Understanding the molecular basis of fragile X syndrome.
about
A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2PAltered synaptic plasticity in a mouse model of fragile X mental retardationSpinocerebellar ataxia type 8: molecular genetic comparisons and haplotype analysis of 37 families with ataxiaA compelling genetic hypothesis for a complex disease: PRODH2/DGCR6 variation leads to schizophrenia susceptibility.Interactions of the G quartet forming semaphorin 3F RNA with the RGG box domain of the fragile X protein familyLong noncoding RNA in genome regulation: prospects and mechanismsComparative genomics and molecular dynamics of DNA repeats in eukaryotesFragile X (CGG)n repeats induce a transcriptional repression in cis upon a linked promoter: evidence for a chromatin mediated effectCytogenetic abnormalities and fragile-X syndrome in Autism Spectrum DisorderPacBio Sequencing and Its ApplicationsModulation of actin dynamics by Rac1 to target cognitive functionIdentification of RTG2 as a modifier gene for CTG*CAG repeat instability in Saccharomyces cerevisiaeDevelopment of Genetic Testing for Fragile X Syndrome and Associated Disorders, and Estimates of the Prevalence of FMR1 Expansion MutationsThe fragile X gene and its functionHaplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autismThe fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif.The fragile X mental retardation protein inhibits translation via interacting with mRNAUnique profile of ordered arrangements of repetitive elements in the C57BL/6J mouse genome implicating their functional roles.Identification of FMRP-associated mRNAs using yeast three-hybrid system.Methylation of novel markers of fragile X alleles is inversely correlated with FMRP expression and FMR1 activation ratio.Modulation of trinucleotide repeat instability by DNA polymerase β polymorphic variant R137Q.The tandem Agenet domain of fragile X mental retardation protein interacts with FUS.E3 Ubiquitin Ligases Neurobiological Mechanisms: Development to DegenerationThe fragile X mental retardation protein is required for type-I metabotropic glutamate receptor-dependent translation of PSD-95.Whole genome microarray analysis of gene expression in subjects with fragile X syndrome.Maternal Factors that Induce Epigenetic Changes Contribute to Neurological Disorders in OffspringAging in fragile X syndrome.Enriched environment promotes behavioral and morphological recovery in a mouse model for the fragile X syndrome.iPSC-derived forebrain neurons from FXS individuals show defects in initial neurite outgrowthEnhanced endocannabinoid signaling elevates neuronal excitability in fragile X syndrome.Demethylation, reactivation, and destabilization of human fragile X full-mutation alleles in mouse embryocarcinoma cells.FMR1 gene and fragile X syndrome.Altered differentiation of neural stem cells in fragile X syndromeA small molecule that targets r(CGG)(exp) and improves defects in fragile X-associated tremor ataxia syndrome.Different approaches to relating genotype to phenotype in developmental disorders.A converging-methods approach to fragile X syndrome.A screen for modifiers of decapentaplegic mutant phenotypes identifies lilliputian, the only member of the Fragile-X/Burkitt's Lymphoma family of transcription factors in Drosophila melanogasterFragile X mental retardation: misregulation of protein synthesis in the developing brain?Circuit and plasticity defects in the developing somatosensory cortex of FMR1 knock-out mice.Variation in the vasopressin V1a receptor promoter and expression: implications for inter- and intraspecific variation in social behaviour.
P2860
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P2860
Understanding the molecular basis of fragile X syndrome.
description
2000 nî lūn-bûn
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2000 թուականի Ապրիլին հրատարակուած գիտական յօդուած
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2000 թվականի ապրիլին հրատարակված գիտական հոդված
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2000年の論文
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2000年論文
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2000年論文
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2000年論文
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2000年論文
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2000年論文
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2000年论文
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name
Understanding the molecular basis of fragile X syndrome.
@ast
Understanding the molecular basis of fragile X syndrome.
@en
type
label
Understanding the molecular basis of fragile X syndrome.
@ast
Understanding the molecular basis of fragile X syndrome.
@en
prefLabel
Understanding the molecular basis of fragile X syndrome.
@ast
Understanding the molecular basis of fragile X syndrome.
@en
P356
P1476
Understanding the molecular basis of fragile X syndrome.
@en
P304
P356
10.1093/HMG/9.6.901
P577
2000-04-01T00:00:00Z