Page last updated: 2024-10-20

spermidine and Thalassemia

spermidine has been researched along with Thalassemia in 2 studies

Thalassemia: A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains. There are several genetic types with clinical pictures ranging from barely detectable hematologic abnormality to severe and fatal anemia.

Research Excerpts

ExcerptRelevanceReference
"Spermine levels were high in the SS lysates but not detectable in SC or AA lysates."1.26Polyamines and membrane proteins in sickle cell disease. ( Kremzner, LT; Natta, CL, 1982)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19902 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Natta, CL2
Kremzner, LT2
Motyczka, AA1

Other Studies

2 other studies available for spermidine and Thalassemia

ArticleYear
Polyamines and membrane proteins in sickle cell disease.
    Blood cells, 1982, Volume: 8, Issue:2

    Topics: Anemia, Sickle Cell; Erythrocytes, Abnormal; Hemoglobin A; Hemoglobin C; Hemoglobin, Sickle; Humans;

1982
Polyamines in sickle cell disease.
    Biochemical medicine, 1980, Volume: 23, Issue:2

    Topics: Anemia, Sickle Cell; Erythrocyte Membrane; Erythrocytes; Hemoglobin C Disease; Humans; Polyamines; P

1980