Předmět: |
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Zdroj: |
Mental Health Weekly Digest; 6/21/2024, p1105-1105, 1p |
Abstrakt: |
A new study from the University of North Carolina Chapel Hill explores the regional and cellular organization of the autism-associated protein UBE3A/E6AP and its antisense transcript in the brain of the developing rhesus monkey. The research focuses on Angelman syndrome (AS), a neurogenetic disorder caused by mutations or deletions in the maternally-inherited UBE3A allele. The study found that UBE3A is silenced in neurons during development by a noncoding transcript, and the absence of UBE3A results in severe neurological symptoms. The findings suggest that early-life intervention may be optimal for overcoming the loss of UBE3A linked to AS. [Extracted from the article] |
Databáze: |
Complementary Index |
Externí odkaz: |
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