, U. (2002) · Cancer Letters · doi:10.1016/s0304-3835(02)00037-x · Cited by 31
Kosaka, T., Heizmann, C. W., & Barnstable, C. J. (1989) · Experimental Brain Research · doi:10.1007/bf00230685 · Cited by 30
Morawski, M., Brückner, G., Jäger, C., Seeger, G., Künzle, H., & Arendt, T. (2009) · Neuroscience · doi:10.1016/j.neuroscience.2009.08.018 · Cited by 28
Self-citationPreuss, T. M., Gray, D., & Cusick, C. G. (1998) · Somatosensory & Motor Research · doi:10.1080/08990229870772 · Cited by 22
MURAKAMI, T., Ohtsuka, A., Su, W., TAGUCHI, T., Oohashi, T., Murakami, T., Abe, K., & Ninomiya, Y. (1999) · Archivum histologicum japonicum · doi:10.1679/aohc.62.273 · Cited by 21
Perineuronal Nets of Proteoglycans in the Adult Mouse Brain are Digested by Collagenase.
MURAKAMI, T., Murakami, T., SU, W. D., Ohtsuka, A., Abe, K., & Ninomiya, Y. (1999) · Archivum histologicum japonicum · doi:10.1679/aohc.62.199 · Cited by 18
Postnatal development of perineuronal nets in wild-type mice and in a mutant deficient in tenascin-R
Br�ckner, G., Grosche, J., Schmidt, S., H�rtig, W., Margolis, R. U., Delpech, B., Seidenbecher, C. I., Czaniera, R., & Schachner, M. (2000) · The Journal of Comparative Neurology · doi:10.1002/1096-9861(20001225)428:4
Hagihara (1999) · doi:10.1002/(sici)1096-9861(19990726)410:2
Flagged first, then by citations
1 of the 77 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
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
Perineuronal nets protect fast-spiking interneurons against oxidative stress
Cabungcal, J.-H., Steullet, P., Morishita, H., Kraftsik, R., Cuenod, M., Hensch, T. K., & Do, K. Q. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1300454110 · Cited by 512
Casting a Wide Net: Role of Perineuronal Nets in Neural Plasticity
Sorg, B. A., Berretta, S., Blacktop, J. M., Fawcett, J. W., Kitagawa, H., Kwok, J. C. F., & Miquel, M. (2016) · The Journal of Neuroscience · doi:10.1523/jneurosci.2351-16.2016 · Cited by 454
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
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
Metadata
- Authors
- Giamanco, K. A., Morawski, M., & Matthews, R. T.
- Affiliations
- SUNY Upstate Medical University (US)
- Leipzig University (DE)
- Venue
- Neuroscience
- Publisher
- Elsevier BV
- Published
- 2010-11
- Volume
- 170
- Issue
- 4
- Pages
- 1314-1327
- ISSN
- 0306-4522 (ISSN-L)
- OpenAlex
- W2033004840
- Cited by
- 207
- References
- 77
- Citations by year
- 2026: 3 · 2025: 15 · 2024: 13 · 2023: 15 · 2022: 15 · 2021: 14 · 2020: 15 · 2019: 9 · 2018: 17 · 2017: 16 · 2016: 15 · 2015: 14 · 2014: 12 · 2013: 11 · 2012: 17
- FWCI
- 4.75
- Type
- journal article
- Language
- en
- Open access
- green
- zenodo.org
- Licence
- Locations
- Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Zenodo (CERN European Organization for Nuclear Research) (submittedVersion, other-oa)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Proteoglycans and glycosaminoglycans research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- perineuronal nets, aggrecan, chondroitin sulfate proteoglycans, hyaluronic acid, HAPLN1, tenascin-R, brevican, Wisteria floribunda agglutinin, chondroitinase, organotypic slice cultures
- MeSH terms
- Proteoglycan Link Protein, Animals, Cells, Cultured, Chondroitin Sulfates, Extracellular Matrix, gamma-Aminobutyric Acid, Hyaluronic Acid, Interneurons, Neurons, Parvalbumins, Proteoglycans, Extracellular Matrix Proteins, Mice, Knockout, Tenascin, Mice, Aggrecans, In Vitro Techniques
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