isomethyleugenol has been researched along with Chromosomal Triplication in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (25.00) | 18.7374 |
| 1990's | 2 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Benedetti, D; Bomben, R; Caldana, C; D'Arena, G; Dal Bo, M; Del Poeta, G; Di Raimondo, F; Gaidano, G; Gattei, V; Hartmann, TN; Hutterer, E; Pozzato, G; Pozzo, F; Rossi, D; Rossi, FM; Tissino, E; Zaja, F; Zucchetto, A | 1 |
| Anisowicz, A; Gadi, IK; Harrison, JJ; Raffeld, M; Sager, R | 1 |
| Bliek, J; Boavida, M; Coad, N; Feinberg, AP; Hoovers, JM; Little, P; Mannens, M; Redeker, E; Steenman, M; Verjaal, M | 1 |
| Artifoni, L; Aviv, H; Baccichetti, C; Bernasconi, F; Franzoni, E; Robinson, WP; Schinzel, AA; Shih, LY; Suslak, L; Wagstaff, J | 1 |
4 other study(ies) available for isomethyleugenol and Chromosomal Triplication
| Article | Year |
|---|---|
CD49d is overexpressed by trisomy 12 chronic lymphocytic leukemia cells: evidence for a methylation-dependent regulation mechanism.
Topics: Azacitidine; B-Lymphocytes; Cell Proliferation; Cells, Cultured; Chromosomes, Human, Pair 12; Decitabine; Disease Progression; Gene Expression Regulation, Leukemic; Humans; Integrin alpha4; Leukemia, Lymphocytic, Chronic, B-Cell; Methylation; Sequence Analysis, DNA; Signal Transduction; Survival Analysis; Trisomy | 2013 |
Azacytidine-induced tumorigenesis of CHEF/18 cells: correlated DNA methylation and chromosome changes.
Topics: Adipose Tissue; Animals; Azacitidine; Cell Line; Chromosome Aberrations; Chromosome Disorders; Cricetinae; DNA, Neoplasm; Karyotyping; Methylation; Mice; Mice, Nude; Neoplasms, Experimental; Trisomy | 1983 |
Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia.
Topics: Beckwith-Wiedemann Syndrome; Child; Chromosome Aberrations; Chromosome Mapping; Chromosomes, Human, Pair 11; DNA; Female; Gene Expression; Genes, Tumor Suppressor; Humans; In Situ Hybridization, Fluorescence; Insulin; Insulin-Like Growth Factor II; Karyotyping; Male; Methylation; Neoplastic Syndromes, Hereditary; Parents; Pedigree; Polymorphism, Restriction Fragment Length; Sex Factors; Translocation, Genetic; Trisomy; Wilms Tumor | 1994 |
Uniparental disomy explains the occurrence of the Angelman or Prader-Willi syndrome in patients with an additional small inv dup(15) chromosome.
Topics: Angelman Syndrome; Child; Child, Preschool; Chromosome Deletion; Chromosome Inversion; Chromosomes, Human, Pair 15; Fathers; Humans; Karyotyping; Male; Methylation; Mothers; Prader-Willi Syndrome; Trisomy | 1993 |