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Blood
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August 1, 1992
Clonal origin of abnormal granulocytes in paroxysmal nocturnal hemoglobinuria
M Bessler, P Hillmen, L Luzzatto
Cell
|
January 10, 1997
Somatic mutations in paroxysmal nocturnal hemoglobinuria: a blessing in disguise?
L Luzzatto, M Bessler, B Rotoli
Blood Cells, Molecules & Diseases
|
January 1, 1996
Hematologically important mutations: glucose-6-phosphate dehydrogenase
E Beutler, T Vulliamy, L Luzzatto
Trends in Genetics : TIG
|
April 1, 1992
The molecular basis of glucose-6-phosphate dehydrogenase deficiency
T Vulliamy, P Mason, L Luzzatto
Leukemia Research
|
January 1, 1992
The "n-1" model for myelodysplastic syndromes
L Luzzatto, F Colonna, I Reilly
Leukemia
|
April 1, 1987
Immunoglobulin gene rearrangements in hairy cell leukemia and other chronic B cell lymphoproliferative disorders
L Foroni, D Catovsky, L Luzzatto
Proceedings of the National Academy of Sciences of the United States of America
|
April 1, 1972
Genetic variants of glucose 6-phosphate dehydrogenase from human erythrocytes: unique properties of the A - variant isolated from "deficient" cells
O Babalola, R Cancedda, L Luzzatto
Human Mutation
|
January 1, 1993
Variants of glucose-6-phosphate dehydrogenase are due to missense mutations spread throughout the coding region of the gene
T Vulliamy, E Beutler, L Luzzatto
British Journal of Haematology
|
July 1, 1980
Genetic and biochemical heterogeneity of beta-thalassaemia in Naples
G Pepe, L Lupi, L Luzzatto
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
March 4, 2000
Human mutations in glucose 6-phosphate dehydrogenase reflect evolutionary history
R Notaro, A Afolayan, L Luzzatto
Page
of 26
Search research articles
Search
Showing results (61-70 of 259) with videos related to
Sort By:
Page
of 26
Blood
|
August 1, 1992
Clonal origin of abnormal granulocytes in paroxysmal nocturnal hemoglobinuria
M Bessler, P Hillmen, L Luzzatto
Cell
|
January 10, 1997
Somatic mutations in paroxysmal nocturnal hemoglobinuria: a blessing in disguise?
L Luzzatto, M Bessler, B Rotoli
Blood Cells, Molecules & Diseases
|
January 1, 1996
Hematologically important mutations: glucose-6-phosphate dehydrogenase
E Beutler, T Vulliamy, L Luzzatto
Trends in Genetics : TIG
|
April 1, 1992
The molecular basis of glucose-6-phosphate dehydrogenase deficiency
T Vulliamy, P Mason, L Luzzatto
Leukemia Research
|
January 1, 1992
The "n-1" model for myelodysplastic syndromes
L Luzzatto, F Colonna, I Reilly
Leukemia
|
April 1, 1987
Immunoglobulin gene rearrangements in hairy cell leukemia and other chronic B cell lymphoproliferative disorders
L Foroni, D Catovsky, L Luzzatto
Proceedings of the National Academy of Sciences of the United States of America
|
April 1, 1972
Genetic variants of glucose 6-phosphate dehydrogenase from human erythrocytes: unique properties of the A - variant isolated from "deficient" cells
O Babalola, R Cancedda, L Luzzatto
Human Mutation
|
January 1, 1993
Variants of glucose-6-phosphate dehydrogenase are due to missense mutations spread throughout the coding region of the gene
T Vulliamy, E Beutler, L Luzzatto
British Journal of Haematology
|
July 1, 1980
Genetic and biochemical heterogeneity of beta-thalassaemia in Naples
G Pepe, L Lupi, L Luzzatto
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology
|
March 4, 2000
Human mutations in glucose 6-phosphate dehydrogenase reflect evolutionary history
R Notaro, A Afolayan, L Luzzatto
Page
of 26