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Nature Communications|January 17, 2018
Author Correction: Myoblasts and macrophages are required for therapeutic morpholino antisense oligonucleotide delivery to dystrophic muscleJames S Novak, Marshall W Hogarth, Jessica F Boehler, et al.Current Therapeutic Research, Clinical and Experimental|June 14, 2019
Effects of Periodic Intensive Insulin Therapy: An Updated ReviewShu Dong, Hien Lau, Cody Chavarria, et al.Aging Cell|June 5, 2021
Human muscle stem cells are refractory to agingJames S Novak, Davi A G Mázala, Marie Nearing, et al.Human Molecular Genetics|November 15, 2015
Effect of genetic background on the dystrophic phenotype in mdx miceWilliam D Coley, Laurent Bogdanik, Maria Candida Vila, et al.Plos One|June 25, 2010
Functional and molecular effects of arginine butyrate and prednisone on muscle and heart in the mdx mouse model of Duchenne Muscular DystrophyAlfredo D Guerron, Rashmi Rawat, Arpana Sali, et al.Mucosal Immunology|June 30, 2024
Human intestinal stromal cells promote homeostasis in normal mucosa but inflammation in Crohn's disease in a retinoic acid-deficient mannerLesley E Smythies, Olga V Belyaeva, Katie L Alexander, et al.Journal of Neuromuscular Diseases|September 27, 2021
Effects of Chronic, Maximal Phosphorodiamidate Morpholino Oligomer (PMO) Dosing on Muscle Function and Dystrophin Restoration in a Mouse Model of Duchenne Muscular DystrophyMargaret E Benny Klimek, Maria Candida Vila, Katie Edwards, et al.Pageof 5