threonine has been researched along with Anemia, Cooley's in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (66.67) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (33.33) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Dadheech, S; Hussien, MD; Jain, S; Jyothy, A; Munshi, A; Rao, AV; Shaheen, U | 1 |
Falick, AM; Houston, ML; Lane, PA; McKinna, JD; Witkowska, HE | 1 |
Aoki, Y; Imai, K; Kikuchi, M; Kishikawa, M; Mawjood, AH; Miyazaki, A; Nakagawa, T; Nakanishi, T; Shimizu, A | 1 |
3 other study(ies) available for threonine and Anemia, Cooley's
Article | Year |
---|---|
Three most common nonsynonymous UGT1A6*2 polymorphisms (Thr181Ala, Arg184Ser and Ser7Ala) and therapeutic response to deferiprone in β-thalassemia major patients.
Topics: Adolescent; Alanine; Amino Acid Substitution; Arginine; beta-Thalassemia; Child; Child, Preschool; Deferiprone; Female; Gene Frequency; Genetic Association Studies; Glucuronosyltransferase; Humans; Iron Chelating Agents; Iron Overload; Isoenzymes; Male; Mutation, Missense; Polymorphism, Single Nucleotide; Pyridones; Serine; Threonine; Treatment Outcome | 2013 |
Hemoglobin D Ibadan-beta zero thalassemia: detection by neonatal screening and confirmation by electrospray-ionization mass spectrometry.
Topics: beta-Thalassemia; Globins; Hemoglobins, Abnormal; Humans; Infant, Newborn; Isoelectric Focusing; Lysine; Male; Mass Spectrometry; Neonatal Screening; Point Mutation; Threonine | 1993 |
Compound heterozygosity for beta(+)-thalassemia [-31 (A-->G)] and a new variant with low oxygen affinity, Hb Sagami [beta139(H17)Asn-->Thr].
Topics: Asparagine; Base Sequence; beta-Thalassemia; Hemoglobins, Abnormal; Heterozygote; Humans; Japan; Male; Mass Spectrometry; Middle Aged; Oxygen; Point Mutation; Polymerase Chain Reaction; Threonine | 1999 |