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The Journal of General Virology|May 1, 1989
Epstein-Barr virus DNA sequences in precursor monocyte-macrophage cell lines established from the bone marrow of children with maturation defects of haematopoiesisR P Revoltella, E Vigneti, A Fruscalzo, et al.
Immunogenetics|January 1, 1995
Differences in peptide-binding specificity of two ankylosing spondylitis-associated HLA-B27 subtypesD Fruci, R H Butler, G Greco, et al.
Immunogenetics|January 1, 1994
The peptide binding specificity of HLA-B27 subtypesN Tanigaki, D Fruci, E Vigneti, et al.
Neuroreport|August 1, 1993
NGF is released into plasma during human pregnancy: an oxytocin-mediated response?P Luppi, R Levi-Montalcini, L Bracci-Laudiero, et al.
American Journal of Human Genetics|June 23, 1998
Sequence homology between 4qter and 10qter loci facilitates the instability of subtelomeric KpnI repeat units implicated in facioscapulohumeral muscular dystrophyS Cacurri, N Piazzo, G Deidda, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 10, 2001
Nerve growth factor displays stimulatory effects on human skin and lung fibroblasts, demonstrating a direct role for this factor in tissue repairA Micera, E Vigneti, D Pickholtz, et al.
Leukemia|April 1, 1996
Two brc-abl junction peptides bind HLA-A3 molecules and allow specific induction of human cytotoxic T lymphocytesG Greco, D Fruci, D Accapezzato, et al.
Neuromuscular Disorders : NMD|June 26, 1999
Molecular analysis of 4q35 rearrangements in fascioscapulohumeral muscular dystrophy (FSHD): application to family studies for a correct genetic advice and a reliable prenatal diagnosis of the diseaseG Galluzzi, G Deidda, S Cacurri, et al.
Annals of Neurology|June 9, 1999
Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number of KpnI repeats at the 4q35 locus and clinical phenotypeE Ricci, G Galluzzi, G Deidda, et al.
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