Abnormal elevation of FMR1 mRNA is associated with psychological symptoms in individuals with the fragile X premutation. - Wikidata - awgldk - TriplyDB

Abnormal elevation of FMR1 mRNA is associated with psychological symptoms in individuals with the fragile X premutation.

Abnormal elevation of FMR1 mRNA is associated with psychological symptoms in individuals with the fragile X premutation.

http://www.wikidata.org/entity/Q46224818

about

Cognitive, anxiety and mood disorders in the fragile X-associated tremor/ataxia syndrome Fragile X syndrome: the FMR1 CGG repeat distribution among world populations Advances in the treatment of fragile X syndrome Fragile X-associated tremor/ataxia syndrome.RNA-mediated neurodegeneration in fragile X-associated tremor/ataxia syndrome Unstable mutations in the FMR1 gene and the phenotypes The role of AGG interruptions in the transcription of FMR1 premutation alleles The fragile X mental retardation 1 gene (FMR1): historical perspective, phenotypes, mechanism, pathology, and epidemiology Fragile X: a family of disorders.Fragile X-associated tremor/ataxia syndrome: clinical features, genetics, and testing guidelines.A review of fragile X premutation disorders: expanding the psychiatric perspective Mouse models of fragile X-associated tremor ataxia.Fragile X-associated tremor/ataxia syndrome: clinical phenotype, diagnosis, and treatment Fibroblast phenotype in male carriers of FMR1 premutation alleles Reduced vagal tone in women with the FMR1 premutation is associated with FMR1 mRNA but not depression or anxiety.Evidence for RNA-mediated toxicity in the fragile X-associated tremor/ataxia syndrome.Clinical involvement in daughters of men with fragile X-associated tremor ataxia syndrome.Broad clinical involvement in a family affected by the fragile X premutation.Lifetime prevalence of mood and anxiety disorders in fragile X premutation carriers Biomarkers in the Study of Families of Individuals with Developmental Disabilities.Psychological symptoms correlate with reduced hippocampal volume in fragile X premutation carriers.Towards an Understanding of Neuropsychiatric Manifestations in Fragile X Premutation Carriers Advances in understanding the molecular basis of FXTAS The primary cognitive deficit among males with fragile X-associated tremor/ataxia syndrome (FXTAS) is a dysexecutive syndrome.Nuclear accumulation of stress response mRNAs contributes to the neurodegeneration caused by Fragile X premutation rCGG repeats Dementia in fragile X-associated tremor/ataxia syndrome (FXTAS): comparison with Alzheimer's disease.Visual motion processing deficits in infants with the fragile X premutation.Aripiprazole in autism spectrum disorders and fragile X syndrome.Identification of expanded alleles of the FMR1 gene among high-risk population in Indonesia by using blood spot screening Teasing apart the heterogeneity of autism: Same behavior, different brains in toddlers with fragile X syndrome and autism.Emerging topics in FXTAS.Fragile X and autism: Intertwined at the molecular level leading to targeted treatments.A combination of ascorbic acid and α-tocopherol to test the effectiveness and safety in the fragile X syndrome: study protocol for a phase II, randomized, placebo-controlled trial Eye movements reveal impaired inhibitory control in adult male fragile X premutation carriers asymptomatic for FXTAS.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.Molecular Advances Leading to Treatment Implications for Fragile X Premutation Carriers A voxel-based morphometry study of grey matter loss in fragile X-associated tremor/ataxia syndrome.Initiation of translation of the FMR1 mRNA Occurs predominantly through 5'-end-dependent ribosomal scanning FMR1 CGG repeat length predicts motor dysfunction in premutation carriers.

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P2860

Abnormal elevation of FMR1 mRNA is associated with psychological symptoms in individuals with the fragile X premutation.

http://www.wikidata.org/entity/Q46224818

description

2005 nî lūn-bûn

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2005年の論文

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年學術文章

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2005年學術文章

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name

Abnormal elevation of FMR1 mRN ...... ith the fragile X premutation.

@en

Abnormal elevation of FMR1 mRN ...... ith the fragile X premutation.

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type

label

Abnormal elevation of FMR1 mRN ...... ith the fragile X premutation.

@en

Abnormal elevation of FMR1 mRN ...... ith the fragile X premutation.

@nl

prefLabel

Abnormal elevation of FMR1 mRN ...... ith the fragile X premutation.

@en

Abnormal elevation of FMR1 mRN ...... ith the fragile X premutation.

@nl

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P1433

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

P1476

Abnormal elevation of FMR1 mRN ...... ith the fragile X premutation.

@en

P2093

Cathlin Rice

http://www.w3.org/2001/XMLSchema#string

Dahlia Weinberg

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Danuta Z Loesch

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David Hessl

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Deborah A Hall

http://www.w3.org/2001/XMLSchema#string

Elizabeth Berry-Kravis

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Emma Gould

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Flora Tassone

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Foster Lewin

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Ingrid Barbato

http://www.w3.org/2001/XMLSchema#string

P2860

FMR1 RNA within the intranuclear inclusions of fragile X-associated tremor/ataxia syndrome (FXTAS).

Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X.

FMR1 gene premutation is a frequent genetic cause of late-onset sporadic cerebellar ataxia.

P304

115-121

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scholarly article

P356

10.1002/AJMG.B.30241

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1

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139B

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2005-11-01T00:00:00Z

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16184602

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