"Pseudo-abnormal" hemoglobins.
نویسندگان
چکیده
منابع مشابه
The Metabolism of the Individual C14 Labeled Hemoglobins in Patients with H-thalassemia, with Observations on Radiochromate Binding to the Hemoglobins during Red Cell Survival.
Patients with thalassemia may have abnormal alterations in the proportions of the structurally normal hemoglobins F and A2, or, in more rare circumstances, new hemoglobins of abnormal structure may appear. Such abnormal hemoglobins have not been shown to have substitutions of single amino acids in the polypeptide chain, as exemplified by hemoglobins S and C. Rather, they occur as unusual combin...
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The presence of HbS was reported in Turkey for the first time in the late fifties by Aksoy et al. This was followed by other reports by the same author revealing the presence of several other abnormal hemoglobins in Turkey. So far up to present 42 abnormal hemoglobins have been identified in the Turkish population. In addition to the studies conducted in Turkey, many European researchers report...
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Two previous reviews by Altay and Akar concerning the " Abnormal Hemoglobins in Turkey " appeared in the journal several years ago [1,2]. Since then, several other variants have been reported in both international and national journals. The aim of this mini-review was to compile the newly published abnormal hemoglobins in the Turkish population since these two previous papers [1,2]. During the ...
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We looked for abnormal hemoglobins in blood samples sent for diagnosis of anemia. Identification of the hemoglobins was made using electrophoretic, chromatographic and molecular procedures. The 2020 blood samples were of patients from various regions of Brazil and from some other Latin American countries. Among the abnormal hemoglobins that we found, 3.5% are known to be rare, while 51% had an ...
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Hemoglobin is an important protein found in the red cells of many animals. In humans, the hemoglobin is mainly distributed in the red blood cell. Single amino acid substitution is the main pathogenesis of most hemoglobin disorders. Here, the author used a new gene ontology technology to predict the molecular function and biological process of four important hemoglobin disorders with single subs...
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عنوان ژورنال:
- Blood
دوره 17 شماره
صفحات -
تاریخ انتشار 1961