A citation-based method for searching scientific literature

Steven J Coultrap, Ronald K Freund, Heather O'Leary, Jennifer L Sanderson, Katherine W Roche, Mark L Dell'Acqua, K Ulrich Bayer. Cell Rep 2014
Times Cited: 127



Y Hayashi, S H Shi, J A Esteban, A Piccini, J C Poncer, R Malinow. Science 2000
Times Cited: 1178




List of shared articles



Times cited

Role of Ca2+/Calmodulin-Dependent Protein Kinase Type II in Mediating Function and Dysfunction at Glutamatergic Synapses.
Archana G Mohanan, Sowmya Gunasekaran, Reena Sarah Jacob, R V Omkumar. Front Mol Neurosci 2022
2

CaMKII: a central molecular organizer of synaptic plasticity, learning and memory.
Ryohei Yasuda, Yasunori Hayashi, Johannes W Hell. Nat Rev Neurosci 2022
7

0

CaMKIIα as a Promising Drug Target for Ischemic Grey Matter.
Nane Griem-Krey, Andrew N Clarkson, Petrine Wellendorph. Brain Sci 2022
0

Protein kinase D promotes activity-dependent AMPA receptor endocytosis in hippocampal neurons.
Carlos O Oueslati Morales, Attila Ignácz, Norbert Bencsik, Zsofia Sziber, Anikó Erika Rátkai, Wolfgang S Lieb, Stephan A Eisler, Attila Szűcs, Katalin Schlett, Angelika Hausser. Traffic 2021
1

Structure, Function, and Pharmacology of Glutamate Receptor Ion Channels.
Kasper B Hansen, Lonnie P Wollmuth, Derek Bowie, Hiro Furukawa, Frank S Menniti, Alexander I Sobolevsky, Geoffrey T Swanson, Sharon A Swanger, Ingo H Greger, Terunaga Nakagawa,[...]. Pharmacol Rev 2021
71

Long-term Memory Upscales Volume of Postsynaptic Densities in the Process that Requires Autophosphorylation of αCaMKII.
Małgorzata Alicja Śliwińska, Anna Cały, Malgorzata Borczyk, Magdalena Ziółkowska, Edyta Skonieczna, Magdalena Chilimoniuk, Tytus Bernaś, K Peter Giese, Kasia Radwanska. Cereb Cortex 2020
9

Interactions between calmodulin and neurogranin govern the dynamics of CaMKII as a leaky integrator.
Mariam Ordyan, Tom Bartol, Mary Kennedy, Padmini Rangamani, Terrence Sejnowski. PLoS Comput Biol 2020
8

CaM Kinase: Still Inspiring at 40.
K Ulrich Bayer, Howard Schulman. Neuron 2019
116

Loss of MsrB1 perturbs spatial learning and long-term potentiation/long-term depression in mice.
Tengrui Shi, Yujie Yang, Zhonghao Zhang, Lei Zhang, Jianxi Song, Yongjing Ping, Xiubo Du, Guoli Song, Qiong Liu, Nan Li. Neurobiol Learn Mem 2019
7


The AMPA Receptor Code of Synaptic Plasticity.
Graham H Diering, Richard L Huganir. Neuron 2018
347

Wip1 phosphatase modulates both long-term potentiation and long-term depression through the dephosphorylation of CaMKII.
Zhi-Yong He, Wei-Yan Hu, Ming Zhang, Zara Zhuyun Yang, Hong-Mei Zhu, Da Xing, Quan-Hong Ma, Zhi-Cheng Xiao. Cell Adh Migr 2016
3

Non-ionotropic signaling by the NMDA receptor: controversy and opportunity.
John A Gray, Karen Zito, Johannes W Hell. F1000Res 2016
17