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Blood Advances|April 1, 2026
Transthyretin V122I Variant and Protein Affects Cardiac Severity and Mortality in Sickle Cell DiseaseHaiou Li, Shijinqui Gao, Xunde Wang, et al.
Blood Cells, Molecules & Diseases|June 9, 2012
A novel 506kb deletion causing εγδβ thalassemiaHelen Rooks, Barnaby Clark, Steve Best, et al.
Biochemical and Biophysical Research Communications|April 8, 2021
NLRP3 inflammasome and bruton tyrosine kinase inhibition interferes with upregulated platelet aggregation and in vitro thrombus formation in sickle cell miceSebastian Vogel, Sayuri Kamimura, Taruna Arora, et al.
Human Mutation|August 6, 2016
Loss of Major DNase I Hypersensitive Sites in Duplicated β-globin Gene Cluster Incompletely Silences HBB Gene ExpressionN Scott Reading, Claire Shooter, Jihyun Song, et al.
International Journal of Laboratory Hematology|August 29, 2018
GlycA is not a useful biomarker of inflammation in sickle cell diseaseJulie K Weisman, Daveena Meeks, Laurel Mendelsohn, et al.
The American Journal of Cardiology|February 8, 2011
Seeking optimal relation between oxygen saturation and hemoglobin concentration in adults with cyanosis from congenital heart diseaseCraig S Broberg, Ananda R Jayaweera, Gerhard P Diller, et al.
Plos One|January 17, 2009
Genetic variation on chromosome 6 influences F cell levels in healthy individuals of African descent and HbF levels in sickle cell patientsLisa E Creary, Pinar Ulug, Stephan Menzel, et al.
Thorax|April 1, 2014
Pulmonary function, CT and echocardiographic abnormalities in sickle cell diseaseAlan Lunt, Sujal R Desai, Athol U Wells, et al.
Journal of Magnetic Resonance Imaging : JMRI|October 20, 2021
Evaluation of Hepatic Iron Overload Using a Contemporary 0.55 T MRI SystemAdrienne E Campbell-Washburn, Christine Mancini, Anna Conrey, et al.
Blood|October 1, 2016
Reversible binding of hemoglobin to band 3 constitutes the molecular switch that mediates O2 regulation of erythrocyte propertiesHaiyan Chu, Mary M McKenna, Nathan A Krump, et al.
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