The DOI matches its Crossref record; 50 of the 50 references it cites were found in a registry or an index.
Sensory Deprivation Alters Aggrecan and Perineuronal Net Expression in the Mouse Barrel Cortex
Open accessAbstract
An important role for the neural extracellular matrix in modulating cortical activity-dependent synaptic plasticity has been established by a number of recent studies. However, identification of the critical molecular components of the neural matrix that mediate these processes is far from complete. Of particular interest is the perineuronal net (PN), an extracellular matrix component found surrounding the cell body and proximal neurites of a subset of neurons. Because of the apposition of the PN to synapses and expression of this structure coincident with the close of the critical period, it has been hypothesized that nets could play uniquely important roles in synapse stabilization and maturation. Interestingly, previous work has also shown that expression of PNs is dependent on appropriate sensory stimulation in the visual system. Here, we investigated whether PNs in the mouse barrel cortex are expressed in an activity-dependent manner by manipulating sensory input through whisker trimming. Importantly, this manipulation did not lead to a global loss of PNs but instead led to a specific decrease in PNs, detected with the antibody Cat-315, in layer IV of the barrel cortex. In addition, we identified a key activity-regulated component of PNs is the proteoglycan aggrecan. We also demonstrate that these Cat-315-positive neurons virtually all also express parvalbumin. Together, these data are in support of an important role for aggrecan in the activity-dependent formation of PNs on parvalbumin-expressing cells and suggest a role for expression of these nets in regulating the close of the critical period.
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?
In the citing paper
“CSPG-enriched PNNs form in an activity-dependent manner during late postnatal development, completing neuronal maturation.32, 33, 34”
From Aggrecan and chondroitin-6-sulfate abnormalities in schizophrenia and bipolar disorder: a postmortem study on the amygdala (2015) · cites this paper as [32]
In the citing paper
“The role of ECM in cortical plasticity has been previously reported (Pizzorusso et al. 2002;Nagy et al. 2006;McRae et al. 2007;Rivera et al. 2010)”
From Genetic Reduction of Matrix Metalloproteinase-9 Promotes Formation of Perineuronal Nets Around Parvalbumin-Expressing Interneurons and Normalizes Auditory Cortex Responses in Developing Fmr1 Knock-Out Mice (2018) · cites this paper as McRae et al. 2007
In the citing paper
“the expression of PNNs in the mouse barrel cortex during development was dependent on appropriate sensory stimulation (McRae et al., 2007)”
From Perineuronal nets and schizophrenia: The importance of neuronal coatings (2014) · cites this paper as McRae et al., 2007
In the citing paper
“Sensory deprivation in adult mice, however, did not alter aggrecan expression, indicating that once established, maintenance of PNNs does not require normal sensory input (McRae et al., 2007)”
From Perineuronal nets and schizophrenia: The importance of neuronal coatings (2014) · cites this paper as McRae et al., 2007
In the citing paper
“sensory deprivation by whisker trimming within the first 30 days of birth was found to decrease the number of aggrecan-positive PNNs around parvalbumin-expressing cells in layer IV of the mouse barrel cortex and prolong the critical period (McRae et al., 2007)”
From Perineuronal nets and schizophrenia: The importance of neuronal coatings (2014) · cites this paper as McRae et al., 2007
In the citing paper
“its expression is dependent on neuronal activity during a maturationally based ‘critical period’”
From Perineuronal nets and schizophrenia: The importance of neuronal coatings (2014) · cites this paper as McRae et al., 2007
In the citing paper
“The organization of specific ECM molecules into PNNs in vivo requires the presence of appropriate stimuli and occurs during postnatal development, in concomitance with the end of the critical period for experience-dependent plasticity (Carulli et al., 2010;Kalb and Hockfield, 1990;McRae et al., 2007;Pizzorusso et al., 2002;Ye and Miao, 2013).”
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 McRae et al., 2007
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
West, M. J., Slomianka, L., & Gundersen, H. J. G. (1991) · The Anatomical Record · doi:10.1002/ar.1092310411 · Cited by 2,994
SINGLE-CELL RESPONSES IN STRIATE CORTEX OF KITTENS DEPRIVED OF VISION IN ONE EYE
Wiesel, T. N., & Hubel, D. H. (1963) · Journal of Neurophysiology · doi:10.1152/jn.1963.26.6.1003 · Cited by 2,628
Critical period plasticity in local cortical circuits
Hensch, T. K. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1787 · Cited by 2,323
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
Wiesel, T. N., & Hubel, D. H. (1963) · Journal of Neurophysiology · doi:10.1152/jn.1963.26.6.978 · Cited by 1,291
Lecticans: organizers of the brain extracellular matrix
Yamaguchi, Y. (2000) · Cellular and Molecular Life Sciences · doi:10.1007/pl00000690 · Cited by 642
A critical period for experience-dependent synaptic plasticity in rat barrel cortex
Fox, K. D. (1992) · Journal of Neuroscience · doi:10.1523/jneurosci.12-05-01826.1992 · Cited by 420
Kawaguchi, Y., & Kondo, S. (2002) · Journal of Neurocytology · doi:10.1023/a:1024126110356 · Cited by 395
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
Cited by
Sorted by citations
Items 201–272 of 272
Experience-dependent regulation of tissue-type plasminogen activator in the mouse barrel cortex
Chen, C., Chu, P., & Brumberg, J. C. (2015) · Neuroscience Letters · doi:10.1016/j.neulet.2015.05.050 · Cited by 9
Self-citationHryciw, T., Geremia, N. M., Walker, M. A., Xu, X., & Brown, A. M. (2018) · Journal of Neurotrauma · doi:10.1089/neu.2018.5928 · Cited by 9
Ueno, H., Suemitsu, S., Murakami, S., Kitamura, N., Wani, K., Matsumoto, Y., Okamoto, M., & Ishihara, T. (2019) · International Journal of Radiation Biology · doi:10.1080/09553002.2019.1564081 · Cited by 9
A new paradigm for the reversible blockage of whisker sensory transmission
Gener, T., Reig, R., & Sanchez-Vives, M. V. (2008) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2008.08.012 · Cited by 9
Contribution of perineuronal nets to hyperexcitability in pilocarpine‐induced status epilepticus
Woo, A. M., Fleischel, E. J., Patel, D. C., & Sontheimer, H. W. (2025) · Epilepsia · doi:10.1111/epi.18489 · Cited by 8
Orchestrating the Matrix: The Role of Glial Cells and Systemic Signals in Perineuronal Net Dynamics
Totaro, V., Pizzorusso, T., & Tognini, P. (2025) · Neurochemical Research · doi:10.1007/s11064-025-04506-8 · Cited by 9
Synaptic Mechanisms of Activity-Dependent Remodeling in Visual Cortex during Monocular Deprivation
Rittenhouse, C. D., & Majewska, A. K. (2009) · Journal of Experimental Neuroscience · doi:10.4137/jen.s2559 · Cited by 9
Ma, C., Kwan, P., Wu, K. L., Shum, D. K., & Chan, Y. (2018) · Brain Structure and Function · doi:10.1007/s00429-018-1795-x · Cited by 7
Imbriglio, T., Verhaeghe, R., Martinello, K., Pascarelli, M. T., Chece, G., Bucci, D., Notartomaso, S., Quattromani, M. J., Mascio, G., Scalabrì, F., et al. (2019) · The FASEB Journal · doi:10.1096/fj.201901093rrr · Cited by 7
Experience-dependent control of synaptic remodeling and structural plasticity by glia
Vita, D. J., Ferro, A., & Cheadle, L. (2025) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2025.103059 · Cited by 6
Sakata, J. T., Alonge, K. M., Diethorn, E. J., Krishnan, K., Milman, N., Ramsaran, A. I., Wan, X., & Sorg, B. A. (2025) · Journal of Neuroscience · doi:10.1523/jneurosci.1367-25.2025 · Cited by 8
Extracellular matrix remodelling in neurological diseases
Kwok, J. C. F., & Dityatev, A. E. (2026) · Nature Reviews Neurology · doi:10.1038/s41582-026-01209-8 · Cited by 9
Perineuronal Net Microscopy: From Brain Pathology to Artificial Intelligence
Paveliev, M., Egorchev, A. A., Musin, F., Lipachev, N., Melnikova, A., Gimadutdinov, R. M., Kashipov, A., Molotkov, D., Chickrin, D. E., & Aganov, A. V. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25084227 · Cited by 8
Lipachev, N., Melnikova, A., Fedosimova, S. V., Arnst, N., Kochneva, A., Shaikhutdinov, N., Dvoeglazova, A., Андреевна, Т. А., Олегович, М. М., Aganov, A. V., et al. (2022) · Neuroscience Research · doi:10.1016/j.neures.2022.06.005 · Cited by 6
Perineuronal Nets: From Structure to Neurological Disorders
Li, X., Li, N., Zhao, P., Ren, D., Luo, B., & Zhou, T. G. (2023) · Current Medicinal Chemistry · doi:10.2174/0109298673258290231009111633 · Cited by 6
Models of vocal learning in the songbird: Historical frameworks and the stabilizing critic
Nick, T. A. (2014) · Developmental Neurobiology · doi:10.1002/dneu.22189 · Cited by 6
The Structural and Compositional Changes of Chondroitin Sulfate Chains in the Aged Mouse Hippocampus
Suzuki, Y., Kerever, A., Tanaka, T., Higashi, K., & Arikawa‐Hirasawa, E. (2019) · Juntendō Igaku/Juntendo igaku · doi:10.14789/jmj.2019.65.jmj18-oa13 · Cited by 6
Perineuronal nets: Cruise from a honeycomb to the safety nets
John, U., Patro, N., & Patro, I. K. (2022) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2022.10.004 · Cited by 6
Contactin-1 is a critical neuronal cell surface receptor for perineuronal net structure
Sinha, A., Nickerson, G. A., Bouyain, S., & Matthews, R. T. (2025) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2025.108504 · Cited by 5
Self-citationMueller, A. L., Davis, A., Carlson, S. S., & Robinson, F. R. (2014) · PLoS ONE · doi:10.1371/journal.pone.0086154 · Cited by 5
Component-specific reduction in perineuronal nets in senescence-accelerated mouse strains
Ueno, H., Takahashi, Y., Murakami, S., Wani, K., Miyazaki, T., Matsumoto, Y., Okamoto, M., & Ishihara, T. (2023) · IBRO Neuroscience Reports · doi:10.1016/j.ibneur.2023.01.002 · Cited by 5
Lemieux, S. P., Lev‐Ram, V., Tsien, R. Y., & Ellisman, M. H. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.11.29.569151 · Cited by 6
Experience-Dependent Synaptic Plasticity in the Developing Cerebral Cortex
Aoki, C. J., & Erişir, A. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-418675-0.00013-4 · Cited by 5
Functional maturation of neocortical inhibitory interneurons
Larimer, P., & Hasenstaub, A. R. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-823672-7.00019-3 · Cited by 5
Sharmin, S., Pradhan, J., Zhang, Z., Bellingham, M. C., Simmons, D. G., & Piper, M. (2021) · Experimental Neurology · doi:10.1016/j.expneurol.2021.113734 · Cited by 4
Fisher, K. M., Garner, J. P., & Darian‐Smith, C. (2022) · The Journal of Comparative Neurology · doi:10.1002/cne.25395 · Cited by 4
Wéber, I., Dakos, A., Mészár, Z., Matesz, C., & Birinyi, A. (2024) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2024.1369103 · Cited by 3
Perineuronal Nets: Old Structures, New Functions
Tewari, B. P., Chaunsali, L., & Sontheimer, H. W. (2026) · The Neuroscientist · doi:10.1177/10738584261421180 · Cited by 3
Long‐Term Memory Engrams From Development to Adulthood
Yu, A. L., & DeNardo, L. A. (2025) · Hippocampus · doi:10.1002/hipo.70032 · Cited by 4
Ueno, H., Kitano, E., Mori, S., Takahashi, Y., Murakami, S., Wani, K., Matsumoto, Y., Okamoto, M., & Ishihara, T. (2025) · IBRO Neuroscience Reports · doi:10.1016/j.ibneur.2025.10.012 · Cited by 3
Fingolimod increases parvalbumin-positive neurons in adult mice
Ueno, H., Takahashi, Y., Murakami, S., Wani, K., Matsumoto, Y., Okamoto, M., & Ishihara, T. (2022) · IBRO Neuroscience Reports · doi:10.1016/j.ibneur.2022.06.005 · Cited by 3
Zhang, S., Larsen, B., Sydnor, V. J., Zeng, T., An, L., Yan, X., Kong, R., Kong, X., Gur, R. C., Gur, R. E., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.06.22.546023 · Cited by 3
Perineuronal nets in motor circuitry regulate the performance of learned vocalizations in songbirds
Wan, X., Wang, A. S., Storch, D.-S., Li, V. Y., & Sakata, J. T. (2025) · Communications Biology · doi:10.1038/s42003-025-07520-2 · Cited by 2
Distribution of perineuronal nets in the adult rat neocortex
Budhu, K., Gomes, H., Borukhov, Y., Chu, P., & Brumberg, J. C. (2025) · Somatosensory & Motor Research · doi:10.1080/08990220.2025.2476945 · Cited by 2
Self-citationKitano, E., Ueno, H., Takahashi, Y., Mori, S., Murakami, S., Wani, K., Matsumoto, Y., Ochi, A., Hatano, T., Okamoto, M., et al. (2025) · Neuroscience · doi:10.1016/j.neuroscience.2025.03.029 · Cited by 3
Hussain, A., & Razak, K. A. (2025) · Neuroscience · doi:10.1016/j.neuroscience.2025.05.026 · Cited by 4
Adolescent neurocognitive development
Ravindranath, O., Parr, A. C., Perica, M. I., Elliott, S., & Luna, B. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-818872-9.00105-9 · Cited by 4
Nakayama, K., Mubuchi, A., & Miyata, S. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.05.29.656756 · Cited by 2
ÖZKAN, Ş., Öz, P., Erdogan, Y., Akpinar, M., Sahsahi, A., & Gecen, Z. (2024) · International Journal of Developmental Neuroscience · doi:10.1002/jdn.10404 · Cited by 1
Ueno, H., Kitano, E., Mori, S., Takahashi, Y., Murakami, S., Wani, K., Matsumoto, Y., Okamoto, M., & Ishihara, T. (2025) · Neuroscience · doi:10.1016/j.neuroscience.2025.08.017 · Cited by 1
X-ray Diffraction Reveals Periodicity in Murine Neocortex
Murokh, S., Willerson, E., Lazarev, A., Lazarev, P., Mourokh, L. G., & Brumberg, J. C. (2024) · Journal of Neuroscience Methods · doi:10.1016/j.jneumeth.2025.110582 · Cited by 1
Self-citationTakiguchi, M., Yoshimura, A., & Funakoshi, K. (2026) · Developmental Neuroscience · doi:10.1159/000550632 · Cited by 1
Reduced expression of perineuronal nets in the normotopic somatosensory cortex of the tish rat
Grosenbaugh, D. K., Skwarzyńska, D., Burnsed, J. C., & Goodkin, H. P. (2022) · Brain Research · doi:10.1016/j.brainres.2022.148179 · Cited by 1
Sinapsien ikuspegi modernoa: zelulaz kanpoko matrizearen funtzioa konexio neuronalean
Nuñez-delMoral, A., & Erdozain, A. M. (2018) · EKAIA Euskal Herriko Unibertsitateko Zientzi eta Teknologi Aldizkaria · doi:10.1387/ekaia.19676 · Cited by 1
Regulation of somatosensory cortex development downstream of glutamate
Petrie, A. (2009) · OpenGrey (Institut de l'Information Scientifique et Technique) · Cited by 1
Common Gene Variants in Schizophrenia Susceptibility with Focus on Neurodevelopment
Kähler, A. K. (2009) · NORA - Norwegian Open Research Archives · Cited by 1
The Role of Perineuronal Nets in Regulating Barrel Cortex Physiology
Chu, P. (2015) · CUNY Academic Works (City University of New York) · Cited by 1
Plasticity after injury to the central nervous system
Selzer, M. A., Clarke, S., Cohen, L. G., Kwakkel, G., & Miller, R. H. (2014) · Cambridge University Press eBooks · doi:10.1017/cbo9780511995583.014
A Role for Focal Adhesions and Extracellular Matrix in Traumatic Axonal Injury
Hemphill, M. A. (2014) · Digital Access to Scholarship at Harvard (DASH) (Harvard University)
Synaptic Specificity and Plasticity in Parvalbumin-Basket Cell Circuits
Bogart, L. J. (2015) · Digital Access to Scholarship at Harvard (DASH) (Harvard University)
Lanton, R. A. (2015) · NORA - Norwegian Open Research Archives
Karthikeyan, S. S. (2017) · uO Research (University of Ottawa) · doi:10.20381/ruor-21084
Baruchin, L. J., Kohl, M. M., & Butt, S. J. B. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.02.18.431791
Potential involvement of perineuronal nets in brain aging
Yamada, J., & Jinno, S. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-817990-1.00015-9
PERINEURONAL NETS IN HIPPOCAMPAL AREA CA2: REGULATION BY ACTIVITY AND DISEASE
Carstens, K. E. (2018) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/khgn-dw13
Mechanisms of Experience-dependent Prevention of Plasticity in Visual Circuits
Balmer, T. S. (2022) · Digital Archive @ GSU · doi:10.57709/5814205
Wéber, I., Dakos, A., Mészár, Z., Matesz, C., & Birinyi, A. (2023) · Research Square · doi:10.21203/rs.3.rs-3184150/v1
ÖZKAN, Ş., Öz, P., Erdogan, Y., Akpinar, M., Sahsahi, A., & Gecen, Z. (2024) · SSRN Electronic Journal · doi:10.2139/ssrn.4741610
X-ray Diffraction Reveals Periodicity in Murine NeocortexPreprint
Murokh, S., Willerson, E., Lazarev, A., Lazarev, P. I., & Brumberg, J. C. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.10.13.618071
Self-citationUeno, H., Takahashi, Y., Mori, S., Kitano, E., Murakami, S., Wani, K., Matsumoto, Y., Okamoto, M., & Ishihara, T. (2025) · IBRO Neuroscience Reports · doi:10.1016/j.ibneur.2025.01.012
Berrouschot, V., Sonntag, M., Reimann, K., Jäger, C., Martin, S., Holzer, M., Stieler, J., & Morawski, M. (2025) · Scientific Reports · doi:10.1038/s41598-025-14942-9
Microglia: Key Players in Perineuronal Net Dynamics
Garmendia-Berges, M., & Puerta, E. (2025) · IntechOpen eBooks · doi:10.5772/intechopen.1012413 · Cited by 1
Synaptic changes upon removal of extracellular perineuronal nets in adult mouse visual cortex
Faini, G. (2017) · theses.fr (ABES) · doi:10.70675/7b38d504z7edfz47dezbf9az0a8668ae448a
Devienne, G. F. (2019) · theses.fr (ABES) · doi:10.70675/453418efzc908z49e0zba6fz71fefaa50691
Vibrotactile Control of Spontaneous Gap Crossing in Premature Rat PupsPreprint
Odrinskaya, М. S., Манолова, А. О., & Midzyanovskaya, I. S. (2026) · Qeios · doi:10.32388/pvdryp
Ashar, M. S., Anwar, M., Singh, A. K., Pradhan, R., Gupta, A., Chakrawarty, A., Haldar, P., Tripathi, M., & Dey, S. (2026) · Journal of Alzheimer s Disease · doi:10.1177/13872877261470815
Maternal separation reshapes layer-specific PV-PNN architecture in the mouse barrel cortex
Zhan, X., Miao, J., Chu, P., Tan, P., & Chen, C. (2026) · Neuroscience Letters · doi:10.1016/j.neulet.2026.138732
Zhan, X., Tan, P., Tan, T., & Chen, C.-C. (2026) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2026.1932616
Heterogeneity of interneuron circuit function in sensory processing and synaptic plasticity
Li, P. (2011) · DigitalGeorgetown (Georgetown University Library)
Metadata
- Authors
- McRae, P. A., Rocco, M. M., Kelly, G., Brumberg, J. C., & Matthews, R. T.
- Affiliations
- Yale University (US)
- The Graduate Center, CUNY (US)
- Queens College, CUNY (US)
- SUNY Upstate Medical University (US)
- Corresponding author
- Matthews, Russell T.
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2007-05-16
- Volume
- 27
- Issue
- 20
- Pages
- 5405-5413
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6672348
- OpenAlex
- W1985654472
- Cited by
- 272
- References
- 50
- Citations by year
- 2026: 7 · 2025: 17 · 2024: 8 · 2023: 11 · 2022: 20 · 2021: 18 · 2020: 14 · 2019: 17 · 2018: 18 · 2017: 22 · 2016: 10 · 2015: 20 · 2014: 23 · 2013: 9 · 2012: 14
- FWCI
- 4.78
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- CUNY Academic Works (City University of New York) (submittedVersion, cc-by)
- Funders
- American Psychological Association
- National Institute of Neurological Disorders and Stroke (NS 007224-21S1, T32NS007224)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Proteoglycans and glycosaminoglycans research
- Keywords
- perineuronal nets, aggrecan, sensory deprivation, whisker trimming, barrel cortex, parvalbumin, extracellular matrix, activity-dependent synaptic plasticity, critical period, layer 4, proteoglycans
- MeSH terms
- Animals, Animals, Newborn, Cerebral Cortex, Extracellular Matrix, Neuronal Plasticity, Sensory Deprivation, Vibrissae, Gene Expression Regulation, Developmental, Mice, Aggrecans
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