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This metallophosphatase is a hybrid-type catalyst having two Zn II atoms as active metal sites with different coordination environments (Fig

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6.1 mtDNA as a biomarker for ART toxicity, metabolic complications, and immunological failure Quantifying mtDNA damage provides a mechanistic insight into ART-related toxicities and may support personalized management

In vivo experiments of prion-disease model mice showed cytotoxicity of PERK-dependent reactive astrocytes against neurons