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A Iolascon

Showing results (131-140 of 154) with videos related to

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British Journal of Haematology|June 3, 1998
Frequent de novo monoallelic expression of beta-spectrin gene (SPTB) in children with hereditary spherocytosis and isolated spectrin deficiencyE Miraglia del Giudice, C Lombardi, M Francese, et al.
International Journal of Laboratory Hematology|March 20, 2015
ICSH guidelines for the laboratory diagnosis of nonimmune hereditary red cell membrane disordersM-J King, L Garçon, J D Hoyer, et al.
Birth Defects Original Article Series|January 1, 1987
Clinical and biochemical study of thalassemia intermedia in Campania (southern Italy)A Iolascon, L Pinto, B Nobili, et al.
British Journal of Haematology|January 1, 1997
Novel band 3 variants (bands 3 Foggia, Napoli I and Napoli II) associated with hereditary spherocytosis and band 3 deficiency: status of the D38A polymorphism within the EPB3 locusE Miraglia del Giudice, A Vallier, P Maillet, et al.
British Journal of Haematology|April 1, 1996
Cytoskeletal behaviour in spectrin and in band 3 deficient spherocytic red cells: evidence for differentiated splenic conditioning roleD Ingrosso, S D'Angelo, S Perrotta, et al.
Oncogene|October 2, 2007
Phosphorylation of nm23-H1 by CKI induces its complex formation with h-prune and promotes cell motilityL Garzia, A D'Angelo, A Amoresano, et al.
Blood|May 15, 1996
The cisternae decorating the red blood cell membrane in congenital dyserythropoietic anemia (type II) originate from the endoplasmic reticulumN Alloisio, P Texier, L Denoroy, et al.
Biochemical and Biophysical Research Communications|February 3, 1997
Expression of G1-phase cell cycle genes during hematopoietic lineageF Della Ragione, A Borriello, S Mastropietro, et al.
American Journal of Human Genetics|August 27, 1998
Genomewide search for dehydrated hereditary stomatocytosis (hereditary xerocytosis): mapping of locus to chromosome 16 (16q23-qter)M Carella, G Stewart, J F Ajetunmobi, et al.
British Journal of Haematology|May 1, 1994
Glucose 6-phosphate dehydrogenase deficiency and red cell membrane defects: additive or synergistic interaction in producing chronic haemolytic anaemiaF Alfinito, V Calabro, M D Cappellini, et al.
Pageof 16

Showing results (131-140 of 154) with videos related to

Sort By:
Pageof 16
British Journal of Haematology|June 3, 1998
Frequent de novo monoallelic expression of beta-spectrin gene (SPTB) in children with hereditary spherocytosis and isolated spectrin deficiencyE Miraglia del Giudice, C Lombardi, M Francese, et al.
International Journal of Laboratory Hematology|March 20, 2015
ICSH guidelines for the laboratory diagnosis of nonimmune hereditary red cell membrane disordersM-J King, L Garçon, J D Hoyer, et al.
Birth Defects Original Article Series|January 1, 1987
Clinical and biochemical study of thalassemia intermedia in Campania (southern Italy)A Iolascon, L Pinto, B Nobili, et al.
British Journal of Haematology|January 1, 1997
Novel band 3 variants (bands 3 Foggia, Napoli I and Napoli II) associated with hereditary spherocytosis and band 3 deficiency: status of the D38A polymorphism within the EPB3 locusE Miraglia del Giudice, A Vallier, P Maillet, et al.
British Journal of Haematology|April 1, 1996
Cytoskeletal behaviour in spectrin and in band 3 deficient spherocytic red cells: evidence for differentiated splenic conditioning roleD Ingrosso, S D'Angelo, S Perrotta, et al.
Oncogene|October 2, 2007
Phosphorylation of nm23-H1 by CKI induces its complex formation with h-prune and promotes cell motilityL Garzia, A D'Angelo, A Amoresano, et al.
Blood|May 15, 1996
The cisternae decorating the red blood cell membrane in congenital dyserythropoietic anemia (type II) originate from the endoplasmic reticulumN Alloisio, P Texier, L Denoroy, et al.
Biochemical and Biophysical Research Communications|February 3, 1997
Expression of G1-phase cell cycle genes during hematopoietic lineageF Della Ragione, A Borriello, S Mastropietro, et al.
American Journal of Human Genetics|August 27, 1998
Genomewide search for dehydrated hereditary stomatocytosis (hereditary xerocytosis): mapping of locus to chromosome 16 (16q23-qter)M Carella, G Stewart, J F Ajetunmobi, et al.
British Journal of Haematology|May 1, 1994
Glucose 6-phosphate dehydrogenase deficiency and red cell membrane defects: additive or synergistic interaction in producing chronic haemolytic anaemiaF Alfinito, V Calabro, M D Cappellini, et al.
Pageof 16