about
Control of muscle formation by the fusogenic micropeptide myomixer.KLHL41 stabilizes skeletal muscle sarcomeres by nonproteolytic ubiquitination.Single-cut genome editing restores dystrophin expression in a new mouse model of muscular dystrophy.Correction of diverse muscular dystrophy mutations in human engineered heart muscle by single-site genome editing.Cullin3-RING ubiquitin ligase activity is required for striated muscle function in mice.Gene editing restores dystrophin expression in a canine model of Duchenne muscular dystrophyThe DWORF micropeptide enhances contractility and prevents heart failure in a mouse model of dilated cardiomyopathyCRISPR-Cas9 corrects Duchenne muscular dystrophy exon 44 deletion mutations in mice and human cellsEnhanced CRISPR-Cas9 correction of Duchenne muscular dystrophy in mice by a self-complementary AAV delivery systemThe intestinal microbiota programs diurnal rhythms in host metabolism through histone deacetylase 3Genetic and epigenetic regulation of cardiomyocytes in development, regeneration and diseaseTrout myomaker contains 14 minisatellites and two sequence extensions but retains fusogenic function
P50
Q33112265-B7747EDD-0299-49CC-ACB8-218E1E5609CBQ41560314-997E2A77-DB8A-40B1-B58B-76EA44A6D4A2Q47153293-86832C79-BEF5-46BE-80C5-88CBAB20365EQ48041681-60E600AA-3FF5-4832-A7AC-1BCB6EB27873Q52321986-F07F6B9F-0709-48F7-835B-F152C8E657FEQ56986031-F9E4D637-AFDF-43A7-A72E-33C6CD3A128AQ57288455-38398F17-B494-41DB-9A71-A910F7DBD825Q64059247-A53BFAC3-DA92-41FD-B84F-75FE0B33EDCFQ90017264-2386E97B-B1A2-43C5-8E58-B7B75AEBD828Q90658279-C3CDE3B8-00EF-43AB-900C-FF726BA366C1Q90679951-86ED28AC-C03C-4886-8BD0-17717AD0B181Q92021900-3039D19C-819E-4E75-979F-1F2207EB29A6
P50
description
investigador
@es
researcher
@en
name
Eric N Olson
@en
type
label
Eric N Olson
@en
prefLabel
Eric N Olson
@en
P31
P496
0000-0003-1151-8262