Compounds > threonine

threonine and Muscle Disorders

threonine has been researched along with Muscle Disorders in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's2 (40.00)18.2507
2000's1 (20.00)29.6817
2010's1 (20.00)24.3611
2020's1 (20.00)2.80

Authors

AuthorsStudies
Arayamethakorn, S; Bordini, M; Davoli, R; Malila, Y; Petracci, M; Rungrassamee, W; Sanpinit, P; Sirri, F; Soglia, F; Thanatsang, KV; Zappaterra, M1
Kärppä, M; Kytövuori, L; Majamaa, K; Saari, M1
Goebel, HH; Gross, M; Kölle, P; Lochmüller, H; Mahnke-Zizelman, DK; Mortier, W; Pongratz, D; Reichmann, H; Rötzer, E; Sabina, RL1
Bardet, J; Diry, C; Heron, B; Kamoun, P; Marsac, C; Munnich, A; Parvy, P; Ponsot, G; Rabier, D; Rotig, A; Rustin, P; Saudubray, JM1
Aguilera, I; Arenas, J; Bautista, J; Campos, Y; García-Lozano, JR; Núñez-Roldán, A1

Other Studies

5 other study(ies) available for threonine and Muscle Disorders

ArticleYear
Differential expression patterns of genes associated with metabolisms, muscle growth and repair in Pectoralis major muscles of fast- and medium-growing chickens.
    PloS one, 2022, Volume: 17, Issue:10

    Topics: AMP-Activated Protein Kinases; Animals; Chickens; Matrix Metalloproteinase 14; Muscular Diseases; Pectoralis Muscles; Poultry Diseases; Serine; Threonine

2022
Mutation m.15923A>G in the MT-TT gene causes mild myopathy - case report of an adult-onset phenotype.
    BMC neurology, 2018, Sep-20, Volume: 18, Issue:1

    Topics: Adult; Age of Onset; DNA, Mitochondrial; Humans; Male; Muscle, Skeletal; Muscular Diseases; Mutation; Phenotype; RNA, Transfer; Threonine

2018
A G468-T AMPD1 mutant allele contributes to the high incidence of myoadenylate deaminase deficiency in the Caucasian population.
    Neuromuscular disorders : NMD, 2002, Volume: 12, Issue:6

    Topics: Alleles; AMP Deaminase; Blotting, Western; DNA Probes; DNA, Complementary; Electromyography; Genotype; Glycine; Humans; Metabolic Diseases; Muscle, Skeletal; Muscular Diseases; Mutation; Phenotype; Polymerase Chain Reaction; Threonine; White People

2002
Persistent hypocitrullinaemia as a marker for mtDNA NARP T 8993 G mutation?
    Journal of inherited metabolic disease, 1998, Volume: 21, Issue:3

    Topics: Abnormalities, Multiple; Ataxia; Biomarkers; Child, Preschool; Citrulline; DNA, Mitochondrial; Female; Glycine; Humans; Infant; Male; Muscular Diseases; Mutation; Retinitis Pigmentosa; Threonine

1998
A novel missense mutation 15747 T>C in the mitochondrial cytochrome b gene.
    Human mutation, 1999, Volume: 14, Issue:6

    Topics: Amino Acid Substitution; Cytochrome b Group; Humans; Isoleucine; Molecular Sequence Data; Muscular Diseases; Mutation, Missense; Polymerase Chain Reaction; Threonine

1999