arginine has been researched along with Anemia, Hemolytic, Hereditary in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 2 (66.67) | 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 |
|---|---|
| Fujii, H; Kanno, H; Miwa, S | 1 |
| Forget, BG; Gallagher, PG; Marchesi, SL; Mohandas, N; Morrow, JS; Petruzzi, MJ; Weed, SA; Zhang, Z | 1 |
| Jacobs, AS; Ranney, HM; Udem, L; Zalusky, R | 1 |
3 other study(ies) available for arginine and Anemia, Hemolytic, Hereditary
| Article | Year |
|---|---|
Low substrate affinity of pyruvate kinase variant (PK Sapporo) caused by a single amino acid substitution (426 Arg-->Gln) associated with hereditary hemolytic anemia.
Topics: Amino Acid Sequence; Anemia, Hemolytic, Congenital; Arginine; Base Sequence; Cloning, Molecular; DNA; Exons; Female; Genetic Variation; Glutamine; Homozygote; Humans; Kinetics; Molecular Sequence Data; Oligodeoxyribonucleotides; Point Mutation; Polymerase Chain Reaction; Pyruvate Kinase; Restriction Mapping; Reticulocytes | 1993 |
Mutation of a highly conserved residue of betaI spectrin associated with fatal and near-fatal neonatal hemolytic anemia.
Topics: Anemia, Hemolytic, Congenital; Arginine; Base Sequence; Conserved Sequence; Erythrocyte Membrane; Female; Homozygote; Humans; Hydrops Fetalis; Laos; Leucine; Male; Membrane Proteins; Models, Molecular; Muscle, Skeletal; Pedigree; Peptide Mapping; Point Mutation; Polymerase Chain Reaction; Protein Conformation; Sequence Analysis, DNA; Spectrin | 1997 |
Hemoglobin Riverdale-Bronx an unstable hemoglobin resulting from the substitution of arginine for glycine at helical residue B6 of the B beta polypeptide chain.
Topics: Amino Acid Sequence; Anemia, Hemolytic, Congenital; Arginine; Binding Sites; Electrophoresis; Erythrocytes; Female; Glycine; Hemoglobins, Abnormal; Humans; Middle Aged | 1968 |