isomethyleugenol has been researched along with Orphan Diseases 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 |
|---|---|
| Flanagan, C; Kerr, K; Maxwell, AP; McAneney, H; McKnight, AJ | 1 |
| Afenjar, A; Bienvenu, T; Billuart, P; Giurgea, I; Goldenberg, A; Hamroune, J; Lebrun, N; Mietton, L; Saintpierre, B | 1 |
1 review(s) available for isomethyleugenol and Orphan Diseases
| Article | Year |
|---|---|
Differential methylation as a diagnostic biomarker of rare renal diseases: a systematic review.
Topics: Biomarkers; Glomerulonephritis, IGA; Glomerulonephritis, Membranous; Humans; Kidney; Kidney Diseases; Methylation; Polycystic Kidney, Autosomal Dominant; Proteinuria; Rare Diseases | 2019 |
1 other study(ies) available for isomethyleugenol and Orphan Diseases
| Article | Year |
|---|---|
RNA Sequencing and Pathway Analysis Identify Important Pathways Involved in Hypertrichosis and Intellectual Disability in Patients with Wiedemann-Steiner Syndrome.
Topics: Adolescent; Adult; Child; Female; Fibroblasts; Gene Expression Regulation; Histone-Lysine N-Methyltransferase; Histones; Humans; Hypertrichosis; Intellectual Disability; Loss of Function Mutation; Lysine; Male; Methylation; Middle Aged; Myeloid-Lymphoid Leukemia Protein; Nitric Oxide Synthase Type III; Rare Diseases; Sequence Analysis, RNA; Signal Transduction; Syndrome; Transcription, Genetic; Young Adult | 2018 |