arginine has been researched along with Muscular Diseases in 34 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (11.76) | 18.7374 |
| 1990's | 3 (8.82) | 18.2507 |
| 2000's | 17 (50.00) | 29.6817 |
| 2010's | 9 (26.47) | 24.3611 |
| 2020's | 1 (2.94) | 2.80 |
| Authors | Studies |
|---|---|
| Bobeck, EA; Meyer, MM | 1 |
| Bogeski, I; Bonhenry, D; Butorac, C; Cappello, S; Ettrich, RH; Frischauf, I; Groschner, K; Hochreiter, A; Litviňuková, M; Lunz, V; Muik, M; Pammer, T; Reha, D; Romanin, C; Schindl, R; Schober, R; Stallinger, A; Svobodová, B; Tociu, L; Zayats, V | 1 |
| Meluzzi, A; Petracci, M; Sirri, F; Soglia, F; Zampiga, M | 1 |
| Blanc, RS; Richard, S | 1 |
| Levitsky, D; Nevzorov, I; Redwood, C | 1 |
| Abbs, S; Al-Sarraj, S; Buk, S; Dirksen, RT; Feng, L; Ghassemi, F; Hanna, M; Jungbluth, H; Lane, RJ; Lillis, S; Loy, RE; Matthews, E; Meissner, G; Mills, K; Muntoni, F; Norwood, F; Rose, MR; Sewry, CA; Treves, S; Zhou, H | 1 |
| Brewer, J; Davis, M; Kumar, KR; Mastaglia, FL; Mina, K; Needham, M; Ng, K; Staples, C; Sue, CM | 1 |
| Clarke, NF; Kennedy, P; Kornberg, A; Kreissl, M; Labarre-Vila, A; McLean, C; Monnier, N; North, KN; Waddell, LB | 1 |
| de Theije, C; Harding, HP; Köhler, SE; Lamers, MC; Lamers, WH; Lindsey, P; Marion, V; Ron, D; Sankaranarayanan, S; van Dijk, P | 1 |
| Allred, P; Baloh, RH; Bell, S; Cooper, P; Harms, MB; Lopate, G; Ma, D; Pestronk, A; Sommerville, RB; Weihl, CC | 1 |
| Bonakdar, N; Czonstke, M; Fabry, B; Goldmann, WH; Jungbauer, T; Koch, TM; Lautscham, L; Luczak, J; Mainka, A; Schröder, R | 1 |
| Arima, M; Chui, DH; Kotorii, S; Santa, Y; Tabira, T; Takahashi, K; Uyama, E | 1 |
| Bonuccelli, G; Capozza, F; Lisanti, MP; Minetti, C; Scherer, PE; Sotgia, F; Woodman, SE | 1 |
| WOODY, NC | 1 |
| Henriksson, KG; Lindberg, C; Lindvall, B; Oldfors, A; Tajsharghi, H; Thornell, LE | 1 |
| Bonaglia, MC; Bresolin, N; Cagliani, R; Comi, GP; D'Angelo, MG; Fortunato, F; Giorda, R; Locatelli, F; Prelle, A; Rodolico, C; Sironi, M; Toscano, A | 1 |
| Galli, L; Marbini, A; Pietrini, V; Sorrentino, V | 1 |
| Birkebaek, N; Gonzalez, I; Schmidt, MR; Sunde, L | 1 |
| Barraza, C; Fee, DB; Figueroa, KP; Pulst, SM; So, YT | 1 |
| Bonne, G; Brown, SC; Burke, MM; Kinali, M; McKenna, W; Mercuri, E; Messina, S; Muntoni, F; Nihoyannopoulos, P; Piercy, RJ; Poulton, J; Richard, P; Sewry, C | 1 |
| Fidziańska, A; Goudeau, B; Hausmanowa-Petrusewicz, I; Kotowicz, J; Sadowska, M; Vicart, P; Walczak, E | 1 |
| Barbier, R; Caron, O; Dollfus, H; Fleury, M; Mohr, M; Tranchant, C; Warter, JM; Ziegler, F | 1 |
| Angelini, C; Borsato, C; Cenacchi, G; Gavassini, BF; Melacini, P; Pegoraro, E; Stramare, R; Vianello, A | 1 |
| Carrithers, JA; Haus, JM; Trappe, SW; Trappe, TA | 1 |
| Al-Tassan, NA; Khalil, DS; Khan, AO | 1 |
| Deutz, NE; Pouw, EM; Schols, AM; Wouters, EF | 1 |
| Donnelly, A; Haan, E; Manson, J; Mulley, J | 1 |
| Bado, M; Bruno, C; DiMauro, S; DiRocco, M; Lamba, LD; Marino, C; Minetti, C; Shanske, S; Stella, G; Tsujino, S; van Diggelen, OP | 1 |
| Abe, M; Higuchi, I; Morisaki, H; Morisaki, T; Osame, M | 1 |
| Babül, A; Sayan, H; Ugurlu, B | 1 |
| Inoue, R; Kakimoto, Y; Kanazawa, A; Miyake, M; Sato, M | 1 |
| Cederbaum, SD; Cotton, ME; Shaw, KN; Valente, M | 1 |
| Bryan, GT; Hopwood, NJ; Lockhart, LH | 1 |
| Selleslag, D | 1 |
2 review(s) available for arginine and Muscular Diseases
| Article | Year |
|---|---|
Regenerating muscle with arginine methylation.
Topics: Aging; Animals; Arginine; Humans; Methylation; Muscle Proteins; Muscles; Muscular Diseases; Myoblasts; Protein-Arginine N-Methyltransferases; Regeneration | 2017 |
Stability of two beta-tropomyosin isoforms: effects of mutation Arg91Gly.
Topics: Animals; Arginine; Glycine; Humans; Muscular Diseases; Mutation; Protein Isoforms; Protein Stability; Protein Structure, Tertiary; Tropomyosin | 2008 |
32 other study(ies) available for arginine and Muscular Diseases
| Article | Year |
|---|---|
Dietary inositol-stabilized arginine silicate numerically reduced woody breast severity in male Ross 708 broilers without altering growth.
Topics: Animal Feed; Animals; Arginine; Chickens; Diet; Male; Meat; Muscular Diseases; Myoglobin; Pectoralis Muscles; Poultry Diseases | 2023 |
Transmembrane helix connectivity in Orai1 controls two gates for calcium-dependent transcription.
Topics: Animals; Arginine; Calcium; Cell Membrane; Drosophila melanogaster; Genomics; HCT116 Cells; HEK293 Cells; Humans; Ion Channel Gating; Molecular Dynamics Simulation; Muscular Diseases; Mutation; Neoplasm Proteins; Neoplasms; ORAI1 Protein; Patch-Clamp Techniques; Protein Structure, Secondary; Stromal Interaction Molecule 1; Transcriptional Activation | 2017 |
Effect of different arginine-to-lysine ratios in broiler chicken diets on the occurrence of breast myopathies and meat quality attributes.
Topics: Animal Feed; Animal Nutritional Physiological Phenomena; Animals; Arginine; Chickens; Diet; Food Quality; Lysine; Male; Meat; Muscular Diseases; Poultry Diseases | 2019 |
Multi-minicore disease and atypical periodic paralysis associated with novel mutations in the skeletal muscle ryanodine receptor (RYR1) gene.
Topics: Adult; Arginine; Caffeine; Calcium; Calcium Channels; Calcium Channels, L-Type; Cell Line, Transformed; DNA Mutational Analysis; Electron Transport Complex IV; Family Health; Female; Humans; Lysine; Male; Membrane Potentials; Muscle, Skeletal; Muscular Diseases; Mutation; NAV1.4 Voltage-Gated Sodium Channel; Patch-Clamp Techniques; Phosphodiesterase Inhibitors; Ryanodine; Ryanodine Receptor Calcium Release Channel; Sodium Channels; Transfection; Tritium | 2010 |
Two Australian families with inclusion-body myopathy, Paget's disease of bone and frontotemporal dementia: novel clinical and genetic findings.
Topics: Adenosine Triphosphatases; Adult; Alkaline Phosphatase; Arginine; Australia; Cell Cycle Proteins; Creatine Kinase; Electrodiagnosis; Family Health; Female; Frontotemporal Dementia; Humans; Inclusion Bodies; Leucine; Magnetic Resonance Imaging; Male; Middle Aged; Muscle, Skeletal; Muscular Diseases; Mutation; Osteitis Deformans; Tryptophan; Valosin Containing Protein | 2010 |
Evidence for a dominant negative disease mechanism in cap myopathy due to TPM3.
Topics: Adolescent; Arginine; Child, Preschool; Cysteine; Humans; Male; Muscle, Skeletal; Muscular Diseases; Mutation; Tropomyosin | 2010 |
Arginine deficiency causes runting in the suckling period by selectively activating the stress kinase GCN2.
Topics: Amino Acid Metabolism, Inborn Errors; Animals; Animals, Suckling; Arginase; Arginine; B-Lymphocytes; Growth Hormone; Hair Diseases; Hypoglycemia; Insulin-Like Growth Factor I; Mechanistic Target of Rapamycin Complex 1; Mice; Mice, Knockout; Multiprotein Complexes; Muscular Diseases; Protein Serine-Threonine Kinases; Proteins; Signal Transduction; Syndrome; TOR Serine-Threonine Kinases | 2011 |
Exome sequencing reveals DNAJB6 mutations in dominantly-inherited myopathy.
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.
Topics: Arginine; Cell Adhesion; Cells, Cultured; Cytoskeleton; Desmin; Humans; Muscular Diseases; Mutation, Missense; Myoblasts; Proline; Stress, Mechanical | 2012 |
Genetic, clinical and pathological studies of CADASIL in Japan: a partial contribution of Notch3 mutations and implications of smooth muscle cell degeneration for the pathogenesis.
Topics: Age of Onset; Arginine; Arteries; Brain; Cerebral Arterial Diseases; Cerebral Infarction; Cysteine; DNA Mutational Analysis; Family Health; Female; Humans; Immunohistochemistry; Japan; Lysine; Magnetic Resonance Imaging; Male; Microscopy, Electron; Muscular Diseases; Mutation; Phenylalanine; Proto-Oncogene Proteins; Receptor, Notch3; Receptors, Cell Surface; Receptors, Notch | 2003 |
Phenotypic behavior of caveolin-3 R26Q, a mutant associated with hyperCKemia, distal myopathy, and rippling muscle disease.
Topics: Amino Acid Substitution; Animals; Arginine; Caveolin 3; Caveolins; Chlorocebus aethiops; COS Cells; Creatine Kinase; Gene Expression Regulation; Glutamine; Mice; Muscle Proteins; Muscular Diseases; Muscular Dystrophies; Mutation; NIH 3T3 Cells; Phenotype | 2003 |
HYPERLYSINEMIA.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Alcohols; Aminobutyrates; Anemia; Arginine; Asthenia; Blood Chemical Analysis; Child; Chromatography; Genetics, Medical; Growth; Humans; Hyperlysinemias; Infant; Lysine; Maple Syrup Urine Disease; Muscular Diseases; Ornithine; Seizures; Urine | 1964 |
Myosin storage myopathy associated with a heterozygous missense mutation in MYH7.
Topics: Adenosine Triphosphatases; Aged; Arginine; Blotting, Western; DNA Mutational Analysis; Family Health; Female; Heterozygote; Humans; Immunohistochemistry; Male; Microscopy, Electron; Molecular Motor Proteins; Molecular Sequence Data; Muscle Fibers, Slow-Twitch; Muscular Diseases; Mutation, Missense; Myosin Heavy Chains; Protein Isoforms; Sequence Alignment; Staining and Labeling; Tryptophan | 2003 |
Molecular analysis of LGMD-2B and MM patients: identification of novel DYSF mutations and possible founder effect in the Italian population.
Topics: Adult; Aged; Arginine; DNA Mutational Analysis; Dysferlin; Female; Founder Effect; Frameshift Mutation; Genetic Testing; Genotype; Humans; Italy; Male; Membrane Proteins; Middle Aged; Muscle Proteins; Muscular Diseases; Muscular Dystrophies; Mutation; Mutation, Missense; Pedigree; Phenotype; Tryptophan | 2003 |
Adult onset multi/minicore myopathy associated with a mutation in the RYR1 gene.
Topics: Arginine; Creatine Kinase; Cysteine; DNA Mutational Analysis; Electromyography; Humans; Male; Microscopy, Electron; Middle Aged; Muscle, Skeletal; Muscular Diseases; Mutation; Ryanodine Receptor Calcium Release Channel; Succinate Dehydrogenase | 2004 |
Barth syndrome without 3-methylglutaconic aciduria.
Topics: Arginine; Cardiomyopathies; Chromosomes, Human, X; Fatal Outcome; Glutarates; Glycine; Humans; Infant, Newborn; Male; Muscular Diseases; Mutation; Mutation, Missense; Pedigree; Syndrome | 2004 |
Phenotypic variability associated with Arg26Gln mutation in caveolin3.
Topics: Aged; Aged, 80 and over; Amino Acid Sequence; Amino Acid Substitution; Arginine; Caveolin 3; Caveolins; Female; Genetic Variation; Glutamine; Humans; Male; Muscular Diseases; Mutation; Pedigree; Phenotype | 2004 |
Extreme variability of skeletal and cardiac muscle involvement in patients with mutations in exon 11 of the lamin A/C gene.
Topics: Adult; Amino Acid Substitution; Arginine; Cardiomyopathy, Hypertrophic; Child; Child, Preschool; Disease Progression; DNA Mutational Analysis; Electrodiagnosis; Exons; Fatal Outcome; Female; Genetic Testing; Heart; Humans; Lamin Type A; Male; Middle Aged; Muscle, Skeletal; Muscular Diseases; Mutation; Myocardium; Phenotype; Protein Structure, Tertiary | 2005 |
A novel desmin R355P mutation causes cardiac and skeletal myopathy.
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 |
Myopathy with tubular aggregates and gyrate atrophy of the choroid and retina due to hyperornithinaemia.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Arginine; Diet, Protein-Restricted; Gyrate Atrophy; Humans; Male; Muscular Diseases; Ornithine; Ornithine-Oxo-Acid Transaminase; Pyridoxine; Vitamin B Complex | 2007 |
MYH7 gene mutation in myosin storage myopathy and scapulo-peroneal myopathy.
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 |
Collagen, cross-linking, and advanced glycation end products in aging human skeletal muscle.
Topics: Actins; Activities of Daily Living; Adult; Age Factors; Aged; Aged, 80 and over; Aging; Amino Acids; Arginine; Collagen; Female; Glycation End Products, Advanced; Humans; Lysine; Male; Muscle Contraction; Muscle Strength; Muscular Diseases; Myofibrils; Myosins; Quadriceps Muscle | 2007 |
Congential fibrosis of the extraocular muscles type I (CFEOM1) on the Arabian Peninsula.
Topics: Adult; Arabs; Arginine; Blepharoptosis; Child, Preschool; Female; Fibrosis; Heterozygote; Humans; Kinesins; Male; Muscular Diseases; Mutation; Nerve Tissue Proteins; Oculomotor Muscles; Ophthalmoplegia; Pedigree; Saudi Arabia; Tryptophan | 2008 |
Plasma and muscle amino acid levels in relation to resting energy expenditure and inflammation in stable chronic obstructive pulmonary disease.
Topics: Acute-Phase Proteins; Acute-Phase Reaction; Adipose Tissue; Aged; Alanine; Amino Acids; Arginine; Carrier Proteins; Case-Control Studies; Citrulline; Energy Metabolism; Glutamic Acid; Glutamine; Humans; Lipopolysaccharides; Lung Diseases, Obstructive; Membrane Glycoproteins; Middle Aged; Muscle, Skeletal; Muscular Diseases; Ornithine; Proteins; Rest | 1998 |
A novel mutation in exon b (R259C) of the MTM1 gene is associated with a mild myotubular myopathy. Mutation in brief no. 125. Online.
Topics: Alleles; Amino Acid Substitution; Arginine; Cysteine; Exons; Female; Humans; Male; Muscular Diseases; Mutation; Polymerase Chain Reaction; Protein Tyrosine Phosphatases; Protein Tyrosine Phosphatases, Non-Receptor; X Chromosome | 1998 |
A novel missense mutation in the glycogen branching enzyme gene in a child with myopathy and hepatopathy.
Topics: 1,4-alpha-Glucan Branching Enzyme; Amino Acid Substitution; Arginine; Base Sequence; Cytoplasmic Granules; Glutamine; Glycogen Storage Disease Type IV; Heterozygote; Humans; Infant; Liver; Liver Diseases; Male; Muscle, Skeletal; Muscular Diseases; Mutation, Missense | 1999 |
First missense mutations (R388W and R425H) of AMPD1 accompanied with myopathy found in a Japanese patient.
Topics: Adult; AMP Deaminase; Arginine; Female; Genetic Carrier Screening; Histidine; Humans; Japan; Middle Aged; Muscular Diseases; Mutation, Missense; Transfection; Tryptophan | 2000 |
Effects of nitric oxide donor and inhibitor on prostaglandin E2-like activity, malondialdehyde and reduced glutathione levels after skeletal muscle ischemia-reperfusion.
Topics: Animals; Arginine; Dinoprostone; Enzyme Inhibitors; Glutathione; Kinetics; Lipid Peroxidation; Male; Malondialdehyde; Muscle, Skeletal; Muscular Diseases; NG-Nitroarginine Methyl Ester; Nitric Oxide Donors; Nitric Oxide Synthase; Rats; Rats, Wistar; Reperfusion Injury | 2001 |
Decrease of 3-methylhistidine and increase of NG,NG-dimethylarginine in the urine of patients with muscular dystrophy.
Topics: Adolescent; Adult; Amino Acids; Arginine; Child; Histidine; Humans; Methylhistidines; Middle Aged; Motor Neurons; Muscular Diseases; Muscular Dystrophies; Neuromuscular Diseases | 1979 |
Argininosuccinic aciduria.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Chromatography, Thin Layer; Citric Acid Cycle; Diet Therapy; Humans; Infant; Intellectual Disability; Karyotyping; Male; Muscle Tonus; Muscular Diseases; Nitrogen; Seizures; Succinates; Urea | 1973 |
Acquired hypothyroidism with muscular hypertrophy and precocious testicular enlargement.
Topics: Arginine; Child; Follicle Stimulating Hormone; Growth Hormone; Humans; Hypothyroidism; Luteinizing Hormone; Male; Muscular Diseases; Physical Exertion; Sleep; Testicular Diseases; Testosterone; Thyroid Hormones; Thyrotropin | 1974 |
A case of fusariosis in an immunocompromised patient successfully treated with liposomal amphotericin B.
Topics: Abscess; Amphotericin B; Antibodies, Monoclonal; Antibodies, Monoclonal, Murine-Derived; Antifungal Agents; Antineoplastic Combined Chemotherapy Protocols; Benzamides; Combined Modality Therapy; Cytarabine; Foot Dermatoses; Fusarium; Humans; Imatinib Mesylate; Immunocompromised Host; Liposomes; Male; Middle Aged; Muscular Diseases; Onychomycosis; Peripheral Blood Stem Cell Transplantation; Piperazines; Precursor Cell Lymphoblastic Leukemia-Lymphoma; Pyrimidines; Recurrence; Remission Induction; Reoperation; Rituximab; Teniposide; Triazoles; Voriconazole | 2006 |