thymine has been researched along with Anemia, Cooley's in 6 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "A beta-thalassemia intermedia phenotype can be caused by multiple genotypes." | 1.30 | Double heterozygosity for the codon beta 39 C-to-T nonsense mutation and a triplicate alpha-globin gene locus can cause "dominantly" inherited beta-thalassemia intermedia. ( Files, JC; Harrell, A; Li, J; Plonczynski, M; Rhodes, SL; Safaya, S; Steinberg, MH, 1999) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 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 | 1 (16.67) | 2.80 |
| Authors | Studies |
|---|---|
| Zarkada, E | 1 |
| Yfanti, E | 1 |
| Teli, A | 1 |
| Balassopoulou, A | 1 |
| Sinopoulou, K | 1 |
| Theodoridou, S | 1 |
| Irenge, LM | 1 |
| Derclaye, I | 1 |
| Heusterspreute, M | 1 |
| Gala, JL | 1 |
| Philippe, M | 1 |
| Rhodes, SL | 1 |
| Plonczynski, M | 1 |
| Harrell, A | 1 |
| Li, J | 1 |
| Safaya, S | 1 |
| Files, JC | 1 |
| Steinberg, MH | 1 |
| Beris, P | 1 |
| Kitundu, MN | 1 |
| Baysal, E | 1 |
| Oner, C | 1 |
| Lanclos, KD | 1 |
| Dimovski, AJ | 1 |
| Kutlar, F | 1 |
| Huisman, TH | 1 |
| Fedorov, AN | 1 |
| Rasulov, EM | 1 |
| Bocharova, TN | 1 |
| Smirnova, EA | 1 |
| Limborska, SA | 1 |
| Costa, FF | 1 |
| Figueredo, MS | 1 |
| Sonati, MF | 1 |
| Kimura, EM | 1 |
| Martins, CS | 1 |
6 other studies available for thymine and Anemia, Cooley's
| Article | Year |
|---|---|
Rare Pathogenic β
Topics: beta-Globins; beta-Thalassemia; Codon, Terminator; DNA Mutational Analysis; Emigrants and Immigrants | 2022 |
Beta-thalassaemia in indigenous Belgians: an update.
Topics: Adenine; Amino Acid Substitution; Anemia; Anemia, Hypochromic; Belgium; Beta-Globulins; beta-Thalass | 1997 |
Double heterozygosity for the codon beta 39 C-to-T nonsense mutation and a triplicate alpha-globin gene locus can cause "dominantly" inherited beta-thalassemia intermedia.
Topics: alpha-Thalassemia; beta-Thalassemia; Codon; Cytosine; Female; Globins; Heterozygote; Humans; Mutatio | 1999 |
Black beta-thalassemia homozygotes with specific sequence variations in the 5' hypersensitive site-2 of the locus control region have high levels of fetal hemoglobin.
Topics: Adenine; Adolescent; Adult; Aged; Aged, 80 and over; Base Sequence; beta-Thalassemia; Black People; | 1992 |
The T-->A mutation at position -30 of the beta-globin gene found in a Karachai patient with beta-thalassemia intermedia.
Topics: Adenine; Adult; beta-Thalassemia; Female; Georgia (Republic); Globins; Humans; Mutation; Thymine | 1992 |
The IVS-I-110 (G-->T) and codon 39 (C-->T) beta-thalassemia mutations in association with alpha-thal-2 (-3.7 Kb) and Hb Hasharon [alpha 47(CE5)Asp-->His] in a Brazilian patient.
Topics: alpha-Thalassemia; Base Sequence; beta-Thalassemia; Brazil; Codon; Cytosine; Female; Guanine; Hemogl | 1992 |