Development of a fluorescence immunochromatographic assay for the detection of zeta globin in the blood of (−−SEA) α-thalassemia carriers
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Hematology,Molecular Biology,Molecular Medicine
Reference23 articles.
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3. The severe form of alpha thalassaemia is caused by a haemoglobin gene deletion;Ottolenghi;Nature,1974
4. Quantities of adult, fetal and embryonic globin chains in the blood of eighteen- to twenty-week-old human fetuses;Kutlar;J. Chromatogr.,1991
5. Embryonic zeta-globin chains in adults: a marker for alpha-thalassemia-1 haplotype due to a greater than 17.5-kb deletion;Chui;N. Engl. J. Med.,1986
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1. LC–MS/MS-Based Absolute Quantitation of Hemoglobin Subunits from Dried Blood Spots Reveals Novel Biomarkers for α-Thalassemia Silent Carriers;Analytical Chemistry;2023-06-07
2. Quantification of human embryonic ζ-globin chains in Southeast Asian deletion (--SEA) carriers;Journal of Clinical Pathology;2022-08-25
3. A smartphone-based enzyme-linked immunochromatographic sensor for rapid quantitative detection of carcinoembryonic antigen;Sensors and Actuators B: Chemical;2021-02
4. Impact of the detection of ζ-globin chains and hemoglobin Bart’s using immunochromatographic strip tests for α0-thalassemia (--SEA) differential diagnosis;PLOS ONE;2019-10-29
5. Immunostick Test for Detecting ζ-Globin Chains and Screening of the Southeast Asian α-Thalassemia 1 Deletion;Biological Procedures Online;2019-08-01
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