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Together these results establish 4HNE as the biological ligand for GDAP1, provide mechanistic insight into 4HNE binding, and demonstrate that altered 4HNE recognition is the likely mechanism underlying CMT-causing mutants such as T157P near the 4HNE binding site

In vivo, PL-Au@P-ZnO NRs with US suppress tumor growth without causing systemic toxicity

Optimal exposure windows, dose scheduling, and the potential for hormetic effects or long-term consequences are poorly defined, impeding the rational design of exercise mimetic administration strategies

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Anemia and red blood cell transfusions, cerebral oxygenation, brain injury and development, and neurodevelopmental outcome in preterm infants: a systematic review