diepoxybutane has been researched along with Bone Marrow Diseases in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (50.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Alter, BP; Fargo, JH; Giri, N; Olson, SB; Rochowski, A; Savage, SA | 1 |
| D'Andrea, AD; Haining, N; Montes de Oca, R; Moreau, LA; Nathan, DG; Shimamura, A; Svenson, JL | 1 |
| Cho, D; Cho, SH; Hong, WP; Hwang, TJ; Kim, CJ; Kook, H; Park, JY; Ryang, DW; Yoon, WS | 1 |
| Bungey, J; Dokal, I; Hows, J; Luzzatto, L; Oscier, D; Williamson, P | 1 |
1 trial(s) available for diepoxybutane and Bone Marrow Diseases
| Article | Year |
|---|---|
Fanconi anemia screening by diepoxybutane and mitomicin C tests in Korean children with bone marrow failure syndromes.
Topics: Adolescent; Bone Marrow Diseases; Child; Child, Preschool; Epoxy Compounds; Fanconi Anemia; Female; Humans; Infant; Infant, Newborn; Korea; Male; Mitomycin; Mutagens | 1998 |
3 other study(ies) available for diepoxybutane and Bone Marrow Diseases
| Article | Year |
|---|---|
Comparison of chromosome breakage in non-mosaic and mosaic patients with Fanconi anemia, relatives, and patients with other inherited bone marrow failure syndromes.
Topics: Adolescent; Adult; Aged; Anemia, Aplastic; Bone Marrow Diseases; Bone Marrow Failure Disorders; Child; Child, Preschool; Chromosome Breakage; Cohort Studies; Epoxy Compounds; Fanconi Anemia; Female; Genetic Carrier Screening; Genotype; Hemoglobinuria, Paroxysmal; Humans; Infant; Lymphocytes; Male; Middle Aged; Mitomycin; Mosaicism; Mutagens; Young Adult | 2014 |
A novel diagnostic screen for defects in the Fanconi anemia pathway.
Topics: Blotting, Western; Bone Marrow Diseases; Cell Line, Transformed; Chromosome Breakage; Chromosomes, Human; DNA, Complementary; Epoxy Compounds; Fanconi Anemia; Fanconi Anemia Complementation Group D2 Protein; Genetic Heterogeneity; Genetic Testing; Genetic Vectors; Humans; Lymphocytes; Microscopy, Fluorescence; Mitomycin; Nuclear Proteins; Protein Processing, Post-Translational; Retroviridae; Transfection; Ubiquitin | 2002 |
Dyskeratosis congenita fibroblasts are abnormal and have unbalanced chromosomal rearrangements.
Topics: Adolescent; Adult; Bone Marrow Diseases; Cell Survival; Cells, Cultured; Child; Chromosome Aberrations; Chromosome Disorders; Chromosome Mapping; Epoxy Compounds; Female; Fibroblasts; Gene Rearrangement; Genetic Linkage; Humans; Karyotyping; Male; Mutagens; Pedigree; Polymorphism, Restriction Fragment Length; Skin; X Chromosome | 1992 |