leucine has been researched along with Anemia, Cooley's in 8 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (12.50) | 18.7374 |
1990's | 4 (50.00) | 18.2507 |
2000's | 2 (25.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 1 (12.50) | 2.80 |
Authors | Studies |
---|---|
Crehuá Gaudiza, E; Quintero García, D; Sebastián Cuevas, FJ | 1 |
Grosso, M; Izzo, P; Morelli, E; Palumbo, I; Puzone, S; Sessa, R | 1 |
BURKA, ER; MARKS, PA | 1 |
Adams, JG; Coleman, MB; Harrell, A; Lu, ZH; Plonczynski, M; Smith, CM; Steinberg, MH | 1 |
Batelaan, D; Bernini, LF; Giordano, PC; Harteveld, CL; Van Delft, P | 1 |
Anguita, E; Arrizabalaga, B; Atuxta, L; Carreño, DL; González, AF; Ropero, P; Sánchez, J; Villegas, A | 1 |
Cho, HI; Hattori, Y; Kim, BK; Kim, SI; Lee, NY; Ohba, Y | 1 |
Agosti, S; Baffico, M; Cao, A; Melevendi, C; Murru, S; Pirastu, M; Poddie, D; Sciarratta, GV | 1 |
8 other study(ies) available for leucine and Anemia, Cooley's
Article | Year |
---|---|
Hepatitis C and beta-thalassemia major in children: experience with glecaprevir/pibrentasvir.
Topics: Aminoisobutyric Acids; Antiviral Agents; Benzimidazoles; beta-Thalassemia; Child; China; Cyclopropanes; Genotype; Hepacivirus; Hepatitis C; Hepatitis C, Chronic; Humans; Lactams, Macrocyclic; Leucine; Proline; Pyrrolidines; Quinoxalines; Sulfonamides | 2021 |
Defective mRNA levels are responsible for a beta-thalassemia phenotype associated with Hb Federico II, a novel hemoglobin variant [beta-106 (G8) Leu->Val].
Topics: beta-Thalassemia; Codon; Female; Hemoglobins; Hemoglobins, Abnormal; Heterozygote; Humans; Leucine; Male; Models, Genetic; Mutation; Pedigree; Phenotype; Sequence Analysis, DNA; Valine | 2008 |
RIBOSOMES ACTIVE IN PROTEIN SYNTHESIS IN HUMAN RETICULOCYTES: A DEFECT IN THALASSEMIA MAJOR.
Topics: Anemia; Anemia, Sickle Cell; beta-Thalassemia; Carbon Isotopes; Hemoglobins; Humans; Isoleucine; Leucine; Nucleoproteins; Proteins; Reticulocytes; Ribosomes; Thalassemia | 1963 |
Two missense mutations in the beta-globin gene can cause severe beta thalassemia. Hemoglobin Medicine Lake (beta 32[B14]leucine-->glutamine; 98 [FG5] valine-->methionine).
Topics: Amino Acid Sequence; Base Sequence; beta-Thalassemia; DNA Primers; Erythrocytes; Erythrocytes, Abnormal; Female; Globins; Glutamine; Hemoglobins, Abnormal; Humans; Infant; Leucine; Male; Methionine; Molecular Sequence Data; Point Mutation; Polymerase Chain Reaction; Polymorphism, Genetic; Reticulocyte Count; Sequence Tagged Sites; Valine | 1995 |
Haemoglobinopathy analyses in the Netherlands: a report of an in vitro globin chain biosynthesis survey using a rapid, modified method.
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 |
Hb Johnstown [beta 109 (G11) Val-->Leu]: second case described and associated for the first time with beta(0)-thalassemia in two Spanish families.
Topics: Adult; Aged; beta-Thalassemia; Female; Hemoglobins, Abnormal; Humans; Leucine; Male; Middle Aged; Mutation; Spain; Valine | 2000 |
A family case of beta-thalassemia minor and hemoglobin Queens: alpha 34 (B15) Leu-Arg.
Topics: Adult; Arginine; beta-Thalassemia; Female; Hemoglobins, Abnormal; Humans; Korea; Leucine; Male; Pedigree | 1992 |
A novel beta-globin structural mutant, Hb Brescia (beta 114 Leu-Pro), causing a severe beta-thalassemia intermedia phenotype.
Topics: Adolescent; Base Sequence; beta-Thalassemia; Erythrocytes; Female; Globins; Hemoglobins, Abnormal; Humans; Italy; Leucine; Macromolecular Substances; Male; Molecular Sequence Data; Proline | 1992 |