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Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2019

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Palabras clave – provistas por la editorial

autism spectrum disorders (ASD); cancer; overlapping genes and gene profiling; super-pathways; phenotypes and diseases; molecular functions and processes; 15q11.2 BP1-BP2 microdeletion (Burnside-Butler) syndrome; imprinting; parent-of-origin effects; phenotype-genotype correlation; autism; developmental delays; motor delays; microbiome; gut; ProSAP2; Phelan McDermid Syndrome; gut–brain interaction; leaky gut; IL-6; SHANK; collapsin response mediator protein 4; autism spectrum disorder; neurodevelopmental disorder; whole-exome sequencing; animal model; sex different phenotypes; 15q11.2 BP1–BP2 microdeletion (Burnside–Butler syndrome); NIPA1; NIPA2; CYFIP1; TUBGCP5 genes; Prader–Willi and Angelman syndromes; magnesium transporters and supplementation; potential treatment options; intellectual disability; AMPA receptors; NMDA receptors; guanine nucleotide exchange factor; synaptic plasticity; Autism spectrum disorder; ASD; Obesity; Overweight; Body mass index; BMI; autism candidate genes; synaptotagmin-like protein 4 (SYTL4); transmembrane protein 187 (TMEM187); SYTL4-protein structure; STRING-protein-protein interaction; expression profile; microRNA- interactions; autism spectrum disorders; biological networks; genomics; multi-omics; network diffusion; data integration; genetics; quantitative traits; stratification by trait severity; heterogeneity reduction; case-control association analysis; fragile X syndrome; RNA toxicity; DNA methylation; mosaicism; pediatrics; MS-QMA; AmplideX; cytokine; monocyte; β-glucan; T cell cytokine; trained immunity; maternal immune activation; epigenetics; mice; postnatal VPA injection; SAM; gene expression; nanostring

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Información

Tipo de recurso:

libros

ISBN electrónico

978-3-0365-3610-1

País de edición

Suiza