isomethyleugenol has been researched along with Agammaglobulinemia in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (16.67) | 18.7374 |
| 1990's | 5 (83.33) | 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 |
|---|---|
| Conley, ME; Parolini, O; Rohrer, J; Shapiro, LH | 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 |
| Alterman, LA; de Alwis, M; Genet, S; Jones, A; Kinnon, C; Levinsky, RJ; Lovering, R; Malcolm, S; Middleton-Price, H; Morgan, G | 1 |
| Abe, T; Kamachi, Y; Matsuoka, H; Torii, S; Tsuge, I | 1 |
| Civin, CI; Fearon, ER; Pardoll, DM; Vogelstein, B; Winkelstein, JA | 1 |
6 other study(ies) available for isomethyleugenol and Agammaglobulinemia
| Article | Year |
|---|---|
B-cell-specific demethylation of BTK, the defective gene in X-linked agammaglobulinemia.
Topics: Agammaglobulinaemia Tyrosine Kinase; Agammaglobulinemia; B-Lymphocytes; Base Sequence; Cell Line; Deoxyribonuclease HpaII; Deoxyribonucleases, Type II Site-Specific; DNA Primers; Genetic Linkage; Humans; Lymphocyte Activation; Methylation; Molecular Sequence Data; Protein-Tyrosine Kinases; T-Lymphocytes; X Chromosome | 1995 |
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 determination for X-linked agammaglobulinemia using X inactivation analysis of purified B cells.
Topics: Agammaglobulinemia; B-Lymphocytes; Base Sequence; Cell Separation; DNA; DNA Primers; Dosage Compensation, Genetic; Female; Genetic Carrier Screening; Genetic Linkage; Humans; Methylation; Molecular Sequence Data; Polymerase Chain Reaction; Receptors, Androgen; X Chromosome | 1993 |
X chromosome inactivation analysis to distinguish sporadic cases of X-linked agammaglobulinaemia from common variable immunodeficiency.
Topics: Adult; Agammaglobulinemia; B-Lymphocytes; Child, Preschool; Diagnosis, Differential; DNA; Dosage Compensation, Genetic; Female; Humans; Hypoxanthine Phosphoribosyltransferase; Immunologic Deficiency Syndromes; Infant; Male; Methylation; Phosphoglycerate Kinase; Polymorphism, Genetic; X Chromosome | 1993 |
Carrier detection in X-linked agammaglobulinemia by analysis of X-chromosome inactivation.
Topics: Agammaglobulinemia; B-Lymphocytes; Dosage Compensation, Genetic; Female; Genetic Carrier Screening; Genetic Linkage; Humans; Male; Methylation; Polymorphism, Restriction Fragment Length; T-Lymphocytes; X Chromosome | 1987 |