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Blood|July 1, 2021
Treatment of sickle cell disease by increasing oxygen affinity of hemoglobinEric R Henry, Belhu Metaferia, Quan Li, et al.American Journal of Hematology|September 18, 2007
Population analysis of the alpha hemoglobin stabilizing protein (AHSP) gene identifies sequence variants that alter expression and functionCamila O dos Santos, Suiping Zhou, Rodrigo Secolin, et al.Plos One|November 6, 2014
Genome wide association study of fetal hemoglobin in sickle cell anemia in TanzaniaSiana Nkya Mtatiro, Tarjinder Singh, Helen Rooks, et al.Human Genetics|October 18, 2002
Genetic basis of inosine triphosphate pyrophosphohydrolase deficiencySatoshi Sumi, Anthony M Marinaki, Monica Arenas, et al.Haematologica|March 7, 2024
Functional and multi-omics signatures of mitapivat efficacy upon activation of pyruvate kinase in red blood cells from patients with sickle cell diseaseAngelo D'Alessandro, Kang Le, Maureen Lundt, et al.Nature Genetics|September 4, 2007
A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15Stephan Menzel, Chad Garner, Ivo Gut, et al.Blood|November 12, 2010
Genetics of fetal hemoglobin in Tanzanian and British patients with sickle cell anemiaJulie Makani, Stephan Menzel, Siana Nkya, et al.Haematologica|December 3, 2016
Associations between environmental factors and hospital admissions for sickle cell diseaseFrédéric B Piel, Sanjay Tewari, Valentine Brousse, et al.Proceedings of the National Academy of Sciences of the United States of America|June 13, 2020
Allosteric control of hemoglobin S fiber formation by oxygen and its relation to the pathophysiology of sickle cell diseaseEric R Henry, Troy Cellmer, Emily B Dunkelberger, et al.Blood Advances|September 12, 2024
Activating pyruvate kinase improves red blood cell integrity by reducing band 3 tyrosine phosphorylationKang Le, Xunde Wang, Jonathan Chu, et al.Pageof 20