The genetics of hemoglobin A2regulation in sickle cell anemia-Reference-Cited by-同舟云学术

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The genetics of hemoglobin A2regulation in sickle cell anemia

Published:2014-08-04 Issue:11 Volume:89 Page:1019-1023
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am. J. Hematol.

Author:

Griffin Paula J.¹,Sebastiani Paola¹,Edward Heather²,Baldwin Clinton T.²,Gladwin Mark T.³,Gordeuk Victor R.⁴,Chui David H.K.²,Steinberg Martin H.²

Affiliation:

1. Department of Biostatistics; Boston University School of Public Health; Boston Massachusetts

2. Department of Medicine; Boston University School of Medicine; Boston Massachusetts

3. Division of Pulmonary, Allergy and Critical Care Medicine; University of Pittsburgh; Pittsburgh Pennsylvania

4. Department of Medicine and Comprehensive Sickle Cell Center; University of Illinois; Chicago Illinois

Funder

Foundation for the National Institutes of Health

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajh.23811/fullpdf

Reference58 articles.

1. Hemoglobin A2: Origin, evolution, and aftermath;Steinberg;Blood,1991

2. HbA2 levels in normal adults are influenced by two distinct genetic mechanisms;Menzel;Br J Haematol,2013

3. The distribution of hemoglobin A2;Heller;Ann NY Acad Sci,1968

4. Sparing effect of hemoglobin F and hemoglobin A 2 on the polymerization of hemoglobin S at physiologic ligand saturations;Poillon;Proc Natl Acad Sci USA,1993

5. Structural basis for the inhibitory effects of hemoglobin F and hemoglobin A2 on the polymerization of hemoglobin S;Nagel;Proc Natl Acad Sci USA,1979

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1. Genetic Variation and Sickle Cell Disease Severity;JAMA Network Open;2023-10-18

2. Experimental Babesia rossi infection induces hemolytic, metabolic, and viral response pathways in the canine host;BMC Genomics;2021-08-16

3. Haemoglobin switching modulator SNPs rs5006884 is associated with increased HbA2 in β-thalassaemia carriers;Archives of Medical Science;2021-07-16

4. Unique Polymorphisms at BCL11A, HBS1L-MYB and HBB Loci Associated with HbF in Kuwaiti Patients with Sickle Cell Disease;Journal of Personalized Medicine;2021-06-17

5. Elevated Hb A2 is Not Always Indicative of β-Thalassemia;Hemoglobin;2021-05-04

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