lysine has been researched along with Elliptocytosis, Hereditary in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (50.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Alloisio, N; Baklouti, F; Dalla Venezia, N; Delaunay, J; Ducluzeau, MT; Lefrançois, P; Lorenzo, F; Morlé, L; Roda, L | 1 |
Abe, Y; Askin, D; Bruce, LJ; Hamasaki, N; Hamasaki, T; Kuma, H; Tanner, MJ | 1 |
2 other study(ies) available for lysine and Elliptocytosis, Hereditary
Article | Year |
---|---|
Protein 4.1 deficiency associated with an altered binding to the spectrin-actin complex of the red cell membrane skeleton.
Topics: Actins; Amino Acid Sequence; Base Sequence; Cloning, Molecular; Cytoskeletal Proteins; DNA Mutational Analysis; Elliptocytosis, Hereditary; Erythrocyte Membrane; Female; France; Humans; Lysine; Male; Membrane Proteins; Molecular Sequence Data; Neuropeptides; Pedigree; Protein Conformation; Recombinant Fusion Proteins; Sequence Deletion; Spectrin | 1994 |
Molecular basis and functional consequences of the dominant effects of the mutant band 3 on the structure of normal band 3 in Southeast Asian ovalocytosis.
Topics: Amino Acid Sequence; Anion Exchange Protein 1, Erythrocyte; Biotin; Chromatography, High Pressure Liquid; Elliptocytosis, Hereditary; Erythrocyte Membrane; Erythrocytes, Abnormal; Heterozygote; Humans; Hydrolysis; Lysine; Molecular Sequence Data; Mutation; Succinimides | 2002 |