A citation-based method for searching scientific literature

Qixu Cai, Tomohisa Hosokawa, Menglong Zeng, Yasunori Hayashi, Mingjie Zhang. Structure 2020
Times Cited: 6







List of co-cited articles
21 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


SHANK proteins: roles at the synapse and in autism spectrum disorder.
Patricia Monteiro, Guoping Feng. Nat Rev Neurosci 2017
236
50

SHANK proteins limit integrin activation by directly interacting with Rap1 and R-Ras.
Johanna Lilja, Thomas Zacharchenko, Maria Georgiadou, Guillaume Jacquemet, Nicola De Franceschi, Emilia Peuhu, Hellyeh Hamidi, Jeroen Pouwels, Victoria Martens, Fatemeh Hassani Nia,[...]. Nat Cell Biol 2017
68
50

Novel de novo SHANK3 mutation in autistic patients.
Julie Gauthier, Dan Spiegelman, Amélie Piton, Ronald G Lafrenière, Sandra Laurent, Judith St-Onge, Line Lapointe, Fadi F Hamdan, Patrick Cossette, Laurent Mottron,[...]. Am J Med Genet B Neuropsychiatr Genet 2009
218
33

Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders.
Christelle M Durand, Catalina Betancur, Tobias M Boeckers, Juergen Bockmann, Pauline Chaste, Fabien Fauchereau, Gudrun Nygren, Maria Rastam, I Carina Gillberg, Henrik Anckarsäter,[...]. Nat Genet 2007
949
33

Reconstituted Postsynaptic Density as a Molecular Platform for Understanding Synapse Formation and Plasticity.
Menglong Zeng, Xudong Chen, Dongshi Guan, Jia Xu, Haowei Wu, Penger Tong, Mingjie Zhang. Cell 2018
110
33

The emerging role of SHANK genes in neuropsychiatric disorders.
Audrey Guilmatre, Guillaume Huguet, Richard Delorme, Thomas Bourgeron. Dev Neurobiol 2014
148
33

SHANK3 mutations identified in autism lead to modification of dendritic spine morphology via an actin-dependent mechanism.
C M Durand, J Perroy, F Loll, D Perrais, L Fagni, T Bourgeron, M Montcouquiol, N Sans. Mol Psychiatry 2012
189
33


Association of CaV1.3 L-type calcium channels with Shank.
Hua Zhang, Anton Maximov, Yu Fu, Fang Xu, Tie-Shan Tang, Tatiana Tkatch, D James Surmeier, Ilya Bezprozvanny. J Neurosci 2005
103
33

C-terminal synaptic targeting elements for postsynaptic density proteins ProSAP1/Shank2 and ProSAP2/Shank3.
Tobias M Boeckers, Thomas Liedtke, Christina Spilker, Thomas Dresbach, Jürgen Bockmann, Michael R Kreutz, Eckart D Gundelfinger. J Neurochem 2005
83
33

Shank3-mutant mice lacking exon 9 show altered excitation/inhibition balance, enhanced rearing, and spatial memory deficit.
Jiseok Lee, Changuk Chung, Seungmin Ha, Dongmin Lee, Do-Young Kim, Hyun Kim, Eunjoon Kim. Front Cell Neurosci 2015
84
33

An architectural framework that may lie at the core of the postsynaptic density.
Marisa K Baron, Tobias M Boeckers, Bianca Vaida, Salem Faham, Mari Gingery, Michael R Sawaya, Danielle Salyer, Eckart D Gundelfinger, James U Bowie. Science 2006
200
33

Synaptic scaffolding proteins in rat brain. Ankyrin repeats of the multidomain Shank protein family interact with the cytoskeletal protein alpha-fodrin.
T M Böckers, M G Mameza, M R Kreutz, J Bockmann, C Weise, F Buck, D Richter, E D Gundelfinger, H J Kreienkamp. J Biol Chem 2001
99
33


Shank expression is sufficient to induce functional dendritic spine synapses in aspiny neurons.
Gautier Roussignol, Fabrice Ango, Stefano Romorini, Jian Cheng Tu, Carlo Sala, Paul F Worley, Joël Bockaert, Laurent Fagni. J Neurosci 2005
213
33

Modeling autism by SHANK gene mutations in mice.
Yong-Hui Jiang, Michael D Ehlers. Neuron 2013
277
33

SHANK3 overexpression causes manic-like behaviour with unique pharmacogenetic properties.
Kihoon Han, J Lloyd Holder, Christian P Schaaf, Hui Lu, Hongmei Chen, Hyojin Kang, Jianrong Tang, Zhenyu Wu, Shuang Hao, Sau Wai Cheung,[...]. Nature 2013
215
33


Social deficits in Shank3-deficient mouse models of autism are rescued by histone deacetylase (HDAC) inhibition.
Luye Qin, Kaijie Ma, Zi-Jun Wang, Zihua Hu, Emmanuel Matas, Jing Wei, Zhen Yan. Nat Neurosci 2018
70
33

Postsynaptic ProSAP/Shank scaffolds in the cross-hair of synaptopathies.
Andreas M Grabrucker, Michael J Schmeisser, Michael Schoen, Tobias M Boeckers. Trends Cell Biol 2011
148
33

Sharpin, a novel postsynaptic density protein that directly interacts with the shank family of proteins.
S Lim, C Sala, J Yoon, S Park, S Kuroda, M Sheng, E Kim. Mol Cell Neurosci 2001
107
33

Structural basis for activation and non-canonical catalysis of the Rap GTPase activating protein domain of plexin.
Yuxiao Wang, Heath G Pascoe, Chad A Brautigam, Huawei He, Xuewu Zhang. Elife 2013
46
16

Ras and Rap Signal Bidirectional Synaptic Plasticity via Distinct Subcellular Microdomains.
Lei Zhang, Peng Zhang, Guangfu Wang, Huaye Zhang, Yajun Zhang, Yilin Yu, Mingxu Zhang, Jian Xiao, Piero Crespo, Johannes W Hell,[...]. Neuron 2018
34
16

The Ras-RasGAP complex: structural basis for GTPase activation and its loss in oncogenic Ras mutants.
K Scheffzek, M R Ahmadian, W Kabsch, L Wiesmüller, A Lautwein, F Schmitz, A Wittinghofer. Science 1997
16

The Rap-RapGAP complex: GTP hydrolysis without catalytic glutamine and arginine residues.
Andrea Scrima, Christoph Thomas, Delia Deaconescu, Alfred Wittinghofer. EMBO J 2008
83
16



Ras and Rap control AMPA receptor trafficking during synaptic plasticity.
J Julius Zhu, Yi Qin, Mingming Zhao, Linda Van Aelst, Roberto Malinow. Cell 2002
592
16

CaM Kinase: Still Inspiring at 40.
K Ulrich Bayer, Howard Schulman. Neuron 2019
67
16

Mechanisms of CaMKII action in long-term potentiation.
John Lisman, Ryohei Yasuda, Sridhar Raghavachari. Nat Rev Neurosci 2012
600
16

Supramodular structure and synergistic target binding of the N-terminal tandem PDZ domains of PSD-95.
Jia-Fu Long, Hidehito Tochio, Ping Wang, Jing-Song Fan, Carlo Sala, Martin Niethammer, Morgan Sheng, Mingjie Zhang. J Mol Biol 2003
112
16

Phase Separation-Mediated TARP/MAGUK Complex Condensation and AMPA Receptor Synaptic Transmission.
Menglong Zeng, Javier Díaz-Alonso, Fei Ye, Xudong Chen, Jia Xu, Zeyang Ji, Roger A Nicoll, Mingjie Zhang. Neuron 2019
40
16

Phase separation at the synapse.
Xudong Chen, Xiandeng Wu, Haowei Wu, Mingjie Zhang. Nat Neurosci 2020
38
16

The CaMKII/NMDA receptor complex controls hippocampal synaptic transmission by kinase-dependent and independent mechanisms.
Salvatore Incontro, Javier Díaz-Alonso, Jillian Iafrati, Marta Vieira, Cedric S Asensio, Vikaas S Sohal, Katherine W Roche, Kevin J Bender, Roger A Nicoll. Nat Commun 2018
49
16

Supramolecular organization of NMDA receptors and the postsynaptic density.
René Aw Frank, Seth Gn Grant. Curr Opin Neurobiol 2017
58
16

Contribution of SHANK3 mutations to autism spectrum disorder.
Rainald Moessner, Christian R Marshall, James S Sutcliffe, Jennifer Skaug, Dalila Pinto, John Vincent, Lonnie Zwaigenbaum, Bridget Fernandez, Wendy Roberts, Peter Szatmari,[...]. Am J Hum Genet 2007
428
16

The molecular basis of CaMKII function in synaptic and behavioural memory.
J Lisman, H Schulman, H Cline. Nat Rev Neurosci 2002
16

Mechanisms of Ca2+/calmodulin-dependent kinase II activation in single dendritic spines.
Jui-Yun Chang, Yoshihisa Nakahata, Yuki Hayano, Ryohei Yasuda. Nat Commun 2019
9
16

Long-Term Potentiation: From CaMKII to AMPA Receptor Trafficking.
Bruce E Herring, Roger A Nicoll. Annu Rev Physiol 2016
199
16

Dendritic spine geometry is critical for AMPA receptor expression in hippocampal CA1 pyramidal neurons.
M Matsuzaki, G C Ellis-Davies, T Nemoto, Y Miyashita, M Iino, H Kasai. Nat Neurosci 2001
16

The Postsynaptic Density: There Is More than Meets the Eye.
Ayse Dosemeci, Richard J Weinberg, Thomas S Reese, Jung-Hwa Tao-Cheng. Front Synaptic Neurosci 2016
41
16

Structural and molecular remodeling of dendritic spine substructures during long-term potentiation.
Miquel Bosch, Jorge Castro, Takeo Saneyoshi, Hitomi Matsuno, Mriganka Sur, Yasunori Hayashi. Neuron 2014
317
16


Reciprocal Activation within a Kinase-Effector Complex Underlying Persistence of Structural LTP.
Takeo Saneyoshi, Hitomi Matsuno, Akio Suzuki, Hideji Murakoshi, Nathan G Hedrick, Emily Agnello, Rory O'Connell, Margaret M Stratton, Ryohei Yasuda, Yasunori Hayashi. Neuron 2019
34
16

Neuronal L-Type Calcium Channel Signaling to the Nucleus Requires a Novel CaMKIIα-Shank3 Interaction.
Tyler L Perfitt, Xiaohan Wang, Matthew T Dickerson, Jason R Stephenson, Terunaga Nakagawa, David A Jacobson, Roger J Colbran. J Neurosci 2020
10
16

Transcellular Nanoalignment of Synaptic Function.
Thomas Biederer, Pascal S Kaeser, Thomas A Blanpied. Neuron 2017
122
16


An essential role for postsynaptic calmodulin and protein kinase activity in long-term potentiation.
R C Malenka, J A Kauer, D J Perkel, M D Mauk, P T Kelly, R A Nicoll, M N Waxham. Nature 1989
794
16

A mechanism for tunable autoinhibition in the structure of a human Ca2+/calmodulin- dependent kinase II holoenzyme.
Luke H Chao, Margaret M Stratton, Il-Hyung Lee, Oren S Rosenberg, Joshua Levitz, Daniel J Mandell, Tanja Kortemme, Jay T Groves, Howard Schulman, John Kuriyan. Cell 2011
148
16

Mechanistic basis of MAGUK-organized complexes in synaptic development and signalling.
Jinwei Zhu, Yuan Shang, Mingjie Zhang. Nat Rev Neurosci 2016
97
16


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.