isomethyleugenol has been researched along with Choreoathetosis Self-Mutilation Hyperuricemia Syndrome in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (50.00) | 18.7374 |
1990's | 2 (50.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Migeon, BR; Wolf, SF | 1 |
Jiralerspong, S; Patel, PI | 1 |
Goto, H; Ogasawara, N; Yamada, Y | 1 |
Jolly, DJ | 1 |
2 review(s) available for isomethyleugenol and Choreoathetosis Self-Mutilation Hyperuricemia Syndrome
Article | Year |
---|---|
Regulation of the hypoxanthine phosphoribosyltransferase gene: in vitro and in vivo approaches.
Topics: Animals; Arthritis, Gouty; Base Sequence; Brain; Cells, Cultured; DNA-Binding Proteins; Enzyme Induction; Erythroid-Specific DNA-Binding Factors; Female; Gene Expression Regulation, Enzymologic; Humans; Hypoxanthine Phosphoribosyltransferase; Lesch-Nyhan Syndrome; Male; Mammals; Methylation; Mice; Mice, Knockout; Mice, Transgenic; Molecular Sequence Data; Nerve Tissue Proteins; Promoter Regions, Genetic; Pseudogenes; Purines; Rodentia; Species Specificity; Transcription Factors; X Chromosome; YY1 Transcription Factor | 1996 |
The role of the HPRT gene in human disease.
Topics: Amino Acid Sequence; Animals; Base Sequence; Brain; Chromosome Mapping; Gene Expression Regulation; Genes; Genetic Engineering; Gout; Humans; Hypoxanthine Phosphoribosyltransferase; Lesch-Nyhan Syndrome; Methylation; Mice; Neurotransmitter Agents; Purines; X Chromosome | 1986 |
2 other study(ies) available for isomethyleugenol and Choreoathetosis Self-Mutilation Hyperuricemia Syndrome
Article | Year |
---|---|
Implications for X-chromosome regulation from studies of human X-chromosome DNA.
Topics: Adult; Animals; Cells, Cultured; Cloning, Molecular; DNA; Female; Fibroblasts; Humans; Hybrid Cells; Karyotyping; Lesch-Nyhan Syndrome; Male; Methylation; Mice; Sex Chromosomes; X Chromosome | 1983 |
HPRT gene mutations in a female Lesch-Nyhan patient.
Topics: Adolescent; Base Sequence; Chromosome Deletion; DNA; Dosage Compensation, Genetic; Female; Humans; Hypoxanthine Phosphoribosyltransferase; Lesch-Nyhan Syndrome; Methylation; Molecular Sequence Data; X Chromosome | 1991 |