The DOI matches its Crossref record; 54 of the 54 references it cites were found in a registry or an index.
Modulation of Perineuronal Nets and Parvalbumin with Developmental Song Learning
Open accessAbstract
Neural circuits and behavior are shaped during developmental phases of maximal plasticity known as sensitive or critical periods. Neural correlates of sensory critical periods have been identified, but their roles remain unclear. Factors that define critical periods in sensorimotor circuits and behavior are not known. Birdsong learning in the zebra finch occurs during a sensitive period similar to that for human speech. We now show that perineuronal nets, which correlate with sensory critical periods, surround parvalbumin-positive neurons in brain areas that are dedicated to singing. The percentage of both total and parvalbumin-positive neurons with perineuronal nets increased with development. In HVC (this acronym is the proper name), a song area important for sensorimotor integration, the percentage of parvalbumin neurons with perineuronal nets correlated with song maturity. Shifting the vocal critical period with tutor song deprivation decreased the percentage of neurons that were parvalbumin positive and the relative staining intensity of both parvalbumin and a component of perineuronal nets. Developmental song learning shares key characteristics with sensory critical periods, suggesting shared underlying mechanisms.
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 cited source says what the claim attributes to it.
In the citing paper
“the percentage of parvalbumin neurons with PNNs correlated with song maturity”
From Perineuronal nets and schizophrenia: The importance of neuronal coatings (2014) · cites this paper as Balmer et al., 2009
In the citing paper
“The implementation of this adult form of ECM coincides with the closure of critical periods of postnatal development, during which neuronal circuits are shaped by experience, and culminates with the maturation of PNNs and PNN-like perisynaptic ECM aggregates (Balmer et al., 2009; Gogolla et al., 2009; Gundelfinger et al., 2010; McRae et al., 2007; Nowicka et al., 2009; Pizzorusso et al., 2002;”
From Losing the sugar coating: Potential impact of perineuronal net abnormalities on interneurons in schizophrenia (2015) · cites this paper as Balmer et al., 2009
In the citing paper
“the percentage of both total and parvalbumin-positive neurons with PNNs increased with development (Balmer et al., 2009)”
From Perineuronal nets and schizophrenia: The importance of neuronal coatings (2014) · cites this paper as Balmer et al., 2009
In the citing paper
“shifting the vocal critical period with tutor song deprivation decreased the percentage of neurons that were parvalbumin positive and the relative staining intensity of both parvalbumin and PNNs (Balmer et al., 2009)”
From Perineuronal nets and schizophrenia: The importance of neuronal coatings (2014) · cites this paper as Balmer et al., 2009
In the citing paper
“PNNs have been observed throughout the CNS of different organisms, including frogs, birds and mammals (Celio et al., 1998;Balmer et al., 2009;Gaál et al., 2014;Morawski et al., 2009).”
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 Balmer et al., 2009
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
The efficiency of systematic sampling in stereology and its prediction*
Gundersen, H. J. G., & Jensen, E. B. V. (1987) · Journal of Microscopy · doi:10.1111/j.1365-2818.1987.tb02837.x · Cited by 3,519
Dynamic predictions: Oscillations and synchrony in top–down processing
Engel, A. K., Fries, P., & Singer, W. (2001) · Nature Reviews Neuroscience · doi:10.1038/35094565 · Cited by 3,454
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
Top-Down Versus Bottom-Up Control of Attention in the Prefrontal and Posterior Parietal Cortices
Buschman, T. J., & Miller, E. K. (2007) · Science · doi:10.1126/science.1138071 · Cited by 2,380
Critical period plasticity in local cortical circuits
Hensch, T. K. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1787 · Cited by 2,323
Sensitive periods in the development of the brain and behavior
Knudsen, E. I. (2004) · Journal of Cognitive Neuroscience · doi:10.1162/0898929042304796 · Cited by 1,842
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
Birdsong and human speech: common themes and mechanisms
Doupe, A. J., & Kuhl, P. K. (1999) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.22.1.567 · Cited by 1,633
Temporal structure in spatially organized neuronal ensembles: a role for interneuronal networks
Buzsáki, G., & Chrobak, J. J. (1995) · Current Opinion in Neurobiology · doi:10.1016/0959-4388(95)80012-3 · Cited by 878
The Role of Auditory Feedback in the Control of Vocalization in the White-Crowned Sparrow 1
Konishi, M. (1965) · Zeitschrift für Tierpsychologie · doi:10.1111/j.1439-0310.1965.tb01688.x · Cited by 832
Cited by
Sorted by citations
Importance of investing in adolescence from a developmental science perspective
Dahl, R. E., Allen, N. B., Wilbrecht, L., & Suleiman, A. B. (2018) · Nature · doi:10.1038/nature25770 · Cited by 1,196
Adolescence as a neurobiological critical period for the development of higher-order cognition
Larsen, B., & Luna, B. (2018) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2018.09.005 · Cited by 853
Critical periods in speech perception: New directions
Werker, J. F., & Hensch, T. K. (2015) · Annual Review of Psychology · doi:10.1146/annurev-psych-010814-015104 · Cited by 774
Balancing Plasticity/Stability Across Brain Development
Takesian, A. E., & Hensch, T. K. (2013) · Progress in Brain Research · doi:10.1016/b978-0-444-63327-9.00001-1 · Cited by 667
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
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
Fear erasure in mice requires synergy between antidepressant drugs and extinction training
Karpova, N. N., Pickenhagen, A., Lindholm, J., Tiraboschi, E., Kulesskaya, N., Ágústsdóttir, A., Antila, H., Popova, D., Akamine, Y., Sullivan, R., et al. (2011) · Science · doi:10.1126/science.1214592 · Cited by 382
Otx2 Binding to Perineuronal Nets Persistently Regulates Plasticity in the Mature Visual Cortex
Beurdeley, M., Spatazza, J., Lee, H. H. C., Sugiyama, S., Bernard, C., Di Nardo, A. A., Hensch, T. K., & Prochiantz, A. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0394-12.2012 · Cited by 398
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
Autism: A “Critical Period” Disorder?
LeBlanc, J. J., & Fagiolini, M. (2011) · Neural Plasticity · doi:10.1155/2011/921680 · Cited by 301
Lensjø, K. K., Lepperød, M. E., Dick, G., Hafting, T., & Fyhn, M. (2017) · The Journal of Neuroscience · doi:10.1523/jneurosci.2504-16.2016 · Cited by 281
Callaghan, B. L., & Tottenham, N. (2016) · Neuropsychopharmacology · doi:10.1038/npp.2015.204 · Cited by 268
Reinhard, S. M., Razak, K., & Ethell, I. M. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00280 · Cited by 219
Perineuronal Nets Enhance the Excitability of Fast-Spiking Neurons
Balmer, T. S. (2016) · eneuro · doi:10.1523/eneuro.0112-16.2016 · Cited by 220
Self-citationErasing Fear Memories with Extinction Training: Figure 1.
Quirk, G. J., Paré, D., Richardson, R., Herry, C., Monfils, M., Schiller, D., & Vicentic, A. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.4268-10.2010 · Cited by 233
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
Aggrecan Directs Extracellular Matrix-Mediated Neuronal Plasticity
Rowlands, D., Lensjø, K. K., Dinh, T., Yang, S., Andrews, M. R., Hafting, T., Fyhn, M., Fawcett, J. W., & Dick, G. (2018) · The Journal of Neuroscience · doi:10.1523/jneurosci.1122-18.2018 · Cited by 204
Translating Birdsong: Songbirds as a Model for Basic and Applied Medical Research
Brainard, M. S., & Doupe, A. J. (2013) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-060909-152826 · Cited by 225
Cognitive-Affective Functions of the Cerebellum
Rudolph, S., Badura, A., Lutzu, S., Pathak, S. S., Thieme, A. G., Verpeut, J. L., Wagner, M. J., Yang, Y., & Fioravante, D. (2023) · Journal of Neuroscience · doi:10.1523/jneurosci.1451-23.2023 · Cited by 215
The extracellular matrix and perineuronal nets in memory
Fawcett, J. W., Fyhn, M., Jendelova, P., Kwok, J. C. F., Ruzicka, J., & Sorg, B. A. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01634-3 · Cited by 169
Extracellular matrix abnormalities in schizophrenia
Berretta, S. (2012) · Neuropharmacology · doi:10.1016/j.neuropharm.2011.08.010 · Cited by 179
Early life nutrition and neural plasticity
Georgieff, M. K., Brunette, K. E., & Tran, P. V. (2015) · Development and Psychopathology · doi:10.1017/s0954579415000061 · Cited by 177
Happel, M. F. K., Niekisch, H., Castiblanco Rivera, L. L., Ohl, F. W., Deliano, M., & Frischknecht, R. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1310272111 · Cited by 176
Berretta, S., Pantazopoulos, H., Markota, M., Brown, C., & Batzianouli, E. T. (2015) · Schizophrenia Research · doi:10.1016/j.schres.2014.12.040 · Cited by 152
Geissler, M., Gottschling, C., Aguado, A., Rauch, U., Wetzel, C. H., Hatt, H., & Faissner, A. (2013) · The Journal of Neuroscience · doi:10.1523/jneurosci.3275-12.2013 · Cited by 140
The perineuronal net component of the extracellular matrix in plasticity and epilepsy
McRae, P. A., & Porter, B. E. (2012) · Neurochemistry International · doi:10.1016/j.neuint.2012.08.007 · Cited by 143
Lensjø, K. K., Christensen, A. C., Tennøe, S., Fyhn, M., & Hafting, T. (2017) · eneuro · doi:10.1523/eneuro.0379-16.2017 · Cited by 133
Wingert, J. C., & Sorg, B. A. (2021) · Frontiers in Synaptic Neuroscience · doi:10.3389/fnsyn.2021.673210 · Cited by 129
Brain ageing changes proteoglycan sulfation, rendering perineuronal nets more inhibitory
Foscarin, S., Raha-Chowdhury, R., Fawcett, J. W., & Kwok, J. C. F. (2017) · Aging · doi:10.18632/aging.101256 · Cited by 139
Oohashi, T., Edamatsu, M., Bekku, Y., & Carulli, D. (2015) · Experimental Neurology · doi:10.1016/j.expneurol.2015.09.010 · Cited by 131
Riga, D., Kramvis, I., Koskinen, M. K., van Bokhoven, P., van der Harst, J. E., Heistek, T. S., Jaap Timmerman, A., van Nierop, P., van der Schors, R. C., Pieneman, A. W., et al. (2017) · Science Translational Medicine · doi:10.1126/scitranslmed.aai8753 · Cited by 128
An Extracellular Perspective on CNS Maturation: Perineuronal Nets and the Control of Plasticity
Carulli, D., & Verhaagen, J. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22052434 · Cited by 136
The Interstitial System of the Brain in Health and Disease
Shetty, A. K., & Zanirati, G. (2020) · Aging and Disease · doi:10.14336/ad.2020.0103 · Cited by 121
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
Fretham, S. J. B., Carlson, E. S., Wobken, J. D., Tran, P. V., Petryk, A., & Georgieff, M. K. (2012) · Hippocampus · doi:10.1002/hipo.22004 · Cited by 98
Neural ECM molecules in synaptic plasticity, learning, and memory
Senkov, O., Anđjus, P. R., Radenović, L., Soriano, E., & Dityatev, A. E. (2014) · Progress in brain research · doi:10.1016/b978-0-444-63486-3.00003-7 · Cited by 96
Baker, K., Gray, A. R., & Richardson, R. (2017) · Behavioral Neuroscience · doi:10.1037/bne0000203 · Cited by 100
Larsen, B., Cui, Z., Adebimpe, A., Pines, A., Alexander-Bloch, A., Bertolero, M., Calkins, M. E., Gur, R. E., Gur, R. C., Mahadevan, A. S., et al. (2022) · Science Advances · doi:10.1126/sciadv.abj8750 · Cited by 80
Developmental Changes in EEG Phenotypes in a Mouse Model of Fragile X Syndrome
Wen, T. H., Lovelace, J. W., Ethell, I. M., Binder, D. K., & Razak, K. A. (2018) · Neuroscience · doi:10.1016/j.neuroscience.2018.11.047 · Cited by 81
Diverse functions of perineuronal nets
Karetko, M., & Skangiel-Kramska, J. (2009) · Acta Neurobiologiae Experimentalis · doi:10.55782/ane-2009-1766 · Cited by 76
Mix, A., Benali, A., Eysel, U. T., & Funke, K. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07425.x · Cited by 78
Mirzadeh, Z., Alonge, K. M., Cabrales, E., Herranz‐Pérez, V., Scarlett, J. M., Brown, J. M., Hassouna, R., Matsen, M. E., Hồng, N. T., García‐Verdugo, J. M., et al. (2019) · Nature Metabolism · doi:10.1038/s42255-018-0029-0 · Cited by 82
Circadian Rhythms of Perineuronal Net Composition
Pantazopoulos, H., Gisabella, B., Rexrode, L., Benefield, D., Yıldız, E., Seltzer, P., Valeri, J., Chelini, G., Reich, A., Ardelt, M., et al. (2020) · eNeuro · doi:10.1523/eneuro.0034-19.2020 · Cited by 77
Yamada, J., & Jinno, S. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.08.061 · Cited by 71
Beebe, N. L., Young, J. W., Mellott, J. G., & Schofield, B. R. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.0217-16.2016 · Cited by 69
Slaker, M. L., Jorgensen, E. T., Hegarty, D. M., Liu, X., Kong, Y., Zhang, F., Linhardt, R. J., Brown, T. E., Aicher, S. A., & Sorg, B. A. (2018) · eneuro · doi:10.1523/eneuro.0221-18.2018 · Cited by 64
“Several studies have demonstrated an important contribution of PNNs to learning and memory (Balmer et al., 2009; Fawcett, 2009; Gogolla et al., 2009; Romberg et al., 2013; Banerjee et al., 2017; Foscarin et al., 2017).”
BackgroundSlaker, M. L., Barnes, J., Sorg, B. A., & Grimm, J. W. (2016) · PLoS ONE · doi:10.1371/journal.pone.0168256 · Cited by 57
Perineuronal net degradation rescues CA2 plasticity in a mouse model of Rett syndrome
Carstens, K. E., Lustberg, D. J., Shaughnessy, E. K., McCann, K. E., Alexander, G. M., & Dudek, S. M. (2021) · Journal of Clinical Investigation · doi:10.1172/jci137221 · Cited by 57
Bath, K. G., Russo, S. J., Pleil, K. E., Wohleb, E. S., Duman, R. S., & Radley, J. J. (2017) · Neurobiology of Stress · doi:10.1016/j.ynstr.2017.05.001 · Cited by 59
Age-Related Deterioration of Perineuronal Nets in the Primary Auditory Cortex of Mice
Brewton, D. H., Kokash, J., Jimenez, O., Pena, E. R., & Razak, K. A. (2016) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2016.00270 · Cited by 54
Diurnal changes in perineuronal nets and parvalbumin neurons in the rat medial prefrontal cortex
Harkness, J. H., Gonzalez, A. E., Bushana, P. N., Jorgensen, E. T., Hegarty, D. M., Nardo, A. A. D., Prochiantz, A., Wisor, J. P., Aicher, S. A., Brown, T. E., et al. (2021) · Brain Structure and Function · doi:10.1007/s00429-021-02229-4 · Cited by 55
Hyperexcitability and homeostasis in fragile X Syndrome.
Liu, X., Kumar, V., Tsai, N.-P., & Auerbach, B. D. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2021.805929 · Cited by 53
Umemori, J., Winkel, F., Ċastrén, E., & Karpova, N. N. (2015) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2015.05.006 · Cited by 56
Yu, Z., Chen, N., Hu, D., Chen, W., Yuan, Y., Meng, S., Zhang, W., Lu, L., Han, Y., & Shi, J. (2020) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2020.00004 · Cited by 52
Horita, H., Kobayashi, M., Liu, W.-C., Oka, K., Jarvis, E. D., & Wada, K. (2012) · PLoS ONE · doi:10.1371/journal.pone.0042173 · Cited by 51
Critical Period Regulation by Thyroid Hormones: Potential Mechanisms and Sex-Specific Aspects
Batista, G., & Hensch, T. K. (2019) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2019.00077 · Cited by 50
Perineuronal Nets: Subtle Structures with Large Implications
Carceller, H., Gramuntell, Y., Klimczak, P., & Nácher, J. (2022) · The Neuroscientist · doi:10.1177/10738584221106346 · Cited by 54
Callaghan, B. L., Graham, B. M., Li, S., & Richardson, R. (2013) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2013.00090 · Cited by 50
Perineuronal Nets Play a Role in Regulating Striatal Function in the Mouse
Lee, H., Leamey, C. A., & Sawatari, A. (2012) · PLoS ONE · doi:10.1371/journal.pone.0032747 · Cited by 47
Expression of aggrecan components in perineuronal nets in the mouse cerebral cortex
Ueno, H., Fujii, K., Suemitsu, S., Murakami, S., Kitamura, N., Wani, K., Aoki, S., Okamoto, M., Ishihara, T., & Takao, K. (2018) · IBRO Reports · doi:10.1016/j.ibror.2018.01.002 · Cited by 49
Convergent Differential Regulation of Parvalbumin in the Brains of Vocal Learners
Hara, E., Rivas, M. V., Ward, J. M., Okanoya, K., & Jarvis, E. D. (2012) · PLoS ONE · doi:10.1371/journal.pone.0029457 · Cited by 49
Karetko-Sysa, M., Skangiel-Kramska, J., & Nowicka, D. (2011) · Experimental Neurology · doi:10.1016/j.expneurol.2011.05.022 · Cited by 45
Neuroplasticity and MRI: A perfect match
Hamaide, J., Groof, G. D., & der Linden, A. V. (2015) · NeuroImage · doi:10.1016/j.neuroimage.2015.08.005 · Cited by 49
Mori, C., & Wada, K. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.1804-14.2015 · Cited by 39
Age‐dependent sexual dimorphism in hippocampal cornu ammonis‐1 perineuronal net expression in rats
Griffiths, B. B., Madden, A. M. K., Edwards, K. A., Zup, S. L., & Stary, C. M. (2019) · Brain and Behavior · doi:10.1002/brb3.1265 · Cited by 38
Karetko, M., Skangiel-Kramska, J., & Nowicka, D. (2014) · Neuroscience · doi:10.1016/j.neuroscience.2014.07.049 · Cited by 37
Bitanihirwe, B. K. Y., Mauney, S. A., & Woo, T.-U. W. (2016) · Biological Psychiatry · doi:10.1016/j.biopsych.2016.03.1047 · Cited by 40
From molecules to behavior: Implications for perineuronal net remodeling in learning and memory
Sanchez, B., Kraszewski, P., Lee, S., & Cope, E. C. (2023) · Journal of Neurochemistry · doi:10.1111/jnc.16036 · Cited by 41
White, S. A. (2009) · Brain and Language · doi:10.1016/j.bandl.2009.10.002 · Cited by 37
Cornez, G., Madison, F. N., der Linden, A. V., Cornil, C. A., Yoder, K. M., Ball, G. F., & Balthazart, J. (2017) · Developmental Neurobiology · doi:10.1002/dneu.22485 · Cited by 37
Nguyen, A., Khaleel, H. M., & Razak, K. A. (2017) · Hearing Research · doi:10.1016/j.heares.2017.04.015 · Cited by 36
Chondroitin Sulfate Proteoglycan Tenascin-R Regulates Glutamate Uptake by Adult Brain Astrocytes
Okuda, H., Tatsumi, K., Morita, S., Shibukawa, Y., Korekane, H., Horii-Hayashi, N., Wada, Y., Taniguchi, N., & Wanaka, A. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.504787 · Cited by 33
Fear Erasure Facilitated by Immature Inhibitory Neuron Transplantation
Yang, W., Liu, T., Cao, J.-W., Chen, X.-F., Liu, X., Wang, M., Su, X., Zhang, S., Qiu, B., Hu, W., et al. (2016) · Neuron · doi:10.1016/j.neuron.2016.11.018 · Cited by 33
The protein tyrosine phosphatase RPTPζ/phosphacan is critical for perineuronal net structure
Eill, G. J., Sinha, A., Morawski, M., Viapiano, M. S., & Matthews, R. T. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ra119.010830 · Cited by 32
The protein tyrosine phosphatase RPTPζ/phosphacan is critical for perineuronal net structure
Eill, G. J., Sinha, A., Morawski, M., Viapiano, M. S., & Matthews, R. T. (2020) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)49907-8 · Cited by 32
Distinct roles for hyaluronan in neural stem cell niches and perineuronal nets
Su, W., Matsumoto, S. G., Sorg, B. A., & Sherman, L. S. (2018) · Matrix Biology · doi:10.1016/j.matbio.2018.01.022 · Cited by 33
Perineuronal nets and GABAergic cells in the inferior colliculus of guinea pigs
Foster, N. L., Mellott, J. G., & Schofield, B. R. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2013.00053 · Cited by 30
Microglia shape AgRP neuron postnatal development via regulating perineuronal net plasticity
Sun, J. Y., Wang, X., Sun, R., Xiao, X., Wang, Y., Peng, Y., & Gao, Y. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02326-2 · Cited by 30
Seasonal changes of perineuronal nets and song learning in adult canaries (Serinus canaria)
Cornez, G., Collignon, C., Müller, W., Ball, G. F., Cornil, C. A., & Balthazart, J. (2019) · Behavioural Brain Research · doi:10.1016/j.bbr.2019.112437 · Cited by 30
Boerma, T., ter Haar, S. M., Ganga, R., Wijnen, F. N. K., Blom, E., & Wierenga, C. J. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105398 · Cited by 36
Recent Advances in the Genetics of Vocal Learning
Condro, M. C., & White, S. A. (2014) · Comparative Cognition & Behavior Reviews · doi:10.3819/ccbr.2014.90003 · Cited by 27
Sexually dimorphic perineuronal nets in the rodent and primate reproductive circuit
Ciccarelli, A., Weijers, D., Kwan, W. C., Warner, C. E., Bourne, J. A., & Gross, C. T. (2021) · The Journal of Comparative Neurology · doi:10.1002/cne.25167 · Cited by 28
Cornez, G., ter Haar, S. M., Cornil, C. A., & Balthazart, J. (2015) · PLoS ONE · doi:10.1371/journal.pone.0123199 · Cited by 28
Mueller, A. L., Davis, A., Sovich, S., Carlson, S. S., & Robinson, F. R. (2016) · Neural Plasticity · doi:10.1155/2016/6021428 · Cited by 29
Vocal motor changes beyond the sensitive period for song plasticity
James, L. S., & Sakata, J. T. (2014) · Journal of Neurophysiology · doi:10.1152/jn.00217.2014 · Cited by 29
Cornez, G., Jonckers, E., ter Haar, S. M., der Linden, A. V., Cornil, C. A., & Balthazart, J. (2018) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2018.0849 · Cited by 27
Mafi, A. M., Hofer, L. N., Russ, M. G., Young, J. W., & Mellott, J. G. (2020) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2020.00027 · Cited by 25
Cornez, G., Collignon, C., Müller, W., Cornil, C. A., Ball, G. F., & Balthazart, J. (2020) · eNeuro · doi:10.1523/eneuro.0361-19.2020 · Cited by 26
Bíró, L., Miskolczi, C., Szebik, H., Bruzsik, B., Varga, Z. K., Szente, L., Tóth, M., Halász, J., & Mikics, É. (2023) · Neurobiology of Stress · doi:10.1016/j.ynstr.2023.100546 · Cited by 28
Net gain and loss: influence of natural rewards and drugs of abuse on perineuronal nets
Brown, T. E., & Sorg, B. A. (2022) · Neuropsychopharmacology · doi:10.1038/s41386-022-01337-x · Cited by 25
Cornez, G., Shevchouk, O. T., Ghorbanpoor, S., Ball, G. F., Cornil, C. A., & Balthazart, J. (2019) · Hormones and Behavior · doi:10.1016/j.yhbeh.2019.104643 · Cited by 25
Song learning and plasticity in songbirds
Rundstrom, P., & Creanza, N. (2021) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2021.02.003 · Cited by 24
The Role and Modulation of Spinal Perineuronal Nets in the Healthy and Injured Spinal Cord
Sánchez-Ventura, J., Lane, M. A., & Udina, E. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.893857 · Cited by 26
Glial regulation of critical period plasticity
Starkey, J., Horstick, E. J., & Ackerman, S. D. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1247335 · Cited by 31
Neural Circuits Underlying Vocal Learning in Songbirds
Sakata, J. T., & Yazaki‐Sugiyama, Y. (2020) · Springer handbook of auditory research · doi:10.1007/978-3-030-34683-6_2 · Cited by 26
Sexually dimorphic perineuronal net expression in the songbird
Meyer, C., Boroda, E., & Nick, T. A. (2013) · Basal Ganglia · doi:10.1016/j.baga.2013.10.002 · Cited by 22
Self-citationLondon, S. E. (2017) · Behavioural Processes · doi:10.1016/j.beproc.2017.11.008 · Cited by 23
Steinzeig, A., Cannarozzo, C., & Ċastrén, E. (2019) · European Journal of Neuroscience · doi:10.1111/ejn.14512 · Cited by 21
Dopamine D1 Receptor Activation Drives Plasticity in the Songbird Auditory Pallium
Macêdo-Lima, M., Boyd, H. M., & Remage‐Healey, L. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.2823-20.2021 · Cited by 24
Sultana, R., Brooks, C. B., Shrestha, A., Ogundele, O. M., & Lee, C. C. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222011140 · Cited by 23
Metadata
- Authors
- Balmer, T. S., Carels, V. M., Frisch, J. L., & Nick, T. A.
- Affiliations
- University of Minnesota (US)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2009-10-14
- Volume
- 29
- Issue
- 41
- Pages
- 12878-12885
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC2769505
- OpenAlex
- W2080602594
- Cited by
- 181
- References
- 53
- Citations by year
- 2026: 4 · 2025: 5 · 2024: 9 · 2023: 13 · 2022: 11 · 2021: 15 · 2020: 13 · 2019: 13 · 2018: 13 · 2017: 14 · 2016: 12 · 2015: 16 · 2014: 11 · 2013: 11 · 2012: 7
- FWCI
- 4.61
- 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)
- Funders
- University of Minnesota
- National Institute on Deafness and Other Communication Disorders (R01DC007384, K02DC008521)
- National Institute of Neurological Disorders and Stroke (R01NS050436)
- Topics
- Life Sciences › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Animal Vocal Communication and Behavior
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neuroscience and Music Perception
- Keywords
- perineuronal nets, parvalbumin, zebra finch, critical period, HVC, sensorimotor integration, neuroplasticity
- MeSH terms
- Age Factors, Animals, Animals, Newborn, Cell Count, Critical Period, Psychological, Female, Learning, Male, Nerve Net, Neuronal Plasticity, Neurons, Parvalbumins, Social Isolation, Vocalization, Animal, Entropy, Finches, High Vocal Center, 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