A Study on Molecular Basis of Hypochromic Microcytic Anemia in Myanmar
スポンサーリンク
概要
著者
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Harano Keiko
Department Of Biochemistry Kawasaki Medical School
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Harano Keiko
Department Of Clinical Nutrition Faculty Of Health Science And Technology Kawasaki University Of Med
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Kyaw SHWE
Department of Clinical Nutrition, Faculty of Health Science and Technology, Kawasaki University of M
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Kyaw Shwe
Department Of Clinical Nutrition Faculty Of Health Science And Technology Kawasaki University Of Med
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HARANO Keiko
Department of Biochemistry and Department of Clinical Pathology, Kawasaki Medical School
関連論文
- Band 4.2 Komatsu: 523 GAT → TAT (175 Asp → Tyr) in exon 4 of the band 4.2 gane associated with total deficiency of band 4.2, hemolytic anemia with ovalostomatocytosis and marked disruption of the cytoskeletal network
- Detection and Differentiation of Malaria Parasites in DNA Extracted from Blood Samples by the Polymerase Chain Reaction (PCR)
- Molecular Aspects of α-Thalassemia in Myanmar
- Aberrant mRNA Spliced in a β^0-Thalassemic Gene Having a G→A Mutation at βIVS II-1
- Molecular Aspects of Transfusion Dependent Thalassemic Children in Myanmar : Analysis of Common β-Thalassemia in Myanmar by Amplification Refractory Mutation System (ARMS)
- Adult Onset, Chronic Anemias of Undermined Etiology, Myanmar
- Prevalence of Hemoglobin E Among the Children Taking Regular Blood Transfusion at the Day Care Room, Yangon Children Hospital, Myanmar
- An Insight into Heterozygous β-Thalassemia, Myanmar
- Hb Nishinomiya [Leu-Gly-Inserted between Codons 69 (E13) and 70 (E14) of β] : A Novel Unstable Hemoglobin with Reduced Oxygen Affinity Found in a Patient with Spherocytic Hemolysis
- Haplotypes of the β^E-Globin Gene Cluster Found in Myanmar
- An Automated Hb A_2 Analyzer, HLC-723G7, for Diagnosis of β-Thalassemia
- Malaria Parasites Detected in Myanmar Thalassemia Patients
- Hemoglobinopathies and Malaria Infection in Myanmar
- A Rare Super-Unstable Hemoglobin Variant, Hb Monroe [β30(B12)Arg→Thr], Found in Two Myanmar Children
- A Case Report of Diagnosis of α-thalassemia-2
- Identification of a Rare Hemoglobin Variant, Hb Nagasaki [β17(A14)Lys→Glu], Found in a Japanese by the Techniques of Protein Chemistry and the DNA Analysis
- Determination of Hemoglobin A_ Content by an Automated Hemoglobin Analyzer, HLC-723G7, Myanmar
- Hemoglobin Pitie-Salpetriere [β34 (B16) Val→Phe] Showing Erythrocytosis and Mild Hemolysis in a Japanese Man
- A Study on Molecular Basis of Hypochromic Microcytic Anemia in Myanmar
- Application of an Automated Hemoglobin Analyzer, HLC-723G7, for Clinical Samples
- Normal glucose tolerance with high HbA1c levels observed in two cases of Hb variants
- A case of hemoglobin Hiroshima (β146 histidine to aspartic acid) with compensatory erythremia and undetectable HbA_
- Hemoglobin Variant HbE Found in Two South Asian Diabetic Patients
- Improved method for quantiation of biosynthesized human globin chains in reticulocytes by use of urea cellulose acetate membrane electrophoresis.