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

BH3 mimetics activate multiple pro-autophagic pathways

BH3 类似物激活多种促自噬途径

S A Malik, I Orhon, E Morselli, A Criollo, S Shen, G Mariño, A BenYounes, P Bénit, P Rustin, M C Maiuri, G Kroemer

Stabilization of hypoxia-inducible factor-1alpha protein in hypoxia occurs independently of mitochondrial reactive oxygen species production

缺氧条件下缺氧诱导因子-1α蛋白的稳定化与线粒体活性氧的产生无关。

Chua, Yee Liu; Dufour, Eric; Dassa, Emmanuel P; Rustin, Pierre; Jacobs, Howard T; Taylor, Cormac T; Hagen, Thilo

Deferiprone targets aconitase: implication for Friedreich's ataxia treatment

去铁酮靶向乌头酸酶:对弗里德赖希共济失调治疗的意义

Goncalves, Sergio; Paupe, Vincent; Dassa, Emmanuel P; Rustin, Pierre

Succinate dehydrogenase deficiency in human

人类琥珀酸脱氢酶缺乏症

Brière, J-J; Favier, J; El Ghouzzi, V; Djouadi, F; Bénit, P; Gimenez, A-P; Rustin, P

Use of neoadjuvant chemotherapy prior to radical hysterectomy in cervical cancer: monitoring tumour shrinkage and molecular profile on magnetic resonance and assessment of 3-year outcome

宫颈癌根治性子宫切除术前新辅助化疗的应用:磁共振监测肿瘤缩小情况和分子特征,并评估3年疗效

deSouza, N M; Soutter, W P; Rustin, G; Mahon, M M; Jones, B; Dina, R; McIndoe, G A

Control of mitochondrial membrane permeabilization by adenine nucleotide translocator interacting with HIV-1 viral protein rR and Bcl-2

腺嘌呤核苷酸转运蛋白与 HIV-1 病毒蛋白 rR 和 Bcl-2 相互作用控制线粒体膜通透性

E Jacotot, K F Ferri, C El Hamel, C Brenner, S Druillennec, J Hoebeke, P Rustin, D Métivier, C Lenoir, M Geuskens, H L Vieira, M Loeffler, A S Belzacq, J P Briand, N Zamzami, L Edelman, Z H Xie, J C Reed, B P Roques, G Kroemer

Branched chain amino acids induce apoptosis in neural cells without mitochondrial membrane depolarization or cytochrome c release: implications for neurological impairment associated with maple syrup urine disease

支链氨基酸在不引起线粒体膜去极化或细胞色素c释放的情况下诱导神经细胞凋亡:对枫糖尿症相关神经功能障碍的启示

Jouvet, P; Rustin, P; Taylor, D L; Pocock, J M; Felderhoff-Mueser, U; Mazarakis, N D; Sarraf, C; Joashi, U; Kozma, M; Greenwood, K; Edwards, A D; Mehmet, H

Mutation of the fumarase gene in two siblings with progressive encephalopathy and fumarase deficiency

两名患有进行性脑病和富马酸酶缺乏症的兄弟姐妹,其富马酸酶基因发生突变。

Bourgeron, T; Chretien, D; Poggi-Bach, J; Doonan, S; Rabier, D; Letouzé, P; Munnich, A; Rötig, A; Landrieu, P; Rustin, P

Keratin gene mutations in human skin disease

人类皮肤病中的角蛋白基因突变

Stevens, H P; Rustin, M H