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British Journal of Haematology|February 24, 2005
Heterogeneity of the epsilon gamma delta beta-thalassaemias: characterization of three novel English deletionsHelen Rooks, Jean Bergounioux, Laurence Game, et al.Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|May 20, 2020
A comparison of cine CMR imaging at 0.55 T and 1.5 TW Patricia Bandettini, Sujata M Shanbhag, Christine Mancini, et al.British Journal of Haematology|July 20, 2016
ASH1L (a histone methyltransferase protein) is a novel candidate globin gene regulator revealed by genetic study of an English family with beta-thalassaemia unlinked to the beta-globin locusAmandine Breton, Andria Theodorou, Suleyman Aktuna, et al.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.Pageof 18