isomethyleugenol has been researched along with Wiskott-Aldrich Syndrome in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 3 (75.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Candotti, F; D'Silva, S; Kottangada, P; Ramgopal, A; Sadhukhan, S; Sarkar, K; Selvakumar, A; Taylor, MD; Vyas, YM | 1 |
| Chen, ZY; Craig, IW; Hendriks, RW; Hinds, H; Schuurman, RK | 1 |
| Chen, ZY; Craig, IW; Hendriks, RW; Hinds, H; Kraakman, ME; Schuurman, RK | 1 |
| Boyd, Y; Carter, J; Espanol, T; Goodship, J; Levinsky, RJ; Malcolm, S | 1 |
4 other study(ies) available for isomethyleugenol and Wiskott-Aldrich Syndrome
| Article | Year |
|---|---|
Nuclear role of WASp in the pathogenesis of dysregulated TH1 immunity in human Wiskott-Aldrich syndrome.
Topics: Actins; Cell Differentiation; Cell Nucleus; Cells, Cultured; Cellular Reprogramming; Chromatin; DNA; Epigenesis, Genetic; Genetic Loci; Genome, Human; Histones; Humans; Immunity; Methylation; Mutant Proteins; Promoter Regions, Genetic; Protein Binding; Protein Transport; T-Box Domain Proteins; Th1 Cells; Transcription, Genetic; Wiskott-Aldrich Syndrome; Wiskott-Aldrich Syndrome Protein | 2010 |
Carrier detection in X-linked immunodeficiencies. I: A PCR-based X chromosome inactivation assay at the MAOA locus.
Topics: Agammaglobulinemia; Chromosome Mapping; Dinucleoside Phosphates; Dosage Compensation, Genetic; Exons; Female; Genetic Carrier Screening; Genetic Linkage; Humans; Immunologic Deficiency Syndromes; Male; Methylation; Monoamine Oxidase; Polymerase Chain Reaction; Severe Combined Immunodeficiency; Wiskott-Aldrich Syndrome; X Chromosome | 1993 |
Carrier detection in X-linked immunodeficiencies. II: An X inactivation assay based on differential methylation of a line-1 repeat at the DXS255 locus.
Topics: Agammaglobulinemia; Chromosome Mapping; Dinucleoside Phosphates; Dosage Compensation, Genetic; Female; Genetic Carrier Screening; Genetic Linkage; Humans; Immunologic Deficiency Syndromes; Male; Methylation; Repetitive Sequences, Nucleic Acid; Severe Combined Immunodeficiency; Wiskott-Aldrich Syndrome; X Chromosome | 1993 |
Carrier detection in Wiskott-Aldrich syndrome: combined use of M27 beta for X-inactivation studies and as a linked probe.
Topics: Alleles; DNA Probes; Dosage Compensation, Genetic; Female; Genetic Carrier Screening; Humans; Male; Methylation; Nucleic Acid Hybridization; Pedigree; Wiskott-Aldrich Syndrome; X Chromosome | 1991 |