Page last updated: 2024-11-08

serine and Iron Overload

serine has been researched along with Iron Overload in 2 studies

Serine: A non-essential amino acid occurring in natural form as the L-isomer. It is synthesized from GLYCINE or THREONINE. It is involved in the biosynthesis of PURINES; PYRIMIDINES; and other amino acids.
serine : An alpha-amino acid that is alanine substituted at position 3 by a hydroxy group.

Iron Overload: An excessive accumulation of iron in the body due to a greater than normal absorption of iron from the gastrointestinal tract or from parenteral injection. This may arise from idiopathic hemochromatosis, excessive iron intake, chronic alcoholism, certain types of refractory anemia, or transfusional hemosiderosis. (From Churchill's Illustrated Medical Dictionary, 1989)

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 (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Dadheech, S1
Rao, AV1
Shaheen, U1
Hussien, MD1
Jain, S1
Jyothy, A1
Munshi, A1
Zhou, L1
Liu, Y1
Zou, C1
Ma, N1
Hui, Y1
Lv, G1
Zhang, H1
Zhou, H1
Gao, X1

Other Studies

2 other studies available for serine and Iron Overload

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
The effect of the Gly139His, Gly143His, and Ser142His mouse heme oxygenase-1 mutants on the HO reaction in vivo and in vitro.
    Anatomical record (Hoboken, N.J. : 2007), 2011, Volume: 294, Issue:1

    Topics: Amino Acid Substitution; Anemia; Animals; Animals, Newborn; Chlorocebus aethiops; COS Cells; Female;

2011