about
The fragile-X premutation: a maturing perspective.Study of the Genetic Etiology of Primary Ovarian Insufficiency: FMR1 GeneEpigenetics and human disease: translating basic biology into clinical applicationsPremutation in the Fragile X Mental Retardation 1 (FMR1) Gene Affects Maternal Zn-milk and Perinatal Brain Bioenergetics and Scaffolding.Comprehensive neurocognitive endophenotyping strategies for mouse models of genetic disordersCNS 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.Fragile X-associated primary ovarian insufficiency: evidence for additional genetic contributions to severity.Concise review: Fragile X proteins in stem cell maintenance and differentiationRare intranuclear inclusions in the brains of 3 older adult males with fragile x syndrome: implications for the spectrum of fragile x-associated disordersMouse models of the fragile x premutation and the fragile X associated tremor/ataxia syndrome.The FMR1 gene and fragile X-associated tremor/ataxia syndrome.Molecular diagnosis of neurogenetic disorders involving trinucleotide repeat expansions.Characterising repetitive behaviours in young boys with fragile X syndrome.SIRT1 inhibition alleviates gene silencing in Fragile X mental retardation syndromeReciprocal changes in DNA methylation and hydroxymethylation and a broad repressive epigenetic switch characterize FMR1 transcriptional silencing in fragile X syndromeMethylation-specific multiplex ligation-dependent probe amplification enables a rapid and reliable distinction between male FMR1 premutation and full-mutation alleles.Investigation of phenotypes associated with mood and anxiety among male and female fragile X premutation carriers.The FMR1 premutation and attention-deficit hyperactivity disorder (ADHD): evidence for a complex inheritanceCo-occurring diagnoses among FMR1 premutation allele carriers.No evidence for a difference in neuropsychological profile among carriers and noncarriers of the FMR1 premutation in adults under the age of 50Neurocognitive endophenotypes in CGG KI and Fmr1 KO mouse models of Fragile X-Associated disorders: an analysis of the state of the fieldReduced activity-dependent protein levels in a mouse model of the fragile X premutation.Autism spectrum disorders: the quest for genetic syndromes.Premature recruitment of oocyte pool and increased mTOR activity in Fmr1 knockout mice and reversal of phenotype with rapamycin.Investigating the relationship between FMR1 allele length and cognitive ability in children: a subtle effect of the normal allele range on the normal ability range?Influence of intermediate and uninterrupted FMR1 CGG expansions in premature ovarian failure manifestation.
P2860
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P2860
description
2003 nî lūn-bûn
@nan
2003 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Expression of the FMR1 gene.
@ast
Expression of the FMR1 gene.
@en
type
label
Expression of the FMR1 gene.
@ast
Expression of the FMR1 gene.
@en
prefLabel
Expression of the FMR1 gene.
@ast
Expression of the FMR1 gene.
@en
P356
P1476
Expression of the FMR1 gene.
@en
P2093
Hagerman PJ
P304
P356
10.1159/000072846
P577
2003-01-01T00:00:00Z