Page last updated: 2024-08-17

lysine and Thalassemia

lysine has been researched along with Thalassemia in 12 studies

Research

Studies (12)

TimeframeStudies, this research(%)All Research%
pre-199011 (91.67)18.7374
1990's1 (8.33)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Dozy, AM; Kan, YW; Roy, KL; Temple, GF1
Headlee, ME; Henson, J; Huisman, TH; Lam, H; Wilson, JB; Yi-Tao, Z1
Conner, R; Fairbanks, VF; Hoyer, JD; Thibodeau, SN; Viker, KA; Wick, MJ1
Gaburro, D; Vigi, V; Volpato, S1
Hunter, AR; Jackson, RJ1
Gacon, G; Labie, D; Najman, A; Wajcman, H1
Bonenti, G1
Anderson, WF; Gilbert, JM; Nienhuis, AW; Thornton, AG1
Barclay, GP; Charlesworth, D; Lehmann, H1
Bargellesi, A; Conconi, F; Pontremoli, S1
Honig, GR; Mason, RG; Rowan, BQ1
Bradley, TB; Jacobs, AS; Ramot, B; Ranney, HM1

Other Studies

12 other study(ies) available for lysine and Thalassemia

ArticleYear
Construction of a functional human suppressor tRNA gene: an approach to gene therapy for beta-thalassaemia.
    Nature, 1982, Apr-08, Volume: 296, Issue:5857

    Topics: Anticodon; Genes; Humans; Lysine; Mutation; Peptide Chain Termination, Translational; RNA, Transfer; Suppression, Genetic; Thalassemia; Transcription, Genetic

1982
Identification of hemoglobin G-Philadelphia (alpha 68 Asn replaced by Lys) and hemoglobin Matsue-Oki (alpha 75 Asp replaced by Asn) in a black infant.
    Biochimica et biophysica acta, 1982, Oct-05, Volume: 707, Issue:2

    Topics: Adolescent; Adult; Asparagine; Aspartic Acid; Black People; Child; Female; Genetic Carrier Screening; Genetic Variation; Hemoglobins, Abnormal; Humans; Infant; Lysine; Male; Mutation; Pedigree; Peptide Fragments; Thalassemia

1982
Hb Tak confirmed by DNA analysis: not expressed as thalassemia in a Hb Tak/Hb E compound heterozygote.
    Hemoglobin, 1998, Volume: 22, Issue:1

    Topics: Adult; Amino Acid Substitution; Cambodia; Genetic Carrier Screening; Glutamic Acid; Hemoglobin A; Hemoglobin E; Hemoglobins, Abnormal; Humans; Lysine; Male; Mutation; Sequence Analysis, DNA; Thalassemia

1998
Diagnosis of beta thalassaemia in the newborn by means of haemoglobin synthesis.
    Acta paediatrica Scandinavica, 1970, Volume: 59, Issue:5

    Topics: Alpha-Globulins; Beta-Globulins; Chromatography; Erythrocyte Count; Female; Hemoglobins; Humans; Infant, Newborn; Infant, Newborn, Diseases; Leucine; Lysine; Male; Osmotic Fragility; Thalassemia; Tritium; Valine

1970
Control of haemoglobin synthesis: coordination of alpha and beta chain synthesis.
    Hamatologie und Bluttransfusion, 1972, Volume: 10

    Topics: Animals; Carbon Radioisotopes; Chromatography, Gel; Cycloheximide; Globins; Heme; Hemoglobins; Humans; Iron; Lysine; Peptide Chain Initiation, Translational; Peptide Fragments; Puromycin; Rabbits; Reticulocytes; Thalassemia; Tritium

1972
Hemoglobin E: its oxygen affinity in relation with the ionic environment.
    FEBS letters, 1974, Apr-15, Volume: 41, Issue:1

    Topics: Binding Sites; Chromatography, Gel; Chromatography, Ion Exchange; Diphosphoglyceric Acids; Erythrocytes; Female; France; Glutamates; Hemoglobins, Abnormal; Heterozygote; Humans; Indonesia; Kinetics; Lysine; Male; Oxygen; Oxyhemoglobins; Pedigree; Protein Binding; Spectrophotometry; Thalassemia

1974
[Considerations on the beta-lysine bactericidal power of the blood of children with thalassemia major].
    Minerva pediatrica, 1968, Oct-13, Volume: 20, Issue:41

    Topics: Bacillus subtilis; Child; Child, Preschool; Humans; Infant; Lysine; Thalassemia

1968
Cell-free hemoglobin synthesis in beta-thalassemia.
    Proceedings of the National Academy of Sciences of the United States of America, 1970, Volume: 67, Issue:4

    Topics: Anemia, Hemolytic, Autoimmune; Anemia, Sickle Cell; Animals; Carbon Isotopes; Cell-Free System; Chromatography; Hemoglobins; Humans; In Vitro Techniques; Leucine; Lysine; Methylcellulose; Rabbits; Reticulocytes; Ribosomes; Thalassemia; Tritium

1970
Abnormal haemoglobins in Zambia. A new haemoglobin Zambia alpha-60 (E9) lysine--asparagine.
    British medical journal, 1969, Dec-06, Volume: 4, Issue:5683

    Topics: Adult; Anemia, Sickle Cell; Asparagine; Blood Protein Electrophoresis; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Infant; Lysine; Thalassemia; Zambia

1969
Excess of alpha-globin synthesis in homozygous beta-thalassemia. Its cytoplasmic molecular forms.
    European journal of biochemistry, 1968, Volume: 5, Issue:3

    Topics: Adult; Blood Proteins; Centrifugation, Density Gradient; Child; Child, Preschool; Chromatography, Ion Exchange; Cytoplasm; Erythrocytes; Globins; Heme; Hemoglobins; Hemolysis; Homozygote; Humans; Infant, Newborn; Infant, Premature; Leucine; Lysine; Peptides; Thalassemia; Tritium; Valine

1968
Unequal synthesis of complementary globin chains of human fetal hemoglobin by the effect of L-O-methylthreonine.
    The Journal of biological chemistry, 1969, Apr-25, Volume: 244, Issue:8

    Topics: Blood Proteins; Carbon Isotopes; Chromatography, Gel; Complement System Proteins; Depression, Chemical; Erythroblastosis, Fetal; Female; Fetal Hemoglobin; Globins; Heme; Hemolysis; Humans; In Vitro Techniques; Infant, Newborn; Isoleucine; Leucine; Lysine; Peptide Biosynthesis; Pregnancy; Solubility; Thalassemia; Threonine

1969
Hemoglobin NYU, a delta chain variant, alpha 2 delta 2 lys.
    The Journal of clinical investigation, 1969, Volume: 48, Issue:11

    Topics: Adolescent; Asparagine; Blood Protein Disorders; Blood Protein Electrophoresis; Chemical Phenomena; Chemistry; Chromatography; Female; Gels; Hemoglobins, Abnormal; Humans; Israel; Jews; Lysine; Male; New York City; Pedigree; Protein Hydrolysates; Starch; Thalassemia

1969