isomethyleugenol has been researched along with Peutz-Jeghers Syndrome 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 | 0 (0.00) | 29.6817 |
| 2010's | 2 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chen, C; Chen, S; Li, N; Liu, C; Liu, J; Lu, H; Pan, J; Shi, H; Wan, H; Wang, D; Wang, F; Wang, Z; Wei, J; Wu, L; Yang, L; Zhang, X; Zhou, X; Zhou, Y; Zhu, M | 1 |
| Al-Sohaily, S; Biankin, A; Kohonen-Corish, M; Leong, R; Warusavitarne, J | 1 |
1 review(s) available for isomethyleugenol and Peutz-Jeghers Syndrome
| Article | Year |
|---|---|
Molecular pathways in colorectal cancer.
Topics: Adenomatous Polyposis Coli; Cell Transformation, Neoplastic; Chromosomal Instability; Colorectal Neoplasms; Colorectal Neoplasms, Hereditary Nonpolyposis; CpG Islands; Hamartoma Syndrome, Multiple; Humans; Methylation; Microsatellite Instability; Peutz-Jeghers Syndrome | 2012 |
1 other study(ies) available for isomethyleugenol and Peutz-Jeghers Syndrome
| Article | Year |
|---|---|
Genetic Screening and Analysis of LKB1 Gene in Chinese Patients with Peutz-Jeghers Syndrome.
Topics: Adult; AMP-Activated Protein Kinase Kinases; Asian People; China; Exons; Female; Genetic Testing; Germ-Line Mutation; Humans; Male; Methylation; Mutation; Peutz-Jeghers Syndrome; Protein Serine-Threonine Kinases; Quality of Life; Sequence Deletion | 2016 |