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Acta Neuropathologica Communications
|
October 20, 2020
rAAV-related therapy fully rescues myonuclear and myofilament function in X-linked myotubular myopathy
Jacob A Ross, Hichem Tasfaout, Yotam Levy, et al.
Iscience
|
July 23, 2024
Dystrophin deficiency impairs cell junction formation during embryonic myogenesis from pluripotent stem cells
Elise Mozin, Emmanuelle Massouridès, Virginie Mournetas, et al.
Carcinogenesis
|
April 27, 2013
Aneuploidy, oncogene amplification and epithelial to mesenchymal transition define spontaneous transformation of murine epithelial cells
Hesed M Padilla-Nash, Nicole E McNeil, Ming Yi, et al.
Biorxiv : the Preprint Server for Biology
|
December 18, 2023
Dystrophin deficiency impairs cell junction formation during embryonic myogenesis
Elise Mozin, Emmanuelle Massouridès, Virginie Mournetas, et al.
Current Research in Toxicology
|
February 13, 2025
An automated platform for simultaneous, longitudinal analysis of engineered neuromuscular tissues for applications in neurotoxin potency testing
Jacob W Fleming, Molly C McCloskey, Kevin Gray, et al.
Advanced Healthcare Materials
|
June 13, 2025
Bioengineered Human Cardiac Ventricular Model with Transmural Helical Remodeling
Nisa P Williams, Kevin M Beussman, John R Foster, et al.
Biorxiv : the Preprint Server for Biology
|
February 14, 2024
Structure-guided engineering of a fast genetically encoded sensor for real-time H<sub>2</sub>O<sub>2</sub> monitoring
Justin Daho Lee, Woojin Won, Kandace Kimball, et al.
JCI Insight
|
November 6, 2025
Myosin inhibition partially rescues the myofiber proteome in X-linked myotubular myopathy
Elise Gerlach Melhedegaard, Fanny Rostedt, Charlotte Gineste, et al.
Biology Open
|
August 19, 2024
High mobility group box 1 (HMGB1) is a potential disease biomarker in cell and mouse models of Duchenne muscular dystrophy
Rebecca A Slick, Jessica Sutton, Margaret Haberman, et al.
Cardiovascular Research
|
May 4, 2019
Absence of full-length dystrophin impairs normal maturation and contraction of cardiomyocytes derived from human-induced pluripotent stem cells
J Manuel Pioner, Xuan Guan, Jordan M Klaiman, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 69) with videos related to
Sort By:
Page
of 7
Acta Neuropathologica Communications
|
October 20, 2020
rAAV-related therapy fully rescues myonuclear and myofilament function in X-linked myotubular myopathy
Jacob A Ross, Hichem Tasfaout, Yotam Levy, et al.
Iscience
|
July 23, 2024
Dystrophin deficiency impairs cell junction formation during embryonic myogenesis from pluripotent stem cells
Elise Mozin, Emmanuelle Massouridès, Virginie Mournetas, et al.
Carcinogenesis
|
April 27, 2013
Aneuploidy, oncogene amplification and epithelial to mesenchymal transition define spontaneous transformation of murine epithelial cells
Hesed M Padilla-Nash, Nicole E McNeil, Ming Yi, et al.
Biorxiv : the Preprint Server for Biology
|
December 18, 2023
Dystrophin deficiency impairs cell junction formation during embryonic myogenesis
Elise Mozin, Emmanuelle Massouridès, Virginie Mournetas, et al.
Current Research in Toxicology
|
February 13, 2025
An automated platform for simultaneous, longitudinal analysis of engineered neuromuscular tissues for applications in neurotoxin potency testing
Jacob W Fleming, Molly C McCloskey, Kevin Gray, et al.
Advanced Healthcare Materials
|
June 13, 2025
Bioengineered Human Cardiac Ventricular Model with Transmural Helical Remodeling
Nisa P Williams, Kevin M Beussman, John R Foster, et al.
Biorxiv : the Preprint Server for Biology
|
February 14, 2024
Structure-guided engineering of a fast genetically encoded sensor for real-time H<sub>2</sub>O<sub>2</sub> monitoring
Justin Daho Lee, Woojin Won, Kandace Kimball, et al.
JCI Insight
|
November 6, 2025
Myosin inhibition partially rescues the myofiber proteome in X-linked myotubular myopathy
Elise Gerlach Melhedegaard, Fanny Rostedt, Charlotte Gineste, et al.
Biology Open
|
August 19, 2024
High mobility group box 1 (HMGB1) is a potential disease biomarker in cell and mouse models of Duchenne muscular dystrophy
Rebecca A Slick, Jessica Sutton, Margaret Haberman, et al.
Cardiovascular Research
|
May 4, 2019
Absence of full-length dystrophin impairs normal maturation and contraction of cardiomyocytes derived from human-induced pluripotent stem cells
J Manuel Pioner, Xuan Guan, Jordan M Klaiman, et al.
Page
of 7