Cited by 112Neuroscience and Music PerceptionAnimal Vocal Communication and BehaviorHearing, Cochlea, Tinnitus, Genetics

The DOI matches its Crossref record; 67 of the 67 references it cites were found in a registry or an index.

Improved cortical entrainment to infant communication calls in mothers compared with virgin mice

Liu, Robert C., Linden, Jennifer F., Schreiner, Christoph E.·2006·European Journal of Neuroscience

DOI 10.1111/j.1460-9568.2006.04840.x

Open this paper in CoChat — free account

Abstract

There is a growing interest in the use of mice as a model system for species‐specific communication. In particular, ultrasonic calls emitted by mouse pups communicate distress, and elicit a search and retrieval response from mothers. Behaviorally, mothers prefer and recognize these calls in two‐alternative choice tests, in contrast to pup‐naïve females that do not have experience with pups. Here, we explored whether one particular acoustic feature that defines these calls − the repetition rate of calls within a bout − is represented differently in the auditory cortex of these two animal groups. Multiunit recordings in anesthetized CBA/CaJ mice revealed that: (i) neural entrainment to repeated stimuli extended up to the natural pup call repetition rate (5 Hz) in mothers; but (ii) neurons in naïve females followed repeated stimuli well only at slower repetition rates; and (iii) entrained responses to repeated pup calls were less sensitive to natural pup call variability in mothers than in pup‐naïve females. In the broader context, our data suggest that auditory cortical responses to communication sounds are plastic, and that communicative significance is correlated with an improved cortical representation.

Integrity signals

Registry

Crossref · 10.1111/j.1460-9568.2006.04840.x

Cites

67 of 67 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

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?

An Introduction to the Bootstrap
Efron, B., & Tibshirani, R. J. (1994) · doi:10.1201/9780429246593 · Cited by 40,500
An Introduction to the Bootstrap
Efron, B., & Tibshirani, R. J. (1993) · doi:10.1007/978-1-4899-4541-9 · Cited by 21,230
The Cognitive neurosciences
(2005) · Choice Reviews Online · doi:10.5860/choice.43-0626 · Cited by 4,726
Control Methods Used in a Study of the Vowels
Peterson, G. E., & Barney, H. L. (1952) · The Journal of the Acoustical Society of America · doi:10.1121/1.1906875 · Cited by 2,837 · cited 2×
“Here, we explored whether one particular acoustic feature that defines these calls ) the repetition rate of calls within a bout ) is represented differently in the auditory cortex of these two animal groups.”
Background
A Cross-Language Study of Voicing in Initial Stops: Acoustical Measurements
Lisker, L., & Abramson, A. S. (1964) · WORD · doi:10.1080/00437956.1964.11659830 · Cited by 2,602
The Cognitive neurosciences
(1995) · Choice Reviews Online · doi:10.5860/choice.32-5931 · Cited by 2,337
Estrogen Actions in the Central Nervous System
McEwen, B. S., & Alves, S. E. (1999) · Endocrine Reviews · doi:10.1210/edrv.20.3.0365 · Cited by 1,504
Cortical Map Reorganization Enabled by Nucleus Basalis Activity
Kilgard, M. P., & Merzenich, M. M. (1998) · Science · doi:10.1126/science.279.5357.1714 · Cited by 1,197
Roles of estradiol and progesterone in regulation of hippocampal dendritic spine density during the estrous cycle in the rat
Woolley, C. S., & McEwen, B. S. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903360210 · Cited by 1,073
The Neurobiology of Parental Behavior
(2003) · Hormones, Brain, and Behavior · doi:10.1007/b97533 · Cited by 684
Ultrasonic Songs of Male Mice
Holy, T. E., & Guo, Z. (2005) · PLoS Biology · doi:10.1371/journal.pbio.0030386 · Cited by 673
Estrogen Actions in the Central Nervous System
McEwen, B. S. (1999) · Endocrine Reviews · doi:10.1210/er.20.3.279 · Cited by 640
Specific long-term memory traces in primary auditory cortex
Weinberger, N. M. (2004) · Nature reviews. Neuroscience · doi:10.1038/nrn1366 · Cited by 606
Cortical remodelling induced by activity of ventral tegmental dopamine neurons
Bao, S., Chan, V. T., & Merzenich, M. M. (2001) · Nature · doi:10.1038/35083586 · Cited by 569
Estradiol increases choline acetyltransferase activity in specific basal forebrain nuclei and projection areas of female rats
Luine, V. N. (1985) · Experimental Neurology · doi:10.1016/0014-4886(85)90108-6 · Cited by 523
Ovarian steroid deprivation results in a reversible learning impairment and compromised cholinergic function in female Sprague-Dawley rats
Singh, M., Meyer, E. M., Millard, W. J., & Simpkins, J. W. (1994) · Brain Research · doi:10.1016/0006-8993(94)91694-2 · Cited by 477
The Auditory psychobiology of the mouse
Willott, J. F. (1983) · Medical Entomology and Zoology · Cited by 460
Thalamocortical transformation of responses to complex auditory stimuli
Creutzfeldt, O. D., Hellweg, F.-C., & Schreiner, C. E. (1980) · Experimental Brain Research · doi:10.1007/bf00237072 · Cited by 359
Self-citation
Change in pattern of ongoing cortical activity with auditory category learning
Ohl, F. W., Scheich, H., & Freeman, W. J. (2001) · Nature · doi:10.1038/35089076 · Cited by 345
Representation of amplitude modulation in the auditory cortex of the cat. II. Comparison between cortical fields
Schreiner, C. E., & Urbas, J. V. (1988) · Hearing Research · doi:10.1016/0378-5955(88)90146-3 · Cited by 329
Self-citation
Infant Rodent Ultrasounds ? A Gate to the Understanding of Sound Communication
Ehret, G. (2005) · Behavior Genetics · doi:10.1007/s10519-004-0853-8 · Cited by 325
The auditory cortex of the house mouse: left-right differences, tonotopic organization and quantitative analysis of frequency representation
Stiebler, I., Neulist, R., Fichtel, I., & Ehret, G. (1997) · Journal of Comparative Physiology A · doi:10.1007/s003590050140 · Cited by 316
Plasticity of temporal information processing in the primary auditory cortex
Kilgard, M. P., & Merzenich, M. M. (1998) · Nature Neuroscience · doi:10.1038/3729 · Cited by 298
Representation of amplitude modulation in the auditory cortex of the cat. I. The anterior auditory field (AAF)
Schreiner, C. E., & Urbas, J. V. (1986) · Hearing Research · doi:10.1016/0378-5955(86)90221-2 · Cited by 292
Self-citation
Between sound and perception: reviewing the search for a neural code
Eggermont, J. J. (2001) · Hearing Research · doi:10.1016/s0378-5955(01)00259-3 · Cited by 273
Spectrotemporal Structure of Receptive Fields in Areas AI and AAF of Mouse Auditory Cortex
Linden, J. F., Liu, R. C., Sahani, M., Schreiner, C. E., & Merzenich, M. M. (2003) · Journal of Neurophysiology · doi:10.1152/jn.00751.2002 · Cited by 255
Self-citation
Ultra-sounds in young rodents. I. Changes with age in albino mice
Noirot, É. (1966) · Animal Behaviour · doi:10.1016/s0003-3472(66)80045-3 · Cited by 254
Motherhood and the hormones of pregnancy modify concentrations of hippocampal neuronal dendritic spines
Kinsley, C. H., Trainer, R., Stafisso-Sandoz, G., Quadros, P. S., Keyser‐Marcus, L., Hearon, C., Meyer, E. A. A., Hester, N. W., Morgan, M. D., & Kozub, F. J. (2005) · Hormones and Behavior · doi:10.1016/j.yhbeh.2005.05.017 · Cited by 248
Age-Related Alteration in Processing of Temporal Sound Features in the Auditory Midbrain of the CBA Mouse
Walton, J. P., Frisina, R. D., & O’Neill, W. E. (1998) · Journal of Neuroscience · doi:10.1523/jneurosci.18-07-02764.1998 · Cited by 238
Steroid-Dependent Auditory Plasticity Leads to Adaptive Coupling of Sender and Receiver
Sisneros, J. A., Forlano, P. M., Deitcher, D. L., & Bass, A. H. (2004) · Science · doi:10.1126/science.1097218 · Cited by 227
Ultrasonic Communication in Rodents
SEWELL, G. D. (1970) · Nature · doi:10.1038/227410a0 · Cited by 222
Environmental Enrichment Improves Response Strength, Threshold, Selectivity, and Latency of Auditory Cortex Neurons
Engineer, N. D., Percaccio, C. R., Pandya, P. K., Moucha, R., Rathbun, D. L., & Kilgard, M. P. (2004) · Journal of Neurophysiology · doi:10.1152/jn.00059.2004 · Cited by 198
Learning-induced plasticity in animal and human auditory cortex
Ohl, F. W., & Scheich, H. (2005) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2005.07.002 · Cited by 197
Acoustic variability and distinguishability among mouse ultrasound vocalizations
Liu, R. C., Miller, K. D., Merzenich, M. M., & Schreiner, C. E. (2003) · The Journal of the Acoustical Society of America · doi:10.1121/1.1623787 · Cited by 195
Self-citation
Alterations of the cortical representation of the rat ventrum induced by nursing behavior
Xerri, C., Stern, J. M., & Merzenich, M. M. (1994) · Journal of Neuroscience · doi:10.1523/jneurosci.14-03-01710.1994 · Cited by 167
Cholinergic modulation of responses to single tones produces tone‐specific receptive field alterations in cat auditory cortex
Metherate, R., & Weinberger, N. M. (1990) · Synapse · doi:10.1002/syn.890060204 · Cited by 165
Distributed representation of spectral and temporal information in rat primary auditory cortex
Kilgard, M. P., & Merzenich, M. M. (1999) · Hearing Research · doi:10.1016/s0378-5955(99)00061-1 · Cited by 155
Age-Related Alterations in the Neural Coding of Envelope Periodicities
Walton, J. P., Simon, H., & Frisina, R. D. (2002) · Journal of Neurophysiology · doi:10.1152/jn.2002.88.2.565 · Cited by 152
Acetylcholine produces stimulus-specific receptive field alterations in cat auditory cortex
Metherato, R., & Weinberger, N. M. (1989) · Brain Research · doi:10.1016/0006-8993(89)90210-2 · Cited by 145
Rate and synchronization measures of periodicity coding in cat primary auditory cortex
Eggermont, J. J. (1991) · Hearing Research · doi:10.1016/0378-5955(91)90165-6 · Cited by 145
Cholinergic modulation of frequency receptive fields in auditory cortex: I. Frequency‐specific effects of muscarinic agonists
McKenna, T. M., Ashe, J. H., & Weinberger, N. M. (1989) · Synapse · doi:10.1002/syn.890040105 · Cited by 137
Temporal organization of ultrasonic vocalizations in infant mice
Elwood, R. W., & Keeling, F. (1982) · Developmental Psychobiology · doi:10.1002/dev.420150306 · Cited by 135
Reward-dependent plasticity in the primary auditory cortex of adult monkeys trained to discriminate temporally modulated signals
Beitel, R. E., Schreiner, C. E., Cheung, S. W., Wang, X., & Merzenich, M. M. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1334187100 · Cited by 129
Self-citation
Ultrasound recognition in house mice: Key-Stimulus configuration and recognition mechanism
Ehret, G., & Haack, B. (1982) · Journal of Comparative Physiology A · doi:10.1007/bf00619131 · Cited by 124
Categorical perception of mouse-pup ultrasounds in the temporal domain
Ehret, G. (1992) · Animal Behaviour · doi:10.1016/s0003-3472(05)80101-0 · Cited by 124
Comparison of the auditory sensitivity of neurons in the cochlear nucleus and inferior colliculus of young and aging C57BL/6J and CBA/J mice
Willott, J. F., Parham, K., & Hunter, K. P. (1991) · Hearing Research · doi:10.1016/0378-5955(91)90215-u · Cited by 113
The Maternal Brain
Kinsley, C. H., & Lambert, K. G. (2006) · Scientific American · doi:10.1038/scientificamerican0106-72 · Cited by 111
Categorical perception of mouse pup ultrasound by lactating females
Ehret, G., & Haack, B. (1981) · Die Naturwissenschaften · doi:10.1007/bf01047208 · Cited by 98
Sound analysis of ultrasonic distress calls of mouse pups as a function of their age
Noirot, É., & Pye, D. (1969) · Animal Behaviour · doi:10.1016/0003-3472(69)90020-7 · Cited by 95
Responses of adult mice to models of infant calls.
Smith, J. C. (1976) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0077287 · Cited by 89
Genetic and Developmental Influences on Infant Mouse Ultrasonic Calling. II. Developmental Patterns in the Calls of Mice 2–12 Days of Age
Hahn, M. E., Karkowski, L. M., Weinreb, L., Henry, A., Schanz, N., & Hahn, E. M. (1998) · Behavior Genetics · doi:10.1023/a:1021679615792 · Cited by 88
Sex and parental experience determine the onset of an instinctive behavior in mice
Ehret, G., Koch, M., Haack, B., & Markl, H. S. (1987) · Die Naturwissenschaften · doi:10.1007/bf00367047 · Cited by 88
Mice and humans perceive multiharmonic communication sounds in the same way
Ehret, G., & Riecke, S. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.012361999 · Cited by 80
Temporal response features of cat auditory cortex neurons contributing to sensitivity to tones delivered in the presence of continuous noise
Phillips, D. P. (1985) · Hearing Research · doi:10.1016/0378-5955(85)90145-5 · Cited by 79
Time-critical integration of formants for perception of communication calls in mice
Geissler, D. B., & Ehret, G. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.122606499 · Cited by 77
Ultrasound in Rodents
SEWELL, G. D. (1968) · Nature · doi:10.1038/217682a0 · Cited by 75
Long-term cortical plasticity evoked by electric stimulation and acetylcholine applied to the auditory cortex
Ma, X., & Suga, N. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0503851102 · Cited by 72
Vocalizations in newborn mice: Genetic analysis
Roubertoux, P. L., Martin, B., Roy, I. L., Beau, J., Pérez-Díaz, F., Cohen‐Salmon, C., Marchaland, C., & Carlier, M. (1996) · Behavior Genetics · doi:10.1007/bf02359487 · Cited by 68
Direct, complex effects of estrogens on basal forebrain cholinergic neurons
Bora, S. H., Liu, Z., Kecojević, A., Merchenthaler, I. J., & Koliatsos, V. E. (2005) · Experimental Neurology · doi:10.1016/j.expneurol.2005.03.015 · Cited by 67
Basal Forebrain Cholinergic Input Is Not Essential for Lesion-Induced Plasticity in Mature Auditory Cortex
Kamke, M. R., Brown, M., & Irvine, D. R. F. (2005) · Neuron · doi:10.1016/j.neuron.2005.09.014 · Cited by 51
Ultrasound‐induced Parental Behaviour in House Mice is Controlled by Female Sex Hormones and Parental Experience
Ehret, G., & Koch, M. (1989) · Ethology · doi:10.1111/j.1439-0310.1989.tb00731.x · Cited by 47
Enhanced contrast sensitivity in auditory cortex as cats learn to discriminate sound frequencies
Witte, R. S., & Kipke, D. R. (2005) · Cognitive Brain Research · doi:10.1016/j.cogbrainres.2004.10.018 · Cited by 47
Perception and recognition discriminated in the mouse auditory cortex by c-Fos labeling
Fichtel, I., & Ehret, G. (1999) · Neuroreport · doi:10.1097/00001756-199908020-00022 · Cited by 39
Decreased Input-Specific Plasticity of the Auditory Cortex in Mice Lacking M1 Muscarinic Acetylcholine Receptors
Zhang, Y. F., Hamilton, S. E., Nathanson, N. M., & Yan, J. (2005) · Cerebral Cortex · doi:10.1093/cercor/bhj067 · Cited by 35
Electrical Cochlear Stimulation in the Deaf Cat: Comparisons Between Psychophysical and Central Auditory Neuronal Thresholds
Beitel, R. E., Snyder, R. L., Schreiner, C. E., Raggio, M. W., & Leake, P. A. (2000) · Journal of Neurophysiology · doi:10.1152/jn.2000.83.4.2145 · Cited by 28
Self-citation
Inhibition of the expression of conditioned cardiac responses in the developing rat
Hunt, P. S., Hess, M. F., & Campbell, B. A. (1998) · Developmental Psychobiology · doi:10.1002/(sici)1098-2302(199811)33:3 · Cited by 19
Morphological plasticity in the maternal brain: Comment on Kinsley et al.; motherhood and the hormones of pregnancy modify concentrations of hippocampal neuronal dendritic spines
Woodside, B. C. (2005) · Hormones and Behavior · doi:10.1016/j.yhbeh.2005.09.001 · Cited by 10

Sorted by citations

Oxytocin enables maternal behaviour by balancing cortical inhibition
Marlin, B. J., Mitre, M., D’amour, J. A., Chao, M. V., & Froemke, R. C. (2015) · Nature · doi:10.1038/nature14402 · Cited by 744
Unusual repertoire of vocalizations in the BTBR T+tf/J mouse model of autism
Scattoni, M. L., Gandhy, S. U., Ricceri, L., & Crawley, J. N. (2008) · PLoS ONE · doi:10.1371/journal.pone.0003067 · Cited by 550
Ultrasonic vocalizations: A tool for behavioural phenotyping of mouse models of neurodevelopmental disorders
Scattoni, M. L., Crawley, J. N., & Ricceri, L. (2008) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2008.08.003 · Cited by 473
Neural control of maternal and paternal behaviors
Dulac, C., O’Connell, L. A., & Wu, Z. (2014) · Science · doi:10.1126/science.1253291 · Cited by 457
Multisensory Integration of Natural Odors and Sounds in the Auditory Cortex
Cohen, L., Rothschild, G., & Mizrahi, A. (2011) · Neuron · doi:10.1016/j.neuron.2011.08.019 · Cited by 192

See all 112

Authors: Liu, R. C., Linden, J. F., & Schreiner, C. E.
Affiliations: Emory University (US)
University of California, San Francisco (US)
Corresponding author: Liu, Robert C.
ORCID: Liu, Robert C.
Linden, Jennifer F.
Schreiner, Christoph E.
Venue: European Journal of Neuroscience
Publisher: Wiley
Published: 2006-06
Volume: 23
Issue: 11
Pages: 3087-3097
ISSN: 0953-816X (ISSN-L)
1460-9568
DOI: 10.1111/j.1460-9568.2006.04840.x
OpenAlex: W2141066586
Cited by: 112
References: 67
Citations by year: 2026: 2 · 2025: 1 · 2024: 4 · 2023: 11 · 2022: 4 · 2021: 5 · 2020: 10 · 2019: 7 · 2018: 6 · 2017: 6 · 2016: 7 · 2015: 6 · 2014: 5 · 2013: 12 · 2012: 3
FWCI: 1.78
Type: journal article
Language: en
Open access: closed
Licence: onlinelibrary.wiley.com/termsAndConditions#vor (vor, 8 d)
Locations: European Journal of Neuroscience (publishedVersion)
PubMed (publishedVersion)
UCL Discovery (University College London) (submittedVersion)
Funders: National Institute on Deafness and Other Communication Disorders (F32DC005279, R01DC002260, F32 DC05279, DC002260)
National Institute of Neurological Disorders and Stroke (NS 34835, P01NS034835)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Neuroscience and Music Perception
Life Sciences › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Animal Vocal Communication and Behavior
Life Sciences › Neuroscience › Sensory Systems › Hearing, Cochlea, Tinnitus, Genetics
Keywords: maternal behavior, ultrasonic vocalizations, auditory cortex, neural entrainment, maternal experience, auditory plasticity, virgin females
MeSH terms: Acoustic Stimulation, Animals, Animals, Newborn, Auditory Cortex, Behavior, Animal, Evoked Potentials, Auditory, Female, Male, Maternal Behavior, Mice, Inbred CBA, Sound Localization, Sound Spectrography, Ultrasonics, Vocalization, Animal, Recognition, Psychology, Mice

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

Improved cortical entrainment to infant communication calls in mothers compared with virgin mice

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks