leucine and Muscular Dystrophy

leucine has been researched along with Muscular Dystrophy in 36 studies

Research

Studies (36)

TimeframeStudies, this research(%)All Research%
pre-199028 (77.78)18.7374
1990's4 (11.11)18.2507
2000's3 (8.33)29.6817
2010's1 (2.78)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Aoki, MS; Baptista, IL; Carlassara, EO; Miyabara, EH; Moriscot, AS; Pereira, MG1
Ameye, L; Young, MF1
KABARA, JJ1
DEVI, A; RAINA, PL; SINGH, A1
Allard, B; Berthier, C; Couchoux, H; Jacquemond, V; Legrand, C1
Berlinguet, L; Srivastava, U1
Walser, M1
Brooke, MH; Dodson, WE; Fenichel, GM; Griggs, RC; Mendell, JR; Miller, JP; Moxley, RT; Province, MA1
Marusyk, H; Mion, CS; Monckton, G; Zatz, M1
Edwards, RH; Halliday, D; Matthews, DE; Millward, DJ; Rennie, MJ; Wolman, SL1
Dubowitz, V; Statham, HE; Witkowski, JA1
Marusyk, H; Monckton, G; Pehowich, E1
Hirano, K; Sakamoto, Y1
Darmaun, D; Hammond, D; Hankard, RG; Haymond, MW1
Bowe, MA; Fallon, JR; Mendis, DB1
Boegman, RJ; Wood, PL1
Marusyk, H; Monckton, G3
Satoyoshi, E1
Griggs, RC; Halliday, D; Herr, BE; Jozefowicz, R; Kingston, W; Nair, KS1
Kanaoka, Y; Murata, M; Oguma, K; Sato, E; Sota, K; Tamai, M; Yokoo, C1
Cheng, KN; Dworzak, F; Gibson, JN; Halliday, D; Pacy, PJ; Rennie, MJ1
Bayreuther, K; Rodemann, HP; Schumacher, E1
Ishida, J; Kai, M; Ohkura, Y1
Bradley, WG; Jaros, E1
Austin, L; Komiya, Y1
Blum, KU1
Edel'shteĭn, EA1
Ichinose, M; Ishii, N; Mori, K; Takamoyi, M; Takaoka, Y1
Gusev, EI1
Nakahara, M; Yamada, S1
Srivastava, U1
Gross, S; Maskaleris, ML; Milhorat, AT1
Devi, A; Mukundan, MA; Srivastava, U1

Reviews

4 review(s) available for leucine and Muscular Dystrophy

ArticleYear
Mice deficient in small leucine-rich proteoglycans: novel in vivo models for osteoporosis, osteoarthritis, Ehlers-Danlos syndrome, muscular dystrophy, and corneal diseases.
    Glycobiology, 2002, Volume: 12, Issue:9

    Topics: Animals; Corneal Diseases; Ehlers-Danlos Syndrome; Leucine; Mice; Mice, Knockout; Models, Molecular; Muscular Dystrophies; Osteoarthritis; Osteoporosis; Proteoglycans

2002
Therapeutic aspects of branched-chain amino and keto acids.
    Clinical science (London, England : 1979), 1984, Volume: 66, Issue:1

    Topics: Amino Acids, Branched-Chain; Animals; Brain; Chickens; Dogs; Hepatic Encephalopathy; Humans; Intestinal Absorption; Keto Acids; Kidney Failure, Chronic; Leucine; Liver; Muscular Dystrophies; Proteins; Rats; Swine

1984
Therapeutic trials on progressive muscular dystrophy.
    Internal medicine (Tokyo, Japan), 1992, Volume: 31, Issue:7

    Topics: Animals; Child; Child, Preschool; Cricetinae; Double-Blind Method; Drug Evaluation, Preclinical; Humans; Incidence; Japan; Leucine; Life Expectancy; Male; Mice; Muscular Dystrophies; Muscular Dystrophy, Animal; Prevalence; Protease Inhibitors; Single-Blind Method

1992
Measuring human muscle protein synthesis.
    Nutrition reviews, 1989, Volume: 47, Issue:3

    Topics: Adult; Carbon Isotopes; Humans; Leucine; Male; Muscle Proteins; Muscular Dystrophies

1989

Trials

3 trial(s) available for leucine and Muscular Dystrophy

ArticleYear
Clinical investigation in Duchenne muscular dystrophy: IV. Double-blind controlled trial of leucine.
    Muscle & nerve, 1984, Volume: 7, Issue:7

    Topics: Child; Clinical Trials as Topic; Contracture; Double-Blind Method; Enzymes; Humans; Leucine; Muscles; Muscular Dystrophies; Time Factors

1984
Therapeutic trials on progressive muscular dystrophy.
    Internal medicine (Tokyo, Japan), 1992, Volume: 31, Issue:7

    Topics: Animals; Child; Child, Preschool; Cricetinae; Double-Blind Method; Drug Evaluation, Preclinical; Humans; Incidence; Japan; Leucine; Life Expectancy; Male; Mice; Muscular Dystrophies; Muscular Dystrophy, Animal; Prevalence; Protease Inhibitors; Single-Blind Method

1992
Rate of protein synthesis in skeletal muscle of normal man and patients with muscular dystrophy: a reassessment.
    Clinical science (London, England : 1979), 1988, Volume: 74, Issue:3

    Topics: Adult; Female; Food; Humans; Intestinal Absorption; Leucine; Male; Muscle Proteins; Muscles; Muscular Dystrophies

1988

Other Studies

30 other study(ies) available for leucine and Muscular Dystrophy

ArticleYear
Leucine supplementation improves skeletal muscle regeneration after cryolesion in rats.
    PloS one, 2014, Volume: 9, Issue:1

    Topics: 3-Phosphoinositide-Dependent Protein Kinases; Administration, Oral; Animals; Cold Temperature; Dietary Supplements; Forkhead Box Protein O3; Forkhead Transcription Factors; Gene Expression; Hindlimb; Leucine; Male; Muscle Contraction; Muscle, Skeletal; Muscular Dystrophies; Proto-Oncogene Proteins c-akt; Rats; Rats, Wistar; Regeneration; Signal Transduction; TOR Serine-Threonine Kinases; Ubiquitination

2014
BRAIN CHOLESTEROL. VI. THE EFFECT OF HEREDITARY DYSTROPHIA MUSCULARIS ON (C14)LEUCINE AND (2-3H)ACETATE INCORPORATION.
    Texas reports on biology and medicine, 1964, Volume: 22

    Topics: Acetates; Animals; Brain; Carbon Isotopes; Cholesterol; Intestines; Kidney; Leucine; Lipid Metabolism; Liver; Metabolism; Mice; Muscles; Muscular Dystrophies; Research; Spleen

1964
ABNORMAL PROTEIN AND NUCLEIC ACID METABOLISM AS A CAUSE OF CATARACT FORMATION INDUCED BY NUTRITIONAL DEFICIENCY IN RABBITS.
    The British journal of ophthalmology, 1965, Volume: 49

    Topics: Animals; Carbon Isotopes; Cataract; DNA; Eye Proteins; Histocytochemistry; Lens, Crystalline; Leucine; Malnutrition; Metabolism; Muscular Dystrophies; Nucleosides; Proteins; Rabbits; Radiometry; Research; RNA; Thymidine; Uridine; Vitamin E Deficiency

1965
Loss of caveolin-3 induced by the dystrophy-associated P104L mutation impairs L-type calcium channel function in mouse skeletal muscle cells.
    The Journal of physiology, 2007, May-01, Volume: 580, Issue:Pt.3

    Topics: Animals; Calcium Channels, L-Type; Caveolin 3; Cells, Cultured; Electric Conductivity; Embryo, Mammalian; Leucine; Mice; Muscle Cells; Muscle Fibers, Skeletal; Muscle, Skeletal; Muscular Dystrophies; Mutation; Proline; Tissue Distribution

2007
Effect of various amino acids on the incorporation of 14C-L-leucine in the tissue proteins of normal and dystrophic mice.
    Canadian journal of biochemistry, 1967, Volume: 45, Issue:12

    Topics: Amino Acids; Animals; Antineoplastic Agents; Aspartic Acid; Brain; Carbon Isotopes; Cycloparaffins; Dactinomycin; Glutamates; Glycine; Kidney; Leucine; Liver; Male; Mice; Muscle Proteins; Muscular Dystrophies; Pancreas; Spleen; Stimulation, Chemical

1967
Results of blind testing a method to detect carriers of the Duchenne muscular dystrophy gene.
    American journal of human genetics, 1984, Volume: 36, Issue:4

    Topics: Adult; Aged; Creatine Kinase; Female; Genetic Carrier Screening; Heterozygote; Humans; Leucine; Male; Middle Aged; Muscles; Muscular Dystrophies; Pyruvate Kinase

1984
Effects of Duchenne muscular dystrophy on muscle protein synthesis.
    Nature, 1982, Mar-11, Volume: 296, Issue:5853

    Topics: Adolescent; Adult; Aged; Child; Creatinine; Humans; Leucine; Male; Methylhistidines; Middle Aged; Muscle Proteins; Muscular Dystrophies

1982
Protein degradation in skin fibroblasts from patients with Duchenne muscular dystrophy.
    The Biochemical journal, 1980, Oct-15, Volume: 192, Issue:1

    Topics: Adolescent; Adult; Cell Cycle; Cells, Cultured; Child; Child, Preschool; Fibroblasts; Humans; Infant; Leucine; Muscular Dystrophies; Proteins; Skin

1980
A method for the detection of carriers of Duchenne muscular dystrophy--a preliminary report.
    American journal of human genetics, 1981, Volume: 33, Issue:6

    Topics: Adolescent; Adult; Autoradiography; Biopsy; Child; Creatine Kinase; Female; Genetic Carrier Screening; Humans; Leucine; Middle Aged; Muscles; Muscular Dystrophies; Tritium

1981
Urinary excretion of acid-soluble peptides in children with Duchenne muscular dystrophy.
    Acta paediatrica Japonica : Overseas edition, 1994, Volume: 36, Issue:6

    Topics: Adolescent; Age Factors; Aminopeptidases; Antineoplastic Agents; Child; Child, Preschool; Chromatography, Paper; Female; Humans; Leucine; Male; Methylhistidines; Muscle, Skeletal; Muscular Dystrophies; Peptides; Placebos; Proteins

1994
Oral glutamine slows down whole body protein breakdown in Duchenne muscular dystrophy.
    Pediatric research, 1998, Volume: 43, Issue:2

    Topics: Administration, Oral; Adolescent; Child; Glutamine; Humans; Indicator Dilution Techniques; Leucine; Male; Muscular Dystrophies; Proteins

1998
The small leucine-rich repeat proteoglycan biglycan binds to alpha-dystroglycan and is upregulated in dystrophic muscle.
    The Journal of cell biology, 2000, Feb-21, Volume: 148, Issue:4

    Topics: Amino Acid Sequence; Animals; Biglycan; Binding Sites; Chondroitin Sulfates; Cytoskeletal Proteins; Dystroglycans; Dystrophin; Extracellular Matrix Proteins; Glycosylation; Humans; Leucine; Membrane Glycoproteins; Mice; Mice, Mutant Strains; Molecular Sequence Data; Molecular Weight; Muscles; Muscular Dystrophies; Neuromuscular Junction; Protein Binding; Proteoglycans; Repetitive Sequences, Amino Acid; Synapses; Torpedo; Up-Regulation

2000
Increased axoplasmic flow in experimental ischemic myopathy.
    Experimental neurology, 1975, Volume: 48, Issue:1

    Topics: Animals; Aorta, Abdominal; Axonal Transport; Creatine Kinase; Ischemia; Leucine; Ligation; Lipids; Male; Muscular Dystrophies; Proteins; Rats; Sciatic Nerve; Serotonin; Spinal Cord; Tritium

1975
The incorporation of 3H (G) L-leucine into single muscle fibers in Duchenne dystrophy and Charcot-Marie Tooth disease.
    The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques, 1979, Volume: 6, Issue:1

    Topics: Adolescent; Adult; Biopsy; Charcot-Marie-Tooth Disease; Humans; In Vitro Techniques; Leucine; Middle Aged; Muscles; Muscular Atrophy; Muscular Dystrophies

1979
An autoradiographic study of muscular dystrophy, motor neuron disease and Charcot-Marie-Tooth disease.
    The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques, 1977, Volume: 4, Issue:1

    Topics: Charcot-Marie-Tooth Disease; Humans; Leucine; Motor Neurons; Muscles; Muscular Dystrophies; Neuromuscular Diseases

1977
Myofibrillar incorporation of 3H (G) L-leucine in pgrogressive muscular dystrophy and motor neuron disease.
    Neurology, 1976, Volume: 26, Issue:3

    Topics: Humans; Leucine; Motor Neurons; Muscle Proteins; Muscular Dystrophies; Myofibrils; Myosins; Neuromuscular Diseases

1976
Mechanism of muscle wasting in myotonic dystrophy.
    Annals of neurology, 1990, Volume: 27, Issue:5

    Topics: Adult; Atrophy; Biopsy; Humans; Leucine; Male; Middle Aged; Muscle Proteins; Muscular Dystrophies

1990
Efficient synthetic method for ethyl (+)-(2S,3S)-3-[(S)-3-methyl- 1-(3-methylbutylcarbamoyl)butylcarbamoyl]-2-oxiranecarb oxylate (EST), a new inhibitor of cysteine proteinases.
    Chemical & pharmaceutical bulletin, 1987, Volume: 35, Issue:3

    Topics: Chemical Phenomena; Chemistry; Cysteine Endopeptidases; Endopeptidases; Leucine; Muscular Dystrophies; Protease Inhibitors

1987
Abnormal protein metabolism in skin fibroblasts in vitro from patients with Duchenne muscular dystrophy.
    Biochemical and biophysical research communications, 1987, May-29, Volume: 145, Issue:1

    Topics: Adolescent; Cells, Cultured; Child; Fibroblasts; Humans; Leucine; Male; Muscular Dystrophies; Protein Biosynthesis; Proteins; Reference Values; Skin; Tritium

1987
Determination of p-hydroxybestatin in human serum by high-performance liquid chromatography using fluorescence detection.
    Journal of chromatography, 1985, Nov-08, Volume: 344

    Topics: Chemical Phenomena; Chemistry; Child; Chromatography, High Pressure Liquid; Enkephalin, Leucine; Enkephalin, Methionine; Humans; Leucine; Muscular Dystrophies; Spectrometry, Fluorescence; Temperature

1985
Axoplasmic flow in axonal neuropathies. II. Axoplasmic flow in mice with motor neuron disease and muscular dystrophy.
    Brain : a journal of neurology, 1973, Volume: 96, Issue:2

    Topics: Amyotrophic Lateral Sclerosis; Animals; Autoradiography; Axonal Transport; Leucine; Mice; Motor Neurons; Muscular Dystrophies; Nerve Degeneration; Nerve Tissue Proteins; Silver; Spinal Nerve Roots; Tritium

1973
Axoplasmic flow of protein in the sciatic nerve of normal and dystrophic mice.
    Experimental neurology, 1974, Volume: 43, Issue:1

    Topics: Animals; Axonal Transport; Carbon Radioisotopes; Leucine; Mice; Mice, Inbred Strains; Muscles; Muscular Dystrophies; Nerve Tissue Proteins; Sciatic Nerve

1974
[Blood cells as indicators of metabolic disorders].
    Zeitschrift fur klinische Chemie und klinische Biochemie, 1967, Volume: 5, Issue:5

    Topics: Acidosis; Adrenal Insufficiency; Alcoholism; Alkalosis; Diabetes Mellitus; Down Syndrome; Electrolytes; Erythrocytes; Galactosemias; Glucosephosphate Dehydrogenase; Glycogen Storage Disease; Humans; Hyperaldosteronism; Hypertension; Hyperthyroidism; Kidney Failure, Chronic; Leucine; Leukocytes; Maple Syrup Urine Disease; Metabolic Diseases; Muscular Dystrophies; Paralyses, Familial Periodic; Potassium; Sodium; Vitamin B Deficiency

1967
[On the current treatment of progressive muscular dystrophies in children].
    Zhurnal nevropatologii i psikhiatrii imeni S.S. Korsakova (Moscow, Russia : 1952), 1968, Volume: 68, Issue:2

    Topics: Adolescent; Alkaloids; Child; Cholinesterase Inhibitors; Creatine; Ganglionic Blockers; Glutamates; Humans; Leucine; Male; Methionine; Muscular Dystrophies

1968
[Progressive muscular dystrophy and current status of study of pancreatic extract].
    Nihon rinsho. Japanese journal of clinical medicine, 1974, Apr-10, Volume: 32, Issue:4

    Topics: Animals; Biological Assay; Cells, Cultured; Female; Humans; Leucine; Male; Mice; Muscular Dystrophies; Pancreatic Extracts; Rabbits; RNA; Swine; Tritium

1974
[Hyperaminoaciduria in children suffering from progressive muscular dystrophy].
    Zhurnal nevropatologii i psikhiatrii imeni S.S. Korsakova (Moscow, Russia : 1952), 1967, Volume: 67, Issue:7

    Topics: Adolescent; Alanine; Amino Acid Metabolism, Inborn Errors; Arginine; Aspartic Acid; Child; Child, Preschool; Creatine; Creatinine; Female; Glutamates; Histidine; Humans; Leucine; Lysine; Male; Methionine; Muscular Dystrophies; Nitrogen; Phenylalanine; Serine; Threonine; Tryptophan; Tyrosine; Valine

1967
Studies on progressive muscular dystrophy. IV. Effects of original amino acids mixture on progressive muscular dystrophy.
    Arzneimittel-Forschung, 1967, Volume: 17, Issue:6

    Topics: Adenosine Triphosphate; Adolescent; Adult; Amino Acids; Arginine; Asparagine; Aspartic Acid; Blood Proteins; Child; Deficiency Diseases; Glutamates; Glycine; Histidine; Humans; Isoleucine; Leucine; Lysine; Male; Methionine; Muscles; Muscular Dystrophies; Phenylalanine; Threonine; Tryptophan; Tyrosine; Valine

1967
Biochemical changes in progressive muscular dystrophy. VII. Studies on the biosynthesis of protein and RNA in various cellular fractions of the muscle of normal and dystrophic mice.
    Canadian journal of biochemistry, 1968, Volume: 46, Issue:1

    Topics: Animals; Carbon Isotopes; Leucine; Mice; Microsomes; Mitochondria, Muscle; Muscles; Muscular Dystrophies; Myofibrils; Protein Biosynthesis; Proteins; RNA; Uridine

1968
Urinary amino acid and peptide excretion patterns in patients with muscular dystrophy (Duchenne). A preliminary study with the autoanalyzer.
    Clinical chemistry, 1969, Volume: 15, Issue:7

    Topics: Adolescent; Alanine; Amino Acid Metabolism, Inborn Errors; Aspartic Acid; Autoanalysis; Child; Child, Preschool; Glutamates; Glycine; Histidine; Humans; Isoleucine; Leucine; Lysine; Male; Muscular Dystrophies; Peptides; Phenylalanine; Serine; Threonine; Tyrosine; Valine

1969
Biochemical changes in progressive muscular dystrophy. IV. Nucleic acid and protein metabolism in the lenses of animals exhibiting nutritional and hereditary muscular dystrophy.
    Experimental eye research, 1966, Volume: 5, Issue:1

    Topics: Aminohydrolases; Animals; Body Weight; Carbon Isotopes; DNA; Eye Proteins; In Vitro Techniques; Lens, Crystalline; Leucine; Leucyl Aminopeptidase; Mice; Muscular Dystrophies; Rabbits; RNA; Thymidine; Uridine; Vitamin E Deficiency

1966