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

Monitoring in real time and far-red imaging of H(2)O(2) dynamics with subcellular resolution

以亚细胞分辨率实时监测和远红外成像H₂O₂动态变化

Lee, Justin Daho; Nguyen, Amanda; Gibbs, Chelsea E; Jin, Zheyu Ruby; Wang, Yuxuan; Moghadasi, Aida; Wait, Sarah J; Choi, Hojun; Evitts, Kira M; Asencio, Anthony; Bremner, Samantha B; Zuniga, Shani; Chavan, Vedant; Pranoto, Inez K A; Williams, C Andrew; Smith, Annette; Moussavi-Harami, Farid; Regnier, Michael; Baker, David; Young, Jessica E; Mack, David L; Nance, Elizabeth; Boyle, Patrick M; Berndt, Andre

Dystrophin Loss in Engineered Heart Tissues Recapitulates Clinically Relevant Aspects of Dystrophic Cardiomyopathy.

工程化心脏组织中肌营养不良蛋白的缺失重现了营养不良性心肌病的临床相关方面。

Goldstein Alex J, Leahy Thomas P, Mack David L, Sniadecki Nathan J

Myosin inhibition partially rescues the myofiber proteome in X-linked myotubular myopathy

肌球蛋白抑制可部分挽救X连锁肌管性肌病中的肌纤维蛋白质组。

Gerlach Melhedegaard, Elise; Rostedt, Fanny; Gineste, Charlotte; Seaborne, Robert Ae; Dugdale, Hannah F; Belhac, Vladimir; Zanoteli, Edmar; Lawlor, Michael W; Mack, David L; Wallgren-Pettersson, Carina; Hessel, Anthony L; Jungbluth, Heinz; Laporte, Jocelyn; Saito, Yoshihiko; Nishino, Ichizo; Ochala, Julien; Laitila, Jenni

Direct cell reprogramming by a designed agonist inducing HER2-FGFR proximity

通过设计激动剂诱导HER2-FGFR邻近性,从而实现直接细胞重编程。

Keshri, Riya; Exposit, Marc; Abedi, Mohamad; Hicks, Derrick R; Foreman, Zachary; Phal, Ashish; Lim, Yen Chian; Barrett, Philip; Sniezek, Catherine; Lin, Jinlong; Schlichthaerle, Thomas; Robinson, Alexander J; Detraux, Damien; Ching, Tung Chan; Wu, Keija; Coventry, Brian; Chang, Lemuel; Smith, Alec S T; Mack, David L; Schweppe, Devin K; Martin, Beatriz Estrada; Hristova, Kalina; Mathieu, Julie; Baker, David; Ruohola-Baker, Hannele

Incomplete-penetrant hypertrophic cardiomyopathy MYH7 G256E mutation causes hypercontractility and elevated mitochondrial respiration

MYH7 G256E 突变导致不完全外显的肥厚型心肌病,引起心肌收缩力增强和线粒体呼吸增强。

Lee, Soah; Vander Roest, Alison S; Blair, Cheavar A; Kao, Kerry; Bremner, Samantha B; Childers, Matthew C; Pathak, Divya; Heinrich, Paul; Lee, Daniel; Chirikian, Orlando; Mohran, Saffie E; Roberts, Brock; Smith, Jacqueline E; Jahng, James W; Paik, David T; Wu, Joseph C; Gunawardane, Ruwanthi N; Ruppel, Kathleen M; Mack, David L; Pruitt, Beth L; Regnier, Michael; Wu, Sean M; Spudich, James A; Bernstein, Daniel

Uncovering the Embryonic Origins of Duchenne Muscular Dystrophy

揭示杜氏肌营养不良症的胚胎起源

Barrett, Philip; Louie, Ke'ale W; Dupont, Jean-Baptiste; Mack, David L; Maves, Lisa

Current insights in ultra-rare adenylosuccinate synthetase 1 myopathy - meeting report on the First Clinical and Scientific Conference. 3 June 2024, National Centre for Advancing Translational Science, Rockville, Maryland, the United States of America

罕见腺苷酸琥珀酸合成酶1型肌病最新研究进展——首届临床与科学会议报告。2024年6月3日,美国马里兰州罗克维尔市国家转化科学促进中心。

Rybalka, Emma; Park, Hyung Jun; Nalini, Atchayaram; Baskar, Dipti; Polavarapu, Kiran; Durmus, Hacer; Xia, Yang; Wan, Linlin; Shieh, Perry B; Moghadaszadeh, Behzad; Beggs, Alan H; Mack, David L; Smith, Alec S T; Hanna-Rose, Wendy; Jinnah, Hyder A; Timpani, Cara A; Shen, Min; Upadhyay, Jaymin; Brault, Jeffrey J; Hall, Matthew D; Baweja, Naveen; Kakkar, Priyanka

Corrigendum: Calcium handling maturation and adaptation to increased substrate stiffness in human iPSC-derived cardiomyocytes: the impact of full-length dystrophin deficiency

更正:人诱导多能干细胞来源的心肌细胞中钙离子处理成熟及对底物刚度增加的适应:全长肌营养不良蛋白缺乏的影响

Pioner, Josè Manuel; Santini, Lorenzo; Palandri, Chiara; Langione, Marianna; Grandinetti, Bruno; Querceto, Silvia; Martella, Daniele; Mazzantini, Costanza; Scellini, Beatrice; Giammarino, Lucrezia; Lupi, Flavia; Mazzarotto, Francesco; Gowran, Aoife; Rovina, Davide; Santoro, Rosaria; Pompilio, Giulio; Tesi, Chiara; Parmeggiani, Camilla; Regnier, Michael; Cerbai, Elisabetta; Mack, David L; Poggesi, Corrado; Ferrantini, Cecilia; Coppini, Raffaele

Editorial: Modeling neuromuscular diseases to determine molecular drivers of pathology and for drug discovery

社论:构建神经肌肉疾病模型以确定病理的分子驱动因素并用于药物发现

Smith, Alec S T; McCain, Megan L; Bothwell, Mark; Mack, David L

Erratum: Voluntary wheel running complements microdystrophin gene therapy to improve muscle function in mdx mice

更正:自愿轮跑可辅助微型肌营养不良蛋白基因疗法改善 mdx 小鼠的肌肉功能

Hamm, Shelby E; Fathalikhani, Daniel D; Bukovec, Katherine E; Addington, Adele K; Zhang, Haiyan; Perry, Justin B; McMillan, Ryan P; Lawlor, Michael W; Prom, Mariah J; Vanden Avond, Mark A; Kumar, Suresh N; Coleman, Kirsten E; Dupont, J B; Mack, David L; Brown, David A; Morris, Carl A; Gonzalez, J Patrick; Grange, Robert W