The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndrome
about
MicroRNA-277 modulates the neurodegeneration caused by Fragile X premutation rCGG repeatsUse of model systems to understand the etiology of fragile X-associated primary ovarian insufficiency (FXPOI)Fragile-X-associated tremor/ataxia syndrome (FXTAS) in females with the FMR1 premutationThe fragile-X premutation: a maturing perspective.Facile FMR1 mRNA structure regulation by interruptions in CGG repeatsThe multiple molecular facets of fragile X-associated tremor/ataxia syndromeRNA-mediated neurodegeneration in fragile X-associated tremor/ataxia syndromeUnstable mutations in the FMR1 gene and the phenotypesThe unstable repeats--three evolving faces of neurological diseaseReversibility of neuropathology and motor deficits in an inducible mouse model for FXTAS.Study of the Genetic Etiology of Primary Ovarian Insufficiency: FMR1 GeneDetection and Quantification of the Fragile X Mental Retardation Protein 1 (FMRP)Translational regulation of the human achaete-scute homologue-1 by fragile X mental retardation proteinUsing mouse models of autism spectrum disorders to study the neurotoxicology of gene-environment interactionsComprehensive neurocognitive endophenotyping strategies for mouse models of genetic disordersCGG repeat in the FMR1 gene: size mattersAging in individuals with the FMR1 mutation.X-linked mental retardation (XLMR): from clinical conditions to cloned genes.Mouse models of fragile X-associated tremor ataxia.Fibroblast phenotype in male carriers of FMR1 premutation allelesFragile X-Associated Tremor/Ataxia Syndrome: From Molecular Pathogenesis to Development of Therapeutics.CNS expression of murine fragile X protein (FMRP) as a function of CGG-repeat size.Evidence for RNA-mediated toxicity in the fragile X-associated tremor/ataxia syndrome.Histone deacetylases suppress CGG repeat-induced neurodegeneration via transcriptional silencing in models of fragile X tremor ataxia syndrome.Advances in understanding the molecular basis of FXTASSmall CGG repeat expansion alleles of FMR1 gene are associated with parkinsonismNuclear accumulation of stress response mRNAs contributes to the neurodegeneration caused by Fragile X premutation rCGG repeatsTemporal 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.RNA-protein interactions in unstable microsatellite diseases.Cerebral protein synthesis in a knockin mouse model of the fragile X premutation.Premutation CGG-repeat expansion of the Fmr1 gene impairs mouse neocortical development.A small molecule that targets r(CGG)(exp) and improves defects in fragile X-associated tremor ataxia syndrome.Repeat associated non-ATG (RAN) translation: new starts in microsatellite expansion disorders.Activation of mTOR ameliorates fragile X premutation rCGG repeat-mediated neurodegenerationThe ubiquitin ligase Praja1 reduces NRAGE expression and inhibits neuronal differentiation of PC12 cellsUbiquitin-positive intranuclear inclusions in neuronal and glial cells in a mouse model of the fragile X premutation.Motor deficits on a ladder rung task in male and female adolescent and adult CGG knock-in miceMouse models of the fragile x premutation and the fragile X associated tremor/ataxia syndrome.
P2860
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P2860
The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndrome
description
2003 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի մայիսին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2003
@ast
im Mai 2003 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2003/05/01)
@sk
vědecký článek publikovaný v roce 2003
@cs
wetenschappelijk artikel (gepubliceerd op 2003/05/01)
@nl
наукова стаття, опублікована в травні 2003
@uk
مقالة علمية (نشرت في مايو 2003)
@ar
name
The FMR1 CGG repeat mouse disp ...... ebellar tremor/ataxia syndrome
@ast
The FMR1 CGG repeat mouse disp ...... ebellar tremor/ataxia syndrome
@en
The FMR1 CGG repeat mouse disp ...... ebellar tremor/ataxia syndrome
@nl
type
label
The FMR1 CGG repeat mouse disp ...... ebellar tremor/ataxia syndrome
@ast
The FMR1 CGG repeat mouse disp ...... ebellar tremor/ataxia syndrome
@en
The FMR1 CGG repeat mouse disp ...... ebellar tremor/ataxia syndrome
@nl
prefLabel
The FMR1 CGG repeat mouse disp ...... ebellar tremor/ataxia syndrome
@ast
The FMR1 CGG repeat mouse disp ...... ebellar tremor/ataxia syndrome
@en
The FMR1 CGG repeat mouse disp ...... ebellar tremor/ataxia syndrome
@nl
P2093
P3181
P356
P1476
The FMR1 CGG repeat mouse disp ...... ebellar tremor/ataxia syndrome
@en
P2093
Andre T. Hoogeveen
Ben A. Oostra
Edwin J. Mientjes
Flora Tassone
Ingeborg M. Nieuwenhuizen
Joan Holstege
Leontine van Unen
Lies-Anne W. F. M. Severijnen
Marianne Hoogeveen-Westerveld
Mariette Schrier
P304
P3181
P356
10.1093/HMG/DDG114
P577
2003-05-01T00:00:00Z