A genetic variant that disrupts MET transcription is associated with autism - Wikidata - wikimedia - TriplyDB

A genetic variant that disrupts MET transcription is associated with autism

A genetic variant that disrupts MET transcription is associated with autism

http://www.wikidata.org/entity/Q24674115

about

Recent advances in the pathogenesis of syndromic autisms The Role of the Neurobiologist in Redefining the Diagnosis of Autism Advances in autism genetics: on the threshold of a new neurobiology Prenatal stress and risk for autism Autism: many genes, common pathways?Autism and brain development The role of immune dysfunction in the pathophysiology of autism The new neurobiology of autism: cortex, connectivity, and neuronal organization Genetics of autistic disorders: review and clinical implications The Tangled Tale of Genes and Environment: Moore's Current developments in the genetics of autism: from phenome to genome The genetic and neurobiologic compass points toward common signaling dysfunctions in autism spectrum disorders Synaptic Wnt/GSK3β Signaling Hub in Autism Consensus paper: pathological role of the cerebellum in autism Networking in autism: leveraging genetic, biomarker and model system findings in the search for new treatments Cytokine dysregulation in autism spectrum disorders (ASD): possible role of the environment Complete or partial reduction of the Met receptor tyrosine kinase in distinct circuits differentially impacts mouse behavior Early-Life Stress Paradigm Transiently Alters Maternal Behavior, Dam-Pup Interactions, and Offspring Vocalizations in Mice.Circuit-specific intracortical hyperconnectivity in mice with deletion of the autism-associated Met receptor tyrosine kinase A new synaptic player leading to autism risk: Met receptor tyrosine kinase A familial heterozygous null mutation of MET in autism spectrum disorder Autoantibodies in autism spectrum disorders (ASD)MET receptor tyrosine kinase controls dendritic complexity, spine morphogenesis, and glutamatergic synapse maturation in the hippocampus Decreased Serum Hepatocyte Growth Factor (HGF) in Autistic Children with Severe Gastrointestinal Disease Involvement of the PRKCB1 gene in autistic disorder: significant genetic association and reduced neocortical gene expression Immunologic and neurodevelopmental susceptibilities of autism Synaptic and extrasynaptic location of the receptor tyrosine kinase met during postnatal development in the mouse neocortex and hippocampus Evidence of cell-nonautonomous changes in dendrite and dendritic spine morphology in the met-signaling-deficient mouse forebrain Animal models of autism spectrum disorders: information for neurotoxicologists Environmental toxicants and autism spectrum disorders: a systematic review Protocadherin α (PCDHA) as a novel susceptibility gene for autism Gene expression profiling of lymphoblasts from autistic and nonaffected sib pairs: altered pathways in neuronal development and steroid biosynthesis Hepatocyte growth factor and c-Met promote dendritic maturation during hippocampal neuron differentiation via the Akt pathway Language Impairments in ASD Resulting from a Failed Domestication of the Human Brain Recent Advances in the Genetics of Vocal Learning Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism Social Neuroscience: Progress and Implications for Mental Health Multi-Scale Molecular Deconstruction of the Serotonin Neuron System.Environmental Enrichment Therapy for Autism: Outcomes with Increased Access.Ras and Rap signaling in synaptic plasticity and mental disorders.

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P2860

A genetic variant that disrupts MET transcription is associated with autism

http://www.wikidata.org/entity/Q24674115

description

2006 nî lūn-bûn

@nan

2006 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2006 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

2006年の論文

@ja

2006年論文

@yue

2006年論文

@zh-hant

2006年論文

@zh-hk

2006年論文

@zh-mo

2006年論文

@zh-tw

2006年论文

@wuu

name

A genetic variant that disrupts MET transcription is associated with autism

@ast

A genetic variant that disrupts MET transcription is associated with autism

@en

A genetic variant that disrupts MET transcription is associated with autism

@nl

type

label

A genetic variant that disrupts MET transcription is associated with autism

@ast

A genetic variant that disrupts MET transcription is associated with autism

@en

A genetic variant that disrupts MET transcription is associated with autism

@nl

prefLabel

A genetic variant that disrupts MET transcription is associated with autism

@ast

A genetic variant that disrupts MET transcription is associated with autism

@en

A genetic variant that disrupts MET transcription is associated with autism

@nl

P1433

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P1476

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P2860

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P932

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P3181

P356

PNAS.0605296103

P1433

Proceedings of the National Academy of Sciences of the United States of America

P1476

A genetic variant that disrupts MET transcription is associated with autism

@en

P2093

Carmela Bravaccio

http://www.w3.org/2001/XMLSchema#string

Cindy Schneider

http://www.w3.org/2001/XMLSchema#string

Daniel B Campbell

http://www.w3.org/2001/XMLSchema#string

Pat Levitt

http://www.w3.org/2001/XMLSchema#string

Raun Melmed

http://www.w3.org/2001/XMLSchema#string

Roberto Militerni

http://www.w3.org/2001/XMLSchema#string

Simona Trillo

http://www.w3.org/2001/XMLSchema#string

P2860

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

Searching for ways out of the autism maze: genetic, epigenetic and environmental clues

Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors

A genomewide screen of 345 families for autism-susceptibility loci.

Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism

Support for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locus

An autosomal genomic screen for autism. Collaborative linkage study of autism

HGF/SF-met signaling in the control of branching morphogenesis and invasion

Met, metastasis, motility and more

The genetics of autism

P304

16834-9

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scholarly article

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3475203

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10.1073/PNAS.0605296103

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P407

P433

45

http://www.w3.org/2001/XMLSchema#string

P478

103

http://www.w3.org/2001/XMLSchema#string

P50

James S. Sutcliffe

Antonio M Persico

P577

2006-11-07T00:00:00Z

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P5875

6742904

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P698

17053076

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P932

1838551

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