Excitatory Synaptic Input to Hilar Mossy Cells under Basal and Hyperexcitable Conditions
Hedrick, Tristan P, Nobis, William P, Foote, Kendall M, Ishii, Toshiyuki, Chetkovich, Dane M, Swanson, Geoffrey T
Published in eNeuro (01.11.2017)
Published in eNeuro (01.11.2017)
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A Pathogenic Missense Mutation in Kainate Receptors Elevates Dendritic Excitability and Synaptic Integration through Dysregulation of SK Channels
Nomura, Toshihiro, Taniguchi, Sakiko, Wang, Yi-Zhi, Yeh, Nai-Hsing, Wilen, Anika P, Castillon, Charlotte C M, Foote, Kendall M, Xu, Jian, Armstrong, John N, Savas, Jeffrey N, Swanson, Geoffrey T, Contractor, Anis
Published in The Journal of neuroscience (22.11.2023)
Published in The Journal of neuroscience (22.11.2023)
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Phosphorylation of the HCN channel auxiliary subunit TRIP8b is altered in an animal model of temporal lobe epilepsy and modulates channel function
Foote, Kendall M., Lyman, Kyle A., Han, Ye, Michailidis, Ioannis E., Heuermann, Robert J., Mandikian, Danielle, Trimmer, James S., Swanson, Geoffrey T., Chetkovich, Dane M.
Published in The Journal of biological chemistry (25.10.2019)
Published in The Journal of biological chemistry (25.10.2019)
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HCN channels in the hippocampus regulate active coping behavior
Fisher, Daniel W., Han, Ye, Lyman, Kyle A., Heuermann, Robert J., Bean, Linda A., Ybarra, Natividad, Foote, Kendall M., Dong, Hongxin, Nicholson, Daniel A., Chetkovich, Dane M.
Published in Journal of neurochemistry (01.09.2018)
Published in Journal of neurochemistry (01.09.2018)
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Clustered mutations in the GRIK2 kainate receptor subunit gene underlie diverse neurodevelopmental disorders
Stolz, Jacob R., Foote, Kendall M., Veenstra-Knol, Hermine E., Pfundt, Rolph, ten Broeke, Sanne W., de Leeuw, Nicole, Roht, Laura, Pajusalu, Sander, Part, Reelika, Rebane, Ionella, Õunap, Katrin, Stark, Zornitza, Kirk, Edwin P., Lawson, John A., Lunke, Sebastian, Christodoulou, John, Louie, Raymond J., Rogers, R. Curtis, Davis, Jessica M., Innes, A. Micheil, Wei, Xing-Chang, Keren, Boris, Mignot, Cyril, Lebel, Robert Roger, Sperber, Steven M., Sakonju, Ai, Dosa, Nienke, Barge-Schaapveld, Daniela Q.C.M., Peeters-Scholte, Cacha M.P.C.D., Ruivenkamp, Claudia A.L., van Bon, Bregje W., Kennedy, Joanna, Low, Karen J., Ellard, Sian, Pang, Lewis, Junewick, Joseph J., Mark, Paul R., Carvill, Gemma L., Swanson, Geoffrey T.
Published in American journal of human genetics (04.11.2021)
Published in American journal of human genetics (04.11.2021)
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Journal Article
Clustered mutations in the GRIK2 kainate receptor subunit gene underlie diverse neurodevelopmental disorders
Stolz, Jacob R., Foote, Kendall M., Veenstra-Knol, Hermine E., Pfundt, Rolph, ten Broeke, Sanne W., de Leeuw, Nicole, Roht, Laura, Pajusalu, Sander, Part, Reelika, Rebane, Ionella, Õunap, Katrin, Stark, Zornitza, Kirk, Edwin P., Lawson, John A., Lunke, Sebastian, Christodoulou, John, Louie, Raymond J., Rogers, R. Curtis, Davis, Jessica M., Innes, A. Micheil, Wei, Xing-Chang, Keren, Boris, Mignot, Cyril, Lebel, Robert Roger, Sperber, Steven M., Sakonju, Ai, Dosa, Nienke, Barge-Schaapveld, Daniela Q.C.M., Peeters-Scholte, Cacha M.P.C.D., Ruivenkamp, Claudia A.L., van Bon, Bregje W., Kennedy, Joanna, Low, Karen J., Ellard, Sian, Pang, Lewis, Junewick, Joseph J., Mark, Paul R., Carvill, Gemma L., Swanson, Geoffrey T.
Published in American journal of human genetics (02.09.2021)
Published in American journal of human genetics (02.09.2021)
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