Mechanistic relationships between Drosophila fragile X mental retardation protein and metabotropic glutamate receptor A signaling.
about
Temporal requirements of the fragile X mental retardation protein in the regulation of synaptic structureMatrix metalloproteinases and minocycline: therapeutic avenues for fragile X syndrome.Learning and behavioral deficits associated with the absence of the fragile X mental retardation protein: what a fly and mouse model can teach us.The pathophysiology of fragile X (and what it teaches us about synapses)From Learning to Memory: What Flies Can Tell Us about Intellectual Disability TreatmentElevated levels of the vesicular monoamine transporter and a novel repetitive behavior in the Drosophila model of fragile X syndromeFragile X mental retardation protein has a unique, evolutionarily conserved neuronal function not shared with FXR1P or FXR2PArgonaute2 suppresses Drosophila fragile X expression preventing neurogenesis and oogenesis defects.Lithium: a promising treatment for fragile X syndrome.Age-dependent cognitive impairment in a Drosophila fragile X model and its pharmacological rescuePharmacological and genetic reversal of age-dependent cognitive deficits attributable to decreased presenilin functionThe nonsense-mediated decay pathway maintains synapse architecture and synaptic vesicle cycle efficacy.The fragile X mental retardation protein developmentally regulates the strength and fidelity of calcium signaling in Drosophila mushroom body neuronsIncreasing our understanding of human cognition through the study of Fragile X Syndrome.Pharmacological reversal of synaptic plasticity deficits in the mouse model of fragile X syndrome by group II mGluR antagonist or lithium treatment.Behavioral and synaptic circuit features in a zebrafish model of fragile X syndrome.Toward fulfilling the promise of molecular medicine in fragile X syndromeThe metabotropic glutamate receptor activates the lipid kinase PI3K in Drosophila motor neurons through the calcium/calmodulin-dependent protein kinase II and the nonreceptor tyrosine protein kinase DFakActivity-dependent FMRP requirements in development of the neural circuitry of learning and memory.Neural circuit architecture defects in a Drosophila model of Fragile X syndrome are alleviated by minocycline treatment and genetic removal of matrix metalloproteinaseIn vivo neuronal function of the fragile X mental retardation protein is regulated by phosphorylationPathological plasticity in fragile X syndrome.The Drosophila DmGluRA is required for social interaction and memoryUsing Drosophila as a tool to identify Pharmacological Therapies for Fragile X SyndromeMultiple Drug Treatments That Increase cAMP Signaling Restore Long-Term Memory and Aberrant Signaling in Fragile X Syndrome Models.Metabotropic glutamate receptor-mediated use-dependent down-regulation of synaptic excitability involves the fragile X mental retardation protein.Limbic epileptogenesis in a mouse model of fragile X syndrome.Fragile X mental retardation protein regulates trans-synaptic signaling in DrosophilaTemporal requirements of the fragile x mental retardation protein in modulating circadian clock circuit synaptic architecture.The fragile X mental retardation protein in circadian rhythmicity and memory consolidation.Translational control of long-lasting synaptic plasticity and memory.The state of synapses in fragile X syndrome.Impaired activity-dependent neural circuit assembly and refinement in autism spectrum disorder genetic models.Activity-dependent modulation of neural circuit synaptic connectivity.2-Methyl-6-(phenylethynyl) pyridine (MPEP) reverses maze learning and PSD-95 deficits in Fmr1 knock-out mice.Mechanisms of translational regulation in synaptic plasticity.Fragile X syndrome and model organisms: identifying potential routes of therapeutic intervention.The complex genetics in autism spectrum disorders.Candidate genes for individual recognition in Polistes fuscatus paper wasps.Dynamics of glutamatergic signaling in the mushroom body of young adult Drosophila.
P2860
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P2860
Mechanistic relationships between Drosophila fragile X mental retardation protein and metabotropic glutamate receptor A signaling.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
Mechanistic relationships betw ...... lutamate receptor A signaling.
@en
type
label
Mechanistic relationships betw ...... lutamate receptor A signaling.
@en
prefLabel
Mechanistic relationships betw ...... lutamate receptor A signaling.
@en
P2093
P2860
P1476
Mechanistic relationships betw ...... lutamate receptor A signaling.
@en
P2093
Elvin Woodruff
Kendal Broadie
Luyuan Pan
Ping Liang
P2860
P304
P356
10.1016/J.MCN.2008.01.003
P577
2008-01-17T00:00:00Z