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Loss of Snord115 mitigates Snord116-driven sleep abnormalities in mouse models of Prader-Willi syndrome
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DOI:10.1016/j.nbd.2026.107551.png)
Abstract
En 中文
• Snord116 deletion disrupts sleep architecture in mice. • Snord115 loss suppresses Snord116-dependent REM sleep abnormalities. • REM sleep changes occur independently of MCH neuron decrease. • Hypothalamic transcriptomic changes are limited across genotypes.
Keywords:
snoRNA
SNORD116
SNORD115
Prader-Willi syndrome
REM sleep
Hypocretin
MCH
Journal
IF:
5.6
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6.7K
Citations:
2.1W
