The DOI matches its Crossref record; 37 of the 37 references it cites were found in a registry or an index.
Laminar Specificity of Functional Input to Distinct Types of Inhibitory Cortical Neurons
Open accessAbstract
Despite the presence of numerous inhibitory cell types, laminar excitatory input has only been characterized for limited identified types, and it is unknown whether there are differences between cell types in their laminar sources of inhibitory input. In the present study, we characterized sources of local input to nine distinct types of layer 2/3 inhibitory neurons in living slices of mouse somatosensory cortex. Whole-cell recordings from identified cell types, facilitated by use of transgenic mice expressing green fluorescent protein in limited inhibitory neuron populations, were combined with laser scanning photostimulation. We found that each inhibitory cell type received distinct excitatory and inhibitory laminar input patterns. Excitatory inputs could be grouped into three categories. All inhibitory cell types received strong excitation from layer 2/3, and for calretinin (CR)-positive Martinotti cells and burst-spiking interneurons, this was their dominant source of excitatory input. Three other cell types, including fast-spiking basket cells, CR-negative Martinotti cells, and bipolar interneurons, also received strong excitatory input from layer 4. The remaining four inhibitory cell types, including chandelier cells, neurogliaform cells, irregular spiking basket cells, and regular spiking presumptive basket cells, received strong excitatory input from layer 5A and not layer 4. Laminar sources of inhibitory input varied between cell types and could not be predicted from the sources of excitatory input. Thus, there are cell-type specific differences in laminar sources of both excitation and inhibition, and complementary input patterns from layer 4 versus layer 5A suggest cell type differences in their relationships to lemniscal versus paralemniscal pathways.
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 source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“some reports have found different excitatory input sources and in vivo responses between PV FS basket and chandelier INs”
From GABAergic Interneurons in the Neocortex: From Cellular Properties to Circuits (2016) · cites this paper as Xu and Callaway, 2009
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“L2/3 bipolar INs have been shown to receive inputs from several layers, which was less common for most other cell types studied (Xu and Callaway, 2009).”
From GABAergic Interneurons in the Neocortex: From Cellular Properties to Circuits (2016) · cites this paper as Xu and Callaway, 2009
The cited source says what the claim attributes to it.
In the citing paper
“Although so far only minor electrophysiological or morphological differences between CR+ and CR- Sst INs have been identified, distinct excitatory input patterns have been found (Xu and Callaway, 2009; Xu et al., 2006).”
From GABAergic Interneurons in the Neocortex: From Cellular Properties to Circuits (2016) · cites this paper as Xu and Callaway, 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
Interneurons of the neocortical inhibitory system
Markram, H., Toledo-Rodriguez, M., Wang, Y., Gupta, A., Silberberg, G., & Wu, C. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1519 · Cited by 2,954
Petilla terminology: nomenclature of features of GABAergic interneurons of the cerebral cortex
The Petilla Interneuron Nomenclature Group (PING) (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2402 · Cited by 1,491
Two networks of electrically coupled inhibitory neurons in neocortex
Gibson, J. R., Beierlein, M., & Connors, B. W. (1999) · Nature · doi:10.1038/47035 · Cited by 1,404
Organizing principles for a diversity of GABAergic interneurons and synapses in the neocortex
Gupta, A., Wang, Y., & Markram, H. (2000) · Science · doi:10.1126/science.287.5451.273 · Cited by 1,036
Somogyi, P., Tamás, G., Luján, R., & Buhl, E. H. (1998) · Brain Research Reviews · doi:10.1016/s0165-0173(97)00061-1 · Cited by 876
Disynaptic Inhibition between Neocortical Pyramidal Cells Mediated by Martinotti Cells
Silberberg, G., & Markram, H. (2007) · Neuron · doi:10.1016/j.neuron.2007.02.012 · Cited by 768
Excitatory cortical neurons form fine-scale functional networks
Yoshimura, Y., Dantzker, J. L. M., & Callaway, E. M. (2005) · Nature · doi:10.1038/nature03252 · Cited by 601
Self-citationChattopadhyaya, B., Di Cristo, G., Higashiyama, H., Knott, G. W., Kuhlman, S. J., Welker, E., & Huang, Z. J. (2004) · The Journal of Neuroscience · doi:10.1523/jneurosci.1851-04.2004 · Cited by 596
Pyramidal cell communication within local networks in layer 2/3 of rat neocortex.
Holmgren, C., Harkany, T., Svennenfors, B., & Zilberter, Y. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2003.044784 · Cited by 573
Synaptic basis for intense thalamocortical activation of feedforward inhibitory cells in neocortex
Cruikshank, S. J., Lewis, T. J., & Connors, B. W. (2007) · Nature Neuroscience · doi:10.1038/nn1861 · Cited by 558
Cited by
Sorted by citations
GABAergic Interneurons in the Neocortex: From Cellular Properties to Circuits
Tremblay, R., Lee, S., & Rudy, B. (2016) · Neuron · doi:10.1016/j.neuron.2016.06.033 · Cited by 2,033
Three groups of interneurons account for nearly 100% of neocortical GABAergic neurons
Rudy, B., Fishell, G., Lee, S., & Hjerling‐Leffler, J. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20853 · Cited by 1,420
Principles of connectivity among morphologically defined cell types in adult neocortex
Jiang, X., Shen, S., Cadwell, C. R., Berens, P., Sinz, F., Ecker, A. S., Patel, S., & Tolias, A. S. (2015) · Science · doi:10.1126/science.aac9462 · Cited by 908
Parallel processing strategies of the primate visual system
Nassi, J. J., & Callaway, E. M. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2619 · Cited by 802
Self-citationBroadly tuned response properties of diverse inhibitory neuron subtypes in mouse visual cortex
Kerlin, A. M., Andermann, M. L., Berezovskii, V. K., & Reid, R. C. (2010) · Neuron · doi:10.1016/j.neuron.2010.08.002 · Cited by 613
Dense Inhibitory Connectivity in Neocortex
Fino, E., & Yuste, R. (2011) · Neuron · doi:10.1016/j.neuron.2011.02.025 · Cited by 532
Distinct behavioural and network correlates of two interneuron types in prefrontal cortex
Kvitsiani, D., Ranade, S., Hangya, B., Taniguchi, H., Huang, J. Z., & Kepecs, A. (2013) · Nature · doi:10.1038/nature12176 · Cited by 516
Xu, X., Roby, K. D., & Callaway, E. M. (2010) · Journal of Comparative Neurology · doi:10.1002/cne.22229 · Cited by 429
Self-citationUnique functional properties of somatostatin-expressing GABAergic neurons in mouse barrel cortex
Gentet, L. J., Kremer, Y., Taniguchi, H., Huang, Z. J., Staiger, J. F., & Petersen, C. C. H. (2012) · Nature Neuroscience · doi:10.1038/nn.3051 · Cited by 438
Membrane potential dynamics of GABAergic neurons in the barrel cortex of behaving mice
Gentet, L. J., Avermann, M., Matyas, F., Staiger, J. F., & Petersen, C. C. H. (2010) · Neuron · doi:10.1016/j.neuron.2010.01.006 · Cited by 429
Sound-Driven Synaptic Inhibition in Primary Visual Cortex
Iurilli, G., Ghezzi, D., Olcese, U., Lassi, G., Nazzaro, C., Tonini, R., Tucci, V., Benfenati, F., & Medini, P. (2012) · Neuron · doi:10.1016/j.neuron.2011.12.026 · Cited by 424
Layer-Specific Entrainment of Gamma-Band Neural Activity by the Alpha Rhythm in Monkey Visual Cortex
Spaak, E., Bonnefond, M., Maier, A., Leopold, D. A., & Jensen, O. (2012) · Current Biology · doi:10.1016/j.cub.2012.10.020 · Cited by 385
Somatostatin-expressing neurons in cortical networks
Urban-Ciecko, J., & Barth, A. L. (2016) · Nature Reviews Neuroscience · doi:10.1038/nrn.2016.53 · Cited by 374
Feldmeyer, D., Brecht, M., Helmchen, F., Petersen, C. C. H., Poulet, J. F. A., Staiger, J. F., Luhmann, H. J., & Schwarz, C. (2013) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2012.11.002 · Cited by 354
“L2/3, as tactile information of L4 microcircuits is not only transferred to supragranular pyramidal neurons, but also with high efficacy to several types of L2/3 inhibitory neurons (Helmstaedter et al., 2008; Xu and Callaway, 2009; Xu et al., 2010) (Fig.”
BackgroundNeural elements for predictive coding
Shipp, S. (2016) · Frontiers in Psychology · doi:10.3389/fpsyg.2016.01792 · Cited by 340
Long‐range connectivity of mouse primary somatosensory barrel cortex
Aronoff, R., Matyas, F., Mateo, C., Ciron, C., Schneider, B., & Petersen, C. C. H. (2010) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2010.07264.x · Cited by 323
Ibrahim, L. A., Mesik, L., Ji, X., Fang, Q., Li, H.-F., Li, Y.-T., Zingg, B., Zhang, L. I., & Tao, H. W. (2016) · Neuron · doi:10.1016/j.neuron.2016.01.027 · Cited by 298
Optogenetic astrocyte activation modulates response selectivity of visual cortex neurons in vivo
Perea, G., Yang, A., Boyden, E. S., & Sur, M. (2014) · Nature Communications · doi:10.1038/ncomms4262 · Cited by 245
The columnar and laminar organization of inhibitory connections to neocortical excitatory cells
Kätzel, D., Zemelman, B. V., Buetfering, C., Wölfel, M., & Miesenböck, G. (2011) · Nature Neuroscience · doi:10.1038/nn.2687 · Cited by 241
Synaptic Computation and Sensory Processing in Neocortical Layer 2/3
Petersen, C. C. H., & Crochet, S. (2013) · Neuron · doi:10.1016/j.neuron.2013.03.020 · Cited by 249
Mechanisms of Inhibition within the Telencephalon: “Where the Wild Things Are”
Fishell, G., & Rudy, B. (2011) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-061010-113717 · Cited by 233
Distinct molecular programs regulate synapse specificity in cortical inhibitory circuits
Favuzzi, E., Deogracias, R., Marques–Smith, A., Maeso, P. A., Jézéquel, J., Exposito-Alonso, D., Balia, M., Kroon, T., Hinojosa, A. J., Maraver, E. F., et al. (2019) · Science · doi:10.1126/science.aau8977 · Cited by 224
Mejias, J. F., Murray, J. D., Kennedy, H., & Wang, X.-J. (2016) · Science Advances · doi:10.1126/sciadv.1601335 · Cited by 227
Ma, W., Liu, B., Li, Y.-T., Huang, Z. J., Zhang, L. I., & Tao, H. W. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.3248-10.2010 · Cited by 221
Microcircuits of excitatory and inhibitory neurons in layer 2/3 of mouse barrel cortex
Avermann, M., Tomm, C., Matéo, C., Wulfram Gerstner, B., & Petersen, C. C. H. (2012) · Journal of Neurophysiology · doi:10.1152/jn.00917.2011 · Cited by 233
Sun, Y., Nguyen, A. Q., Nguyen, J. P., Le, L., Saur, D., Choi, J., Callaway, E. M., & Xu, X. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.02.030 · Cited by 218
Self-citationPrönneke, A., Scheuer, B., Wagener, R. J., Möck, M., Witte, M., & Staiger, J. F. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv202 · Cited by 204
Complementary control of sensory adaptation by two types of cortical interneurons
Natan, R. G., Briguglio, J. J., Mwilambwe-Tshilobo, L., Jones, S. I., Aizenberg, M., Goldberg, E. M., & Geffen, M. N. (2015) · eLife · doi:10.7554/elife.09868 · Cited by 200
Genetics and Function of Neocortical GABAergic Interneurons in Neurodevelopmental Disorders
Rossignol, E. (2011) · Neural Plasticity · doi:10.1155/2011/649325 · Cited by 192
Somatostatin-Expressing Inhibitory Interneurons in Cortical Circuits
Yavorska, I., & Wehr, M. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00076 · Cited by 185
Integration of GABAergic interneurons into cortical cell assemblies: lessons from embryos and adults
Bartolini, G., Ciceri, G., & Marín, O. (2013) · Neuron · doi:10.1016/j.neuron.2013.08.014 · Cited by 185
Brain-Wide Maps of Synaptic Input to Cortical Interneurons
Wall, N. R., Parra, M. D. L., Sorokin, J. M., Taniguchi, H., Huang, Z. J., & Callaway, E. M. (2016) · Journal of Neuroscience · doi:10.1523/jneurosci.3967-15.2016 · Cited by 186
Self-citationDevelopment and specification of GABAergic cortical interneurons
Kelsom, C., & Lu, W. (2013) · Cell & Bioscience · doi:10.1186/2045-3701-3-19 · Cited by 193
Marques-Smith, A., Lyngholm, D., Kaufmann, A.-K., Stacey, J. A., Hoerder-Suabedissen, A., Becker, E. B. E., Wilson, M. C., Molnár, Z., & Butt, S. J. B. (2016) · Neuron · doi:10.1016/j.neuron.2016.01.015 · Cited by 173
Common Origins of Hippocampal Ivy and Nitric Oxide Synthase Expressing Neurogliaform Cells
Tricoire, L., Pelkey, K. A., Daw, M. I., Sousa, V. H., Miyoshi, G., Jeffries, B., Cauli, B., Fishell, G., & McBain, C. J. (2010) · The Journal of Neuroscience · doi:10.1523/jneurosci.5123-09.2010 · Cited by 171
Microglia Elimination Increases Neural Circuit Connectivity and Activity in Adult Mouse Cortex
Liu, Y., Spangenberg, E. E., Tang, B., Holmes, T. C., Green, K. N., & Xu, X. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.2140-20.2020 · Cited by 169
Self-citationDepolarizing effect of neocortical chandelier neurons
Woodruff, A. (2009) · Frontiers in Neural Circuits · doi:10.3389/neuro.04.015.2009 · Cited by 163
Multiple Transmitter Receptors in Regions and Layers of the Human Cerebral Cortex
Zilles, K., & Palomero‐Gallagher, N. (2017) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2017.00078 · Cited by 150
A Laminar Organization for Selective Cortico-Cortical Communication
D’Souza, R. D., & Burkhalter, A. (2017) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2017.00071 · Cited by 138
Inhibitory Circuits in Cortical Layer 5
Naka, A., & Adesnik, H. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00035 · Cited by 143
Receptive fields and functional architecture in the retina
Balasubramanian, V., & Sterling, P. (2009) · The Journal of Physiology · doi:10.1113/jphysiol.2009.170704 · Cited by 126
State-dependent function of neocortical chandelier cells
Woodruff, A. R., McGarry, L. M., Vogels, T. P., Inan, M., Anderson, S. A., & Yuste, R. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.3894-11.2011 · Cited by 115
Sensory inputs control the integration of neurogliaform interneurons into cortical circuits
De Marco García, N. V., Priya, R., Tuncdemir, S. N., Fishell, G., & Karayannis, T. (2015) · Nature Neuroscience · doi:10.1038/nn.3946 · Cited by 117
Traumatic Brain Injury and Neuronal Functionality Changes in Sensory Cortex
Carron, S. F., Alwis, D. S., & Rajan, R. (2016) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2016.00047 · Cited by 115
Lodato, S., Tomassy, G. S., De Leonibus, E., Uzcategui, Y. G., Andolfi, G., Armentano, M., Touzot, A., Gaztelu, J. M., Arlotta, P., Menendez de la Prida, L., et al. (2011) · The Journal of Neuroscience · doi:10.1523/jneurosci.6580-10.2011 · Cited by 112
State-dependent function of neocortical chandelier cells
Woodruff, A. R., Vogels, T. P., McGarry, L. M., Inan, M., Anderson, S. A., & Yuste, R. (2010) · Columbia Academic Commons (Columbia University) · doi:10.7916/d8416wck · Cited by 111
Genetic dissection of GABAergic neural circuits in mouse neocortex
Taniguchi, H. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00008 · Cited by 106
Matéo, C., Avermann, M., Gentet, L. J., Zhang, F., Deisseroth, K. A., & Petersen, C. C. H. (2011) · Current Biology · doi:10.1016/j.cub.2011.08.028 · Cited by 100
The Enigmatic Function of Chandelier Cells
Woodruff, A. R., Anderson, S. A., & Yuste, R. (2010) · Frontiers in Neuroscience · doi:10.3389/fnins.2010.00201 · Cited by 97
GABAergic interneurons form transient layer-specific circuits in early postnatal neocortex
Anastasiades, P. G., Marques-Smith, A., Lyngholm, D., Lickiss, T., Raffiq, S., Kätzel, D., Miesenböck, G., & Butt, S. J. B. (2016) · Nature Communications · doi:10.1038/ncomms10584 · Cited by 87
Otsuka, T., & Kawaguchi, Y. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.2219-09.2009 · Cited by 99
Hsu, Y. A., Tempest, L., Quina, L. A., Wei, A. D., Zeng, H., & Turner, E. E. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.2927-13.2013 · Cited by 95
Lee, A. J., Wang, G., Jiang, X., Johnson, S. M., Hoang, E. T., Lanté, F., Stornetta, R. L., Beenhakker, M. P., Shen, Y., & Julius Zhu, J. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhu020 · Cited by 94
Dense and Overlapping Innervation of Pyramidal Neurons by Chandelier Cells
Inan, M., Blázquez‐Llorca, L., Merchán-Pérez, Á., Anderson, S. A., DeFelipe, J., & Yuste, R. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.4049-12.2013 · Cited by 94
Veit, J., Handy, G., Mossing, D. P., Doiron, B., & Adesnik, H. (2022) · Neuron · doi:10.1016/j.neuron.2022.10.036 · Cited by 84
A whole-brain monosynaptic input connectome to neuron classes in mouse visual cortex
Yao, S., Wang, Q., Hirokawa, K. E., Ouellette, B., Ahmed, R., Bomben, J., Brouner, K., Casal, L., Caldejon, S., Cho, A., et al. (2022) · Nature Neuroscience · doi:10.1038/s41593-022-01219-x · Cited by 91
Revisiting enigmatic cortical calretinin-expressing interneurons
Cauli, B., Zhou, X., Tricoire, L., Toussay, X., & Staiger, J. F. (2014) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00052 · Cited by 86
Nienborg, H., Hasenstaub, A. R., Nauhaus, I., Taniguchi, H., Huang, Z. J., & Callaway, E. M. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.5320-12.2013 · Cited by 89
Self-citationXu, X., Olivas, N. D., Ikrar, T., Peng, T., Holmes, T. C., Nie, Q., & Shi, Y. (2016) · The Journal of Physiology · doi:10.1113/jp271891 · Cited by 83
Self-citationInhibitory Regulation of Dendritic Activity in vivo
Palmer, L. M., Murayama, M., & Larkum, M. E. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00026 · Cited by 88
Apicella, A. J., Wickersham, I. R., Seung, H. S., & Shepherd, G. M. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.0011-12.2012 · Cited by 86
Höfflin, F., Jäck, A., Riedel, C., Mack-Bucher, J., Roos, J., Corcelli, C., Schultz, C., Wahle, P., & Engelhardt, M. (2017) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2017.00332 · Cited by 78
Neurons on the Move: Migration and Lamination of Cortical Interneurons
Faux, C. H., Rakić, S., Andrews, W. D., & Britto, J. M. (2012) · Neurosignals · doi:10.1159/000334489 · Cited by 88
Mòdol, L., Cobianchi, S., & Navarro, X. (2014) · Pain · doi:10.1016/j.pain.2014.05.004 · Cited by 79
Jang, H. J., Chung, H., Rowland, J. M., Richards, B. A., Kohl, M. M., & Kwag, J. (2020) · Science Advances · doi:10.1126/sciadv.aay5333 · Cited by 73
Recording of brain activity across spatial scales
Lewis, C., Bosman, C. A., & Fries, P. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.12.007 · Cited by 78
Functional diversity of supragranular GABAergic neurons in the barrel cortex
Gentet, L. J. (2012) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00052 · Cited by 83
Synapse-specific inhibitory control of hippocampal feedback inhibitory circuit
Chamberland, S. (2010) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2010.00130 · Cited by 75
Plasticity of Binocularity and Visual Acuity Are Differentially Limited by Nogo Receptor
Stephany, C.-É., Chan, L. L.-H., Parivash, S. N., Dorton, H. M., Piechowicz, M., Qiu, S., & McGee, A. W. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.0545-14.2014 · Cited by 72
Antonio, A. S., Liban, K., Ikrar, T., Tsyganovskiy, E., & Xu, X. (2013) · The Journal of Comparative Neurology · doi:10.1002/cne.23486 · Cited by 72
Self-citationMesik, L., Ma, W., Li, L., Ibrahim, L. A., Huang, Z. J., Zhang, L. I., & Tao, H. W. (2015) · Frontiers in Neural Circuits · doi:10.3389/fncir.2015.00022 · Cited by 74
Towards a “canonical” agranular cortical microcircuit
Beul, S. F., & Hilgetag, C. C. (2015) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2014.00165 · Cited by 71
Mechanisms underlying the response of mouse cortical networks to optogenetic manipulation
Mahrach, A., Chen, G., Li, N., van Vreeswijk, C., & Hansel, D. (2020) · eLife · doi:10.7554/elife.49967 · Cited by 68
Cortical Circuits of Callosal GABAergic Neurons
Rock, C., Zurita, H., Lebby, S., Wilson, C. J., & Apicella, A. J. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx025 · Cited by 73
Electrophysiological Heterogeneity of Fast-Spiking Interneurons: Chandelier versus Basket Cells
Povysheva, N. V., Zaitsev, A. V., González‐Burgos, G., & Lewis, D. A. (2013) · PLoS ONE · doi:10.1371/journal.pone.0070553 · Cited by 70
Parvalbumin and GABA Microcircuits in the Mouse Superior Colliculus
Villalobos, C. A., Wu, Q., Lee, P. H., May, P. J., & Basso, M. A. (2018) · Frontiers in Neural Circuits · doi:10.3389/fncir.2018.00035 · Cited by 62
Griffen, T. C. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00091 · Cited by 64
Ninomiya, T., Dougherty, K., Godlove, D. C., Schall, J. D., & Maier, A. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00624.2014 · Cited by 60
Li, Y., Aimone, J. B., Xu, X., Callaway, E. M., & Gage, F. H. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1120754109 · Cited by 62
Self-citationCircuit asymmetries underlie functional lateralization in the mouse auditory cortex
Levy, R. B., Marquarding, T., Reid, A. P., Pun, C. M., Renier, N., & Oviedo, H. V. (2019) · Nature Communications · doi:10.1038/s41467-019-10690-3 · Cited by 65
Liu, Y., Ehrengruber, M. U., Negwer, M., Shao, H., Cetin, A. H., & Lyon, D. C. (2013) · Current Biology · doi:10.1016/j.cub.2013.07.033 · Cited by 52
Wood, L., & Shepherd, G. M. (2010) · Neurobiology of Disease · doi:10.1016/j.nbd.2010.01.018 · Cited by 57
Oligodendrocytes as Regulators of Neuronal Networks during Early Postnatal Development
Doretto, S., Malerba, M., Ramos, M., Ikrar, T., Kinoshita, C., Mei, C. D., Tirotta, E., Xu, X., & Borrelli, E. (2011) · PLoS ONE · doi:10.1371/journal.pone.0019849 · Cited by 54
Self-citationPeng, Y. W., Lu, Z., Li, G., Piechowicz, M., Anderson, M. J., Uddin, Y., Wu, J., & Qiu, S. (2016) · Molecular Psychiatry · doi:10.1038/mp.2015.182 · Cited by 55
Eto, K., Ishibashi, H., Yoshimura, T., Watanabe, M., Miyamoto, A., Ikenaka, K., Moorhouse, A. J., & Nabekura, J. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.2104-12.2012 · Cited by 50
Anastasiades, P. G., & Butt, S. J. B. (2012) · The Journal of Neuroscience · doi:10.1523/jneurosci.1262-12.2012 · Cited by 49
Poorthuis, R. B., & Mansvelder, H. D. (2013) · Biochemical Pharmacology · doi:10.1016/j.bcp.2013.07.003 · Cited by 54
Apicella, A. J., & Marchionni, I. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.811484 · Cited by 45
Distinct Circuits for Recovery of Eye Dominance and Acuity in Murine Amblyopia
Stephany, C.-É., Ma, X., Dorton, H. M., Wu, J., Solomon, A. M., Frantz, M. G., Qiu, S., & McGee, A. W. (2018) · Current Biology · doi:10.1016/j.cub.2018.04.055 · Cited by 47
Cell Type-Specific Control of Neuronal Responsiveness by Gamma-Band Oscillatory Inhibition
Otte, S. L., Hasenstaub, A. R., & Callaway, E. M. (2010) · Journal of Neuroscience · doi:10.1523/jneurosci.4818-09.2010 · Cited by 43
Self-citationLocal and Long-Range Circuit Connections to Hilar Mossy Cells in the Dentate Gyrus
Sun, Y., Grieco, S. F., Holmes, T. C., & Xu, X. (2017) · eNeuro · doi:10.1523/eneuro.0097-17.2017 · Cited by 40
Self-citationXu, X., Olivas, N. D., Levi, R., Ikrar, T., & Nenadić, Z. (2010) · Journal of Neurophysiology · doi:10.1152/jn.00992.2009 · Cited by 41
Self-citationLayer 5 Callosal Parvalbumin-Expressing Neurons: A Distinct Functional Group of GABAergic Neurons
Zurita, H., Feyen, P., & Apicella, A. J. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00053 · Cited by 42
Kirkcaldie, M. (2011) · Elsevier eBooks · doi:10.1016/b978-0-12-369497-3.10004-4 · Cited by 45
Spatial distribution of neurons innervated by chandelier cells
Blázquez‐Llorca, L., Woodruff, A. R., Inan, M., Anderson, S. A., Yuste, R., DeFelipe, J., & Merchán-Pérez, Á. (2014) · Brain Structure and Function · doi:10.1007/s00429-014-0828-3 · Cited by 36
Age-related neurochemical changes in the rhesus macaque inferior colliculus
Engle, J. R., Gray, D. T., Turner, H. N., Udell, J. B. M., & Recanzone, G. H. (2014) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2014.00073 · Cited by 39
Brill, J., & Huguenard, J. R. (2010) · Cerebral Cortex · doi:10.1093/cercor/bhq040 · Cited by 38
A comprehensive data-driven model of cat primary visual cortex
Antolík, J., Cagnol, R., Rózsa, T., Monier, C., Frégnac, Y., & Davison, A. P. (2024) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1012342 · Cited by 35
Chandelier Cells in Functional and Dysfunctional Neural Circuits
Wang, Y., Zhang, P., & Wyskiel, D. R. (2016) · Frontiers in Neural Circuits · doi:10.3389/fncir.2016.00033 · Cited by 40
Igarashi, J., YAMAURA, H., & Yamazaki, T. (2019) · Frontiers in Neuroinformatics · doi:10.3389/fninf.2019.00071 · Cited by 36
Metadata
- Authors
- Xu, X., & Callaway, E. M.
- Affiliations
- Salk Institute for Biological Studies (US)
- Corresponding author
- Callaway, Edward M.
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2009-01-07
- Volume
- 29
- Issue
- 1
- Pages
- 70-85
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC2656387
- OpenAlex
- W2124626486
- Cited by
- 218
- References
- 37
- Citations by year
- 2026: 4 · 2025: 6 · 2024: 7 · 2023: 11 · 2022: 10 · 2021: 4 · 2020: 14 · 2019: 8 · 2018: 6 · 2017: 13 · 2016: 22 · 2015: 17 · 2014: 21 · 2013: 17 · 2012: 17
- FWCI
- 8.18
- 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
- National Institutes of Health
- National Institute of Mental Health (MH063912, R01MH063912)
- National Institute on Drug Abuse (R00DA023700, K99DA023700)
- National Eye Institute (EY-010742, R01EY010742)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- inhibitory interneurons, laminar specificity, somatosensory cortex, layer 2/3, layer 4, Martinotti cells, basket cells, chandelier cells, neurogliaform cells, calretinin, excitatory synaptic input, inhibitory synaptic input, lemniscal pathway
- MeSH terms
- Action Potentials, Analysis of Variance, Animals, Animals, Newborn, Dendrites, Electric Stimulation, Mice, Transgenic, Nerve Net, Neural Inhibition, Neurons, Photic Stimulation, Proteins, RNA, Messenger, Somatosensory Cortex, Somatostatin, Models, Statistical, Patch-Clamp Techniques, Statistics, Nonparametric, Excitatory Postsynaptic Potentials, Green Fluorescent Proteins, Mice, S100 Calcium Binding Protein G, Calbindin 2, 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