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Proceedings of the National Academy of Sciences of the United States of America|June 27, 2007
Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adultsSwee Lay Thein, Stephan Menzel, Xu Peng, et al.
JCI Insight|January 20, 2026
Pyruvate kinase deficiency modifies sickle hemoglobin carrier and sickle cell disease phenotypes in miceXunde Wang, Meghann Smith, Sayuri Kamimura, et al.
British Journal of Haematology|February 19, 2016
Reduced rate of sickle-related complications in Brazilian patients carrying HbF-promoting alleles at the BCL11A and HMIP-2 lociFlávia C Leonardo, Ana F Brugnerotto, Igor F Domingos, et al.
Blood Advances|January 28, 2020
American Society of Hematology 2020 guidelines for sickle cell disease: transfusion supportStella T Chou, Mouaz Alsawas, Ross M Fasano, et al.
Annals of Human Genetics|July 30, 2014
Global genetic architecture of an erythroid quantitative trait locus, HMIP-2Stephan Menzel, Helen Rooks, Diana Zelenika, et al.
Blood. Red Cells & Iron|March 11, 2026
Long-term mitapivat treatment is safe and efficacious in patients with sickle cell diseaseAnna Conrey, Nancy Asomaning, Ingrid Frey, et al.
Plos One|August 13, 2013
Genome wide association analysis of a founder population identified TAF3 as a gene for MCHC in humansGiorgio Pistis, Shawntel U Okonkwo, Michela Traglia, et al.
Hemasphere|April 16, 2026
Lower efficacy of transfusion of red blood cells from donors with sickle cell traitMonika Dzieciatkowska, Daniel Stephenson, Ariel Hay, et al.
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