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Identification and Characterization of Genetic Components in Autism Spectrum Disorders 2019

The Identification of the Genetic Components of Autism Spectrum Disorders 2019 will serve as a resource for laboratory and clinical scientists as well as translational-based researchers, primary healthcare providers or physicians, psychologists/psychiatrists, neurologists, developmental pediatrician...

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Guardat en:
Autor corporatiu: Butler, Merlin G.
Format: Livro
Idioma:Inglês
Publicat: MDPI - Multidisciplinary Digital Publishing Institute 2022
Matèries:
thema EDItEUR::G Reference, Information and Interdisciplinary subjects::GP Research and information: general
thema EDItEUR::P Mathematics and Science::PS Biology, life sciences
thema EDItEUR::P Mathematics and Science::PS Biology, life sciences::PSA Life sciences: general issues::PSAK Genetics (non-medical)
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
Accés en línia:https://directory.doabooks.org/handle/20.500.12854/81036
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