valine has been researched along with Hemoglobinopathies in 11 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 8 (72.73) | 18.7374 |
| 1990's | 3 (27.27) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cossu, G; Ferranti, P; Malorni, A; Manca, L; Marino, G; Masala, B; Parlapiano, A; Pucci, P | 1 |
| Davies, SC; Galactéros, F; Henthorn, JS; Kister, J; Promé, D; Wajcman, H | 1 |
| Beris, P; Darbellay, R; Deutsch, S; Frutiger, A; Kister, J; Offord, R; Wajcman, H | 1 |
| Arends, T; Lehmann, H; Plowman, D; Stathopoulou, R | 1 |
| Cohen-Solal, M; Creyssel, R; Delphin, D; Gaillard, L; Rosa, J | 1 |
| Arous, N; Blouquit, Y; Feingold, J; Galacteros, F; Garin, J; Keclard, L; Merault, G; Poyart, C; Rosa, J | 1 |
| Reed, RE; Rucknagel, DL; Winter, WP | 1 |
| Rieder, RF | 1 |
| Blecher, TE; Dacie, JV; French, EA; Gordon-Smith, EC; Lehmann, H; Wiltshirre, BG | 1 |
| Ramot, B; Shchory, M | 1 |
| Ranney, HM | 1 |
1 review(s) available for valine and Hemoglobinopathies
| Article | Year |
|---|---|
Variation in beta-alpha synthesis ratios in thalassemia and hemoglobinopathies.
Topics: Anemia, Hemolytic, Autoimmune; Anemia, Sickle Cell; Bone Marrow; Bone Marrow Cells; Carbon Radioisotopes; Erythrocyte Aging; Erythrocytes; Globins; Hemoglobin C Disease; Hemoglobinopathies; Heterozygote; Homozygote; Humans; Leucine; Peptide Chain Termination, Translational; Peptide Fragments; RNA, Messenger; Thalassemia; Tritium; Trypsin; Valine | 1974 |
10 other study(ies) available for valine and Hemoglobinopathies
| Article | Year |
|---|---|
Hemoglobin Ozieri: a new alpha-chain variant (alpha 71(E20)Ala-->Val). Characterization using FAB- and electrospray-mass spectrometric techniques.
Topics: Alanine; Base Sequence; Fetal Blood; Globins; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Infant, Newborn; Isoelectric Focusing; Italy; Mass Spectrometry; Mutation; Valine | 1993 |
Hb Uxbridge [beta 20 (B2)Val-->Gly]: a new variant with mild increase in oxygen affinity found during a neonatal screening program.
Topics: Female; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Infant, Newborn; Neonatal Screening; Oxygen; Point Mutation; Valine | 1996 |
Hb Iraq-Halabja beta10 (A7) Ala-->Val (GCC-->GTC): a new beta-chain silent variant in a family with multiple Hb disorders.
Topics: Adult; Alanine; Amino Acid Substitution; Child; Child, Preschool; Female; Genetic Variation; Genotype; Globins; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Macromolecular Substances; Male; Middle Aged; Models, Molecular; Pedigree; Phenotype; Point Mutation; Protein Conformation; Protein Structure, Secondary; RNA, Messenger; Valine | 1999 |
Haemoglobin North Shore-Caracas beta 134 (H12) valine replaced by glutamic acid.
Topics: Amino Acid Sequence; Amino Acids; Child; Glutamates; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Male; Peptide Fragments; Valine | 1977 |
[Lyon hemoglobin: discovery of an abnormal hemoglobin due to deletion of aminoacids (beta 17-18 (A 14-15) lys-val equals 0)].
Topics: Adolescent; Amino Acid Sequence; Anemia, Hypochromic; Blood Protein Electrophoresis; Chromatography; Chromosome Aberrations; Genes, Dominant; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Kinetics; Lysine; Male; Mutation; Oxygen; Valine | 1975 |
Hemoglobin La Desirade alpha A2 beta 2 129 (H7) Ala----Val: a new unstable hemoglobin.
Topics: Alanine; Amino Acid Sequence; Black People; Chromatography, High Pressure Liquid; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Isoelectric Focusing; Oxygen; Pedigree; Valine | 1986 |
Haemoglobin inkster (alpha2 85aspartic acid leads to valine beta2) coexisting with beta-thalassaemia in a Caucasian family.
Topics: Amino Acid Sequence; Aspartic Acid; Chromatography, Gel; Chromatography, Ion Exchange; Chromatography, Paper; Cyanogen Bromide; Edetic Acid; Electrophoresis, Paper; Electrophoresis, Starch Gel; Genetics, Medical; Globins; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Models, Structural; Mutation; Thalassemia; Trypsin; Valine | 1974 |
Haemoglobin Nottingham, beta FG 5 (98) valgly: a new unstable haemoglobin producing severe haemolysis.
Topics: Child, Preschool; Female; Glycine; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Infant; Valine | 1973 |
Globin chain synthesis in the marrow and reticulocytes of beta thalassemia, hemoglobin H disease, and beta delta thalassemia.
Topics: Bone Marrow; Bone Marrow Cells; Carbon Isotopes; Chromatography; Globins; Hemoglobinometry; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Leucine; Reticulocytes; Thalassemia; Valine | 1972 |
Interactions of other hemoglobin variants with sickle-cell hemoglobin.
Topics: Anemia, Sickle Cell; Binding Sites; Gels; Glutamates; Hemoglobin C; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Models, Theoretical; Oxygen; Polymers; Valine | 1970 |