about
CNS expression of murine fragile X protein (FMRP) as a function of CGG-repeat size.Advances in understanding the molecular basis of FXTASTemporal ordering deficits in female CGG KI mice heterozygous for the fragile X premutation.Mouse models of the fragile X premutation and fragile X-associated tremor/ataxia syndromeFragile X and autism: Intertwined at the molecular level leading to targeted treatments.Activation of mTOR ameliorates fragile X premutation rCGG repeat-mediated neurodegenerationUbiquitin-positive intranuclear inclusions in neuronal and glial cells in a mouse model of the fragile X premutation.Current research, diagnosis, and treatment of fragile X-associated tremor/ataxia syndrome.Motor deficits on a ladder rung task in male and female adolescent and adult CGG knock-in miceAbnormal dendrite and spine morphology in primary visual cortex in the CGG knock-in mouse model of the fragile X premutationImmune dysregulation as a cause of autoinflammation in fragile X premutation carriers: link between FMRI CGG repeat number and decreased cytokine responses.Regulation of molecular pathways in the Fragile X Syndrome: insights into Autism Spectrum DisordersWidespread non-central nervous system organ pathology in fragile X premutation carriers with fragile X-associated tremor/ataxia syndrome and CGG knock-in mice.Female CGG knock-in mice modeling the fragile X premutation are impaired on a skilled forelimb reaching taskRNA-binding protein misregulation in microsatellite expansion disordersClustered burst firing in FMR1 premutation hippocampal neurons: amelioration with allopregnanolone.Spatiotemporal processing deficits in female CGG KI mice modeling the fragile X premutation.Signaling defects in iPSC-derived fragile X premutation neuronsEarly mitochondrial abnormalities in hippocampal neurons cultured from Fmr1 pre-mutation mouse model.Distribution and frequency of intranuclear inclusions in female CGG KI mice modeling the fragile X premutationImpaired activity-dependent FMRP translation and enhanced mGluR-dependent LTD in Fragile X premutation miceNeurodegeneration the RNA wayIntranuclear inclusions in a fragile X mosaic maleMolecular pathogenesis of fragile X-associated tremor/ataxia syndromeMurine hippocampal neurons expressing Fmr1 gene premutations show early developmental deficits and late degeneration.Fragile X-associated tremor/ataxia syndrome (FXTAS): pathology and mechanisms.CAG repeat RNA as an auxiliary toxic agent in polyglutamine disorders.Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS) Motor Dysfunction Modeled in MiceWhat has been learned from mouse models of the Fragile X Premutation and Fragile X-associated tremor/ataxia syndrome?Upregulation of cystathione β-synthase and p70S6K/S6 in neonatal hypoxic ischemic brain injury.
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P2860
description
2009 nî lūn-bûn
@nan
2009 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Mouse models of fragile X-associated tremor ataxia.
@ast
Mouse models of fragile X-associated tremor ataxia.
@en
type
label
Mouse models of fragile X-associated tremor ataxia.
@ast
Mouse models of fragile X-associated tremor ataxia.
@en
prefLabel
Mouse models of fragile X-associated tremor ataxia.
@ast
Mouse models of fragile X-associated tremor ataxia.
@en
P2860
P1476
Mouse models of fragile X-associated tremor ataxia.
@en
P2093
Rob Willemsen
Robert F Berman
P2860
P304
P356
10.2310/JIM.0B013E3181AF59D6
P577
2009-12-01T00:00:00Z