deoxyuridine triphosphate has been researched along with HbS Disease in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 1 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Barron-Casella, EA; Casella, JF; Fortenberry, YM; Keefer, JR; Purvis, SH | 1 |
Brown, S; Christiano, AM; Day, NS; Lanzano, P; Piomelli, S; Tadin, M | 1 |
2 other study(ies) available for deoxyuridine triphosphate and HbS Disease
Article | Year |
---|---|
Identification of Aptamers That Bind to Sickle Hemoglobin and Inhibit Its Polymerization.
Topics: Anemia, Sickle Cell; Antisickling Agents; Aptamers, Nucleotide; Cell-Free System; Deoxycytosine Nucleotides; Deoxyuracil Nucleotides; DNA, Complementary; Dose-Response Relationship, Drug; Drug Discovery; Hemoglobin, Sickle; Humans; Polymerization; Pyrimidines; SELEX Aptamer Technique | 2017 |
Rapid prenatal diagnosis of sickle cell diseases using oligonucleotide ligation assay coupled with laser-induced capillary fluorescence detection.
Topics: Anemia, Sickle Cell; Base Sequence; Deoxyuracil Nucleotides; DNA; DNA Ligases; Electrophoresis, Capillary; Female; Genotype; Globins; Hemoglobin A; Hemoglobin C; Hemoglobin, Sickle; Humans; Molecular Sequence Data; Oligonucleotides; Point Mutation; Polymerase Chain Reaction; Pregnancy; Prenatal Diagnosis; Sensitivity and Specificity; Templates, Genetic | 2002 |