25 results for “autism”. Showing 25 of 39,449.
The Face of Autism in Israel.
autism. Typically, diagnosis is at age 2. The autism intervention
Single-cell genomics identifies cell type-specific molecular changes in autism.
autism to identify autism-associated transcriptomic changes in specific cell
Interneuron Transplantation Rescues Social Behavior Deficits without Restoring Wild-Type Physiology in a Mouse Model of Autism with Excessive Synaptic Inhibition.
autism models, suggesting that autism may be treated by correcting
Mesenchymal stem cell-derived extracellular vesicles alleviate autism by regulating microglial glucose metabolism reprogramming and neuroinflammation through PD-1/PD-L1 interaction.
autism spectrum disorder (ASD), and this process includes crucial metabolic
Tau reduction attenuates autism-like features in Fmr1 knockout mice.
autism spectrum disorder (ASD) and resulted from a loss of the FMR1
Autism gene variants disrupt enteric neuron migration and cause gastrointestinal dysmotility.
autism and gastrointestinal distress is well-established, yet the molecular
Interaction between MAOA and FOXP2 in association with autism and verbal communication in a Korean population.
autism spectrum disorder. Forkhead box protein P2 (FOXP2), a transcription
Neuroanatomical Diversity of Corpus Callosum and Brain Volume in Autism: Meta-analysis, Analysis of the Autism Brain Imaging Data Exchange Project, and Simulation.
autism have been often reported to have a smaller corpus
An autistic endophenotype results in complex immune dysfunction in healthy siblings of autistic children.
autism. Because it is becoming apparent that autism is associated
Inherited and multiple de novo mutations in autism/developmental delay risk genes suggest a multifactorial model.
autism risk genes in probands from the Autism Clinical and Genetic
Interneuron Dysfunction in Syndromic Autism: Recent Advances.
Autism is an extremely heterogeneous disorder, but its frequent cooccurrence
Neurodegeneration in Autism: A Study of Clusterin, Very Long-Chain Fatty Acids, and Carnitine.
autism spectrum disorder (ASD) with and without regression. By exploring
Association of mouse Dlg4 (PSD-95) gene deletion and human DLG4 gene variation with phenotypes relevant to autism spectrum disorders and Williams' syndrome.
autism spectrum disorders and other neurodevelopmental disorders to synaptic abnormalities
Role of JAK-STAT and PPAR-Gamma Signalling Modulators in the Prevention of Autism and Neurological Dysfunctions.
autism. Thus, PPAR-gamma agonist upregulation may be associated with
Sodium butyrate facilitates CRHR2 expression to alleviate HPA axis hyperactivity in autism-like rats induced by prenatal lipopolysaccharides through histone deacetylase inhibition.
autism and LPS-exposed rat model of autism exhibited lower
Fecundity of patients with schizophrenia, autism, bipolar disorder, depression, anorexia nervosa, or substance abuse vs their unaffected siblings.
autism, bipolar disorder, depression, anorexia nervosa, or substance abuse and their
De novo TBR1 mutations in sporadic autism disrupt protein functions
autism cases. Coupling these novel genetic data to empirical assays
SYN2 is an autism predisposing gene: loss-of-function mutations alter synaptic vesicle cycling and axon outgrowth.
autism spectrum disorders (ASDs) has been identified, many of which
Prenatal Exposure to COVID-19 mRNA Vaccine BNT162b2 Induces Autism-Like Behaviors in Male Neonatal Rats: Insights into WNT and BDNF Signaling Perturbations.
autism-related neurobehavioral outcomes in a rat model. Pregnant rats
[Autism. Neurobiological aspects].
Autism is a neurodevelopmental disorder with a neurobiological basis, characterized
High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility.
Autism spectrum disorders are a group of highly heritable neurodevelopmental
The Parvalbumin Hypothesis of Autism Spectrum Disorder
autism spectrum disorder (ASD)-a type of neurodevelopmental disorder-is increasing
Reversal of memory and autism-related phenotypes in Tsc2+/- mice via inhibition of Nlgn1.
autism and is caused by loss of function mutations in the TSC1
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
autism spectrum disorders (ASD) have a strong genetic component; however
Systemic auto-antibodies in children with autism.
autism. A subset of anti-ds-DNA antibodies has been