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L Luzzatto

Showing results (91-100 of 259) with videos related to

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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.
The New England Journal of Medicine|November 5, 1981
Uracil in DNA in megaloblastic anemiaL Luzzatto, A O Falusi, E A Joju
Blood|October 1, 1984
Two populations of erythroid cell progenitors in paroxysmal nocturnal hemoglobinuriaB Rotoli, R Robledo, N Scarpato, et al.
Blood Cells, Molecules & Diseases|August 1, 1997
Hematologically important mutations: glucose-6-phosphate dehydrogenaseT Bulliamy, L Luzzatto, A Hirono, et al.
British Journal of Haematology|September 1, 1991
Acquired beta thalassaemia trait in MDSC Hoyle, J Kaeda, J Leslie, 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 Luzzatto
Lancet (London, England)|April 16, 1994
Somatic mutations and cellular selection in paroxysmal nocturnal haemoglobinuriaM Bessler, P Mason, P Hillmen, et al.
Nature: New Biology|February 3, 1971
Synthesis of haemoglobins specified by allelic genes in human heterozygotesG J Esan, T A Adesina, L Luzzatto
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 Luzzatto
Tropical and Geographical Medicine|December 1, 1970
Haemophilia in NigeriaE M Essien, A O Folami, L Luzzatto
Pageof 26

Showing results (91-100 of 259) with videos related to

Sort By:
Pageof 26
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.
The New England Journal of Medicine|November 5, 1981
Uracil in DNA in megaloblastic anemiaL Luzzatto, A O Falusi, E A Joju
Blood|October 1, 1984
Two populations of erythroid cell progenitors in paroxysmal nocturnal hemoglobinuriaB Rotoli, R Robledo, N Scarpato, et al.
Blood Cells, Molecules & Diseases|August 1, 1997
Hematologically important mutations: glucose-6-phosphate dehydrogenaseT Bulliamy, L Luzzatto, A Hirono, et al.
British Journal of Haematology|September 1, 1991
Acquired beta thalassaemia trait in MDSC Hoyle, J Kaeda, J Leslie, 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 Luzzatto
Lancet (London, England)|April 16, 1994
Somatic mutations and cellular selection in paroxysmal nocturnal haemoglobinuriaM Bessler, P Mason, P Hillmen, et al.
Nature: New Biology|February 3, 1971
Synthesis of haemoglobins specified by allelic genes in human heterozygotesG J Esan, T A Adesina, L Luzzatto
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 Luzzatto
Tropical and Geographical Medicine|December 1, 1970
Haemophilia in NigeriaE M Essien, A O Folami, L Luzzatto
Pageof 26