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Biochimica Et Biophysica Acta|February 13, 1992
Purification and properties of human glucose-6-phosphate dehydrogenase made in E. coliJ M Bautista, P J Mason, L LuzzattoTumori|October 31, 1990
Parental occupation and other environmental factors in the etiology of leukemias and non-Hodgkin's lymphomas in childhood: a case-control studyC Magnani, G Pastore, L Luzzatto, et al.Early Human Development|November 1, 1987
Neonatal jaundice and severity of glucose-6-phosphate dehydrogenase deficiency in Sardinian babiesT Meloni, S Cutillo, U Testa, et al.Blood|October 1, 1984
Two populations of erythroid cell progenitors in paroxysmal nocturnal hemoglobinuriaB Rotoli, R Robledo, N Scarpato, et al.FEBS Letters|June 5, 1995
Human glucose-6-phosphate dehydrogenase. Lysine 205 is dispensable for substrate binding but essential for catalysisJ M Bautista, P J Mason, L LuzzattoThe Journal of Biological Chemistry|May 25, 1976
Genetic variants of human erythrocyte glucose-6-phosphate dehydrogenase. Kinetic and thermodynamic parameters of variants A, B, and A- in relation to quaternary structureA O Babalola, J G Beetlestone, L LuzzattoHaematologica|April 5, 2007
Erythopoietin treatment during complement inhibition with eculizumab in a patient with paroxysmal nocturnal hemoglobinuriaA Hill, S J Richards, R P Rother, et al.Leukemia|October 20, 2006
Flow cytometric protein expression profiling as a systematic approach for developing disease-specific assays: identification of a chronic lymphocytic leukaemia-specific assay for use in rituximab-containing regimensA C Rawstron, R de Tute, A S Jack, et al.Blood|August 26, 1998
Lymphocyte subset analysis and glycosylphosphatidylinositol phenotype in patients with paroxysmal nocturnal hemoglobinuriaS J Richards, D R Norfolk, D M Swirsky, et al.Leukemia & Lymphoma|July 28, 2016
Rearrangement of T-cell Receptor (Delta, Gamma and Beta) Genes and its Significance in T-cell Chronic LeukaemiasA K Singh, M Laffan, S Eridani, et al.Pageof 162