Compounds > proline

proline and Muscular Diseases

proline has been researched along with Muscular Diseases in 12 studies

Research

Studies (12)

TimeframeStudies, this research(%)All Research%
pre-19902 (16.67)18.7374
1990's0 (0.00)18.2507
2000's7 (58.33)29.6817
2010's3 (25.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Arné-Bes, MC; Delisle, MB; Figarella-Branger, D; Heitz, F; Levade, T; Pellissier, JF; Richard, P; Uro-Coste, E1
Calvo, MI; Gil, AG; Goicoechea, M; López de Cerain, A; López de Munain, A; Uriarte-Pueyo, I1
Bertini, E; Bushby, K; D'Amico, A; Goldfarb, LG; Lee, HS; Lochmüller, H; McKenna, C; Odgerel, Z; Paola, F; Rankin, J; Sarkozy, A; Straub, V1
Allred, P; Baloh, RH; Bell, S; Cooper, P; Harms, MB; Lopate, G; Ma, D; Pestronk, A; Sommerville, RB; Weihl, CC1
Bonakdar, N; Czonstke, M; Fabry, B; Goldmann, WH; Jungbauer, T; Koch, TM; Lautscham, L; Luczak, J; Mainka, A; Schröder, R1
Blancato, JK; Dagvadorj, A; Goldfarb, LG; Goudeau, B; Hilton-Jones, D; Nagle, JW; Shatunov, A; Simon-Casteras, M; Squier, W; Vicart, P1
Chen, CM; Chen, ST; Lee-Chen, GJ; Lin, CY; Lin, TC; Ro, LS; Wu, YR1
Fidziańska, A; Goudeau, B; Hausmanowa-Petrusewicz, I; Kotowicz, J; Sadowska, M; Vicart, P; Walczak, E1
Aebi, U; Bär, H; Herrmann, H; Kostareva, A; Mücke, N; Sjöberg, G1
Horváth, R; Jaksch, M; Lochmüller, H; Müller-Höcker, J; Schoser, BG; Völpel, M1
Burden, AC; Samanta, A1
Mitchell, R; Ofeigsson, OJ; Patrick, RS1

Other Studies

12 other study(ies) available for proline and Muscular Diseases

ArticleYear
Striking phenotypic variability in two familial cases of myosin storage myopathy with a MYH7 Leu1793pro mutation.
    Neuromuscular disorders : NMD, 2009, Volume: 19, Issue:2

    Topics: Amino Acid Substitution; Cardiac Myosins; Cardiomyopathies; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Genetic Variation; Genotype; Heart; Humans; Leucine; Middle Aged; Muscle Hypotonia; Muscle, Skeletal; Muscular Diseases; Mutation; Myocardium; Myosin Heavy Chains; Phenotype; Proline; Young Adult

2009
Negative evidence for stachydrine or Galeopsis ladanum L. seeds as the causal agents of coturnism after quail meat ingestion.
    Journal of agricultural and food chemistry, 2009, Nov-25, Volume: 57, Issue:22

    Topics: Animals; Diet; Humans; Lamiaceae; Male; Meat; Muscle Weakness; Muscular Diseases; Myoglobinuria; Plant Extracts; Proline; Quail; Rats; Rats, Wistar; Rhabdomyolysis; Seeds

2009
Inheritance patterns and phenotypic features of myofibrillar myopathy associated with a BAG3 mutation.
    Neuromuscular disorders : NMD, 2010, Volume: 20, Issue:7

    Topics: Actin Cytoskeleton; Adaptor Proteins, Signal Transducing; Adolescent; Adult; Apoptosis Regulatory Proteins; Child; DNA Mutational Analysis; Family Health; Female; Genotype; Humans; Leucine; Male; Microscopy, Electron, Scanning; Muscular Diseases; Mutation; Phenotype; Proline; Sural Nerve; Young Adult

2010
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
Biomechanical characterization of a desminopathy in primary human myoblasts.
    Biochemical and biophysical research communications, 2012, Mar-23, Volume: 419, Issue:4

    Topics: Arginine; Cell Adhesion; Cells, Cultured; Cytoskeleton; Desmin; Humans; Muscular Diseases; Mutation, Missense; Myoblasts; Proline; Stress, Mechanical

2012
Respiratory insufficiency in desminopathy patients caused by introduction of proline residues in desmin c-terminal alpha-helical segment.
    Muscle & nerve, 2003, Volume: 27, Issue:6

    Topics: Adult; Aged; Base Sequence; Cell Line; Desmin; DNA Mutational Analysis; Female; Genetic Testing; Humans; Intermediate Filaments; Male; Middle Aged; Molecular Sequence Data; Muscle Fibers, Skeletal; Muscle Weakness; Muscular Diseases; Mutation; Proline; Protein Structure, Secondary; Respiratory Insufficiency; Respiratory Muscles; Respiratory Paralysis; Sequence Homology, Amino Acid

2003
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
A novel desmin R355P mutation causes cardiac and skeletal myopathy.
    Neuromuscular disorders : NMD, 2005, Volume: 15, Issue:8

    Topics: Adult; alpha-Crystallin B Chain; Arginine; Desmin; DNA Mutational Analysis; Humans; Immunohistochemistry; Intermediate Filament Proteins; Male; Microscopy, Electron, Transmission; Muscle Weakness; Muscle, Skeletal; Muscular Diseases; Mutation; Myocardium; Nerve Tissue Proteins; Proline; Protein Kinases; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger

2005
Severe muscle disease-causing desmin mutations interfere with in vitro filament assembly at distinct stages.
    Proceedings of the National Academy of Sciences of the United States of America, 2005, Oct-18, Volume: 102, Issue:42

    Topics: 3T3 Cells; Amino Acid Sequence; Animals; Cytoskeleton; Desmin; Humans; Intermediate Filaments; Mice; Molecular Sequence Data; Muscular Diseases; Mutation; Proline; Protein Structure, Secondary; Recombinant Proteins; Sequence Alignment

2005
Mutations in mtDNA-encoded cytochrome c oxidase subunit genes causing isolated myopathy or severe encephalomyopathy.
    Neuromuscular disorders : NMD, 2005, Volume: 15, Issue:12

    Topics: Adult; DNA Mutational Analysis; Electron Transport Complex IV; Glutamic Acid; Humans; Immunohistochemistry; Male; Mitochondrial Encephalomyopathies; Muscle, Skeletal; Muscular Diseases; Mutation; Proline; Reverse Transcriptase Polymerase Chain Reaction; Rhabdomyolysis; RNA, Messenger; Serine

2005
Fever, myalgia, and arthralgia in a patient on captopril and allopurinol.
    Lancet (London, England), 1984, Mar-24, Volume: 1, Issue:8378

    Topics: Aged; Allopurinol; Captopril; Drug Synergism; Fever; Humans; Joint Diseases; Male; Muscular Diseases; Pain; Proline

1984
Observations on the cold water treatment of cutaneous burns.
    The Journal of pathology, 1972, Volume: 108, Issue:2

    Topics: Animals; Back; Burns; Cell Nucleus; Collagen; Connective Tissue; Connective Tissue Cells; Cryosurgery; Epithelial Cells; Epithelium; Hydroxyproline; Muscular Diseases; Necrosis; Proline; Rats; Skin; Skin Ulcer; Thymidine; Tritium; Water; Wound Healing

1972