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A Bioinspired Robotic Finger for Multimodal Tactile Sensing Powered by Fiber Optic Sensors

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Multimodal cortical neuronal cell type classification

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Cortical Reorganization after Limb Loss: Bridging the Gap between Basic Science and Clinical Recovery

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The synaptic inputs and thalamic projections of two classes of layer 6 corticothalamic neurons in primary somatosensory cortex of the mouse

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Distal activity patterns shape the spatial specificity of neurovascular coupling

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Direction selectivity of inhibitory interneurons in mouse barrel cortex differs between interneuron subtypes.

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Connectivity of single neurons classifies cell subtypes in mouse brains

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Tactile cognition in rodents

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Touch-evoked traveling waves establish a translaminar spacetime code

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Intersectional strategy to study cortical inhibitory parvalbumin-expressing interneurons

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Cortical VIP+/ChAT+ interneurons: From genetics to function

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A layered microcircuit model of somatosensory cortex with three interneuron types and cell-type-specific short-term plasticity

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Effects of optogenetic inhibition of a small fraction of parvalbumin-positive interneurons on the representation of sensory stimuli in mouse barrel cortex

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Learning-related congruent and incongruent changes of excitation and inhibition in distinct cortical areas

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<i>Sncg</i>,<i>Mybpc1</i>, and<i>Parm1</i>Classify subpopulations of VIP-expressing interneurons in layers 2/3 of the somatosensory cortex

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Functional gradients facilitate tactile sensing in elephant whiskers.

Schulz, A. K., Kaufmann, L., Smith, L. T., Philip, D. S., David, H., Lazovic, J., Brecht, M., Richter, G., & Kuchenbecker, K. J. (2025) · Science · doi:10.1126/science.adx8981 · Cited by 12

Biologically informed cortical models predict optogenetic perturbations

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Correlation of zero echo time functional MRI with neuronal activity in rats

Valjakka, J. S., Paasonen, J., Salo, R., Paasonen, E., Stenroos, P., Gureviciene, I., Kettunen, M., Idiyatullin, D., Tanila, H., Michaeli, S., et al. (2025) · Journal of Cerebral Blood Flow and Metabolism · doi:10.1177/0271678x251314682 · Cited by 10 · see citing works

Distinct roles of cortical layer 5 subtypes in associative learning

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Axonal and Dendritic Morphology of Excitatory Neurons in Layer 2/3 Mouse Barrel Cortex Imaged Through Whole-Brain Two-Photon Tomography and Registered to a Digital Brain Atlas

Liu, Y., Foustoukos, G., Crochet, S., & Petersen, C. C. H. (2022) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2021.791015 · Cited by 18 · see citing works

Identification of a Developmental Switch in Information Transfer between Whisker S1 and S2 Cortex in Mice

Cai, L., Yang, J.-W., Wang, C.-F., Chou, S.-J., Luhmann, H. J., & Karayannis, T. (2021) · Journal of Neuroscience · doi:10.1523/jneurosci.2246-21.2022 · Cited by 10 · see citing works

Neuronal Connectivity as a Determinant of Cell Types and SubtypesPreprint

Liu, L., Yun, Z.-X., Manubens-Gil, L., Chen, H.-B., Xiong, F., Dong, H.-W., Zeng, H.-K., Hawrylycz, M., Ascoli, G., & Peng, H. (2023) · bioRxiv · doi:10.21203/rs.3.rs-2960606/v1 · Cited by 9 · see citing works

Cortical VIP+ Interneurons in the Upper and Deeper Layers Are Transcriptionally Distinct

Wu, J., Zhao, Z., Shi, Y., & He, M. (2022) · Journal of Molecular Neuroscience · doi:10.1007/s12031-022-02040-8 · Cited by 8 · see citing works

The tuning of tuning: How adaptation influences single cell information transfer

Zeldenrust, F., Calcini, N., Xuan, Y., Bijlsma, A., & Celikel, T. (2024) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1012043 · Cited by 18 · see citing works

Thalamocortical feedback selectively controls pyramidal neuron excitability

Brandalise, F., Chéreau, R., Chen, I.-W., van Oorschot, D., Raig, C. M., Bawa, T., Mule, N., Pagès, S., Markopoulos, F., & Holtmaat, A. J. D. G. (2025) · Nature Communications · doi:10.1038/s41467-025-60835-w · Cited by 9 · see citing works

Multihead self-attention in cortico-thalamic circuits

Granier, A., & Senn, W. (2025) · arXiv.org · doi:10.48550/arxiv.2504.06354 · Cited by 8

Reactivated thalamocortical plasticity alters neural activity in sensory-motor cortex during post-critical period

Jie, H., Petrus, E., Pothayee, N., & Koretsky, A. P. (2025) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2025.102735 · Cited by 6 · see citing works

Activation of M1 cholinergic receptors in mouse somatosensory cortex enhances information processing and detection behaviour

Mishra, W., Kheradpezhouh, E., & Arabzadeh, E. (2024) · Communications Biology · doi:10.1038/s42003-023-05699-w · Cited by 13 · see citing works

Functional and structural synaptic remodeling mechanisms underlying somatotopic organization and reorganization in the thalamus

Ueta, Y., & Miyata, M. (2023) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2023.105332 · Cited by 8 · see citing works

Velocity of Conduction Between Columns and Layers in Barrel Cortex Reported by Parvalbumin Interneurons

Scheuer, K. S., Judge, J., Zhao, X., & Jackson, M. (2023) · bioRxiv · doi:10.1101/2022.07.27.501767 · Cited by 8

Translational neuronal ensembles: Neuronal microcircuits in psychology, physiology, pharmacology and pathology

Lara-González, E., Padilla-Orozco, M., Fuentes-Serrano, A., Bargas, J., & Duhne, M. (2022) · Frontiers in Systems Neuroscience · doi:10.3389/fnsys.2022.979680 · Cited by 8 · see citing works

Mechanisms Underlying Target Selectivity for Cell Types and Subcellular Domains in Developing Neocortical Circuits

Gutman-Wei, A. Y., & Brown, S. P. (2021) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.728832 · Cited by 8 · see citing works

The postsubiculum as a head-direction cortex

Duszkiewicz, A. J., Fricker, D., Burgalossi, A., & Peyrache, A. (2025) · Trends in Neurosciences · doi:10.1016/j.tins.2025.09.004 · Cited by 4 · see citing works

Syngap1 promotes cognitive function through regulation of cortical sensorimotor dynamics

Vaissière, T., Michaelson, S. D., Creson, T. K., Goins, J., Fürth, D., Balázsfi, D., Rojas, C., Golovin, R. M., Meletis, K., Miller, C. A., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-56125-0 · Cited by 12 · see citing works

Separation of bimodal fMRI responses in mouse somatosensory areas into V1 and non-V1 contributions

Dinh, T. N. A., Moon, H. S., & Kim, S. (2024) · Scientific Reports · doi:10.1038/s41598-024-56305-w · Cited by 10 · see citing works

Axonal connections between S1 barrel, M1, and S2 cortex in the newborn mouse

Gellért, L., Luhmann, H. J., & Kilb, W. (2023) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2023.1105998 · Cited by 7 · see citing works

Early alterations of the neuronal network processing whisker‐related sensory signal during absence epileptogenesis

Laghouati, E., Studer, F., Depaulis, A., & Guillemain, I. (2021) · Epilepsia · doi:10.1111/epi.17151 · Cited by 7 · see citing works

Layers 4 and 3 neurons of the bilateral whisker-barrel cortex in a conditional Robo3 mutant mouse line

Tsytsarev, V., Kwon, S. E., Plachez, C., Zhao, S., O'Connor, D. H., & Erzurumlu, R. (2022) · Neuroscience · doi:10.1016/j.neuroscience.2022.05.018 · Cited by 6

Molecular mechanisms regulating the spatial configuration of neurites

Hasegawa, K., & Kuwako, K.-I. (2022) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2022.02.015 · Cited by 7 · see citing works

Brain Structure and Function: the first 15 years—a retrospective

Záborszky, L. (2021) · Brain Structure and Function · doi:10.1007/s00429-021-02362-0 · Cited by 6 · see citing works

‘Backpropagation and the brain’ realized in cortical error neuron microcircuits

Max, K., Jaras, I., Granier, A., Wilmes, K., & Petrovici, M. A. (2025) · bioRxiv · doi:10.1101/2025.07.11.664263 · Cited by 5

Dynamic redistribution of AMPA receptors toward memory-related neuronal ensembles in mice barrel cortex during sensory learning.

Li, J., Zhou, R., Wang, J.-P., Zhang, X., Li, Y., Li, C., He, B., Li, C., Li, C.-Y., Long, S., et al. (2025) · Neuron · doi:10.1016/j.neuron.2025.06.002 · Cited by 5 · see citing works

Aging alters calcium signaling in vascular mural cells and drives remodeling of neurovascular coupling in the awake brain

Zhang, X., Tao, L., Nygaard, A. H., Dong, Y., Groves, T., Hong, X., Goddard, C. M., He, C., Postnov, D. D., Allodi, I., et al. (2025) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1177/0271678x251320455 · Cited by 4 · see citing works

Synaptotagmin 7 sculpts short-term plasticity at a high probability synapse

Chiu, D. N., & Carter, B. C. (2024) · Journal of Neuroscience · doi:10.1523/jneurosci.1756-23.2023 · Cited by 11 · see citing works

Whole-brain mapping of long-range inputs to the VIP-expressing inhibitory neurons in the primary motor cortex

Lee, C., Côté, S. L., Raman, N., Chaudhary, H., Mercado, B. C., & Chen, S. X. (2023) · Frontiers in Neural Circuits · doi:10.3389/fncir.2023.1093066 · Cited by 5 · see citing works

Normal connectivity of thalamorecipient networks in barrel equivalents of the reeler cortex

Meeuwissen, A., Möck, M., Staiger, J. F., & Guy, J. (2023) · Cerebral Cortex · doi:10.1093/cercor/bhad072 · Cited by 4 · see citing works

Retrosplenial cortex enables context-dependent goal-directed sensorimotor transformation

Bech, P., Dard, R. F., Lebert, J. M., Smith, L., Bisi, A., Renard, A., Crochet, S., & Petersen, C. C. H. (2026) · eLife · doi:10.1101/2025.10.31.685738

Topographic correspondence between retinotopic and whisker somatosensory map in mouse higher visual area and its development

Matsumoto, H., Murakami, T., & Ohki, K. (2025) · Frontiers in Neural Circuits · doi:10.3389/fncir.2025.1552130 · Cited by 4 · see citing works

Development of spontaneous and sensory evoked network activity in rodent cerebral cortex in vivo

Nigi, E., Yang, J., Luhmann, H. J., & Sinning, A. (2025) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2025.1648685 · Cited by 5 · see citing works

Reward history guides focal attention in whisker somatosensory cortex

Ramamurthy, D. L., Rodriguez, L., Cen, C., Li, S., Chen, A., & Feldman, D. E. (2025) · Nature Communications · doi:10.1038/s41467-025-60592-w · Cited by 5 · see citing works

Type-I nNOS neurons orchestrate cortical neural activity and vasomotion

Turner, K. L., Brockway, D. F., Hossain, M. S., Griffith, K. R., Greenawalt, D., Zhang, Q.-G., Gheres, K. W., Crowley, N. A., & Drew, P. (2025) · bioRxiv · doi:10.1101/2025.01.21.634042 · Cited by 4

Permanent tactile sensory loss reduces neuronal activity in the amygdala and ventral hippocampus and alters anxiety-like behaviors

Ibarra-Castañeda, N., Lopez-Virgen, V., López, N. A. M., & González-Pérez, Ó. (2025) · Behavioural Brain Research · doi:10.1016/j.bbr.2025.115456 · Cited by 3 · see citing works

Recovery kinetics of short-term depression of GABAergic and glutamatergic synapses at layer 2/3 pyramidal cells in the mouse barrel cortex

Lombardi, A., Wang, Q., Stüttgen, M. C., Mittmann, T., Luhmann, H. J., & Kilb, W. (2023) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2023.1254776 · Cited by 5 · see citing works

Membrane potential dynamics of excitatory and inhibitory neurons in mouse barrel cortex during active whisker sensing

Kiritani, T., Pala, A., Gasselin, C., Crochet, S., & Petersen, C. C. H. (2023) · PLoS ONE · doi:10.1371/journal.pone.0287174 · Cited by 5 · see citing works

Whisker trimming induces anti-anxiety like status via activation of dorsomedial hypothalamus nucleus in mice

Wang, J., Shan, W., Chen, X., & Zuo, Z. (2022) · Brain Research · doi:10.1016/j.brainres.2022.147946 · Cited by 5 · see citing works

Local inhibitory dynamics underpin temporal integration and functional segregation between barrels and septa in the mouse barrel cortex

Argunşah, A. Ö., Stachniak, T. J., Yang, J., Cai, L., van der Bourg, A., Kästli, R., & Karayannis, T. (2026) · eLife · doi:10.1101/2024.01.23.576792

Probabilistic Perceptual Decisions during Navigation Are Driven by a Small Subpopulation of Neurons in a Single Cortical Column of the Primary Somatosensory CortexPreprint

Armstrong, A. G., & Vlasov, Y. A. (2025) · Journal of Neuroscience · doi:10.1101/2025.02.17.638764 · Cited by 3 · see citing works

Inhibitory circuit motifs of cortical somatosensory layer 5 SST interneurons are uniform within layers but specific across layers

Preuss, F., Walker, F., Möck, M., Witte, M., & Staiger, J. F. (2025) · The Journal of Physiology · doi:10.1113/jp288309 · Cited by 3 · see citing works

IP3R2-Mediated Astrocytic Ca2+ Transients Are Critical to Sustain Modulatory Effects of Locomotion on Neurons in Mouse Somatosensory Cortex

de la Puebla, M. F., Zhang, X., Nagelhus, E. A., Bjørås, M., & Tang, W. (2025) · Cells · doi:10.3390/cells14141103 · Cited by 3 · see citing works

Making sense of vertebrate senses from a neural crest and cranial placode evo-devo perspective

Edens, B. M., & Bronner-Fraser, M. E. (2025) · Trends in Neurosciences · doi:10.1016/j.tins.2024.12.008 · Cited by 5 · see citing works

Cortical Coding of Gustatory and Thermal Signals in Active Licking Mice

Nash, A. N., Shakeshaft, M., Bouaichi, C. G., Odegaard, K. E., Needham, T., Bauer, M., Bertram, R., & Vincis, R. (2024) · bioRxiv · doi:10.1101/2024.04.27.591293 · Cited by 3

Astrocyte modulation of synaptic plasticity mediated by activity-dependent Sonic hedgehog signaling

Le, A. D., Fu, M., Kumar, R., Zacharias, G., & Garcia, A. D. R. (2024) · bioRxiv · doi:10.1101/2024.04.05.588352 · Cited by 3

Distinct brain-wide presynaptic networks underlie the functional identity of individual cortical neuronsPreprint

Inácio, A. R. L., Lam, K. C., Zhao, Y., Pereira, F., Gerfen, C. R., & Lee, S. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.05.25.542329 · Cited by 6 · see citing works

Stimulus Feature-Specific Control of Layer 2/3 Subthreshold Whisker Responses by Layer 4 in the Mouse Primary Somatosensory Cortex

Varani, S., Vecchia, D., Zucca, S., Forli, A., & Fellin, T. (2021) · Cerebral Cortex · doi:10.1093/cercor/bhab297 · Cited by 8 · see citing works

Dual color mesoscopic imaging reveals spatiotemporally heterogeneous coordination of cholinergic and neocortical activityPreprint

Lohani, S., Moberly, A. H., Benisty, H., Landa, B., Jing, M., Li, Y., Higley, M., & Cardin, J. A. (2020) · bioRxiv · doi:10.1101/2020.12.09.418632 · Cited by 3 · see citing works

Can we study whisker movements to gain insights into the natural sensory behaviours of mammals?

Grant, R. A. (2025) · Journal of Physiology · doi:10.1113/jp288053 · Cited by 2 · see citing works

The canine vibrissal system as a highly innervated and functional sensory organ

Döring, D., Müller, H., Franzmeier, S., Matiasek, K., Blutke, A., & Reese, S. (2025) · Scientific Reports · doi:10.1038/s41598-025-91629-1 · Cited by 2

Behavioral adaptations after unilateral whisker denervation

Wright, P., McCall, E. C., Collier, S., Johnson, F. R., Iyer, L., Koretsky, A. P., & Petrus, E. (2025) · Behavioural Brain Research · doi:10.1016/j.bbr.2025.115435 · Cited by 2 · see citing works

Spatially integrated cortico-subcortical tracing data for analyses of rodent brain topographical organization

Øvsthus, M., van Swieten, M. M. H., Puchades, M. A., Tocco, C., Studer, M., Bjaalie, J. G., & Leergaard, T. B. (2024) · Scientific Data · doi:10.1038/s41597-024-04060-y · Cited by 3 · see citing works

The posterior intralaminar thalamic nucleus promotes nose‐to‐nose contacts leading to prosocial reception in the sequence of mouse social interaction

Arakawa, H., & Tokashiki, M. (2024) · European Journal of Neuroscience · doi:10.1111/ejn.16520 · Cited by 4 · see citing works

Inter and intralaminar excitation of parvalbumin interneurons in mouse barrel cortex

Scheuer, K. S., Jansson, A. M., Zhao, X., & Jackson, M. B. (2024) · PLoS ONE · doi:10.1371/journal.pone.0289901 · Cited by 3 · see citing works

Higher-order thalamocortical projections selectively control excitability via NMDAR and mGluRI-mediated mechanismsPreprint

Brandalise, F., Chéreau, R., Raig, C. M., Bawa, T., Mule, N., Pagès, S., Markopoulos, F., & Holtmaat, A. J. D. G. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.12.20.572353 · Cited by 2 · see citing works

Deep cortical microinfarction induced by femtosecond laser in mice: Long-term secondary pathological changes in corresponding superficial cortex

Liu, Z., He, B., Wang, X., Peng, J., Sun, Q., & Luo, C. (2023) · Neuroscience Letters · doi:10.1016/j.neulet.2023.137170 · Cited by 2 · see citing works

Syngap1 Regulates Cortical Circuit Assembly by Controlling Membrane ExcitabilityPreprint

Arora, V., Michaelson, S. D., Aceti, M., Kilinic, M., Miller, C. A., & Rumbaugh, G. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.12.06.519295 · Cited by 8 · see citing works

Synchronous inhibitory synaptic inputs to layer II/III pyramidal neurons in the murine barrel cortex

Yamamoto, K., Nakaya, Y., Sugawara, S., & Kobayashi, M. (2021) · Brain Research · doi:10.1016/j.brainres.2021.147686 · Cited by 2 · see citing works

Neural correlates of perceptual decision-making in the primary somatosensory cortex

Armstrong, A. G., & Vlasov, Y. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2514107123 · Cited by 1 · see citing works

Cortico-subcortical multi-head self-attention as a substrate for cognitive performancePreprint

Babu, V. K., Granier, A., Proix, T., Balvočius, T., Woodman, M., Saudargienė, A., Jirsa, V., & Senn, W. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.08.06.743205

Postnatal sensory experience and barrel cortex alterations anticipate autistic traits in a mouse model of CDKL5 deficiency disorder

Raspanti, A., Pizzo, R., Gurgone, A., Giraudo, C., Sagona, G., Macioce, A., Battaglia, A., Katsanou, L., Comai, D., Medici, G., et al. (2026) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2026.102949 · Cited by 1 · see citing works

Contextual gating of whisker-evoked responses by frontal cortex supports flexible decision making

Ghaderi, P., Crochet, S., & Petersen, C. C. H. (2026) · Nature Communications · doi:10.1038/s41467-026-73622-y · Cited by 1

Cell-type-selective synaptogenesis during the development of layer 6 corticothalamic neuron connectivity in the mammalian neocortex

Gutman-Wei, A. Y., Sudarsanam, S., Cabalinan, A. G., Shahid, N., Shi, A., Guzman-Clavel, L., Spindler-Krage, S. M., Agarwal, A., Kolodkin, A. L., & Brown, S. P. (2026) · Cell Reports · doi:10.1016/j.celrep.2025.116792 · Cited by 2 · see citing works

Cerebellar climbing fibers impact experience-dependent plasticity in the mouse primary somatosensory cortexPreprint

Silbaugh, A. M., Koster, K. P., & Hansel, C. (2025) · eLife · doi:10.7554/elife.109183 · Cited by 2 · see citing works

Cerebellar climbing fibers impact experience-dependent plasticity in the mouse primary somatosensory cortex

Silbaugh, A. M., Koster, K. P., & Hansel, C. (2025) · eLife · doi:10.1101/2025.04.18.649578 · Cited by 2 · see citing works

Task-Optimized Convolutional Recurrent Networks Align with Tactile Processing in the Rodent Brain

Chung, T., Shen, Y.-C., Kong, N. C. L., & Nayebi, A. (2025) · Neural Information Processing Systems · doi:10.48550/arxiv.2505.18361 · Cited by 1

Functional thalamocortical innervation of VIP- and SST-expressing GABAergic interneurons in mouse barrel cortex

Feyerabend, M., Witte, M., Möck, M., & Staiger, J. F. (2025) · iScience · doi:10.1016/j.isci.2025.112539 · Cited by 1 · see citing works

Gestational Chlorpyrifos Exposure Imparts Lasting Alterations to the Rat Somatosensory CortexPreprint

Koenig, J. A., Haga, C., Cramer, N., & Keller, A. (2025) · Journal of Neuroscience · doi:10.1101/2025.02.19.639085 · Cited by 1 · see citing works

Cortical coding of gustatory and thermal signals in active licking mice

Nash, A. N., Shakeshaft, M., Bouaichi, C. G., Odegaard, K. E., Needham, T., Bauer, M., Bertram, R., & Vincis, R. (2025) · The Journal of Physiology · doi:10.1113/jp287499 · Cited by 3 · see citing works

Fxr1 Deletion from Cortical Parvalbumin Interneurons Modifies Their Excitatory Synaptic Responses

Scheuer, K. S., Jansson, A. M., Shen, M., Zhao, X., & Jackson, M. B. (2025) · eNeuro · doi:10.1523/eneuro.0363-24.2024 · Cited by 1 · see citing works

The Anterolateral Barrel Subfield Differs from the Posteromedial Barrel Subfield in the Morphology and Cell Density of Parvalbumin-Positive GABAergic Interneurons

Shigematsu, N., Miyamoto, Y., Esumi, S., & Fukuda, T. (2024) · eNeuro · doi:10.1523/eneuro.0518-22.2024 · Cited by 2 · see citing works

Learning Successor Features with Distributed Hebbian Temporal Memory

Dzhivelikian, E., Kuderov, P., & Panov, A. (2023) · International Conference on Learning Representations · doi:10.48550/arxiv.2310.13391 · Cited by 1

What Does Physiological Mean?

Petersen, O. (2023) · Function · doi:10.1093/function/zqad042 · Cited by 1

Inter and Intralaminar Excitation of Parvalbumin Interneurons in Mouse Barrel Cortex

Scheuer, K. S., Jansson, A., Zhao, X.-Y., & Jackson, M. (2023) · bioRxiv · doi:10.1101/2023.06.02.543448 · Cited by 1 · see citing works

Activation of M1 cholinergic receptors in mouse somatosensory cortex enhances information processing and improves detection behaviourPreprint

Mishra, W., Kheradpezhouh, E., & Arabzadeh, E. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.06.06.543981

Repetitively burst-spiking neurons in reeler mice show conserved but also highly variable morphological features of layer Vb-fated “thick-tufted” pyramidal cells

Staiger, J. F., Sachkova, A., Möck, M., Guy, J., & Witte, M. (2022) · Frontiers in Neuroanatomy · doi:10.3389/fnana.2022.1000107 · Cited by 1 · see citing works