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Items: 1 to 20 of 27

1.
Identification of new ciliary signaling pathways in the brain and insights into neurological disorders
Abdelhalim Loukil, Emma Ebright, Akiyoshi Uezu, Yudong Gao, Scott H Soderling, Sarah C. Goetz
Version 1. bioRxiv. Preprint. 2023 Dec 21. doi: 10.1101/2023.12.20.572700
PMCID:
PMC10769350
AbstractArticlePDF–11M
2.
Impaired OTUD7A-dependent Ankyrin regulation mediates neuronal dysfunction in mouse and human models of the 15q13.3 microdeletion syndrome
Brianna K. Unda, Leon Chalil, Sehyoun Yoon, Savannah Kilpatrick, Courtney Irwin, Sansi Xing, Nadeem Murtaza, Anran Cheng, Chad Brown, Alexandria Afonso, Elizabeth McCready, Gabriel M. Ronen, Jennifer Howe, Aurélie Caye-Eude, Alain Verloes, Brad W. Doble, Laurence Faivre, Antonio Vitobello, Stephen W. Scherer, Yu Lu, Peter Penzes, Karun K. Singh
Mol Psychiatry. 2023; 28(4): 1747–1769. Published online 2023 Jan 6. doi: 10.1038/s41380-022-01937-5
PMCID:
PMC10208958
AbstractArticlePDF–7.0M
3.
Rescue of neuropsychiatric phenotypes in a mouse model of 16p11.2 duplication syndrome by genetic correction of an epilepsy network hub
Marc P. Forrest, Marc Dos Santos, Nicolas H. Piguel, Yi-Zhi Wang, Nicole A. Hawkins, Vikram A. Bagchi, Leonardo E. Dionisio, Sehyoun Yoon, Dina Simkin, Maria Dolores Martin-de-Saavedra, Ruoqi Gao, Katherine E. Horan, Alfred L. George, Jr., Mark S. LeDoux, Jennifer A. Kearney, Jeffrey N. Savas, Peter Penzes
Nat Commun. 2023; 14: 825. Published online 2023 Feb 17. doi: 10.1038/s41467-023-36087-x
PMCID:
PMC9938216
AbstractArticlePDF–5.3M
4.
Expression and Interaction Proteomics of GluA1- and GluA3-Subunit-Containing AMPARs Reveal Distinct Protein Composition
Sophie J. F. van der Spek, Nikhil J. Pandya, Frank Koopmans, Iryna Paliukhovich, Roel C. van der Schors, Mylene Otten, August B. Smit, Ka Wan Li
Cells. 2022 Nov; 11(22): 3648. Published online 2022 Nov 17. doi: 10.3390/cells11223648
PMCID:
PMC9688267
AbstractArticlePDF–1.7M
5.
Deficiency of transmembrane AMPA receptor regulatory protein γ-8 leads to attention-deficit hyperactivity disorder-like behavior in mice
Wan-Jun Bai, Xing-Guang Luo, Bao-Hua Jin, Kang-Sheng Zhu, Wen-Yan Guo, Xiao-Que Zhu, Xia Qin, Zu-Xiao Yang, Jiao-Jiao Zhao, Si-Ruan Chen, Ri Wang, Jie Hao, Fei Wang, Yun Stone Shi, De-Zhi Kong, Wei Zhang
Zool Res. 2022 Sep 18; 43(5): 851–870. doi: 10.24272/j.issn.2095-8137.2022.122
PMCID:
PMC9486526
AbstractArticlePDF–8.0M
6.
SNP rs10420324 in the AMPA receptor auxiliary subunit TARP γ-8 regulates the susceptibility to antisocial personality disorder
Shi-Xiao Peng, Yue-Ying Wang, Min Zhang, Yan-Yu Zang, Dan Wu, Jingwen Pei, Yansong Li, Jiapei Dai, Xiaoyun Guo, Xingguang Luo, Ning Zhang, Jian-Jun Yang, Chen Zhang, Xiang Gao, Na Liu, Yun Stone Shi
Sci Rep. 2021; 11: 11997. Published online 2021 Jun 7. doi: 10.1038/s41598-021-91415-9
PMCID:
PMC8184779
AbstractArticlePDF–7.9M
7.
Gating and modulation of a hetero-octameric AMPA glutamate receptor
Danyang Zhang, Jake F. Watson, Peter M. Matthews, Ondrej Cais, Ingo H. Greger
Nature. Author manuscript; available in PMC 2021 Dec 1.
Published in final edited form as: Nature. 2021 Jun 1; 594(7863): 454–458. Published online 2021 Jun 2. doi: 10.1038/s41586-021-03613-0
PMCID:
PMC7611729
AbstractArticlePDF–6.2M
8.
TARP γ-2 and γ-8 Differentially Control AMPAR Density Across Schaffer Collateral/Commissural Synapses in the Hippocampal CA1 Area
Miwako Yamasaki, Masahiro Fukaya, Maya Yamazaki, Hirotsugu Azechi, Rie Natsume, Manabu Abe, Kenji Sakimura, Masahiko Watanabe
J Neurosci. 2016 Apr 13; 36(15): 4296–4312. doi: 10.1523/JNEUROSCI.4178-15.2016
PMCID:
PMC6601775
AbstractArticlePDF–12M
9.
LTP requires postsynaptic PDZ-domain interactions with glutamate receptor/auxiliary protein complexes
Nengyin Sheng, Michael A. Bemben, Javier Díaz-Alonso, Wucheng Tao, Yun Stone Shi, Roger A. Nicoll
Proc Natl Acad Sci U S A. 2018 Apr 10; 115(15): 3948–3953. Published online 2018 Mar 26. doi: 10.1073/pnas.1800719115
PMCID:
PMC5899490
AbstractArticlePDF–1.0M
10.
SynDIG4/Prrt1 Is Required for Excitatory Synapse Development and Plasticity Underlying Cognitive Function
Lucas Matt, Lyndsey M. Kirk, George Chenaux, David J. Speca, Kyle R. Puhger, Michael C. Pride, Mohammad Qneibi, Tomer Haham, Kristopher E. Plambeck, Yael Stern-Bach, Jill L. Silverman, Jacqueline N. Crawley, Johannes W. Hell, Elva Díaz
Cell Rep. Author manuscript; available in PMC 2018 Mar 16.
Published in final edited form as: Cell Rep. 2018 Feb 27; 22(9): 2246–2253. doi: 10.1016/j.celrep.2018.02.026
PMCID:
PMC5856126
AbstractArticlePDF–955K
11.
Control of AMPA receptor activity by the extracellular loops of auxiliary proteins
Irene Riva, Clarissa Eibl, Rudolf Volkmer, Anna L Carbone, Andrew JR Plested
eLife. 2017; 6: e28680. Published online 2017 Aug 30. doi: 10.7554/eLife.28680
PMCID:
PMC5599240
AbstractArticlePDF–3.2M
12.
CaMKII phosphorylation of TARPγ-8 is a mediator of LTP and learning and memory
Joongkyu Park, Andres E. Chavez, Yann S. Mineur, Megumi Morimoto-Tomita, Stefano Lutzu, Kwang S. Kim, Marina R. Picciotto, Pablo E. Castillo, Susumu Tomita
Neuron. Author manuscript; available in PMC 2017 Oct 5.
Published in final edited form as: Neuron. 2016 Oct 5; 92(1): 75–83. Published online 2016 Sep 22. doi: 10.1016/j.neuron.2016.09.002
PMCID:
PMC5059846
AbstractArticlePDF–1.1M
13.
Cornichon proteins determine the subunit composition of synaptic AMPA receptors
Bruce E. Herring, Yun Shi, Young Ho Suh, Chan-Ying Zheng, Sabine M. Blankenship, Katherine W. Roche, Roger A. Nicoll
Neuron. Author manuscript; available in PMC 2014 Mar 20.
Published in final edited form as: Neuron. 2013 Mar 20; 77(6): 1083–1096. doi: 10.1016/j.neuron.2013.01.017
PMCID:
PMC3652566
AbstractArticlePDF–2.6M
14.
PDZ binding of TARP©-8 controls synaptic transmission, but not synaptic plasticity
Akio Sumioka, Travis Brown, Akihiko Kato, David S. Bredt, Julie A. Kauer, Susumu Tomita
Nat Neurosci. Author manuscript; available in PMC 2012 May 1.
Published in final edited form as: Nat Neurosci. 2011 Nov; 14(11): 1410–1412. Published online 2011 Oct 16. doi: 10.1038/nn.2952
PMCID:
PMC3206644
AbstractArticlePDF–437K
15.
Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium
Pascale Gaudet, Michael S. Livstone, Suzanna E. Lewis, Paul D. Thomas
Brief Bioinform. 2011 Sep; 12(5): 449–462. Published online 2011 Aug 27. doi: 10.1093/bib/bbr042
PMCID:
PMC3178059
AbstractArticlePDF–1.0M
16.
The stoichiometry of AMPA receptors and TARPs varies by neuronal cell type
Yun Shi, Wei Lu, Aaron D. Milstein, Roger A. Nicoll
Neuron. Author manuscript; available in PMC 2011 Jun 21.
Published in final edited form as: Neuron. 2009 Jun 11; 62(5): 633–640. doi: 10.1016/j.neuron.2009.05.016
PMCID:
PMC3119531
AbstractArticlePDF–666K
17.
Critical role for TARPs in early development despite broad functional redundancy
Karen Menuz, Geoffrey A. Kerchner, Jessica L. O’Brien, Roger A. Nicoll
Neuropharmacology. Author manuscript; available in PMC 2011 Jun 9.
Published in final edited form as: Neuropharmacology. 2009 Jan; 56(1): 22–29. Published online 2008 Jun 27. doi: 10.1016/j.neuropharm.2008.06.037
PMCID:
PMC3111090
AbstractArticlePDF–621K
18.
Cardiac L-type calcium channel (Cav1.2) associates with γ subunits
Lin Yang, Alexander Katchman, John P. Morrow, Darshan Doshi, Steven O. Marx
FASEB J. 2011 Mar; 25(3): 928–936. doi: 10.1096/fj.10-172353
PMCID:
PMC3042847
AbstractArticle
19.
Hippocampal AMPA receptor gating controlled by both TARP and cornichon proteins
Akihiko S. Kato, Martin B. Gill, Michelle T. Ho, Hong Yu, Yuan Tu, Edward R. Siuda, He Wang, Yue-Wei Qian, Eric S. Nisenbaum, Susumu Tomita, David S. Bredt
Neuron. Author manuscript; available in PMC 2011 Dec 22.
Published in final edited form as: Neuron. 2010 Dec 22; 68(6): 1082–1096. doi: 10.1016/j.neuron.2010.11.026
PMCID:
PMC3034222
AbstractArticlePDF–3.5M
20.
A High-Resolution Anatomical Atlas of the Transcriptome in the Mouse Embryo
Graciana Diez-Roux, Sandro Banfi, Marc Sultan, Lars Geffers, Santosh Anand, David Rozado, Alon Magen, Elena Canidio, Massimiliano Pagani, Ivana Peluso, Nathalie Lin-Marq, Muriel Koch, Marchesa Bilio, Immacolata Cantiello, Roberta Verde, Cristian De Masi, Salvatore A. Bianchi, Juliette Cicchini, Elodie Perroud, Shprese Mehmeti, Emilie Dagand, Sabine Schrinner, Asja Nürnberger, Katja Schmidt, Katja Metz, Christina Zwingmann, Norbert Brieske, Cindy Springer, Ana Martinez Hernandez, Sarah Herzog, Frauke Grabbe, Cornelia Sieverding, Barbara Fischer, Kathrin Schrader, Maren Brockmeyer, Sarah Dettmer, Christin Helbig, Violaine Alunni, Marie-Annick Battaini, Carole Mura, Charlotte N. Henrichsen, Raquel Garcia-Lopez, Diego Echevarria, Eduardo Puelles, Elena Garcia-Calero, Stefan Kruse, Markus Uhr, Christine Kauck, Guangjie Feng, Nestor Milyaev, Chuang Kee Ong, Lalit Kumar, MeiSze Lam, Colin A. Semple, Attila Gyenesei, Stefan Mundlos, Uwe Radelof, Hans Lehrach, Paolo Sarmientos, Alexandre Reymond, Duncan R. Davidson, Pascal Dollé, Stylianos E. Antonarakis, Marie-Laure Yaspo, Salvador Martinez, Richard A. Baldock, Gregor Eichele, Andrea Ballabio
PLoS Biol. 2011 Jan; 9(1): e1000582. Published online 2011 Jan 18. doi: 10.1371/journal.pbio.1000582
PMCID:
PMC3022534
AbstractArticlePDF–3.8M

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