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Seminars in Hematology|June 13, 1998
Genetic treatment of severe hemoglobinopathies: the combat against transgene variegation and transgene silencingS Rivella, M SadelainImmuno-Oncology Technology|June 27, 2022
Function and evolution of the prototypic CD28ζ and 4-1BBζ chimeric antigen receptorsJ Feucht, M SadelainTrends in Cardiovascular Medicine|November 16, 2001
A promising genetic approach to the treatment of beta-thalassemiaC May, M SadelainSeminars in Hematology|October 18, 2001
Toward gene therapy for disorders of globin synthesisJ Tisdale, M SadelainCurrent Opinion in Hematology|March 1, 1996
The dual pathogenesis of paroxysmal nocturnal hemoglobinuriaL Luzzatto, M BesslerThe Journal of Clinical Investigation|December 1, 1992
Anomalous rearrangements of the immunoglobulin heavy chain genes in human leukemias support the loop-out mechanism of class switchM Laffan, L LuzzattoLeukemia|August 2, 2001
The cellular pathogenesis of paroxysmal nocturnal haemoglobinuriaA Karadimitris, L LuzzattoMolecular and Biochemical Parasitology|June 1, 1990
Expression and characterization of glucose-6-phosphate dehydrogenase of Plasmodium falciparumB Kurdi-Haidar, L LuzzattoNature|February 6, 1985
Adaptation of Plasmodium falciparum to glucose 6-phosphate dehydrogenase-deficient host red cells by production of parasite-encoded enzymeE A Usanga, L LuzzattoPageof 22