4-trifluoromethylaniline has been researched along with Fanconi Anemia in 1 studies
*Fanconi Anemia: Congenital disorder affecting all bone marrow elements, resulting in ANEMIA; LEUKOPENIA; and THROMBOPENIA, and associated with cardiac, renal, and limb malformations as well as dermal pigmentary changes. Spontaneous CHROMOSOME BREAKAGE is a feature of this disease along with predisposition to LEUKEMIA. There are at least 7 complementation groups in Fanconi anemia: FANCA, FANCB, FANCC, FANCD1, FANCD2, FANCE, FANCF, FANCG, and FANCL. (from Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=227650, August 20, 2004) [MeSH]
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Blafkova, J; Cmejla, R; Jelinek, J; Petrtylova, K; Pospisilova, D; Stopka, T | 1 |
1 other study(ies) available for 4-trifluoromethylaniline and Fanconi Anemia
| Article | Year |
|---|---|
Ribosomal proteins S3a, S13, S16, and S24 are not mutated in patients with Diamond-Blackfan anemia.
Topics: Aniline Compounds; Eukaryotic Initiation Factor-2; Fanconi Anemia; Humans; Mutation; Reverse Transcriptase Polymerase Chain Reaction; Ribosomal Proteins; RNA; Sequence Analysis, DNA | 2001 |