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Hematti, P

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Human fetal neurons displayed progressive loss throughout 6 d after L-Glu, as evidenced by microscopic examination [73]

Mitochondrial dysfunction is apparent as intramitochondrial iron deposition within the erythroid precursor, the hallmark ringed sideroblast. Mitochondrial cytopathy comprises a genetically heterogeneous group of disorders in which mitochondrial DNA shows deletions, duplications, and other mutations, of either sporadic or inherited origin (Fig

Intracellular pool of vascular endothelial growth factor in human neutrophils
