beta-thalassemia如何读 英:['bi:təθəlɑ:s'i:mɪə] 美:['bitəθəlɑs'imɪr] beta-thalassemia是什么意思 n.β地中海贫血症 beta-thalassemia英英释义 noun thalassemia in which the longer hemoglobin chain is affected and which comprises Cooley's anemia in the homozygous ...
Beta-thalassemias are a group of hereditary blood disorders characterized by anomalies in the synthesis of the beta chains of hemoglobin resulting in variable phenotypes ranging from severe anemia to clinically asymptomatic individuals. The total annual incidence of symptomatic individuals is estimated at ...
Evaluation of hemoglobin agarose electrophoresis and Hb-F alkali denaturation test in diagnosis of β-Thalassemia; 全自动血红蛋白电泳与Hb-F碱变性试验在β地中海贫血中的应用及评价 3) Beta-thalassemia β地中海贫血 1. Amniotic fluid gene detection in prenatal diagnosis of alpha-and beta-thalassemia; ...
Beta-thalassemia (β-thalassemia) is characterized by reduced synthesis of the hemoglobin subunit beta (hemoglobin beta chain) that results in microcytic hypochromic anemia, an abnormal peripheral blood smear with nucleated red blood cells, and reduced amounts of hemoglobin A (HbA) on hemoglobin analy...
A recently initiated collaboration between Russian and American institutions has resulted in the characterization of several known or new -thalassemia alleles and unstable hemoglobin types. Nine known -thalassemia alleles were present which have also been found in Mediterranean, East Asian, and Black ...
Beta-thalassemia is caused by the reduced (beta+) or absent (beta0) synthesis of the beta globin chains of the hemoglobin tetramer. Three clinical and hematological conditions of increasing severity are recognized, i.e., the beta-thalassemia carrier state, thalassemia intermedia, and thalassemia ma...
Ayi, K.et al.Enhanced phagocytosis of ring-parasitized mutant erythrocytes: A common mechanism that may explain protection againstFalciparumMalaria in sickle trait and beta-thalassemia trait.Blood104(10), 3364–3371.(2004). PubMedGoogle Scholar ...
Hemoglobinopathies and Thalassemias John Old, in Emery and Rimoin's Principles and Practice of Medical Genetics (Sixth Edition), 2013 71.2.1 Primary and Secondary Structures The primary structure of each globin chain is its amino acid sequence; it is composed of 141 amino acids in α- and...
James F. ReynoldsAmerican Journal of Medical GeneticsPootrakul, S., Muang-sup, V., Fucharoen, S., and Wasi, P. (1988). Cord blood study on beta- thalassemia and hemoglobin E. Am. J. Med. Genet. 29:49.Pootrakul S, Muang-sup V, Fucharoen S, Wasi P. Cord blood study on β-...
Romana M,Keclard L,Froger A,et al.Spectrum of β-Thalassemia Mutations in Guadeloupe (French West Indies) and Interactions with Other Hemoglobinopathies[... M Romana,L Kéclard,A Froger,... - 《Annals of the New York Academy of Sciences》 被引量: 12发表: 2010年 加载更多来源...