MOI, PAOLO
MOI, PAOLO
A decisional algorithm to start iron chelation in patients with beta thalassemia
2014-01-01 Danjou, Fabrice; Cabantchik, Zi; Origa, Raffaella; Moi, Paolo; Marcias, M; Barella, S; Defraia, E; Dessì, C; Foschini, Ml; Giagu, N; Leoni, Gb; Morittu, M; Galanello, R.
A genetic score for the prediction of beta-thalassemia severity
2015-01-01 Danjou, Fabrice; Francavilla, M; Anni, Franco; Satta, Stefania; Demartis, Fr; Perseu, L; Manca, Matteo; Sollaino, Mc; Manunza, Laura; Mereu, E; Marceddu, G; Pissard, S; Joly, P; Thuret, I; Origa, Raffaella; Borg, J; Forni, Gl; Piga, A; Lai, Me; Badens, C; Moi, Paolo; Galanello, R.
A homozygous nonsense mutation of the human growth hormone receptor gene in a Sardinian boy with Laron-type dwarfism
1997-01-01 Putzolu, M; Meloni, A; Loche, S; Pischedda, C; Cao, A; Moi, Paolo
A missense (T577I) mutation in the luteinizing hormone receptor gene associated with familial male-limited precocious puberty
1996-01-01 Cocco, S; Meloni, A; Marini, MARIA GIUSEPPINA; Cao, A; Moi, Paolo
A novel high-content immunofluorescence assay as a tool to identify at the single cell level γ-globin inducing compounds
2015-01-01 Durlak, Marta; Fugazza, Cristina; Elangovan, Sudharshan; Marini, Maria Giuseppina; Marongiu, Maria Franca; Moi, Paolo; Fraietta, Ivan; Cappella, Paolo; Barbarani, Gloria; Font Monclus, Isaura; Mauri, Mario; Ottolenghi, Sergio; Gasparri, Fabio; Ronchi, Antonella
A novel missense mutation (C84R) in a patient with type II vitamin D-dependent rickets
2010-01-01 Asunis, I; Marini, MARIA GIUSEPPINA; Porcu, Loredana; Meloni, A; Cabriolu, Annalisa; Cao, A; Moi, Paolo
A novel silent beta-thalassemia mutation in the distal CACCC box affects the binding and responsiveness to EKLF
2004-01-01 Moi, Paolo; Faà, V; Marini, MARIA GIUSEPPINA; Asunis, I; Ibba, G; Cao, A; Rosatelli, MARIA CRISTINA
A novel splicing defect (IVS6+1G > T) in a patient with pseudovitamin D deficiency rickets
2002-01-01 Porcu, Loredana; Meloni, A; Casula, L; Asunis, I; Marini, MARIA GIUSEPPINA; Cao, A; Moi, P.
A validated cellular biobank for β-thalassemia
2016-01-01 Cosenza, Lucia Carmela; Breda, Laura; Breveglieri, Giulia; Zuccato, Cristina; Finotti, Alessia; Lampronti, Ilaria; Borgatti, Monica; Chiavilli, Francesco; Gamberini, Maria Rita; Satta, Stefania; Manunza, Laura; De Martis, Franca Rosa; Moi, Paolo; Rivella, Stefano; Gambari, Roberto; Bianchi, Nicoletta
An initiation codon mutation (AUG----GUG) of the human alpha 1-globin gene. Structural characterization and evidence for a mild thalassemic phenotype
1987-01-01 Moi, Paolo; Cash, Fe; Liebhaber, Sa; Cao, A; Pirastu, M.
Beta-thalassaemia unlinked to the beta-globin gene interacts with sickle-cell trait in a Portuguese family
1995-01-01 Pacheco, P; Peres, Mj; Faustino, P; Pischedda, C; Gonçalves, J; Carvajales Ramos, M; Seixas, T; Martins, Mc; Moi, Paolo; Lavinha, J.
beta-Thalassemia mutation at -90C-->T impairs the interaction of the proximal CACCC box with both erythroid and nonerythroid factors
1996-01-01 Faustino, P; Lavinha, J; Marini, MARIA GIUSEPPINA; Moi, Paolo
cAMP differentially regulates gamma-globin gene expression in erythroleukemic cells and primary erythroblasts through c-Myb expression
2006-01-01 Kuroyanagi, Y; Kaneko, Y; Muta, K; Park, Bs; Moi, Paolo; Ausenda, S; Cappellini, Md; Ikuta, T.
Causes of hospital admission in children and adults with transfusion-dependent thalassemia in Sardinia, 2000-2015
2017-01-01 Origa, Raffaella; Anni, Franco; Mereu, Luca; Follesa, Ilenia; Campus, Simona; Dessì, Carlo; Foschini, Maria Loreta; Leoni, Giovanbattista; Moi, Paolo; Morittu, Maddalena; Orecchia, Valeria; Perra, Maria; Zappu, Antonietta; Podda, Rosa Anna
Changes in HbA2 and HbF in alpha thalassemia carriers with KLF1 mutation
2017-01-01 Satta, Stefania; Paglietti, MARIA ELISABETTA; Sollaino, Maria Carla; Barella, Susanna; Moi, Paolo; Desogus, Maria Franca; Demartis, FRANCA ROSA; Manunza, Laura; Origa, Raffaella
Children of a lesser god or miracles? An emotional and behavioural profile of children born to mothers on dialysis in Italy: A multicentre nationwide study 2000-12
2015-01-01 Piccoli, Giorgina Barbara; Postorino, Valentina; Cabiddu, Gianfranca; Ghiotto, Sara; Guzzo, Gabriella; Roggero, Simona; Manca, Eleonora; Puddu, Rosalba; Meloni, Francesca; Attini, Rossella; Moi, Paolo; Maxia, Stefania; Piga, Antonio; Mazzone, Luigi; Pani, Antonello; Postorino, Maurizio; Castellino, Santina; Gernone, Giuseppe; Guida, Bruna; Calabria, Santo; Galliani, Marco; Manisco, Gianfranco; Di Tullio, Massimo; Vernaglione, Luigi; Chiappini, Maria Grazia; Proietti, Emanuela; Saffiotti, Stefano; Gangeni, Concetta; Brunati, Chiara; Montoli, Alberto; Esposito, Ciro; Montagna, Giovanni; Tata, Salvatore; Romano, Paolo; Amatruda, Ottavio; Cervini, Paolo; Casiraghi, Erika; Fabbrini, Paolo; Pieruzzi, Federico; Di Benedetto, Attilio; Alfisi, Giuseppina; Heidempergher, Marco; Buskermolen, Monique; Leveque, Alessandro; Autuly, Valerie; Giofrè, Francesco; Alati, Giovanni; Lombardi, Luigi; Riccio, Mara; Riccio, Ivano; Stingone, Antonio; D'Angelo, Benito; Lucchi, Leonardo; Stipo, Lucia; Loi, Valentina
Chromosomal localization of the human NF-E2 family of bZIP transcription factors by fluorescence in situ hybridization
1995-01-01 Chan, Jy; Cheung, Mc; Moi, Paolo; Chan, K; Kan, Yw
Cloning MafF by recognition site screening with the NFE2 tandem repeat of HS2: analysis of its role in globin and GCSl genes regulation
2002-01-01 Marini, MARIA GIUSEPPINA; Asunis, I; Chan, K; Chan, Jy; Kan, Yw; Porcu, Loredana; Cao, A; Moi, Paolo
CLONING OF A SMALL HUMAN MAF PROTEIN THAT HETERODIMERIZES SPECIFICALLY WITH NRF1
1994-01-01 Moi, Paolo; Chan, K; Marini, G; Casula, L; Melis, A; Cao, A.
Cloning, characterization, DNA binding, mapping and mutation analysis of the human erythroid kruppel-like factor (EKLF) gene
1996-01-01 Moi, P; Azunis, I; Saba, Luisella; Padiglia, Alessandra; Senes, G; Pischedda, C; Nucaro, Al; Cao, A; Rosatelli, MARIA CRISTINA
| Titolo | Data di pubblicazione | Autore(i) | Rivista | Editore |
|---|---|---|---|---|
| A decisional algorithm to start iron chelation in patients with beta thalassemia | 1-gen-2014 | Danjou, Fabrice; Cabantchik, Zi; Origa, Raffaella; Moi, Paolo; Marcias, M; Barella, S; Defraia, E; Dessì, C; Foschini, Ml; Giagu, N; Leoni, Gb; Morittu, M; Galanello, R. | HAEMATOLOGICA | - |
| A genetic score for the prediction of beta-thalassemia severity | 1-gen-2015 | Danjou, Fabrice; Francavilla, M; Anni, Franco; Satta, Stefania; Demartis, Fr; Perseu, L; Manca, Matteo; Sollaino, Mc; Manunza, Laura; Mereu, E; Marceddu, G; Pissard, S; Joly, P; Thuret, I; Origa, Raffaella; Borg, J; Forni, Gl; Piga, A; Lai, Me; Badens, C; Moi, Paolo; Galanello, R. | HAEMATOLOGICA | - |
| A homozygous nonsense mutation of the human growth hormone receptor gene in a Sardinian boy with Laron-type dwarfism | 1-gen-1997 | Putzolu, M; Meloni, A; Loche, S; Pischedda, C; Cao, A; Moi, Paolo | JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION | - |
| A missense (T577I) mutation in the luteinizing hormone receptor gene associated with familial male-limited precocious puberty | 1-gen-1996 | Cocco, S; Meloni, A; Marini, MARIA GIUSEPPINA; Cao, A; Moi, Paolo | HUMAN MUTATION | - |
| A novel high-content immunofluorescence assay as a tool to identify at the single cell level γ-globin inducing compounds | 1-gen-2015 | Durlak, Marta; Fugazza, Cristina; Elangovan, Sudharshan; Marini, Maria Giuseppina; Marongiu, Maria Franca; Moi, Paolo; Fraietta, Ivan; Cappella, Paolo; Barbarani, Gloria; Font Monclus, Isaura; Mauri, Mario; Ottolenghi, Sergio; Gasparri, Fabio; Ronchi, Antonella | PLOS ONE | - |
| A novel missense mutation (C84R) in a patient with type II vitamin D-dependent rickets | 1-gen-2010 | Asunis, I; Marini, MARIA GIUSEPPINA; Porcu, Loredana; Meloni, A; Cabriolu, Annalisa; Cao, A; Moi, Paolo | EXPERIMENTAL AND CLINICAL ENDOCRINOLOGY & DIABETES | - |
| A novel silent beta-thalassemia mutation in the distal CACCC box affects the binding and responsiveness to EKLF | 1-gen-2004 | Moi, Paolo; Faà, V; Marini, MARIA GIUSEPPINA; Asunis, I; Ibba, G; Cao, A; Rosatelli, MARIA CRISTINA | BRITISH JOURNAL OF HAEMATOLOGY | - |
| A novel splicing defect (IVS6+1G > T) in a patient with pseudovitamin D deficiency rickets | 1-gen-2002 | Porcu, Loredana; Meloni, A; Casula, L; Asunis, I; Marini, MARIA GIUSEPPINA; Cao, A; Moi, P. | JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION | - |
| A validated cellular biobank for β-thalassemia | 1-gen-2016 | Cosenza, Lucia Carmela; Breda, Laura; Breveglieri, Giulia; Zuccato, Cristina; Finotti, Alessia; Lampronti, Ilaria; Borgatti, Monica; Chiavilli, Francesco; Gamberini, Maria Rita; Satta, Stefania; Manunza, Laura; De Martis, Franca Rosa; Moi, Paolo; Rivella, Stefano; Gambari, Roberto; Bianchi, Nicoletta | JOURNAL OF TRANSLATIONAL MEDICINE | - |
| An initiation codon mutation (AUG----GUG) of the human alpha 1-globin gene. Structural characterization and evidence for a mild thalassemic phenotype | 1-gen-1987 | Moi, Paolo; Cash, Fe; Liebhaber, Sa; Cao, A; Pirastu, M. | THE JOURNAL OF CLINICAL INVESTIGATION | - |
| Beta-thalassaemia unlinked to the beta-globin gene interacts with sickle-cell trait in a Portuguese family | 1-gen-1995 | Pacheco, P; Peres, Mj; Faustino, P; Pischedda, C; Gonçalves, J; Carvajales Ramos, M; Seixas, T; Martins, Mc; Moi, Paolo; Lavinha, J. | BRITISH JOURNAL OF HAEMATOLOGY | - |
| beta-Thalassemia mutation at -90C-->T impairs the interaction of the proximal CACCC box with both erythroid and nonerythroid factors | 1-gen-1996 | Faustino, P; Lavinha, J; Marini, MARIA GIUSEPPINA; Moi, Paolo | BLOOD | - |
| cAMP differentially regulates gamma-globin gene expression in erythroleukemic cells and primary erythroblasts through c-Myb expression | 1-gen-2006 | Kuroyanagi, Y; Kaneko, Y; Muta, K; Park, Bs; Moi, Paolo; Ausenda, S; Cappellini, Md; Ikuta, T. | BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS | - |
| Causes of hospital admission in children and adults with transfusion-dependent thalassemia in Sardinia, 2000-2015 | 1-gen-2017 | Origa, Raffaella; Anni, Franco; Mereu, Luca; Follesa, Ilenia; Campus, Simona; Dessì, Carlo; Foschini, Maria Loreta; Leoni, Giovanbattista; Moi, Paolo; Morittu, Maddalena; Orecchia, Valeria; Perra, Maria; Zappu, Antonietta; Podda, Rosa Anna | ANNALS OF HEMATOLOGY | - |
| Changes in HbA2 and HbF in alpha thalassemia carriers with KLF1 mutation | 1-gen-2017 | Satta, Stefania; Paglietti, MARIA ELISABETTA; Sollaino, Maria Carla; Barella, Susanna; Moi, Paolo; Desogus, Maria Franca; Demartis, FRANCA ROSA; Manunza, Laura; Origa, Raffaella | BLOOD CELLS, MOLECULES, & DISEASES | - |
| Children of a lesser god or miracles? An emotional and behavioural profile of children born to mothers on dialysis in Italy: A multicentre nationwide study 2000-12 | 1-gen-2015 | Piccoli, Giorgina Barbara; Postorino, Valentina; Cabiddu, Gianfranca; Ghiotto, Sara; Guzzo, Gabriella; Roggero, Simona; Manca, Eleonora; Puddu, Rosalba; Meloni, Francesca; Attini, Rossella; Moi, Paolo; Maxia, Stefania; Piga, Antonio; Mazzone, Luigi; Pani, Antonello; Postorino, Maurizio; Castellino, Santina; Gernone, Giuseppe; Guida, Bruna; Calabria, Santo; Galliani, Marco; Manisco, Gianfranco; Di Tullio, Massimo; Vernaglione, Luigi; Chiappini, Maria Grazia; Proietti, Emanuela; Saffiotti, Stefano; Gangeni, Concetta; Brunati, Chiara; Montoli, Alberto; Esposito, Ciro; Montagna, Giovanni; Tata, Salvatore; Romano, Paolo; Amatruda, Ottavio; Cervini, Paolo; Casiraghi, Erika; Fabbrini, Paolo; Pieruzzi, Federico; Di Benedetto, Attilio; Alfisi, Giuseppina; Heidempergher, Marco; Buskermolen, Monique; Leveque, Alessandro; Autuly, Valerie; Giofrè, Francesco; Alati, Giovanni; Lombardi, Luigi; Riccio, Mara; Riccio, Ivano; Stingone, Antonio; D'Angelo, Benito; Lucchi, Leonardo; Stipo, Lucia; Loi, Valentina | NEPHROLOGY DIALYSIS TRANSPLANTATION | - |
| Chromosomal localization of the human NF-E2 family of bZIP transcription factors by fluorescence in situ hybridization | 1-gen-1995 | Chan, Jy; Cheung, Mc; Moi, Paolo; Chan, K; Kan, Yw | HUMAN GENETICS | - |
| Cloning MafF by recognition site screening with the NFE2 tandem repeat of HS2: analysis of its role in globin and GCSl genes regulation | 1-gen-2002 | Marini, MARIA GIUSEPPINA; Asunis, I; Chan, K; Chan, Jy; Kan, Yw; Porcu, Loredana; Cao, A; Moi, Paolo | BLOOD CELLS, MOLECULES, & DISEASES | - |
| CLONING OF A SMALL HUMAN MAF PROTEIN THAT HETERODIMERIZES SPECIFICALLY WITH NRF1 | 1-gen-1994 | Moi, Paolo; Chan, K; Marini, G; Casula, L; Melis, A; Cao, A. | BLOOD | - |
| Cloning, characterization, DNA binding, mapping and mutation analysis of the human erythroid kruppel-like factor (EKLF) gene | 1-gen-1996 | Moi, P; Azunis, I; Saba, Luisella; Padiglia, Alessandra; Senes, G; Pischedda, C; Nucaro, Al; Cao, A; Rosatelli, MARIA CRISTINA | - | - |