MARINI, MARIA GIUSEPPINA
MARINI, MARIA GIUSEPPINA
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
DeltaN133p53 expression levels in relation to haplotypes of the TP53 internal promoter region
2010-01-01 Bellini, I; Pitto, L; Marini, MARIA GIUSEPPINA; Porcu, L; Moi, P; Garritano, S; Boldrini, L; Rainaldi, G; Fontanini, G; Chiarugi, M; Barale, R; Gemignani, F; Landi, S.
Regulation of the human HBA genes by KLF4 in erythroid cell lines
2010-01-01 Marini, MARIA GIUSEPPINA; Porcu, Loredana; Asunis, I; Loi, Mg; Ristaldi, Ms; Porcu, S; Ikuta, T; Cao, A; Moi, P.
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
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
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.
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
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