Impaired binding of AHSP to α chain variants: Hb Groene Hart illustrates a mechanism leading to unstable hemoglobins with α thalassemic like syndrome-Reference-Cited by-同舟云学术

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Impaired binding of AHSP to α chain variants: Hb Groene Hart illustrates a mechanism leading to unstable hemoglobins with α thalassemic like syndrome

Published:2006-11 Issue:3 Volume:37 Page:173-179
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Vasseur-Godbillon Corinne,Marden Michael C.,Giordano Piero,Wajcman Henri,Baudin-Creuza Véronique

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference29 articles.

1. An abundant erythroid protein that stabilizes free α-haemoglobin;Kihm;Nature,2002

2. NMR structure of the alpha-hemoglobin stabilizing protein: insights into conformational heterogeneity and binding;Santiveri;J. Biol. Chem.,2004

3. Biophysical characterization of the alpha-globin binding protein alpha-hemoglobin stabilizing protein;Gell;J. Biol. Chem.,2002

4. Loss of alpha-hemoglobin-stabilizing protein impairs erythropoiesis and exacerbates beta-thalassemia;Kong;J. Clin. Invest.,2004

5. Evaluation of alpha hemoglobin stabilizing protein (AHSP) as a genetic modifier in patients with beta thalassemia;Viprakasit;Blood,2004

Cited by 37 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Hemoglobinopathy gone astray—three novel forms of α-thalassemia in Norwegian patients characterized by quantitative real-time PCR and DNA sequencing;Scandinavian Journal of Clinical and Laboratory Investigation;2021-11-18

2. Effect of Mutations on mRNA and Globin Stability: The Cases of Hb Bernalda/Groene Hart and Hb Southern Italy;Genes;2020-07-31

3. Alpha-hemoglobin-stabilizing protein (AHSP): a modulatory factor in β-thalassemia;International Journal of Hematology;2020-01-01

4. Curating the gnomAD database: Report of novel variants in the globin‐coding genes and bioinformatics analysis;Human Mutation;2019-10-14

5. Molecular Genetics of the α‐Thalassaemias;eLS;2018-10-15

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