alpha-Thalassemiabeta-Globinsnitric oxide synthase type IIIhemoglobinsnitric oxidesickle cell traitSevere malaria is associated with impaired nitric oxide (NO) synthase (NOS)鈥揹ependent vasodilation, and reversal of this deficit improves survival in murine models. Malaria might have selected for ...
Alpha+-thalassemia trait caused by a nonsense mutation in the alpha2-globin gene: codon 54 (CAG>TAG). 来自 国家科技图书文献中心 喜欢 0 阅读量: 134 作者:B Eng,L Walker,JS Waye 摘要:We report a new alpha-thalassemia (alpha-thal) point mutation detected in a woman with alpha(+)-thal ...
Coexisting β-Thalassemia Trait, Gilbert Syndrome and Alpha-Globin Gene Triplication in a Child with Non-Transfusion Dependent Thalassemia Phenotype View further author informationhttps://orcid.org/0000-0002-1009-7649deepakbansaldr@gmail.comDeepak BansalView further author informationJasbir Kaur HiraView ...
The level of Hb C in the erythrocytes of individuals with Hb C trait decreases significantly in the presence of coexisting alpha-thalassemia. This relationship may result from the higher affinity of beta A than beta C for limiting amounts of alpha-globin during hemoglobin assembly. This mechanism...
Confirmation of the validity of using birth MCV for the diagnosis of alpha thalassemia trait.Confirmation of the validity of using birth MCV for the diagnosis of alpha thalassemia trait.doi:10.4081/hr.2009.e20HbBartshighperformanceliquidchromatographyMCHMCV...
Previous studies have shown that subjects with sickle cell trait (SCT), alpha-thalassemia (alpha-t), and the dual hemoglobinopathy (SCT/alpha-t) manifest subtle, albeit significant, differences during exercise. To better understand such differences, we assessed skeletal muscle histomorphological and ...
alpha‐thalassemia 1 traitmean corpuscular volume (MCV)polymerase chain reaction (PCR)thalassemia screeningAim: To identify the optimal cutoff of mean corpuscular volume (MCV) for screening of alpha-thalassemia 1 trait. Methods: The database of pregnant women who attended antenatal care clinic at ...
Alpha thalassemia trait masquerading as hemoglobin H disease due to co-existing primary myelofibrosisArticleDear Editor, The patient was a 29-year old Southern Chinese who was screened for thalassemia after his wife had been diagnosed as an alpha thalassemia carrier during antenatal check-up. He was...
alpha-Thalassaemia trait should be considered in all patients of 'high-risk' ethnic origins with a blood picture suggestive of beta-thalassaemia trait but in whom the levels of Hb A2 and Hb F are within normal limits. 展开 关键词: Humans Thalassemia Fetal Hemoglobin Blood Cell Count Infant, ...
Hegde U.M., White J.M., Hart G.H., Marsh G.W. Diagnosis of alpha-thalassemia trait from Coulter Counter `S' indices. J. Clin. Pathol. 1977; 30: 884-889.Hegde UM, White JM, Hart GH, Marsh GW: Diagnosis of alpha- thalassemia trait from Coulter counter'S' indices. J Clin Path...