Distinct genetic risk based on association of MET in families with co-occurring autism and gastrointestinal conditions
about
Maternal infection and immune involvement in autismGenetics of autistic disorders: review and clinical implicationsThe Impact of Neuroimmune Alterations in Autism Spectrum DisorderNetworking in autism: leveraging genetic, biomarker and model system findings in the search for new treatmentsCircuit-specific intracortical hyperconnectivity in mice with deletion of the autism-associated Met receptor tyrosine kinaseA new synaptic player leading to autism risk: Met receptor tyrosine kinaseA familial heterozygous null mutation of MET in autism spectrum disorderDecreased Serum Hepatocyte Growth Factor (HGF) in Autistic Children with Severe Gastrointestinal DiseaseThe clinical-basic interface in defining pathogenesis in disorders of neurodevelopmental origin.Myeloid dendritic cells frequencies are increased in children with autism spectrum disorder and associated with amygdala volume and repetitive behaviors.Rigid-compulsive behaviors are associated with mixed bowel symptoms in autism spectrum disorder.Association of genetic variation in the MET proto-oncogene with schizophrenia and general cognitive ability.Effects of food on physical and sleep complaints in children with ADHD: a randomised controlled pilot studyPrenatal polycyclic aromatic hydrocarbon exposure leads to behavioral deficits and downregulation of receptor tyrosine kinase, MET.Characterizing genes with distinct methylation patterns in the context of protein-protein interaction network: application to human brain tissues.The mind-body-microbial continuumSynaptic microcircuit dysfunction in genetic models of neurodevelopmental disorders: focus on Mecp2 and Met.Prader-Willi syndrome and autism spectrum disorders: an evolving story.Risperidone-related improvement of irritability in children with autism is not associated with changes in serum of epidermal growth factor and interleukin-13.Association of a MET genetic variant with autism-associated maternal autoantibodies to fetal brain proteins and cytokine expression.Maladaptive Behavior and Gastrointestinal Disorders in Children with Autism Spectrum Disorder.Gastrointestinal dysfunction in autism: parental report, clinical evaluation, and associated factors.Autism Linked to Increased Oncogene Mutations but Decreased Cancer Rate.Patterns of Risk for Multiple Co-Occurring Medical Conditions Replicate Across Distinct Cohorts of Children with Autism Spectrum Disorder.Enrichment of elevated plasma F2t-isoprostane levels in individuals with autism who are stratified by presence of gastrointestinal dysfunction.Association of maternal report of infant and toddler gastrointestinal symptoms with autism: evidence from a prospective birth cohort.Prenatal expression of MET receptor tyrosine kinase in the fetal mouse dorsal raphe nuclei and the visceral motor/sensory brainstemShort-chain fatty acid fermentation products of the gut microbiome: implications in autism spectrum disorders.The Genetic Intersection of Neurodevelopmental Disorders and Shared Medical Comorbidities - Relations that Translate from Bench to BedsideTranscriptional regulation of the MET receptor tyrosine kinase gene by MeCP2 and sex-specific expression in autism and Rett syndrome.Gastrointestinal tract abnormalities induced by prenatal valproic Acid exposure in rat offspringThe conundrums of understanding genetic risks for autism spectrum disordersThe bacterial peptidoglycan-sensing molecule Pglyrp2 modulates brain development and behaviorMedical comorbidities in autism: challenges to diagnosis and treatment.A review of candidate urinary biomarkers for autism spectrum disorder.MET receptor tyrosine kinase as an autism genetic risk factor.Immune dysregulation in autism spectrum disorder.Distinct projection targets define subpopulations of mouse brainstem vagal neurons that express the autism-associated MET receptor tyrosine kinase.The Pleiotropic MET Receptor Network: Circuit Development and the Neural-Medical Interface of Autism.Brief Report: Association Between Autism Spectrum Disorder, Gastrointestinal Problems and Perinatal Risk Factors Within Sibling Pairs.
P2860
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P2860
Distinct genetic risk based on association of MET in families with co-occurring autism and gastrointestinal conditions
description
2009 nî lūn-bûn
@nan
2009 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի մարտին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Distinct genetic risk based on ...... nd gastrointestinal conditions
@ast
Distinct genetic risk based on ...... nd gastrointestinal conditions
@en
Distinct genetic risk based on ...... nd gastrointestinal conditions
@nl
type
label
Distinct genetic risk based on ...... nd gastrointestinal conditions
@ast
Distinct genetic risk based on ...... nd gastrointestinal conditions
@en
Distinct genetic risk based on ...... nd gastrointestinal conditions
@nl
prefLabel
Distinct genetic risk based on ...... nd gastrointestinal conditions
@ast
Distinct genetic risk based on ...... nd gastrointestinal conditions
@en
Distinct genetic risk based on ...... nd gastrointestinal conditions
@nl
P2093
P3181
P356
P1433
P1476
Distinct genetic risk based on ...... nd gastrointestinal conditions
@en
P2093
Daniel B Campbell
Harland Winter
Margaret Bauman
Pat Levitt
Timothy M Buie
P304
P3181
P356
10.1542/PEDS.2008-0819
P407
P577
2009-03-01T00:00:00Z