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Impairment of autophagic degradation and mitochondrial dysfunction are also significant factors, as evidenced by accumulation of autophagosomes and suppression of mitochondrial oxygen consumption rates in DOX-treated hearts [14]
One of the main issues is dosage transparency
Methylcobalamin degrades more rapidly under the same conditions
At week 4, the combination group achieved a larger OHIP14 K reduction than either monotherapy
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