Page last updated: 2024-08-17

lysine and Anemia, Sickle Cell

lysine has been researched along with Anemia, Sickle Cell in 13 studies

Research

Studies (13)

Timeframe	Studies, this research(%)	All Research%
pre-1990	10 (76.92)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (7.69)	29.6817
2010's	2 (15.38)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Adanho, CSA; Adekile, AD; Adorno, EV; Barbosa, CG; Ferreira, JRD; Fonseca, CA; Goncalves, MS; Lyra, IM; Mafili, VV; Ndidi, US; Pitanga, TN; Santana, SS; Santiago, RP; Yahouédéhou, SCMA	1
Becchi, M; Francina, A; Joly, P; Préhu, C; Riou, J; Wajcman, H; Zanella-Cleon, I	1
Biemond, BJ; Brandjes, DP; Fijnvandraat, K; Nur, E; Otten, HM; Schalkwijk, CG; Schnog, JJ	1
BEALE, D; IRVINE, D; LEHMANN, H; WATSON-WILLIAMS, EJ	1
Manning, JM; Nigen, AM	1
Fales, FW; Grush, OC; Sophianopoulos, AJ; Sophianopoulos, JA; Wilson, JS	1
Gardner, LI	1
Itano, HA; Suzuki, H	1
Levy, HL	1
Alter, BP; Kan, YW; Nathan, DG	1
Moon, RB; Nelson, MJ; Powars, DF; Richards, JH	1
Anderson, WF; Gilbert, JM; Nienhuis, AW; Thornton, AG	1
Barclay, GP; Charlesworth, D; Lehmann, H	1

Reviews

2 review(s) available for lysine and Anemia, Sickle Cell

Article	Year
Genetically expressed abnormalities in the fetus. Clinical obstetrics and gynecology, 1974, Volume: 17, Issue:3 Topics: Adrenal Insufficiency; Amino Acid Metabolism, Inborn Errors; Amino Acids, Sulfur; Ammonia; Anemia, Sickle Cell; Anencephaly; Carbohydrate Metabolism, Inborn Errors; Fabry Disease; Female; Fetal Diseases; Fetus; Gangliosides; Gaucher Disease; Humans; Karyotyping; Lipid Metabolism, Inborn Errors; Lipidoses; Lysine; Metabolism, Inborn Errors; Mucopolysaccharidoses; Polyploidy; Pregnancy; Propionates; Sphingolipidoses; Turner Syndrome; Vitamin B 12	1974
Genetic screening. Advances in human genetics, 1973, Volume: 4 Topics: Amino Acid Metabolism, Inborn Errors; Anemia, Sickle Cell; Arginine; Carbohydrate Metabolism, Inborn Errors; Cystinuria; Erythrocytes; Fanconi Syndrome; Galactosemias; Genetics, Population; Glucosephosphate Dehydrogenase; Glycine; Hartnup Disease; Heterozygote; Histidine; Homocystine; Humans; Lysine; Maple Syrup Urine Disease; Mass Screening; Methods; Ornithine; Phenylalanine; Phenylketonurias; Succinates; Tyrosine	1973

Article

Year

Genetically expressed abnormalities in the fetus.

Clinical obstetrics and gynecology, 1974, Volume: 17, Issue:3

Topics: Adrenal Insufficiency; Amino Acid Metabolism, Inborn Errors; Amino Acids, Sulfur; Ammonia; Anemia, Sickle Cell; Anencephaly; Carbohydrate Metabolism, Inborn Errors; Fabry Disease; Female; Fetal Diseases; Fetus; Gangliosides; Gaucher Disease; Humans; Karyotyping; Lipid Metabolism, Inborn Errors; Lipidoses; Lysine; Metabolism, Inborn Errors; Mucopolysaccharidoses; Polyploidy; Pregnancy; Propionates; Sphingolipidoses; Turner Syndrome; Vitamin B 12

1974

Genetic screening.

Advances in human genetics, 1973, Volume: 4

Topics: Amino Acid Metabolism, Inborn Errors; Anemia, Sickle Cell; Arginine; Carbohydrate Metabolism, Inborn Errors; Cystinuria; Erythrocytes; Fanconi Syndrome; Galactosemias; Genetics, Population; Glucosephosphate Dehydrogenase; Glycine; Hartnup Disease; Heterozygote; Histidine; Homocystine; Humans; Lysine; Maple Syrup Urine Disease; Mass Screening; Methods; Ornithine; Phenylalanine; Phenylketonurias; Succinates; Tyrosine

1973

Other Studies

11 other study(ies) available for lysine and Anemia, Sickle Cell

Article	Year
Effect of N(Epsilon)-(carboxymethyl)lysine on Laboratory Parameters and Its Association with Disease markers, 2019, Volume: 2019 Topics: Anemia, Sickle Cell; Antisickling Agents; Aspartate Aminotransferases; beta-Globins; Child; Creatinine; Female; Genotype; Haplotypes; Humans; Hydroxyurea; Inflammation; L-Lactate Dehydrogenase; Leukocytes; Lysine; Male	2019
Strategy for identification by mass spectrometry of a new human hemoglobin variant with two mutations in Cis in the beta-globin chain: Hb S-Clichy [beta6(A3)Glu-->Val; beta8(A5)Lys-->Thr]. Hemoglobin, 2009, Volume: 33, Issue:3 Topics: Anemia, Sickle Cell; beta-Globins; Chromatography, Liquid; Female; Glutamic Acid; Hemoglobin, Sickle; Hemoglobins, Abnormal; Humans; Lysine; Mass Spectrometry; Middle Aged; Mutation; Spectrometry, Mass, Electrospray Ionization; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Threonine; Valine	2009
Plasma levels of advanced glycation end products are associated with haemolysis-related organ complications in sickle cell patients. British journal of haematology, 2010, Volume: 151, Issue:1 Topics: Adolescent; Adult; Anemia, Sickle Cell; Arginine; Biomarkers; Female; Glycation End Products, Advanced; Hemolysis; Humans; Lysine; Male; Middle Aged; Oxidative Stress; Young Adult	2010
A NEW HAEMOGLOBIN, D IBADAN (BETA-87 THREONINE -- LYSINE), PRODUCING NO SICKLE-CELL HAEMOGLOBIN D DISEASE WITH HAEMOGLOBIN S. Nature, 1965, Mar-27, Volume: 205 Topics: Anemia, Sickle Cell; Chromatography; Electrophoresis; Genetics, Medical; Hemoglobin, Sickle; Hemoglobins; Hemoglobins, Abnormal; Humans; Lysine; Nigeria; Threonine	1965
Inhibition of erythrocyte sickling in vitro by DL-glyceraldehyde. Proceedings of the National Academy of Sciences of the United States of America, 1977, Volume: 74, Issue:1 Topics: Anemia, Sickle Cell; Erythrocytes, Abnormal; Gels; Glyceraldehyde; Hemoglobin, Sickle; Humans; Lysine; Oxygen; Valine	1977
Two new antisickling agents and the use of amino acid salts. Clinical biochemistry, 1974, Volume: 7, Issue:2 Topics: Anemia, Sickle Cell; Arginine; Aspartic Acid; Drug Synergism; Edetic Acid; Glucose; Glutamates; Hemoglobins, Abnormal; Homozygote; Humans; Hydrogen-Ion Concentration; Lysine; Osmolar Concentration	1974
Delayed removal of N-terminal methionine from nascent globin chains in sickle-cell anemia reticulocytes. Proceedings of the National Academy of Sciences of the United States of America, 1973, Volume: 70, Issue:7 Topics: Anemia, Sickle Cell; Animals; Chromatography; Hemoglobin, Sickle; Hemoglobins; Hemoglobins, Abnormal; Humans; In Vitro Techniques; Lysine; Methionine; Peptide Biosynthesis; Peptide Chain Elongation, Translational; Peptides; Rabbits; Reticulocytes; Sulfur Isotopes; Tritium; Valine	1973
Inhibition of hemoglobin synthesis by cyanate in vitro. Blood, 1974, Volume: 43, Issue:1 Topics: Amino Acids; Anemia, Sickle Cell; Biological Transport; Bone Marrow; Carbon Radioisotopes; Cell-Free System; Cells, Cultured; Cyanates; Globins; Hemoglobins; Humans; Iontophoresis; Leucine; Lysine; Methionine; Polyribosomes; Reticulocytes; RNA, Transfer	1974
13C magnetic resonance studies of hemoglobin carbamylation. Physiological chemistry and physics, 1974, Volume: 6, Issue:1 Topics: Adult; Amino Acid Sequence; Anemia, Sickle Cell; Binding Sites; Carbon Isotopes; Carbon Monoxide; Carboxyhemoglobin; Cyanates; Evaluation Studies as Topic; Fourier Analysis; Hemoglobins; Heparin; Humans; Hydrogen-Ion Concentration; Lysine; Magnetic Resonance Spectroscopy; Methods; Protein Binding; Protein Conformation; Valine	1974
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