نتایج جستجو برای: hba2
تعداد نتایج: 435 فیلتر نتایج به سال:
Background and purpose: Throughout the world 5.2% of the population is carrier for a main hemoglobin disorder. Mazandaran province in North of Iran is highly influenced by heterozygote advantage resulting in high prevalence of hemoglobinopathies. Hemoglobin E is one of the beta globin variants that can cause severe anemia such as thalassemia major. Materials and methods: This descriptive st...
BACKGROUND Muscle satellite cells (MSCs) represent a devoted stem cell population that is responsible for postnatal muscle growth and skeletal muscle regeneration. An important characteristic of MSCs is that they encompass multi potential mesenchymal stem cell activity and are able to differentiate into myocytes and adipocytes. To achieve a global view of the genes differentially expressed in M...
Background: β-Thalassaemia syndromes are a group of hereditary disorders characterised by a genetic deficiency in the synthesis of β-globin chains due to a defect in β-globin genes. The objective of this study was to determine the haematological features of β-thalassaemia trait (BTT), and to determine the sensitivity of Mean Corpuscular Volume (MCV), Mean Corpuscular Haemoglobin (MCH) and Mentz...
Abstract Background Western Kenya, being a malaria-endemic region, has high prevalence of hemoglobinopathies mostly sickle cell and thalassemia. The hemoglobin fractions or variants, HbA, HbA2, HbF, serve as biomarkers for the detection are commonly used in laboratory screening diagnosis these diseases. Diagnosis diseases entails accurate precise representation patient’s condition. This is main...
With their complex life cycle and highly derived body plan, echinoderms are unique among bilaterians. Although early development has been intensively studied, the molecular mechanisms underlying development of the adult echinoderm and its unusual radial body plan are largely unknown. To investigate the evolution of developmental changes in gene expression underlying radial body plan development...
Cyanide can react with globin hemochromogen in two different ways. In the first reaction cyanide combines with globin hemochromogen without displacing or competing with globin. In the second reaction cyanide displaces globin.
BACKGROUND Haemoglobinopathies are the commonest hereditary disorders in India and pose a major health problem. Both beta thalassaemia and structural haemoglobin variants are relatively common in northwestern India. Here we report a 29-year-old Sindhi female who was referred to us for a haemoglobinopathy work up and genetic counseling since her spouse was a classical beta thalassaemia carrier. ...
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