Compounds > valine

valine and Muscle Disorders

valine 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's0 (0.00)18.2507
2000's4 (80.00)29.6817
2010's1 (20.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Antozzi, C; Brancati, F; D Apice, MR; Federici, L; Maggi, L; Marshall, CR; Massa, R; Minassian, BA; Mora, M; Morandi, L; Novelli, G; Pasanisi, MB; Ruggieri, A; Sangiuolo, F; Saredi, S; Scherer, SW; Terracciano, C; Zanotti, S1
Feng, Y; Luo, XG; Ren, Y; Wang, H1
Catteruccia, M; Di Giacopo, R; Lo Monaco, M; Sanna, T; Santorelli, FM; Sauchelli, D; Servidei, S; Tessa, A; Verbo, A1
Chen, CM; Chen, ST; Lee-Chen, GJ; Lin, CY; Lin, TC; Ro, LS; Wu, YR1
Cooper, ST; Domazetovska, A; Hutchinson, DO; Ilkovski, B; Kumar, V; North, KN; Peckham, M; Robinson, PJ; Sparrow, JC; Valova, VA; Vandebrouck, A1

Other Studies

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

ArticleYear
Complete loss of the DNAJB6 G/F domain and novel missense mutations cause distal-onset DNAJB6 myopathy.
    Acta neuropathologica communications, 2015, Jul-25, Volume: 3

    Topics: Adult; Aged; DNA Mutational Analysis; Family Health; Female; Genetic Predisposition to Disease; HSP40 Heat-Shock Proteins; HSP70 Heat-Shock Proteins; Humans; Italy; Male; Middle Aged; Models, Molecular; Molecular Chaperones; Muscular Diseases; Mutation, Missense; Nerve Tissue Proteins; Phenylalanine; Tomography Scanners, X-Ray Computed; Valine; Young Adult

2015
Permanent myopathy caused by mutation of SCN4A Metl592Val: Observation on myogenesis in vitro and on effect of basic fibroblast growth factor on the muscle.
    Neuroscience bulletin, 2009, Volume: 25, Issue:2

    Topics: Adult; Cell Proliferation; Cells, Cultured; Creatine Kinase; Dose-Response Relationship, Drug; Fibroblast Growth Factor 2; Humans; L-Lactate Dehydrogenase; Male; Methionine; Middle Aged; Muscle Development; Muscular Diseases; Mutation; Myoblasts; NAV1.4 Voltage-Gated Sodium Channel; Sodium Channels; Valine

2009
Rippling muscle disease and cardiomyopathy associated with a mutation in the CAV3 gene.
    Neuromuscular disorders : NMD, 2009, Volume: 19, Issue:11

    Topics: Adult; Alanine; Cardiomyopathies; Caveolin 3; Electrocardiography; Electromyography; Family Health; Female; Genetic Predisposition to Disease; Humans; Magnetic Resonance Imaging; Male; Middle Aged; Muscle, Skeletal; Muscular Diseases; Mutation; Valine; Young Adult

2009
Phenotypic features and genetic findings in 2 chinese families with Miyoshi distal myopathy.
    Archives of neurology, 2004, Volume: 61, Issue:10

    Topics: Adolescent; Adult; Asian People; Distal Myopathies; DNA Mutational Analysis; Dysferlin; Exons; Family Health; Female; Genetic Linkage; Genotype; Glycine; Humans; Immunohistochemistry; Leucine; Magnetic Resonance Imaging; Male; Membrane Proteins; Muscle Proteins; Muscle, Skeletal; Muscular Diseases; Mutation; Pedigree; Phenotype; Polymorphism, Single-Stranded Conformational; Proline; Valine

2004
Intranuclear rod myopathy: molecular pathogenesis and mechanisms of weakness.
    Annals of neurology, 2007, Volume: 62, Issue:6

    Topics: Actin Cytoskeleton; Actins; Adaptation, Physiological; Animals; Animals, Genetically Modified; Cell Line; Cytoplasm; Drosophila; Humans; Methionine; Mice; Muscle Weakness; Muscle, Skeletal; Muscular Diseases; Protein Isoforms; Regeneration; Sarcomeres; Transfection; Valine

2007