2005
DOI: 10.1080/09720073.2005.11890875
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Haemoglobin Variants in North Indian Populations

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Cited by 3 publications
(4 citation statements)
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“…Tebal tipisnya pita protein terlihat pada sampel eritrosit burung merpati hias yang memiliki protein utama berupa hemoglobin. Protein hemoglobin memiliki berat molekul 63-66 kDa [16]. Berdasarkan berat molekul protein hemoglobin tersebut, pada jenis burung merpati hias yang terekspresi adalah pada jenis American Fantail dan Indian Fantail dengan berat molekul 65,6 kDa.…”
Section: Pembahasanunclassified
“…Tebal tipisnya pita protein terlihat pada sampel eritrosit burung merpati hias yang memiliki protein utama berupa hemoglobin. Protein hemoglobin memiliki berat molekul 63-66 kDa [16]. Berdasarkan berat molekul protein hemoglobin tersebut, pada jenis burung merpati hias yang terekspresi adalah pada jenis American Fantail dan Indian Fantail dengan berat molekul 65,6 kDa.…”
Section: Pembahasanunclassified
“…Haemoglobin (Hb), the red respiratory protein found in mammalian erythrocytes is one of the most informative molecules in primate blood [1]. In adult humans, the most common haemoglobin type is a tetramer known as haemoglobin-A consists of four separate polypeptide chains of amino acids and each subunit is composed of a protein chain tightly associated with a non-protein haeme group that fix oxygen.…”
Section: Introductionmentioning
confidence: 99%
“…Haemoglobin variants are a part of the normal embryonic and fetal development which can also be pathologic mutant forms caused by variations in genetics of haemoglobin in a population. Haemoglobinopathies covers a group of hereditary disorders in which the structure (qualitative change) or the rate of synthesis (quantitative change) of one of the normal haemoglobin chain is altered [1]. Haemoglobinopathies causes varying degrees of microcytic anemia that can range from insignificant to life threatening [2].…”
Section: Introductionmentioning
confidence: 99%
“…The structure of haemoglobin variants is similar to normal haemoglobin (HbA) except there is alteration in the sequence of amino acids usually in the β-chain. Haemoglobinopathies can be divided into two groups -the structural haemoglobin variants due to single point mutation in the globin structure (like HbS , C, D, and E) and the thalassemia, where the rate of synthesis of globin chain is inefficient [1] . The clinical spectrums of the disorders vary from asymptomatic conditions to serious disorders like death in utero.…”
Section: Introductionmentioning
confidence: 99%