Channelrhodopsin-2-assisted circuit mapping of long-range callosal projections

Millisecond-timescale, genetically targeted optical control of neural activity

Boyden, E. S., Zhang, F., Bamberg, E., Nagel, G., & Deisseroth, K. A. (2005) · Nature Neuroscience · doi:10.1038/nn1525 · Cited by 5,015

Improved monomeric red, orange and yellow fluorescent proteins derived from Discosoma sp. red fluorescent protein

Shaner, N. C., Campbell, R. E., Steinbach, P. A., Giepmans, B. N. G., Palmer, A. E., & Tsien, R. Y. (2004) · Nature Biotechnology · doi:10.1038/nbt1037 · Cited by 4,619

Synaptic Activity and the Construction of Cortical Circuits

Katz, L. C., & Shatz, C. J. (1996) · Science · doi:10.1126/science.274.5290.1133 · Cited by 3,048

A variant of yellow fluorescent protein with fast and efficient maturation for cell-biological applications

Nagai, T., Ibata, K., Park, E. S., Kubota, M., Mikoshiba, K., & Miyawaki, A. (2002) · Nature Biotechnology · doi:10.1038/nbt0102-87 · Cited by 2,769

Channelrhodopsin-2, a directly light-gated cation-selective membrane channel

Nagel, G., Szellas, T., Huhn, W., Kateriya, S., Adeishvili, N., Berthold, P. R., Ollig, D., Hegemann, P., & Bamberg, E. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1936192100 · Cited by 2,730

NEURONAL CIRCUITS OF THE NEOCORTEX

Douglas, R. J., & Martin, K. A. C. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144152 · Cited by 1,886

Intrinsic firing patterns of diverse neocortical neurons

Connors, B. W., & Gutnick, M. J. (1990) · Trends in Neurosciences · doi:10.1016/0166-2236(90)90185-d · Cited by 1,440

Red fluorescent protein

CHAFFEY, N. J. (2001) · Trends in Plant Science · doi:10.1016/s1360-1385(01)01902-1 · Cited by 1,045

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

A Quantitative Map of the Circuit of Cat Primary Visual Cortex

Binzegger, T., Douglas, R. J., & Martin, K. A. C. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1400-04.2004 · Cited by 893

WTR: A Toolkit for Functional Anterograde Transneuronal Circuit MappingPreprint

Chen, C., Liu, R., Yi-Luo, A., Cao, X., Hu, J., Guan, S., Chang, S.-Y., Cui, X., Zhou, W., Zhao, F., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.03.23.713595 · Cited by 1

GABAergic signaling in cortical feedback to the olfactory bulb

Mazo, C. (2017) · theses.fr (ABES) · doi:10.70675/2ebf44fdz7471z4669zbc58zdbe2e8e66849 · Cited by 1

Optical Imaging and Control of Neurons

Song, Y. (2012) · Springer eBooks · doi:10.1007/978-94-007-3965-9_14

Optical analysis of synaptic plasticity in rat hippocampus

Zhang, Y. (2008) · edoc (University of Basel) · doi:10.5451/unibas-004414662

Transfer at C. elegans Synapses

Narayan, A. (2010) · CaltechTHESIS (California Institute of Technology) · doi:10.7907/cb9q-mc14

Optogenetics: Molecular and Optical Tools for Controlling Life with Light

Boyden, E. S. (2013) · Conference on Lasers and Electro-Optics · doi:10.1364/cleo_at.2013.af1l.1

Optogenetic approaches for deciphering the neural circuits of the cortex

Brown, S. P. (2014) · Conference on Lasers and Electro-Optics · doi:10.1364/cleo_at.2014.af1b.1

Channelrhodopsin as a Noble Biomaterial Useful for the Operation and Performance Test of the Ionchannel Devices

Uno, H., Wang, Z.-H., Takada, N., Ishizuka, T., Yawo, H., & Urisu, T. (2012) · MATERIALS TRANSACTIONS · doi:10.2320/matertrans.n-m2012814

Strategies for recovering exact structure of neural circuits with broadly targeted fluorescent connectivity probesPreprint

Mishchenko, Y. (2009) · Nature Precedings · doi:10.1038/npre.2009.2669.2

Behavioural effects of single-cell stimulation in Barrel cortex

Tanke, N. (2014) · EUR Research Repository (Erasmus University Rotterdam)

Activity Regulation in the Study of Neural Plasticity

Komai, S. (2015) · Springer eBooks · doi:10.1007/978-4-431-55516-2_20

Discovery and Development of Spectrally Diverse Channelrhodopsins (ChR) for Neurobiological Applications

Lin, J. Y., Knutsen, P. M., & Muller, A. (2015) · Biological and medical physics, biomedical engineering · doi:10.1007/978-3-319-12913-6_5

Optical Recording and Photo Modulation in the Study of Dynamics in Neural Circuits

Xu, H. (2010) · doi:10.7301/z0db8025

Uncrossed cortical and thalamic circuits to mediate sensory processing weeks after stroke

Aminoltejari, K. (2011) · cIRcle (University of British Columbia) · doi:10.14288/1.0072024

Optogenetic Stimulation of Neurons in the Brainstem of Freely Behaving Rats and Mice

Abbott, S. B. G. (2012) · Neuromethods · doi:10.1007/978-1-62703-233-9_1

Photoswitchable Voltage-Gated Ion Channels

Fortin, D. L., & Krämer, R. (2011) · Neuromethods · doi:10.1007/978-1-61779-031-7_11

Encoding of saltatory tactile velocity in the adult orofacial somatosensory system

Custead, R. (2016) · Lincoln (University of Nebraska)

Neocortical Circuit Interrogation with Optogenetics

Fenno, L. E., & Deisseroth, K. A. (2013) · Neuromethods · doi:10.1007/978-1-62703-785-3_11

Development of High-Throughput Screening Device for Neurodegenerative Diseases

Urisu, T., Wang, Z., Uno, H., Nagaoka, Y., Kobayashi, K., Goto-Saitoh, M., Suzuki, Y., & Urabe, Y. (2016) · Springer eBooks · doi:10.1007/978-4-431-56429-4_4

Revolutionizing Causal Circuitry Neurostimulation Utilizing the Optogenetic Technique Through Advanced Microsystems Development

Kale, R. P., Paek, S. B., Tye, S. J., & Kouzani, A. Z. (2017) · Series in bioengineering · doi:10.1007/978-981-10-3957-7_3

Optogenetic approaches in neurobiology

Borisova, E. V., Epifanova, E. A., Tutukova, S., Salina, V. A., & Babaev, A. A. (2016) · Molecular Genetics Microbiology and Virology · doi:10.3103/s0891416816040029

Engineering of TEV Protease for Manipulation of Biosystems

Chen, X. (2014) · TSpace (University of Toronto)

Extracellular unit recording study in characterizing activity of optogenetically identified parvalbumin expressing neurons in dentate gyrus of freely moving mice

Lit, K. K. (2017) · doi:10.32657/10356/72720

Oscillations in routing and chaos

Palmigiano, A. (2017) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-6513

Anatomical and functional analysis of non-retinal tectal afferents in larval zebrafish

Heap, L. A. (2017) · The University of Queensland · doi:10.14264/uql.2017.805

Optimal dissection of a model circuit

Sakaba, T. (2018) · The Journal of Physiology · doi:10.1113/jp276895

Molecular and structural determinants that contribute to channel function and gating in channelrhodopsin-2

Richards, R. (2016) · Digital WPI

PACAP neurons in the ventral premammillary nucleus regulate reproductive function in the female mouse

Ross, R. A., Leon, S., Madara, J. C., Schafer, D. M., Fergani, C., Maguire, C., Verstegen, A. M. J., Brengle, E., Kong, D., Herbison, A. E., et al. (2019) · Yearbook of pediatric endocrinology · doi:10.1530/ey.16.7.1

Thalamic encoding of complex sensory patterns and its possible role in cognitionPreprint

Castejon, C., Martín-Cortecero, J., & Núñez, Á. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.08.19.257667

Input-specific organization of cellular and subcellular connectivity in superficial layers of the prefrontal cortex

Little, J. P. (2013) · ProQuest Demo Repository

Development of Glutamatergic and GABAergic Synapses

Sassoé‐Pognetto, M., & Patrizi, A. (2021) · Springer eBooks · doi:10.1007/978-3-030-23810-0_12

A Platform for Spatiotemporal “Matrix” Stimulation in Brain Networks Reveals Novel Forms of Circuit Plasticity

Wilson, N. R., Wang, F. L., Chen, N., Yan, S. X., Daitch, A. L., Shi, B., Sharma, S., & Sur, M. (2022) · Frontiers in Neural Circuits · doi:10.3389/fncir.2021.792228

Neural Circuits Underlying the Pathophysiology of Major Depression

Amidfar, M., & Kim, Y. (2022) · Neuromethods · doi:10.1007/978-1-0716-2083-0_3

Development of Glutamatergic and GABAergic Synapses

Sassoé‐Pognetto, M., & Patrizi, A. (2019) · Springer eBooks · doi:10.1007/978-3-319-97911-3_12-2

Neurophotonics

Mascaro, A. L. A., Silvestri, L., Sacconi, L., Calamai, M., & Pavone, F. S. (2015) · Wiley eBooks · doi:10.1002/9783527600441.oe1009

Topological zones define basolateral amygdala synaptic input and functional organization of the claustrum

Ham, G. X. (2021) · DR-NTU (Nanyang Technological University) · doi:10.32657/10356/155180

Optogenetics

Cardin, J. A. (2014) · Springer eBooks · doi:10.1007/978-1-4614-7320-6_524-1

S1 Microcircuits

Feldmeyer, D. (2015) · Atlantis Press eBooks · doi:10.2991/978-94-6239-133-8_42 · Cited by 1

Faculty Opinions recommendation of Progenitor hyperpolarization regulates the sequential generation of neuronal subtypes in the developing neocortex.

Hippenmeyer, S. (2018) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.733715075.793551739

Optogenetics

Michaelides, M., & Bonci, A. (2016) · Springer eBooks · doi:10.1007/978-1-4939-3474-4_172

Optogenetics

Cardin, J. A. (2015) · Springer eBooks · doi:10.1007/978-1-4614-6675-8_524

Optogenetics

Michaelides, M., & Bonci, A. (2015) · Springer eBooks · doi:10.1007/978-1-4614-6434-1_172-1

Faculty Opinions recommendation of Studies of cortical connectivity using optical circuit mapping methods.

Duffin, J. (2017) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.732084138.793539459

In vivo imaging of synaptogenesis

Munz, M., Kutsarova, E., & Ruthazer, E. S. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-823672-7.00002-8

Optogenetic approaches in neurobiology

Borisova, E. V., Epifanova, E. A., Tutukov, S. A., Salina, V. A., & Babaev, A. A. (2016) · Molecular Genetics Microbiology and Virology (Russian) · doi:10.18821/0208-0613-2016-34-4-128-132

Faculty Opinions recommendation of New rabies virus variants for monitoring and manipulating activity and gene expression in defined neural circuits.

Pickering, A. E. (2011) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.13399006.14768127

Channelrhodopsin: Potential Applications in Vision Restoration

Pan, Z., & Dizhoor, A. M. (2009) · Wiley eBooks · doi:10.1002/9780470015902.a0021388

Faculty Opinions recommendation of Progenitor hyperpolarization regulates the sequential generation of neuronal subtypes in the developing neocortex.

Robertson, S. P. (2019) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.733715075.793557713

Faculty Opinions recommendation of Neural substrates of awakening probed with optogenetic control of hypocretin neurons.

Mayford, M. R. (2007) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1096940.553246

Optogenetics

Cardin, J. A. (2022) · Springer eBooks · doi:10.1007/978-1-0716-1006-0_524

Modeling and application of electrochemical ammonia recovery

Rodrigues, M. (2022) · doi:10.18174/575597

Optogenetics

Michaelides, M., & Bonci, A. (2022) · Springer eBooks · doi:10.1007/978-3-030-88832-9_172

Decision letter: A striatal circuit balances learned fear in the presence and absence of sensory cues

(2022) · eLife · doi:10.7554/elife.75703.sa1

eLife Assessment: Reward contingency gates selective cholinergic suppression of amygdala neurons

Bradfield, L. A. (2023) · eLife · doi:10.7554/elife.89093.1.sa3

Reward contingency gates selective cholinergic suppression of amygdala neuronsPreprint

Kimchi, E. Y., Burgos-Robles, A., Matthews, G. A., Chakoma, T. L., Patarino, M., Weddington, J., Siciliano, C. A., Yang, W., Foutch, S., Simons, R., et al. (2023) · eLife · doi:10.7554/elife.89093.1

The Diversity and Synaptic Connectivity of Somatostatin-Containing Inhibitory Interneurons in the Somatosensory (Barrel) Cortex

Hostetler, R. E. (2023) · The Research Repository @ WVU (West Virginia University) · doi:10.33915/etd.12253

Decision letter: Criticality supports cross-frequency cortical-thalamic information transfer during conscious states

(2023) · eLife · doi:10.7554/elife.86547.sa1

Reviewer #3 (Public Review): Rabies virus-based barcoded neuroanatomy resolved by single-cell RNA and in situ sequencing

(2024) · eLife · doi:10.7554/elife.87866.3.sa3

Reviewer #2 (Public Review): Patch-walking: Coordinated multi-pipette patch clamp for efficiently finding synaptic connections

(2024) · eLife · doi:10.7554/elife.97399.1.sa1

eLife Assessment: Patch-walking: Coordinated multi-pipette patch clamp for efficiently finding synaptic connections

Smith, J. C. (2024) · eLife · doi:10.7554/elife.97399.1.sa3

Patch-walking: Coordinated multi-pipette patch clamp for efficiently finding synaptic connectionsPreprint

Yip, M. C., Gonzalez, M. M., Lewallen, C. F., Landry, C. R., Kolb, I., Yang, B., Stoy, W. A., Fong, M., Rowan, M. J., Boyden, E. S., et al. (2024) · eLife · doi:10.7554/elife.97399.1

Reviewer #1 (Public Review): Patch-walking: Coordinated multi-pipette patch clamp for efficiently finding synaptic connections

(2024) · eLife · doi:10.7554/elife.97399.1.sa2

Reviewer #3 (Public Review): Patch-walking: Coordinated multi-pipette patch clamp for efficiently finding synaptic connections

(2024) · eLife · doi:10.7554/elife.97399.1.sa0

Reviewer #2 (Public Review): Single neurons and networks in the claustrum integrate input from widespread cortical sources

Shelton, A. M., Oliver, D. K., Lazarte, I. P., et al. (2024) · eLife · doi:10.7554/elife.98002.1.sa1

Reviewer #1 (Public Review): Single neurons and networks in the claustrum integrate input from widespread cortical sources

Shelton, A. M., Oliver, D. K., Lazarte, I. P., et al. (2024) · eLife · doi:10.7554/elife.98002.1.sa2

Reviewer #3 (Public Review): Single neurons and networks in the claustrum integrate input from widespread cortical sources

Shelton, A. M., Oliver, D. K., Lazarte, I. P., et al. (2024) · eLife · doi:10.7554/elife.98002.1.sa0

eLife Assessment: Single neurons and networks in the claustrum integrate input from widespread cortical sources

Bathellier, B. (2024) · eLife · doi:10.7554/elife.98002.1.sa3

Cell class-specific long-range axonal projections of neurons in mouse whisker-related somatosensory corticesPreprint

Liu, Y., Bech, P., Tamura, K., Délez, L. T., Crochet, S., & Petersen, C. C. H. (2024) · eLife · doi:10.7554/elife.97602.2

Fabrication and characterization of ultra-flexible optoelectrodes for chronic opto-electric neural interfaces

Liu, Y., Ma, H., Artem, I., Shi, Y.-Z., Meng, L., Xu, M., & He, F. (2024) · Conference on Biomedical Photonics and Cross-Fusion (BPC) · doi:10.1117/12.3039744

Functional study of residual iCre activity relevant for split-Cre applications

Minetti, A., Barsotti, N., & Pasqualetti, M. (2024) · Current Research in Biotechnology · doi:10.1016/j.crbiot.2024.100263

From Circuits to Drug Targets: The Promise of Opto- and Chemogenetics for Drug Discovery

Kätzel, D. (2024) · Royal Society of Chemistry eBooks · doi:10.1039/9781837672059-00185 · Cited by 1

WTR: An Anterograde Tracing Toolkit for Neural Circuits MappingPreprint

Chen, C., Yi-Luo, A., Liu, R., Cao, X., Chang, S., Guan, S., Cui, X., Hu, J., Zhou, W. J., Zhao, F., et al. (2024) · SSRN Electronic Journal · doi:10.2139/ssrn.5055156

Characterization of direct Purkinje cell outputs to the brainstemPreprint

Chen, C. H., Yao, Z., Wu, S., & Regehr, W. G. (2025) · eLife · doi:10.7554/elife.101825.2

Modulating Interhemispheric Connectivity Through Chemogenetic Stimulation: A fMRI-fMRS StudyPreprint

Just, N. (2025) · Research Square · doi:10.21203/rs.3.rs-6369938/v1

A cortical–hippocampal communication undergoes rebalancing after new learningPreprint

Hall, A. F., & Wang, D. V. (2025) · eLife · doi:10.7554/elife.107370

A cortical–hippocampal communication undergoes rebalancing after new learningPreprint

Hall, A. F., & Wang, D. V. (2025) · eLife · doi:10.7554/elife.107370.1

Emerging bioelectronics and optogenetics for neurogastroenterology

Liu, H., Luo, W., Xu, M., Zhang, S., Xue, J., Chen, Q., Zhao, Y., Hu, N., & Gao, Z. (2025) · Biosensors and Bioelectronics · doi:10.1016/j.bios.2025.117795

Separation of Scales and the Improbability of Quantum Foundations for ConsciousnessPreprint

Harkiolakis, N. (2025) · SSRN Electronic Journal · doi:10.2139/ssrn.5353957

Neural Circuit Remodeling Underlying Enhanced Feeding During Pregnancy in MicePreprint

Inada, K., Tasaka, G., Hagihara, M., Kobayashi, K., Yukinaga, H., & Miyamichi, K. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.08.07.669199

Hypothalamic recurrent inhibition regulates functional states of stress effector neurons

Ichiyama, A., Mestern, S., Füzesi, T., Allman, B. L., Nicola, W., Bains, J. S., Muller, L., & Inoue, W. (2026) · Cell Reports · doi:10.1016/j.celrep.2026.117741

Postnatal Development of Pyramidal Neurons Excitability and Synaptic Inputs in Mouse Gustatory Cortical Circuits

Schiff, H. C., & Maffei, A. (2026) · eNeuro · doi:10.1523/eneuro.0329-25.2026

CS - plasticity and behavioral-state integration in the posterior insula during auditory fear learningPreprint

Osypenko, D., Palchaudhuri, S., Kochubey, O., & Schneggenburger, R. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.09.25.678609

Neuronal architecture of the mouse insular cortex underlying its diverse functionsPreprint

Jongbloets, B. C., Chen, Y., Gingerich, I. K., Muniak, M. A., & Mao, T. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.10.23.683697

Synaptic Silencing with Transactivation of Tetanus Neurotoxin for Pathway-Selective Manipulation

Isa, T., Isa, K., & Vanduffel, W. (2025) · Methods in molecular biology · doi:10.1007/978-1-0716-4807-0_15

Experience-dependent plasticity of layer 2/3 circuits in developing somatosensory neocortex

Wen, J. A. (2018) · KiltHub Repository · doi:10.1184/r1/6716537

Dendritic Integration and Reciprocal Inhibition in the Retina

Grimes, W. N. (2008) · University Libraries (University of Maryland)

Additional file 5 of A symbiotic footprint in the plant root microbiome

Hartman, K., Schmid, M. W., Bodenhausen, N., Bender, S. F., Valzano‐Held, A., Schlaeppi, K., & van der Heijden, M. G. A. (2024) · Figshare · doi:10.6084/m9.figshare.26607802

Additional file 8 of A symbiotic footprint in the plant root microbiome

Hartman, K., Schmid, M. W., Bodenhausen, N., Bender, S. F., Valzano‐Held, A., Schlaeppi, K., & van der Heijden, M. G. A. (2024) · Figshare · doi:10.6084/m9.figshare.26607811

Additional file 4 of A symbiotic footprint in the plant root microbiome

Hartman, K., Schmid, M. W., Bodenhausen, N., Bender, S. F., Valzano‐Held, A., Schlaeppi, K., & van der Heijden, M. G. A. (2024) · Figshare · doi:10.6084/m9.figshare.26607799

Additional file 7 of A symbiotic footprint in the plant root microbiome

Hartman, K., Schmid, M. W., Bodenhausen, N., Bender, S. F., Valzano‐Held, A., Schlaeppi, K., & van der Heijden, M. G. A. (2024) · Figshare · doi:10.6084/m9.figshare.26607808

Additional file 1 of A symbiotic footprint in the plant root microbiome

Hartman, K., Schmid, M. W., Bodenhausen, N., Bender, S. F., Valzano‐Held, A., Schlaeppi, K., & van der Heijden, M. G. A. (2024) · Figshare · doi:10.6084/m9.figshare.26607790

Additional file 6 of A symbiotic footprint in the plant root microbiome

Hartman, K., Schmid, M. W., Bodenhausen, N., Bender, S. F., Valzano‐Held, A., Schlaeppi, K., & van der Heijden, M. G. A. (2024) · Figshare · doi:10.6084/m9.figshare.26607805

Additional file 2 of A symbiotic footprint in the plant root microbiome

Hartman, K., Schmid, M. W., Bodenhausen, N., Bender, S. F., Valzano‐Held, A., Schlaeppi, K., & van der Heijden, M. G. A. (2024) · Figshare · doi:10.6084/m9.figshare.26607793

Additional file 3 of A symbiotic footprint in the plant root microbiome

Hartman, K., Schmid, M. W., Bodenhausen, N., Bender, S. F., Valzano‐Held, A., Schlaeppi, K., & van der Heijden, M. G. A. (2024) · Figshare · doi:10.6084/m9.figshare.26607796

G-protein subtype selectivity in dopamine D1 receptor

Nguyen, A. M. (2025) · Digital Repository Service (Northeastern University) · doi:10.17760/d20791815

Early adversity promotes adolescent avoidance behavior by enhancing prefrontal–amygdala communication through CRH⁺ glutamatergic neuronsPreprint

Goodpaster, C. M., Zeidler, Z., Gongwer, M. W., Bland, C. J., Shari, M., Klune, C. B., Jones, N. S., Ramirez, M., Batul-Alturki, M., Hundley, R., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2025.12.23.696229

A neuronal population in the bed nucleus of the stria terminalis mediating pup-directed aggression in male micePreprint

Inada, K., Sato, H., Hagihara, M., & Miyamichi, K. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.02.26.708360

Transformation and recombination of neural information in a brain networkPreprint

Jiang, Y., Ke, Y., Wen, J., Medrano, J., Tu, W., Stallings, B., Bricault, S., Dong, A., Chung, S. K., & Jasanoff, A. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.03.04.709604

投射先特異的な単一神経細胞を起点とした狂犬病ウイルストレーシング法

正木, 佑. (2022) · Institutional Repositories DataBase (IRDB)

Behavioral and synaptic consequences following removal of the Il1rapl1 gene in mice, a model of intellectual disability

Houbaert, X. (2014) · theses.fr (ABES) · doi:10.70675/e01f6a8dze8a0z4d04z90e1z3d1812752374

Long-term channelrhodopsin-2 (ChR2) expression can induce abnormal axonal morphology and targeting in cerebral cortex

Miyashita, T., Shao, Y. R., Chung, J. E., Pourzia, O., & Feldman, D. E. (2013) · Frontiers in Neural Circuits · doi:10.3389/fncir.2013.00008 · Cited by 123

High-speed mapping of synaptic connectivity using photostimulation in Channelrhodopsin-2 transgenic mice

Wang, H., Peça, J., Matsuzaki, M., Matsuzaki, K., Noguchi, J., Qiu, L., Wang, D., Zhang, F., Boyden, E. S., Deisseroth, K. A., et al. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0700384104 · Cited by 384

Optical Elucidation of Neural Microcircuitry

Urabe, H. (2009) · doi:10.7301/z0rr1whb

An engineered channelrhodopsin optimized for axon terminal activation and circuit mapping

Hamada, S., Nagase, M., Yoshizawa, T., Hagiwara, A., Isomura, Y., Watabe, A. M., & Ohtsuka, T. (2021) · Communications Biology · doi:10.1038/s42003-021-01977-7 · Cited by 23

High-speed optogenetic circuit mapping

Augustine, G. J., Chen, S., Gill, H., Katarya, M., Kim, J., Kudolo, J., Lee, L. M., Lee, H., Lo, S. Q., Nakajima, R., et al. (2013) · Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE · doi:10.1117/12.2012404 · Cited by 2