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Mouse Genetic Models of Human Brain DisordersGenetics of Autism Spectrum Disorder: Current Status and Possible Clinical ApplicationsAutism spectrum disorder in Phelan-McDermid syndrome: initial characterization and genotype-phenotype correlationsAn evo-devo approach to thyroid hormones in cerebral and cerebellar cortical development: etiological implications for autismPhelan-McDermid Syndrome and SHANK3: Implications for Treatment.Elucidating the role of neurotensin in the pathophysiology and management of major mental disorders.Strategies to develop putative biomarkers to characterize the female phenotype with autism spectrum disorders.Genetic insights into the functional elements of language.Autism-Associated Insertion Mutation (InsG) of Shank3 Exon 21 Causes Impaired Synaptic Transmission and Behavioral Deficits.Linkage analysis in a Dutch population isolate shows no major gene for left-handedness or atypical language lateralizationNovel Therapeutic Approach for Autism Spectrum Disorder: Focus on SHANK3Shank Modulates Postsynaptic Wnt Signaling to Regulate Synaptic Development.Epigenetics and autism.Epigenetic findings in autism: new perspectives for therapy.MLPA analysis in a cohort of patients with autism.Resting state EEG abnormalities in autism spectrum disorders.Editorial. New Targets of Medical Treatment in Psychiatric Disorders.The complex genetics in autism spectrum disorders.Phelan-McDermid syndrome data network: Integrating patient reported outcomes with clinical notes and curated genetic reports.DNA methylation analysis in constitutional disorders: Clinical implications of the epigenome.Endosomal system genetics and autism spectrum disorders: A literature review.Constitutional Epi/Genetic Conditions: Genetic, Epigenetic, and Environmental Factors.Stem cell-derived neurons from autistic individuals with SHANK3 mutation show morphogenetic abnormalities during early development.Prospective study of autism phenomenology and the behavioural phenotype of Phelan-McDermid syndrome: comparison to fragile X syndrome, Down syndrome and idiopathic autism spectrum disorder.Early postnatal exposure to airborne fine particulate matter induces autism-like phenotypes in male rats.Framework for assessing individuals with rare genetic disorders associated with profound intellectual and multiple disabilities (PIMD): the example of Phelan McDermid Syndrome.SHANK3 Regulates Intestinal Barrier Function Through Modulating ZO-1 Expression Through the PKCε-dependent Pathway.Aberrant cognitive phenotypes and altered hippocampal BDNF expression related to epigenetic modifications in mice lacking the post-synaptic scaffolding protein SHANK1: Implications for autism spectrum disorder.De novo SHANK3 mutation causes Rett syndrome-like phenotype in a female patient.Persistent 6-OH-BDE-47 exposure impairs functional neuronal maturation and alters expression of neurodevelopmentally-relevant chromatin remodelers.
P2860
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P2860
description
article científic
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article scientifique
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articol științific
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articolo scientifico
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artigo científico
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artigo científico
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artigo científico
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artikel ilmiah
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artikull shkencor
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artículo científico
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name
SHANK3 as an autism spectrum disorder-associated gene.
@en
type
label
SHANK3 as an autism spectrum disorder-associated gene.
@en
prefLabel
SHANK3 as an autism spectrum disorder-associated gene.
@en
P1476
SHANK3 as an autism spectrum disorder-associated gene.
@en
P2093
Chikako Waga
Shigeo Uchino
P304
P356
10.1016/J.BRAINDEV.2012.05.013
P577
2012-06-29T00:00:00Z