Sort   by:  
 Page size 
ProteomicsProteomics Analysis of Saliva from Children with Autism Spectrum Disorder
In the current work, saliva samples were collected from children with different degrees of ASD and healthy children and proteomics approaches were applied to generate data on differentially expressed proteins between groups which will serve as a basis for future validation studies as protein markers...
ORGANISM(S): Homo sapiens (Human) 
2022-02-14 | PXD030065 | Pride
Austism spectrum disorder Saliva Biomarker 
GenomicsMitochondrial DNA mutations contribute to autism and also to the characteristics of mitochondrial disorders present in patients with autism spectrum disorders
Intellectual disability (ID) is common among autism spectrum disorder (ASD) patients. Also, evidence from many fields of medicine has documented multiple non-CNS physiological abnormalities associated with ASD, suggesting that, in some individuals, ASD arises from systemic, rather than organ-specifi...
EGAS00001002750 | EGA
Genomicsec1a94c2-4912-49d9-8640-39b211629678 - samples
Sequences from 95 subjects presenting intellectual disability (ID) and 98 subjects presenting intellectual disability and a diagnosis of autism spectrum disorder (ASD). The mtDNA was amplified by long-range PCR with 3 pairs of primers producing overlapping fragments. The three fragments were mixed i...
EGAD00001004213 | EGA
TranscriptomicsMicroarray profiling of primary neurons transduced with shRNA for multiple ASD-implicated genes
Austism spectrum disorder (ASD) is a heterogeneous behavioral disease most commonly characterized by severe impairment of social engagement and the presence of repetitive activities. The molecular etiology of ASD is still largely unknown despite a strong genetic component. Part of the difficulty in...
ORGANISM(S): Mus musculus 
2013-05-23 | E-GEOD-47150 | biostudies-arrayexpress
TranscriptomicsMicroarray profiling of primary neurons transduced with shRNA for multiple ASD-implicated genes
Austism spectrum disorder (ASD) is a heterogeneous behavioral disease most commonly characterized by severe impairment of social engagement and the presence of repetitive activities. The molecular etiology of ASD is still largely unknown despite a strong genetic component. Part of the difficulty in ...
ORGANISM(S): Mus musculus 
2013-05-23 | GSE47150 | GEO
GenomicsMus musculus
Microarray profiling of primary neurons transduced with shRNA for multiple ASD-implicated genes
PRJNA204967 | ENA
Sort   by:  
 Page size