The expression of various genes encoding complex I-driving proteins, such as NDUFC1, NDUFB4, NDUFB10, NDUFB11, NDUFA12, NDUFA13, NDUFS7, NDUFS2, and NDUFA7 , showed the most pronounced reduction in IC-B cells in ABMR ( Figure 4D )
2021;16(12):e0261552
Therefore, we hypothesized that L-GSH supplementation, in conjunction with RIF therapy, would improve the control M
Conclusion: We generated a representative human developmental model of Alagille syndrome using complex liver organoids derived from iPSCs
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