University of Cagliari
Genetic modifying factors in β-thalassemia
2000-01-01 Cao, A; Moi, Paolo
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.
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 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
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
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
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.
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.
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
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
Isolation of NF-E2-related factor 2 (Nrf2), a NF-E2-like basic leucine zipper transcriptional activator that binds to the tandem NF-E2/AP1 repeat of the beta-globin locus control region
1994-01-01 Moi, Paolo; Chan, K; Asunis, I; Cao, A; Kan, Yw
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.
INTERETHNIC POLYMORPHISM OF THE BETA-GLOBIN GENE LOCUS-CONTROL REGION (LCR) IN SICKLE-CELL-ANEMIA PATIENTS
1993-01-01 Perichon, B; Ragusa, A; Lapoumeroulie, C; Romand, A; Moi, Paolo; Ikuta, T; Labie, D; Elion, J; Krishnamoorthy, R.
Delta-thalassemia due to a mutation in an erythroid-specific binding protein sequence 3' to the delta-globin gene
1992-01-01 Moi, Paolo; Loudianos, G; Lavinha, J; Murru, S; Cossu, P; Casu, R; Oggiano, L; Longinotti, M; Cao, A; Pirastu, M.
NORMAL DELTA-GLOBIN GENE-SEQUENCES IN SARDINIAN NONDELETIONAL DELTA-BETA-THALASSEMIA
1992-01-01 Loudianos, G; Moi, Paolo; Lavinha, J; Galanello, R; Cao, A; Pirastu, M.
Dissection of the enhancer activity of beta-globin 5' DNase I-hypersensitive site 2 in transgenic mice
1992-01-01 Liu, D; Chang, Jc; Moi, Paolo; Liu, W; Kan, Yw; Curtin, Pt
Synergistic enhancement of globin gene expression by activator protein-1-like proteins
1990-01-01 Moi, Paolo; Kan, Yw
Interaction of heterozygous beta zero-thalassemia with single functional alpha-globin gene
1988-01-01 Galanello, R; Paglietti, E; Melis, M. A; Crobu, M. G; Addis, M; Moi, Paolo; Cao, A.
Delineation of the molecular basis of delta- and normal HbA2 beta-thalassemia
1988-01-01 Moi, Paolo; Paglietti, MARIA ELISABETTA; Sanna, A; Brancati, C; Tagarelli, A; Galanello, R; Cao, A; Pirastu, M.
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.
Molecular characterization of a normal Hb A2 beta-thalassaemia determinant in a Sardinian family.
1987-01-01 Oggiano, L; Pirastu, M; Moi, Paolo; Longinotti, M; Perseu, L; Cao, A.
Molecular pathology of haemoglobin H disease in Sardinians
1986-01-01 Paglietti, MARIA ELISABETTA; Galanello, R; Moi, Paolo; Pirastu, M; Cao, A.
Phenotype-genotype correlation in haemoglobin H disease in childhood
1983-01-01 Galanello, R; Pirastu, M; Melis, Ma; Paglietti, MARIA ELISABETTA; Moi, Paolo; Cao, A.
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