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Accession: PRJNA254971 ID: 254971

Disruption of human-specific synaptogenesis program in autism [RNA-seq]

To test the connection between the molecular mechanisms underlying autistic disorder and human cognitive evolution, we analyzed the gene expression changes taking place during prefrontal cortex development in autism patients and healthy controls, as well as non-human primates. More...
AccessionPRJNA254971; GEO: GSE59288
Data TypeTranscriptome or Gene expression
ScopeMultispecies
PublicationsLiu X et al., "Disruption of an Evolutionarily Novel Synaptic Expression Pattern in Autism.", PLoS Biol, 2016 Sep;14(9):e1002558
SubmissionRegistration date: 10-Jul-2014
Partner Institute for Computational Biology
RelevanceUnknown
Project Data:
Resource NameNumber
of Links
Sequence data
SRA Experiments73
Publications
PubMed1
PMC1
Other datasets
BioSample73
GEO DataSets1
GEO Data Details
ParameterValue
Data volume, Supplementary Mbytes3
SRA Data Details
ParameterValue
Data volume, Gbases69
Data volume, Mbytes47794

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