Sfoglia per Autore
Porfirie
2004-01-01 Moi, Paolo
Difetti enzimatici del globulo rosso e anemie megaloblastiche congenite
2004-01-01 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
The distal beta-globin CACCC box is required for maximal stimulation of the beta-globin gene by EKLF
2004-01-01 Marini, MARIA GIUSEPPINA; Asunis, I; Porcu, L; Salgo, Mg; Loi, Mg; Brucchietti, A; Cao, A; Moi, Paolo
Negative regulation of gamma-globin gene expression by cyclic AMP-dependent pathway in erythroid cells
2004-01-01 Inoue, A; Kuroyanagi, Y; Terui, K; Moi, Paolo; Ikuta, T.
Regulation of the globin genes
2002-01-01 Cao, A; Moi, Paolo
Nuclear factor-erythroid 2 (NF-E2) expression in normal and malignant megakaryocytopoiesis
2002-01-01 Catani, L; Vianelli, N; Amabile, M; Pattacini, L; Valdrè, L; Fagioli, Me; Poli, M; Gugliotta, L; Moi, Paolo; Marini, MARIA GIUSEPPINA; Martinelli, G; Tura, S; Baccarani, M.
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.
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
Genetic modifying factors in β-thalassemia
2000-01-01 Cao, A; Moi, Paolo
Regulation of mouse p45 NF-E2 transcription by an erythroid-specific GATA-dependent intronic alternative promoter
2000-01-01 Moroni, E; Mastrangelo, T; Razzini, R; Cairns, L; Moi, Paolo; Ottolenghi, S; Giglioni, B.
Molecular characterization of Wilson disease in the Sardinian population - Evidence of a founder effect
1999-01-01 Loudianos, G; Dessi, V; Lovicu, M; Angius, A; Figus, A; Lilliu, F; De Virgiliis, S; Nurchi, ANNA MARIA; Deplano, A; Moi, Paolo; Pirastu, M; Cao, A.
Mutations in the Zn finger of EKLF that retain binding to the DNA reduce its ability to transactivate the γ-globin gene
1998-01-01 Moi, Paolo; Asunis, I; Casula, S; Marini, Mg; AND CAO, A.
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
hMAF, a small human transcription factor that heterodimerizes specifically with Nrf1 and Nrf2
1997-01-01 Marini, MARIA GIUSEPPINA; Chan, K; Casula, L; Kan, Yw; Cao, A; Moi, Paolo
Human EKLF binding and transactivation from wild type and mutant CACCC boxes
1996-01-01 Moi, P; Senes, G; Azunis, I; Casula, S; Saba, Luisella; Rosatelli, MARIA CRISTINA; 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
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
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
Isolation of a differentially regulated splicing isoform of human NF-E2.
1995-01-01 Pischedda, C; Cocco, S; Melis, A; Marini, MARIA GIUSEPPINA; Kan, Yw; Cao, A; Moi, Paolo
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