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

Spatial proteomics reveals recombinant human laminin-111 restores adhesion signaling to laminin-α2-deficient muscle

空间蛋白质组学揭示重组人层粘连蛋白-111可恢复层粘连蛋白-α2缺陷肌肉的粘附信号传导。

Hailey J Hermann,Ryan D Wuebbles,Marisela Dagda,Axel Muñoz,Lauren L Parker,Paula C Guzman,Lola T Byrne,Steven A Moore,Dean J Burkin

The Influence of a Genetic Variant in CCDC78 on LMNA-Associated Skeletal Muscle Disease

CCDC78 基因变异对 LMNA 相关骨骼肌疾病的影响

Nathaniel P Mohar, Efrem M Cox, Emily Adelizzi, Steven A Moore, Katherine D Mathews, Benjamin W Darbro, Lori L Wallrath

DUX4 double whammy: The transcription factor that causes a rare muscular dystrophy also kills the precursors of the human nose

DUX4双重打击:这种转录因子不仅会导致一种罕见的肌肉萎缩症,还会杀死人类鼻子的前体细胞。

Kaoru Inoue ,Hamed Bostan ,MaKenna R Browne ,Owen F Bevis ,Carl D Bortner ,Steven A Moore ,Aaron A Stence ,Negin P Martin ,Shih-Heng Chen ,Adam B Burkholder ,Jian-Liang Li ,Natalie D Shaw

A De Novo Sequence Variant in Barrier-to-Autointegration Factor Is Associated with Dominant Motor Neuronopathy

自我整合障碍因子的新生序列变异与显性运动神经元病相关

Agathe Marcelot, Felipe Rodriguez-Tirado, Philippe Cuniasse, Mei-Ling Joiner, Simona Miron, Alexey A Soshnev, Mimi Fang, Miles A Pufall, Katherine D Mathews, Steven A Moore, Sophie Zinn-Justin, Pamela K Geyer

Cross-sectional Neuromuscular Phenotyping Study of Patients With Arhinia With SMCHD1 Variants

患有 SMCHD1 变异的 Arhinia 患者的横断面神经肌肉表型研究

Payam Mohassel, Ning Chang, Kaoru Inoue, Angela Delaney, Ying Hu, Sandra Donkervoort, Dimah Saade, B Jeanne Billioux, Brooke Meader, Rita Volochayev, Chamindra G Konersman, Angela M Kaindl, Chie-Hee Cho, Bianca Russell, Adrian Rodriguez, K Wade Foster, A Reghan Foley, Steven A Moore, Peter L Jones, 

The inflammatory pathology of dysferlinopathy is distinct from calpainopathy, Becker muscular dystrophy, and inflammatory myopathies

肌营养不良症的炎症病理与钙蛋白酶病、贝克尔肌营养不良症和炎症性肌病不同

Nicole Becker, Steven A Moore, Karra A Jones

Comparison between MR and CT imaging used to correct for skull-induced phase aberrations during transcranial focused ultrasound

比较磁共振成像和计算机断层扫描成像在经颅聚焦超声中校正颅骨引起的相位差方面的应用

Leung, Steven A; Moore, David; Gilbo, Yekaterina; Snell, John; Webb, Taylor D; Meyer, Craig H; Miller, G Wilson; Ghanouni, Pejman; Butts Pauly, Kim

Lysosomes and the pathogenesis of merosin-deficient congenital muscular dystrophy

溶酶体与美罗星缺乏型先天性肌营养不良症的发病机制

Sarah J Smith, Lacramioara Fabian, Adeel Sheikh, Ramil Noche, Xiucheng Cui, Steven A Moore, James J Dowling

Evaluating hip disarticulation outcomes in a 51-patient series

评估 51 例患者髋关节离断术的疗效

Huffman, Allison; Schneeberger, Steven; Goodyear, Evelyn; West, Julie M; O'Brien, Andrew L; Scharschmidt, Thomas J; Mayerson, Joel L; Schulz, Steven A; Moore, Amy M

Sphingosine Phosphate Lyase Is Upregulated in Duchenne Muscular Dystrophy, and Its Inhibition Early in Life Attenuates Inflammation and Dystrophy in Mdx Mice

鞘氨醇磷酸裂解酶在杜氏肌营养不良症中上调,生命早期抑制该酶可减轻 Mdx 小鼠的炎症和营养不良

Anabel S De la Garza-Rodea, Steven A Moore, Jesus Zamora-Pineda, Eric P Hoffman, Karishma Mistry, Ashok Kumar, Jonathan B Strober, Piming Zhao, Jung H Suh, Julie D Saba