glutamine has been researched along with Anemia, Hemolytic, Congenital in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (50.00) | 18.7374 |
1990's | 1 (50.00) | 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 |
Braunsteiner, H; Lehmann, H; Lorkin, PA; Pietschmann, H | 1 |
2 other study(ies) available for glutamine and Anemia, Hemolytic, Congenital
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 |
Structure of haemoglobin Wien beta 130 (H8) tyrosine-aspartic acid: an unstable haemoglobin variant.
Topics: Adult; Amino Acid Sequence; Amino Acids; Anemia, Hemolytic, Congenital; Aspartic Acid; Austria; Carboxypeptidases; Electrophoresis, Paper; Electrophoresis, Starch Gel; Fetal Hemoglobin; Genetic Variation; Glutamine; Hemoglobins, Abnormal; Humans; Male; Trypsin | 1974 |