Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Paolo Moi

Showing results (11-20 of 40) with videos related to

Pageof 4
Sort By:
British Journal of Haematology|September 24, 2004
The distal beta-globin CACCC box is required for maximal stimulation of the beta-globin gene by EKLFMaria Giuseppina Marini, Isadora Asunis, Loredana Porcu, et al.
Blood Cells, Molecules & Diseases|December 20, 2002
Cloning MafF by recognition site screening with the NFE2 tandem repeat of HS2: analysis of its role in globin and GCSl genes regulationM Giuseppina Marini, Isadora Asunis, Kaimin Chan, et al.
Blood|August 9, 2011
KLF1 gene mutations cause borderline HbA(2)Lucia Perseu, Stefania Satta, Paolo Moi, et al.
Haematologica|January 29, 2011
Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrinStefania Satta, Lucia Perseu, Paolo Moi, et al.
British Journal of Haematology|March 25, 2010
Regulation of the human HBA genes by KLF4 in erythroid cell linesM Giuseppina Marini, Loredana Porcu, Isadora Asunis, et al.
Acta Haematologica|May 30, 2015
Thalassemia Major: Who Is Afraid of Serum Ferritin below 500 μg/l?Francesca Pinna, Roberto Carta, Maddalena Morittu, et al.
Blood Cells, Molecules & Diseases|March 27, 2017
Changes in HbA2 and HbF in alpha thalassemia carriers with KLF1 mutationStefania Satta, Maria Elisabetta Paglietti, Maria Carla Sollaino, et al.
Blood|October 15, 2016
Current growth patterns in children and adolescents with thalassemia majorRaffaella Origa, Fabrice Danjou, Valeria Orecchia, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|June 21, 2018
Quality of life in Sardinian patients with transfusion-dependent Thalassemia: a cross-sectional studyFrancesca Floris, Federica Comitini, GiovanBattista Leoni, et al.
Haematologica|July 23, 2013
In vivo activation of the human δ-globin gene: the therapeutic potential in β-thalassemic miceMaria F Manchinu, Maria F Marongiu, Daniela Poddie, et al.
Pageof 4

Showing results (11-20 of 40) with videos related to

Sort By:
Pageof 4
British Journal of Haematology|September 24, 2004
The distal beta-globin CACCC box is required for maximal stimulation of the beta-globin gene by EKLFMaria Giuseppina Marini, Isadora Asunis, Loredana Porcu, et al.
Blood Cells, Molecules & Diseases|December 20, 2002
Cloning MafF by recognition site screening with the NFE2 tandem repeat of HS2: analysis of its role in globin and GCSl genes regulationM Giuseppina Marini, Isadora Asunis, Kaimin Chan, et al.
Blood|August 9, 2011
KLF1 gene mutations cause borderline HbA(2)Lucia Perseu, Stefania Satta, Paolo Moi, et al.
Haematologica|January 29, 2011
Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrinStefania Satta, Lucia Perseu, Paolo Moi, et al.
British Journal of Haematology|March 25, 2010
Regulation of the human HBA genes by KLF4 in erythroid cell linesM Giuseppina Marini, Loredana Porcu, Isadora Asunis, et al.
Acta Haematologica|May 30, 2015
Thalassemia Major: Who Is Afraid of Serum Ferritin below 500 μg/l?Francesca Pinna, Roberto Carta, Maddalena Morittu, et al.
Blood Cells, Molecules & Diseases|March 27, 2017
Changes in HbA2 and HbF in alpha thalassemia carriers with KLF1 mutationStefania Satta, Maria Elisabetta Paglietti, Maria Carla Sollaino, et al.
Blood|October 15, 2016
Current growth patterns in children and adolescents with thalassemia majorRaffaella Origa, Fabrice Danjou, Valeria Orecchia, et al.
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|June 21, 2018
Quality of life in Sardinian patients with transfusion-dependent Thalassemia: a cross-sectional studyFrancesca Floris, Federica Comitini, GiovanBattista Leoni, et al.
Haematologica|July 23, 2013
In vivo activation of the human δ-globin gene: the therapeutic potential in β-thalassemic miceMaria F Manchinu, Maria F Marongiu, Daniela Poddie, et al.
Pageof 4