Description
The authors identify functional homologs between species but don’t explain what sequence or structural features enable this conservation. This knowledge gap limits translation of lncRNA-based therapies from mouse models to human patients.
Gap type: open_question Source paper: hUC-MSC-derived exosomes ameliorate Alzheimer’s disease pathology through lncRNA-9969-mediated multi-target protection involving neuronal autophagy and microglial modulation. (2026, Alzheimer’s research & therapy, PMID:41540476)