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

Efficient Cas9 nuclease-based editing in skeletal muscle via lipid nanoparticle delivery

通过脂质纳米颗粒递送在骨骼肌中高效进行基于Cas9核酸酶的基因编辑

Iyer, Sukanya; Daman, Katelyn; Sun, Yehui; Tutto, Amanda; Holbrook, Sarah E; Joynt, Anya T; Yan, Jing; Ambegaokar, Prajakta; Guo, Dongsheng; Liu, Pengpeng; Stauffer, Jennifer; Maitland, Stacy A; Lee, Sang M; Gallagher, Thomas L; Cox, Gregory A; Keeler, Allison M; Siegwart, Daniel J; Emerson, Charles P; Wolfe, Scot A

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

Identification of quantitative trait loci for survival in the mutant dynactin p150Glued mouse model of motor neuron disease

在运动神经元疾病的突变型动力蛋白p150Glued小鼠模型中鉴定生存相关的数量性状基因座

Alexander, Guillermo M; Heiman-Patterson, Terry D; Bearoff, Frank; Sher, Roger B; Hennessy, Laura; Terek, Shannon; Caccavo, Nicole; Cox, Gregory A; Philip, Vivek M; Blankenhorn, Elizabeth A

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

Functional rescue in a mouse model of congenital muscular dystrophy with megaconial myopathy

在先天性肌营养不良伴巨锥肌病的鼠模型中实现功能性挽救

Sayed-Zahid, Ambreen A; Sher, Roger B; Sukoff Rizzo, Stacey J; Anderson, Laura C; Patenaude, Kathryn E; Cox, Gregory A

Genetic background effects on disease onset and lifespan of the mutant dynactin p150Glued mouse model of motor neuron disease

遗传背景对突变型动力蛋白p150Glued小鼠运动神经元疾病模型的发病和寿命的影响

Heiman-Patterson, Terry D; Blankenhorn, Elizabeth P; Sher, Roger B; Jiang, Juliann; Welsh, Priscilla; Dixon, Meredith C; Jeffrey, Jeremy I; Wong, Philip; Cox, Gregory A; Alexander, Guillermo M

A congenital muscular dystrophy with mitochondrial structural abnormalities caused by defective de novo phosphatidylcholine biosynthesis

一种先天性肌营养不良症,伴有线粒体结构异常,由磷脂酰胆碱从头合成缺陷引起。

Mitsuhashi, Satomi; Ohkuma, Aya; Talim, Beril; Karahashi, Minako; Koumura, Tomoko; Aoyama, Chieko; Kurihara, Mana; Quinlivan, Ros; Sewry, Caroline; Mitsuhashi, Hiroaki; Goto, Kanako; Koksal, Burcu; Kale, Gulsev; Ikeda, Kazutaka; Taguchi, Ryo; Noguchi, Satoru; Hayashi, Yukiko K; Nonaka, Ikuya; Sher, Roger B; Sugimoto, Hiroyuki; Nakagawa, Yasuhito; Cox, Gregory A; Topaloglu, Haluk; Nishino, Ichizo

Rhabdomyosarcomas in aging A/J mice.

老年A/J小鼠的横纹肌肉瘤

Sher Roger B, Cox Gregory A, Mills Kevin D, Sundberg John P

Anisotropic regulation of Ankrd2 gene expression in skeletal muscle by mechanical stretch

机械拉伸对骨骼肌中Ankrd2基因表达的各向异性调控

Mohamed, Junaith S; Lopez, Michael A; Cox, Gregory A; Boriek, Aladin M