Eliana Vigneti

Progress in the molecular diagnosis of facioscapulohumeral muscular dystrophy and correlation between the number ofKpnI repeats at the 4q35 locus and clinical phenotype

Enzo Ricci, Giuliana Galluzzi, Giancarlo Deidda et al. · Annals of Neurology · 1999 · 296 citations

Ecori Fragment Size, Rare Diseases, Facioscapulohumeral Muscular Dystrophy +15

Nerve growth factor displays stimulatory effects on human skin and lung fibroblasts, demonstrating a direct role for this factor in tissue repair

Alessandra Micera, Eliana Vigneti, Dalia Pickholtz et al. · Proceedings of the National Academy of Sciences · 2001 · 239 citations · Full text

Tissue Engineering, Engineering, Peripheral Nerve Injury +24

Physical Mapping Evidence for a Duplicated Region on Chromosome 10qter Showing High Homology with the Facioscapulohumeral Muscular Dystrophy Locus on Chromosome 4qter

Giancarlo Deidda, S. Cacurri, Paola Grisanti et al. · European Journal of Human Genetics · 1995 · 102 citations

Biology, Chromosome Dynamics, Genetic Disorder +8

Nerve growth factor release by human synovial fibroblasts prior to and following exposure to tumor necrosis factor-alpha, interleukin-1 beta and cholecystokinin-8: the possible role of NGF in the inflammatory response.

Luigi Manni, Thomas Lundeberg, Silvana Fiorito et al. · PubMed · 2004 · 101 citations

Two brc-abl junction peptides bind HLA-A3 molecules and allow specific induction of human cytotoxic T lymphocytes.

Giulia Greco, Doriana Fruci, Daniele Accapezzato et al. · PubMed · 1996 · 88 citations