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

Copper delivery to the CNS by CuATSM effectively treats motor neuron disease in SOD(G93A) mice co-expressing the Copper-Chaperone-for-SOD.

CuATSM 将铜输送到中枢神经系统可有效治疗共表达 SOD 铜伴侣蛋白的 SOD(G93A) 小鼠的运动神经元疾病

Williams Jared R, Trias Emiliano, Beilby Pamela R, Lopez Nathan I, Labut Edwin M, Bradford C Samuel, Roberts Blaine R, McAllum Erin J, Crouch Peter J, Rhoads Timothy W, Pereira Cliff, Son Marjatta, Elliott Jeffrey L, Franco Maria Clara, Estévez Alvaro G, Barbeito Luis, Beckman Joseph S

The death domain-containing kinase RIP1 regulates p27(Kip1) levels through the PI3K-Akt-forkhead pathway

含有死亡结构域的激酶RIP1通过PI3K-Akt-forkhead通路调控p27(Kip1)的水平。

Park, Seongmi; Ramnarain, Deepti B; Hatanpaa, Kimmo J; Mickey, Bruce E; Saha, Debabrata; Paulmurugan, Ramasamy; Madden, Christopher J; Wright, Paul S; Bhai, Salman; Ali, M Aktar; Puttaparthi, Krishna; Hu, Wei; Elliott, Jeffrey L; Stuve, Olaf; Habib, Amyn A

Biological effects of CCS in the absence of SOD1 enzyme activation: implications for disease in a mouse model for ALS.

CCS 在 SOD1 酶未激活的情况下的生物学效应:对 ALS 小鼠模型疾病的影响

Proescher Jody B, Son Marjatta, Elliott Jeffrey L, Culotta Valeria C

Overexpression of CCS in G93A-SOD1 mice leads to accelerated neurological deficits with severe mitochondrial pathology

G93A-SOD1小鼠中CCS的过表达会导致神经功能缺陷加速发展,并伴有严重的线粒体病理。

Son, Marjatta; Puttaparthi, Krishna; Kawamata, Hibiki; Rajendran, Bhagya; Boyer, Philip J; Manfredi, Giovanni; Elliott, Jeffrey L

Assessing the role of immuno-proteasomes in a mouse model of familial ALS

评估免疫蛋白酶体在家族性ALS小鼠模型中的作用。

Puttaparthi, Krishna; Van Kaer, Luc; Elliott, Jeffrey L

Disease progression in a transgenic model of familial amyotrophic lateral sclerosis is dependent on both neuronal and non-neuronal zinc binding proteins

在家族性肌萎缩侧索硬化症的转基因模型中,疾病进展依赖于神经元和非神经元锌结合蛋白。

Puttaparthi, Krishna; Gitomer, William L; Krishnan, Uma; Son, Marjatta; Rajendran, Bhagya; Elliott, Jeffrey L