Neuropathologic features in the hippocampus and cerebellum of three older men with fragile X syndrome - Wikidata - wikimedia - TriplyDB

Neuropathologic features in the hippocampus and cerebellum of three older men with fragile X syndrome

Neuropathologic features in the hippocampus and cerebellum of three older men with fragile X syndrome

http://www.wikidata.org/entity/Q34610850

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Conceptualizing neurodevelopmental disorders through a mechanistic understanding of fragile X syndrome and Williams syndrome Autism spectrum disorders and neuropathology of the cerebellum Ephrin-B3 coordinates timed axon targeting and amygdala spinogenesis for innate fear behaviour.Antipurinergic therapy corrects the autism-like features in the poly(IC) mouse model Identification and characterisation of Simiate, a novel protein linked to the fragile X syndrome Comprehensive neurocognitive endophenotyping strategies for mouse models of genetic disorders CGG repeat in the FMR1 gene: size matters Saccade adaptation abnormalities implicate dysfunction of cerebellar-dependent learning mechanisms in Autism Spectrum Disorders (ASD).Rare intranuclear inclusions in the brains of 3 older adult males with fragile x syndrome: implications for the spectrum of fragile x-associated disorders Autism Spectrum Disorder (ASD) and Fragile X Syndrome (FXS): Two Overlapping Disorders Reviewed through Electroencephalography-What Can be Interpreted from the Available Information?Altered mTOR signaling and enhanced CYFIP2 expression levels in subjects with fragile X syndrome.Is autism a disease of the cerebellum? An integration of clinical and pre-clinical research.Intranuclear inclusions in a fragile X mosaic male Does microglial dysfunction play a role in autism and Rett syndrome?Reorganization of circuits underlying cerebellar modulation of prefrontal cortical dopamine in mouse models of autism spectrum disorder Neurocognitive endophenotypes in CGG KI and Fmr1 KO mouse models of Fragile X-Associated disorders: an analysis of the state of the field Advancing drug discovery for neuropsychiatric disorders using patient-specific stem cell models.Pathways to drug development for autism spectrum disorders.Perspectives in Pediatric Pathology, Chapter 15. Macrorchidism as the Expression of Several Congenital and Acquired Pathologies.Cerebellar and Striatal Pathologies in Mouse Models of Autism Spectrum Disorder.Autism spectrum disorder: neuropathology and animal models.Gray matter textural heterogeneity as a potential in-vivo biomarker of fine structural abnormalities in Asperger syndrome.Decreased home cage movement and oromotor impairments in adult Fmr1-KO mice.Pathophysiological and neurobehavioral characteristics of a propionic acid-mediated autism-like rat model.Delayed myelination in a mouse model of fragile X syndrome.

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Neuropathologic features in the hippocampus and cerebellum of three older men with fragile X syndrome

http://www.wikidata.org/entity/Q34610850

description

2011 nî lūn-bûn

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2011 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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2011 թվականի փետրվարին հրատարակված գիտական հոդված

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2011年の論文

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Molecular Autism

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Celestine S Navarro

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Claudia M Greco

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Cynthia Schumann

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Flora Tassone

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Lee-Way Jin

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Paul J Hagerman

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Randi J Hagerman

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P2860

Autistic phenotypes and genetic testing: state-of-the-art for the clinical geneticist

Neuroanatomy of autism

The fragile X syndrome protein represses activity-dependent translation through CYFIP1, a new 4E-BP

Fragile X syndrome: loss of local mRNA regulation alters synaptic development and function

New insights into fragile X syndrome: from molecules to neurobehaviors

The role of fragile X mental retardation protein in major mental disorders.

The neuroanatomy and neuroendocrinology of fragile X syndrome.

Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile-X syndrome: a quantitative examination.

Fragile x mental retardation protein regulates proliferation and differentiation of adult neural stem/progenitor cells.

The neuropathology of autism: defects of neurogenesis and neuronal migration, and dysplastic changes

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10.1186/2040-2392-2-2

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