Fig. 7
- ID
- ZDB-IMAGE-250304-7
- Publication
- Chen et al., 2025 - NDUFB7 mutations cause brain neuronal defects, lactic acidosis, and mitochondrial dysfunction in humans and zebrafish
- All Figures
- Figures for Chen et al., 2025
Fig. 7 Knockdown of Ndufb7 reduces the oxygen consumption rate.
We treated one-cell stage zebrafish embryos without or with indicated Ndufb7 translational-blocking morpholino oligonucleotides (tMO), and Ndufb7 mRNA or Mitoquinone mesylate (MitoQ) as described in Fig.