nadp has been researched along with Thalassemias in 14 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 13 (92.86) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (7.14) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Roos, D; van Zwieten, R; Verhoeven, AJ | 1 |
| SWARUP, S | 1 |
| KLEIHAUER, E | 1 |
| Benatti, U; De Flora, A; Filippi, G; Lenzerini, L; Morelli, A; Piazza, A; Pontremoli, S; Rinaldi, A; Siniscalco, M | 1 |
| Anderson, BB; Clements, JE; Fashola, R; Perry, GM; Salsini, G; Studds, C; Vullo, C | 1 |
| Canestrari, F; Coppa, GV; Cucchiarini, L; Felici, L; Fornaini, G; Giorgi, PL; Magnani, M; Stocchi, O; Stocchi, V | 1 |
| Biermé, R; Gherardi, M; Gourdin, D; Ruffié, J; Vergnes, H; Yoshida, A | 1 |
| Luzzatto, L | 1 |
| Alessio, L; Dioguardi, N; Fiorelli, G; Pabis, A; Sulis, E | 1 |
| Chatterjea, JB; Ghosh, SK; Swarup, S | 1 |
| Gabuzda, TG; Gardner, FH; Laforet, MT | 1 |
| Sartori, E; Zacchello, F | 1 |
| Itie, R; Orsini, A; Perrimond, H; Vovan, L | 1 |
| Baur, EW; Moutlsky, AG; Yoshida, A | 1 |
2 review(s) available for nadp and Thalassemias
| Article | Year |
|---|---|
Inborn defects in the antioxidant systems of human red blood cells.
Topics: Anemia, Hemolytic; Antioxidants; Erythrocytes; Erythropoiesis; Glucosephosphate Dehydrogenase Deficiency; Glutathione; Humans; Malaria; NADP; Oxidation-Reduction; Oxidative Stress; Reactive Oxygen Species; Sickle Cell Trait; Thalassemia | 2014 |
Genetic heterogeneity and pathophysiology of G6PD deficiency.
Topics: Binding Sites; Erythrocytes; Genes; Glucosephosphate Dehydrogenase Deficiency; Half-Life; Humans; Kinetics; Metabolism, Inborn Errors; Models, Biological; Molecular Conformation; Mutation; NADP; Protein Binding; Thalassemia | 1974 |
12 other study(ies) available for nadp and Thalassemias
| Article | Year |
|---|---|
ERYTHROCYTE ENZYMES IN THALASSAEMIA.
Topics: Cholinesterases; Clinical Enzyme Tests; Erythrocytes; Glucosephosphate Dehydrogenase; Glutathione; Hemoglobins; Hemoglobins, Abnormal; Humans; Methemoglobin; NADP; Oxidoreductases; Thalassemia | 1963 |
[ON SOME NEW METHODS IN THE DIAGNOSIS OF HEMATOLOGICAL DISEASES].
Topics: Anemia; Anemia, Hemolytic; Clinical Enzyme Tests; Clinical Laboratory Techniques; Fetal Hemoglobin; Hemoglobins; Hemoglobins, Abnormal; Humans; Methemoglobinemia; NAD; NADP; Thalassemia | 1963 |
Genetic variation in the quantitative levels of an NADP (H)-binding protein (FX) in human erythrocytes.
Topics: Adult; Age Factors; Blood Proteins; Carbohydrate Epimerases; Carrier Proteins; Child; Erythrocytes; Female; Genes; Genetic Linkage; Genetic Variation; Glucosephosphate Dehydrogenase; Glucosephosphate Dehydrogenase Deficiency; Humans; Ketone Oxidoreductases; Male; Mathematics; NADP; Sex Factors; Thalassemia; X Chromosome | 1981 |
Genetic and other influences on red-cell flavin enzymes, pyridoxine phosphate oxidase and glutathione reductase in families with beta-thalassaemia.
Topics: Adult; Erythrocytes; Flavin-Adenine Dinucleotide; Glutathione Reductase; Heterozygote; Humans; Kinetics; Middle Aged; NADP; Oxidoreductases Acting on CH-NH Group Donors; Pyridoxaminephosphate Oxidase; Thalassemia | 1989 |
Redox and energetic state of red blood cells in G6PD deficiency, heterozygous beta-thalassemia and the combination of both.
Topics: Adenine Nucleotides; Child, Preschool; Erythrocytes; Glucosephosphate Dehydrogenase Deficiency; Glutathione; Heterozygote; Humans; Male; NAD; NADP; Oxidation-Reduction; Thalassemia | 1986 |
Glucose-6-phosphate dehydrogenase Toulouse. A new variant with marked instability and severe deficiency discovered in a family of Mediterranean ancestry.
Topics: Child; Electrophoresis, Starch Gel; Favism; France; Genetic Variation; Glucosephosphate Dehydrogenase; Glucosephosphate Dehydrogenase Deficiency; Glutathione; Humans; Hydrogen-Ion Concentration; Italy; Male; Mutation; NADP; Pedigree; Temperature; Thalassemia | 1974 |
[Favism, hemoglobin H, alpha-thalassemia and hemoglobinopathy in various Sardinian families. Studies on glucose-6-phosphate dehydrogenase].
Topics: Electrophoresis; Erythrocytes; Favism; Glucosephosphate Dehydrogenase; Hemoglobinopathies; Hemoglobins, Abnormal; Hemolysis; Humans; Italy; NADP; Thalassemia | 1969 |
Stability of erythrocytic reduced glutathione and nicotinadenine dinucleotide phosphate in HbE-thalassaemia disease.
Topics: Erythrocytes; Glucosephosphate Dehydrogenase; Glutathione; Glutathione Reductase; Hemoglobins, Abnormal; Humans; NADP; Thalassemia | 1966 |
Oxidative precipitation of hemoglobin H and its relation to reduced glutathione.
Topics: Chemical Precipitation; Cyanides; Erythrocytes; Female; Glutathione; Hemoglobins, Abnormal; Humans; Male; NAD; NADP; Oxidation-Reduction; Thalassemia | 1967 |
[Non-spherocytic congenital hemolytic anemias due to G6PD deficiency. Clinical and hematologic aspects and mechanism of hyperhemolysis].
Topics: Age Factors; Anemia, Hemolytic, Congenital Nonspherocytic; Erythrocyte Aging; Erythrocytes; Glucosephosphate Dehydrogenase Deficiency; Hemoglobinometry; Humans; NADP; Thalassemia | 1968 |
[Free nucleotides of erythrocytes in anemias in children. Results of 64 examinations].
Topics: Adenine Nucleotides; Adenosine Triphosphate; Anemia, Hemolytic; Anemia, Hemolytic, Congenital; Anemia, Sickle Cell; Child; Chromatography, Ion Exchange; Elliptocytosis, Hereditary; Erythrocytes; Glucosephosphate Dehydrogenase Deficiency; Hemoglobin C; Hemoglobin C Disease; Hemoglobinopathies; Humans; Hypersplenism; Methods; NAD; NADP; Spectrophotometry; Spherocytosis, Hereditary; Thalassemia | 1969 |
A Philippino glucose-6-phosphate dehydrogenase variant (G6PD Union) with enzyme deficiency and altered substrate specificity.
Topics: Asian People; Coenzymes; Electrophoresis; Erythrocytes; Galactose; Gels; Glucosephosphate Dehydrogenase; Glucosephosphate Dehydrogenase Deficiency; Hexosephosphates; Humans; Hydrogen-Ion Concentration; Immune Sera; Male; Metabolism, Inborn Errors; NADP; Neutralization Tests; Pedigree; Starch; Terminology as Topic; Thalassemia | 1970 |