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

Single-cell RNA-sequencing reveals early mitochondrial dysfunction unique to motor neurons shared across FUS- and TARDBP-ALS

单细胞RNA测序揭示了FUS-ALS和TARDBP-ALS患者运动神经元中特有的早期线粒体功能障碍。

Christoph Schweingruber ,Jik Nijssen ,Jonas Mechtersheimer ,Stefan Reber ,Mélanie Lebœuf ,Niamh L O'Brien ,Irene Mei ,Erin Hedges ,Michaela Keuper ,Julio Aguila Benitez ,Vlad Radoi ,Martin Jastroch ,Marc-David Ruepp # ,Eva Hedlund #

Lysosomal Dysfunction in Amyotrophic Lateral Sclerosis: A Familial Case Linked to the p.G376D TARDBP Mutation

肌萎缩侧索硬化症中的溶酶体功能障碍:与 p.G376D TARDBP 突变相关的家族病例

Roberta Romano ,Victoria Stefania Del Fiore ,Giorgia Ruotolo ,Martina Mazzoni ,Jessica Rosati ,Francesca Luisa Conforti ,Cecilia Bucci

Atypical TDP-43 protein expression in an ALS pedigree carrying a p.Y374X truncation mutation in TARDBP

在携带TARDBP基因p.Y374X截断突变的ALS家系中,TDP-43蛋白表达异常。

Johnathan Cooper-Knock ,Thomas H Julian ,Emily Feneberg ,J Robin Highley ,Maurice Sidra ,Martin R Turner ,Kevin Talbot ,Olaf Ansorge ,Scott P Allen ,Tobias Moll ,Tatyana Shelkovnikova ,Lydia Castelli ,Guillaume M Hautbergue ,Christopher Hewitt ,Janine Kirby ,Stephen B Wharton ,Richard J Mead ,Pamela J Shaw

Impairment of Mitochondrial Calcium Buffering Links Mutations in C9ORF72 and TARDBP in iPS-Derived Motor Neurons from Patients with ALS/FTD

线粒体钙缓冲功能障碍与肌萎缩侧索硬化症/额颞叶痴呆症患者诱导多能干细胞来源的运动神经元中C9ORF72和TARDBP基因突变相关。

Ruxandra Dafinca ,Paola Barbagallo ,Lucy Farrimond ,Ana Candalija ,Jakub Scaber ,Nida'a A Ababneh ,Chaitra Sathyaprakash ,Jane Vowles ,Sally A Cowley ,Kevin Talbot