In vivo neuronal function of the fragile X mental retardation protein is regulated by phosphorylation
about
Matrix 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)Characterization of fragile X mental retardation protein recruitment and dynamics in Drosophila stress granulesCellular and molecular characterization of multipolar Map5-expressing cells: a subset of newly generated, stage-specific parenchymal cells in the mammalian central nervous systemTherapeutic Strategies in Fragile X Syndrome: From Bench to Bedside and BackFMRP S499 is phosphorylated independent of mTORC1-S6K1 activity.Fragile X mental retardation protein regulates translation by binding directly to the ribosomeEvidence for a fragile X mental retardation protein-mediated translational switch in metabotropic glutamate receptor-triggered Arc translation and long-term depression.Metabotropic Glutamate Receptor and Fragile X Signaling in a Female Model of Escalated Aggression.A fully automated Drosophila olfactory classical conditioning and testing system for behavioral learning and memory assessmentMammalian FMRP S499 Is Phosphorylated by CK2 and Promotes Secondary Phosphorylation of FMRP.Impaired activity-dependent neural circuit assembly and refinement in autism spectrum disorder genetic models.RNA-binding proteins involved in RNA localization and their implications in neuronal diseases.Fragile X mental retardation protein and synaptic plasticityRNA-binding proteins and translational regulation in axons and growth cones.Fruitful research: drug target discovery for neurodegenerative diseases in Drosophila.Importance of gene dosage in controlling dendritic arbor formation during development.GABAergic circuit dysfunction in the Drosophila Fragile X syndrome model.ESCRT-III Membrane Trafficking Misregulation Contributes To Fragile X Syndrome Synaptic Defects.Characterization of Fragile X Mental Retardation Protein granules formation and dynamics in Drosophila.Biophysical characterization of G-quadruplex forming FMR1 mRNA and of its interactions with different fragile X mental retardation protein isoforms.Fragile X Mental Retardation Protein Regulates Activity-Dependent Membrane Trafficking and Trans-Synaptic Signaling Mediating Synaptic Remodeling.Unraveling the Pathways to Neuronal Homeostasis and Disease: Mechanistic Insights into the Role of RNA-Binding Proteins and Associated Factors
P2860
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P2860
In vivo neuronal function of the fragile X mental retardation protein is regulated by phosphorylation
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
In vivo neuronal function of t ...... s regulated by phosphorylation
@ast
In vivo neuronal function of t ...... s regulated by phosphorylation
@en
type
label
In vivo neuronal function of t ...... s regulated by phosphorylation
@ast
In vivo neuronal function of t ...... s regulated by phosphorylation
@en
prefLabel
In vivo neuronal function of t ...... s regulated by phosphorylation
@ast
In vivo neuronal function of t ...... s regulated by phosphorylation
@en
P2093
P2860
P356
P1476
In vivo neuronal function of t ...... s regulated by phosphorylation
@en
P2093
Ashley J Williamson
Christopher M Adkins
Kendal Broadie
Marisa C Gray
R Lane Coffee
Terry L Page
P2860
P304
P356
10.1093/HMG/DDR527
P577
2011-11-11T00:00:00Z