arginine and Muscular Dystrophies, Limb-Girdle

arginine has been researched along with Muscular Dystrophies, Limb-Girdle in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (50.00)29.6817
2010's3 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Cole, AR; Keep, NH; Orengo, C; Sula, A; Yeats, C1
Beil, T; Grabher, C; Middel, V; Nienhaus, GU; Rastegar, S; Reischl, M; Roostalu, U; Shahid, M; Strähle, U; Takamiya, M; Zhou, L1
Hayashi, YK; Matsuda, C; Minami, N; Mitsuhashi, H; Nishino, I; Noguchi, S; Nonaka, I; Shalaby, S1
Allred, P; Baloh, RH; Bell, S; Cooper, P; Harms, MB; Lopate, G; Ma, D; Pestronk, A; Sommerville, RB; Weihl, CC1
Chrobáková, T; Fajkusová, L; Havlová, M; Hermanová, M; Kroupová, I; Maríková, T; Mazanec, R; Stanek, J; Vondrácek, P; Zámecník, J1
Angelini, C; Fanin, M; Fulizio, L; Nascimbeni, AC1

Other Studies

6 other study(ies) available for arginine and Muscular Dystrophies, Limb-Girdle

ArticleYear
Crystal structures of the human Dysferlin inner DysF domain.
    BMC structural biology, 2014, Jan-17, Volume: 14

    Topics: Arginine; Crystallography, X-Ray; Dysferlin; Humans; Hydrogen Bonding; Membrane Proteins; Models, Molecular; Muscle Proteins; Muscular Dystrophies, Limb-Girdle; Mutation, Missense; Protein Conformation; Protein Folding; Protein Structure, Secondary; Protein Structure, Tertiary; Sequence Alignment; Tryptophan

2014
Dysferlin-mediated phosphatidylserine sorting engages macrophages in sarcolemma repair.
    Nature communications, 2016, 09-19, Volume: 7

    Topics: Animals; Animals, Genetically Modified; Arginine; Dysferlin; Embryo, Nonmammalian; HeLa Cells; Humans; Macrophages; Membrane Proteins; Muscular Dystrophies, Limb-Girdle; Phosphatidylserines; Sarcolemma; Zebrafish; Zebrafish Proteins

2016
Defective myotilin homodimerization caused by a novel mutation in MYOT exon 9 in the first Japanese limb girdle muscular dystrophy 1A patient.
    Journal of neuropathology and experimental neurology, 2009, Volume: 68, Issue:6

    Topics: Actinin; Animals; Arginine; Chlorocebus aethiops; Connectin; COS Cells; Cytoskeletal Proteins; DNA Mutational Analysis; Exons; Female; Humans; Immunoprecipitation; Japan; Lysine; Male; Microfilament Proteins; Middle Aged; Molecular Sequence Data; Muscle Proteins; Muscular Dystrophies, Limb-Girdle; Mutation, Missense; NAD; Protein Structure, Tertiary; Serine; Transfection; Two-Hybrid System Techniques

2009
Exome sequencing reveals DNAJB6 mutations in dominantly-inherited myopathy.
    Annals of neurology, 2012, Volume: 71, Issue:3

    Topics: Adolescent; Adult; Amino Acid Sequence; Arginine; Exome; Female; Genes, Dominant; Genome-Wide Association Study; HSP40 Heat-Shock Proteins; Humans; Male; Middle Aged; Molecular Chaperones; Molecular Sequence Data; Muscular Diseases; Muscular Dystrophies, Limb-Girdle; Mutation; Nerve Tissue Proteins; Pedigree; Proline; Protein Structure, Tertiary; Sequence Analysis, DNA; Young Adult

2012
Mutations in Czech LGMD2A patients revealed by analysis of calpain3 mRNA and their phenotypic outcome.
    Neuromuscular disorders : NMD, 2004, Volume: 14, Issue:10

    Topics: Adolescent; Adult; Aged; Arginine; Blotting, Western; Calpain; Child; Czech Republic; DNA Mutational Analysis; Dysferlin; Exons; Female; Humans; Immunohistochemistry; Isoenzymes; Male; Membrane Proteins; Middle Aged; Muscle Proteins; Muscle, Skeletal; Muscular Dystrophies, Limb-Girdle; Mutation; Phenotype; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger; Tryptophan

2004
The frequency of limb girdle muscular dystrophy 2A in northeastern Italy.
    Neuromuscular disorders : NMD, 2005, Volume: 15, Issue:3

    Topics: Alanine; Arginine; Blotting, Western; Calpain; DNA Mutational Analysis; Family Health; Glutamine; Haplotypes; Humans; Isoenzymes; Italy; Linkage Disequilibrium; Muscle Proteins; Muscular Dystrophies, Limb-Girdle; Mutation; Prevalence; Retrospective Studies

2005