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Laura Breda

Showing results (21-30 of 48) with videos related to

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Annals of Hematology|March 31, 2012
A combined approach for β-thalassemia based on gene therapy-mediated adult hemoglobin (HbA) production and fetal hemoglobin (HbF) inductionCristina Zuccato, Laura Breda, Francesca Salvatori, et al.
Annals of the New York Academy of Sciences|August 18, 2010
A preclinical approach for gene therapy of beta-thalassemiaLaura Breda, Dorothy A Kleinert, Carla Casu, et al.
Free Radical Biology & Medicine|November 30, 2007
Protective role of calreticulin in HFE hemochromatosisJorge P Pinto, Pedro Ramos, Sérgio F de Almeida, et al.
Blood|July 14, 2016
Forced chromatin looping raises fetal hemoglobin in adult sickle cells to higher levels than pharmacologic inducersLaura Breda, Irene Motta, Silvia Lourenco, et al.
British Journal of Haematology|August 31, 2006
Downregulation of hepcidin and haemojuvelin expression in the hepatocyte cell-line HepG2 induced by thalassaemic seraOrly Weizer-Stern, Konstantin Adamsky, Ninette Amariglio, et al.
Journal of Biomedical Science|August 19, 2004
Complexation to cationic microspheres of double-stranded peptide nucleic acid-DNA chimeras exhibiting decoy activityCarlo Mischiati, Alessia Sereni, Alessia Finotti, et al.
Analytical and Bioanalytical Chemistry|July 6, 2019
Development and characterization of cellular biosensors for HTS of erythroid differentiation inducers targeting the transcriptional activity of γ-globin and β-globin gene promotersGiulia Breveglieri, Francesca Salvatori, Alessia Finotti, et al.
Cell|August 16, 2014
Reactivation of developmentally silenced globin genes by forced chromatin loopingWulan Deng, Jeremy W Rupon, Ivan Krivega, et al.
Annals of the New York Academy of Sciences|December 13, 2005
Exploring the role of hepcidin, an antimicrobial and iron regulatory peptide, in increased iron absorption in beta-thalassemiaLaura Breda, Sara Gardenghi, Ella Guy, et al.
Biotechnology and Applied Biochemistry|February 17, 2009
Development of K562 cell clones expressing beta-globin mRNA carrying the beta039 thalassaemia mutation for the screening of correctors of stop-codon mutationsFrancesca Salvatori, Vera Cantale, Giulia Breveglieri, et al.
Pageof 5

Showing results (21-30 of 48) with videos related to

Sort By:
Pageof 5
Annals of Hematology|March 31, 2012
A combined approach for β-thalassemia based on gene therapy-mediated adult hemoglobin (HbA) production and fetal hemoglobin (HbF) inductionCristina Zuccato, Laura Breda, Francesca Salvatori, et al.
Annals of the New York Academy of Sciences|August 18, 2010
A preclinical approach for gene therapy of beta-thalassemiaLaura Breda, Dorothy A Kleinert, Carla Casu, et al.
Free Radical Biology & Medicine|November 30, 2007
Protective role of calreticulin in HFE hemochromatosisJorge P Pinto, Pedro Ramos, Sérgio F de Almeida, et al.
Blood|July 14, 2016
Forced chromatin looping raises fetal hemoglobin in adult sickle cells to higher levels than pharmacologic inducersLaura Breda, Irene Motta, Silvia Lourenco, et al.
British Journal of Haematology|August 31, 2006
Downregulation of hepcidin and haemojuvelin expression in the hepatocyte cell-line HepG2 induced by thalassaemic seraOrly Weizer-Stern, Konstantin Adamsky, Ninette Amariglio, et al.
Journal of Biomedical Science|August 19, 2004
Complexation to cationic microspheres of double-stranded peptide nucleic acid-DNA chimeras exhibiting decoy activityCarlo Mischiati, Alessia Sereni, Alessia Finotti, et al.
Analytical and Bioanalytical Chemistry|July 6, 2019
Development and characterization of cellular biosensors for HTS of erythroid differentiation inducers targeting the transcriptional activity of γ-globin and β-globin gene promotersGiulia Breveglieri, Francesca Salvatori, Alessia Finotti, et al.
Cell|August 16, 2014
Reactivation of developmentally silenced globin genes by forced chromatin loopingWulan Deng, Jeremy W Rupon, Ivan Krivega, et al.
Annals of the New York Academy of Sciences|December 13, 2005
Exploring the role of hepcidin, an antimicrobial and iron regulatory peptide, in increased iron absorption in beta-thalassemiaLaura Breda, Sara Gardenghi, Ella Guy, et al.
Biotechnology and Applied Biochemistry|February 17, 2009
Development of K562 cell clones expressing beta-globin mRNA carrying the beta039 thalassaemia mutation for the screening of correctors of stop-codon mutationsFrancesca Salvatori, Vera Cantale, Giulia Breveglieri, et al.
Pageof 5