Transfer of Human α- to β-Hemoglobin via Its Chaperone Protein
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference18 articles.
1. Disorders of Hemoglobin;Thein,2000
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2. Structure and function of haemoglobins;Blood Cells, Molecules, and Diseases;2018-05
3. Red blood cells free α-haemoglobin pool: a biomarker to monitor the β-thalassemia intermedia variability. The ALPHAPOOL study;British Journal of Haematology;2017-06-23
4. Rôle du chaperon moléculaire de l’alpha-hémoglobine dans la formation de l’hémoglobine et l’expression clinique de certaines hémoglobinopathies;Transfusion Clinique et Biologique;2015-03
5. Role of α-Globin H Helix in the Building of Tetrameric Human Hemoglobin: Interaction with α-Hemoglobin Stabilizing Protein (AHSP) and Heme Molecule;PLoS ONE;2014-11-04
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