isomethyleugenol has been researched along with Dwarfism in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Abdel-Hamid, MS; Abdel-Salam, GM; Afifi, HH; Alkuraya, FS; Alomar, R; Emam, BA; Guy, MP; Ismail, SI; Phizicky, EM; Shaheen, R | 1 |
| Chen, JK; Cheung, P; Gozani, O; Ishibe-Murakami, S; Kuo, AJ; Patel, DJ; Song, J; Yamazoe, S | 1 |
| Calvert, GD | 1 |
3 other study(ies) available for isomethyleugenol and Dwarfism
| Article | Year |
|---|---|
Mutation in WDR4 impairs tRNA m(7)G46 methylation and causes a distinct form of microcephalic primordial dwarfism.
Topics: Dwarfism; Exome; Facies; GTP-Binding Proteins; Humans; Methylation; Microcephaly; Mutation, Missense; RNA, Transfer; Saccharomyces cerevisiae | 2015 |
The BAH domain of ORC1 links H4K20me2 to DNA replication licensing and Meier-Gorlin syndrome.
Topics: Animals; Carrier Proteins; Cell Cycle; Cell Line; Chromatin; Congenital Microtia; Crystallography, X-Ray; Disease Models, Animal; DNA Replication; Dwarfism; Ear; Growth Disorders; Histones; Humans; Lysine; Methylation; Micrognathism; Models, Molecular; Origin Recognition Complex; Patella; Protein Structure, Tertiary; Replication Origin; Zebrafish; Zebrafish Proteins | 2012 |
Trimethylaminuria and inherited Noonan's syndrome.
Topics: Abnormalities, Multiple; Adult; Amines; Blood Coagulation Disorders; Cryptorchidism; Dwarfism; Humans; Male; Methylation; Pedigree; Turner Syndrome | 1973 |