isomethyleugenol has been researched along with Muscular Dystrophy, Facioscapulohumeral in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Ball, AR; Balog, J; Chen, YY; Chien, R; de Greef, JC; Donovan, PJ; Frants, RR; Gregson, HC; Kimonis, VE; Kong, X; Lock, LF; Pyle, A; Robertson, KD; Schmiesing, JA; van der Maarel, SM; Winokur, ST; Yokomori, K; Zeng, W | 1 |
| Enthoven, L; Felicetti, L; Frants, RR; Jeanpierre, M; Padberg, GW; Ricci, E; Rossi, M; van der Maarel, SM; van Overveld, PG; Winokur, ST | 1 |
2 other study(ies) available for isomethyleugenol and Muscular Dystrophy, Facioscapulohumeral
| Article | Year |
|---|---|
Specific loss of histone H3 lysine 9 trimethylation and HP1gamma/cohesin binding at D4Z4 repeats is associated with facioscapulohumeral dystrophy (FSHD).
Topics: Animals; Cell Cycle Proteins; Chromosomal Proteins, Non-Histone; Cohesins; Cricetinae; Euchromatin; HeLa Cells; Heterochromatin; Histones; Humans; Methylation; Methyltransferases; Mice; Models, Molecular; Muscular Dystrophy, Facioscapulohumeral; Polymerase Chain Reaction; Repressor Proteins; Tandem Repeat Sequences; Tumor Cells, Cultured | 2009 |
Variable hypomethylation of D4Z4 in facioscapulohumeral muscular dystrophy.
Topics: Age Factors; Alleles; Chromosomes, Human, Pair 4; Genetic Variation; Humans; Linear Models; Methylation; Muscular Dystrophy, Facioscapulohumeral; Repetitive Sequences, Nucleic Acid; Restriction Mapping | 2005 |