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Lucio Luzzatto

Showing results (121-130 of 140) with videos related to

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Blood Cells, Molecules & Diseases|August 14, 2016
Favism, the commonest form of severe hemolytic anemia in Palestinian children, varies in severity with three different variants of G6PD deficiency within the same communityN Scott Reading, Mahmoud M Sirdah, Mohammad E Shubair, et al.
The Journal of Allergy and Clinical Immunology|September 7, 2015
Genetic predisposition to hemophagocytic lymphohistiocytosis: Report on 500 patients from the Italian registryValentina Cetica, Elena Sieni, Daniela Pende, et al.
Blood|February 2, 2013
Glycosylphosphatidylinositol-specific, CD1d-restricted T cells in paroxysmal nocturnal hemoglobinuriaLucia Gargiulo, Maria Papaioannou, Michela Sica, et al.
Developmental Cell|October 27, 2009
LRF is an essential downstream target of GATA1 in erythroid development and regulates BIM-dependent apoptosisTakahiro Maeda, Keisuke Ito, Taha Merghoub, et al.
Haematologica|December 3, 2011
Thrombolytic therapy is effective in paroxysmal nocturnal hemoglobinuria: a series of nine patients and a review of the literatureDavid J Araten, Rosario Notaro, Howard T Thaler, et al.
Human Genomics|July 24, 2023
COVID-19 annual update: a narrative reviewMichela Biancolella, Vito Luigi Colona, Lucio Luzzatto, et al.
Cytometry. Part B, Clinical Cytometry|January 3, 2013
A systematic analysis of bone marrow cells by flow cytometry defines a specific phenotypic profile beyond GPI deficiency in paroxysmal nocturnal hemoglobinuriaFrancesco Mannelli, Sara Bencini, Benedetta Peruzzi, et al.
Genes & Cancer|July 23, 2011
A Role for PML in Innate ImmunityAndrea Lunardi, Mirella Gaboli, Marco Giorgio, et al.
Blood|May 9, 2014
Transcriptional and epigenetic basis for restoration of G6PD enzymatic activity in human G6PD-deficient cellsKalliopi Makarona, Valentina S Caputo, Joana R Costa, et al.
Haematologica|September 17, 2013
Polymorphism of the complement receptor 1 gene correlates with the hematologic response to eculizumab in patients with paroxysmal nocturnal hemoglobinuriaTommaso Rondelli, Antonio M Risitano, Régis Peffault de Latour, et al.
Pageof 14

Showing results (121-130 of 140) with videos related to

Sort By:
Pageof 14
Blood Cells, Molecules & Diseases|August 14, 2016
Favism, the commonest form of severe hemolytic anemia in Palestinian children, varies in severity with three different variants of G6PD deficiency within the same communityN Scott Reading, Mahmoud M Sirdah, Mohammad E Shubair, et al.
The Journal of Allergy and Clinical Immunology|September 7, 2015
Genetic predisposition to hemophagocytic lymphohistiocytosis: Report on 500 patients from the Italian registryValentina Cetica, Elena Sieni, Daniela Pende, et al.
Blood|February 2, 2013
Glycosylphosphatidylinositol-specific, CD1d-restricted T cells in paroxysmal nocturnal hemoglobinuriaLucia Gargiulo, Maria Papaioannou, Michela Sica, et al.
Developmental Cell|October 27, 2009
LRF is an essential downstream target of GATA1 in erythroid development and regulates BIM-dependent apoptosisTakahiro Maeda, Keisuke Ito, Taha Merghoub, et al.
Haematologica|December 3, 2011
Thrombolytic therapy is effective in paroxysmal nocturnal hemoglobinuria: a series of nine patients and a review of the literatureDavid J Araten, Rosario Notaro, Howard T Thaler, et al.
Human Genomics|July 24, 2023
COVID-19 annual update: a narrative reviewMichela Biancolella, Vito Luigi Colona, Lucio Luzzatto, et al.
Cytometry. Part B, Clinical Cytometry|January 3, 2013
A systematic analysis of bone marrow cells by flow cytometry defines a specific phenotypic profile beyond GPI deficiency in paroxysmal nocturnal hemoglobinuriaFrancesco Mannelli, Sara Bencini, Benedetta Peruzzi, et al.
Genes & Cancer|July 23, 2011
A Role for PML in Innate ImmunityAndrea Lunardi, Mirella Gaboli, Marco Giorgio, et al.
Blood|May 9, 2014
Transcriptional and epigenetic basis for restoration of G6PD enzymatic activity in human G6PD-deficient cellsKalliopi Makarona, Valentina S Caputo, Joana R Costa, et al.
Haematologica|September 17, 2013
Polymorphism of the complement receptor 1 gene correlates with the hematologic response to eculizumab in patients with paroxysmal nocturnal hemoglobinuriaTommaso Rondelli, Antonio M Risitano, Régis Peffault de Latour, et al.
Pageof 14