日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Mutations in mitochondrial ferredoxin FDX2 suppress frataxin deficiency.

线粒体铁氧还蛋白 FDX2 的突变可抑制弗拉塔辛缺乏症。

Meisel Joshua D, Joshi Pallavi R, Spelbring Amy N, Wang Hong, Wellner Sandra M, Wiesenthal Presli P, Miranda Maria, McCoy Jason G, Barondeau David P, Ruvkun Gary, Mootha Vamsi K

Hypoxia and intra-complex genetic suppressors rescue complex I mutants by a shared mechanism.

缺氧和复合物内遗传抑制因子通过共同的机制拯救复合物 I 突变体

Meisel Joshua D, Miranda Maria, Skinner Owen S, Wiesenthal Presli P, Wellner Sandra M, Jourdain Alexis A, Ruvkun Gary, Mootha Vamsi K