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

Exploring the evidence for the use of protein biomarkers of muscular damage and disease progression in Duchenne and Becker muscular dystrophy: a systematic review and meta-analysis protocol

探索蛋白质生物标志物在杜氏肌营养不良症和贝克尔肌营养不良症肌肉损伤和疾病进展中的应用证据:系统评价和荟萃分析方案

Mondello, Stefania; McGill, Amelia; Lu, Ange; Spitali, Pietro; Russell, Alan J; Belfiore-Oshan, Ramona; Martin, Paige B

Clinically relevant mouse models of severe spinal muscular atrophy with respiratory distress type 1.

具有临床意义的重度脊髓性肌萎缩症伴呼吸窘迫1型小鼠模型

Holbrook Sarah E, Hicks Amy N, Martin Paige B, Hines Timothy J, Castro Harold P, Cox Gregory A

Poly-alanine-tailing is a modifier of neurodegeneration caused by Listerin mutation.

聚丙氨酸尾部修饰是李斯特林突变引起的神经退行性疾病的修饰因子

Hung Hao-Chih, Costas-Insua Carlos, Holbrook Sarah E, Stauffer Jennifer E, Martin Paige B, Müller Tina A, Schroeder David G, Kigoshi-Tansho Yu, Xu Haifei, Rudolf Rüdiger, Cox Gregory A, Joazeiro Claudio A P

Author Correction: NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease

作者更正:NEMF基因突变会损害核糖体相关的质量控制,而这些突变与神经肌肉疾病有关。

Martin, Paige B; Kigoshi-Tansho, Yu; Sher, Roger B; Ravenscroft, Gianina; Stauffer, Jennifer E; Kumar, Rajesh; Yonashiro, Ryo; Müller, Tina; Griffith, Christopher; Allen, William; Pehlivan, Davut; Harel, Tamar; Zenker, Martin; Howting, Denise; Schanze, Denny; Faqeih, Eissa A; Almontashiri, Naif A M; Maroofian, Reza; Houlden, Henry; Mazaheri, Neda; Galehdari, Hamid; Douglas, Ganka; Posey, Jennifer E; Ryan, Monique; Lupski, James R; Laing, Nigel G; Joazeiro, Claudio A P; Cox, Gregory A