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

Mifepristone alone and in combination with scAAV9-SMN1 gene therapy improves disease phenotypes in Smn(2B/-) spinal muscular atrophy mice

米非司酮单独使用或与scAAV9-SMN1基因疗法联合使用,均可改善Smn(2B/-)脊髓性肌萎缩症小鼠的疾病表型。

Sutton, Emma R; McCallion, Eve; Hoolachan, Joseph M; Çetin, Özge; Pacheco-Torres, Paloma; Rashid, Saman; Bouhmidi, Sihame; Haynes, Katie; Churchill, Lauren; Scaife, Taylor; Chaytow, Helena; Huang, Yu-Ting; Duguez, Stephanie; Schneider, Bernard L; Gillingwater, Thomas H; Dimitriadi, Maria; Bowerman, Melissa

Genome-Wide Gene-Set Analysis Identifies Molecular Mechanisms Associated with ALS

全基因组基因集分析揭示与肌萎缩侧索硬化症相关的分子机制

Vasilopoulou, Christina; McDaid-McCloskey, Sarah L; McCluskey, Gavin; Duguez, Stephanie; Morris, Andrew P; Duddy, William

Serum Neurofilaments in Motor Neuron Disease and Their Utility in Differentiating ALS, PMA and PLS.

运动神经元疾病中的血清神经丝及其在区分 ALS、PMA 和 PLS 中的应用

McCluskey Gavin, Morrison Karen E, Donaghy Colette, McConville John, McCarron Mark O, McVerry Ferghal, Duddy William, Duguez Stephanie

Extracellular Vesicles in Amyotrophic Lateral Sclerosis

肌萎缩侧索硬化症中的细胞外囊泡

McCluskey, Gavin; Morrison, Karen E; Donaghy, Colette; Rene, Frederique; Duddy, William; Duguez, Stephanie

The Role of Sphingomyelin and Ceramide in Motor Neuron Diseases

鞘磷脂和神经酰胺在运动神经元疾病中的作用

McCluskey, Gavin; Donaghy, Colette; Morrison, Karen E; McConville, John; Duddy, William; Duguez, Stephanie

Genome-Wide Gene-Set Analysis Approaches in Amyotrophic Lateral Sclerosis

肌萎缩侧索硬化症的全基因组基因集分析方法

Vasilopoulou, Christina; Duguez, Stephanie; Duddy, William

The Cellular and Molecular Signature of ALS in Muscle

肌萎缩侧索硬化症在肌肉中的细胞和分子特征

Anakor, Ekene; Duddy, William John; Duguez, Stephanie

Exosomes in Ageing and Motor Neurone Disease: Biogenesis, Uptake Mechanisms, Modifications in Disease and Uses in the Development of Biomarkers and Therapeutics

衰老和运动神经元疾病中的外泌体:生物发生、摄取机制、疾病中的改变及其在生物标志物和治疗方法开发中的应用

Anakor, Ekene; Le Gall, Laura; Dumonceaux, Julie; Duddy, William John; Duguez, Stephanie

Understanding Neuromuscular Health and Disease: Advances in Genetics, Omics, and Molecular Function

了解神经肌肉健康与疾病:遗传学、组学和分子功能方面的进展

Duddy, William J; Duguez, Stephanie

GGPS1 Mutations Cause Muscular Dystrophy/Hearing Loss/Ovarian Insufficiency Syndrome

GGPS1基因突变导致肌营养不良/听力丧失/卵巢功能不全综合征

Foley, A Reghan; Zou, Yaqun; Dunford, James E; Rooney, Jachinta; Chandra, Goutam; Xiong, Hui; Straub, Volker; Voit, Thomas; Romero, Norma; Donkervoort, Sandra; Hu, Ying; Markello, Thomas; Horn, Adam; Qebibo, Leila; Dastgir, Jahannaz; Meilleur, Katherine G; Finkel, Richard S; Fan, Yanbin; Mamchaoui, Kamel; Duguez, Stephanie; Nelson, Isabelle; Laporte, Jocelyn; Santi, Mariarita; Malfatti, Edoardo; Maisonobe, Thierry; Touraine, Philippe; Hirano, Michio; Hughes, Imelda; Bushby, Kate; Oppermann, Udo; Böhm, Johann; Jaiswal, Jyoti K; Stojkovic, Tanya; Bönnemann, Carsten G