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.
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“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
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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
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Obray, J. D., Denton, A. R., Carroll-Deaton, J., Marquardt, K., Chandler, L. J., & Scofield, M. D. (2024) · Alcohol · doi:10.1016/j.alcohol.2024.12.006 · Cited by 9
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Talwalkar, A., Haden, G., & Duncan, K. A. (2024) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2024.102418 · Cited by 3
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Hayase, S., Shao, C., Kobayashi, M., Mori, C., Liu, W., & Wada, K. (2021) · Molecular Brain · doi:10.1186/s13041-021-00869-5 · Cited by 3
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Sakata, J. T., & Balthazart, J. (2026) · Hormones and Behavior · doi:10.1016/j.yhbeh.2026.105923 · Cited by 1
Rahman, T. (2026) · Hormones and Behavior · doi:10.1016/j.yhbeh.2026.105999 · Cited by 1
Cummings, J. A. (2016) · doi:10.14418/wes01.1.1210 · Cited by 1
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Chu, P. (2015) · CUNY Academic Works (City University of New York) · Cited by 1
Wiersma, A. M. (2017) · ERA: Education and Research Archive (University of Alberta) · doi:10.7939/r3v698s16 · Cited by 1
Critical period plasticity and sensory function in a neuroligin-3 model of autism
LeBlanc, J. J. (2013) · Digital Access to Scholarship at Harvard (DASH) (Harvard University)
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Bogart, L. J. (2015) · Digital Access to Scholarship at Harvard (DASH) (Harvard University)
Karthikeyan, S. S. (2017) · uO Research (University of Ottawa) · doi:10.20381/ruor-21084
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Mencio, C. P., Tran, V. M., Quintero, M. V., Koketsu, M., Goller, F., & Kuberan, B. (2017) · Developmental Neurobiology · doi:10.1002/dneu.22547
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Steinzeig, A., Cannarozzo, C., & Ċastrén, E. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/487553
The Role of Perineuronal Nets in Learning and Memory
Nath, M. (2018) · TSpace (University of Toronto)
Orije, J. E. M. J., Raymaekers, S. R., Majumadar, G., Groof, G. D., Jonckers, E., Ball, G. F., Verhoye, M., Darras, V., & der Linden, A. V. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.10.21.465109
Mechanisms of Experience-dependent Prevention of Plasticity in Visual Circuits
Balmer, T. S. (2022) · Digital Archive @ GSU · doi:10.57709/5814205
Self-citationDisinhibition enables vocal repertoire expansion after a critical periodPreprint
Heim, F., Mendoza, E., Koparkar, A., & Vallentin, D. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.04.04.588109
Zhang, H., Cicvaric, A., Bassett, T. E., Wood, E. M., Petrovic, Z., & Radulović, J. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-15754-7.00066-3
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
Tschida, K. (2011) · DukeSpace (Duke University)
Morandi-Raikova, A., Aydın, R., Parada, C. D. C., Rowland, H. M., Vallortigara, G., Mayer, U., & Salva, O. R. (2026) · Heliyon · doi:10.1016/j.heliyon.2026.e44526
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Sikder, S., & Bozdagi-Gunal, O. (2026) · Brain Science Advances · doi:10.26599/bsa.2026.905017
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
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