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Potential Role of Selenoenzymes and Antioxidant Metabolism in relation to Autism Etiology and PathologyTwo knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis.Molecular handoffs in nitrergic neurotransmissionAbsence of strong strain effects in behavioral analyses of Shank3-deficient miceStudying autism in rodent models: reconciling endophenotypes with comorbiditiesReduced excitatory neurotransmission and mild autism-relevant phenotypes in adolescent Shank3 null mutant miceDevelopmental trajectories in children with and without autism spectrum disorders: the first 3 years.Co-expression profiling of autism genes in the mouse brain.DNA methylation profiling in the thalamus and hippocampus of postnatal malnourished mice, including effects related to long-term potentiation.Autism spectrum disorder and epilepsy: Disorders with a shared biology.Epigenetic understanding of gene-environment interactions in psychiatric disorders: a new concept of clinical genetics.Functional annotation of the human brain methylome identifies tissue-specific epigenetic variation across brain and bloodGenetic removal of p70 S6 kinase 1 corrects molecular, synaptic, and behavioral phenotypes in fragile X syndrome mice.Neurobiological sequelae of witnessing stressful events in adult mice.Reduction in parvalbumin expression not loss of the parvalbumin-expressing GABA interneuron subpopulation in genetic parvalbumin and shank mouse models of autismTranslational approaches to the biology of Autism: false dawn or a new era?Working up autism: the practical role of medical genetics.Gene-environment interactions and epigenetic pathways in autism: the importance of one-carbon metabolism.The genetic landscape of autism spectrum disorders.A blueprint for research on Shankopathies: a view from research on autism spectrum disorder.Synaptic Signaling in Learning and Memory.Touchscreen learning deficits and normal social approach behavior in the Shank3B model of Phelan-McDermid Syndrome and autismNovel Shank3 mutant exhibits behaviors with face validity for autism and altered striatal and hippocampal function.De novo SHANK3 mutation causes Rett syndrome-like phenotype in a female patient.
P2860
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P2860
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
@zh
2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
2011年學術文章
@zh-hant
name
SHANK3, the synapse, and autism.
@en
SHANK3, the synapse, and autism.
@nl
type
label
SHANK3, the synapse, and autism.
@en
SHANK3, the synapse, and autism.
@nl
prefLabel
SHANK3, the synapse, and autism.
@en
SHANK3, the synapse, and autism.
@nl
P356
P1476
SHANK3, the synapse, and autism.
@en
P304
P356
10.1056/NEJMCIBR1104261
P407
P577
2011-07-01T00:00:00Z