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Tumori|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 LuzzattoProceedings of the National Academy of Sciences of the United States of America|September 16, 1998
Very late DNA replication in the human cell cycleR J Widrow, R S Hansen, H Kawame, et al.Proceedings of the National Academy of Sciences of the United States of America|April 1, 1982
Transformation with DNA from 5-azacytidine-reactivated X chromosomesL Venolia, S M Gartler, E R Wassman, et al.The Journal of Biological Chemistry|June 6, 1997
5-Azadeoxycytidine-induced chromatin remodeling of the inactive X-linked HPRT gene promoter occurs prior to transcription factor binding and gene reactivationM D Litt, R S Hansen, I K Hornstra, et al.Blood|January 1, 1993
Production and characterization of lymphoblastoid cell lines with the paroxysmal nocturnal hemoglobinuria phenotypeP Hillmen, M Bessler, D H Crawford, et al.Pageof 24