Researchers took to social media to discuss a new tool for recording brain activity in freely moving mice and a study linking a mutation in the gene MBD5 to epilepsy and intellectual disability. That and more in this week’s Community Newsletter.
Researchers on social media reacted to a new version of the Neuropixels probe and a study of sex differences in the brain. That and more in this week’s Community Newsletter.
This week on social media, researchers discussed a genome-wide association study of the human cerebral cortex, how astrocytes integrate calcium signals, and more.
Researchers reacted to a study of brain mitochondria and behavior in mice and a study of brain structure differences in autism and other conditions. That and more in this week’s Community Newsletter.
Researchers took to social media to discuss how cognitive maps form during learning. There was also talk about a study of peripheral nerves in mice missing PTEN, an autism-linked gene. That and more in this week’s Community Newsletter.
A look back at NeuroDev’s first year gathering genomic and phenotypic data in Kenya and South Africa and a study on an underlying cause of repetitive behaviors in fragile X model mice absorbed researchers’ attention on social media this week. That and more in this week’s Community Newsletter.
This week on social media, researchers discussed research on sensory issues in fragile X mice, and they considered yet another study of epidurals and autism. That and more in this week’s Community Newsletter.
Researchers discussed a study of the integrated stress response in fragile X syndrome and a new how-to guide for quantitative bioimaging — plus more in this week’s Community Newsletter.
A new technique to map the entire body of a mouse and a high-resolution 4D imaging method for living brain tissue samples piqued researchers’ interest on social media this week — that and more in this issue of Community Newsletter.
This week on social media, researchers discussed sample size in neuroimaging studies and the potential of antisense oligonucleotides to restore the protein lost in fragile X syndrome.