Cited by 530Neuroscience and Neuropharmacology ResearchNeurogenesis and neuroplasticity mechanismsVisual perception and processing mechanisms

The DOI matches its Crossref record; 15 of the 15 references it cites were found in a registry or an index.

A specific ‘axo-axonal’ interneuron in the visual cortex of the rat

Somogyi, P.·1977·Brain Research

DOI 10.1016/0006-8993(77)90808-3

Open this paper in CoChat — free account

Integrity signals

Registry

Crossref · 10.1016/0006-8993(77)90808-3

Cites

15 of 15 references verified0 citation errors · 0 not checkable

Statistics

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

Claims the paper makes

We couldn’t retrieve this paper’s full text, 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?

Characteristics of Excitatory and Inhibitory Synapses in the Central Nervous System of the Cat
UCHIZONO, K. (1965) · Nature · doi:10.1038/207642a0 · Cited by 917
The ‘module-concept’ in cerebral cortex architecture
Szentágothai, J. (1975) · Brain Research · doi:10.1016/0006-8993(75)90122-5 · Cited by 614
Varieties and distribution of non‐pyramidal cells in the somatic sensory cortex of the squirrel monkey
Jones, E. G. (1975) · The Journal of Comparative Neurology · doi:10.1002/cne.901600204 · Cited by 593
Conceptual Models of Neural Organization.
Pritchard, J. J. (1976) · Europe PMC (PubMed Central) · Cited by 514
THE AXON HILLOCK AND THE INITIAL SEGMENT
Palay, S. L., Sotelo, C., Peters, A., & Orkand, P. M. (1968) · The Journal of Cell Biology · doi:10.1083/jcb.38.1.193 · Cited by 489
Conceptual models of neural organization.
Szentágothai, J., & Arbib, M. A. (1974) · PubMed · Cited by 329
Electron microscopy of presynaptic organelles of the spinal cord.
Eg, G. (1963) · PubMed · Cited by 312
TWO INHIBITORY MECHANISMS IN THE MAUTHNER NEURONS OF GOLDFISH
Furukawa, T., & Furshpan, E. J. (1963) · Journal of Neurophysiology · doi:10.1152/jn.1963.26.1.140 · Cited by 303
THE SMALL PYRAMIDAL NEURON OF THE RAT CEREBRAL CORTEX
Peters, A., Proskauer, C. C., & Kaiserman‐Abramof, I. R. (1968) · The Journal of Cell Biology · doi:10.1083/jcb.39.3.604 · Cited by 272
Fine structure of the synaptic endings on the Mauthner cell of the goldfish
Nakajima, Y. (1974) · The Journal of Comparative Neurology · doi:10.1002/cne.901560402 · Cited by 162

Show all 15 references

Research works printed but not linked: 2

Hámori, 1965, The Purkinje cell basket: ultrastructure of an inhibitory synapse, Acta Biol. Acad. Sci. hung., 15, 465
Schober, 1975, Die visuelle Kortex der Ratte Cytoarchitektonik und stereotaktische Parameter, Z. mikrosk.-anat. Forsch., 89, 431

Sorted by citations

Items 201–300 of 530

Selectivity of neuronal [3H]GABA accumulation in the visual cortex as revealed by Golgi staining of the labeled neurons
Somogyi, P., Freund, T. ́. F., Halász, N., & ́rdy, Z. ́. F. K. (1981) · Brain Research · doi:10.1016/0006-8993(81)90849-0 · Cited by 75
Self-citation
Large Volume Electron Microscopy and Neural Microcircuit Analysis
Kubota, Y., Sohn, J., & Kawaguchi, Y. (2018) · Frontiers in Neural Circuits · doi:10.3389/fncir.2018.00098 · Cited by 74
The chandelier cell, form and function
Inan, M., & Anderson, S. A. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.01.009 · Cited by 83
Golgi preparations as a tool in neuropathology with particular reference to investigations of the human telencephalic cortex
Braak, H., & Braak, E. (1985) · Progress in Neurobiology · doi:10.1016/0301-0082(85)90001-2 · Cited by 73
Strategically Positioned Inhibitory Synapses of Axo-axonic Cells Potently Control Principal Neuron Spiking in the Basolateral Amygdala
Veres, J. M., Nagy, G. A., Vereczki, V., Andrási, T., & Hájos, N. (2014) · Journal of Neuroscience · doi:10.1523/jneurosci.2232-14.2014 · Cited by 66
Quantitative ultrastructural analysis of basket and axo-axonic cell terminals in the mouse hippocampus
Takács, V. T., Szőnyi, A., Freund, T. F., Nyíri, G., & Gulyás, A. I. (2014) · Brain Structure and Function · doi:10.1007/s00429-013-0692-6 · Cited by 71
Local circuit neurons of macaque monkey striate cortex: III. Neurons of laminae 4B, 4A, and 3B
Lund, J. S., & Yoshioka, T. (1991) · The Journal of Comparative Neurology · doi:10.1002/cne.903110206 · Cited by 69
Untitled work
Fashena, D. (1999) · doi:10.1002/(sici)1096-9861(19990412)406:3
Target cell specificity of synaptic connections in the hippocampus
Frotscher, M. (1991) · Hippocampus · doi:10.1002/hipo.450010202 · Cited by 66
Alterations in excitatory and gabaergic inhibitory connections in hippocampal transplants
Freund, T. F., & Buzsáki, G. (1988) · Neuroscience · doi:10.1016/0306-4522(88)90275-8 · Cited by 66
Quantification of synapses formed with apical dendrites of golgi-impregnated pyramidal cells: Variability in thalamocortical inputs, but consistency in the ratios of asymmetrical to symmetrical synapses
Hersch, S. M., & White, E. L. (1981) · Neuroscience · doi:10.1016/0306-4522(81)90069-5 · Cited by 66
The Cerebral Neocortex
Eccles, J. C. (1984) · Cerebral cortex · doi:10.1007/978-1-4615-6610-6_1 · Cited by 66
Modulation of bistratified cell IPSPs and basket cell IPSPs by pentobarbitone sodium, diazepam and Zn2+: dual recordings in slices of adult rat hippocampus
Pawelzik, H., Bannister, A. P., Deuchars, J., Ilia, M., & Thomson, A. M. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00772.x · Cited by 63
Different types of 3H-GABA accumulating neurons in the visual cortex of the rat. Characterization by combined autoradiography and Golgi impregnation
Somogyi, P., Freund, T. F., & Kisv�rday, Z. F. (1984) · Experimental Brain Research · doi:10.1007/bf00235817 · Cited by 65
Self-citation
GABAergic innervation of the rat fascia dentata: A novel type of interneuron in the granule cell layer with extensive axonal arborization in the molecular layer
Soriano, E., & Frotscher, M. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903340305 · Cited by 63
Interneuron Types and Their Circuits in the Basolateral Amygdala
Hájos, N. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.687257 · Cited by 66
Polyribosomes associated with synaptic specializations on axon initial segments: localization of protein-synthetic machinery at inhibitory synapses
Steward, O., & Ribak, C. (1986) · Journal of Neuroscience · doi:10.1523/jneurosci.06-10-03079.1986 · Cited by 63
GABAergic synapses: their plasticity and role in sensory cortex - See more at: http://journal.frontiersin.org/Journal/10.3389/fncel.2014.00091/abstract#sthash.l5jGe6MC.dpuf
Griffen, T. C. (2014) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2014.00091 · Cited by 64
Cortical Orofacial Motor Representation in Old World Monkeys, Great Apes, and Humans
Sherwood, C., Holloway, R., Erwin, J., & Hof, P. (2004) · Brain, Behavior and Evolution · doi:10.1159/000075673 · Cited by 36
The Current Status of Somatostatin-Interneurons in Inhibitory Control of Brain Function and Plasticity
Scheyltjens, I., & Arckens, L. (2016) · Neural Plasticity · doi:10.1155/2016/8723623 · Cited by 71
Excitatory and inhibitory connections show selectivity in the neocortex
Watts, J., & Thomson, A. M. (2004) · The Journal of Physiology · doi:10.1113/jphysiol.2004.076984 · Cited by 62
The chandelier cell of the human visual cortex: A Golgi study
Marín‐Padilla, M. (1987) · The Journal of Comparative Neurology · doi:10.1002/cne.902560106 · Cited by 62
Altered Cortical GABA Neurotransmission in Schizophrenia: Insights into Novel Therapeutic Strategies
Stan, A. D., & Lewis, D. A. (2012) · Current Pharmaceutical Biotechnology · doi:10.2174/138920112800784925 · Cited by 64
Total Number and Ratio of GABAergic Neuron Types in the Mouse Lateral and Basal Amygdala
Vereczki, V., Müller, K., Krizsán, É., Máté, Z., Fekete, Z., Rovira-Esteban, L., Veres, J. M., Erdélyi, F., & Hájos, N. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.2700-20.2021 · Cited by 65
Histological and cytological study of the bed nuclei of the stria terminalis in adult rat. II. Oval nucleus: Extrinsic inputs, cell types, neuropil, and neuronal modules
Larriva-Sahd, J. A. (2006) · The Journal of Comparative Neurology · doi:10.1002/cne.21011 · Cited by 61
Perisomatic GABAergic synapses of basket cells effectively control principal neuron activity in amygdala networks
Veres, J. M., Nagy, G. A., & Hájos, N. (2017) · eLife · doi:10.7554/elife.20721 · Cited by 63
Corticotropin‐releasing factor immunoreactivity in monkey neocortex: An immunohistochemical analysis
Lewis, D. A., Foote, S. L., & Cha, C. I. (1989) · The Journal of Comparative Neurology · doi:10.1002/cne.902900412 · Cited by 61
From bugs to brain: unravelling the GABA signalling networks in the brain–gut–microbiome axis
Belelli, D., Lambert, J. J., Wan, M. L. Y., Monteiro, A. R., Nutt, D., & Swinny, J. D. (2024) · Brain · doi:10.1093/brain/awae413 · Cited by 69
Axon initial segments of the granule cell in the rat dentate gyrus: synaptic contacts on bundles of axon initial segments
Kosaka, T. (1983) · Brain Research · doi:10.1016/0006-8993(83)90527-9 · Cited by 60
The role of dendritic inhibition in shaping the plasticity of excitatory synapses
Bar-Ilan, L., Gidon, A., & Segev, I. (2013) · Frontiers in Neural Circuits · doi:10.3389/fncir.2012.00118 · Cited by 61
Theoretical relation between axon initial segment geometry and excitability
Goethals, S., & Brette, R. (2020) · eLife · doi:10.7554/elife.53432 · Cited by 58
Patchy intrinsic projections in visual cortex, area 18, of the cat: Morphological and immunocytochemical evidence for an excitatory function
LeVay, S. (1988) · The Journal of Comparative Neurology · doi:10.1002/cne.902690210 · Cited by 59
Morphological Diversity Strongly Constrains Synaptic Connectivity and Plasticity
Reimann, M., Trautmann, A.-L., Ramaswamy, S., Muller, E. B., & Markram, H. (2017) · Cerebral Cortex · doi:10.1093/cercor/bhx150 · Cited by 56
Differential distribution of parvalbumin-immunoreactive pericellular clusters of terminal boutons in developing and adult monkey neocortex
Akil, M., & Lewis, D. A. (1992) · Experimental Neurology · doi:10.1016/0014-4886(92)90058-x · Cited by 58
Parvalbumin and parvalbumin chandelier interneurons in autism and other psychiatric disorders
Juárez, P., & Martínez‐Cerdeño, V. (2022) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2022.913550 · Cited by 56
Assortment of GABAergic Plasticity in the Cortical Interneuron Melting Pot
Méndez, P., & Bacci, A. (2011) · Neural Plasticity · doi:10.1155/2011/976856 · Cited by 61
Examining neocortical circuits: Some background and facts
Peters, A. (2002) · Journal of Neurocytology · doi:10.1023/a:1024157522651 · Cited by 59
Laminar distribution and neuronal targets of GABAergic axon terminals in cat primary auditory cortex (AI)
Prieto, J. J., Peterson, B. A., & Winer, J. A. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903440305 · Cited by 56
Lack of Molecular-Anatomical Evidence for GABAergic Influence on Axon Initial Segment of Cerebellar Purkinje Cells by the Pinceau Formation
Iwakura, A., Uchigashima, M., Miyazaki, T., Yamasaki, M., & Watanabe, M. (2012) · Journal of Neuroscience · doi:10.1523/jneurosci.1651-12.2012 · Cited by 56
Thalamocortical and other synapses involving nonspiny multipolar cells of mouse SmI cortex
White, E. L., Benshalom, G., & Hersch, S. M. (1984) · The Journal of Comparative Neurology · doi:10.1002/cne.902290303 · Cited by 56
Ketamine Administration During the Second Postnatal Week Alters Synaptic Properties of Fast-Spiking Interneurons in the Medial Prefrontal Cortex of Adult Mice
Jeevakumar, V., & Kroener, S. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu293 · Cited by 59
Shedding Light on Chandelier Cell Development, Connectivity, and Contribution to Neural Disorders
Gallo, N. B., Paul, A., & Aelst, L. V. (2020) · Trends in Neurosciences · doi:10.1016/j.tins.2020.05.003 · Cited by 55
Axonal patterns and topography of short‐axon neurons in visual areas 17, 18, and 19 of the cat
Meyer, G. (1983) · The Journal of Comparative Neurology · doi:10.1002/cne.902200405 · Cited by 55
Interneuron development and dysfunction
Yang, J., Yang, X. W., & Tang, K. (2021) · FEBS Journal · doi:10.1111/febs.15872 · Cited by 54
Robust correlations between action potential duration and the properties of synaptic connections in layer 4 interneurones in neocortical slices from juvenile rats and adult rat and cat
Ali, A. B., Bannister, A. P., & Thomson, A. M. (2007) · The Journal of Physiology · doi:10.1113/jphysiol.2006.124214 · Cited by 53
The Distribution of Chandelier Cell Axon Terminals that Express the GABA Plasma Membrane Transporter GAT-1 in the Human Neocortex
Inda, M. C., DeFelipe, J., & Muñoz, A. (2006) · Cerebral Cortex · doi:10.1093/cercor/bhl114 · Cited by 54
Mapping pathologic circuitry in schizophrenia
Glausier, J. R., & Lewis, D. A. (2018) · Handbook of clinical neurology · doi:10.1016/b978-0-444-63639-3.00025-6 · Cited by 53
Smooth or sparsely spined cells with myelinated axons in rat visual cortex
Peters, A., & Proskauer, C. C. (1980) · Neuroscience · doi:10.1016/0306-4522(80)90126-8 · Cited by 54
Synaptic connections of axo-axonic (chandelier) cells in human epileptic temporal cortex
Kisvárday, Z. F., Adams, C. B. T., & Smith, A. D. (1986) · Neuroscience · doi:10.1016/0306-4522(86)90131-4 · Cited by 53
Postnatal development of synaptic structure proteins in pyramidal neuron axon initial segments in monkey prefrontal cortex
Cruz, D. A., Lovallo, E., Stockton, S. D., Rasband, M. N., & Lewis, D. A. (2009) · The Journal of Comparative Neurology · doi:10.1002/cne.22006 · Cited by 51
The Neurotensin Agonist PD149163 Increases Fos Expression in the Prefrontal Cortex of the Rat
Petrie, K. A., Bubser, M., Casey, C. D., Davis, M. D., Roth, B. L., & Deutch, A. Y. (2004) · Neuropsychopharmacology · doi:10.1038/sj.npp.1300494 · Cited by 52
Axo‐axonic synapses formed by somatostatin‐expressing GABAergic neurons in rat and monkey visual cortex
Gonchar, Y., Turney, S. G., Price, J. L., & Burkhalter, A. (2001) · The Journal of Comparative Neurology · doi:10.1002/cne.1425 · Cited by 52
Parvalbumin‐producing cortical interneurons receive inhibitory inputs on proximal portions and cortical excitatory inputs on distal dendrites
Kameda, H., Hioki, H., Tanaka, Y. H., Tanaka, T., Sohn, J., Sonomura, T., Furuta, T., Fujiyama, F., & Kaneko, T. (2012) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2012.08027.x · Cited by 51
GABAergic neuron-specific whole-brain transduction by AAV-PHP.B incorporated with a new GAD65 promoter
Hoshino, C., Konno, A., Hosoi, N., Kaneko, R., Mukai, R., Nakai, J., & Hirai, H. (2021) · Molecular Brain · doi:10.1186/s13041-021-00746-1 · Cited by 57
Target and temporal pattern selection at neocortical synapses
Thomson, A. M., Bannister, A. P., Mercer, A., & Morris, O. T. (2002) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2002.1163 · Cited by 49
Laminar and cellular localization of cytochrome oxidase in the cat striate cortex
Kageyama, G. H., & Wong‐Riley, M. T. T. (1986) · The Journal of Comparative Neurology · doi:10.1002/cne.902450202 · Cited by 51
IPSPs elicited in CA1 pyramidal cells by putative basket cells in slices of adult rat hippocampus
Ali, A. B., Bannister, A. P., & Thomson, A. M. (1999) · European Journal of Neuroscience · doi:10.1046/j.1460-9568.1999.00592.x · Cited by 51
Regulation of Chandelier Cell Cartridge and Bouton Development via DOCK7-Mediated ErbB4 Activation
Tai, Y., Janas, J. A., Wang, C.-L., & Aelst, L. V. (2014) · Cell Reports · doi:10.1016/j.celrep.2013.12.034 · Cited by 49
Linearity of synaptic interactions in the assembly of receptive fields in cat visual cortex
Ferster, D. (1994) · Current Opinion in Neurobiology · doi:10.1016/0959-4388(94)90058-2 · Cited by 49
Development, morphology and topography of chandeller cells in the auditory cortex of the cat
Carlos, J., López‐Mascaraque, L., & Valverde, F. (1985) · Developmental Brain Research · doi:10.1016/0165-3806(85)90182-8 · Cited by 49
Chapter 14: The patchy intrinsic projections of visual cortex
LeVay, S. (1988) · Progress in brain research · doi:10.1016/s0079-6123(08)60474-4 · Cited by 49
Polysynaptic subcircuits in the neocortex: spatial and temporal diversity
Silberberg, G. (2008) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2008.08.009 · Cited by 46
Different kinds of axon terminals forming symmetric synapses with the cell bodies and initial axon segments of layer II/III pyramidal cells. I. Morphometric analysis
Peters, A., & Harriman, K. M. (1990) · Journal of Neurocytology · doi:10.1007/bf01217295 · Cited by 48
Developmental changes in the relationship between type 2 synapses and spiny neurons in the monkey visual cortex
Mates, S. L., & Lund, J. S. (1983) · The Journal of Comparative Neurology · doi:10.1002/cne.902210108 · Cited by 47
Neurodevelopmental mutation of giant ankyrin-G disrupts a core mechanism for axon initial segment assembly
Yang, R., Walder-Christensen, K. K., Lalani, S., Yan, H., García-Prieto, I. D., Álvarez, S., Fernández‐Jaén, A., Speltz, L., Jiang, Y.-H., & Bennett, V. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1909989116 · Cited by 44
Mammals
Voogd, J., Nieuwenhuys, R., van Dongen, P. A. M., & ten Donkelaar, H. J. (1998) · Springer eBooks · doi:10.1007/978-3-642-18262-4_22 · Cited by 46
Properties of horizontal axo‐axonic cells in stratum oriens of the hippocampal CA1 area of rats in vitro
Ganter, P., Szűcs, P., Paulsen, O., & Somogyi, P. (2004) · Hippocampus · doi:10.1002/hipo.10170 · Cited by 47
Self-citation
Modulatory and inhibitory processes in the visual cortex
Sillito, A. M., Salt, T. E., & Kemp, J. A. (1985) · Vision Research · doi:10.1016/0042-6989(85)90062-8 · Cited by 46
Subgroups of parvalbumin-expressing interneurons in layers 2/3 of the visual cortex
Helm, J. S., Akgül, G., & Wollmuth, L. P. (2012) · Journal of Neurophysiology · doi:10.1152/jn.00782.2012 · Cited by 45
Relationship between orientation tuning and spatial frequency in neurones of cat area 17
Vidyasagar, T. R., & Sig�enza, J. A. (1985) · Experimental Brain Research · doi:10.1007/bf00237851 · Cited by 41
Does inhibition balance excitation in neocortex?
Trevelyan, A. J., & Watkinson, O. T. (2004) · Progress in Biophysics and Molecular Biology · doi:10.1016/j.pbiomolbio.2004.06.008 · Cited by 38
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
GABA Targets for the Treatment of Cognitive Dysfunction in Schizophrenia
Volk, D. W., & Lewis, D. A. (2005) · Current Neuropharmacology · doi:10.2174/1570159052773396 · Cited by 38
A quantitative analysis of parvalbumin neurons in rabbit auditory neocortex
McMullen, N. T., Smelser, C. B., & de Venecia, R. K. (1994) · The Journal of Comparative Neurology · doi:10.1002/cne.903490402 · Cited by 38
A model of striate response properties based on geniculate anisotropies
Vidyasagar, T. R. (1987) · Biological Cybernetics · doi:10.1007/bf00318712 · Cited by 38
Neurons of the basolateral amygdala: A Golgi study in the opossum (Didelphis virginiana)
McDonald, A. J., & Culberson, J. L. (1981) · American Journal of Anatomy · doi:10.1002/aja.1001620404 · Cited by 38
Laminar interactions during neocortical epileptogenesis
Ebersole, J. S., & Chatt, A. B. (1984) · Brain Research · doi:10.1016/0006-8993(84)91425-2 · Cited by 38
Golgi, Cajal, and the fine structure of the nervous system
Peters, A. (2006) · Brain Research Reviews · doi:10.1016/j.brainresrev.2006.12.002 · Cited by 39
Chandelier cells in the hippocampal formation of the rat: The entorhinal area and subicular complex
Soriano, E., Martı́nez, A., Fariñas, I., & Frotscher, M. (1993) · The Journal of Comparative Neurology · doi:10.1002/cne.903370110 · Cited by 38
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
The underside of the cerebral cortex: layer V/VI spiny inverted neurons
Mendizabal‐Zubiaga, J., Reblet, C., & Bueno‐López, J. (2007) · Journal of Anatomy · doi:10.1111/j.1469-7580.2007.00779.x · Cited by 36
New perspectives on the functional anatomical organization of the basolateral amygdala
Carlsen, J. (1989) · Acta Neurologica Scandinavica · doi:10.1111/j.1600-0404.1989.tb08018.x · Cited by 36
5‐HT1A receptor localization on the axon hillock of cervical spinal motoneurons in primates
Kheck, N. M., Gannon, P. J., & Azmitia, E. C. (1995) · The Journal of Comparative Neurology · doi:10.1002/cne.903550205 · Cited by 36
Chandelier cell anatomy and function reveal a variably distributed but common signalPreprint
Schneider-Mizell, C. M., Bodor, Á. L., Collman, F., Brittain, D., Bleckert, A., Dorkenwald, S., Turner, N. L., Macrina, T., Lee, K., Lu, R., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.03.31.018952 · Cited by 37
Robust Short-Latency Perisomatic Inhibition onto Neocortical Pyramidal Cells Detected by Laser-Scanning Photostimulation
Brill, J., & Huguenard, J. R. (2009) · Journal of Neuroscience · doi:10.1523/jneurosci.6098-08.2009 · Cited by 38
Molecular and Electrophysiological Characterization of GABAergic Interneurons Expressing the Transcription Factor COUP-TFII in the Adult Human Temporal Cortex
Varga, C., Tamás, G., Barzó, P., Oláh, S., & Somogyi, P. (2015) · Cerebral Cortex · doi:10.1093/cercor/bhv045 · Cited by 34
Self-citation
Chandelier neurons within the rabbits' cerebral cortex
Ib, M.-P., T�mb�l, T., & Petsche, H. (1983) · Anatomy and Embryology · doi:10.1007/bf00317950 · Cited by 35
Plasticity of the Axon Initial Segment: Fast and Slow Processes with Multiple Functional Roles
Petersen, A. V., Cotel, F., & Perrier, J. (2016) · The Neuroscientist · doi:10.1177/1073858416648311 · Cited by 35
Structure of the nucleus olfactorius anterior of the hedgehog (Erinaceus europaeus)
Valverde, F., López‐Mascaraque, L., & Carlos, J. (1989) · The Journal of Comparative Neurology · doi:10.1002/cne.902790407 · Cited by 34
Double immunofluorescence, peroxidase labelling and ultrastructural analysis of interneurones following prolonged electrophysiological recordings in vitro
Hughes, D. I., Bannister, A. P., Pawelzik, H., & Thomson, A. M. (2000) · Journal of Neuroscience Methods · doi:10.1016/s0165-0270(00)00254-5 · Cited by 34
Neural Circuitry of the Prefrontal Cortex in Schizophrenia
Lewis, D. A. (1995) · Archives of General Psychiatry · doi:10.1001/archpsyc.1995.03950160019004 · Cited by 34
Thalamic inputs to identified commissural neurons in the monkey somatic sensory cortex
Hendry, S. H. C., & Jones, E. G. (1983) · Journal of Neurocytology · doi:10.1007/bf01148466 · Cited by 34
Regulation of the E/I-balance by the neural matrisome
Mueller-Buehl, C., Wegrzyn, D., Bauch, J., & Faissner, A. (2023) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2023.1102334 · Cited by 35
Regulation of Synapse Development byVgatDeletion from ErbB4-Positive Interneurons
Lin, T. W., Tan, Z., Barik, A., Yin, D., Brudvik, E., Wang, H., Xiong, W., & Mei, L. (2018) · Journal of Neuroscience · doi:10.1523/jneurosci.0669-17.2018 · Cited by 37
Localization of NPY-immunoreactivity in the cat's visual cortex
W�hle, P., Meyer, G., & Albus, K. (1986) · Experimental Brain Research · doi:10.1007/bf00239525 · Cited by 33
A community-based transcriptomics classification and nomenclature of neocortical cell types
Yuste, R., Hawrylycz, M., Aalling, N., Aguilar-Valles, A., Arendt, D., Armañanzas, R., Ascoli, G. A., Bielza, C., Bokharaie, V., Bergmann, T. B., et al. (2020) · Nature Neuroscience · doi:10.1038/s41593-020-0685-8 · Cited by 32
Self-citation
The nature and origin of orientation specificity in neurons of the visual pathways
Henry, G. H., Michalski, A., Wimborne, B., & McCart, R. (1994) · Progress in Neurobiology · doi:10.1016/0301-0082(94)90061-2 · Cited by 32
GABA Neurons and Their Role in Activity-Dependent Plasticity of Adult Primate Visual Cortex
Jones, E. G., Hendry, S. H. C., DeFelipe, J., & Benson, D. L. (1994) · Cerebral cortex · doi:10.1007/978-1-4757-9628-5_3 · Cited by 32
The Cortical Neuron as an Electrophysiological Unit
Gutnick, M. J., & Crill, W. E. (1995) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195083309.003.0003 · Cited by 32
Modularity Induced Gating and Delays in Neuronal Networks
Idelson, M. S., Cohen, G., Ben‐Jacob, E., & Hanein, Y. (2016) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004883 · Cited by 26

Authors: Somogyi, P.
Affiliations: Semmelweis University (HU)
Corresponding author: Somogyi, P.
ORCID: Somogyi, P.
Venue: Brain Research
Publisher: Elsevier BV
Published: 1977-11
Volume: 136
Issue: 2
Pages: 345-350
ISSN: 0006-8993 (ISSN-L)
DOI: 10.1016/0006-8993(77)90808-3
OpenAlex: W2077544618
Cited by: 530
References: 15
Citations by year: 2026: 7 · 2025: 14 · 2024: 13 · 2023: 16 · 2022: 8 · 2021: 22 · 2020: 9 · 2019: 8 · 2018: 10 · 2017: 18 · 2016: 14 · 2015: 12 · 2014: 20 · 2013: 10 · 2012: 13
FWCI: 1.64
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Brain Research (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
Life Sciences › Neuroscience › Cognitive Neuroscience › Visual perception and processing mechanisms
Keywords: chandelier cells, GABAergic interneurons, visual cortex, pyramidal neurons, inhibitory synapse formation, synaptic plasticity, brain development, inhibitory circuits, rats
MeSH terms: Animals, Axons, Interneurons, Pyramidal Tracts, Synapses, Visual Cortex, Rats

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

A specific ‘axo-axonal’ interneuron in the visual cortex of the rat

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