LOX-1 and cancer: an indissoluble liaison

por Murdocca, M., De Masi, C., Pucci, S., Mango, R., Novelli, G., Di Natale, C., Sangiuolo, F.
Publicado 2021

Direct PCR: a new pharmacogenetic approach for the inexpensive testing of HLA-B*57:01

por Cascella, R, Strafella, C, Ragazzo, M, Zampatti, S, Borgiani, P, Gambardella, S, Pirazzoli, A, Novelli, G, Giardina, E
Publicado 2015

Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment

por Columbaro, M., Capanni, C., Mattioli, E., Novelli, G., Parnaik, V. K., Squarzoni, S., Maraldi, N. M., Lattanzi, G.
Publicado 2005

Laminopathies: many diseases, one gene. Report of the first Italian Meeting Course on Laminopathies

por Lattanzi, G., Benedetti, S., Bertini, E., Boriani, G., Mazzanti, L., Novelli, G., Pasquali, R., Pini, A., Politano, L.
Publicado 2011

TNFAIP3 Gene Polymorphisms in Three Common Autoimmune Diseases: Systemic Lupus Erythematosus, Rheumatoid Arthritis, and Primary Sjogren Syndrome—Association with Disease Susceptibi...

por Ciccacci, C., Latini, A., Perricone, C., Conigliaro, P., Colafrancesco, S., Ceccarelli, F., Priori, R., Conti, F., Perricone, R., Novelli, G., Borgiani, P.
Publicado 2019

Clusterin silencing restores myoblasts viability and down modulates the inflammatory process in osteoporotic disease

por Pucci, S., Greggi, C., Polidoro, C., Piro, M. C., Celi, M., Feola, M., Gasbarra, E., Iundusi, R., Mastrangeli, F., Novelli, G., Orlandi, A., Tarantino, U.
Publicado 2019

Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria

por Cenni, V., Capanni, C., Columbaro, M., Ortolani, M., D'Apice, M.R., Novelli, G., Fini, M., Marmiroli, S., Scarano, E., Maraldi, N.M., Squarzoni, S., Prencipe, S., Lattanzi, G.
Publicado 2011

Erratum - Autophagic Degradation of Farnesylated Prelamin a as a Therapeutic Approach to Lamin-Linked Progeria

por Cenni, V., Capanni, C., Columbaro, M., Ortolani, M., D’Apice, M.R., Novelli, G., Fini, M., Marmiroli, S., Scarano, E., Maraldi, N.M., Squarzoni, S., Prencipe, S., Lattanzi, G.
Publicado 2013

Evidence for an Association between the SRD5A2 (Type II Steroid 5α-Reductase) Locus and Prostate Cancer in Italian Patients

por Margiotti, K., Sangiuolo, F., De Luca, A., Froio, F., Pearce, C. L., Ricci-Barbini, V., Micali, F., Bonafè, M., Franceschi, C., Dallapiccola, B., Novelli, G., Reichardt, J. K. V.
Publicado 2000

Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeria

por Dominici, S., Fiori, V., Magnani, M., Schena, E., Capanni, C., Camozzi, D., D’Apice, M.R., Le Dour, C., Auclair, M., Caron, M., Novelli, G., Vigouroux, C., Maraldi, N.M., Lattanzi, G.
Publicado 2009

MBNL1(42) and MBNL1(43) gene isoforms, overexpressed in DM1-patient muscle, encode for nuclear proteins interacting with Src family kinases

por Botta, A, Malena, A, Tibaldi, E, Rocchi, L, Loro, E, Pena, E, Cenci, L, Ambrosi, E, Bellocchi, M C, Pagano, M A, Novelli, G, Rossi, G, Monaco, H L, Gianazza, E, Pantic, B, Romeo, V, Marin, O, Brunati, A M, Vergani, L
Publicado 2013