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Nature Medicine
|
March 19, 2013
Macrophages support pathological erythropoiesis in polycythemia vera and β-thalassemia
Pedro Ramos, Carla Casu, Sara Gardenghi, et al.
The Journal of Clinical Investigation
|
November 25, 2010
Hepcidin as a therapeutic tool to limit iron overload and improve anemia in β-thalassemic mice
Sara Gardenghi, Pedro Ramos, Maria Franca Marongiu, et al.
Blood
|
February 15, 2007
Ineffective erythropoiesis in beta-thalassemia is characterized by increased iron absorption mediated by down-regulation of hepcidin and up-regulation of ferroportin
Sara Gardenghi, Maria F Marongiu, Pedro Ramos, et al.
Haematologica
|
May 23, 2020
2'-O-methoxyethyl splice-switching oligos correct splicing from IVS2-745 β-thalassemia patient cells restoring HbA production and chain rebalance
Alisa Dong, Valentina Ghiaccio, Irene Motta, et al.
Blood
|
May 16, 2008
Decreased differentiation of erythroid cells exacerbates ineffective erythropoiesis in beta-thalassemia
Ilaria V Libani, Ella C Guy, Luca Melchiori, et al.
Molecular Therapy. Nucleic Acids
|
April 2, 2025
Effective gene therapy for metachromatic leukodystrophy achieved with minimal lentiviral genomic integrations
Lucas Tricoli, Sunetra Sase, Julia L Hacker, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
January 30, 2021
Lentiviral vector ALS20 yields high hemoglobin levels with low genomic integrations for treatment of beta-globinopathies
Laura Breda, Valentina Ghiaccio, Naoto Tanaka, et al.
Blood
|
July 1, 2024
Use of HSC-targeted LNP to generate a mouse model of lethal α-thalassemia and treatment via lentiviral gene therapy
Maxwell E Chappell, Laura Breda, Lucas Tricoli, et al.
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of 5
Search research articles
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Showing results (41-50 of 48) with videos related to
Sort By:
Page
of 5
You have reached the last page of results.
This site can display upto 48 results.
Nature Medicine
|
March 19, 2013
Macrophages support pathological erythropoiesis in polycythemia vera and β-thalassemia
Pedro Ramos, Carla Casu, Sara Gardenghi, et al.
The Journal of Clinical Investigation
|
November 25, 2010
Hepcidin as a therapeutic tool to limit iron overload and improve anemia in β-thalassemic mice
Sara Gardenghi, Pedro Ramos, Maria Franca Marongiu, et al.
Blood
|
February 15, 2007
Ineffective erythropoiesis in beta-thalassemia is characterized by increased iron absorption mediated by down-regulation of hepcidin and up-regulation of ferroportin
Sara Gardenghi, Maria F Marongiu, Pedro Ramos, et al.
Haematologica
|
May 23, 2020
2'-O-methoxyethyl splice-switching oligos correct splicing from IVS2-745 β-thalassemia patient cells restoring HbA production and chain rebalance
Alisa Dong, Valentina Ghiaccio, Irene Motta, et al.
Blood
|
May 16, 2008
Decreased differentiation of erythroid cells exacerbates ineffective erythropoiesis in beta-thalassemia
Ilaria V Libani, Ella C Guy, Luca Melchiori, et al.
Molecular Therapy. Nucleic Acids
|
April 2, 2025
Effective gene therapy for metachromatic leukodystrophy achieved with minimal lentiviral genomic integrations
Lucas Tricoli, Sunetra Sase, Julia L Hacker, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
January 30, 2021
Lentiviral vector ALS20 yields high hemoglobin levels with low genomic integrations for treatment of beta-globinopathies
Laura Breda, Valentina Ghiaccio, Naoto Tanaka, et al.
Blood
|
July 1, 2024
Use of HSC-targeted LNP to generate a mouse model of lethal α-thalassemia and treatment via lentiviral gene therapy
Maxwell E Chappell, Laura Breda, Lucas Tricoli, et al.
Page
of 5