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L Luzzatto

Showing results (121-130 of 259) with videos related to

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Acta Haematologica|January 1, 1976
Erythrocyte enzymes in neonatal juandiceU Bienzle, C E Effiong, V E Aimaku, et al.
British Journal of Haematology|June 1, 1994
Myelodysplasia in a patient with pre-existing paroxysmal nocturnal haemoglobinuria: a clonal disease originating from within a clonal diseaseL Longo, M Bessler, P Beris, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1985
Tissue-specific levels of human glucose-6-phosphate dehydrogenase correlate with methylation of specific sites at the 3' end of the geneG Battistuzzi, M D'Urso, D Toniolo, et al.
Cancer|October 1, 1991
Analysis of beta, gamma, and delta T-cell receptor genes in mycosis fungoides and Sezary syndromeS J Whittaker, N P Smith, R R Jones, et al.
Nature|December 24, 1981
cDNA sequences of human glucose 6-phosphate dehydrogenase cloned in pBR322M G Persico, D Toniolo, C Nobile, et al.
Annals of Human Genetics|October 1, 1989
A new genetic polymorphism in the 16S ribosomal RNA gene of human mitochondrial DNAA B Mehta, T Vulliamy, E C Gordon-Smith, et al.
Blood Cells, Molecules & Diseases|October 29, 1998
The spectrum of somatic mutations in the PIG-A gene in paroxysmal nocturnal hemoglobinuria includes large deletions and small duplicationsK Nafa, M Bessler, H Castro-Malaspina, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1979
Genetic heterogeneity of "normal" human erythrocyte glucose-6-phosphate dehydrogenase: an isoelectrophoretic polymorphismG Modiano, G Battistuzzi, G J Esan, et al.
British Journal of Haematology|February 13, 2001
PNH cells are as sensitive to T-cell-mediated lysis as their normal counterparts: implications for the pathogenesis of paroxysmal nocturnal haemoglobinuriaA Karadimitris, R Notaro, G Koehne, et al.
Journal of Internal Medicine|January 1, 1994
Tissue plasminogen activator for hepatic vein thrombosis in paroxysmal nocturnal haemoglobinuriaM F McMullin, P Hillmen, J Jackson, et al.
Pageof 26

Showing results (121-130 of 259) with videos related to

Sort By:
Pageof 26
Acta Haematologica|January 1, 1976
Erythrocyte enzymes in neonatal juandiceU Bienzle, C E Effiong, V E Aimaku, et al.
British Journal of Haematology|June 1, 1994
Myelodysplasia in a patient with pre-existing paroxysmal nocturnal haemoglobinuria: a clonal disease originating from within a clonal diseaseL Longo, M Bessler, P Beris, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 1, 1985
Tissue-specific levels of human glucose-6-phosphate dehydrogenase correlate with methylation of specific sites at the 3' end of the geneG Battistuzzi, M D'Urso, D Toniolo, et al.
Cancer|October 1, 1991
Analysis of beta, gamma, and delta T-cell receptor genes in mycosis fungoides and Sezary syndromeS J Whittaker, N P Smith, R R Jones, et al.
Nature|December 24, 1981
cDNA sequences of human glucose 6-phosphate dehydrogenase cloned in pBR322M G Persico, D Toniolo, C Nobile, et al.
Annals of Human Genetics|October 1, 1989
A new genetic polymorphism in the 16S ribosomal RNA gene of human mitochondrial DNAA B Mehta, T Vulliamy, E C Gordon-Smith, et al.
Blood Cells, Molecules & Diseases|October 29, 1998
The spectrum of somatic mutations in the PIG-A gene in paroxysmal nocturnal hemoglobinuria includes large deletions and small duplicationsK Nafa, M Bessler, H Castro-Malaspina, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1979
Genetic heterogeneity of "normal" human erythrocyte glucose-6-phosphate dehydrogenase: an isoelectrophoretic polymorphismG Modiano, G Battistuzzi, G J Esan, et al.
British Journal of Haematology|February 13, 2001
PNH cells are as sensitive to T-cell-mediated lysis as their normal counterparts: implications for the pathogenesis of paroxysmal nocturnal haemoglobinuriaA Karadimitris, R Notaro, G Koehne, et al.
Journal of Internal Medicine|January 1, 1994
Tissue plasminogen activator for hepatic vein thrombosis in paroxysmal nocturnal haemoglobinuriaM F McMullin, P Hillmen, J Jackson, et al.
Pageof 26