about
Mice that lack the C-terminal region of Reelin exhibit behavioral abnormalities related to neuropsychiatric disorders.CRISPR/Cas9-mediated heterozygous knockout of the autism gene CHD8 and characterization of its transcriptional networks in cerebral organoids derived from iPS cells.Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism.The ApoE receptors Vldlr and Apoer2 in central nervous system function and disease.Developmental Neurotoxicity of Traffic-Related Air Pollution: Focus on Autism.Autism, epilepsy, and synaptopathies: a not rare association.A de novo splice site mutation in EHMT1 resulting in Kleefstra syndrome with pharmacogenomics screening and behavior therapy for regressive behaviors.The de novo autism spectrum disorder RELN R2290C mutation reduces Reelin secretion and increases protein disulfide isomerase expression.Immunoexcitotoxicity as the central mechanism of etiopathology and treatment of autism spectrum disorders: A possible role of fluoride and aluminum.Serum Cytokine and Growth Factor Levels in Children with Autism Spectrum Disorder.
P2860
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P2860
description
2016 nî lūn-bûn
@nan
2016 թուականին հրատարակուած գիտական յօդուած
@hyw
2016 թվականին հրատարակված գիտական հոդված
@hy
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
name
RELN Mutations in Autism Spectrum Disorder
@ast
RELN Mutations in Autism Spectrum Disorder
@en
RELN Mutations in Autism Spectrum Disorder
@nl
type
label
RELN Mutations in Autism Spectrum Disorder
@ast
RELN Mutations in Autism Spectrum Disorder
@en
RELN Mutations in Autism Spectrum Disorder
@nl
prefLabel
RELN Mutations in Autism Spectrum Disorder
@ast
RELN Mutations in Autism Spectrum Disorder
@en
RELN Mutations in Autism Spectrum Disorder
@nl
P2860
P3181
P356
P1476
RELN Mutations in Autism Spectrum Disorder
@en
P2093
Brian W Howell
Dawn B Lammert
P2860
P3181
P356
10.3389/FNCEL.2016.00084
P407
P577
2016-01-01T00:00:00Z