Journal
CELL
Volume 184, Issue 21, Pages 5303-5305Publisher
CELL PRESS
DOI: 10.1016/j.cell.2021.09.027
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The study reveals that adeno-associated viruses, engineered for glia-specific expression, can become widely active in endogenous neurons, posing a challenge for researchers in their quest for efficient conversion of glia into neurons for brain repair.
In this issue of Cell, Wang et al. come to the unsettling conclusion that adeno-associated viruses, despite being engineered for glia-specific expression, can become widely active in endogenous neurons, misleading researchers in their quest for efficient conversion of glia into neurons for brain repair.
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