| The tripartite motif family identifies cell compartments A Reymond, G Meroni, A Fantozzi, G Merla, S Cairo, L Luzi, D Riganelli, ... The EMBO journal 20 (9), 2140-2151, 2001 | 1606 | 2001 |
| TRIM/RBCC, a novel class of ‘single protein RING finger’E3 ubiquitin ligases G Meroni, G Diez‐Roux Bioessays 27 (11), 1147-1157, 2005 | 823 | 2005 |
| A cluster of sulfatase genes on Xp22. 3: mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy B Franco, G Meroni, G Parenti, J Levilliers, L Bernard, M Gebbia, L Cox, ... Cell 81 (1), 15-25, 1995 | 336 | 1995 |
| Genomic analysis of the TRIM family reveals two groups of genes with distinct evolutionary properties M Sardiello, S Cairo, B Fontanella, A Ballabio, G Meroni BMC evolutionary biology 8 (1), 1-22, 2008 | 313 | 2008 |
| The sulfatase gene family G Parenti, G Meroni, A Ballabio Current opinion in genetics & development 7 (3), 386-391, 1997 | 220 | 1997 |
| TRIM family: Pleiotropy and diversification through homomultimer and heteromultimer formation LM Napolitano, G Meroni IUBMB life 64 (1), 64-71, 2012 | 198 | 2012 |
| Rox, a novel bHLHZip protein expressed in quiescent cells that heterodimerizes with Max, binds a non‐canonical E box and acts as a transcriptional repressor G Meroni, A Reymond, M Alcalay, G Borsani, A Tanigami, R Tonlorenzi, ... The EMBO journal 16 (10), 2892-2906, 1997 | 172 | 1997 |
| Functional characterization of the Opitz syndrome gene product (midin): evidence for homodimerization and association with microtubules throughout the cell cycle S Cainarca, S Messali, A Ballabio, G Meroni Human molecular genetics 8 (8), 1387-1396, 1999 | 157 | 1999 |
| Pharmacological enhancement of mutated α-glucosidase activity in fibroblasts from patients with Pompe disease G Parenti, A Zuppaldi, MG Pittis, MR Tuzzi, I Annunziata, G Meroni, ... Molecular Therapy 15 (3), 508-514, 2007 | 148 | 2007 |
| A mutation of β-actin that alters depolymerization dynamics is associated with autosomal dominant developmental malformations, deafness, and dystonia V Procaccio, G Salazar, S Ono, ML Styers, M Gearing, A Davila, ... The American Journal of Human Genetics 78 (6), 947-960, 2006 | 142 | 2006 |
| BTBD1 and BTBD2 colocalize to cytoplasmic bodies with the RBCC/tripartite motif protein, TRIM5δ L Xu, L Yang, PK Moitra, K Hashimoto, P Rallabhandi, S Kaul, G Meroni, ... Experimental cell research 288 (1), 84-93, 2003 | 138 | 2003 |
| Phosphorylation and microtubule association of the Opitz syndrome protein mid-1 is regulated by protein phosphatase 2A via binding to the regulatory subunit α4 J Liu, TD Prickett, E Elliott, G Meroni, DL Brautigan Proceedings of the National Academy of Sciences 98 (12), 6650-6655, 2001 | 134 | 2001 |
| Functional interactions between ubiquitin E2 enzymes and TRIM proteins LM Napolitano, EG Jaffray, RT Hay, G Meroni Biochemical Journal 434 (2), 309-319, 2011 | 130 | 2011 |
| X‐linked Opitz syndrome: Novel mutations in the MID1 gene and redefinition of the clinical spectrum F De Falco, S Cainarca, G Andolfi, R Ferrentino, C Berti, ... American Journal of Medical Genetics Part A 120 (2), 222-228, 2003 | 120 | 2003 |
| Mutations that impair interaction properties of TRIM32 associated with limb‐girdle muscular dystrophy 2H V Saccone, M Palmieri, L Passamano, G Piluso, G Meroni, L Politano, ... Human mutation 29 (2), 240-247, 2008 | 119 | 2008 |
| TRIM27 negatively regulates NOD2 by ubiquitination and proteasomal degradation B Zurek, I Schoultz, A Neerincx, LM Napolitano, K Birkner, E Bennek, ... PloS one 7 (7), e41255, 2012 | 117 | 2012 |
| Mlx, a new Max-like bHLHZip family member: the center stage of a novel transcription factors regulatory pathway? G Meroni, S Cairo, G Merla, S Messali, R Brent, A Ballabio, A Reymond Oncogene 19 (29), 3266-3277, 2000 | 103 | 2000 |
| Zinc‐finger‐based transcriptional repression of rhodopsin in a model of dominant retinitis pigmentosa C Mussolino, D Sanges, E Marrocco, C Bonetti, U Di Vicino, V Marigo, ... EMBO molecular medicine 3 (3), 118-128, 2011 | 88 | 2011 |
| Mig12, a novel Opitz syndrome gene product partner, is expressed in the embryonic ventral midline and co-operates with Mid1 to bundle and stabilize microtubules C Berti, B Fontanella, R Ferrentino, G Meroni BMC cell biology 5 (1), 1-12, 2004 | 84 | 2004 |
| Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome L Pinson, J Auge, S Audollent, G Mattei, H Etchevers, N Gigarel, F Razavi, ... Journal of Medical Genetics 41 (5), 381-386, 2004 | 83 | 2004 |
