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This suggests that the effects of Wnt/-catenin signaling shift as the cochlea matures, emphasizing its context-dependent role

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Maternal riboflavin deficiency, resulting in transient neonatal-onset glutaric aciduria Type 2, is caused by a microdeletion in the riboflavin transporter gene GPR172B

germ-free or antibiotic-treated mice had impaired microglial clearance of A plaques, which could be restored by supplying acetate [100]

Additionally, established procedures help support reliable batch-to-batch performance and standardized research material preparation

More importantly, the mechanistic rationale fits acute repair better than it fits osteoarthritis