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L Luzzatto

Showing results (241-250 of 259) with videos related to

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Human Molecular Genetics|June 1, 1992
G6PD Kalyan and G6PD Kerala; two deficient variants in India caused by the same 317 Glu-->Lys mutationA Ahluwalia, C M Corcoran, T J Vulliamy, et al.
Il Giornale Di Chirurgia|March 17, 2004
[Is the Lauren classification an independent parameter for the prognostic evaluation of surgically treated gastric cancer patients? Analysis of a case series]G Midiri, E Eleuteri, M Coppola, et al.
Il Giornale Di Chirurgia|July 31, 2003
[From molecular biology to new treatment approaches to colorectal cancer: basic research, experimental trials and surgical implications]E Giarnieri, G Midiri, V A Cirolla, et al.
Acta Crystallographica. Section D, Biological Crystallography|March 25, 1999
Solution of the structure of tetrameric human glucose 6-phosphate dehydrogenase by molecular replacementS W Au, C E Naylor, S Gover, et al.
The Journal of Clinical Investigation|April 1, 1979
Defects in DNA and globin messenger RNA in homozygotes for hemoglobin LeporeF Ramirez, J G Mears, U Nudel, et al.
British Journal of Haematology|July 23, 1998
Clinical and haematological consequences of recurrent G6PD mutations and a single new mutation causing chronic nonspherocytic haemolytic anaemiaT J Vulliamy, J S Kaeda, D Ait-Chafa, et al.
British Journal of Haematology|February 15, 2002
Association of clonal T-cell large granular lymphocyte disease and paroxysmal nocturnal haemoglobinuria (PNH): further evidence for a pathogenetic link between T cells, aplastic anaemia and PNHA Karadimitris, K Li, R Notaro, et al.
British Medical Journal (Clinical Research Ed.)|June 8, 1985
Seroconversion of human T cell lymphotrophic virus III (HTLV-III) in patients with haemophilia: a longitudinal studyS E Ball, J M Hows, A M Worsley, et al.
American Journal of Human Genetics|December 1, 1995
A new glucose-6-phosphate dehydrogenase variant, G6PD Orissa (44 Ala-->Gly), is the major polymorphic variant in tribal populations in IndiaJ S Kaeda, G P Chhotray, M R Ranjit, et al.
British Journal of Haematology|March 2, 1999
Bone marrow transplants for paroxysmal nocturnal haemoglobinuriaR Saso, J Marsh, L Cevreska, et al.
Pageof 26

Showing results (241-250 of 259) with videos related to

Sort By:
Pageof 26
Human Molecular Genetics|June 1, 1992
G6PD Kalyan and G6PD Kerala; two deficient variants in India caused by the same 317 Glu-->Lys mutationA Ahluwalia, C M Corcoran, T J Vulliamy, et al.
Il Giornale Di Chirurgia|March 17, 2004
[Is the Lauren classification an independent parameter for the prognostic evaluation of surgically treated gastric cancer patients? Analysis of a case series]G Midiri, E Eleuteri, M Coppola, et al.
Il Giornale Di Chirurgia|July 31, 2003
[From molecular biology to new treatment approaches to colorectal cancer: basic research, experimental trials and surgical implications]E Giarnieri, G Midiri, V A Cirolla, et al.
Acta Crystallographica. Section D, Biological Crystallography|March 25, 1999
Solution of the structure of tetrameric human glucose 6-phosphate dehydrogenase by molecular replacementS W Au, C E Naylor, S Gover, et al.
The Journal of Clinical Investigation|April 1, 1979
Defects in DNA and globin messenger RNA in homozygotes for hemoglobin LeporeF Ramirez, J G Mears, U Nudel, et al.
British Journal of Haematology|July 23, 1998
Clinical and haematological consequences of recurrent G6PD mutations and a single new mutation causing chronic nonspherocytic haemolytic anaemiaT J Vulliamy, J S Kaeda, D Ait-Chafa, et al.
British Journal of Haematology|February 15, 2002
Association of clonal T-cell large granular lymphocyte disease and paroxysmal nocturnal haemoglobinuria (PNH): further evidence for a pathogenetic link between T cells, aplastic anaemia and PNHA Karadimitris, K Li, R Notaro, et al.
British Medical Journal (Clinical Research Ed.)|June 8, 1985
Seroconversion of human T cell lymphotrophic virus III (HTLV-III) in patients with haemophilia: a longitudinal studyS E Ball, J M Hows, A M Worsley, et al.
American Journal of Human Genetics|December 1, 1995
A new glucose-6-phosphate dehydrogenase variant, G6PD Orissa (44 Ala-->Gly), is the major polymorphic variant in tribal populations in IndiaJ S Kaeda, G P Chhotray, M R Ranjit, et al.
British Journal of Haematology|March 2, 1999
Bone marrow transplants for paroxysmal nocturnal haemoglobinuriaR Saso, J Marsh, L Cevreska, et al.
Pageof 26