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RISMutation Screening of the 3’-UTR of SHANK3 in Autism Spectrum Disorder
Single nucleotide mutations and CNVs at the SHANK3 locus have already been associated with Autism Spectrum Disorder (ASD). However, the 3’-untranslated region (3’-UTR) of this gene has not been evaluated in ASD for possible mutations. 3’-UTRs...
Dysregulation of miRNAs and genes in Autism Spectrum Disorder
RNA interplays. Moreover, there is evidence for miRNAs involvement in the pathogenesis of some neurodevelopmental disorders such as schizophrenia. We used Illumina human miRNA arrays (representing 735 miRNAs) to evaluate possible miRNA dysregulation in autism...
An evaluation model for analysing persuasive systems in mobile healthcare
The Profile of Functional Emotional Development of Children with Autism Spectrum Disorders from the Perspective of Developmental, Individual Differences(DIR), Relationship-based Approach
Introduction:The dominant approach in the etiology and treatment of autism spectrum disorder (ASD) is a behavioral approach. Proponents of the behavioral model believe that children with autism in access to capabilities in achieving love, empathy...
Developing a mixed family-focused therapy based on integrated human development model and comparing its effectiveness with Floortime play-therapy on the developmental family functioning and the functional-emotional development of children with autism spec
Introduction: Autism spectrum disorder (ASD) is a major disability of childhood which is the basis of many mental pressures on children and their families. Regarding the unfavorable effects of this disorder on the family system, the present research...
Using video and live modelling to teach motor skill to children with autism spectrum disorder
Observational learning is one of the most important learning tools for the education of people with autism spectrum disorders (ASD). The aim of current study was to investigate the effect of two
kinds of demonstration, namely video and live...
Genetic basis of Autism a neurogenetic complex disease
Autism spectrum disorder (ASD) is a neurogenetic syndrome which the majority of its pre-symptomatic behavioral
markers are investigated in the first year of life. The neural systems associated with these behaviors, include the...
Human PTCHD3 nulls: rare copy number and sequence variants suggest a non-essential gene
sequence assembly. Homozygous deletions (or CNV nulls) that are found in the normal population are of particular interest because they may serve to define non-essential genes in human biology.
Results: In a genomic screen investigating CNV in Autism...