isomethyleugenol has been researched along with Cancer Syndromes, Hereditary in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (66.67) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Auclair-Perrossier, J; Blanché, H; Bodo, S; Bourdeaut, F; Brems, H; Brugières, L; Buhard, O; Buisine, MP; Cabaret, O; Caron, O; Chalastanis, A; Cohen-Haguenauer, O; Colas, C; Collura, A; Coulet, F; Duval, A; Entz-Werle, N; Fedhila, F; Fléjou, JF; Frébourg, T; Gauthier-Villars, M; Gerdes, AM; Goldberg, Y; Grandjouan, S; Guilloux, A; Hamelin, R; Ilencikova, D; Kinzel, M; Knappe, UJ; Lafitte, P; Lavoine, N; Leclerc, J; Leis, A; Lejeune, S; Malka, D; Mathieu-Dramard, M; Mortemousque, I; Muleris, M; Parfait, B; Ruiz-Ponte, C; Sheridan, E; Soubrier, F; Svrcek, M; Tinat, J; Vasen, H; Verloes, A; Vidaud, D; Wafaa, B; Wang, Q; Wimmer, K | 1 |
| Bliek, J; Boavida, M; Coad, N; Feinberg, AP; Hoovers, JM; Little, P; Mannens, M; Redeker, E; Steenman, M; Verjaal, M | 1 |
| Feinberg, AP | 1 |
3 other study(ies) available for isomethyleugenol and Cancer Syndromes, Hereditary
| Article | Year |
|---|---|
Diagnosis of Constitutional Mismatch Repair-Deficiency Syndrome Based on Microsatellite Instability and Lymphocyte Tolerance to Methylating Agents.
Topics: Adaptor Proteins, Signal Transducing; Adenosine Triphosphatases; Adult; Antineoplastic Agents, Alkylating; Biomarkers, Tumor; Brain Neoplasms; Caco-2 Cells; Case-Control Studies; Colorectal Neoplasms; Colorectal Neoplasms, Hereditary Nonpolyposis; DNA Mutational Analysis; DNA Repair Enzymes; DNA-Binding Proteins; Drug Resistance, Neoplasm; Female; Genetic Predisposition to Disease; Genetic Testing; Germ-Line Mutation; HCT116 Cells; Heredity; Humans; Lymphocytes; Male; Methylation; Microsatellite Instability; Mismatch Repair Endonuclease PMS2; Multiplex Polymerase Chain Reaction; MutL Protein Homolog 1; MutS Homolog 2 Protein; Neoplastic Syndromes, Hereditary; Nuclear Proteins; Phenotype; Predictive Value of Tests; Reproducibility of Results; Transfection; Young Adult | 2015 |
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 |
Genomic imprinting and gene activation in cancer.
Topics: Alleles; DNA, Neoplasm; Gene Expression Regulation, Neoplastic; Genes, Tumor Suppressor; Humans; Methylation; Models, Genetic; Neoplasms; Neoplastic Syndromes, Hereditary; Oncogenes; Philadelphia Chromosome; Transcriptional Activation | 1993 |