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 ameliorates neurodegeneration and movement disorder in a mouse model of Parkinson's disease.

缺氧可改善帕金森病小鼠模型中的神经退行性变和运动障碍

Marutani Eizo, Miranda Maria, Durham Timothy J, Kim Sharon H, Russell Dreson L, Wiesenthal Presli P, Lichtenegger Paul, Menard Marissa A, Brzozowski Charlotte F, Li Haobo, Ruvkun Gary, Meisel Joshua D, Volpicelli-Daley Laura, Mootha Vamsi K, Ichinose Fumito

From nematode to Nobel: How community-shared resources fueled the rise of Caenorhabditis elegans as a research organism

从线虫到诺贝尔奖:社区共享资源如何推动秀丽隐杆线虫成为研究生物

Ambros, Victor R; Chalfie, Martin; Daul, Aric L; Fire, Andrew Z; Hall, David H; Horvitz, H Robert; Mello, Craig C; Ruvkun, Gary; Schroeder, Nathan E; Sternberg, Paul W; Rougvie, Ann E

Translation elongation defects activate the Caenorhabditis elegans ZIP-2 bZIP transcription factor-mediated toxin defense

翻译延伸缺陷激活秀丽隐杆线虫 ZIP-2 bZIP 转录因子介导的毒素防御机制

Kniazeva, Marina; Ruvkun, Gary

Decreased SynMuv B gene activity in response to viral infection leads to activation of the antiviral RNAi pathway in C. elegans

线虫中,病毒感染导致 SynMuv B 基因活性降低,进而激活抗病毒 RNAi 通路。

Seetharaman, Ashwin; Galagali, Himani; Linarte, Elizabeth; Liu, Mona H X; Cohen, Jennifer D; Chetal, Kashish; Sadreyev, Ruslan; Tate, Alex J; Montgomery, Taiowa A; Ruvkun, Gary

Mitochondrial fission surveillance is coupled to Caenorhabditis elegans DNA and chromosome segregation integrity.

线粒体分裂监测与秀丽隐杆线虫的DNA和染色体分离完整性相关

Yang Xiaomeng, Wei Ruichen, Meng Fanfan, Liu Dianchen, Gong Xuan, Ruvkun Gary, Wei Wei

The effects of intense light on Caenorhabditis elegans.

强光对秀丽隐杆线虫的影响

Kniazeva Marina, Ruvkun Gary

A spurious fln-2 mutation in a wide variety of commonly used C. elegans strains.

在多种常用的秀丽隐杆线虫品系中发现了一种虚假的fln-2突变

Kniazeva Marina, Ruvkun Gary

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

CMTR-1 RNA methyltransferase mutations activate widespread expression of a dopaminergic neuron-specific mitochondrial complex I gene

CMTR-1 RNA 甲基转移酶突变激活多巴胺能神经元特异性线粒体复合物 I 基因的广泛表达

Joshua D Meisel, Presli P Wiesenthal, Vamsi K Mootha, Gary Ruvkun