Page last updated: 2024-08-17

lysine and Elliptocytosis, Hereditary

lysine has been researched along with Elliptocytosis, Hereditary in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (50.00)18.2507
2000's1 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Alloisio, N; Baklouti, F; Dalla Venezia, N; Delaunay, J; Ducluzeau, MT; Lefrançois, P; Lorenzo, F; Morlé, L; Roda, L1
Abe, Y; Askin, D; Bruce, LJ; Hamasaki, N; Hamasaki, T; Kuma, H; Tanner, MJ1

Other Studies

2 other study(ies) available for lysine and Elliptocytosis, Hereditary

ArticleYear
Protein 4.1 deficiency associated with an altered binding to the spectrin-actin complex of the red cell membrane skeleton.
    The Journal of clinical investigation, 1994, Volume: 94, Issue:4

    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.
    Biochemistry, 2002, Mar-12, Volume: 41, Issue:10

    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