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1860796917925019648
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INTELEK Repository
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Online Access
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https://intelek.unisza.edu.my/intelek/pages/search.php?search=!collection407072
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2014-09-25 11:11:50
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Restricted Document
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10679
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UniSZA
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4757-01-FH02-FP-15-02863.pdf
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AH XSL Formatter V6.1 MR4 Lite for Windows (x64) : 6.1.9.14491 (2013/12/19 12:04JST)
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oai_dc
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https://intelek.unisza.edu.my/intelek/pages/view.php?ref=10679
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10679 https://intelek.unisza.edu.my/intelek/pages/view.php?ref=10679 https://intelek.unisza.edu.my/intelek/pages/search.php?search=!collection407072 Restricted Document Article Journal application/pdf 2 1.6 Adobe Acrobat Pro DC 20 Paper Capture Plug-in AH XSL Formatter V6.1 MR4 Lite for Windows (x64) : 6.1.9.14491 (2013/12/19 12:04JST) 2014-09-25 11:11:50 4757-01-FH02-FP-15-02863.pdf UniSZA Private Access Reasons of Unknown HPLC Peaks during Hemoglobin Analysis for Patients with Beta Thalassemias Journal of Hematology & Thromboembolic Diseases Beta-thalassemias (β-thal) are inherited quantitative disorders of haemoglobin (Hb) leading to underproduction of the beta globin chains of hemoglobin. In β-thal, the synthesis of normal α globin chains from the unaffected α globin gene continues as normal, resulting in the accumulation within the erythroid precursors of excess free α globin chains, which precipitate in the red cell precursors in the bone marrow forming inclusion bodies. Excess free alpha globin chain precipitate as insoluble hemichrome on the inner surface of red cell membrane (membrane-bound), forming inclusions called micro- Heinz bodies or occure as free cytosolic (soluble) hemichrome. 2 5 1-2 http://esciencecentral.org/journals/reasons-of-unknown-hplc-
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Reasons of Unknown HPLC Peaks during Hemoglobin Analysis for Patients with Beta Thalassemias
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| summary |
Beta-thalassemias (β-thal) are inherited quantitative disorders of haemoglobin (Hb) leading to underproduction of the beta globin chains of hemoglobin. In β-thal, the synthesis of normal α globin chains from the unaffected α globin gene continues as normal, resulting in the accumulation within the erythroid precursors of excess free α globin chains, which precipitate in the red cell precursors in the bone marrow forming inclusion bodies. Excess free alpha globin chain precipitate as insoluble hemichrome on the inner surface of red cell membrane (membrane-bound), forming inclusions called micro- Heinz bodies or occure as free cytosolic (soluble) hemichrome.
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| title |
Reasons of Unknown HPLC Peaks during Hemoglobin Analysis for Patients with Beta Thalassemias
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| title_full |
Reasons of Unknown HPLC Peaks during Hemoglobin Analysis for Patients with Beta Thalassemias
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| title_fullStr |
Reasons of Unknown HPLC Peaks during Hemoglobin Analysis for Patients with Beta Thalassemias
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| title_full_unstemmed |
Reasons of Unknown HPLC Peaks during Hemoglobin Analysis for Patients with Beta Thalassemias
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| title_short |
Reasons of Unknown HPLC Peaks during Hemoglobin Analysis for Patients with Beta Thalassemias
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| title_sort |
reasons of unknown hplc peaks during hemoglobin analysis for patients with beta thalassemias
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