Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)
Integrated analysis of transcriptomic and proteomic alterations in mouse models of ALS/FTD identify early metabolic adaptions with similarities to mitochondrial dysfunction disorders
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration ( IF 2.8 ) Pub Date : 2024-01-23 , DOI: 10.1080/21678421.2023.2261979
Anna Matveeva 1, 2 , Orla Watters 2, 3 , Ani Rukhadze 4 , Niraj Khemka 1, 2 , Debora Gentile 4 , Ivan Fernandez Perez 1, 2 , Irene Llorente-Folch 1, 2 , Cliona Farrell 1, 2 , Elide Lo Cacciato 4 , Joshua Jackson 4 , Antonia Piazzesi 4 , Lena Wischhof 4 , Ina Woods 1, 2 , Luise Halang 1, 2 , Marion Hogg 2, 3, 5 , Amaya Garcia Muñoz 6 , Eugène T Dillon 7 , David Matallanas 6 , Ingrid Arijs 8, 9 , Diether Lambrechts 8, 9 , Daniele Bano 4 , Niamh M C Connolly 1, 2 , Jochen H M Prehn 1, 2, 3
Affiliation  

Sporadic and familial amyotrophic lateral sclerosis (ALS) is a fatal progressive neurodegenerative disease that results in loss of motor neurons and, in some patients, associates with frontotempora...

中文翻译:

对 ALS/FTD 小鼠模型转录组和蛋白质组改变的综合分析确定了与线粒体功能障碍疾病相似的早期代谢适应

散发性和家族性肌萎缩侧索硬化症 (ALS) 是一种致命的进行性神经退行性疾病,会导致运动神经元丧失,并且在某些患者中与额颞叶炎有关。
更新日期:2024-01-23
down
wechat
bug