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Items: 1 to 20 of 29

1.
Colorectal cancer promoter methylation alteration affects the expression of glutamate ionotropic receptor AMPA type subunit 4 alternative isoforms potentially relevant in colon tissue
Ana Florencia Vega-Benedetti, Eleonora Loi, Loredana Moi, Angelo Restivo, Francesco Cabras, Simona Deidda, Andrea Pretta, Pina Ziranu, Sandra Orrù, Mario Scartozzi, Luigi Zorcolo, Patrizia Zavattari
Hum Cell. 2022; 35(1): 310–319. Published online 2021 Oct 30. doi: 10.1007/s13577-021-00640-x
PMCID:
PMC8732896
ArticlePDF–1.9M
2.
Genome-wide association study identifies glutamate ionotropic receptor GRIA4 as a risk gene for comorbid nicotine dependence and major depression
Hang Zhou, Zhongshan Cheng, Nicholas Bass, John H. Krystal, Lindsay A. Farrer, Henry R. Kranzler, Joel Gelernter
Transl Psychiatry. 2018; 8: 208. Published online 2018 Oct 4. doi: 10.1038/s41398-018-0258-8
PMCID:
PMC6172277
ArticlePDF–712K
3.
De Novo Variants in GRIA4 Lead to Intellectual Disability with or without Seizures and Gait Abnormalities
Sonja Martin, Adam Chamberlin, Deepali N. Shinde, Maja Hempel, Tim M. Strom, Allison Schreiber, Jessika Johannsen, Lilian Bomme Ousager, Martin J. Larsen, Lars Kjaersgaard Hansen, Ali Fatemi, Julie S. Cohen, Johannes Lemke, Kristina P. Sørensen, Katherine L. Helbig, Davor Lessel, Rami Abou Jamra
Am J Hum Genet. 2017 Dec 7; 101(6): 1013–1020. Published online 2017 Dec 7. doi: 10.1016/j.ajhg.2017.11.004
PMCID:
PMC5812909
ArticlePDF–1.2M
4.
Association of SLC12A1 and GLUR4 Ion Transporters with Neoadjuvant Chemoresistance in Luminal Locally Advanced Breast Cancer
Montserrat Justo-Garrido, Alejandro López-Saavedra, Nicolás Alcaraz, Carlo C. Cortés-González, Luis F. Oñate-Ocaña, Claudia Haydee Sarai Caro-Sánchez, Clementina Castro-Hernández, Cristian Arriaga-Canon, José Díaz-Chávez, Luis A. Herrera
Int J Mol Sci. 2023 Nov; 24(22): 16104. Published online 2023 Nov 9. doi: 10.3390/ijms242216104
PMCID:
PMC10670992
ArticlePDF–4.4M
5.
Neuronal pentraxin 2 supports clear cell renal cell carcinoma by activating the AMPA-selective glutamate receptor-4
Christina A. von Roemeling, Derek C. Radisky, Laura A. Marlow, Simon J. Cooper, Stefan K. Grebe, Panagiotis Z. Anastasiadis, Han W. Tun, John A. Copland
Cancer Res. Author manuscript; available in PMC 2015 Sep 1.
Published in final edited form as: Cancer Res. 2014 Sep 1; 74(17): 4796–4810. Published online 2014 Jun 24. doi: 10.1158/0008-5472.CAN-14-0210
PMCID:
PMC4154999
ArticlePDF–3.9M
6.
Superactivation of AMPA receptors by auxiliary proteins
Anna L. Carbone, Andrew J. R. Plested
Nat Commun. 2016; 7: 10178. Published online 2016 Jan 8. doi: 10.1038/ncomms10178
PMCID:
PMC4729862
ArticlePDF–2.9M
7.
Synaptic AMPA Receptor Plasticity and Behavior
Helmut W. Kessels, Roberto Malinow
Neuron. Author manuscript; available in PMC 2014 Feb 7.
Published in final edited form as: Neuron. 2009 Feb 12; 61(3): 340–350. doi: 10.1016/j.neuron.2009.01.015
PMCID:
PMC3917551
ArticlePDF–69K
8.
Characterization of Phosphorylation Sites on the Glutamate Receptor 4 Subunit of the AMPA Receptors
Ana Luísa Carvalho, Kimihiko Kameyama, Richard L. Huganir
J Neurosci. 1999 Jun 15; 19(12): 4748–4754. doi: 10.1523/JNEUROSCI.19-12-04748.1999
PMCID:
PMC6782640
ArticlePDF–298K
9.
Amyloid-β Receptors: The Good, the Bad, and the Prion Protein
Heledd H. Jarosz-Griffiths, Elizabeth Noble, Jo V. Rushworth, Nigel M. Hooper
J Biol Chem. 2016 Feb 12; 291(7): 3174–3183. Published online 2015 Dec 30. doi: 10.1074/jbc.R115.702704
PMCID:
PMC4751366
ArticlePDF–942K
10.
Altered Glutamate Protein Co-Expression Network Topology Linked to Spine Loss in the Auditory Cortex of Schizophrenia
Matthew L. MacDonald, Ying Ding, Jason Newman, Scott Hemby, Peter Penzes, David A. Lewis, Nathan Yates, Robert A. Sweet
Biol Psychiatry. Author manuscript; available in PMC 2016 Jun 1.
Published in final edited form as: Biol Psychiatry. 2015 Jun 1; 77(11): 959–968. Published online 2014 Nov 26. doi: 10.1016/j.biopsych.2014.09.006
PMCID:
PMC4428927
ArticlePDF–563K
11.
The N-terminal Domain Modulates α-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) Receptor Desensitization
Tommi Möykkynen, Sarah K. Coleman, Artur Semenov, Kari Keinänen
J Biol Chem. 2014 May 9; 289(19): 13197–13205. Published online 2014 Mar 20. doi: 10.1074/jbc.M113.526301
PMCID:
PMC4036331
ArticlePDF–1.2M
12.
Electrophysiological Properties of AMPA Receptors Are Differentially Modulated Depending on the Associated Member of the TARP Family
Sabine Kott, Markus Werner, Christoph Körber, Michael Hollmann
J Neurosci. 2007 Apr 4; 27(14): 3780–3789. doi: 10.1523/JNEUROSCI.4185-06.2007
PMCID:
PMC6672393
ArticlePDF–368K
13.
Surface Expression of GluR-D AMPA Receptor Is Dependent on an Interaction between Its C-Terminal Domain and a 4.1 Protein
Sarah K. Coleman, Chunlin Cai, David G. Mottershead, Jukka-Pekka Haapalahti, Kari Keinänen
J Neurosci. 2003 Feb 1; 23(3): 798–806. doi: 10.1523/JNEUROSCI.23-03-00798.2003
PMCID:
PMC6741938
ArticlePDF–465K
14.
Chromosomal localization of human glutamate receptor genes
JO McNamara, JH Eubanks, JD McPherson, JJ Wasmuth, GA Evans, SF Heinemann
J Neurosci. 1992 Jul 1; 12(7): 2555–2562. doi: 10.1523/JNEUROSCI.12-07-02555.1992
PMCID:
PMC6575855
AbstractPDF–4.6M
15.
Splicing and editing of ionotropic glutamate receptors: a comprehensive analysis based on human RNA-Seq data
Robin Herbrechter, Nadine Hube, Raoul Buchholz, Andreas Reiner
Cell Mol Life Sci. 2021; 78(14): 5605–5630. Published online 2021 Jun 8. doi: 10.1007/s00018-021-03865-z
PMCID:
PMC8257547
ArticlePDF–2.4M
16.
A phylogenetic analysis reveals an unusual sequence conservation within introns involved in RNA editing.
P J Aruscavage, B L Bass
RNA. 2000 Feb; 6(2): 257–269. doi: 10.1017/s1355838200991921
PMCID:
PMC1369911
SummaryPDF–576K
17.
Adjacent asparagines in the NR2-subunit of the NMDA receptor channel control the voltage-dependent block by extracellular Mg2+
Lonnie P Wollmuth, Thomas Kuner, Bert Sakmann
J Physiol. 1998 Jan 1; 506(Pt 1): 13–32. doi: 10.1111/j.1469-7793.1998.013bx.x
PMCID:
PMC2230696
ArticlePDF–959K
18.
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
ArticlePDF–3.5M
19.
Genome-wide meta-analyses of multi-ethnic cohorts identify multiple new susceptibility loci for refractive error and myopia
Virginie J.M. Verhoeven, Pirro G. Hysi, Robert Wojciechowski, Qiao Fan, Jeremy A. Guggenheim, René Höhn, Stuart MacGregor, Alex W. Hewitt, Abhishek Nag, Ching-Yu Cheng, Ekaterina Yonova-Doing, Xin Zhou, M. Kamran Ikram, Gabriëlle H.S. Buitendijk, George McMahon, John P. Kemp, Beate St. Pourcain, Claire L. Simpson, Kari-Matti Mäkelä, Terho Lehtimäki, Mika Kähönen, Andrew D. Paterson, S. Mohsen Hosseini, Hoi Suen Wong, Liang Xu, Jost B. Jonas, Olavi Pärssinen, Juho Wedenoja, Shea Ping Yip, Daniel W. H. Ho, Chi Pui Pang, Li Jia Chen, Kathryn P. Burdon, Jamie E. Craig, Barbara E. K. Klein, Ronald Klein, Toomas Haller, Andres Metspalu, Chiea-Chuen Khor, E-Shyong Tai, Tin Aung, Eranga Vithana, Wan-Ting Tay, Veluchamy A. Barathi, CREAM, Peng Chen, Ruoying Li, Jiemin Liao, Yingfeng Zheng, Rick T. Ong, Angela Döring, DCCT/EDIC Research Group, David M. Evans, Nicholas J. Timpson, Annemieke J.M.H. Verkerk, Thomas Meitinger, Olli Raitakari, Felicia Hawthorne, Tim D. Spector, Lennart C. Karssen, Mario Pirastu, Federico Murgia, Wei Ang, WTCCC2, Aniket Mishra, Grant W. Montgomery, Craig E. Pennell, Phillippa M. Cumberland, Ioana Cotlarciuc, Paul Mitchell, Jie Jin Wang, Maria Schache, Sarayut Janmahasathian, Robert P. Igo, Jr, Jonathan H. Lass, Emily Chew, Sudha K. Iyengar, the Fuchs’ Genetics Multi-Center Study Group, Theo G.M.F. Gorgels, Igor Rudan, Caroline Hayward, Alan F. Wright, Ozren Polasek, Zoran Vatavuk, James F. Wilson, Brian Fleck, Tanja Zeller, Alireza Mirshahi, Christian Müller, Andre’ G. Uitterlinden, Fernando Rivadeneira, Johannes R. Vingerling, Albert Hofman, Ben A. Oostra, Najaf Amin, Arthur A.B. Bergen, Yik-Ying Teo, Jugnoo S. Rahi, Veronique Vitart, Cathy Williams, Paul N. Baird, Tien-Yin Wong, Konrad Oexle, Norbert Pfeiffer, David A. Mackey, Terri L. Young, Cornelia M. van Duijn, Seang-Mei Saw, Joan E. Bailey Wilson, Dwight Stambolian, Caroline C. Klaver, Christopher J. Hammond
Nat Genet. Author manuscript; available in PMC 2013 Sep 1.
Published in final edited form as: Nat Genet. 2013 Mar; 45(3): 314–318. Published online 2013 Feb 10. doi: 10.1038/ng.2554
Correction in:
volume 45 on page 712
PMCID:
PMC3740568
ArticlePDF–575K
20.
Pharmacogenetics of antipsychotic response in the CATIE trial: a candidate gene analysis
Anna C Need, Richard SE Keefe, Dongliang Ge, Iris Grossman, Sam Dickson, Joseph P McEvoy, David B Goldstein
Eur J Hum Genet. 2009 Jul; 17(7): 946–957. Published online 2009 Jan 21. doi: 10.1038/ejhg.2008.264
PMCID:
PMC2986499
ArticlePDF–172K

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