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Clinical Chemistry and Laboratory Medicine|June 2, 2000
Genetic modifying factors in beta-thalassemiaA Cao, P MoiBritish Journal of Haematology|July 1, 1986
Molecular pathology of haemoglobin H disease in SardiniansE Paglietti, R Galanello, P Moi, et al.Proceedings of the National Academy of Sciences of the United States of America|October 11, 1994
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 regionP Moi, K Chan, I Asunis, et al.The Journal of Clinical Investigation|November 1, 1987
An initiation codon mutation (AUG----GUG) of the human alpha 1-globin gene. Structural characterization and evidence for a mild thalassemic phenotypeP Moi, F E Cash, S A Liebhaber, et al.Journal of Endocrinological Investigation|May 1, 1997
A homozygous nonsense mutation of the human growth hormone receptor gene in a Sardinian boy with Laron-type dwarfismM Putzolu, A Meloni, S Loche, et al.Hemoglobin|January 1, 1992
Normal delta-globin gene sequences in Sardinian nondeletional delta beta-thalassemiaG Loudianos, P Moi, J Lavinha, et al.British Journal of Haematology|October 1, 1987
Molecular characterization of a normal Hb A2 beta-thalassaemia determinant in a Sardinian familyL Oggiano, M Pirastu, P Moi, et al.Journal of Medical Genetics|December 1, 1983
Phenotype-genotype correlation in haemoglobin H disease in childhoodR Galanello, M Pirastu, M A Melis, et al.The Journal of Biological Chemistry|June 27, 1997
hMAF, a small human transcription factor that heterodimerizes specifically with Nrf1 and Nrf2M G Marini, K Chan, L Casula, et al.Journal of Endocrinological Investigation|July 12, 2002
A novel splicing defect (IVS6+1G>T) in a patient with pseudovitamin D deficiency ricketsL Porcu, A Meloni, L Casula, et al.Pageof 37