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Koppensteiner, P., Bhandari, P., Önal, C., Borges Merjane, C., Le Monnier, E., Roy, U.,https://doi.org/10.1073/pnas.2301449121__Shigemoto, R. (2024). GABAB receptors induce phasic release from medial habenula terminals through activity-dependent recruitment of release-ready vesicles. Proceedings of the National Academy of Sciences. Proceedings of the National Academy of Sciences.https://doi.org/10.1073/pnas.2301449121 

Chen, J., Kaufmann, W., Chen, C., Arai,https://doi.org/10.1016/j.neuron.2023.12.002__itaru, Kim, O., Shigemoto, R., &; Jonas, P. M. (n.d.). Developmental transformation of C+ channel-vesicle nanotopography at a central GABAergic synapse. Neuron. Elsevier.https://doi.org/10.1016/j.neuron.2023.12.002 

Vierra, N. C., Ribeiro-Silva, L., Kirmiz, M., Van Der List, D., Bhandari, P., Mack, O. A.,https://doi.org/10.1038/s41467-023-40930-6__Trimmer, J. S. (2023). Neuronal ER-plasma membrane junctions couple excitation to C+-activated PKA signaling. Nature Communications. Springer Nature.https://doi.org/10.1038/s41467-023-40930-6 

Eguchi, K., Le Monnier, E., &; Shigemoto, R. (2023). Nanoscale phosphoinositide distribution on cell membranes of mouse cerebellar neurons. The Journal of Neuroscience. Society for Neuroscience.https://doi.org/10.1523/JNEUROSCI.1514-22.2023 

Shigemoto, R. (2023). Transition from tonic to phasic neurotransmitter release by presynaptic GABAB receptor activation in medial habenula terminals. Institute of Science and Technology Austria.https://doi.org/10.15479/AT:ISTA:13173 

Eguchi, K., Montanaro-Punzengruber, J.-C., Le Monnier, E., &; Shigemoto, R. (2022). The number and distinct clustering patterns of voltage-gated Calcium channels in nerve terminals. Frontiers in Neuroanatomy. Frontiers.https://doi.org/10.3389/fnana.2022.846615 

Shigemoto, R. (2022). Electron microscopic visualization of single molecules by tag-mediated metal particle labeling. Microscopy. Oxford Academic.https://doi.org/10.1093/jmicro/dfab048 

Martín-Belmonte, A., Aguado, C., Alfaro-Ruiz, R., Moreno-Martínez, A. E., de la Ossa, L., Aso, E.,https://doi.org/10.1186/s13195-022-01078-5__Luján, R. (2022). Nanoscale alterations in GABAB receptors and GIRK channel organization on the hippocampus of APP/P mice. Alzheimer’s Research &; Therapy. Springer Nature.https://doi.org/10.1186/s13195-022-01078-5 

Fredes Tolorza, F. A., Silva Sifuentes, M. A., Koppensteiner, P., Kobayashi, K., Jösch, M. A., &; Shigemoto, R. (2021). Ventro-dorsal hippocampal pathway gates novelty-induced contextual memory formation. Current Biology. Elsevier.https://doi.org/10.1016/j.cub.2020.09.074 

Schöpf, C. L., Ablinger, C., Geisler, S. M., Stanika, R. I., Campiglio, M., Kaufmann, W.,https://doi.org/10.1073/pnas.1920827118__Obermair, G. J. (2021). Presynaptic ;12;4 subunits are key organizers of glutamatergic synapses. PNAS. National Academy of Sciences.https://doi.org/10.1073/pnas.1920827118 

Fredes, F., &; Shigemoto, R. (2021). The role of hippocampal mossy cells in novelty detection. Neurobiology of Learning and Memory. Elsevier.https://doi.org/10.1016/j.nlm.2021.107486 

Butola, T., Alvanos, T., Hintze, A., Koppensteiner, P., Kleindienst, D., Shigemoto, R.,https://doi.org/10.1523/JNEUROSCI.0586-21.2021__Moser, T. (2021). RIM-binding protein 2 organizes Ca<sup>21</sup> channel topography and regulates release probability and vesicle replenishment at a fast central synapse. Journal of Neuroscience. Society for Neuroscience.https://doi.org/10.1523/JNEUROSCI.0586-21.2021 

Biane, C., Rückerl, F., Abrahamsson, T., Saint-Cloment, C., Mariani, J., Shigemoto, R.,https://doi.org/10.7554/eLife.65954__Cathala, L. (2021). Developmental emergence of two-stage nonlinear synaptic integration in cerebellar interneurons. ELife. eLife Sciences Publications.https://doi.org/10.7554/eLife.65954 

Bhandari, P., Vandael, D. H., Fernández-Fernández, D., Fritzius, T., Kleindienst, D., Önal, H. C.,https://doi.org/10.7554/ELIFE.68274__Koppensteiner, P. (2021). GABAB receptor auxiliary subunits modulate Ca.3-mediated release from medial habenula terminals. ELife. eLife Sciences Publications.https://doi.org/10.7554/ELIFE.68274 

Kaufmann, W., Kleindienst, D., Harada, H., &; Shigemoto, R. (2021). High-Resolution localization and quantitation of membrane proteins by SDS-digested freeze-fracture replica labeling (SDS-FRL). In https://doi.org/10.1007/978-1-0716-1522-5_19__Receptor and Ion Channel Detection in the Brain (Vol. 169, pp. 267–283). New York: Humana.https://doi.org/10.1007/978-1-0716-1522-5_19 

Nakamoto, C., Konno, K., Miyazaki, T., Nakatsukasa, E., Natsume, R., Abe, M.,https://doi.org/10.1002/cne.24792__Watanabe, M. (2020). Expression mapping, quantification, and complex formation of Glu and Glu glutamate receptors in adult mouse brain. Journal of Comparative Neurology. Wiley.https://doi.org/10.1002/cne.24792 

Martín-Belmonte, A., Aguado, C., Alfaro-Ruíz, R., Moreno-Martínez, A. E., De La Ossa, L., Martínez-Hernández, J.,https://doi.org/10.3390/ijms21072459__Luján, R. (2020). Density of GABAB receptors is reduced in granule cells of the hippocampus in a mouse model of Alzheimer’s disease. International Journal of Molecular Sciences. MDPI.https://doi.org/10.3390/ijms21072459 

Eguchi, K., Velicky, P., Saeckl, E., Itakura, M., Fukazawa, Y., Danzl, J. G., &; Shigemoto, R. (2020). Advantages of acute brain slices prepared at physiological temperature in the characterization of synaptic functions. Frontiers in Cellular Neuroscience. Frontiers Media.https://doi.org/10.3389/fncel.2020.00063 

Bao, J., Graupner, M., Astorga, G., Collin, T., Jalil, A., Indriati, D. W.,https://doi.org/10.7554/eLife.56839__Llano, I. (2020). Synergism of type 1 metabotropic and ionotropic glutamate receptors in cerebellar molecular layer interneurons in vivo. ELife. eLife Sciences Publications.https://doi.org/10.7554/eLife.56839 

Martín-Belmonte, A., Aguado, C., Alfaro-Ruíz, R., Moreno-Martínez, A. E., De La Ossa, L., Martínez-Hernández, J.,https://doi.org/10.1111/bpa.12802__Luján, R. (2020). Reduction in the neuronal surface of post and presynaptic GABA&;B&; receptors in the hippocampus in a mouse model of Alzheimer’s disease. Brain Pathology. Wiley.https://doi.org/10.1111/bpa.12802 

Kleindienst, D., Montanaro-Punzengruber, J.-C., Bhandari, P., Case, M. J., Fukazawa, Y., &; Shigemoto, R. (2020). Deep learning-assisted high-throughput analysis of freeze-fracture replica images applied to glutamate receptors and calcium channels at hippocampal synapses. International Journal of Molecular Sciences. MDPI.https://doi.org/10.3390/ijms21186737 

Zenmyo, N., Tokumaru, H., Uchinomiya, S., Fuchida, H., Tabata, S., Hamachi, I.,https://doi.org/10.1246/bcsj.20190034__Ojida, A. (2019). Optimized reaction pair of the CysHis tag and Ni(II)-NTA probe for highly selective chemical labeling of membrane proteins. Bulletin of the Chemical Society of Japan. Bulletin of the Chemical Society of Japan.https://doi.org/10.1246/bcsj.20190034 

Byczkowicz, N., Eshra, A., Montanaro-Punzengruber, J.-C., Trevisiol, A., Hirrlinger, J., Kole, M. H.,https://doi.org/10.7554/eLife.42766__Hallermann, S. (2019). HCN channel-mediated neuromodulation can control action potential velocity and fidelity in central axons. ELife. eLife Sciences Publications.https://doi.org/10.7554/eLife.42766 

Kasugai, Y., Vogel, E., Hörtnagl, H., Schönherr, S., Paradiso, E., Hauschild, M.,https://doi.org/10.1016/j.neuron.2019.08.013__Ferraguti, F. (2019). Structural and functional remodeling of amygdala GABAergic synapses in associative fear learning. Neuron. Elsevier.https://doi.org/10.1016/j.neuron.2019.08.013 

Klotz, L., Wendler, O., Frischknecht, R., Shigemoto, R., Schulze, H., &; Enz, R. (2019). Localization of group II and III metabotropic glutamate receptors at pre- and postsynaptic sites of inner hair cell ribbon synapses. FASEB Journal. FASEB.https://doi.org/10.1096/fj.201901543R 

Tabata, S., Jevtic, M., Kurashige, N., Fuchida, H., Kido, M., Tani, K.,https://doi.org/10.1016/j.isci.2019.11.025__Ojida, A. (2019). Electron microscopic detection of single membrane proteins by a specific chemical labeling. IScience. Elsevier.https://doi.org/10.1016/j.isci.2019.11.025 

Luján, R., Aguado, C., Ciruela, F., Arus, X., Martín Belmonte, A., Alfaro Ruiz, R.,https://doi.org/10.3389/fncel.2018.00311__Fukazawa, Y. (2018). Sk2 channels associate with mGlu1;1 receptors and Ca.1 channels in Purkinje cells. Frontiers in Cellular Neuroscience. Frontiers Media.https://doi.org/10.3389/fncel.2018.00311 

Sawada, K., Kawakami, R., Shigemoto, R., &; Nemoto, T. (2018). Super resolution structural analysis of dendritic spines using three-dimensional structured illumination microscopy in cleared mouse brain slices. European Journal of Neuroscience. Wiley.https://doi.org/10.1111/ejn.13901 

Miklosi, A., Del Favero, G., Bulat, T., Höger, H., Shigemoto, R., Marko, D., &; Lubec, G. (2018). Super resolution microscopical localization of dopamine receptors 1 and 2 in rat hippocampal synaptosomes. Molecular Neurobiology. Springer.https://doi.org/10.1007/s12035-017-0688-y 

Luján, R., Aguado, C., Ciruela, F., Cózar, J., Kleindienst, D., De La Ossa, L.,https://doi.org/10.1007/s00429-017-1568-y__Fukazawa, Y. (2018). Differential association of GABAB receptors with their effector ion channels in Purkinje cells. Brain Structure and Function. Springer.https://doi.org/10.1007/s00429-017-1568-y 

Miki, T., Kaufmann, W., Malagon, G., Gomez, L., Tabuchi, K., Watanabe, M.,https://doi.org/10.1073/pnas.1704470114__Marty, A. (2017). Numbers of presynaptic C+ channel clusters match those of functionally defined vesicular docking sites in single central synapses. PNAS. National Academy of Sciences.https://doi.org/10.1073/pnas.1704470114 

Rubio, M., Matsui, K., Fukazawa, Y., Kamasawa, N., Harada, H., Itakura, M.,https://doi.org/10.1007/s00429-017-1408-0__Shigemoto, R. (2017). The number and distribution of AMPA receptor channels containing fast kinetic Glu and Glu subunits at auditory nerve synapses depend on the target cells. Brain Structure and Function. Springer.https://doi.org/10.1007/s00429-017-1408-0 

Shigemoto, R., &; Jösch, M. A. (2017). The genetic encoded toolbox for electron microscopy and connectomics. WIREs Developmental Biology. Wiley-Blackwell.https://doi.org/10.1002/wdev.288 

Aloisi, E., Le Corf, K., Dupuis, J., Zhang, P., Ginger, M., Labrousse, V.,https://doi.org/10.1038/s41467-017-01191-2__Frick, A. (2017). Altered surface mGlu dynamics provoke synaptic NMDAR dysfunction and cognitive defects in Fmr1 knockout mice. Nature Communications. Nature Publishing Group.https://doi.org/10.1038/s41467-017-01191-2 

Ukai, H., Kawahara, A., Hirayama, K., Case, M. J., Aino, S., Miyabe, M.,https://doi.org/10.1371/journal.pone.0179377__Ito, I. (2017). PirB regulates asymmetries in hippocampal circuitry. PLoS One. Public Library of Science.https://doi.org/10.1371/journal.pone.0179377 

Booker, S., Althof, D., Gross, A., Loreth, D., Müller, J., Unger, A.,https://doi.org/10.1093/cercor/bhw090__Kulik, Á. (2016). KCT auxiliary proteins modulate kinetics of GABAB receptor-mediated inhibition in Cholecystokinin-containing interneurons. Cerebral Cortex. Oxford University Press.https://doi.org/10.1093/cercor/bhw090 

Matsuno, H., Kudoh, M., Watakabe, A., Yamamori, T., Shigemoto, R., &; Nagao, S. (2016). Distribution and structure of synapses on medial vestibular nuclear neurons targeted by cerebellar flocculus purkinje cells and vestibular nerve in mice: Light and electron microscopy studies. PLoS One. Public Library of Science.https://doi.org/10.1371/journal.pone.0164037 

Harada, H., &; Shigemoto, R. (2016). Immunogold protein localization on grid-glued freeze-fracture replicas. In High-Resolution Imaging of Cellular Proteins (Vol. 1474, pp. 203–216). Springer.https://doi.org/10.1007/978-1-4939-6352-2_12 

Mansouri, M., Kasugai, Y., Fukazawa, Y., Bertaso, F., Raynaud, F., Perroy, J.,https://doi.org/10.1111/ejn.12779__Ferraguti, F. (2015). Distinct subsynaptic localization of type 1 metabotropic glutamate receptors at glutamatergic and GABAergic synapses in the rodent cerebellar cortex. European Journal of Neuroscience. Wiley-Blackwell.https://doi.org/10.1111/ejn.12779 

Gómez Gonzalo, M., Navarrete, M., Perea, G., Covelo, A., Martín Fernández, M., Shigemoto, R.,https://doi.org/10.1093/cercor/bhu231__Araque, A. (2015). Endocannabinoids induce lateral long term potentiation of transmitter release by stimulation of gliotransmission. Cerebral Cortex. Oxford University Press.https://doi.org/10.1093/cercor/bhu231 

Nakamura, Y., Harada, H., Kamasawa, N., Matsui, K., Rothman, J., Shigemoto, R.,https://doi.org/10.1016/j.neuron.2014.11.019__Takahashi, T. (2015). Nanoscale distribution of presynaptic C+ channels and its impact on vesicular release during development. Neuron. Elsevier.https://doi.org/10.1016/j.neuron.2014.11.019 

Javdani, F., Holló, K., Hegeds, K., Kis, G., Hegyi, Z., Dócs, K.,https://doi.org/10.1002/cne.23774__Antal, M. (2015). Differential expression patterns of K+Cl- cotransporter 2 in neurons within the superficial spinal dorsal horn of rats. Journal of Comparative Neurology. Wiley-Blackwell.https://doi.org/10.1002/cne.23774 

Edamura, M., Murakami, G., Meng, H., Itakura, M., Shigemoto, R., Fukuda, A., &; Nakahara, D. (2014). Functional deficiency of MHC class i enhances LTP and abolishes LTD in the nucleus accumbens of mice. PLoS One. Public Library of Science.https://doi.org/10.1371/journal.pone.0107099 

Ritzau Jost, A., Delvendahl, I., Rings, A., Byczkowicz, N., Harada, H., Shigemoto, R.,https://doi.org/10.1016/j.neuron.2014.08.036__Hallermann, S. (2014). Ultrafast action potentials mediate kilohertz signaling at a central synapse. Neuron. Elsevier.https://doi.org/10.1016/j.neuron.2014.08.036 

Wang, W., Nakadate, K., Masugi Tokita, M., Shutoh, F., Aziz, W., Tarusawa, E.,https://doi.org/10.1073/pnas.1315541111__Shigemoto, R. (2014). Distinct cerebellar engrams in short-term and long-term motor learning. PNAS. National Academy of Sciences.https://doi.org/10.1073/pnas.1315541111 

Aziz, W., Wang, W., Kesaf, S., Mohamed, A., Fukazawa, Y., &; Shigemoto, R. (2014). Distinct kinetics of synaptic structural plasticity, memory formation, and memory decay in massed and spaced learning. PNAS. National Academy of Sciences.https://doi.org/10.1073/pnas.1303317110 

Hatakeyama, J., Wakamatsu, Y., Nagafuchi, A., Kageyama, R., Shigemoto, R., &; Shimamura, K. (2014). Cadherin-based adhesions in the apical endfoot are required for active Notch signaling to control neurogenesis in vertebrates. Development. Company of Biologists.https://doi.org/10.1242/dev.102988 

Matsukawa, H., Akiyoshi Nishimura, S., Zhang, Q., Luján, R., Yamaguchi, K., Goto, H.,https://doi.org/10.1523/JNEUROSCI.1141-14.2014__Itohara, S. (2014). Netrin-G/NGL complexes encode functional synaptic diversification. Journal of Neuroscience. Society for Neuroscience.https://doi.org/10.1523/JNEUROSCI.1141-14.2014 

Rubio, M., Fukazawa, Y., Kamasawa, N., Clarkson, C., Molnár, E., &; Shigemoto, R. (2014). Target- and input-dependent organization of AMPA and NMDA receptors in synaptic connections of the cochlear nucleus. Journal of Comparative Neurology. Wiley-Blackwell.https://doi.org/10.1002/cne.23654 

Beppu, K., Sasaki, T., Tanaka, K., Yamanaka, A., Fukazawa, Y., Shigemoto, R., &; Matsui, K. (2014). Optogenetic countering of glial acidosis suppresses glial glutamate release and ischemic brain damage. Neuron. Elsevier.https://doi.org/10.1016/j.neuron.2013.11.011 

Budreck, E., Kwon, O., Jung, J., Baudouin, S., Thommen, A., Kim, H.,https://doi.org/10.1073/pnas.1214718110__Kim, J. (2013). Neuroligin-1 controls synaptic abundance of NMDA-type glutamate receptors through extracellular coupling. PNAS. National Academy of Sciences.https://doi.org/10.1073/pnas.1214718110 

Dobi, A., Sartori, S., Busti, D., Van Der Putten, H., Singewald, N., Shigemoto, R., &; Ferraguti, F. (2013). Neural substrates for the distinct effects of presynaptic group III metabotropic glutamate receptors on extinction of contextual fear conditioning in mice. Neuropharmacology. Elsevier.https://doi.org/10.1016/j.neuropharm.2012.05.025 

Indriati, D., Kamasawa, N., Matsui, K., Meredith, A., Watanabe, M., &; Shigemoto, R. (2013). Quantitative localization of Ca.1 (P/Q-Type) voltage-dependent calcium channels in Purkinje cells: Somatodendritic gradient and distinct somatic coclustering with calcium-activated potassium channels. Journal of Neuroscience. Society for Neuroscience.https://doi.org/10.1523/JNEUROSCI.2921-12.2013 

Budisantoso, T., Harada, H., Kamasawa, N., Fukazawa, Y., Shigemoto, R., &; Matsui, K. (2013). Evaluation of glutamate concentration transient in the synaptic cleft of the rat calyx of Held. Journal of Physiology. Wiley-Blackwell.https://doi.org/10.1113/jphysiol.2012.241398 

Booker, S., Gross, A., Althof, D., Shigemoto, R., Bettler, B., Frotscher, M.,https://doi.org/10.1523/JNEUROSCI.1186-12.2013__Vida, I. (2013). Differential GABAB-receptor-mediated effects in perisomatic- and dendrite-targeting parvalbumin interneurons. Journal of Neuroscience. Society for Neuroscience.https://doi.org/10.1523/JNEUROSCI.1186-12.2013 

Sümegi, M., Fukazawa, Y., Matsui, K., Lörincz, A., Eyre, M., Nusser, Z., &; Shigemoto, R. (2012). Virus-mediated swapping of zolpidem-insensitive with zolpidem-sensitive GABA A receptors in cortical pyramidal cells. Journal of Physiology. Wiley-Blackwell.https://doi.org/10.1113/jphysiol.2012.227538 

Saito, Y., Inoue, T., Zhu, G., Kimura, N., Okada, M., Nishimura, M.,https://doi.org/10.1186/1750-1326-7-50__Suzuki, T. (2012). Hyperpolarization-activated cyclic nucleotide gated channels: A potential molecular link between epileptic seizures and A;2 generation in Alzheimer’s disease. Molecular Neurodegeneration. BioMed Central.https://doi.org/10.1186/1750-1326-7-50 

Sasaki, T., Beppu, K., Tanaka, K., Fukazawa, Y., Shigemoto, R., &; Matsui, K. (2012). Application of an optogenetic byway for perturbing neuronal activity via glial photostimulation. PNAS. National Academy of Sciences.https://doi.org/10.1073/pnas.1213458109 

Abrahamsson, T., Cathala, L., Matsui, K., Shigemoto, R., &; Digregorio, D. (2012). Thin dendrites of cerebellar interneurons confer sublinear synaptic integration and a gradient of short-term plasticity. Neuron. Elsevier.https://doi.org/10.1016/j.neuron.2012.01.027 

Ballesteros Merino, C., Lin, M., Wu, W., Ferrándiz Huertas, C., Cabañero, M., Watanabe, M.,https://doi.org/10.1002/hipo.20986__Luján, R. (2012).https://doi.org/10.1002/hipo.20986__Developmental profile of SK2 channel expression and function in C neurons. Hippocampus. Wiley-Blackwell.https://doi.org/10.1002/hipo.20986 

Budisantoso, T., Matsui, K., Kamasawa, N., Fukazawa, Y., &; Shigemoto, R. (2012). Mechanisms underlying signal filtering at a multisynapse contact. Journal of Neuroscience. Society for Neuroscience.https://doi.org/10.1523/JNEUROSCI.5243-11.2012 

Parajuli, L., Nakajima, C., Kulik, Á., Matsui, K., Schneider, T., Shigemoto, R., &; Fukazawa, Y. (2012). Quantitative regional and ultra structural localization of the Cahttps://doi.org/10.1523/JNEUROSCI.1142-12.2012__3 subunit of R type calcium channel in mouse brain. Journal of Neuroscience. Society for Neuroscience.https://doi.org/10.1523/JNEUROSCI.1142-12.2012 

Shinohara, Y., Hosoya, A., Yamasaki, N., Ahmed, H., Hattori, S., Eguchi, M.,https://doi.org/10.1002/hipo.20886__Shigemoto, R. (2012). Right-hemispheric dominance of spatial memory in split-brain mice. Hippocampus. Wiley-Blackwell.https://doi.org/10.1002/hipo.20886 

Fukazawa, Y., &; Shigemoto, R. (2012). Intra-synapse-type and inter-synapse-type relationships between synaptic size and AMPAR expression. Current Opinion in Neurobiology. Elsevier.https://doi.org/10.1016/j.conb.2012.01.006 

Chan, S., Glajch, K., Gertler, T., Guzmán, J., Mercer, J., Lewis, A.,https://doi.org/10.1038/nn.2692__Surmeier, J. (2011). HCN channelopathy in external globus pallidus neurons in models of Parkinson s disease. Nature Neuroscience. Nature Publishing Group.https://doi.org/10.1038/nn.2692 

Szabadits, E., Cserép, C., Szonyi, A., Fukazawa, Y., Shigemoto, R., Watanabe, M.,https://doi.org/10.1523/JNEUROSCI.5938-10.2011__Nyíri, G. (2011). NMDA receptors in hippocampal GABAergic synapses and their role in nitric oxide signaling. Journal of Neuroscience. Society for Neuroscience.https://doi.org/10.1523/JNEUROSCI.5938-10.2011 

Allen, D., Bond, C., Luján, R., Ballesteros Merino, C., Lin, M., Wang, K.,https://doi.org/10.1038/nn.2832__Adelman, J. (2011). The SK2-long isoform directs synaptic localization and function of SK2-containing channels. Nature Neuroscience. Nature Publishing Group.https://doi.org/10.1038/nn.2832 

Fukata, Y., Lovero, K., Iwanaga, T., Watanabe, A., Yokoi, N., Tabuchi, K.,https://doi.org/10.1073/pnas.0914537107__Fukata, M. (2010). Disruption of LG-linked synaptic complex causes abnormal synaptic transmission and epilepsy. PNAS. National Academy of Sciences.https://doi.org/10.1073/pnas.0914537107 

Atherton, J., Kitano, K., Baufreton, J., Fan, K., Wokosin, D., Tkatch, T.,https://doi.org/10.1523/JNEUROSCI.3898-10.2010__Bevan, M. (2010). Selective participation of somatodendritic HCN channels in inhibitory but not excitatory synaptic integration in neurons of the subthalamic nucleus. Journal of Neuroscience. Society for Neuroscience.https://doi.org/10.1523/JNEUROSCI.3898-10.2010 

Kasugai, Y., Swinny, J., Roberts, J., Dalezios, Y., Fukazawa, Y., Sieghart, W.,https://doi.org/10.1111/j.1460-9568.2010.07473.x__Somogyi, P. (2010). Quantitative localisation of synaptic and extrasynaptic GABAA receptor subunits on hippocampal pyramidal cells by freeze-fracture replica immunolabelling. European Journal of Neuroscience. Wiley-Blackwell.https://doi.org/10.1111/j.1460-9568.2010.07473.x 

Dong, Y., Fukazawa, Y., Wang, W., Kamasawa, N., &; Shigemoto, R. (2010). Differential postsynaptic compartments in the laterocapsular division of the central nucleus of amygdala for afferents from the parabrachial nucleus and the basolateral nucleus in the rat. Journal of Comparative Neurology. Wiley-Blackwell.https://doi.org/10.1002/cne.22487 

Furuya, S., Furuya, K., Shigemoto, R., &; Sokabe, M. (2010). Localization of NK1 receptors and roles of substance-P in subepithelial fibroblasts of rat intestinal villi. Cell and Tissue Research. Springer.https://doi.org/10.1007/s00441-010-1056-7 

Parajuli, L., Fukazawa, Y., Watanabe, M., &; Shigemoto, R. (2010). Subcellular distribution of ;11G subunit of T-type calcium channel in the mouse dorsal lateral geniculate nucleus. Journal of Comparative Neurology. Wiley-Blackwell.https://doi.org/10.1002/cne.22461 

Matsuda, K., Miura, E., Miyazaki, T., Kakegawa, W., Emi, K., Narumi, S.,https://doi.org/10.1126/science.1185152__Yuzaki, M. (2010). Cbln1 is a ligand for an orphan glutamate receptor ;42, a bidirectional synapse organizer. Science. American Association for the Advancement of Science.https://doi.org/10.1126/science.1185152 

Loukanov, A., Kamasawa, N., Danev, R., Shigemoto, R., &; Nagayama, K. (2010). Immunolocalization of multiple membrane proteins on a carbon replica with STEM and EDX. Ultramicroscopy. Elsevier.https://doi.org/10.1016/j.ultramic.2010.01.016 

Fernández Alacid, L., Aguado, C., Ciruela, F., Martín, R., Colón, J., Cabañero, M.,https://doi.org/10.1111/j.1471-4159.2009.06229.x__Luján, R. (2009).https://doi.org/10.1111/j.1471-4159.2009.06229.x__Subcellular compartment-specific molecular diversity of pre- and post-synaptic GABAB-activated GIRK channels in Purkinje cells. Journal of Neurochemistry. Wiley-Blackwell.https://doi.org/10.1111/j.1471-4159.2009.06229.x 

Tarusawa, E., Matsui, K., Budisantoso, T., Molnár, E., Watanabe, M., Matsui, M.,https://doi.org/10.1523/JNEUROSCI.6160-08.2009__Shigemoto, R. (2009). Input-specific intrasynaptic arrangements of ionotropic glutamate receptors and their impact on postsynaptic responses. Journal of Neuroscience. Society for Neuroscience.https://doi.org/10.1523/JNEUROSCI.6160-08.2009 

Rives, M., Vol, C., Fukazawa, Y., Tinel, N., Trinquet, E., Ayoub, M.,https://doi.org/10.1038/emboj.2009.177__Prezèau, L. (2009). Crosstalk between GABAB and mGlu1a receptors reveals new insight into GPCR signal integration. EMBO Journal. Wiley-Blackwell.https://doi.org/10.1038/emboj.2009.177 

Fukuda, Y., Fukazawa, Y., Danev, R., Shigemoto, R., &; Nagayama, K. (2009). Tuning of the Zernike phase-plate for visualization of detailed ultrastructure in complex biological specimens. Journal of Structural Biology. Academic Press.https://doi.org/10.1016/j.jsb.2009.08.011 

Grinevich, V., Kolleker, A., Eliava, M., Takada, N., Takuma, H., Fukazawa, Y.,https://doi.org/10.1016/j.jneumeth.2009.07.015__Osten, P. (2009). Fluorescent Arc/Ar.1 indicator mice: A versatile tool to study brain activity changes in vitro and in vivo. Journal of Neuroscience Methods. Elsevier.https://doi.org/10.1016/j.jneumeth.2009.07.015 

Kaufmann, W., Ferraguti, F., Fukazawa, Y., Kasugai, Y., Shigemoto, R., Laake, P.,https://doi.org/10.1002/cne.22066__Ottersen, O. (2009). Large-conductance calcium-activated potassium channels in Purkinje cell plasma membranes are clustered at sites of hypolemmal microdomains. Journal of Comparative Neurology. Wiley-Blackwell.https://doi.org/10.1002/cne.22066 

Guetg, N., Seddik, R., Vigot, R., Turedek, R., Gassmann, M., Vogt, K.,https://doi.org/10.1523/JNEUROSCI.3697-08.2009__Bettler, B. (2009). The GABA a isoform mediates heterosynaptic depression at hippocampal mossy fiber synapses. Journal of Neuroscience. Society for Neuroscience.https://doi.org/10.1523/JNEUROSCI.3697-08.2009 

Pan, B., Dong, Y., Ito, W., Yanagawa, Y., Shigemoto, R., &; Morozov, A. (2009). Selective gating of glutamatergic inputs to excitatory neurons of amygdala by presynaptic GABAb receptor. Neuron. Elsevier.https://doi.org/10.1016/j.neuron.2009.01.029 

Jiang, Y., Horimoto, N., Imura, K., Matsui, K., &; Shigemoto, R. (2009). Bioimaging with two-photon-induced luminescence from triangular nanoplates and nanoparticle aggregates of gold. Advanced Materials. Wiley-Blackwell.https://doi.org/10.1002/adma.200802312 

Tanaka, H., Ma, J., Tanaka, K., Takao, K., Komada, M., Tanda, K.,https://doi.org/10.1523/JNEUROSCI.3216-08.2009__Ikenaka, K. (2009). Mice with altered myelin proteolipid protein gene expression display cognitive deficits accompanied by abnormal neuron-glia interactions and decreased conduction velocities. Journal of Neuroscience. Society for Neuroscience.https://doi.org/10.1523/JNEUROSCI.3216-08.2009 

Tomita, H., Sugano, E., Fukazawa, Y., Isago, H., Sugiyama, Y., Hiroi, T.,https://doi.org/10.1371/journal.pone.0007679__Tamai, M. (2009). Visual properties of transgenic rats harboring the channelrhodopsin-2 gene regulated by the thy-1.2 promoter. PLoS One. Public Library of Science.https://doi.org/10.1371/journal.pone.0007679 

Sano, H., Nagai, Y., Miyakawa, T., Shigemoto, R., &; Yokoi, M. (2008). Increased social interaction in mice deficient of the striatal medium spiny neuron-specific phosphodiesterase 10. Journal of Neurochemistry. Wiley-Blackwell.https://doi.org/10.1111/j.1471-4159.2007.05152.x 

Endo, T., Tarusawa, E., Notomi, T., Kaneda, K., Hirabayashi, M., Shigemoto, R., &; Isa, T. (2008). Dendritic Ih ensures high-fidelity dendritic spike responses of motion-sensitive neurons in rat superior colliculus. Journal of Neurophysiology. American Physiological Society.https://doi.org/10.1152/jn.00556.2007 

Kawakami, R., Dobi, A., Shigemoto, R., &; Ito, I. (2008). Right isomerism of the brain in inversus viscerum mutant mice. PLoS One. Public Library of Science.https://doi.org/10.1371/journal.pone.0001945 

Fukazawa, Y., Tarusawa, E., Matsui, K., &; Shigemoto, R. (2008).  Ultrastructural insights of postsynaptic glutamate receptor organization . Tanpakushitsu Kakusan Koso Protein Nucleic Acid Enzyme. Kyoritsu Shuppan.

Li, X., Kamasawa, N., Ciolofan, C., Olson, C., Lu, S., Davidson, K.,https://doi.org/10.1523/JNEUROSCI.2137-08.2008__Nagy, J. (2008). Connexin45-containing neuronal gap junctions in rodent retina also contain connexin36 in both apposing hemiplaques, forming bihomotypic gap junctions, with scaffolding contributed by zonula occludens-1. Journal of Neuroscience. Society for Neuroscience.https://doi.org/10.1523/JNEUROSCI.2137-08.2008 

Varga, V., Hangya, B., Kránitz, K., Ludányi, A., Zemankovics, R., Katona, I.,https://doi.org/10.1113/jphysiol.2008.155242__Borhegyi, Z. (2008). The presence of pacemaker HCN channels identifies theta rhythmic GABAergic neurons in the medial septum. Journal of Physiology. Wiley-Blackwell.https://doi.org/10.1113/jphysiol.2008.155242 

Antal, M., Fukazawa, Y., Eördögh, M., Muszil, D., Molnár, E., Itakura, M.,https://doi.org/10.1523/JNEUROSCI.1551-08.2008__Shigemoto, R. (2008). Numbers, densities, and colocalization of AMPA- and NMDA-type glutamate receptors at individual synapses in the superficial spinal dorsal horn of rats. Journal of Neuroscience. Society for Neuroscience.https://doi.org/10.1523/JNEUROSCI.1551-08.2008 

Shinohara, Y., Hirase, H., Watanabe, M., Itakura, M., Takahashi, M., &; Shigemoto, R. (2008). Left-right asymmetry of the hippocampal synapses with differential subunit allocation of glutamate receptors. PNAS. National Academy of Sciences.https://doi.org/10.1073/pnas.0807461105 

Kuramoto, E., Fujiyama, F., Unzai, T., Nakamura, K., Hioki, H., Furuta, T.,https://doi.org/10.1002/cne.21216__Kaneko, T. (2007). Metabotropic glutamate receptor 4-immunopositive terminals of medium-sized spiny neurons selectively form synapses with cholinergic interneurons in the rat neostriatum. Journal of Comparative Neurology. Wiley-Blackwell.https://doi.org/10.1002/cne.21216 

Toyono, T., Kataoka, S., Seta, Y., Shigemoto, R., &; Toyoshima, K. (2007). Expression of group II metabotropic glutamate receptors in rat gustatory papillae. Cell and Tissue Research. Springer.https://doi.org/10.1007/s00441-006-0351-9 

Tóth, K., Wittner, L., Urbán, Z., Doyle, W., Buzsáki, G., Shigemoto, R.,https://doi.org/10.1016/j.neuroscience.2006.09.039__Maglóczky, Z. (2007). Morphology and synaptic input of substance P receptor-immunoreactive interneurons in control and epileptic human hippocampus. Neuroscience. Elsevier.https://doi.org/10.1016/j.neuroscience.2006.09.039 

Luyt, K., Slade, T., Dorward, J., Durant, C., Wu, Y., Shigemoto, R.,https://doi.org/10.1111/j.1471-4159.2006.04255.x__Molnár, E. (2007). Developing oligodendrocytes express functional GABAB receptors that stimulate cell proliferation and migration. Journal of Neurochemistry. Wiley-Blackwell.https://doi.org/10.1111/j.1471-4159.2006.04255.x 

Boyes, J., Bolam, J., Shigemoto, R., &; Stanford, I. (2007). Functional presynaptic HCN channels in the rat globus pallidus. European Journal of Neuroscience. Wiley-Blackwell.https://doi.org/10.1111/j.1460-9568.2007.05463.x