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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.
Pediatric Hematology and Oncology|August 3, 2010
Transfusion and chelation practices in sickle cell disease: a regional perspectiveElliott P Vichinsky, Kwaku Ohene-Frempong, Swee Lay Thein, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 26, 2022
Phenotypic screening of the ReFRAME drug repurposing library to discover new drugs for treating sickle cell diseaseBelhu Metaferia, Troy Cellmer, Emily B Dunkelberger, et al.
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