Parallel RNA and DNA analysis after deep-sequencing (PRDD-seq) reveals cell type specific lineage patterns in human brain.
Autism BrainNet
Neuroinflammatory gene expression alterations in anterior cingulate cortical white and gray matter of males with autism spectrum disorder.
Insulin-like growth factor and insulin-like growth factor receptor expression in human idiopathic autism fusiform gyrus tissue.
The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing.
Autism spectrum disorder: Neuropathology and animal models.
T-lymphocytes and cytotoxic astrocyte blebs correlate across autism brains.
Genome-wide DNA methylation profiling identifies convergent molecular signatures associated with idiopathic and syndromic autism in post-mortem human brain tissue.
The microglial innate immune receptor TREM2 is required for synapse elimination and normal brain connectivity.
Autism-like phenotype and risk gene mRNA deadenylation by CPEB4 mis-splicing.
Genome-wide changes in lncRNA, splicing, and regional gene expression patterns in autism.
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