Theta-burst LTP von Larson, John, Munkácsy, Erin

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Engineering a memory with LTD and LTP von Nabavi, Sadegh, Fox, Rocky, Proulx, Christophe D., Lin, John Y., Tsien, Roger Y., Malinow, Roberto

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Robust LiTi2(PO4)3 microflowers as high-rate and long-life cathodes for Mg-based hybrid-ion batteriesElectronic supplementary information (ESI) available: XRD patterns of bare LTP; nitrogen adsorption-desorption isotherms of LTP-F precursor, LTP-F/C and bare LTP; EDS elemental mappings and the EDS spectrum of the residual carbon skeleton after etching the LTP from LTP-F/C; SEM images of the bare LTP; TGA curves of LTP-F/C; the contribution ratio of the plateau discharge capacity of LTP-F/C at di von Xu, Yanan, Xu, Chang, An, Qinyou, Wei, Qiulong, Sheng, Jinzhi, Xiong, Fangyu, Pei, Cunyuan, Mai, Liqiang

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LTP and LTD: An Embarrassment of Riches von Malenka, Robert C., Bear, Mark F.

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Molecular Mechanisms of Early and Late LTP von Baltaci, Saltuk Bugra, Mogulkoc, Rasim, Baltaci, Abdulkerim Kasim

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The SILVA and "All-species Living Tree Project (LTP)" taxonomic frameworks von Yilmaz, Pelin, Parfrey, Laura Wegener, Yarza, Pablo, Gerken, Jan, Pruesse, Elmar, Quast, Christian, Schweer, Timmy, Peplies, Jörg, Ludwig, Wolfgang, Glöckner, Frank Oliver

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Gliogenic LTP spreads widely in nociceptive pathways von Kronschläger, M. T., Drdla-Schutting, R., Gassner, M., Honsek, S. D., Teuchmann, H. L., Sanakühler, J.

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TrkB signalling pathways in LTP and learning von Minichiello, Liliana

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Dopamine agonists rescue Aβ–induced LTP impairment by Src-family tyrosine kinases von Yuan Xiang, PingAn, Janc, Oliwia, Grochowska, Katarzyna M, Kreutz, Michael R, Reymann, Klaus G

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Neuroligin-1 Signaling Controls LTP and NMDA Receptors by Distinct Molecular Pathways von Wu, Xiaoting, Morishita, Wade K., Riley, Ashley M., Hale, William D., Südhof, Thomas C., Malenka, Robert C.

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Chromatin Acetylation, Memory, and LTP Are Impaired in CBP +/− Mice : A Model for the Cognitive Deficit in Rubinstein-Taybi Syndrome and Its Amelioration von Alarcón, Juan M, Malleret, Gaël, Touzani, Khalid, Vronskaya, Svetlana, Ishii, Shunsuke, Kandel, Eric R, Barco, Angel

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Postsynaptic synaptotagmins mediate AMPA receptor exocytosis during LTP von Wu, Dick, Bacaj, Taulant, Morishita, Wade, Goswami, Debanjan, Arendt, Kristin L., Xu, Wei, Chen, Lu, Malenka, Robert C., Südhof, Thomas C.

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LTP POST-Release submission (Preprint) von Mykhaylyuk, Igor, Abraham, Tadele, biswal, subhashree

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BDNF mechanisms in late LTP formation: A synthesis and breakdown von Panja, Debabrata, Bramham, Clive R.

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LTP induction by structural rather than enzymatic functions of CaMKII von Tullis, Jonathan E., Larsen, Matthew E., Rumian, Nicole L., Freund, Ronald K., Boxer, Emma E., Brown, Carolyn Nicole, Coultrap, Steven J., Schulman, Howard, Aoto, Jason, Dell’Acqua, Mark L., Bayer, K. Ulrich

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LTP Induction Boosts Glutamate Spillover by Driving Withdrawal of Perisynaptic Astroglia von Henneberger, Christian, Bard, Lucie, Panatier, Aude, Reynolds, James P., Kopach, Olga, Medvedev, Nikolay I., Minge, Daniel, Herde, Michel K., Anders, Stefanie, Kraev, Igor, Heller, Janosch P., Rama, Sylvain, Zheng, Kaiyu, Jensen, Thomas P., Sanchez-Romero, Inmaculada, Jackson, Colin J., Janovjak, Harald, Ottersen, Ole Petter, Nagelhus, Erlend Arnulf, Oliet, Stephane H.R., Stewart, Michael G., Nägerl, U. Valentin, Rusakov, Dmitri A.

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Sensory-Induced Human LTP-Like Synaptic Plasticity - Using Visual Evoked Potentials to Explore the Relation Between LTP-Like Synaptic Plasticity and Visual Perceptual Learning von Lengali, Lilly, Hippe, Johannes, Hatlestad-Hall, Christoffer, Rygvold, Trine Waage, Sneve, Markus Handal, Andersson, Stein

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Sensory-evoked LTP driven by dendritic plateau potentials in vivo von Gambino, Frédéric, Pagès, Stéphane, Kehayas, Vassilis, Baptista, Daniela, Tatti, Roberta, Carleton, Alan, Holtmaat, Anthony

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Fission’ for LTP von Bray, Natasha

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Discovering long‐term potentiation (LTP) – recollections and reflections on what came after von Lomo, T

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