Sequencing ASMT identifies rare mutations in Chinese Han patients with autism
about
Melatonin in children with autism spectrum disorders: endogenous and pharmacokinetic profiles in relation to sleep.Coherent somatic mutation in autoimmune disease.Understanding melatonin receptor pharmacology: latest insights from mouse models, and their relevance to human disease.Genetic variation in melatonin pathway enzymes in children with autism spectrum disorder and comorbid sleep onset delay.Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders.Melatonin in Children with Autism Spectrum Disorders: How Does the Evidence Fit Together?Altered brain gene expression but not steroid biochemistry in a genetic mouse model of neurodevelopmental disorder.Redox Regulation and the Autistic Spectrum: Role of Tryptophan Catabolites, Immuno-inflammation, Autoimmunity and the Amygdala.Biomarkers in autism spectrum disorder: the old and the new.The Contribution of Missense Mutations in Core and Rim Residues of Protein-Protein Interfaces to Human Disease.A Comparative Genomic and Transcriptomic Survey Provides Novel Insights into N-Acetylserotonin Methyltransferase (ASMT) in Fish.
P2860
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P2860
Sequencing ASMT identifies rare mutations in Chinese Han patients with autism
description
2013 nî lūn-bûn
@nan
2013 թուականին հրատարակուած գիտական յօդուած
@hyw
2013 թվականին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Sequencing ASMT identifies rare mutations in Chinese Han patients with autism
@ast
Sequencing ASMT identifies rare mutations in Chinese Han patients with autism
@en
Sequencing ASMT identifies rare mutations in Chinese Han patients with autism
@nl
type
label
Sequencing ASMT identifies rare mutations in Chinese Han patients with autism
@ast
Sequencing ASMT identifies rare mutations in Chinese Han patients with autism
@en
Sequencing ASMT identifies rare mutations in Chinese Han patients with autism
@nl
prefLabel
Sequencing ASMT identifies rare mutations in Chinese Han patients with autism
@ast
Sequencing ASMT identifies rare mutations in Chinese Han patients with autism
@en
Sequencing ASMT identifies rare mutations in Chinese Han patients with autism
@nl
P2093
P2860
P1433
P1476
Sequencing ASMT identifies rare mutations in Chinese Han patients with autism
@en
P2093
Chenxing Liu
Lifang Wang
Meixiang Jia
Tianlan Lu
Weihua Yue
Yanyan Ruan
P2860
P304
P356
10.1371/JOURNAL.PONE.0053727
P407
P577
2013-01-01T00:00:00Z