Polymerization of Three Hemoglobin A2 Variants Containing Valδ6 and Inhibition of Hemoglobin S Polymerization by Hemoglobin A2-Reference-Cited by-同舟云学术

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Polymerization of Three Hemoglobin A2 Variants Containing Valδ6 and Inhibition of Hemoglobin S Polymerization by Hemoglobin A2

Published:1996-10 Issue:40 Volume:271 Page:24557-24563
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Adachi Kazuhiko,Pang Jian,Reddy Lattupally R.,Bradley Lorelle E.,Chen Quikan,Trifillis Panayiota,Schwartz Elias,Surrey Saul

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference38 articles.

1. Hemoglobin: Molecular, Genetic and Clinical Aspects;Bunn,1986

2. The Sickle Hemoglobins: Science and Medicine.;Embury,1994

3. Role of hybrid tetramer formation in gelation of haemoglobin S

4. Participation of hemoglobins A and F in polymerization of sickle hemoglobin.

5. Structural bases of the inhibitory effects of hemoglobin F and hemoglobin A2 on the polymerization of hemoglobin S.

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2. Delta‐globin gene expression improves sickle cell disease in a humanised mouse model;British Journal of Haematology;2021-05-28

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4. Hemoglobin disorders: lentiviral gene therapy in the starting blocks to enter clinical practice;Experimental Hematology;2018-08

5. Mathematical modeling of erythrocyte chimerism informs genetic intervention strategies for sickle cell disease;American Journal of Hematology;2016-07-14

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