RNA rewrite improves breathing, survival in Rett mice
The technique involves editing the cellular instructions to make MECP2 protein and partially restores its levels in the brainstem.
The technique involves editing the cellular instructions to make MECP2 protein and partially restores its levels in the brainstem.
Mood, anxiety, personality and eating disorders more commonly affect autistic people diagnosed in adulthood than those diagnosed in childhood.
Tickling our brains on Twitter this week were threads about helping neuroscientists learn the programming language Python, a study about autistic schoolchildren, and the possible root of modern humans’ brain power.
A well-studied brain response to sound appears earlier than usual in young children with autism.
Null and replicated results in this month’s newsletter tackle aging, a purported pathway for oxytocin’s effects on autistic people, and a possible autism biomarker.
The prize recognizes Geschwind’s contributions to our understanding of autism genetics.
A 341-repeat mutation from a person with fragile X does not lead to the syndrome’s traits or function the same way in mice, highlighting a need for different animal models.
The brains of mice carrying different mutations in the autism-linked gene TBR1 display different molecular changes yet similar structural changes, resembling those previously found in autistic people with TBR1 mutations.
Sleep disruption early in life has long-lasting consequences for mice missing a copy of the autism-linked gene SHANK3.
Mice with a mutated copy of SHANK3 fail to establish normal sleep patterns during development.