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Somatic Cell and Molecular Genetics|March 1, 1993
Paroxysmal nocturnal hemoglobinuria: correction of abnormal phenotype by somatic cell hybridizationP Hillmen, M Bessler, J Bungey, et al.Acta Cytologica|June 2, 2000
Human papillomavirus infection in atrophic smears. A case reportR Luzzatto, M Poli, M Recktenvald, et al.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 LuzzattoLancet (London, England)|April 16, 1994
Somatic mutations and cellular selection in paroxysmal nocturnal haemoglobinuriaM Bessler, P Mason, P Hillmen, et al.The 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 LuzzattoCritical Reviews in Immunology|October 20, 2001
A unique folate hydrolase, prostate-specific membrane antigen (PSMA): a target for immunotherapy?J Tasch, M Gong, M Sadelain, et al.Pageof 22