isomethyleugenol has been researched along with Thalassemias in 15 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 13 (86.67) | 18.7374 |
| 1990's | 2 (13.33) | 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 |
|---|---|
| Anagnou, NP; DeSimone, J; Humphries, RK; Keller, GH; Keller, P; Ley, TJ; Nienhuis, AW; Turner, PH; Young, NS | 1 |
| Benz, EJ | 1 |
| DeSimone, J; Heller, P; Ley, TJ; Nienhuis, AW; Noguchi, CT; Schechter, AN; Turner, PH | 1 |
| Adamson, JW | 1 |
| DeSimone, J; Heller, P | 1 |
| Flavell, RA | 1 |
| Collins, FS; Weissman, SM | 1 |
| Lim, SK; Maquat, LE | 1 |
| Ao, ZH; Chen, SS; Huang, YW; Jia, PC; Jin, HQ; Liang, CC; Liu, DP; Liu, LJ; Wang, RX; Zha, DY | 1 |
| Karlsson, S; Nienhuis, AW | 1 |
| Cole, JL; Collins, FS; Iannuzzi, MC; Lockwood, WK | 1 |
| Feingold, EA; Forget, BG | 1 |
| Jones, PA | 1 |
| Ley, TJ; Nienhuis, AW | 1 |
| Delgrosso, K; Poncz, M; Schwartz, E; Surrey, S; Sutton, M | 1 |
5 review(s) available for isomethyleugenol and Thalassemias
| Article | Year |
|---|---|
5-Azacytidine and fetal hemoglobin.
Topics: Adult; Anemia, Sickle Cell; Animals; Azacitidine; Carcinogens; Disease Models, Animal; DNA; Fetal Hemoglobin; Gene Expression Regulation; Humans; Male; Methylation; Middle Aged; Papio; Thalassemia | 1984 |
The molecular genetics of human hemoglobin.
Topics: Biological Evolution; Chromosome Deletion; Codon; Deoxyribonuclease I; Gene Conversion; Gene Expression Regulation; Genes; Genetic Linkage; Globins; Hemoglobins; Humans; Methylation; Mutation; Polymorphism, Genetic; Promoter Regions, Genetic; Protein Biosynthesis; RNA Splicing; RNA, Messenger; Thalassemia; Transcription, Genetic | 1984 |
Developmental regulation of human globin genes.
Topics: Azacitidine; Chromatin; Chromosome Deletion; Chromosomes, Human, 16-18; Chromosomes, Human, 6-12 and X; Enhancer Elements, Genetic; Fetal Hemoglobin; Gene Expression Regulation; Genes; Globins; Hemoglobins; Humans; Methylation; Mutation; Poly A; Promoter Regions, Genetic; Protein Biosynthesis; Repetitive Sequences, Nucleic Acid; RNA Caps; RNA Processing, Post-Transcriptional; RNA, Messenger; Thalassemia; Transcription Factors | 1985 |
Altering gene expression with 5-azacytidine.
Topics: Anemia, Sickle Cell; Animals; Azacitidine; Cell Differentiation; Cell Line; DNA; Embryo, Mammalian; Embryo, Nonmammalian; Fetal Hemoglobin; Gene Expression Regulation; Genes; Genes, Regulator; Methylation; Mutation; Neoplasms; Thalassemia; Thymidine Kinase | 1985 |
Induction of hemoglobin F synthesis in patients with beta thalassemia.
Topics: Animals; Azacitidine; DNA; Erythroblasts; Female; Fetal Hemoglobin; Gene Expression Regulation; Globins; Humans; Hydroxyurea; Methylation; Papio; Thalassemia | 1985 |
10 other study(ies) available for isomethyleugenol and Thalassemias
| Article | Year |
|---|---|
5-azacytidine selectively increases gamma-globin synthesis in a patient with beta+ thalassemia.
Topics: Adult; Azacitidine; DNA; Erythropoiesis; Gene Expression Regulation; Globins; Hemoglobins; Humans; Male; Methylation; RNA, Messenger; Stimulation, Chemical; Thalassemia | 1982 |
Clinical management of gene expression.
Topics: Azacitidine; DNA; Fetal Hemoglobin; Gene Expression Regulation; Globins; Humans; Methylation; Thalassemia | 1982 |
5-Azacytidine increases gamma-globin synthesis and reduces the proportion of dense cells in patients with sickle cell anemia.
Topics: Adult; Anemia, Sickle Cell; Azacitidine; Bone Marrow Cells; DNA; Erythrocytes; Fetal Hemoglobin; Globins; Humans; Male; Methylation; Middle Aged; RNA, Messenger; Thalassemia | 1983 |
Hemoglobin--from F to A, and back.
Topics: Anemia, Sickle Cell; Azacitidine; DNA; Fetal Hemoglobin; Humans; Hydroxyurea; Methylation; Thalassemia | 1984 |
The eighteenth Colworth Medal Lecture. The globin genes of rabbit and man.
Topics: Animals; Base Sequence; DNA; DNA, Recombinant; Genes; Genetic Techniques; Globins; HeLa Cells; Humans; Methylation; Operon; Phenotype; Rabbits; RNA, Messenger; Simian virus 40; Thalassemia; Transcription, Genetic | 1983 |
Human beta-globin mRNAs that harbor a nonsense codon are degraded in murine erythroid tissues to intermediates lacking regions of exon I or exons I and II that have a cap-like structure at the 5' termini.
Topics: Animals; Antibodies, Monoclonal; Base Sequence; Codon; Erythroid Precursor Cells; Exons; Exonucleases; Globins; Humans; Methylation; Methyltransferases; Mice; Molecular Sequence Data; Pyrophosphatases; RNA Caps; RNA Processing, Post-Transcriptional; RNA, Messenger; Spleen; Thalassemia | 1992 |
Treatment of severe beta-thalassemia (patients) with myleran.
Topics: Busulfan; Child; DNA; Erythrocyte Count; Female; Fetal Hemoglobin; Globins; Humans; Leukocyte Count; Male; Methylation; Sister Chromatid Exchange; Thalassemia; Time Factors | 1990 |
The deletion in both common types of hereditary persistence of fetal hemoglobin is approximately 105 kilobases.
Topics: Chromatin; Chromosome Deletion; Chromosome Mapping; DNA Restriction Enzymes; Electrophoresis, Agar Gel; Fetal Hemoglobin; Globins; Humans; Methylation; Multigene Family; Thalassemia | 1987 |
The breakpoint of a large deletion causing hereditary persistence of fetal hemoglobin occurs within an erythroid DNA domain remote from the beta-globin gene cluster.
Topics: Amino Acid Sequence; Base Sequence; Blotting, Southern; Chromosome Deletion; Enhancer Elements, Genetic; Erythroid Precursor Cells; Fetal Hemoglobin; Gene Expression Regulation; Globins; Hemoglobinopathies; Humans; Methylation; Molecular Sequence Data; Regulatory Sequences, Nucleic Acid; Restriction Mapping; Thalassemia; Transcription, Genetic | 1989 |
DNA methylation in hereditary persistence of fetal hemoglobin (HPFH-2).
Topics: DNA; Female; Genes; Globins; Hemoglobin, Sickle; Humans; Infant; Male; Methylation; Thalassemia | 1987 |