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FMR1 and the fragile X syndrome: human genome epidemiology review

FMR1 and the fragile X syndrome: human genome epidemiology review

http://www.wikidata.org/entity/Q34362009

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Childhood developmental disorders: an academic and clinical convergence point for psychiatry, neurology, psychology and pediatrics L-acetylcarnitine for treating fragile X syndrome L-acetylcarnitine for fragile X syndrome Folic acid for fragile X syndrome Folic acid for fragile X syndrome Interactions of the G quartet forming semaphorin 3F RNA with the RGG box domain of the fragile X protein family Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles Fragile X syndrome: the FMR1 CGG repeat distribution among world populations Systematic review of pharmacological treatments in fragile X syndrome Transcriptional Reactivation of the FMR1 Gene. A Possible Approach to the Treatment of the Fragile X Syndrome Mouse Genetic Models of Human Brain Disorders Single-Nucleotide Mutations in FMR1 Reveal Novel Functions and Regulatory Mechanisms of the Fragile X Syndrome Protein FMRP Behavioral phenotypes of genetic mouse models of autism.Modeling neurodevelopmental disorders using human neurons The clinical relevance of neuroplasticity in corticostriatal networks during operant learning Matrix metalloproteinases and minocycline: therapeutic avenues for fragile X syndrome.Modeling neurological disorders by human induced pluripotent stem cells Phenobarbital use and neurological problems in FMR1 premutation carriers Regulation of GABAA receptors by fragile X mental retardation protein Early social enrichment rescues adult behavioral and brain abnormalities in a mouse model of fragile X syndrome.Reward processing in autism: a thematic series.Comprehensive analysis of ultrasonic vocalizations in a mouse model of fragile X syndrome reveals limited, call type specific deficits Potential therapeutic interventions for fragile X syndrome Phonological accuracy and intelligibility in connected speech of boys with fragile X syndrome or Down syndrome.Direct magnitude estimation of articulation rate in boys with fragile X syndrome.Use of state administrative data sources to study adolescents and young adults with rare conditions Joint Engagement and Early Language in Young Children With Fragile X Syndrome Automated screening for Fragile X premutation carriers based on linguistic and cognitive computational phenotypes.Gene, brain, and behavior relationships in fragile X syndrome: evidence from neuroimaging studies.Psychiatric symptoms in boys with fragile X syndrome: a comparison with nonsyndromic autism spectrum disorder.GABA-B Agonist Baclofen Normalizes Auditory-Evoked Neural Oscillations and Behavioral Deficits in the Fmr1 Knockout Mouse Model of Fragile X Syndrome.The economic burden of fragile x syndrome: healthcare resource utilization in the United States.The tandem Agenet domain of fragile X mental retardation protein interacts with FUS.IL1RAPL1 gene deletion as a cause of X-linked intellectual disability and dysmorphic features Dynamic Object Representations in Infants with and without Fragile X Syndrome.Abnormal structure or function of the amygdala is a common component of neurodevelopmental disorders.Arginines of the RGG box regulate FMRP association with polyribosomes and mRNA.Four decades of leading-edge research in the reproductive and developmental sciences: the Infant Primate Research Laboratory at the University of Washington National Primate Research Center.Molecular testing for fragile X: analysis of 5062 tests from 1105 fragile X families--performed in 12 clinical laboratories in Spain.Language Development in Individuals with Fragile X Syndrome

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FMR1 and the fragile X syndrome: human genome epidemiology review

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FMR1 and the fragile X syndrome: human genome epidemiology review

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FMR1 and the fragile X syndrome: human genome epidemiology review

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FMR1 and the fragile X syndrome: human genome epidemiology review

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FMR1 and the fragile X syndrome: human genome epidemiology review

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FMR1 and the fragile X syndrome: human genome epidemiology review

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FMR1 and the fragile X syndrome: human genome epidemiology review

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FMR1 and the fragile X syndrome: human genome epidemiology review

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FMR1 and the fragile X syndrome: human genome epidemiology review

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FMR1 and the fragile X syndrome: human genome epidemiology review

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Genetics in Medicine

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A novel RNA-binding nuclear protein that interacts with the fragile X mental retardation (FMR1) protein

A PEDIGREE OF MENTAL DEFECT SHOWING SEX-LINKAGE.

FXR1, an autosomal homolog of the fragile X mental retardation gene

Differential expression of FMR1, FXR1 and FXR2 proteins in human brain and testis

Oligomerization properties of fragile-X mental-retardation protein (FMRP) and the fragile-X-related proteins FXR1P and FXR2P

Isolation of an FMRP-associated messenger ribonucleoprotein particle and identification of nucleolin and the fragile X-related proteins as components of the complex

Technical standards and guidelines for fragile X: the first of a series of disease-specific supplements to the Standards and Guidelines for Clinical Genetics Laboratories of the American College of Medical Genetics. Quality Assurance Subcommittee of

Specific sequences in the fragile X syndrome protein FMR1 and the FXR proteins mediate their binding to 60S ribosomal subunits and the interactions among them

Evidence that fragile X mental retardation protein is a negative regulator of translation

The protein product of the fragile X gene, FMR1, has characteristics of an RNA-binding protein

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