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Human Molecular Genetics|August 14, 2010
Flt-1 haploinsufficiency ameliorates muscular dystrophy phenotype by developmentally increased vasculature in mdx miceMayank Verma, Yoko Asakura, Hiroyuki Hirai, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 18, 2007
Increased survival of muscle stem cells lacking the MyoD gene after transplantation into regenerating skeletal muscleAtsushi Asakura, Hiroyuki Hirai, Boris Kablar, et al.
International Journal of STEM Education|August 2, 2022
Predicting implementation of active learning by tenure-track teaching faculty using robust cluster analysisKameryn Denaro, Petra Kranzfelder, Melinda T Owens, et al.
Annals of Neurology|June 4, 2025
Autosomal Recessive Cerebellar Ataxias: Translating Genes to TherapiesBrent L Fogel, Thomas Klopstock, David R Lynch, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|March 13, 2026
Lafora disease gene therapy: EPM2A but not EPM2B overexpression results in Lafora body formationEsther O Alao, Mehrnaz Sheibani, Jun Wu, et al.
Circulation|February 2, 2018
CD301b/MGL2+ Mononuclear Phagocytes Orchestrate Autoimmune Cardiac Valve Inflammation and FibrosisLee A Meier, Jennifer L Auger, Brianna J Engelson, et al.
The Journal of Clinical Investigation|April 7, 2020
Transcriptional and cytopathological hallmarks of FSHD in chronic DUX4-expressing miceDarko Bosnakovski, Ahmed S Shams, Ce Yuan, et al.
Acta Neuropathologica|February 27, 2024
Myofiber-type-dependent 'boulder' or 'multitudinous pebble' formations across distinct amylopectinosesSharmistha Mitra, Baozhi Chen, John M Shelton, et al.
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