Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism. - Wikidata - awgldk - TriplyDB

Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.

Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.

http://www.wikidata.org/entity/Q37716254

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CHD8 regulates neurodevelopmental pathways associated with autism spectrum disorder in neural progenitors The Evolving Diagnostic and Genetic Landscapes of Autism Spectrum Disorder Prenatal Neurogenesis in Autism Spectrum Disorders A Short Review on the Current Understanding of Autism Spectrum Disorders Functional Evaluations of Genes Disrupted in Patients with Tourette's Disorder.Astrocytes and Microglia and Their Potential Link with Autism Spectrum Disorders Striatal Circuits as a Common Node for Autism Pathophysiology Mutations and Modeling of the Chromatin Remodeler CHD8 Define an Emerging Autism Etiology Functional genomics of human brain development and implications for autism spectrum disorders Moving from capstones toward cornerstones: successes and challenges in applying systems biology to identify mechanisms of autism spectrum disorders Genes, circuits, and precision therapies for autism and related neurodevelopmental disorders The role of cerebellar circuitry alterations in the pathophysiology of autism spectrum disorders Modeling psychiatric disorders for developing effective treatments Switching modes in corticogenesis: mechanisms of neuronal subtype transitions and integration in the cerebral cortex The developmental transcriptome of the human brain: implications for neurodevelopmental disorders From trans to cis: transcriptional regulatory networks in neocortical development Connectivity in Autism: A Review of MRI Connectivity Studies Mutation of the CH1 Domain in the Histone Acetyltransferase CREBBP Results in Autism-Relevant Behaviors in Mice Advancing the understanding of autism disease mechanisms through genetics A Subset of Autism-Associated Genes Regulate the Structural Stability of Neurons.Genetic and genomic analyses as a basis for new diagnostic nosologies Discovery of Rare Mutations in Autism: Elucidating Neurodevelopmental Mechanisms Identification of the BRD1 interaction network and its impact on mental disorder risk Synaptic, transcriptional and chromatin genes disrupted in autism The contribution of de novo coding mutations to autism spectrum disorder MET receptor tyrosine kinase controls dendritic complexity, spine morphogenesis, and glutamatergic synapse maturation in the hippocampus Genome-wide prediction and functional characterization of the genetic basis of autism spectrum disorder TSHZ3 deletion causes an autism syndrome and defects in cortical projection neurons.Loss of Wdfy3 in mice alters cerebral cortical neurogenesis reflecting aspects of the autism pathology FOXG1-Dependent Dysregulation of GABA/Glutamate Neuron Differentiation in Autism Spectrum Disorders Opposing Effects on NaV1.2 Function Underlie Differences Between SCN2A Variants Observed in Individuals With Autism Spectrum Disorder or Infantile Seizures Rare deleterious mutations of the gene EFR3A in autism spectrum disorders.Estrogens Suppress a Behavioral Phenotype in Zebrafish Mutants of the Autism Risk Gene, CNTNAP2.The cerebellum, sensitive periods, and autism.Atypical miRNA expression in temporal cortex associated with dysregulation of immune, cell cycle, and other pathways in autism spectrum disorders BCL11A deletions result in fetal hemoglobin persistence and neurodevelopmental alterations.Putative Microcircuit-Level Substrates for Attention Are Disrupted in Mouse Models of Autism.Merging data from genetic and epigenetic approaches to better understand autistic spectrum disorder.A MARKOV RANDOM FIELD-BASED APPROACH TO CHARACTERIZING HUMAN BRAIN DEVELOPMENT USING SPATIAL-TEMPORAL TRANSCRIPTOME DATA.On joint estimation of Gaussian graphical models for spatial and temporal data.

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Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.

http://www.wikidata.org/entity/Q37716254

description

2013 nî lūn-bûn

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2013年の論文

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年學術文章

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2013年學術文章

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2013年學術文章

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Coexpression networks implicat ...... in the pathogenesis of autism.

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Coexpression networks implicat ...... in the pathogenesis of autism.

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Coexpression networks implicat ...... in the pathogenesis of autism.

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Coexpression networks implicat ...... in the pathogenesis of autism.

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Coexpression networks implicat ...... in the pathogenesis of autism.

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Coexpression networks implicat ...... in the pathogenesis of autism.

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J.CELL.2013.10.020

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A Gulhan Ercan-Sencicek

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A Jeremy Willsey

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Abha R Gupta

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Bernie Devlin

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Candace Bichsel

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Cong Lu

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Ed S Lein

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Ellen J Hoffman

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James P Noonan

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Jeremy A Miller

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P2860

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

TBR1 directly represses Fezf2 to control the laminar origin and development of the corticospinal tract

Rate of de novo mutations and the importance of father's age to disease risk

Strong association of de novo copy number mutations with autism

Fast and accurate short read alignment with Burrows-Wheeler transform

CNVs: harbingers of a rare variant revolution in psychiatric genetics

The Sequence Alignment/Map format and SAMtools

Patterns and rates of exonic de novo mutations in autism spectrum disorders

Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders

Integration of biological networks and gene expression data using Cytoscape

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