Epidermal growth factor-like domain 7 promotes migration and invasion of human trophoblast cells through activation of MAPK, PI3K and NOTCH signaling pathways

Por Massimiani, M., Vecchione, L., Piccirilli, D., Spitalieri, P., Amati, F., Salvi, S., Ferrazzani, S., Stuhlmann, H., Campagnolo, L.
Publicado no Mol Hum Reprod (2015)

Effects of weight loss and exercise on insulin resistance, and intramyocellular triacylglycerol, diacylglycerol and ceramide

Por Dubé, J. J., Amati, F., Toledo, F. G. S., Stefanovic-Racic, M., Rossi, A., Coen, P., Goodpaster, B. H.
Publicado em 2011

Biased T-cell receptor repertoires in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)

Por PIERDOMINICI, M, MAZZETTA, F, CAPRINI, E, MARZIALI, M, DIGILIO, M C, MARINO, B, AIUTI, A, AMATI, F, RUSSO, G, NOVELLI, G, PANDOLFI, F, LUZI, G, GIOVANNETTI, A
Publicado em 2003

Prooxidant Effects of Verbascoside, a Bioactive Compound from Olive Oil Mill Wastewater, on In Vitro Developmental Potential of Ovine Prepubertal Oocytes and Bioenergetic/Oxidative...

Por Dell'Aquila, M. E., Bogliolo, L., Russo, R., Martino, N. A., Filioli Uranio, M., Ariu, F., Amati, F., Sardanelli, A. M., Linsalata, V., Ferruzzi, M. G., Cardinali, A., Minervini, F.
Publicado em 2014

Mutations of UFD1L are not responsible for the majority of cases of DiGeorge Syndrome/velocardiofacial syndrome without deletions within chromosome 22q11.

Por Wadey, R, McKie, J, Papapetrou, C, Sutherland, H, Lohman, F, Osinga, J, Frohn, I, Hofstra, R, Meijers, C, Amati, F, Conti, E, Pizzuti, A, Dallapiccola, B, Novelli, G, Scambler, P
Publicado em 1999

Human homologue sequences to the Drosophila dishevelled segment-polarity gene are deleted in the DiGeorge syndrome.

Por Pizzuti, A., Novelli, G., Mari, A., Ratti, A., Colosimo, A., Amati, F., Penso, D., Sangiuolo, F., Calabrese, G., Palka, G., Silani, V., Gennarelli, M., Mingarelli, R., Scarlato, G., Scambler, P., Dallapiccola, B.
Publicado em 1996