The DOI matches its Crossref record; 34 of the 34 references it cites were found in a registry or an index.
Molecular organization of vomeronasal chemoreception
Open accessAbstract
The vomeronasal organ (VNO) has a key role in mediating the social and defensive responses of many terrestrial vertebrates to species- and sex-specific chemosignals. More than 250 putative pheromone receptors have been identified in the mouse VNO, but the nature of the signals detected by individual VNO receptors has not yet been elucidated. To gain insight into the molecular logic of VNO detection leading to mating, aggression or defensive responses, we sought to uncover the response profiles of individual vomeronasal receptors to a wide range of animal cues. Here we describe the repertoire of behaviourally and physiologically relevant stimuli detected by a large number of individual vomeronasal receptors in mice, and define a global map of vomeronasal signal detection. We demonstrate that the two classes (V1R and V2R) of vomeronasal receptors use fundamentally different strategies to encode chemosensory information, and that distinct receptor subfamilies have evolved towards the specific recognition of certain animal groups or chemical structures. The association of large subsets of vomeronasal receptors with cognate, ethologically and physiologically relevant stimuli establishes the molecular foundation of vomeronasal information coding, and opens new avenues for further investigating the neural mechanisms underlying behaviour specificity.
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
“Vomeronasal receptors (VRs) detect pheromonal cues emitted during social encounters, leading to the activation of distinct neural ensembles in the vomeronasal organ (VNO) (Dulac and Torello, 2003; Holy et al., 2000; Isogai et al., 2011).”
From Neuronal Representation of Social Information in the Medial Amygdala of Awake Behaving Mice (2017) · cites this paper as Isogai et al., 2011
In the citing paper
“In virgin mice, 58% ± 6% (mean ± SD) of the recorded MeApd neurons responded to more than one social stimulus, suggesting the existence of significant signal integration at this level of the VNO pathway compared to the initial narrow tuning demonstrated in most VRs (Isogai et al., 2011) (Figure 4C).”
From Neuronal Representation of Social Information in the Medial Amygdala of Awake Behaving Mice (2017) · cites this paper as Isogai et al., 2011
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
A novel multigene family may encode odorant receptors: A molecular basis for odor recognition
Buck, L., & Axel, R. (1991) · Cell · doi:10.1016/0092-8674(91)90418-x · Cited by 4,987
Imaging neural activity in worms, flies and mice with improved GCaMP calcium indicators
Tian, L., Hires, S. A., Mao, T., Huber, D., Chiappe, M. E., Chalasani, S. H., Petreanu, L., Akerboom, J., McKinney, S. A., Schreiter, E. R., et al. (2009) · Nature Methods · doi:10.1038/nmeth.1398 · Cited by 1,967
Schaeren‐Wiemers, N., & Gerfin-Moser, A. (1993) · Histochemistry and Cell Biology · doi:10.1007/bf00267823 · Cited by 1,151
A novel family of genes encoding putative pheromone receptors in mammals
Dulac, C., & Axel, R. (1995) · Cell · doi:10.1016/0092-8674(95)90161-2 · Cited by 1,001
Self-citationLoss of Sex Discrimination and Male-Male Aggression in Mice Deficient for TRP2
Stowers, L., Holy, T. E., Meister, M., Dulac, C. G., & Koentges, G. (2002) · Science · doi:10.1126/science.1069259 · Cited by 880
Self-citationMolecular detection of pheromone signals in mammals: from genes to behaviour
Dulac, C. G., & Torello, A. T. (2003) · Nature reviews. Neuroscience · doi:10.1038/nrn1140 · Cited by 662
Self-citationUltrasensitive pheromone detection by mammalian vomeronasal neurons
Leinders-Zufall, T., Lane, A. P., Puche, A. C., Ma, W., Novotny, M. V., Shipley, M. T., & Zufall, F. (2000) · Nature · doi:10.1038/35015572 · Cited by 576
Formyl peptide receptor-like proteins are a novel family of vomeronasal chemosensors
Rivière, S., Challet, L., Fluegge, D., Spehr, M., & Rodríguez, I. (2009) · Nature · doi:10.1038/nature08029 · Cited by 392
The effects of owl predation on the foraging behavior of heteromyid rodents
Brown, J. S., Kotler, B. P., Smith, R. J., & Wirtz, W. O. (1988) · Oecologia · doi:10.1007/bf00377036 · Cited by 381
Haga‐Yamanaka, S., Hattori, T., Sato, T., Sato, K., Matsuda, S., Kobayakawa, R., Sakano, H., Yoshihara, Y., Kikusui, T., & Touhara, K. (2010) · Nature · doi:10.1038/nature09142 · Cited by 376
Cited by
Sorted by citations
Galanin neurons in the medial preoptic area govern parental behaviour
Wu, Z., Autry, A. E., Bergan, J. F., Watabe‐Uchida, M., & Dulac, C. G. (2014) · Nature · doi:10.1038/nature13307 · Cited by 610
Self-citationGenomic analyses identify distinct patterns of selection in domesticated pigs and Tibetan wild boars
Li, M., Tian, S., Jin, L. G., Zhou, G., Li, Y., Zhang, Y., Wang, T., Yeung, C. K. L., Chen, L., Ma, J., et al. (2013) · Nature Genetics · doi:10.1038/ng.2811 · Cited by 560
Functional circuit architecture underlying parental behaviour
Kohl, J., Babayan, B. M., Rubinstein, N. D., Autry, A. E., Marin-Rodriguez, B., Kapoor, V., Miyamichi, K., Zweifel, L. S., Luo, L., Uchida, N., et al. (2018) · Nature · doi:10.1038/s41586-018-0027-0 · Cited by 470
Self-citationDetecting Activated Cell Populations Using Single-Cell RNA-Seq
Wu, Y. E., Pan, L., Zuo, Y., Li, X., & Hong, W. (2017) · Neuron · doi:10.1016/j.neuron.2017.09.026 · Cited by 438
Molecular Profiling of Activated Neurons by Phosphorylated Ribosome Capture
Knight, Z. A., Tan, K., Birsoy, K., Schmidt, S. F., Garrison, J. L., Wysocki, R. W., Emiliano, A. B., Ekstrand, M. I., & Friedman, J. M. (2012) · Cell · doi:10.1016/j.cell.2012.10.039 · Cited by 312
Liberles, S. D. (2013) · Annual Review of Physiology · doi:10.1146/annurev-physiol-021113-170334 · Cited by 300
Neuronal Representation of Social Information in the Medial Amygdala of Awake Behaving Mice
Li, Y., Mathis, A., Grewe, B. F., Osterhout, J. A., Ahanonu, B., Schnitzer, M. J., Murthy, V. N., & Dulac, C. (2017) · Cell · doi:10.1016/j.cell.2017.10.015 · Cited by 291
Self-citationCorticoamygdala Transfer of Socially Derived Information Gates Observational Learning
Allsop, S. A., Wichmann, R., Mills, F., Burgos-Robles, A., Chang, C.-J., Felix-Ortiz, A. C., Vienne, A., Beyeler, A., Izadmehr, E. M., Glober, G., et al. (2018) · Cell · doi:10.1016/j.cell.2018.04.004 · Cited by 288
Sex-specific processing of social cues in the medial amygdala
Bergan, J. F., Ben-Shaul, Y., & Dulac, C. (2014) · eLife · doi:10.7554/elife.02743 · Cited by 237
Self-citationCyclic regulation of sensory perception by a female hormone alters behavior
Dey, S., Chamero, P., Pru, J. K., Chien, M.-S., Ibarra-Soria, X., Spencer, K. R., Logan, D. W., Matsunami, H., Peluso, J. J., & Stowers, L. (2015) · Cell · doi:10.1016/j.cell.2015.04.052 · Cited by 204
Kaur, A. W., Ackels, T., Kuo, T.-H., Cichy, A., Dey, S., Hays, C. K., Kateri, M., Logan, D. W., Marton, T. F., Spehr, M., et al. (2014) · Cell · doi:10.1016/j.cell.2014.02.025 · Cited by 207
Representing Sex in the Brain, One Module at a Time
Yang, C. F., & Shah, N. M. (2014) · Neuron · doi:10.1016/j.neuron.2014.03.029 · Cited by 203
Synchronous Evolution of an Odor Biosynthesis Pathway and Behavioral Response
Li, Q., Korzan, W. J., Ferrero, D. M., Chang, R. B., Roy, D. S., Buchi, M., Lemon, J. K., Kaur, A. W., Stowers, L., Fendt, M., et al. (2012) · Current Biology · doi:10.1016/j.cub.2012.10.047 · Cited by 196
The neural circuits of innate fear: detection, integration, action, and memorization
Silva, B. A., Gross, C. T., & Gräff, J. (2016) · Learning & Memory · doi:10.1101/lm.042812.116 · Cited by 186
A labeled-line neural circuit for pheromone-mediated sexual behaviors in mice
Ishii, K. K., Osakada, T., Mori, H., Miyasaka, N., Yoshihara, Y., Miyamichi, K., & Touhara, K. (2017) · Neuron · doi:10.1016/j.neuron.2017.05.038 · Cited by 185
Mouse alarm pheromone shares structural similarity with predator scents
Brechbühl, J., Moine, F., Klaey‐Tassone, M., Nenniger-Tosato, M., Hurni, N., Sporkert, F., Giroud, C., & Broillet, M.-C. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1214249110 · Cited by 176
Wired for behaviors: from development to function of innate limbic system circuitry
Sokolowski, K., & Corbin, J. G. (2012) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2012.00055 · Cited by 181
Genetic and Neural Mechanisms that Inhibit Drosophila from Mating with Other Species
Fan, P., Manoli, D. S., Ahmed, O. M., Chen, Y., Agarwal, N., Kwong, S., Cai, A. G., Neitz, J., Renslo, A., Baker, B. S., et al. (2013) · Cell · doi:10.1016/j.cell.2013.06.008 · Cited by 164
The Olfactory Transcriptomes of Mice
Ibarra-Soria, X., Levitin, M. O., Saraiva, L. R., & Logan, D. W. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004593 · Cited by 156
Pardo‐Bellver, C., Cádiz‐Moretti, B., Novejarque, A., Martínez‐Garciá, F., & Lanuza, E. (2012) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2012.00033 · Cited by 166
Social Control of Hypothalamus-Mediated Male Aggression
Yang, T., Yang, C. F., Chizari, M., Maheswaranathan, N., Burke, K. J., Borius, M., Inoue, S., Chiang, M. C., Bender, K. J., Ganguli, S., et al. (2017) · Neuron · doi:10.1016/j.neuron.2017.06.046 · Cited by 161
Olfactory systems and neural circuits that modulate predator odor fear
Takahashi, L. K. (2014) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2014.00072 · Cited by 172
From genes to social communication: molecular sensing by the vomeronasal organ
Chamero, P., Leinders‐Zufall, T., & Zufall, F. (2012) · Trends in Neurosciences · doi:10.1016/j.tins.2012.04.011 · Cited by 150
Oxytocin signaling in the medial amygdala is required for sex discrimination of social cues
Yao, S., Bergan, J., Lanjuin, A., & Dulac, C. (2017) · eLife · doi:10.7554/elife.31373 · Cited by 151
Self-citationA family of non-GPCR chemosensors defines an alternative logic for mammalian olfaction
Greer, P. L., Bear, D. M., Lassance, J.-M., Bloom, M. L., Tsukahara, T., Pashkovski, S. L., Masuda, F. K., Nowlan, A. C., Kirchner, R., Hoekstra, H. E., et al. (2016) · Cell · doi:10.1016/j.cell.2016.05.001 · Cited by 148
Gur, R., Tendler, A., & Wagner, S. (2014) · Biological Psychiatry · doi:10.1016/j.biopsych.2014.03.022 · Cited by 144
An olfactory cocktail party: figure-ground segregation of odorants in rodents
Rokni, D., Hemmelder, V., Kapoor, V., & Murthy, V. N. (2014) · Nature Neuroscience · doi:10.1038/nn.3775 · Cited by 143
Self-citationTaste and smell processing in the brain
Rolls, E. T. (2019) · Handbook of clinical neurology · doi:10.1016/b978-0-444-63855-7.00007-1 · Cited by 150
The Evolving Neural and Genetic Architecture of Vertebrate Olfaction
Bear, D. M., Lassance, J., Hoekstra, H. E., & Datta, S. R. (2016) · Current Biology · doi:10.1016/j.cub.2016.09.011 · Cited by 133
Molecular profiling of activated olfactory neurons identifies odorant receptors for odors in vivo
Jiang, Y., Gong, N. N., Hu, X. S., Ni, M. J., Pasi, R., & Matsunami, H. (2015) · Nature Neuroscience · doi:10.1038/nn.4104 · Cited by 133
Anholt, R. R. H., & Mackay, T. F. C. (2012) · Annual Review of Genetics · doi:10.1146/annurev-genet-110711-155514 · Cited by 139
Limbic Neurons Shape Sex Recognition and Social Behavior in Sexually Naive Males
Bayless, D. W., Yang, T., Mason, M. M., Susanto, A. A. T., Lobdell, A., & Shah, N. M. (2019) · Cell · doi:10.1016/j.cell.2018.12.041 · Cited by 131
Oxytocin modulation of neural circuits for social behavior
Marlin, B. J., & Froemke, R. C. (2017) · Developmental Neurobiology · doi:10.1002/dneu.22452 · Cited by 130
Multisensory Logic of Infant-Directed Aggression by Males
Isogai, Y., Wu, Z., Love, M. I., Ahn, M. H., Bambah-Mukku, D., Hua, V. J., Farrell, K., & Dulac, C. G. (2018) · Cell · doi:10.1016/j.cell.2018.11.032 · Cited by 137
Self-citationOxytocin mediates entrainment of sensory stimuli to social cues of opposing valence
Choe, H. K., Reed, M. D., Benavidez, N., Montgomery, D., Soares, N., Yim, Y. S., & Choi, G. B. (2015) · Neuron · doi:10.1016/j.neuron.2015.06.022 · Cited by 124
Signal Detection and Coding in the Accessory Olfactory System
Mohrhardt, J., Nagel, M., Fleck, D., Ben‐Shaul, Y., & Spehr, M. (2018) · Chemical Senses · doi:10.1093/chemse/bjy061 · Cited by 121
Simultaneous multiplane imaging with reverberation two-photon microscopy
Beaulieu, D. R., Davison, I. G., Kılıç, K., Bifano, T. G., & Mertz, J. C. (2020) · Nature Methods · doi:10.1038/s41592-019-0728-9 · Cited by 107
From molecules to mating: Rapid evolution and biochemical studies of reproductive proteins
Wilburn, D. B., & Swanson, W. J. (2015) · Journal of Proteomics · doi:10.1016/j.jprot.2015.06.007 · Cited by 110
Integrated action of pheromone signals in promoting courtship behavior in male mice
Haga‐Yamanaka, S., Ma, L., He, J., Qiu, Q., Lavis, L. D., Looger, L. L., & Yu, C. R. (2014) · eLife · doi:10.7554/elife.03025 · Cited by 110
Xiong, Z., Zhu, X., Geng, J., Xu, Y., Wu, R., Li, C., Fan, D., Qin, X. S., Du, Y., Tian, Y., et al. (2021) · Immunity · doi:10.1016/j.immuni.2022.03.001 · Cited by 109
Of Pheromones and Kairomones: What Receptors Mediate Innate Emotional Responses?
Fortes-Marco, L., Lanuza, E., & Martínez‐Garciá, F. (2013) · The Anatomical Record · doi:10.1002/ar.22745 · Cited by 106
Mammalian pheromones: emerging properties and mechanisms of detection
Stowers, L., & Kuo, T.-H. (2015) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2015.02.005 · Cited by 106
Johnson, M. A., Korsak, L. I. T., Roy, D. S., Valenzuela, D. H., Mosley, C., Magklara, A., Lomvardas, S., Liberles, S. D., & Barnea, G. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1206724109 · Cited by 103
Chemical signals in terrestrial vertebrates: search for design features.
Apps, P., Weldon, P., & Kramer, M. (2015) · Natural product reports (Print) · doi:10.1039/c5np00029g · Cited by 80
Antagonism in olfactory receptor neurons and its implications for the perception of odor mixtures
Reddy, G., Zak, J. D., Vergassola, M., & Murthy, V. N. (2018) · eLife · doi:10.7554/elife.34958 · Cited by 94
Self-citationAntagonistic odor interactions in olfactory sensory neurons are widespread in freely breathing mice
Zak, J. D., Reddy, G., Vergassola, M., & Murthy, V. N. (2020) · Nature Communications · doi:10.1038/s41467-020-17124-5 · Cited by 91
Self-citationCádiz‐Moretti, B., Otero‐García, M., Martínez‐Garciá, F., & Lanuza, E. (2014) · Brain Structure and Function · doi:10.1007/s00429-014-0954-y · Cited by 93
The genomic basis of vomeronasal-mediated behaviour
Ibarra-Soria, X., Levitin, M. O., & Logan, D. W. (2013) · Mammalian Genome · doi:10.1007/s00335-013-9463-1 · Cited by 86
Sensory Ecology of Predator-Induced Phenotypic Plasticity
Weiss, L. C. (2019) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2018.00330 · Cited by 83
First evidence for functional vomeronasal 2 receptor genes in primates
Hohenbrink, P., Mundy, N. I., Zimmermann, E., & Radespiel, U. (2012) · Biology Letters · doi:10.1098/rsbl.2012.1006 · Cited by 83
Principles of odor coding in vertebrates and artificial chemosensory systems
Manzini, I., Schild, D., & Natale, C. D. (2021) · Physiological Reviews · doi:10.1152/physrev.00036.2020 · Cited by 90
Nucleus Accumbens Dopamine Signaling Regulates Sexual Preference for Females in Male Mice
Beny, Y., Zilkha, N., Lavi‐Avnon, Y., Bezalel, N., Rogachev, I., Brandis, A. S., Dayan, M., & Kimchi, T. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.11.062 · Cited by 85
Distribution of oxytocin and co-localization with arginine vasopressin in the brain of mice
Otero‐García, M., Agustín‐Pavón, C., Lanuza, E., & Martínez‐Garciá, F. (2015) · Brain Structure and Function · doi:10.1007/s00429-015-1111-y · Cited by 80
Guimarães, A. T. B., Freitas, Í. N., Mubarak, N. M., Rahman, M. M., Rodrigues, F. P., Rodrigues, A. S. D. L., Barceló, ., Islam, A. R. M. T., & Malafaia, G. (2022) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2022.130004 · Cited by 77
Neural control of sexually dimorphic behaviors
Manoli, D. S., Fan, P., Fraser, E. J., & Shah, N. M. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.04.005 · Cited by 78
Neural coding of sex-specific social information in the mouse brain
Li, Y., & Dulac, C. G. (2018) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2018.07.005 · Cited by 76
Self-citationState-dependent responses to sex pheromones in mouse
Stowers, L., & Liberles, S. D. (2016) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2016.04.001 · Cited by 81
Trouillet, A., Keller, M., Weiss, J., Leinders‐Zufall, T., Birnbaumer, L., Zufall, F., & Chamero, P. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1821492116 · Cited by 74
Processing by the main olfactory system of chemosignals that facilitate mammalian reproduction
Baum, M. J., & Cherry, J. A. (2014) · Hormones and Behavior · doi:10.1016/j.yhbeh.2014.06.003 · Cited by 79
Molecular Evolutionary Characterization of a V1R Subfamily Unique to Strepsirrhine Primates
Yoder, A. D., Chan, L. M., dos Reis, M., Larsen, P. A., Campbell, C. R., Rasoloarison, R. M., Barrett, M., Roos, C., Kappeler, P. M., Bielawski, J. P., et al. (2014) · Genome Biology and Evolution · doi:10.1093/gbe/evu006 · Cited by 73
Sexual rejection via a vomeronasal receptor-triggered limbic circuit
Osakada, T., Ishii, K. K., Mori, H., Eguchi, R., Ferrero, D. M., Yoshihara, Y., Liberles, S. D., Miyamichi, K., & Touhara, K. (2018) · Nature Communications · doi:10.1038/s41467-018-07003-5 · Cited by 78
Urocortin-3 neurons in the mouse perifornical area promote infant-directed neglect and aggression
Autry, A. E., Wu, Z., Kapoor, V., Kohl, J., Bambah-Mukku, D., Rubinstein, N. D., Marin-Rodriguez, B., Carta, I., Sedwick, V. M., Tang, M., et al. (2021) · eLife · doi:10.7554/elife.64680 · Cited by 74
Self-citationChemosensory signals and their receptors in the olfactory neural system
Ihara, S., Yoshikawa, K., & Touhara, K. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.08.063 · Cited by 72
Chen, A.-X., Yan, J., Zhang, W., Wang, L. A., Yu, Z., Ding, X., Wang, D., Zhang, M., Zhang, Y., Song, N., et al. (2020) · Neuron · doi:10.1016/j.neuron.2020.08.025 · Cited by 66
Organization of Vomeronasal Sensory Coding Revealed by Fast Volumetric Calcium Imaging
Turaga, D., & Holy, T. E. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.5339-11.2012 · Cited by 66
Experience-Dependent Plasticity Drives Individual Differences in Pheromone-Sensing Neurons
Xu, P. S., Lee, D., & Holy, T. E. (2016) · Neuron · doi:10.1016/j.neuron.2016.07.034 · Cited by 65
Mutual influences between the main olfactory and vomeronasal systems in development and evolution
Suárez, R., García‐González, D., & de Castro, F. (2012) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2012.00050 · Cited by 64
Olfactory marker protein (OMP) regulates formation and refinement of the olfactory glomerular map
Albeanu, D. F., Provost, A. C., Agarwal, P., Soucy, E. R., Zak, J. D., & Murthy, V. N. (2018) · Nature Communications · doi:10.1038/s41467-018-07544-9 · Cited by 62
Self-citationMolecular and neural control of sexually dimorphic social behaviors
Yang, T., & Shah, N. M. (2016) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2016.04.015 · Cited by 61
The evolution of red color vision is linked to coordinated rhodopsin tuning in lycaenid butterflies
Liénard, M. A., Bernard, G. D., Allen, A. A., Lassance, J., Song, S., Childers, R. R., Yu, N., Ye, D., Stephenson, A., Valencia‐Montoya, W. A., et al. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2008986118 · Cited by 57
Gutiérrez‐Castellanos, N., Pardo‐Bellver, C., Martínez‐Garciá, F., & Lanuza, E. (2013) · European Journal of Neuroscience · doi:10.1111/ejn.12393 · Cited by 59
Functional organization of glomerular maps in the mouse accessory olfactory bulb
Hammen, G. F., Turaga, D., Holy, T. E., & Meeks, J. P. (2014) · Nature Neuroscience · doi:10.1038/nn.3738 · Cited by 58
Roles of sex and gonadal steroids in mammalian pheromonal communication
Baum, M. J., & Bakker, J. (2013) · Frontiers in Neuroendocrinology · doi:10.1016/j.yfrne.2013.07.004 · Cited by 58
Xie, Z., Gu, H., Huang, M., Cheng, X., Shang, C., Tao, T., Li, D., Xie, Y., Zhao, J., Lü, W., et al. (2022) · Nature Neuroscience · doi:10.1038/s41593-021-00985-4 · Cited by 56
Ominous odors: olfactory control of instinctive fear and aggression in mice
Stowers, L., Cameron, P. A., & Keller, J. A. (2013) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2013.01.007 · Cited by 59
Visualization of odor-induced neuronal activity by immediate early gene expression
Bepari, A. K., Watanabe, K., Yamaguchi, M., Tamamaki, N., & Takebayashi, H. (2012) · BMC Neuroscience · doi:10.1186/1471-2202-13-140 · Cited by 58
van der Linden, C., Jakob, S., Gupta, P., Dulac, C. G., & Santoro, S. W. (2018) · Nature Communications · doi:10.1038/s41467-018-07120-1 · Cited by 58
Self-citationBaum, M. J. (2012) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2012.00020 · Cited by 56
Zilkha, N., Sofer, Y., Beny, Y., & Kimchi, T. (2016) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2016.04.014 · Cited by 52
Coding of pheromones by vomeronasal receptors
Tirindelli, R. (2021) · Cell and Tissue Research · doi:10.1007/s00441-020-03376-6 · Cited by 53
Behrens, M., Frank, O., Rawel, H. M., Ahuja, G., Potting, C., Hofmann, T. F., Meyerhof, W., & Korsching, S. I. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.573162 · Cited by 52
Faecal bile acids are natural ligands of the mouse accessory olfactory system
Doyle, W. I., Dinser, J. A., Cansler, H. L., Zhang, X., Dinh, D. D., Browder, N. S., Riddington, I. M., & Meeks, J. P. (2016) · Nature Communications · doi:10.1038/ncomms11936 · Cited by 52
Sensory coding mechanisms revealed by optical tagging of physiologically defined neuronal types
Lee, D., Kume, M., & Holy, T. E. (2019) · Science · doi:10.1126/science.aax8055 · Cited by 50
Larsen, P. A., Heilman, A. M., & Yoder, A. D. (2014) · BMC Genomics · doi:10.1186/1471-2164-15-720 · Cited by 50
Innate and learned aspects of pheromone-mediated social behaviours
Beny, Y., & Kimchi, T. (2014) · Animal Behaviour · doi:10.1016/j.anbehav.2014.09.014 · Cited by 55
Oboti, L., Ibarra-Soria, X., Pérez‐Gómez, A., Schmid, A., Pyrski, M. M., Paschek, N., Kircher, S., Logan, D. W., Leinders‐Zufall, T., Zufall, F., et al. (2015) · BMC Biology · doi:10.1186/s12915-015-0211-8 · Cited by 46
Reading Out Olfactory Receptors: Feedforward Circuits Detect Odors in Mixtures without Demixing
Mathis, A., Rokni, D., Kapoor, V., Bethge, M., & Murthy, V. N. (2016) · Neuron · doi:10.1016/j.neuron.2016.08.007 · Cited by 48
Self-citationMorphological and Immunohistochemical Features of the Vomeronasal System in Dogs
Salazar, I., Cifuentes, J. M., & Sánchez‐Quinteiro, P. (2012) · The Anatomical Record · doi:10.1002/ar.22617 · Cited by 46
Arakawa, H., Kelliher, K. R., Zufall, F., & Munger, S. D. (2013) · Chemical Senses · doi:10.1093/chemse/bjt015 · Cited by 46
A Nose for Death: Integrating Trophic and Informational Networks for Conservation and Management
Jones, M. E., Apfelbach, R., Banks, P. B., Cameron, E. Z., Dickman, C. R., Frank, A. S. K., McLean, S., McGregor, I. S., Müller‐Schwarze, D., Parsons, M. H., et al. (2016) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2016.00124 · Cited by 46
Excreted Steroids in Vertebrate Social Communication
Doyle, W. I., & Meeks, J. P. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.2488-17.2018 · Cited by 45
Functional evolution of vertebrate sensory receptors
Baldwin, M. W., & Ko, M. (2020) · Hormones and Behavior · doi:10.1016/j.yhbeh.2020.104771 · Cited by 44
Zebrafish olfactory receptors ORAs differentially detect bile acids and bile salts
Cong, X., Zheng, Q., Ren, W., Chéron, J.-B., Fiorucci, S., Wen, T., Zhang, C., Yu, H., Golebiowski, J., & Yu, Y. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.006483 · Cited by 42
Genomic variation in the vomeronasal receptor gene repertoires of inbred mice
Wynn, E. H., Sánchez-Andrade, G., Carss, K., & Logan, D. W. (2012) · BMC Genomics · doi:10.1186/1471-2164-13-415 · Cited by 38
Bufe, B., Teuchert, Y., Schmid, A., Pyrski, M. M., Pérez‐Gómez, A., Eisenbeis, J., Timm, T., Ishii, T., Lochnit, G., Bischoff, M., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-12842-x · Cited by 45
deCarvalho, T., Akitake, C. M., Thisse, C., Thisse, B., & Halpern, M. E. (2013) · Frontiers in Neural Circuits · doi:10.3389/fncir.2013.00098 · Cited by 41
Sparse and stereotyped encoding implicates a core glomerulus for ant alarm behavior
Hart, T., Frank, D. D., Lopes, L. E., Olivos-Cisneros, L., Lacy, K. D., Trible, W., Ritger, A. L., Valdés-Rodríguez, S., & Kronauer, D. J. C. (2023) · Cell · doi:10.1016/j.cell.2023.05.025 · Cited by 39
Smadja, C. M., Loire, É., Caminade, P., Thoma, M., Latour, Y., Roux, C., Thoß, M., Penn, D. J., Ganem, G., & Boursot, P. (2015) · Molecular Ecology · doi:10.1111/mec.13301 · Cited by 39
Identification of an Intra- and Inter-specific Tear Protein Signal in Rodents
Tsunoda, M., Miyamichi, K., Eguchi, R., Sakuma, Y., Yoshihara, Y., Kikusui, T., Kuwahara, M., & Touhara, K. (2018) · Current Biology · doi:10.1016/j.cub.2018.02.060 · Cited by 38
Neural circuit control of innate behaviors
Wei, X., Jiao, Z., Senol, E., Yao, J., Zhao, M., Zhao, Z., Chen, X., Cao, P., Fu, Y., Gao, Z., et al. (2021) · Science China Life Sciences · doi:10.1007/s11427-021-2043-2 · Cited by 40
Metadata
- Authors
- Isogai, Y., Si, S., Pont-Lezica, L., Tan, T., Kapoor, V., Murthy, V. N., & Dulac, C.
- Affiliations
- Harvard University (US)
- Howard Hughes Medical Institute (US)
- Corresponding author
- Dulac, Catherine
- Venue
- Nature
- Published
- 2011-09-21
- Volume
- 478
- Issue
- 7368
- Pages
- 241-245
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC3192931
- OpenAlex
- W2152243497
- Cited by
- 317
- References
- 34
- Citations by year
- 2026: 10 · 2025: 8 · 2024: 22 · 2023: 21 · 2022: 15 · 2021: 25 · 2020: 24 · 2019: 19 · 2018: 27 · 2017: 16 · 2016: 27 · 2015: 21 · 2014: 31 · 2013: 25 · 2012: 21
- FWCI
- 13.80
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Digital Access to Scholarship at Harvard (DASH) (Harvard University) (submittedVersion, cc-by)
- RePEc: Research Papers in Economics (submittedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Funders
- Howard Hughes Medical Institute
- National Institute on Deafness and Other Communication Disorders (R01DC003903, R01DC009019)
- Topics
- Life Sciences › Neuroscience › Sensory Systems › Olfactory and Sensory Function Studies
- Life Sciences › Neuroscience › Sensory Systems › Ion Channels and Receptors
- Health Sciences › Nursing › Nutrition and Dietetics › Biochemical Analysis and Sensing Techniques
- Keywords
- vomeronasal organ, vomeronasal receptors, pheromone receptors, V1R, V2 receptor, kairomones, pheromones, innate behavior, social behavior, aggression, mating behavior, mice
- MeSH terms
- Animals, Birds, Chemoreceptor Cells, Cues, Female, Gene Expression Regulation, Male, Mammals, Pheromones, Predatory Behavior, Sex Characteristics, Species Specificity, Receptors, Odorant, Vomeronasal Organ, Mice, Early Growth Response Protein 1
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