Page last updated: 2024-11-08

alanine and Anemia, Cooley's

alanine has been researched along with Anemia, Cooley's in 3 studies

Alanine: A non-essential amino acid that occurs in high levels in its free state in plasma. It is produced from pyruvate by transamination. It is involved in sugar and acid metabolism, increases IMMUNITY, and provides energy for muscle tissue, BRAIN, and the CENTRAL NERVOUS SYSTEM.
alanine : An alpha-amino acid that consists of propionic acid bearing an amino substituent at position 2.

Research Excerpts

ExcerptRelevanceReference
"Deferiprone is used as a chelation agent in chronic iron overload in β-thalassemia patients."3.79Three most common nonsynonymous UGT1A6*2 polymorphisms (Thr181Ala, Arg184Ser and Ser7Ala) and therapeutic response to deferiprone in β-thalassemia major patients. ( Dadheech, S; Hussien, MD; Jain, S; Jyothy, A; Munshi, A; Rao, AV; Shaheen, U, 2013)

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (33.33)29.6817
2010's2 (66.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Dadheech, S1
Rao, AV1
Shaheen, U1
Hussien, MD1
Jain, S1
Jyothy, A1
Munshi, A1
Manconi, B1
De Rosa, MC1
Cappabianca, MP1
Olianas, A1
Carelli Alinovi, C1
Mastropietro, F1
Ponzini, D1
Amato, A1
Pellegrini, M1
Pagano, L1
Salzano, AM1
Carbone, V1
Iannelli, D1
Viola, A1
Pollio, F1
Prossomariti, L1
David, O1
Ricco, G1
Pucci, P1

Other Studies

3 other studies available for alanine and Anemia, Cooley's

ArticleYear
Three most common nonsynonymous UGT1A6*2 polymorphisms (Thr181Ala, Arg184Ser and Ser7Ala) and therapeutic response to deferiprone in β-thalassemia major patients.
    Gene, 2013, Dec-01, Volume: 531, Issue:2

    Topics: Adolescent; Alanine; Amino Acid Substitution; Arginine; beta-Thalassemia; Child; Child, Preschool; D

2013
A new beta-chain haemoglobin variant with increased oxygen affinity: Hb Roma [beta115(g17)Ala-->Val].
    Biochimica et biophysica acta, 2010, Volume: 1800, Issue:3

    Topics: Adult; Alanine; Amino Acid Substitution; beta-Globins; beta-Thalassemia; Carrier State; Female; Gene

2010
Hb Cardarelli [beta86(F2)Ala-->Pro]: a new unstable and hyperaffine variant in association with beta(+)-thalassemia.
    Hemoglobin, 2004, Volume: 28, Issue:2

    Topics: Adult; Aged; Alanine; Amino Acid Substitution; beta-Thalassemia; Child; Child, Preschool; Codon; DNA

2004