isomethyleugenol has been researched along with Muscular Dystrophy in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (57.14) | 18.7374 |
| 1990's | 3 (42.86) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Appel, SH; Moore, RB | 1 |
| Azofeifa, J; Cremer, M; Hübner, C; Voit, T | 1 |
| Marchi, J; Nobile, C | 1 |
| Lou, MF | 1 |
| Fenwick, RG; Garcia, CA; Hoffman, EP; Lupski, JR; Zoghbi, HY | 1 |
| Affara, NA; Burmeister, M; Ferguson-Smith, MA; Gillard, EF; Kunkel, LM; Lehrach, H; Monaco, AP; van Ommen, GJ | 1 |
| Perry, SV | 1 |
7 other study(ies) available for isomethyleugenol and Muscular Dystrophy
| Article | Year |
|---|---|
Methylation of erythrocyte membrane phospholipids in patients with myotonic and Duchenne muscular dystrophy.
Topics: Erythrocyte Membrane; Erythrocytes; Humans; Kinetics; Membrane Lipids; Methylation; Muscular Dystrophies; Phosphatidylcholines; Phospholipids; S-Adenosylmethionine | 1980 |
X-chromosome methylation in manifesting and healthy carriers of dystrophinopathies: concordance of activation ratios among first degree female relatives and skewed inactivation as cause of the affected phenotypes.
Topics: Child; Data Interpretation, Statistical; DNA; Dosage Compensation, Genetic; Dystrophin; Female; Heterozygote; Humans; Infant; Male; Methylation; Muscular Dystrophies; Pedigree; Polymorphism, Restriction Fragment Length; X Chromosome | 1995 |
A refined restriction map of YAC clones spanning the entire human dystrophin gene.
Topics: Animals; Chromosomes, Artificial, Yeast; Cloning, Molecular; Dinucleoside Phosphates; Dystrophin; Exons; Gene Deletion; Hominidae; Humans; Methylation; Muscular Dystrophies; Restriction Mapping; Sequence Homology, Nucleic Acid | 1994 |
Human muscular dystrophy: elevation of urinary dimethylarginines.
Topics: Arginine; Creatine; Creatinine; Humans; Methylation; Muscle Proteins; Muscular Dystrophies | 1979 |
Discordance of muscular dystrophy in monozygotic female twins: evidence supporting asymmetric splitting of the inner cell mass in a manifesting carrier of Duchenne dystrophy.
Topics: Adult; Blotting, Southern; Child; Densitometry; Diseases in Twins; DNA; Dosage Compensation, Genetic; Dystrophin; Female; Genetic Carrier Screening; Humans; Male; Methylation; Multigene Family; Muscles; Muscular Dystrophies; Mutation; Pedigree; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Twins, Monozygotic; X Chromosome | 1991 |
A 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy gene.
Topics: Chromosome Deletion; Chromosome Mapping; Cloning, Molecular; Electrophoresis; Genetic Linkage; Humans; Methylation; Muscular Dystrophies; X Chromosome | 1988 |
Development and specialization in muscle and the biochemistry of the dystrophies.
Topics: Amino Acids; Animals; Animals, Newborn; Creatine Kinase; Histidine; Humans; Isoenzymes; Methylation; Muscle Contraction; Muscle Development; Muscle Proteins; Muscles; Muscular Dystrophies; Muscular Dystrophy, Animal; Myofibrils; Rabbits; Vitamin E Deficiency | 1971 |