نتایج جستجو برای: grin1 gene

تعداد نتایج: 1141395  

Journal: :Behavioural brain research 2016
Janitza L Montalvo-Ortiz Kelly A Bordner Becky C Carlyle Joel Gelernter Arthur A Simen Joan Kaufman

Early life neglect increases risk for the development of psychopathologies during childhood and adulthood, including depression and anxiety disorders. We recently reported epigenetic changes in DNA derived from saliva in three genes predicted depression in a cohort of maltreated children: DNA-binding protein inhibitor ID-3 (ID3), Glutamate NMDA Receptor (GRIN1), and Tubulin Polymerization Promo...

2014
R. N. Kalendar A. H. Schulman A. I. Vaido Y. J. Kim K. K. Lee J. W. Kim

Stress can induce structural changes in the brain and contribute to a variety of chronic diseases from post-traumatic stress disorder to depression. The hippocampus is a highly plastic brain region particularly susceptible to the effects of environmental stress. A genomic stress response partly consists in changes in insertion activity of transposable elements. Retrotransposons account for ~45%...

Journal: :Neuropharmacology 2017
Brice Mullier Christian Wolff Zara Amanda Sands Philippe Ghisdal Pierandrea Muglia Rafal Marian Kaminski Véronique Marie André

De novo gain of function mutations in GRIN2B encoding the GluN2B subunit of the N-methyl-d-aspartate (NMDA) receptor have been linked with epileptic encephalopathies, including infantile spasms. We investigated the effects of radiprodil, a selective GluN2B negative allosteric modulator and other non-selective NMDA receptor inhibitors on glutamate currents mediated by NMDA receptors containing m...

Journal: :Journal of neurophysiology 2011
Francesco Mori Michele Ribolsi Hajime Kusayanagi Alberto Siracusano Vilma Mantovani Elena Marasco Giorgio Bernardi Diego Centonze

N-methyl-d-aspartate (NMDA) receptors play crucial roles in glutamate-mediated synaptic transmission and plasticity and are involved in a variety of brain functions. Specific single nucleotide polymorphisms (SNPs) in the genes encoding NMDA receptor subunits have been associated with some neuropsychiatric disorders involving altered glutamate transmission, but how these polymorphisms impact on ...

2011
Francesco Mori Michele Ribolsi Hajime Kusayanagi Alberto Siracusano Elena Marasco Giorgio Bernardi Diego Centonze

33 NMDA receptors play crucial roles in glutamate-mediated synaptic transmission and plasticity, and 34 are involved in a variety of brain functions. Specific single nucleotide polymorphisms (SNPs) in the 35 genes encoding NMDA receptor subunits have been associated with some neuropsychiatric 36 disorders involving altered glutamate transmission, but how these polymorphisms impact on 37 synapti...

Journal: :Pharmacology, biochemistry, and behavior 2009
Viviane Labrie Steven J Clapcote John C Roder

Several compounds that promote activation of the N-methyl-d-aspartate receptor (NMDAR) glycine site have been proposed as treatments for schizophrenia, but the impact of these putative antipsychotics on anxiety remains unclear. In this study, we employed genetic and pharmacological mouse models of altered NMDAR glycine site function to examine the effects of these proposed treatments in uncondi...

2016
Li-Ching Lee Ying-Chun Cho Pei-Jung Lin Ting-Chi Yeh Chun-Yen Chang Ting-Kuang Yeh

Considerable evidence has suggested that the epigenetic regulation of N-methyl-D-aspartate (NMDA) glutamate receptors plays a crucial role in neuropsychiatric disorders. Previous exploratory studies have been primarily based on evidence from patients and have rarely sampled the general population. This exploratory study examined the relationship of single-nucleotide polymorphism (SNP) variation...

2015
MING WEN YONG YAN NING YAN XIAO SHAN CHEN SHI YONG LIU ZHAN HUI FENG

Mutations in RNA‑binding Fox 1 (RBFOX1) are known to be associated with neurodevelopmental disorders including epilepsy, mental retardation and autism spectrum disorder. The deletion of the Rbfox1 gene in mice has been shown to result in heightened susceptibility to seizures. However, other studies have revealed mutations or the downregulation of RBFOX1 in specimens obtained from patients with ...

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