leucine and Hemoglobinopathies

leucine has been researched along with Hemoglobinopathies in 21 studies

Research

Studies (21)

Timeframe	Studies, this research(%)	All Research%
pre-1990	20 (95.24)	18.7374
1990's	1 (4.76)	18.2507
2000's	0 (0.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Batelaan, D; Bernini, LF; Giordano, PC; Harteveld, CL; Van Delft, P	1
Kendall, A; Lehmann, H; Oune, N; Wiltshire, B; Young, S	1
Harris, HF; Huisman, TH; Kutlar, A; Kutlar, F; Wilson, JB	1
Clegg, JB; Knox-Macaulay, HH; Pembrey, ME; Weatherall, DJ	1
Feldman, R; Rieder, RF	1
Dozy, AM; Kan, YW; Todd, D	1
Piddington, SK; White, JM	1
James, GW; Rieder, RF	1
Lang, A; Lehmann, H; White, JM	1
Bank, A; Dow, LW; Grossbard, E; Terada, M	1
Rieder, RF	1
Gallo, E; Mazza, U; Pich, PG; Pinna, G; Pugliatti, L; Ricco, G	1
Benz, EJ; Forget, BG; Swerdlow, PS	1
Cividalli, G; Crookston, MC; Kan, Y; Nathan, DG	1
Chang, H; Cividalli, G; Frigoletto, FD; Hobbins, JC; Kan, YW; Mahoney, MJ; Nathan, DG	1
Ramot, B; Shchory, M	1
Bannister, D; Clegg, JB; MacNeish, AS; Mann, JR; Weatherall, DJ; Wood, WG	1
Clark, KG; Lehmann, H; Lorkin, PA; Wiltshire, BG	1
Atwater, J; Gill, F; Schwartz, E	1
Charlesworth, D; Hollán, SR; Lehmann, H; Lorkin, PA; Miltényi, M; Szelényi, JG	1
Kan, YW; Nathan, DG; Schwartz, E	1

Reviews

1 review(s) available for leucine and Hemoglobinopathies

Article	Year
Variation in beta-alpha synthesis ratios in thalassemia and hemoglobinopathies. Annals of the New York Academy of Sciences, 1974, Volume: 232, Issue:0 Topics: Anemia, Hemolytic, Autoimmune; Anemia, Sickle Cell; Bone Marrow; Bone Marrow Cells; Carbon Radioisotopes; Erythrocyte Aging; Erythrocytes; Globins; Hemoglobin C Disease; Hemoglobinopathies; Heterozygote; Homozygote; Humans; Leucine; Peptide Chain Termination, Translational; Peptide Fragments; RNA, Messenger; Thalassemia; Tritium; Trypsin; Valine	1974

Article

Year

Variation in beta-alpha synthesis ratios in thalassemia and hemoglobinopathies.

Annals of the New York Academy of Sciences, 1974, Volume: 232, Issue:0

Topics: Anemia, Hemolytic, Autoimmune; Anemia, Sickle Cell; Bone Marrow; Bone Marrow Cells; Carbon Radioisotopes; Erythrocyte Aging; Erythrocytes; Globins; Hemoglobin C Disease; Hemoglobinopathies; Heterozygote; Homozygote; Humans; Leucine; Peptide Chain Termination, Translational; Peptide Fragments; RNA, Messenger; Thalassemia; Tritium; Trypsin; Valine

1974

Other Studies

20 other study(ies) available for leucine and Hemoglobinopathies

Article	Year
Haemoglobinopathy analyses in the Netherlands: a report of an in vitro globin chain biosynthesis survey using a rapid, modified method. Clinical and laboratory haematology, 1999, Volume: 21, Issue:4 Topics: alpha-Thalassemia; beta-Thalassemia; Diagnosis, Differential; Gene Frequency; Genetic Testing; Genetic Variation; Globins; Hemoglobin SC Disease; Hemoglobinopathies; Hemoglobins, Abnormal; Heterozygote; Homozygote; Humans; Leucine; Netherlands; Reticulocytes; Tritium	1999
The unstable Hb Genova (beta 28Leu replaced by Pro) in an East African Family. Family study and the effect of splenectomy. Acta haematologica, 1979, Volume: 61, Issue:5 Topics: Adolescent; Adult; Aged; Child; Child, Preschool; Female; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Kenya; Leucine; Male; Middle Aged; Pedigree; Pregnancy; Proline; Splenectomy	1979
The M gamma chain of human fetal hemoglobin. Progress in clinical and biological research, 1987, Volume: 251 Topics: Amino Acid Sequence; Chromatography, High Pressure Liquid; Fetal Hemoglobin; Hemoglobinopathies; Humans; Leucine; Macromolecular Substances; Methionine; Molecular Sequence Data	1987
Thalassaemia in the British. British medical journal, 1973, Jul-21, Volume: 3, Issue:5872 Topics: Adolescent; Anemia; Beta-Globulins; Carbon Isotopes; Diagnosis, Differential; Female; Fetal Hemoglobin; Hemoglobin H; Hemoglobinopathies; Humans; Leucine; Male; Thalassemia; United Kingdom	1973
The interaction of hemoglobin E with beta thalassemia: a study of hemoglobin synthesis in a family of mixed Burmese and Iranian origin. Blood, 1973, Volume: 42, Issue:5 Topics: Carrier State; Cell Survival; Child, Preschool; Chromium Radioisotopes; Electrophoresis, Starch Gel; Erythrocytes; Female; Fetal Hemoglobin; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Iran; Leucine; Myanmar; Pedigree; Peptides; Suppression, Genetic; Thalassemia; Tritium	1973
Haemoglobin Constant Spring synthesis in red cell precursors. British journal of haematology, 1974, Volume: 28, Issue:1 Topics: Adolescent; Adult; Blood Cells; Bone Marrow; Carbon Radioisotopes; Child; Chromatography; Erythrocytes; Erythropoiesis; Female; Globins; Hematopoietic Stem Cells; Hemoglobin H; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Hydrogen-Ion Concentration; Leucine; Male; Reticulocytes	1974
The effect of lead on total globin and alpha- and beta-chain synthesis; in vitro and in vivo. British journal of haematology, 1974, Volume: 27, Issue:3 Topics: Adult; Anemia, Hemolytic, Autoimmune; Anemia, Hypochromic; Depression, Chemical; Female; Globins; Heme; Hemoglobinopathies; Hemoglobins; Humans; In Vitro Techniques; Lead; Leucine; Male; Puromycin; Radioisotopes; Reticulocytes; Tritium	1974
Imbalance in alpha and beta globin synthesis associated with a hemoglobinopathy. The Journal of clinical investigation, 1974, Volume: 54, Issue:4 Topics: Adult; Chromatography, Gel; Electrophoresis, Starch Gel; Erythrocytes; Female; Globins; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Leucine; Tritium	1974
Compensation of chain synthesis by the single chain gene in Hb Lepore trait. Nature: New biology, 1972, Dec-27, Volume: 240, Issue:104 Topics: Amino Acids; Bone Marrow; Bone Marrow Cells; Genes; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Kinetics; Leucine; Peptide Chain Elongation, Translational; Peptides; Protein Biosynthesis; Reticulocytes; RNA, Messenger; Transcription, Genetic; Tritium	1972
Decreased globin messenger RNA activity associated with polyribosomes in thalassaemia. Nature: New biology, 1973, Feb-14, Volume: 241, Issue:111 Topics: Adult; Carbon Isotopes; Cell Fractionation; Cell-Free System; Chromatography; Female; Globins; Hemoglobin H; Hemoglobinopathies; Humans; Leucine; Polyribosomes; Reticulocytes; RNA, Messenger; Thalassemia; Tritium	1973
A case of haemoglobin J Sardegna- -thalassaemia double heterozygosis. Acta haematologica, 1972, Volume: 47, Issue:5 Topics: Amino Acids; Blood Protein Electrophoresis; Carbon Isotopes; Chromatography, DEAE-Cellulose; Glycerophosphates; Hemoglobinopathies; Hemoglobins, Abnormal; Heterozygote; Humans; Italy; Leucine; Male; Oxygen; Pedigree; Peptides; Thalassemia	1972
Globin messenger RNA in hemoglobin H disease. Blood, 1973, Volume: 42, Issue:6 Topics: Adult; Animals; Carbon Radioisotopes; Cell-Free System; Globins; Hemoglobin H; Hemoglobinopathies; Humans; Leucine; Male; Neoplasm Proteins; Neoplasms, Experimental; Potassium Chloride; Rabbits; Reticulocytes; Ribosomes; RNA, Messenger; Thalassemia	1973
Concentration of fetal red blood cells from a mixture of maternal and fetal blood by anti-i serum--an aid to prenatal diagnosis of hemoglobinopathies. Blood, 1974, Volume: 43, Issue:3 Topics: Anemia, Sickle Cell; Blood; Carbon Radioisotopes; Cell Separation; Erythrocytes; Fetal Hemoglobin; Fetus; Gestational Age; Hemagglutination Tests; Hemoglobinopathies; Immune Sera; Isoantibodies; Leucine; Methods; Prenatal Diagnosis; Tritium; Umbilical Cord	1974
In utero diagnosis of hemoglobinopathies. Hemoglobin synthesis in fetal red cells. The New England journal of medicine, 1974, 05-09, Volume: 290, Issue:19 Topics: Amniotic Fluid; Blood; Blood Specimen Collection; Carbon Radioisotopes; Chromatography; Erythrocytes; Extraembryonic Membranes; Female; Fetal Hemoglobin; Fetus; Gestational Age; Globins; Hemoglobin, Sickle; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Leucine; Methods; Needles; Placenta; Pregnancy; Prenatal Diagnosis; Tritium; Ultrasonography	1974
Globin chain synthesis in the marrow and reticulocytes of beta thalassemia, hemoglobin H disease, and beta delta thalassemia. Blood, 1972, Volume: 40, Issue:1 Topics: Bone Marrow; Bone Marrow Cells; Carbon Isotopes; Chromatography; Globins; Hemoglobinometry; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Leucine; Reticulocytes; Thalassemia; Valine	1972
Delta-beta-thalassaemia in a Chinese family. British journal of haematology, 1972, Volume: 23, Issue:4 Topics: Adult; Alanine; Asian People; Black People; Carbon Isotopes; Child; Child, Preschool; Chromatography; Female; Fetal Hemoglobin; Glycine; Hemoglobinopathies; Heterozygote; Humans; Infant; Leucine; Male; Middle Aged; Pedigree; Peptides; Reticulocytes; Thalassemia	1972
Haemoglobin Denmark Hill 95 (G2) Pro-Ala, a variant with unusual electrophoretic and oxygen-binding properties. Biochimica et biophysica acta, 1972, Oct-31, Volume: 278, Issue:3 Topics: Adult; Alanine; Amino Acid Sequence; Amino Acids; Electrophoresis, Paper; Electrophoresis, Starch Gel; Female; Gestational Age; Hemoglobinopathies; Hemoglobins; Hemoglobins, Abnormal; Humans; Hydrogen-Ion Concentration; Infant, Newborn; Leucine; London; Molecular Biology; Mutation; Oxygen; Peptides; Pregnancy; Proline; Protein Binding; Serine	1972
Hemoglobin Lepore trait: globin synthesis in bone marrow and peripheral blood. Science (New York, N.Y.), 1972, Nov-10, Volume: 178, Issue:4061 Topics: Bone Marrow; Carbon Isotopes; Chromatography; Globins; Hemoglobinopathies; Humans; Leucine; Thalassemia	1972
Unstable haemoglobin disease caused by Hb Santa Ana- 88 (F4) Leu leads to Pro. Haematologia, 1970, Volume: 4, Issue:2 Topics: Acetylcholinesterase; Adenosine Triphosphate; Amino Acid Sequence; Anemia, Hemolytic; Blood Group Antigens; Blood Protein Electrophoresis; Cell Membrane Permeability; Cell Survival; Chemistry Techniques, Analytical; Child; Chromium Isotopes; Electrophoresis, Disc; Electrophoresis, Paper; Erythrocytes, Abnormal; Erythropoiesis; Glucosephosphate Dehydrogenase; Glutathione; Hemoglobinopathies; Hemoglobins, Abnormal; Humans; Hungary; Immunogenetics; Iron Isotopes; Leucine; Lipids; Male; Mutation; Proline; Pyrroles	1970
Globin chain synthesis in the alpha thalassemia syndromes. The Journal of clinical investigation, 1969, Volume: 47, Issue:11 Topics: Anemia, Hypochromic; Blood Protein Electrophoresis; Blood Proteins; Carbon Isotopes; Erythrocyte Count; Globins; Hematocrit; Hemoglobinopathies; Hemoglobins; Humans; Leucine; Lymphatic Diseases; Pedigree; Reticulocytes; Thalassemia	1969