MOI, PAOLO

MOI, PAOLO  

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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 - -