Mutation screening and association analysis of six candidate genes for autism on chromosome 7q - Wikidata - wikimedia - TriplyDB

Mutation screening and association analysis of six candidate genes for autism on chromosome 7q

Mutation screening and association analysis of six candidate genes for autism on chromosome 7q

http://www.wikidata.org/entity/Q28291465

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Relationships between gene expression and brain wiring in the adult rodent brain The genetics of autistic disorders and its clinical relevance: a review of the literature Genetics of autistic disorders: review and clinical implications NrCAM in addiction vulnerability: positional cloning, drug-regulation, haplotype-specific expression, and altered drug reward in knockout mice Association of the neuronal cell adhesion molecule (NRCAM) gene variants with autism Xenopus laevis neuronal cell adhesion molecule (nrcam): plasticity of a CAM in the developing nervous system.Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABAT Neural cell adhesion molecule NrCAM is expressed in the mammalian inner ear and modulates spiral ganglion neurite outgrowth in an in vitro alternate choice assay.Impaired sociability and cognitive function in Nrcam-null mice.High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility.Proper migration and axon outgrowth of zebrafish cranial motoneuron subpopulations require the cell adhesion molecule MDGA2A Severity of Demyelinating and Axonal Neuropathy Mouse Models Is Modified by Genes Affecting Structure and Function of Peripheral Nodes A genome-wide association study identifies multiple loci associated with mathematics ability and disability Neural cell adhesion molecule NrCAM regulates Semaphorin 3F-induced dendritic spine remodeling Neuron glia-related cell adhesion molecule (NrCAM) promotes topographic retinocollicular mapping Development of a versatile enrichment analysis tool reveals associations between the maternal brain and mental health disorders, including autism Identification of chromosome 7 inversion breakpoints in an autistic family narrows candidate region for autism susceptibility Identification of novel autism candidate regions through analysis of reported cytogenetic abnormalities associated with autism.Molecular genetics of addiction vulnerability LAMB1 polymorphism is associated with autism symptom severity in Korean autism spectrum disorder patients.The UPF3B gene, implicated in intellectual disability, autism, ADHD and childhood onset schizophrenia regulates neural progenitor cell behaviour and neuronal outgrowth.The Wnt Signaling Pathway and Related Therapeutic Drugs in Autism Spectrum Disorder.

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Mutation screening and association analysis of six candidate genes for autism on chromosome 7q

http://www.wikidata.org/entity/Q28291465

description

2005 nî lūn-bûn

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2005 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2005 թվականի փետրվարին հրատարակված գիտական հոդված

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2005年の論文

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年學術文章

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Mutation screening and associa ...... es for autism on chromosome 7q

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Mutation screening and associa ...... es for autism on chromosome 7q

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Mutation screening and associa ...... es for autism on chromosome 7q

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Mutation screening and associa ...... es for autism on chromosome 7q

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Mutation screening and associa ...... es for autism on chromosome 7q

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Mutation screening and associa ...... es for autism on chromosome 7q

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prefLabel

Mutation screening and associa ...... es for autism on chromosome 7q

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Mutation screening and associa ...... es for autism on chromosome 7q

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SJ.EJHG.5201315

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European Journal of Human Genetics

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Mutation screening and associa ...... es for autism on chromosome 7q

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Agatino Battaglia

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Anthony J Bailey

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Birgitte Viskum

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Demetrios Haracopos

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Elena Bacchelli

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Elena Maestrini

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Ester-Ulsted Sorensen

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Firtz Poustka

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Francesca Blasi

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Gabrielle Barnby

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Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genes

Genetics of austim: complex aetiology for a heterogeneous disorder

Pervasive Developmental Disorders in Preschool Children

Are rare variants responsible for susceptibility to complex diseases?

SRPK2: a differentially expressed SR protein-specific kinase involved in mediating the interaction and localization of pre-mRNA splicing factors in mammalian cells

CASP, the alternatively spliced product of the gene encoding the CCAAT-displacement protein transcription factor, is a Golgi membrane protein related to giantin

PedCheck: a program for identification of genotype incompatibilities in linkage analysis

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

Exon/intron structure and alternative transcripts of the CUTL1 gene

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sj.ejhg.5201315

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Karen Brondum-Nielsen

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