Compounds > arginine

arginine and Autosomal Recessive Emery-Dreifuss Muscular Dystrophy

arginine has been researched along with Autosomal Recessive Emery-Dreifuss Muscular Dystrophy in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Angelini, C; Borsato, C; Cenacchi, G; Gavassini, BF; Melacini, P; Pegoraro, E; Stramare, R; Vianello, A1
Buendia, B; Collas, P; Delbarre, E; Gaustad, KG; Håkelien, AM1

Other Studies

2 other study(ies) available for arginine and Autosomal Recessive Emery-Dreifuss Muscular Dystrophy

ArticleYear
MYH7 gene mutation in myosin storage myopathy and scapulo-peroneal myopathy.
    Neuromuscular disorders : NMD, 2007, Volume: 17, Issue:4

    Topics: Adult; Aged; Arginine; Cardiac Myosins; Child; Family Health; Female; Humans; Infant; Magnetic Resonance Imaging; Male; Microscopy, Electron, Transmission; Middle Aged; Muscle, Skeletal; Muscular Diseases; Muscular Dystrophy, Emery-Dreifuss; Mutation; Myosin Heavy Chains; Myosins; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger; Tryptophan

2007
Expression of the myodystrophic R453W mutation of lamin A in C2C12 myoblasts causes promoter-specific and global epigenetic defects.
    Experimental cell research, 2008, May-01, Volume: 314, Issue:8

    Topics: Amino Acid Substitution; Animals; Arginine; Cell Differentiation; Cell Line; Cell Nucleus; DNA Methylation; Epigenesis, Genetic; Histones; Humans; Lamin Type A; Methylation; Mice; Muscular Dystrophy, Emery-Dreifuss; Mutation, Missense; Myoblasts; Myogenin; Promoter Regions, Genetic; Tryptophan; Up-Regulation; X Chromosome

2008