Molecular cascades and cell type–specific signatures in ASD revealed by single-cell genomics
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Researchers have made discoveries about the molecular mechanisms underlying autism spectrum disorder (ASD) using single-cell genomics. Studies have identified cell type-specific signatures and molecular changes in ASD, with some focusing on the role of microglia and others examining the functions of specific genetic elements. The findings appear to shed light on the genetic risk for autism and its connection to changes in the brain, although the specifics of these connections are still being explored.
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